Publications

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

We provide access to full summary statistics from published 23andMe research.

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  • Nick Brandon, Ooi Sern, Loh Huiwen, Joo Ho Peh, Milne Roger L. et al. Show more authors.Nick Brandon, Ooi Sern, Loh Huiwen, Joo Ho Peh, Milne Roger L, Giles Graham, Gao Chi , Kraft Peter, John Esther M, Swerdlow Anthony, Brenner Hermann, Wu Anna H, Haiman Christopher D, Evans Gareth, Zheng Wei, Fasching Peter A, Castelao Jose Esteban, Kwong Ava, Shen Xia, Czene Kamila, Hall Per, Dunning Alison, Easton Douglas, Hartman Mikael, Li Jingmei Show fewer authors. “The genetic interplay between body mass index, breast size and breast cancer risk: A Mendelian randomization analysis” International Journal of Epidemiology. 21 July 2019. Cancer
  • Li Qingqin S., Tian Chao, McIntyre Matthew H., Suna Yu, 23andMe Research Team. et al. Show more authors.Li Qingqin S., Tian Chao, McIntyre Matthew H., Suna Yu, 23andMe Research Team, Hinds David A., Narayana Vaibhav A. Show fewer authors. “Phenotypic Analysis of 23andMe Survey Data: Treatment-resistant Depression from Participants’ Perspective” Science Direct. 11 June 2019. Psychiatry
  • Haga Susanne B., Kim Esther, Myers Rachel A., and Ginsburg Geoffrey S..Haga Susanne B., Kim Esther, Myers Rachel A., and Ginsburg Geoffrey S. Show fewer authors. “Primary Care Physicians’ Knowledge, Attitudes, and Experience with Personal Genetic Testing” Journal of Personalized Medicine. 29 May 2019. ELSI
  • Warrington Nicole M., Beaumont Robin N., Horikoshi Momoko, Day Felix R., Helgeland Øyvind. et al. Show more authors.Warrington Nicole M., Beaumont Robin N., Horikoshi Momoko, Day Felix R., Helgeland Øyvind, Laurin Charles, Bacelis Jonas, Peng Shouneng, Hao Ke, Feenstra Bjarke, Wood Andrew R., Mahajan Anubha, Tyrrell Jessica, Neil R. Robertson, N. William Rayner, Zhen Qiao, Gunn-Helen Moen, Marc Vaudel, Carmen J. Marsit, Jia Chen, Michael Nodzenski, Theresia M. Schnurr, Mohammad H. Zafarmand, Jonathan P. Bradfield, Niels Grarup, Marjolein N. Kooijman, Ruifang Li-Gao, Frank Geller, Tarunveer S. Ahluwalia, Lavinia Paternoster, Rico Rueedi, Ville Huikari, Jouke-Jan Hottenga, Leo-Pekka Lyytikäinen, Alana Cavadino, Sarah Metrustry, Diana L. Cousminer, Ying Wu, Elisabeth Thiering, Carol A. Wang, Christian T. Have, Natalia Vilor-Tejedor, Peter K. Joshi, Jodie N. Painter, Ioanna Ntalla, Ronny Myhre, Niina Pitkänen, Elisabeth M. van Leeuwen, Raimo Joro, Vasiliki Lagou, Rebecca C. Richmond, Ana Espinosa, Sheila J. Barton, Hazel M. Inskip, John W. Holloway, Loreto Santa-Marina, Xavier Estivill, Wei Ang, Julie A. Marsh, Christoph Reichetzeder, Letizia Marullo, Berthold Hocher, Kathryn L. Lunetta, Joanne M. Murabito, Caroline L. Relton, Manolis Kogevinas, Leda Chatzi, Catherine Allard, Luigi Bouchard, Marie-France Hivert, Ge Zhang, Louis J. Muglia, Jani Heikkinen, EGG Consortium, Camilla S. Morgen, Antoine H. C. van Kampen, Barbera D. C. van Schaik, Frank D. Mentch, Claudia Langenberg, Jian’an Luan, Robert A. Scott, Jing Hua Zhao, Gibran Hemani, Susan