Publications

Sharing our research with the scientific community is key to our mission. Read our scientific publications, white papers, and conference presentations below.

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  • Hysi PG, Valdes AM, Liu F, Furlotte NA, Evans DM. et al. Show more authors.Hysi PG, Valdes AM, Liu F, Furlotte NA, Evans DM, Bataille V, Visconti A, Hemani G, McMahon G, Ring SM, Smith GD, Duffy DL, Zhu G, Gordon SD, Medland SE, Lin BD, Willemsen G, Hottenga JJ, Vuckovic D, Girotto G, Gandin I, Sala C, Concas MP, Brumat M, Gasparini P, Toniolo D, Cocca M, Robino A, Yazar S, Hewitt AW, Chen Y, Zeng C, Uitterlinden AG, Ikram MA, Hamer MA, van Duijn CM, Nijsten T, Mackey DA, Falchi M, Boomsma DI, Martin NG, Hinds DA, Kayser M, Spector TD, The International Visible Trait Genetics Consortium Show fewer authors. “A GWAS meta-analysis of more than 300,000 individuals of European ancestry identifies numerous new genetic loci explaining significant portions of hair color variation and heritability.” Nature Communications. 16 April 2018. Traits
  • Howard DM, Adams MJ, Shirali M, Clarke TK, Marioni RE. et al. Show more authors.Howard DM, Adams MJ, Shirali M, Clarke TK, Marioni RE, Davies G, Coleman JRI, Alloza C, Shen X, Barbu MC, Wigmore EM, Gibson J, Agee M, Alipanahi B, Auton A, Bell RK, Bryc K, Elson SL, Fontanillas P, Furlotte NA, Hinds DA, Huber KE, Kleinman A, Litterman NK, McCreight JC, McIntyre MH, Mountain JL, Noblin ES, Northover CAM, Pitts SJ, Sathirapongsasuti JF, Sazonova OV, Shelton JF, Shringarpure S, Tian C, Tung JY, Vacic V, Wilson CH, Hagenaars SP, Lewis CM, Ward J, Smith DJ, Sullivan PF, Haley CS, Breen G, Deary IJ, McIntosh AM Show fewer authors. “Genome-wide association study of depression phenotypes in UK Biobank (n = 322,580) identifies the enrichment of variants in excitatory synaptic pathways.” Nature Communications. 16 April 2018. Neurology Psychiatry
  • Wu W, the 23andMe Research Team, Amos CI, Lee JE, Wei Q. et al. Show more authors.Wu W, the 23andMe Research Team, Amos CI, Lee JE, Wei Q, Sarin KY, Han J Show fewer authors. “Inverse relationship between vitiligo-related genes and skin cancer risk.” Journal of Investigative Dermatology. 23 March 2018. Cancer Dermatology
  • Fejzo MS, Sazonova OV, Sathirapongsasuti JF, Hallgrímsdóttir IB, Vacic V. et al. Show more authors.Fejzo MS, Sazonova OV, Sathirapongsasuti JF, Hallgrímsdóttir IB, Vacic V, MacGibbon KW, Schoenberg FP, Mancuso N, Slamon DJ, Mullin PM, Agee M, Alipanahi B, Auton A, Bell RK, Bryc K, Elson SL, Fontanillas P, Furlotte NA, Hinds DA, Hromatka BS, Huber KE, Kleinman A, Litterman NK, McIntyre MH, Noblin ES, Northover CAM, Pitts SJ, Shelton JF, Shringarpure S, Tian C, Tung JY, Wilson CH. Show fewer authors. “Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum.” Nature Communications. 21 March 2018. Reproduction
  • Tung JY, Shaw RJ, Hagenkord JM, Hackmann M, Muller M. et al. Show more authors.Tung JY, Shaw RJ, Hagenkord JM, Hackmann M, Muller M, Beachy SH, Pratt VM, Terry SF, Cashion AK, Ginsburg GS. Show fewer authors. “Accelerating precision health by applying the lessons learned from direct-to-consumer genomics to digital health technologies.” National Academy of Medicine Perspectives. 19 March 2018. ELSI
  • Warrier V, Toro R, Chakrabarti B, the iPSYCH-Broad autism group, Børglum AD. et al. Show more authors.Warrier V, Toro R, Chakrabarti B, the iPSYCH-Broad autism group, Børglum AD, Grove J, the 23andMe Research Team, Hinds DA, Bourgeron T, Baron-Cohen S. Show fewer authors. “Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa” Translational Psychiatry. 12 March 2018. Behavior Psychiatry
  • Warrier V and Baron-Cohen S.Warrier V and Baron-Cohen S Show fewer authors. “Genetic contribution to ‘theory of mind’ in adolescence.” Scientific Reports. 22 February 2018. Behavior
  • Turley P, Walters RK, Maghzian O, Okbay A, Lee JJ. et al. Show more authors.Turley P, Walters RK, Maghzian O, Okbay A, Lee JJ, Fontana MA, Nguyen-Viet TA, Wedow R, Zacher M, Furlotte NA, Magnusson P, Oskarsson S, Johannesson M, Visscher PM, Laibson D, Cesarini D, Neale BM, Benjamin DJ, 23andMe Research Team, Social Science Genetic Association Consortium Show fewer authors. “Multi-trait analysis of genome-wide association summary statistics using MTAG.” Nature Genetics. 3 January 2018. Methods
  • Sanchez-Roige S, Fontanillas P, Elson SL, Pandit A, Schmidt EM. et al. Show more authors.Sanchez-Roige S, Fontanillas P, Elson SL, Pandit A, Schmidt EM, Foerster JR, Abecasis GR, Gray JC, de Wit H, Davis LK, MacKillop J, Palmer AA, the 23andMe Research Team Show fewer authors. “Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry.” Nature Neuroscience. 11 December 2017. Behavior
  • Shaffer JR, Li J, Lee MK, Roosenboom J, Orlova E. et al. Show more authors.Shaffer JR, Li J, Lee MK, Roosenboom J, Orlova E, Adhikari K, Agee M, Alipanahi B, Auton A, Bell RK, Bryc K, Elson SL, Fontanillas P, Furlotte NA, Hromatka BS, Huber KE, Kleinman A, Litterman NK, McIntyre MH, Mountain JL, Noblin ES, Northover CAM, Pitts SJ, Sathirapongsasuti JF, Sazonova OV, Shelton JF, Shringarpure S, Tian C, Tung JY, Vacic V, Wilson CH, Gallo C, Poletti G, Schuler-Faccini L, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, González-José R, Pfeffer PE, Wollenschlaeger CA, Hecht JT, Wehby GL, Moreno LM, Ding A, Jin L, Yang Y, Carlson JC, Leslie EJ, Feingold E, Marazita ML, Hinds DA, Cox TC, Wang S, Ruiz-Linares A, Weinberg SM Show fewer authors. “Multiethnic GWAS reveals polygenic architecture of earlobe attachment.” Amerian Journal of Human Genetics. 30 November 2017. Traits
  • Lo MT, Wang Y, Kauppi K, Sanyal N, Fan CC. et al. Show more authors.Lo MT, Wang Y, Kauppi K, Sanyal N, Fan CC, Smeland OB, Schork A, Holland D, Hinds DA, Tung JY, Andreassen OA, Dale AM, Chen CH Show fewer authors. “Modeling prior information of common genetic variants improves gene discovery for neuroticism.” Human Molecular Genetics. 15 November 2017. Behavior
  • Sanchez-Roige S, Fontanillas P, Elson SL, The 23andMe Research Team, Gray JC. et al. Show more authors.Sanchez-Roige S, Fontanillas P, Elson SL, The 23andMe Research Team, Gray JC, de Wit H, Davis LK, MacKillop J, Palmer AA Show fewer authors. “Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20,328 research participants of European ancestry.” Addiction Biology. 23 October 2017. Psychiatry
  • Schormair B, Zhao C, Bell S, Tilch E, Salminen AV. et al. Show more authors. Schormair B, Zhao C, Bell S, Tilch E, Salminen AV, Pütz B, Dauvilliers Y, Stefani A, Högl B, Poewe W, Kemlink D, Sonka K, Bachmann CG, Paulus W, Trenkwalder C, Oertel WH, Hornyak M, Teder-Laving M, Metspalu A, Hadjigeorgiou GM, Polo O, Fietze I, Ross OA, Wszolek Z, Butterworth AS, Soranzo N, Ouwehand WH, Roberts DJ, Danesh J, Allen RP, Earley CJ, Ondo WG, Xiong L, Montplaisir J, Gan-Or Z, Perola M, Vodicka P, Dina C, Franke A, Tittmann L, Stewart AFR, Shah SH, Gieger C, Peters A, Rouleau GA, Berger K, Oexle K, Di Angelantonio E, Hinds DA, Müller-Myhsok B, Winkelmann J, 23andMe Research Team, DESIR study group Show fewer authors. “Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.” The Lancet: Neurology. 13 October 2017. Neurology
  • Ehm MG, Aponte JL, Chiano MN, Yerges-Armstrong LM, Johnson T. et al. Show more authors.Ehm MG, Aponte JL, Chiano MN, Yerges-Armstrong LM, Johnson T, Barker JN, Cook SF, Gupta A, Hinds DA, Li L, Nelson MR, Simpson MA, Tian C, McCarthy LC, Rajpal DK, Waterworth DM Show fewer authors. “Phenome-wide association study using research participants’ self-reported data provides insight into the Th17 and IL-17 pathway.” PLoS ONE. 13 October 2017. Immunity