M. Ring, Amanda J. Bennett, Kyle J. Gaulton, Juan Fernandez-Tajes, Natalie R. van Zuydam, Carolina Medina-Gomez, Hugoline G. de Haan, Frits R. Rosendaal, Zoltán Kutalik, Pedro Marques-Vidal, Shikta Das, Gonneke Willemsen, Hamdi Mbarek, Martina Müller-Nurasyid, Marie Standl, Emil V. R. Appel, Cilius E. Fonvig, Caecilie Trier, Catharina E. M. van Beijsterveldt, Mario Murcia, Mariona Bustamante, Sílvia Bonas-Guarch, David M. Hougaard, Josep M. Mercader, Allan Linneberg, Katharina E. Schraut, Penelope A. Lind, Sarah E. Medland, Beverley M. Shields, Bridget A. Knight, Jin-Fang Chai, Kalliope Panoutsopoulou, Meike Bartels, Friman Sánchez, Jakob Stokholm, David Torrents, Rebecca K. Vinding, Sara M. Willems, Mustafa Atalay, Bo L. Chawes, Peter Kovacs, Inga Prokopenko, Marcus A. Tuke, Hanieh Yaghootkar, Katherine S. Ruth, Samuel E. Jones, Po-Ru Loh, Anna Murray, Michael N. Weedon, Anke Tönjes, Michael Stumvoll, Kim F. Michaelsen, Aino-Maija Eloranta, Timo A. Lakka, Cornelia M. van Duijn, Wieland Kiess, Antje Körner, Harri Niinikoski, Katja Pahkala, Olli T. Raitakari, Bo Jacobsson, Eleftheria Zeggini, George V. Dedoussis, Yik-Ying Teo, Seang-Mei Saw, Grant W. Montgomery, Harry Campbell, James F. Wilson, Tanja G. M. Vrijkotte, Martine Vrijheid, Eco J. C. N. de Geus, M. Geoffrey Hayes, Haja N. Kadarmideen, Jens-Christian Holm, Lawrence J. Beilin, Craig E. Pennell, Joachim Heinrich, Linda S. Adair, Judith B. Borja, Karen L. Mohlke, Johan G. Eriksson, Elisabeth E. Widén, Andrew T. Hattersley, Tim D. Spector, Mika Kähönen, Jorma S. Viikari, Terho Lehtimäki, Dorret I. Boomsma, Sylvain Sebert, Peter Vollenweider, Thorkild I. A. Sørensen, Hans Bisgaard, Klaus Bønnelykke, Jeffrey C. Murray, Mads Melbye, Ellen A. Nohr, Dennis O. Mook-Kanamori, Fernando Rivadeneira, Albert Hofman, Janine F. Felix, Vincent W. V. Jaddoe, Torben Hansen, Charlotta Pisinger, Allan A. Vaag, Oluf Pedersen, André G. Uitterlinden, Marjo-Riitta Järvelin, Christine Power, Elina Hyppönen, Denise M. Scholtens, William L. Lowe Jr, George Davey Smith, Nicholas J. Timpson, Andrew P. Morris, Nicholas J. Wareham, Hakon Hakonarson, Struan F. A. Grant, Timothy M. Frayling, Debbie A. Lawlor, Pål R. Njølstad, Stefan Johansson, Ken K. Ong, Mark I. McCarthy, John R. B. Perry, David M. Evans & Rachel M. Freathy Show fewer authors. “Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic disease” Nature Genetics. 1 May 2019. Reproduction
  • Blauwendraat Cornelis, Heilbron Karl, Vallerga Costanza L., Bandres-Ciga Sara, Rainer von Coelln. et al. Show more authors.Blauwendraat Cornelis, Heilbron Karl, Vallerga Costanza L., Bandres-Ciga Sara, Rainer von Coelln, Pihlstrøm Lasse, Simón-Sánchez Javier, Schulte Claudia, Manu Sharma, Lynne Krohn, Ari Siitonen, Hirotaka Iwaki, Hampton Leonard, Alastair J. Noyce, Manuela Tan, J. Raphael Gibbs, Dena G. Hernandez, Sonja W. Scholz, Joseph Jankovic, Lisa M. Shulman, Suzanne Lesage, Jean-Christophe Corvol, Alexis Brice, Jacobus J. van Hilten, Johan Marinus, The 23andMe Research Team, Pentti Tienari, Kari Majamaa, Mathias Toft, Donald G. Grosset, Thomas Gasser, Peter Heutink, Joshua M Shulman, Nicolas Wood, John Hardy, Huw R Morris, David A. Hinds, Jacob Gratten, Peter M. Visscher, Ziv Gan-Or, Mike A. Nalls, Andrew B. Singleton, for the International Parkinson’s Disease Genomics Consortium (IPDGC) Show fewer authors. “Parkinson’s disease age of onset: defining heritability, identifying genetic loci, implicating α-synuclein mechanisms” Movement Disorders. 7 April 2019. [bioRxiv] Neurology
  • Ferreira Manuel A.R., Mathur Riddhima, Vonk Judith M., Szwajda Agnieszka, Brumpton Ben. et al. Show more authors.Ferreira Manuel A.R., Mathur Riddhima, Vonk Judith M., Szwajda Agnieszka, Brumpton Ben, Granell Raquel, Brew Bronwyn K., Ullemar Vilhelmina, Lu Yi, Jiang Yunxuan, 23andMe Research Team, eQTLGen Consortium, BIOS Consortium, Magnusson Patrik K.E., Karlsson Robert, Hinds David A., Paternoster Lavinia, Koppelman Gerard H., Almqvist Catarina Show fewer authors. “Genetic risk factors for childhood- and adult-onset asthma are partly distinct” American Journal of Human Genetics. 4 April 2019. Immunity
  • Heilbron Karl, Noyce Alastair J., Fontanillas Pierre, Alipanahi Babak, Nalls Mike A.. et al. Show more authors.Heilbron Karl, Noyce Alastair J., Fontanillas Pierre, Alipanahi Babak, Nalls Mike A., The 23andMe Research Team & Cannon Paul Show fewer authors. “The Parkinson’s Phenome: Traits Associated with Parkinson’s in a Deeply Phenotyped Cohort” Nature Parkinson's Disease. 27 March 2019. Neurology
  • Dudding Tom, Haworth Simon, Lind Penelope A., Sathirapongsasuti Fah, 23andMe Research Team. et al. Show more authors.Dudding Tom, Haworth Simon, Lind Penelope A., Sathirapongsasuti Fah, 23andMe Research Team, Tung Joyce Y., Mitchell Ruth, Colodro-Conde Lucía, Medland Sarah E., Scott Gordon, Benjamin Elsworth, Lavinia Paternoster, Paul W. Franks, Steven J. Thomas, Nicholas G. Martin & Nicholas J. Timpson Show fewer authors. “Genome wide analysis for mouth ulcers in representative populations identifies association at immune regulatory loci.” Nature Communications. 5 March 2019. Dermatology
  • Grove Jakob, Ripke Stephan, Als Thomas D., Mattheisen Manuel, Walters Raymond. et al. Show more authors.Grove Jakob, Ripke Stephan, Als Thomas D., Mattheisen Manuel, Walters Raymond, Won Hyejung, Pallesen Jonatan, Agerbo Esben, Andreassen Ole A., Anney Richard, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg-Grauholm, Marie Bækved-Hansen, Felecia Cerrato, Kimberly Chambert, Jane H. Christensen, Claire Churchhouse, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashle Dumont, Jacqueline Goldstein, Christine S. Hansen, Mads Engel Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten B. Pedersen, Marianne G. Pedersen, Timothy Poterba, Jesper B. Poulsen, Beate St Pourcain, Per Qvist, Karola Rehnström, Avi Reichenberg, Jennifer Reichert, Elise B. Robinson, Kathryn Roeder, Panos Roussos, Evald Saemundsen, Sven Sandin, F. Kyle Satterstrom, George D. Smith, Hreinn Stefansson, Kari Stefansson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium, BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 23andMe Research Team, Daniel Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum Show fewer authors. “Common risk variants identified in autism spectrum disorder” Nature Genetics. 25 February 2019. [bioRxiv] Neurology