  • Ferreira MA, Vonk JM, Baurecht H, Marenholz I, Tian C. et al. Show more authors.Ferreira MA, Vonk JM, Baurecht H, Marenholz I, Tian C, Hoffman JD, Helmer Q, Tillander A, Ullemar V, van Dongen J, Lu Y, Rüschendorf F, Esparza-Gordillo J, Medway CW, Mountjoy E, Burrows K, Hummel O, Grosche S, Brumpton BM, Witte JS, Hottenga JJ, Willemsen G, Zheng J, Rodríguez E, Hotze M, Franke A, Revez JA, Beesley J, Matheson MC, Dharmage SC, Bain LM, Fritsche LG, Gabrielsen ME, Balliu B, 23andMe Research Team, AAGC collaborators, BIOS consortium, LifeLines Cohort Study, Nielsen JB, Zhou W, Hveem K, Langhammer A, Holmen OL, Løset M, Abecasis GR, Willer CJ, Arnold A, Homuth G, Schmidt CO, Thompson PJ, Martin NG, Duffy DL, Novak N, Schulz H, Karrasch S, Gieger C, Strauch K, Melles RB, Hinds DA, Hübner N, Weidinger S, Magnusson PKE, Jansen R, Jorgenson E, Lee YA, Boomsma DI, Almqvist C, Karlsson R, Koppelman GH, Paternoster L Show fewer authors. “Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.” Nature Genetics. 13 October 2017. Immunity
  • Tian C, Hromatka BS, Kiefer AK, Eriksson N, Noble SM. et al. Show more authors. Tian C, Hromatka BS, Kiefer AK, Eriksson N, Noble SM, Tung JY, Hinds DA. Show fewer authors. “Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.” Nature Communications. 19 September 2017. Immunity
  • Chang D, Nalls MA, Hallgrímsdóttir IB, Hunkapiller J, van der Brug M. et al. Show more authors. Chang D, Nalls MA, Hallgrímsdóttir IB, Hunkapiller J, van der Brug M, Cai F, International Parkinson's Disease Genomics Consortium, 23andMe Research Team, Kerchner GA, Ayalon G, Bingol B, Sheng M, Hinds D, Behrens TW, Singleton AB, Bhangale TR, Graham RR. Show fewer authors. “A meta-analysis of genome-wide association studies identifies 17 new Parkinson’s disease risk loci” Nature Genetics. 11 September 2017. Neurology
  • Gazal S, Finucane H, Furlotte NA, Loh PR, Palamara PF. et al. Show more authors. Gazal S, Finucane H, Furlotte NA, Loh PR, Palamara PF, Liu X, Schoech A, Bulik-sullivan B, Neale BM, Gusev A, Price AL. Show fewer authors. “Linkage disequilibrium dependent architecture of human complex traits reveals action of negative selection” Nature Genetics. 11 September 2017. Methods
  • Zhang G, Feenstra B, Bacelis J, Liu X, Muglia LM. et al. Show more authors. Zhang G, Feenstra B, Bacelis J, Liu X, Muglia LM, Juodakis J, Miller DE, Litterman N, Jiang P, Russell L, Hinds DA, Hu Y, Weirauch MT, Chen X, Chavan AR, Wagner GP, Pavličev M, Nnamani MC, Maziarz J, Karjalainen MK, Rämet M, Sengpiel V, Geller F, Boyd HA, Palotie A, Momany A, Bedell B, Ryckman KK, Huusko JM, Forney CR, Kottyan LC, Hallman M, Teramo K, Nohr EA, Smith GD, Melbye M, Jacobsson B, Muglia LJ. Show fewer authors. “Genetic associations with gestational duration and spontaneous preterm birth” New England Journal of Medicine. 6 September 2017. Reproduction
  • Hellwege JN, Jeff JM, Wise LA, Gallagher CS, Wellons M. et al. Show more authors. Hellwege JN, Jeff JM, Wise LA, Gallagher CS, Wellons M, Hartmann KE, Jones SF, Torstenson ES, Dickinson S, Ruiz-Narváez EA, Rohland N, Allen A, Reich D, Tandon A, Pasaniuc B, Mancuso N, Im HK, Hinds DA, Palmer JR, Rosenberg L, Denny JC, Roden DM, Stewart EA, Morton CC, Kenny EE, Edwards TL, Velez Edwards DR. Show fewer authors. “A multi-stage genome-wide association study of uterine fibroids in African Americans” Human Genetics. 23 August 2017. Reproduction
  • Boutwell B, Hinds D, Agee M, Alipanahi B, Auton A. et al. Show more authors. Boutwell B, Hinds D, Agee M, Alipanahi B, Auton A, Bell RK, Bryc K, Elson SL, Fontanillas P, Furlotte NA, Hromatka BS, Huber KE, Kleinman A, Litterman NK, McIntyre M, Mountain JM, Northerover CAM, Sathiraspongsasuti JF, Sazonova OV, Shelton JF. Shringarpure S, Tian C, Tung JY, Vacic V, Wilson CH, Tielbeek J, Ong KK, Day FR, Perry JRB Show fewer authors. “Replication and characterization of CADM2 and MSRA genes on human behavior.” Heliyon. 26 July 2017. Behavior
  • Warrier V, Grasby KL, Uzefovsky F, Toro R, Smith P. et al. Show more authors. Warrier V, Grasby KL, Uzefovsky F, Toro R, Smith P, Chakrabarti B, Khadake J, Mawbey-Adamson E, Litterman N, Hottenga J-J, Lubke G, Boomsma DI, Martin NG, Hatemi PK, Medland SE, Hinds DA, Bourgeron T, Baron-Cohen S. Show fewer authors. “Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition.” Molecular Psychiatry. 6 June 2017. Behavior Psychiatry
  • Sapkota Y, Steinthorsdottir V, Morris AP, Fassbender A, Rahmioglu N. et al. Show more authors. Sapkota Y, Steinthorsdottir V, Morris AP, Fassbender A, Rahmioglu N, De Vivo I, Buring JE, Zhang F, Edwards TL, Jones S, O D, Peterse D, Rexrode KM, Ridker PM, Schork AJ, MacGregor S, Martin NG, Becker CM, Adachi S, Yoshihara K, Enomoto T, Takahashi A, Kamatani Y, Matsuda K, Kubo M, Thorleifsson G, Geirsson RT, Thorsteinsdottir U, Wallace LM, iPSYCH-SSI-Broad Group, Yang J, Velez Edwards DR, Nyegaard M, Low S, Zondervan KT, Missmer SA, D'Hooghe T, Montgomery GW, Chasman I, Stefansson K, Tung JY, Nyholt DR. Show fewer authors. “Meta-analysis of 208,000 individuals identifies 18 risk loci for endometriosis and highlights key genes involved in hormone metabolism.” Nature Communications. 24 May 2017. Reproduction
  • Tsoi LC, Stuart PE, Tian C, Gudjonsson JE, Das S. et al. Show more authors. Tsoi LC, Stuart PE, Tian C, Gudjonsson JE, Das S, Zawistowski M, Ellinghaus E, Barker JN, Chandran V, Dand N, Duffin KC, Enerbäck C, Esko T, Franke A, Gladman DD, Hoffmann P, Kingo K, Kõks S, Krueger GG, Lim HW, Metspalu A, Mrowietz U, Mucha S, Rahman P, Reis A, Tejasvi T, Trembath R, Voorhees JJ, Weidinger S, Weichenthal M, Wen X, Eriksson N, Kang HM, Hinds DA, Nair RP, Abecasis GR, Elder JT. Show fewer authors. “Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants.” Nature Communications. 24 May 2017. Dermatology Immunity
  • Smeland OB, Wang Y, Lo M, Li W, Frei O. et al. Show more authors. Smeland OB, Wang Y, Lo M, Li W, Frei O, Witoelar A, Tesli M, Hinds DA, Tung JY, Djurovic S, Chen C, Dale AM, Andreassen OA. Show fewer authors. “Identification of genetic loci shared between schizophrenia and the Big Five personality traits.” Scientific Reports. 22 May 2017. Behavior Psychiatry
  • Felix R Day, Deborah J Thompson, Hannes Helgason, Daniel I Chasman, Hilary Finucane. et al. Show more authors. Felix R Day, Deborah J Thompson, Hannes Helgason, Daniel I Chasman, Hilary Finucane, Patrick Sulem, Katherine S Ruth, Sean Whalen, Abhishek K Sarkar, Eva Albrecht, Elisabeth Altmaier, Marzyeh Amini, Caterina M Barbieri, Thibaud Boutin, Archie Campbell, Ellen Demerath, Ayush Giri, Chunyan He, Jouke J Hottenga, Robert Karlsson, Ivana Kolcic, Po-Ru Loh, Kathryn L Lunetta, Massimo Mangino, Brumat Marco, George McMahon, Sarah E Medland, Ilja M Nolte, Raymond Noordam, Teresa Nutile, Lavinia Paternoster, Natalia Perjakova, Eleonora Porcu, Lynda M Rose, Katharina E Schraut, Ayellet V Segre, Albert V Smith, Lisette Stolk, Alexander Teumer, Irene L Andrulis, Stefania Bandinelli, Matthias W Beckmann, Javier Benitez, Sven Bergmann, Murielle Bochud, Eric Boerwinkle, Stig E Bojesen, Manjeet K Bolla, Judith S Brand, Hiltrud Brauch, Hermann Brenner, Linda Broer, Thomas Bruning, Julie E Buring, Harry Campbell, Eulalia Catamo, Stephen Chanock, Georgia Chenevix-Trench, Tanguy Corre, Fergus J Couch, Diana L Cousminer, Angela Cox, Laura Crisponi, Kamila Czene, George Davey Smith, Eco J C N de Geus, Renee de Mutsert, Immaculata De Vivo, Joe Dennis, Peter Devilee, Isabel dos-Santos-Silva, Alison M Dunning, Johan G Eriksson, Peter A Fasching, Lindsay Fernández-Rhodes, Luigi Ferrucci, Dieter Flesch-Janys, Lude Franke, Marike Gabrielson, Ilaria Gandin, Graham G Giles, Harald Grallert, Daniel F Gudbjartsson, Pascal Guenel, Per Hall, Emily Hallberg, Ute Hamann, Tamara B Harris, Catharina A Hartman, Gerardo Heiss, Maartje J Hooning, John L Hopper, Frank Hu, David J Hunter, M Arfan Ikram, Hae Kyung Im, Marjo-Riitta Jarvelin, Peter K Joshi, David Karasik, Manolis Kellis, Zoltan Kutalik, Genevieve LaChance, Diether Lambrechts, Claudia Langenberg, Lenore J Launer, Joop S E Laven, Stefania Lenarduzzi, Jingmei Li, Penelope A Lind, Sara Lindstrom, YongMei Liu, Jian'an Luan, Reedik Magi, Arto Mannermaa, Hamdi Mbarek, Mark I McCarthy, Christa Meisinger, Thomas Meitinger, Cristina Menni, Andres Metspalu, Kyriaki Michailidou, Lili Milani, Roger L Milne, Grant W Montgomery, Anna M Mulligan, Mike A Nalls, Pau Navarro, Heli Nevanlinna, Dale R Nyholt, Albertine J Oldehinkel, Tracy A O'Mara, Sandosh Padmanabhan, Aarno Palotie, Nancy Pedersen, Annette Peters, Julian Peto, Paul D P Pharoah, Anneli Pouta, Paolo Radice, Iffat Rahman, Susan M Ring, Antonietta Robino, Frits R Rosendaal, Igor Rudan, Rico Rueedi, Daniela Ruggiero, Cinzia F Sala, Marjanka K Schmidt, Robert A Scott, Mitul Shah, Rossella Sorice, Melissa C Southey, Ulla Sovio, Meir Stampfer, Maristella Steri, Konstantin Strauch, Toshiko Tanaka, Emmi Tikkanen, Nicholas J Timpson, Michela Traglia, Therèse Truong, Jonathan P Tyrer, André G Uitterlinden, Digna R Velez Edwards, Veronique Vitart, Uwe Volker, Peter Vollenweider, Qin Wang, Elisabeth Widen, Ko Willems van Dijk, Gonneke Willemsen, Robert Winqvist, Bruce H R Wolffenbuttel, Jing Hua Zhao, Magdalena Zoledziewska, Marek Zygmunt, Behrooz Z Alizadeh, Dorret I Boomsma, Marina Ciullo, Francesco Cucca, Tõnu Esko, Nora Franceschini, Christian Gieger, Vilmundur Gudnason, Caroline Hayward, Peter Kraft, Debbie A Lawlor, Patrik K E Magnusson, Nicholas G Martin, Dennis O Mook-Kanamori, Ellen A Nohr, Ozren Polasek, David Porteous, Alkes L Price, Paul M Ridker, Harold Snieder, Tim D Spector, Doris Stockl, Daniela Toniolo, Sheila Ulivi, Jenny A Visser, Henry Volzke, Nicholas J Wareham, James F Wilson, The LifeLines Cohort Study, The InterAct Consortium, kConFab/AOCS Investigators, Endometrial Cancer Association Consortium, Ovarian Cancer Association Consortium, PRACTICAL consortium, Amanda B Spurdle, Unnur Thorsteindottir, Katherine S Pollard, Douglas F Easton, Joyce Y Tung, Jenny Chang-Claude, David Hinds, Anna Murray, Joanne M Murabito, Kari Stefansson, Ken K Ong, John R B Perry. Show fewer authors. “Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility.” Nature Genetics. 24 April 2017. Cancer Reproduction
  • Heilmann-Heimbach S, Herold C, Hochfeld LM, Hillmer AM, Nyholt DR. et al. Show more authors. Heilmann-Heimbach S, Herold C, Hochfeld LM, Hillmer AM, Nyholt DR, Hecker J, Javed A, Chew EGY, Pechlivanis S, Drichel D, Heng XT, Rosario RCH, Fier HL, Paus R, Rueedi R, Galesloot TE, Moebus S, Anhalt T, Prabhakar S, Li R, Kanoni S, Papanikolaou G, Kutalik Z, Deloukas P, Philpott MP, Waeber G, Spector TD, Vollenweider P, Kiemeney LALM, Dedoussis G, Richards JB, Nothnagel M, Martin NG, Becker T, Hinds DA, Nöthen MM. Show fewer authors. “Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.” Nature Communications. 8 March 2017. Dermatology Traits
  • Jones AV, Tilley M, Gutteridge A, Hyde C, Nagle M. et al. Show more authors. Jones AV, Tilley M, Gutteridge A, Hyde C, Nagle M, Ziemek D, Gorman D, Fauman EB, Chen X, Miller MR, Tian C, Hu Y, Hinds DA, Cox P, Scollen S. Show fewer authors. “GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.” Human Molecular Genetics. 11 February 2017. Immunity
  • Ransohoff KJ, Wu W, Cho HG, Chahal HC, Lin Y. et al. Show more authors. Ransohoff KJ, Wu W, Cho HG, Chahal HC, Lin Y, Dai HJ, Amos CI, Lee JE, Tang JY, Hinds DA, Han J, Wei Q, Sarin KY. Show fewer authors. “Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.” Oncotarget. 9 February 2017. Cancer Dermatology
  • Kreiner E, Waage J, Standl M, Brix S, Pers TH. et al. Show more authors. Kreiner E, Waage J, Standl M, Brix S, Pers TH, Couto Alves A, Warrington NM, Tiesler CM, Fuertes E, Franke L, Hirschhorn JN, James A, Simpson A, Tung JY, Koppelman GH, Postma DS, Pennell CE, Jarvelin MR, Custovic A, Timpson N, Ferreira MA, Strachan DP, Henderson J, Hinds D, Bisgaard H, Bonnelykke K. Show fewer authors. “Shared genetic variants suggest common pathways in allergy and autoimmune diseases.” Journal of Allergy and Clinical Immunology. 7 February 2017. Immunity
  • Trampush JW, Yang ML, Yu J, Knowles E, Davies G. et al. Show more authors. Trampush JW, Yang ML, Yu J, Knowles E, Davies G, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, DeRosse P, Lundervold AJ, Steen VM, Espeseth T, Raikkonen K, Widen E, Palotie A, Eriksson JG, Giegling I, Konte B, Roussos P, Giakoumaki S, Burdick KE, Payton A, Ollier W, Horan M, Chiba-Falek O, Attix DK, Need AC, Cirulli ET, Voineskos AN, Stefanis NC, Avramopoulos D, Hatzimanolis A, Arking DE, Smyrnis N, Bilder RM, Freimer NA, Cannon TD, London E, Poldrack RA, Sabb FW, Congdon E, Conley ED, Scult MA, Dickinson D, Straub RE, Donohoe G, Morris D, Corvin A, Gill M, Hariri AR, Weinberger DR, Pendleton N, Bitsios P, Rujescu D, Lahti J, Le Hellard S, Keller MC, Andreassen OA, Deary IJ, Glahn DC, Malhotra AK, Lencz T. Show fewer authors. “GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.” Molecular Psychiatry. 17 January 2017. Behavior
  • Robinson MR, Kleinman A, Graff M, Vinkhuyzen AAE, Couper D. et al. Show more authors. Robinson MR, Kleinman A, Graff M, Vinkhuyzen AAE, Couper D, Miller MB, Peyrot WJ, Abdellaoui A, Zietsch BP, Nolte IM, Vliet-Ostaptchouk JV, Snieder H, The LifeLines Cohort Study, Genetic Investigation of Anthropometric Traits (GIANT) consortium, Medland SE, Martin NG, Magnusson PKE, Iacono WG, McGue M, North KE, Yang J, Visscher PM. Show fewer authors. “Genetic evidence of assortative mating in humans.” Nature Human Behavior. 9 January 2017.
  • Lo MT, Hinds DA, Tung JY, Franz C, Fan CC. et al. Show more authors. Lo MT, Hinds DA, Tung JY, Franz C, Fan CC, Wang Y, Smeland OB, Schork A, Holland D, Kauppi K, Sanyal N, Escott-Price V, Smith DJ, O'Donovan M, Stefansson H, Bjornsdottir G, Thorgeirsson TE, Stefansson K, McEvoy LK, Dale AM, Andreassen OA, Chen CH. Show fewer authors. “Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders.” Nature Genetics. 5 December 2016. Behavior Psychiatry
  • Jones AV, Hockley JR, Hyde C, Gorman D, Sredic-Rhodes A. et al. Show more authors. Jones AV, Hockley JR, Hyde C, Gorman D, Sredic-Rhodes A, Bilsland J, McMurray G, Furlotte NA, Hu Y, Hinds DA, Cox PJ, Scollen S. Show fewer authors. “Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus.” Pain. 1 November 2016. Neurology Reproduction
  • Eppinga RN, Hagemeijer Y, Burgess S, Hinds DA, Stefansson K. et al. Show more authors. Eppinga RN, Hagemeijer Y, Burgess S, Hinds DA, Stefansson K, Gudbjartsson DF, van Veldhuisen DJ, Munroe PB, Verweij N, van der Harst P. Show fewer authors. “Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality.” Nature Genetics. 31 October 2016. Traits
  • Barban N, Jansen R, de Vlaming R, Vaez A, Mandemakers JJ. et al. Show more authors. Barban N, Jansen R, de Vlaming R, Vaez A, Mandemakers JJ, Tropf FC, Shen X, Wilson JF, Chasman DI, Nolte IM, Tragante V, van der Laan SW, Perry JR, Kong A; BIOS Consortium, Ahluwalia TS, Albrecht E, Yerges-Armstrong L, Atzmon G, Auro K, Ayers K, Bakshi A, Ben-Avraham D, Berger K, Bergman A, Bertram L, Bielak LF, Bjornsdottir G, Bonder MJ, Broer L, Bui M, Barbieri C, Cavadino A, Chavarro JE, Turman C, Concas MP, Cordell HJ, Davies G, Eibich P, Eriksson N, Esko T, Eriksson J, Falahi F, Felix JF, Fontana MA, Franke L, Gandin I, Gaskins AJ, Gieger C, Gunderson EP, Guo X, Hayward C, He C, Hofer E, Huang H, Joshi PK, Kanoni S, Karlsson R, Kiechl S, Kifley A, Kluttig A, Kraft P, Lagou V, Lecoeur C, Lahti J, Li-Gao R, Lind PA, Liu T, Makalic E, Mamasoula C, Matteson L, Mbarek H, McArdle PF, McMahon G, Meddens SF, Mihailov E, Miller M, Missmer SA, Monnereau C, van der Most PJ, Myhre R, Nalls MA, Nutile T, Kalafati IP, Porcu E, Prokopenko I, Rajan KB, Rich-Edwards J, Rietveld CA, Robino A, Rose LM, Rueedi R, Ryan KA, Saba Y, Schmidt D, Smith JA, Stolk L, Streeten E, Tonjes A, Thorleifsson G, Ulivi S, Wedenoja J, Wellmann J, Willeit P, Yao J, Yengo L, Zhao JH, Zhao W, Zhernakova DV, Amin N, Andrews H, Balkau B, Barzilai N, Bergmann S, Biino G, Bisgaard H, Bonnelykke K, Boomsma DI, Buring JE, Campbell H, Cappellani S, Ciullo M, Cox SR, Cucca F, Toniolo D, Davey-Smith G, Deary IJ, Dedoussis G, Deloukas P, van Duijn CM, de Geus EJ, Eriksson JG, Evans DA, Faul JD, Sala CF, Froguel P, Gasparini P, Girotto G, Grabe HJ, Greiser KH, Groenen PJ, de Haan HG, Haerting J, Harris TB, Heath AC, Heikkila K, Hofman A, Homuth G, Holliday EG, Hopper J, Hypponen E, Jacobsson B, Jaddoe VW, Johannesson M, Jugessur A, Kahonen M, Kajantie E, Kardia SL, Keavney B, Kolcic I, Koponen P, Kovacs P, Kronenberg F, Kutalik Z, La Bianca M, Lachance G, Iacono WG, Lai S, Lehtimaki T, Liewald DC; LifeLines Cohort Study, Lindgren CM, Liu Y, Luben R, Lucht M, Luoto R, Magnus P, Magnusson PK, Martin NG, McGue M, McQuillan R, Medland SE, Meisinger C, Mellstrom D, Metspalu A, Traglia M, Milani L, Mitchell P, Montgomery GW, Mook-Kanamori D, de Mutsert R, Nohr EA, Ohlsson C, Olsen J, Ong KK, Paternoster L, Pattie A, Penninx BW, Perola M, Peyser PA, Pirastu M, Polasek O, Power C, Kaprio J, Raffel LJ, Raikkonen K, Raitakari O, Ridker PM, Ring SM, Roll K, Rudan I, Ruggiero D, Rujescu D, Salomaa V, Schlessinger D, Schmidt H, Schmidt R, Schupf N, Smit J, Sorice R, Spector TD, Starr JM, Stockl D, Strauch K, Stumvoll M, Swertz MA, Thorsteinsdottir U, Thurik AR, Timpson NJ, Tung JY, Uitterlinden AG, Vaccargiu S, Viikari J, Vitart V, Volzke H, Vollenweider P, Vuckovic D, Waage J, Wagner GG, Wang JJ, Wareham NJ, Weir DR, Willemsen G, Willeit J, Wright AF, Zondervan KT, Stefansson K, Krueger RF, Lee JJ, Benjamin DJ, Cesarini D, Koellinger PD, den Hoed M, Snieder H, Mills MC. Show fewer authors. “Genome-wide analysis identifies 12 loci influencing human reproductive behavior.” Nature Genetics. 31 October 2016. Behavior Reproduction
  • Li QS, Tian C, Seabrook GR, Drevets WC, Narayan VA.Li QS, Tian C, Seabrook GR, Drevets WC, Narayan VA Show fewer authors. “Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.” Translational Psychiatry. 13 September 2016. Neurology Psychiatry
  • Ferreira MA, Jansen R, Willemsen G, Penninx B, Bain LM. et al. Show more authors. Ferreira MA, Jansen R, Willemsen G, Penninx B, Bain LM, Vicente CT, Revez JA, Matheson MC, Hui J, Tung JY, Baltic S, Le Souef P, Montgomery GW, Martin NG, Robertson CF, James A, Thompson PJ, Boomsma DI, Hopper JL, Hinds DA, Werder RB, Phipps S; Australian Asthma Genetics Consortium Collaborators. Show fewer authors. “Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling.” Journal of Allergy and Clinical Immunology. 20 August 2016. Immunity
  • Chahal HS, Wu W, Ransohoff KJ, Yang L, Hedlin H. et al. Show more authors. Chahal HS, Wu W, Ransohoff KJ, Yang L, Hedlin H, Desai M, Lin Y, Dai HJ, Qureshi AA, Li WQ, Kraft P, Hinds DA, Tang JY, Han J, Sarin KY. Show fewer authors. “Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma.” Nature Communications. 19 August 2016. Cancer Dermatology
  • McIntosh AM, Hall LS, Zeng Y, Adams MJ, Gibson J. et al. Show more authors. McIntosh AM, Hall LS, Zeng Y, Adams MJ, Gibson J, Wigmore E, Hagenaars SP, Davies G, Fernandez-Pujals AM, Campbell AI, Clarke TK, Hayward C, Haley CS, Porteous DJ, Deary IJ, Smith DJ, Nicholl BI, Hinds DA, Jones AV, Scollen S, Meng W, Smith BH, Hocking LJ. Show fewer authors. “Genetic and environmental risk for chronic pain and the contribution of risk variants for major depressive disorder: a family-based mixed-model analysis.” PLoS Medicine. 16 August 2016. Neurology Psychiatry
  • Jones SE, Tyrrell J, Wood AR, Beaumont RN, Ruth KS. et al. Show more authors. Jones SE, Tyrrell J, Wood AR, Beaumont RN, Ruth KS, Tuke MA, Yaghootkar H, Hu Y, Teder-Laving M, Hayward C, Roenneberg T, Wilson JF, Del Greco F, Hicks AA, Shin C, Yun CH, Lee SK, Metspalu A, Byrne EM, Gehrman PR, Tiemeier H, Allebrandt KV, Freathy RM, Murray A, Hinds DA, Frayling TM, Weedon MN. Show fewer authors. “Genome-wide association analyses in 128,266 individuals identifies new morningness and sleep duration loci.” PLoS Genetics. 5 August 2016. Behavior
  • Hyde CL, Nagle MW, Tian C, Chen X, Paciga SA. et al. Show more authors. Hyde CL, Nagle MW, Tian C, Chen X, Paciga SA, Wendland JR, Tung JY, Hinds DA, Perlis RH, Winslow AR. Show fewer authors. “Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.” Nature Genetics. 1 August 2016. Psychiatry
  • Chahal HS, Lin Y, Ransohoff KJ, Hinds DA, Wu W. et al. Show more authors. Chahal HS, Lin Y, Ransohoff KJ, Hinds DA, Wu W, Dai HJ, Qureshi AA, Li WQ, Kraft P, Tang JY, Han J, Sarin KY. Show fewer authors. “Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma.” Nature Communications. 18 July 2016. Cancer Dermatology
  • Hinds DA, Barnholt KE, Mesa RA, Kiefer AK, Do CB. et al. Show more authors. Hinds DA, Barnholt KE, Mesa RA, Kiefer AK, Do CB, Eriksson N, Mountain JL, Francke U, Tung JY, Nguyen HM, Zhang H, Gojenola L, Zehnder JL, Gotlib J. Show fewer authors. “Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms.” Blood Journal. 30 June 2016. Cancer Hematology Rare Diseases
  • Gormley P, Anttila V, Winsvold BS, Palta P, Esko T. et al. Show more authors. Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, Kallela M, Freilinger TM, Ran C, Gordon SG, Stam AH, Steinberg S, Borck G, Koiranen M, Quaye L, Adams HH, Lehtimaki T, Sarin AP, Wedenoja J, Hinds DA, Buring JE, Schurks M, Ridker PM, Hrafnsdottir MG, Stefansson H, Ring SM, Hottenga JJ, Penninx BW, Farkkila M, Artto V, Kaunisto M, Vepsalainen S, Malik R, Heath AC, Madden PA, Martin NG, Montgomery GW, Kurki MI, Kals M, Magi R, Parn K, Hamalainen E, Huang H, Byrnes AE, Franke L, Huang J, Stergiakouli E, Lee PH, Sandor C, Webber C, Cader Z, Muller-Myhsok B, Schreiber S, Meitinger T, Eriksson JG, Salomaa V, Heikkila K, Loehrer E, Uitterlinden AG, Hofman A, van Duijn CM, Cherkas L, Pedersen LM, Stubhaug A, Nielsen CS, Mannikko M, Mihailov E, Milani L, Gobel H, Esserlind AL, Christensen AF, Hansen TF, Werge T; International Headache Genetics Consortium, Kaprio J, Aromaa AJ, Raitakari O, Ikram MA, Spector T, Jarvelin MR, Metspalu A, Kubisch C, Strachan DP, Ferrari MD, Belin AC, Dichgans M, Wessman M, van den Maagdenberg AM, Zwart JA, Boomsma DI, Smith GD, Stefansson K, Eriksson N, Daly MJ, Neale BM, Olesen J, Chasman DI, Nyholt DR, Palotie A. Show fewer authors. “Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.” Nature Genetics. 20 June 2016. Neurology
  • Pickrell JK, Berisa T, Liu JZ, Segurel L, Tung JY. et al. Show more authors. Pickrell JK, Berisa T, Liu JZ, Segurel L, Tung JY, Hinds DA. Show fewer authors. “Detection and interpretation of shared genetic influences on 42 human traits.” Nature Genetics. 16 May 2016. Methods Traits
  • Rietveld CA, Turley P, Chen GB, Emilsson V, Meddens SF. et al. Show more authors. Rietveld CA, Turley P, Chen GB, Emilsson V, Meddens SF, Oskarsson S, Pickrell JK, Thom K, Timshel P, de Vlaming R, Abdellaoui A, Ahluwalia TS, Bacelis J, Baumbach C, Bjornsdottir G, Brandsma JH, Pina Concas M, Derringer J, Furlotte NA, Galesloot TE, Girotto G, Gupta R, Hall LM, Harris SE, Hofer E, Horikoshi M, Huffman JE, Kaasik K, Kalafati IP, Karlsson R, Kong A, Lahti J, van der Lee SJ, deLeeuw C, Lind PA, Lindgren KO, Liu T, Mangino M, Marten J, Mihailov E, Miller MB, van der Most PJ, Oldmeadow C, Payton A, Pervjakova N, Peyrot WJ, Qian Y, Raitakari O, Rueedi R, Salvi E, Schmidt B, Schraut KE, Shi J, Smith AV, Poot RA, St Pourcain B, Teumer A, Thorleifsson G, Verweij N, Vuckovic D, Wellmann J, Westra HJ, Yang J, Zhao W, Zhu Z, Alizadeh BZ, Amin N, Bakshi A, Baumeister SE, Biino G, Bonnelykke K, Boyle PA, Campbell H, Cappuccio FP, Davies G, De Neve JE, Deloukas P, Demuth I, Ding J, Eibich P, Eisele L, Eklund N, Evans DM, Faul JD, Feitosa MF, Forstner AJ, Gandin I, Gunnarsson B, Halldorsson BV, Harris TB, Heath AC, Hocking LJ, Holliday EG, Homuth G, Horan MA, Hottenga JJ, de Jager PL, Joshi PK, Jugessur A, Kaakinen MA, Kahonen M, Kanoni S, Keltigangas-Jarvinen L, Kiemeney LA, Kolcic I, Koskinen S, Kraja AT, Kroh M, Kutalik Z, Latvala A, Launer LJ, Lebreton MP, Levinson DF, Lichtenstein P, Lichtner P, Liewald DC; LifeLines Cohort Study, Loukola A, Madden PA, Magi R, Maki-Opas T, Marioni RE, Marques-Vidal P, Meddens GA, McMahon G, Meisinger C, Meitinger T, Milaneschi Y, Milani L, Montgomery GW, Myhre R, Nelson CP, Nyholt DR, Ollier WE, Palotie A, Paternoster L, Pedersen NL, Petrovic KE, Porteous DJ, Raikkonen K, Ring SM, Robino A, Rostapshova O, Rudan I, Rustichini A, Salomaa V, Sanders AR, Sarin AP, Schmidt H, Scott RJ, Smith BH, Smith JA, Staessen JA, Steinhagen-Thiessen E, Strauch K, Terracciano A, Tobin MD, Ulivi S, Vaccargiu S, Quaye L, van Rooij FJ, Venturini C, Vinkhuyzen AA, Volker U, Volzke H, Vonk JM, Vozzi D, Waage J, Ware EB, Willemsen G, Attia JR, Bennett DA, Berger K, Bertram L, Bisgaard H, Boomsma DI, Borecki IB, Bultmann U, Chabris CF, Cucca F, Cusi D, Deary IJ, Dedoussis GV, van Duijn CM, Eriksson JG, Franke B, Franke L, Gasparini P, Gejman PV, Gieger C, Grabe HJ, Gratten J, Groenen PJ, Gudnason V, van der Harst P, Hayward C, Hinds DA, Hoffmann W, Hypponen E, Iacono WG, Jacobsson B, Jarvelin MR, Jockel KH, Kaprio J, Kardia SL, Lehtimaki T, Lehrer SF, Magnusson PK, Martin NG, McGue M, Metspalu A, Pendleton N, Penninx BW, Perola M, Pirastu N, Pirastu M, Polasek O, Posthuma D, Power C, Province MA, Samani NJ, Schlessinger D, Schmidt R, Sorensen TI, Spector TD, Stefansson K, Thorsteinsdottir U, Thurik AR, Timpson NJ, Tiemeier H, Tung JY, Uitterlinden AG, Vitart V, Vollenweider P, Weir DR, Wilson JF, Wright AF, Conley DC, Krueger RF, Davey Smith G, Hofman A, Laibson DI, Medland SE, Meyer MN, Yang J, Johannesson M, Visscher PM, Esko T, Koellinger PD, Cesarini D, Benjamin DJ. Show fewer authors. “Genome-wide association study identifies 74 loci associated with educational attainment.” Nature. 11 May 2016. Behavior
  • Okbay A, Beauchamp JP, Fontana MA, Lee JJ, Pers TH. et al. Show more authors. Okbay A, Beauchamp JP, Fontana MA, Lee JJ, Pers TH, Fontana MA, Meddens SF, Linner RK, Rietveld CA, Derringer J, Gratten J, Lee JJ, Liu JZ, de Vlaming R, Ahluwalia TS, Buchwald J, Cavadino A, Frazier-Wood AC, Furlotte NA, Garfield V, Geisel MH, Gonzalez JR, Haitjema S, Karlsson R, van der Laan SW, Ladwig KH, Lahti J, van der Lee SJ, Lind PA, Liu T, Matteson L, Mihailov E, Miller MB, Minica CC, Nolte IM, Mook-Kanamori D, van der Most PJ, Oldmeadow C, Qian Y, Raitakari O, Rawal R, Realo A, Rueedi R, Schmidt B, Smith AV, Stergiakouli E, Tanaka T, Taylor K, Wedenoja J, Wellmann J, Westra HJ, Willems SM, Zhao W; LifeLines Cohort Study, Amin N, Bakshi A, Boyle PA, Cherney S, Cox SR, Davies G, Davis OS, Ding J, Direk N, Eibich P, Emeny RT, Fatemifar G, Faul JD, Ferrucci L, Forstner A, Gieger C, Gupta R, Harris TB, Harris JM, Holliday EG, Hottenga JJ, De Jager PL, Kaakinen MA, Kajantie E, Karhunen V, Kolcic I, Kumari M, Launer LJ, Franke L, Li-Gao R, Koini M, Loukola A, Marques-Vidal P, Montgomery GW, Mosing MA, Paternoster L, Pattie A, Petrovic KE, Pulkki-Raback L, Quaye L, Raikkonen K, Rudan I, Scott RJ, Smith JA, Sutin AR, Trzaskowski M, Vinkhuyzen AE, Yu L, Zabaneh D, Attia JR, Bennett DA, Berger K, Bertram L, Boomsma DI, Snieder H, Chang SC, Cucca F, Deary IJ, van Duijn CM, Eriksson JG, Bultmann U, de Geus EJ, Groenen PJ, Gudnason V, Hansen T, Hartman CA, Haworth CM, Hayward C, Heath AC, Hinds DA, Hypponen E, Iacono WG, Jarvelin MR, Jockel KH, Kaprio J, Kardia SL, Keltikangas-Jarvinen L, Kraft P, Kubzansky LD, Lehtimaki T, Magnusson PK, Martin NG, McGue M, Metspalu A, Mills M, de Mutsert R, Oldehinkel AJ, Pasterkamp G, Pedersen NL, Plomin R, Polasek O, Power C, Rich SS, Rosendaal FR, den Ruijter HM, Schlessinger D, Schmidt H, Svento R, Schmidt R, Alizadeh BZ, Sorensen TI, Spector TD, Steptoe A, Terracciano A, Thurik AR, Timpson NJ, Tiemeier H, Uitterlinden AG, Vollenweider P, Wagner GG, Weir DR, Yang J, Conley DC, Smith GD, Hofman A, Johannesson M, Laibson DI, Medland SE, Meyer MN, Pickrell JK, Esko T, Krueger RF, Beauchamp JP, Koellinger PD, Benjamin DJ, Bartels M, Cesarini D. Show fewer authors. “Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.” Nature Genetics. 18 April 2016. Behavior Psychiatry
  • Chen R, Shi L, Hakenberg J, Naughton B, Sklar P. et al. Show more authors. Chen R, Shi L, Hakenberg J, Naughton B, Sklar P, Zhang J, Zhou H, Tian L, Prakash O, Lemire M, Sleiman P, Cheng WY, Chen W, Shah H, Shen Y, Fromer M, Omberg L, Deardorff MA, Zackai E, Bobe JR, Levin E, Hudson TJ, Groop L, Wang J, Hakonarson H, Wojcicki A, Diaz G, Edelmann L, Schadt EE, Friend SH. Show fewer authors. “Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases.” Nature Biotechnology. 11 April 2016. Rare Diseases
  • Hinds DA, Buil A, Ziemek D, Martinez-Perez A, Malik R. et al. Show more authors. Hinds DA, Buil A, Ziemek D, Martinez-Perez A, Malik R, Folkersen L, Germain M, Malarstig A, Brown A, Soria JM, Dichgans M, Bing N, Franco-Cereceda A, Souto JC, Dermitzakis ED, Hamsten A, Worrall BB, Tung JY, METASTROKE Consortium, INVENT Consortium, Sabater-Lleal M. Show fewer authors. “Genome-wide association analysis in 6,135 individuals and 252,827 controls identifies 8 loci associated with thrombosis.” Human Molecular Genetics. 9 February 2016. Hematology
  • Hu Y, Shmygelska A, Tran D, Eriksson N, Tung JY. et al. Show more authors. Hu Y, Shmygelska A, Tran D, Eriksson N, Tung JY, Hinds DA. Show fewer authors. “GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person.” Nature Communications. 2 February 2016. Behavior
  • Minikel EV, Vallabh SM, Lek M, Estrada K, Samocha KE. et al. Show more authors. Minikel EV, Vallabh SM, Lek M, Estrada K, Samocha KE, Sathirapongsasuti JF, McLean CY, Tung JY, Yu LP, Gambetti P, Blevins J, Zhang S, Cohen Y, Chen W, Yamada M, Hamaguchi T, Sanjo N, Mizusawa H, Nakamura Y, Kitamoto T, Collins SJ, Boyd A, Will RG, Knight R, Ponto C, Zerr I, Kraus TF, Eigenbrod S, Giese A, Calero M, de Pedro-Cuesta J, Haik S, Laplanche JL, Bouaziz-Amar E, Brandel JP, Capellari S, Parchi P, Poleggi A, Ladogana A, O'Donnell-Luria AH, Karczewski KJ, Marshall JL, Boehnke M, Laakso M, Mohlke KL, Kahler A, Chambert K, McCarroll S, Sullivan PF, Hultman CM, Purcell SM, Sklar P, van der Lee SJ, Rozemuller A, Jansen C, Hofman A, Kraaij R, van Rooij JG, Ikram MA, Uitterlinden AG, van Duijn CM; Exome Aggregation Consortium (ExAC), Daly MJ, MacArthur DG. Show fewer authors. “Quantifying prion disease penetrance using large population control cohorts.” Science Translational Medicine. 20 January 2016. Neurology Rare Diseases
  • Gharahkhani P, Tung J, Hinds D, Mishra A, Barrett's and Esophageal Adenocarcinoma Consortium (BEACON). et al. Show more authors. Gharahkhani P, Tung J, Hinds D, Mishra A, Barrett's and Esophageal Adenocarcinoma Consortium (BEACON), Vaughan TL, Whiteman DC, MacGregor S; BEACON study investigators. Show fewer authors. “Chronic gastroesophageal reflux disease shares genetic background with esophageal adenocarcinoma and Barrett’s esophagus.” Human Molecular Genetics. 23 December 2015. Cancer
  • Jorgenson E, Makki N, Shen L, Chen DC, Tian C. et al. Show more authors. Jorgenson E, Makki N, Shen L, Chen DC, Tian C, Eckalbar WL, Hinds D, Ahituv N, Avins A. Show fewer authors. “A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia.” Nature Communications. 21 December 2015. Musculoskeletal
  • Day FR, Bulik-Sullivan B, Hinds DA, Finucane HK, Murabito JM. et al. Show more authors. Day FR, Bulik-Sullivan B, Hinds DA, Finucane HK, Murabito JM, Tung JY, Ong KK, Perry JRB. Show fewer authors. “Shared genetic aetiology of puberty timing between sexes and with health-related outcomes.” Nature Communications. 9 November 2015. Reproduction
  • Paternoster L, Standl M, Waage J, Baurecht H, Hotze M. et al. Show more authors. Paternoster L, Standl M, Waage J, Baurecht H, Hotze M, Strachan DP, Curtin JA, Bonnelykke K, Tian C, Takahashi A, Esparza-Gordillo J, Alves AC, Thyssen JP, den Dekker HT, Ferreira MA, Altmaier E, Sleiman PMA, Xiao FL, Gonzalez JR, Marenholz I, Kalb B, Pino-Yanes M, Xu CJ, Carstensen L, Groen-Blokhuis MM, Venturini C, Pennell CE, Barton SJ, Levin AM, Curjuric I, Bustamante M, Kreiner-Moller E, Lockett GA, Bacelis J, Bunyavanich S, Myers RA, Matanovic A, Kumar A, Tung JY, Hirota T, Kubo M, McArdle WL, Henderson AJ, Kemp JP, Zheng J, Smith GD, Ruschendorf F, Bauerfeind A, Lee-Kirsch MA, Arnold A, Homuth G, Schmidt CO, Mangold E, Cichon S, Keil T, Rodriguez E, Peters A, Franke A, Lieb W, Novak N, Folster-Holst R, Horikoshi M, Pekkanen J, Sebert S, Husemoen LL, Grarup N, de Jongste JC, Rivadeneira F, Hofman A, Jaddoe VWV, Pasmans SGMA, Elbert NJ, Uitterlinden AG, Marks GB, Thompson PJ, Matheson MC, Robertson CF, Australian Asthma Genetics Consortium (AAGC), Ried JS, Li J, Zuo XB, Zheng XD, Yin XY, Sun LD, McAleer MA, O'Regan GM, Fahy CMR, Campbell LE, Macek M, Kurek M, Hu D, Eng C, Postma D, Feenstra B, Geller F, Hottenga JJ, Middeldorp CM, Hysi P, Bataille V, Spector T, Tiesler CMT, Thiering E, Pahukasahasram B, Yang JJ, Imboden M, Huntsman S, Vilor-Tejedor N, Relton CL, Myhre R, Nystad W, Custovic A, Weiss ST, Meyers DA, Soderhall C, Melen E, Ober C, Raby BA, Simpson A, Jacobsson B, Holloway JW, Bisgaard H, Sunyer J, Probst-Hensch NM, Williams LK, Godfrey KM, Wang CA, Boomsma DI, Melbye M, Koppelman GH, Jarvis D, McLean WHI, Irvine AD, Zhang XJ, Hakonarson H, Gieger C, Burchard EG, Martin NG, Duijts L, Linneberg A, Jarvelin MR, Nothen MM, Lau S, Hubner N, Lee YA, Tamari M, Hinds DA, Glass D, Brown SJ, Heinrich J, Evans DM, and Stephan Weidinger for the EArly Genetics and Lifecourse Epidemiology (EAGLE) Eczema Consortium. Show fewer authors. “Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.” Nature Genetics. 19 October 2015. Dermatology Immunity
  • Carere DA, VanderWeele T, Moreno TA, Mountain JL, Roberts JS. et al. Show more authors. Carere DA, VanderWeele T, Moreno TA, Mountain JL, Roberts JS, Kraft P, Green RC, the PGen Study Group. Show fewer authors. “The impact of direct-to-consumer personal genomic testing on perceived risk of breast, prostate, colorectal, and lung cancer: findings from the PGen study.” BMC Medical Genomics. 15 October 2015. Cancer
  • Day FR, Hinds DA, Tung JY, Stolk L, Styrkarsdottir U. et al. Show more authors. Day FR, Hinds DA, Tung JY, Stolk L, Styrkarsdottir U, Saxena R, Bjonnes A, Broer L, Dunger DB, Halldorsson BV, Lawlor DA, Laval G, Mathieson I, McCardle WL, Louwers Y, Meun C, Ring S, Scott RA, Sulem P, Uitterlinden AG, Wareham NJ, Thorsteinsdottir U, Welt C, Stefansson K, Laven JSE, Ong KK, Perry JRB. Show fewer authors. “Causal mechanisms and balancing selection inferred from genetic associations with the Polycystic Ovary Syndrome.” Nature Communications. 25 September 2015. Reproduction
  • Zheng HF, Forgetta V, Hsu YH, Estrada K, Rosello-Diez A. et al. Show more authors. Zheng HF, Forgetta V, Hsu YH, Estrada K, Rosello-Diez A, Leo PJ, Dahia CL, Park-Min KH, Tobias JH, Kooperberg C, Kleinman A, Styrkarsdottir U, Liu CT, Uggla C, Evan DS, Nielson CM, Walter K, Pettersson-Kymmer U, McCarthy S, Eriksson J, Kwan T, Jhamai M, Trajanoska K, Memari Y, Min J, Huang J, Danecek P, Wilmot B, Li R, Chou WC, Mokry LE, Moayyeri A, Claussnitzer M, Cheng CH, Cheung W, Medina-Gomez C, Ge B, Chen SH, Choi K, Oei L, Fraser J, Kraaij R, Hibbs MA, Gregson CL, Paquette D, Hofman A, Wibom C, Tranah GJ, Marshall M, Gardiner BB, Cremin K, Auer P, Hsu L, Ring S, Tung JY, Thorleifsson G, Enneman AW, van Schoor NM, de Groot LCPGM, van der Velde N, Melin B, Kemp JP, Christiansen C, Sayers A, Zhou Y, Calderari S, van Rooij J, Carlson C, Peters U, Berlivet S, Dostie J, Uitterlinden AG, Williams SR, Farber C, Grinberg D, LaCroix AZ, Haessler J, Chasman DI, Giulianini F, Rose LM, Ridker PM, Eisman JA, Nguyen TV, Center JR, Nogues X, Garcia-Giralt N, Launer LL, Gudnason V, Mellstrom D, Vandenput L, Amin N, van Duijn CM, Karlsson MK, Ljunggren O, Svensson O, Hallmans G, Rousseau F, Giroux S, Bussiere J, Arp PP, Koromani F, Prince RL, Lewis JR, Langdahl BL, Hermann AP, Jensen JEB, Kaptoge S, Khaw KT, Reeve J, Formosa MM, Xuereb-Anastasi A, Akesson K, McGuigan FE, Garg G, Olmos JM, Zarrabeitia MT, Riancho JA, Ralston SH, Alonso N, Jiang X, Goltzman D, Pastinen T, Grundberg E, Gauguier D, Orwoll ES, Karasik D, Davey-Smith G, AOGC Consortium, Smith AV, Siggeirsdottir K, Harris TB, Zillikens MC, van Meurs JBJ, Thorsteinsdottir U, Maurano MT, Timpson NJ, Soranzo N, Durbin R, Wilson SG, Ntzani EE, Brown MA, Stefansson Kari, Hinds DA, Spector T, Cupples LA, Ohlsson C, Greenwood CMT, UK10K Consortium, Jackson RD, Rowe DW, Loomis CA, Evans DM, Ackert-Bicknell CL, Joyner AL, Duncan EL, Kiel DP, Rivadeneira F, Richards JB. Show fewer authors. “Whole-genome sequencing and deep imputation identifies non-coding variants near Engrailed-1 with large effects on bone mineral density and fracture.” Nature. 14 September 2015. Musculoskeletal
  • Nalls MA, McLean CY, Rick J, Eberly S, Hutten SJ. et al. Show more authors.Nalls MA, McLean CY, Rick J, Eberly S, Hutten SJ, Gwinn K, Sutherland M, Martinez M, Heutink P, Williams NM, Hardy J, Gasser T, Brice A, Price TR, Nicolas A, Keller MF, Molony C, Gibbs JR, Chen-Plotkin A, Suh E, Letson C, Fiandaca MS, Mapstone M, Federoff HJ, Noyce AJ, Morris H, Van Deerlin VM, Weintraub D, Zabetian C, Hernandez DG, Lesage S, Mullins M, Conley ED, Northover CAM, Frasier M, Marek K, Day-Williams AG, Stone DJ, Ioannidis JPA, Singleton AB, for the Parkinson's Disease Biomarkers Program and Parkinson's Progression Marker Initiative investigators Show fewer authors. “Diagnosis of Parkinson’s disease on the basis of clinical and genetic classification: a population-based modelling study.” Lancet Neuro. 10 August 2015. Neurology
  • Nalls MA, McLean CY, Rick J, Eberly S, Hutten SJ. et al. Show more authors. Nalls MA, McLean CY, Rick J, Eberly S, Hutten SJ, Gwinn K, Sutherland M, Martinez M, Heutink P, Williams NM, Hardy J, Gasser T, Brice A, Price TR, Nicolas A, Keller MF, Molony C, Gibbs JR, Chen-Plotkin A, Suh E, Letson C, Fiandaca MS, Mapstone M, Federoff HJ, Noyce AJ, Morris H, Van Deerlin VM, Weintraub D, Zabetian C, Hernandez DG, Lesage S, Mullins M, Conley ED, Northover CAM, Frasier M, Marek K, Day-Williams AG, Stone DJ, Ioannidis JPA, Singleton AB, for the Parkinson's Disease Biomarkers Program and Parkinson's Progression Marker Initiative investigators. Show fewer authors. “Diagnosis of Parkinson’s disease on the basis of clinical and genetic classification: a population-based modelling study.” Lancet Neuro. 10 August 2015.
  • Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY. et al. Show more authors. Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY, Hinds DA, Esko T, Elks CE, Altmaier E, He C, Huffman JE, Mihailov E, Porcu E, Robino A, Rose LM, Schick UM, Stolk L, Teumer A, Thompson DJ, Traglia M, Wang CA, Yerges-Armstrong LM, Antoniou AC, Barbieri C, Coviello AD, Cucca F, Demerath EW, Dunning AM, Gandin I, Grove ML, Gudbjartsson DF, Hocking LJ, Hofman A, Huang J, Jackson RD, Karasik D, Kriebel J, Lange EM, Lange LA, Langenberg C, Li X, Luan J, Magi R, Morrison AC, Padmanabhan S, Pirie A, Polasek O, Porteous D, Reiner AP, Rivadeneira F, Rudan I, Sala CF, Schlessinger D, Scott RA, Stockl D, Visser JA, Volker U, Vozzi D, Wilson JG, Zygmunt M, EPIC-InterAct Consortium, Generation Scotland, Boerwinkle E, Buring JE, Crisponi L, Easton DF, Hayward C, Hu FB, Liu S, Metspalu A, Pennell CE, Ridker PM, Strauch K, Streeten EA, Toniolo D, Uitterlinden AG, Ulivi S, Volzke H, Wareham NJ, Wellons M, Franceschini N, Chasman DI, Thorsteinsdottir U, Murray A, Stefansson K, Murabito JM, Ong KK, Perry JRB. Show fewer authors. “Rare coding variants and X-linked loci associated with age at menarche.” Nature Communications. 4 August 2015. Reproduction
  • Meisel SF, Carere DA, Wardle J, Kalia SS, Moreno TA. et al. Show more authors. Meisel SF, Carere DA, Wardle J, Kalia SS, Moreno TA, Mountain JL, Roberts JS, Green RC; PGen Study Group. Show fewer authors. “Explaining, not just predicting, drives interest in personal genomics.” Genome Medicine. 1 August 2015. ELSI
  • Dorsey ER, Darwin KC, Mohammed S, Donohue S, Tethal A. et al. Show more authors.Dorsey ER, Darwin KC, Mohammed S, Donohue S, Tethal A, Achey MA, Ward S, Caughey E, Conley ED, Eriksson N, Ravina B Show fewer authors. “Virtual research visits and direct-to-consumer genetic testing in Parkinson’s disease.” Digital Health. 27 June 2015. Neurology
  • Dorsey ER, Darwin KC, Mohammed S, Donohue S, Tethal A. et al. Show more authors. Dorsey ER, Darwin KC, Mohammed S, Donohue S, Tethal A, Achey MA, Ward S, Caughey E, Conley ED, Eriksson N, Ravina B. Show fewer authors. “Virtual research visits and direct-to-consumer genetic testing in Parkinson’s disease.” Digital Health. 27 June 2015.
  • Ostergren JE, Gornick MC, Carere DA, Kalia SS, Uhlmann WR. et al. Show more authors. Ostergren JE, Gornick MC, Carere DA, Kalia SS, Uhlmann WR, Ruffin MT, Mountain JL, Green RC, Roberts JS. Show fewer authors. “How well do customers of Direct-to-Consumer Personal Genomic Services understand genetic test results? Findings from the Personal Genomics (PGen) Study.” Public Health Genomics. 16 June 2015. ELSI
  • Arloth J, Bogdan R, Weber P, Frishman G, Menke A. et al. Show more authors. Arloth J, Bogdan R, Weber P, Frishman G, Menke A, Wagner KV, Balsevich G, Schmidt MV, Karbalai N, Czamara D, Altmann A, Trumbach D, Wurst W, Mehta D, Uhr M, Klengel T, Erhardt A, Carey CE, Conley ED, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (PGC), Ruepp A, Muller-Myhsok B, Hariri AR, Binder EB. Show fewer authors. “Genetic differences in the immediate transcriptome response to stress predict risk-related brain function and psychiatric disorders.” Neuron. 3 June 2015. Neurology Psychiatry
  • Chang AL, Raber I, Xu J, Li R, Spitale R. et al. Show more authors. Chang AL, Raber I, Xu J, Li R, Spitale R, Chen J, Kiefer AK, Tian C, Eriksson NK, Hinds DA, Tung JY. Show fewer authors. “Assessment of the genetic basis of rosacea by genome-wide association study.” Journal of Investigative Dermatology. 12 March 2015. Dermatology Immunity
  • Campbell CL, Furlotte NA, Eriksson N, Hinds D, Auton A.Campbell CL, Furlotte NA, Eriksson N, Hinds D, Auton A Show fewer authors. “Escape from crossover interference increases with maternal age.” Nature Communications. 19 February 2015. Methods Reproduction
  • Hromatka BS, Tung JY, Kiefer AK, Do CB, Hinds DA. et al. Show more authors. Hromatka BS, Tung JY, Kiefer AK, Do CB, Hinds DA, Eriksson N. Show fewer authors. “Genetic variants associated with motion sickness point to roles of inner ear development, neurological processes, and glucose homeostasis.” Human Molecular Genetics. 26 January 2015. Neurology
  • Bryc K, Durand EY, Macpherson JM, Reich D, Mountain JL.Bryc K, Durand EY, Macpherson JM, Reich D, Mountain JL Show fewer authors. “The genetic ancestry of African Americans, Latinos, and European Americans across the United States.” AJHG. 18 December 2014. Ancestry
  • Carere DA, Couper MP, Crawford SD, Kalia SS, Duggan JR. et al. Show more authors. Carere DA, Couper MP, Crawford SD, Kalia SS, Duggan JR, Moreno TA, Mountain JL, Roberts JS, Green RC; PGen Study Group.Design. Show fewer authors. “Design, methods, and participant characteristics of the Impact of Personal Genomics (PGen) Study, a prospective cohort study of direct-to-consumer personal genomic testing customers.” Genome Medicine. 3 December 2014. ELSI
  • Fuchsberger C, Abecasis GR, Hinds DA.Fuchsberger C, Abecasis GR, Hinds DA Show fewer authors. “minimac2: faster genotype imputation.” Bioinformatics. 22 October 2014. Methods
  • Durand EY, Do CB, Mountain JL, Macpherson JM.Durand EY, Do CB, Mountain JL, Macpherson JM Show fewer authors. “Ancestry Composition: A novel, efficient pipeline for ancestry deconvolution.” bioRxiv. 18 October 2014. Ancestry Methods
  • Rietveld CA, Conley D, Eriksson N, Esko T, Medland SE. et al. Show more authors. Rietveld CA, Conley D, Eriksson N, Esko T, Medland SE, Vinkhuyzen AA, Yang J, Boardman JD, Chabris CF, Dawes CT, Domingue BW, Hinds DA, Johannesson M, Kiefer AK, Laibson D, Magnusson PK, MMountain JL, Oskarsson S, Rostapshova O, Teumer A, Tung JY, Visscher PM, Benjamin DJ, Cesarini D, Koellinger PD; the Social Science Genetics Association Consortium; the Social Science Genetics Association Consortium. Show fewer authors. “Replicability and robustness of genome-wide-association studies for behavioral traits.” Psychological Science. 6 October 2014. Behavior
  • Nalls MA, Bras J, Hernandez DG, Keller MF, Majounie E. et al. Show more authors. Nalls MA, Bras J, Hernandez DG, Keller MF, Majounie E, Renton AE, Saad M, Jansen I, Guerreiro R, Lubbe S, Plagnol V, Gibbs JR, Schulte C, Pankratz N, Sutherland M, Bertram L, Lill CM, DeStefano AL, Faroud T, Eriksson N, Tung JY, Edsall C, Nichols N, Brooks J, Arepalli S, Pliner H, Letson C, Heutink P, Martinez M, Gasser T, Traynor BJ, Wood N, Hardy J, Singleton AB; the International Parkinson's Disease Genomics Consortium (IPDGC) and the Parkinson's Disease meta-analysis consortium. Show fewer authors. “NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases.” Neurobiology of Aging. 4 August 2014. Neurology
  • Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG. et al. Show more authors. Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, Stefansson H, Liu X, Pliner H, Lee JH, Cheng R; International Parkinson's Disease Genomics Consortium (IPDGC); Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI); 23andMe; GenePD; NeuroGenetics Research Consortium (NGRC); Hussman Institute of Human Genomics (HIHG); The Ashkenazi Jewish Dataset Investigator; Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE); North American Brain Expression Consortium (NABEC); United Kingdom Brain Expression Consortium (UKBEC); Greek Parkinson's Disease Consortium; Alzheimer Genetic Analysis Group, Ikram MA, Ioannidis JP, Hadjigeorgiou GM, Bis JC, Martinez M, Perlmutter JS, Goate A, Marder K, Fiske B, Sutherland M, Xiromerisiou G, Myers RH, Clark LN, Stefansson K, Hardy JA, Heutink P, Chen H, Wood NW, Houlden H, Payami H, Brice A, Scott WK, Gasser T, Bertram L, Eriksson N, Foroud T, Singleton AB. Show fewer authors. “Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease.” Nature Genetics. 27 July 2014. Neurology
  • Durand EY, Eriksson N, McLean CY.Durand EY, Eriksson N, McLean CY Show fewer authors. “Reducing pervasive false positive identical-by-descent segments detected by large-scale pedigree analysis.” Molecular Biology and Evolution. 30 April 2014. Ancestry Methods
  • Ferreira MA, Matheson MC, Tang CS, Granell R, Ang W. et al. Show more authors. Ferreira MA, Matheson MC, Tang CS, Granell R, Ang W, Hui J, Kiefer AK, Duffy DL, Baltic S, Danoy P, Bui M, Price L, Sly PD, Eriksson N, Madden PA, Abramson MJ, Holt PG, Heath AC, Hunter M, Musk B, Robertson CF, Le Souef P, Montgomery GW, Henderson AJ, Tung JY, Dharmage SC, Brown MA, James A, Thompson PJ, Pennell C, Martin NG, Evans DM, Hinds D, Hopper JL, the Australian Asthma Genetics Consortium Collaborators. Show fewer authors. “Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype.” Journal of Allergy and Clinical Immunology. 31 December 2013. Immunity
  • Lubke GH, Laurin C, Walters R, Eriksson N, Hysi P. et al. Show more authors. Lubke GH, Laurin C, Walters R, Eriksson N, Hysi P, Spector TD, Montgomery GW, Martin NG, Medland SE, Boomsma DI. Show fewer authors. “Gradient Boosting as a SNP Filter: an evaluation using simulated and hair morphology data.” Journal of Data Mining in Genomics & Proteomics. 20 October 2013. Methods
  • Wellman CL, Camp M, Jones VM, MacPherson KP, Ihne J. et al. Show more authors. Wellman CL, Camp M, Jones VM, MacPherson KP, Ihne J, Fitzgerald P, Maroun M, Drabant E, Bogdan R, Hariri AR, Holmes A. Show fewer authors. “Convergent effects of mouse Pet-1 deletion and human PET-1 variation on amygdala fear and threat processing.” Experimental Neurology. 4 October 2013. Behavior
  • Revez JA, Bain L, Chapman B, Powell JE, Jansen R. et al. Show more authors. Revez JA, Bain L, Chapman B, Powell JE, Jansen R, Duffy DL, Tung JY, AAGC Collaborators, Penninx BW, Visscher PM, De Geus EJC, Boomsma DI, Hinds DA, Martin NG, Montgomery GW, Ferreira MAR. Show fewer authors. “A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk.” Genes and Immunity. 15 August 2013. Immunity
  • Tung JY, Kiefer AK, Mullins M, Francke U, Eriksson N.Tung JY, Kiefer AK, Mullins M, Francke U, Eriksson N Show fewer authors. “Genome-wide association analysis implicates elastic microfibrils in the development of nonsyndromic striae distensae.” Journal of Investigative Dermatology. 11 July 2013. Dermatology
  • Hinds DA, McMahon G, Kiefer AK, Do CB, Eriksson N. et al. Show more authors. Hinds DA, McMahon G, Kiefer AK, Do CB, Eriksson N, Evans DM, St Pourcain B, Ring SM, Mountain JL, Francke U, Davey-Smith G, Timpson NJ, Tung JY. Show fewer authors. “A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.” Nature Genetics. 30 June 2013. Immunity
  • Pichler I, Del Greco M. F, Gogele M, Lill CM, Bertram L. et al. Show more authors. Pichler I, Del Greco M. F, Gogele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, PD GWAS Consortium, Nalls M, Keller MF, International Parkinson's Disease Genomics Consortium, Wellcome Trust Case Control Consortium 2, Benyamin B, Whitfield JB, Genetics of Iron Status Consortium, Pramstaller PP, Hicks AA, Thompson JR, Minelli C. Show fewer authors. “Serum iron levels and the risk of Parkinson’s disease: a Mendelian randomization study.” PLOS Medicine. 4 June 2013.
  • Pichler I, Del Greco M. F, Gogele M, Lill CM, Bertram L. et al. Show more authors.Pichler I, Del Greco M. F, Gogele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, PD GWAS Consortium, Nalls M, Keller MF, International Parkinson's Disease Genomics Consortium, Wellcome Trust Case Control Consortium 2, Benyamin B, Whitfield JB, Genetics of Iron Status Consortium, Pramstaller PP, Hicks AA, Thompson JR, Minelli C Show fewer authors. “Serum iron levels and the risk of Parkinson’s disease: a Mendelian randomization study.” PLOS Medicine. 4 June 2013. Neurology
  • Nikolova YS, Singhi EK, Drabant EM, Hariri AR.Nikolova YS, Singhi EK, Drabant EM, Hariri AR Show fewer authors. “Reward-related ventral striatum reactivity mediates gender-specific effects of a galanin remote enhancer haplotype on problem drinking.” Genes, Brain and Behavior. 4 April 2013. Psychiatry
  • Kiefer AK, Tung JY, Do CB, Hinds DA, Mountain JL. et al. Show more authors. Kiefer AK, Tung JY, Do CB, Hinds DA, Mountain JL, Francke U, Eriksson N. Show fewer authors. “Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia.” PLoS Genetics. 28 February 2013. Neurology Traits
  • Francke U, Dijamco C, Kiefer AK, Eriksson N, Moiseff BR. et al. Show more authors. Francke U, Dijamco C, Kiefer AK, Eriksson N, Moiseff BR, Tung JY, Mountain JL. Show fewer authors. “Dealing with the unexpected: Consumer responses to direct-access BRCA mutation testing.” PeerJ. 12 February 2013. Cancer ELSI
  • Heilmann S, Kiefer AK, Fricker N, Drichel D, Hillmer AM. et al. Show more authors. Heilmann S, Kiefer AK, Fricker N, Drichel D, Hillmer AM, Herold C, Tung JY, Eriksson N, Redler S, Betz RC, Li R, Karason A, Nyholt DR, Song K, Vermeulen SH, Kanoni S, Dedoussis G, Martin NG, Kiemeny LA, Mooser V, Stefansson K, Richards JB, Becker T, Brockschmidt FF, Hinds DA, Nothen MM. Show fewer authors. “Androgenetic alopecia: identification of four new genetic risk loci and evidence for the contribution of WNT-signaling to its etiology.” Journal of Investigative Dermatology. 28 January 2013. Dermatology
  • Mickey BJ, Heitzeg MM, Langenecker SA, Zubieta JK, Bogdan R. et al. Show more authors. Mickey BJ, Heitzeg MM, Langenecker SA, Zubieta JK, Bogdan R, Nikolova YS, Drabant E, Hariri AR, Bevilacqua L, Goldman D, Doyle GA. Show fewer authors. “Functional genetic variants in the vesicular monoamine transporter 1 modulate emotion processing.” Molecular Psychiatry. 22 January 2013. Behavior
  • Eriksson N, Wu S, Do CB, Kiefer AK, Tung JY. et al. Show more authors. Eriksson N, Wu S, Do CB, Kiefer AK, Tung JY, Mountain JL, Hinds DA, Francke U. Show fewer authors. “A genetic variant near olfactory receptor genes influence cilantro preference.” Flavour. 29 November 2012. Traits
  • Do CB, Hinds DA, Francke U, Eriksson N.Do CB, Hinds DA, Francke U, Eriksson N Show fewer authors. “Comparison of family history and SNP-based methods for predicting risk of polygenic disease.” PLoS Genetics. 11 October 2012. Methods
  • Eriksson N, Benton GM, Do CB, Kiefer AK, Mountain JL. et al. Show more authors. Eriksson N, Benton GM, Do CB, Kiefer AK, Mountain JL, Hinds DA, Francke U, Tung JY. Show fewer authors. “Genetic variants associated with breast size also influence breast cancer risk.” BMC Medical Genetics. 30 June 2012. Cancer Traits
  • Li R, Brockschmidt FF, Kiefer AK, Stefansson H, Nyholt DR. et al. Show more authors. Li R, Brockschmidt FF, Kiefer AK, Stefansson H, Nyholt DR, Song K, Vermeulen SH, Kanoni S, Glass D, Medland SE, Dimitriou M, Waterworth D, Tung JY, Geller F, Heilmann S, Hillmer AM, Bataille V, Eigelshoven S, Hanneken S, Moebus S, Herold C, den Heijer M, Montgomery GW, Deloukas P, Eriksson N, Heath AC, Becker T, Sulem P, Mangino M, Vollenweider P, Spector TD, Dedoussis G, Martin NG, Kiemeney LA, Mooser V, Stefansson K, Hinds DA, Nothen MM, Richards JB. Show fewer authors. “Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.” PLoS Genetics. 31 May 2012. Dermatology
  • Eriksson N, Tung JY, Kiefer AK, Hinds DA, Francke U. et al. Show more authors. Eriksson N, Tung JY, Kiefer AK, Hinds DA, Francke U, Mountain JL, Do CB. Show fewer authors. “Novel associations for hypothyroidism include known autoimmune risk loci.” PLoS One. 6 April 2012. Immunity
  • Henn BM, Hon L, Macpherson JM, Eriksson N, Saxonov S. et al. Show more authors. Henn BM, Hon L, Macpherson JM, Eriksson N, Saxonov S, Pe'er I, Mountain JL. Show fewer authors. “Cryptic distant relatives are common in both isolated and cosmopolitan genetic samples.” PLoS One. 3 April 2012. Ancestry Methods
  • Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S. et al. Show more authors. Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, Biernacka JM, Brice A, DeStefano AL, Do CB, Eriksson N, Factor SA, Farrer MJ, Foroud T, Gasser T, Hamza T, Hardy JA, Heutink P, Hill-Burns EM, Klein C, Latourelle JC, Maraganore DM, Martin ER, Martinez M, Myers RH, Nalls MA, Pankratz N, Payami H, Satake W, Scott WK, Sharma M, Singleton AB, Stefansson K, Toda T, Tung JY, Vance J, Wood NW, Zabetian CP; 23andMe Genetic Epidemiology of Parkinson's Disease Consortium; International Parkinson's Disease Genomics Consortium; Parkinson's Disease GWAS Consortium; Wellcome Trust Case Control Consortium 2), Young P, Tanzi RE, Khoury MJ, Zipp F, Lehrach H, Ioannidis JP, Bertram L. Show fewer authors. “Comprehensive research synopsis and systematic meta-analyses in Parkinson’s Disease: The PDGene database.” PLoS Genetics. 15 March 2012. Neurology
  • Lehmann LS, Kaufman DJ, Sharp RR, Moreno TA, Mountain JL. et al. Show more authors. Lehmann LS, Kaufman DJ, Sharp RR, Moreno TA, Mountain JL, Roberts JS, Green RC. Show fewer authors. “Navigating a research partnership between academia and industry to assess the impact of personalized genetic testing.” Genetics in Medicine. 12 January 2012. ELSI
  • Tung JY, Do CB, Hinds DA, Kiefer AK, Macpherson JM. et al. Show more authors. Tung JY, Do CB, Hinds DA, Kiefer AK, Macpherson JM, Chowdry AB, Francke U, Naughton BT, Mountain JL, Wojcicki A, Eriksson N. Show fewer authors. “Efficient replication of over 180 genetic associations with self-reported medical data.” PLoS One. 17 August 2011. Methods
  • Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM. et al. Show more authors. Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, Mountain JL, Goldman SM, Tanner CM, Langston JW, Wojcicki A, Eriksson N. Show fewer authors. “Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson’s disease.” PLoS Genetics. 23 June 2011. Neurology
  • Henn BM, Gignoux CR, Jobin M, Granka JM, Macpherson JM. et al. Show more authors. Henn BM, Gignoux CR, Jobin M, Granka JM, Macpherson JM, Kidd JM, Rodriguez-Botigue L, Ramachandran S, Hon L, Brisbin A, Lin AA, Underhill PA, Comas D, Kidd KK, Norman PJ, Parham P, Bustamante CD, Mountain JL, Feldman MW. Show fewer authors. “Hunter-gatherer genomic diversity suggests a southern African origin for modern humans.” PNAS. 1 March 2011. Ancestry
  • Eriksson N, Macpherson JM, Tung JY, Hon LS, Naughton B. et al. Show more authors. Eriksson N, Macpherson JM, Tung JY, Hon LS, Naughton B, Saxonov S, Avey L, Wojcicki A, Pe'er I, Mountain J. Show fewer authors. “Web-based, participant-driven studies yield novel genetic associations for common traits.” PLoS Genetics. 24 June 2010. Methods

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