  • Sanchez-Roige S, Fontanillas P, Elson SL, Gray JC, de Wit H. et al. Show more authors.Sanchez-Roige S, Fontanillas P, Elson SL, Gray JC, de Wit H, MacKillop J, Palmer AA. Show fewer authors. “Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes.” Journal of Neuroscience. 4 February 2019. Behavior
  • Howard DM, Adams MJ, Clarke T, Hafferty JD, Gibson J. et al. Show more authors.Howard DM, Adams MJ, Clarke T, Hafferty JD, Gibson J, Shirali M, Coleman JRI, Hagenaars SP, Ward J, Wigmore EM, Alloza C, Shen X, Barbu MC, Xu EY, Whalley HC, Marioni RE, Porteous DJ, Davies G, Deary IJ, Hemani G, Berger K, Teismann H, Rawal R, Arolt V, Baune BT, Dannlowski U, Domschke K, Tian C, Hinds DA, 23andMe Research Team, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Trzaskowski M, Byren EM, Ripke S, Smith DJ, Sullivan PF, Wray NR, Breen G, Lewis CM, McIntosh AM. Show fewer authors. “Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.” Nature Neuroscience. 4 February 2019. Psychiatry
  • Jones SE, Lane JM, Wood AR, van Hees VT, Tyrrell J. et al. Show more authors.Jones SE, Lane JM, Wood AR, van Hees VT, Tyrrell J, Beaumont RN, Jeffries AR, Dashti HS, Hillsdon M, Ruth KS, Tuke MA, Yaghootkar H, Sharp SA, Jie Y, Thompson WD, Harrison JW, Dawes A, Byren EM, Tiemeier H, Allebrandt KV, Bowden J, Ray DW, Freathy RM, Murray A, Mazzotti DR, Gehrman PR, Lawlor DA, Frayling TM, Rutter MK, Hinds DA, Saxena R, Weedon, MN. Show fewer authors. “Genome-wide association analyses of chronotype in 697,828 individuals provides new insights into circadian rhythms in humans and links to disease.” Nature Communications. 29 January 2019. Neurology
  • Liu M, Jiang Y, Wedow R, Li Y, Brazel DM. et al. Show more authors.Liu M, Jiang Y, Wedow R, Li Y, Brazel DM, Chen F, Datta G, Davila-Velderrain J, McGuire D, Tian C, Zhan X, 23andMe Research Team, HUNT All-In Psychiatry, Choquet H, Docherty AR, Faul JD, Foerster JR, Fristche LG, Gabrielsen ME, Gordon SD, Haessler J, Hottenga J, Huang H, Jang S, Jansen PR, Ling Y, Mägi R, Matoba N, McMahon G, Mulas A, Orrù V, Palviainen T, Pandit A, Reginsson GW, Skogholt AH, Smith JA, Taylor AE, Turman C, Willemsen G, Young H, Young KA, Zajac GJM, Zhao W, Zhou W, Bjornsdottir G, Boardman JD, Boehnke M, Boomsma DI, Chen C, Cucca F, Davies GE, Eaton CB, Ehringer MA, Esko T, Fiorillo E, Gillespie NA, Gudbjartsson DF, Haller T, Harris KM, Heath AC, Hewitt JK, Hickie IB, Hokanson JE, Hopfer CJ, Hunger DJ, Iacono WG, Johnson EO, Kamatani Y, Kardia SLR, Keller MC, Kellis M, Kooperberg C, Kraft P, Krauter KS, Laakso M, Lind PA, Luokola A, Lutz SM, Madden PAF, Martin NG, McGue M, McQueen MB, Medland SE, Metspalu A, Mohlke KL, Nielsen JB, Okada Y, Peters U, Polderman TJC, Posthuma D, Reiner AP, Rice JP, Rimm E, Rose RJ, Runarsdottir V, Stallings MC, Stančáková, Stegansson H, Thai KK, Tindle HA, Tyrfingsson T, Wall TL, Weir DR, Weisner C, Whitfield JB, Winsvold BS, Yin J, Zuccolo L, Bierut LJ, Hveem K, Lee JJ, Munafò, Sccone NL, Willer CJ, Corenlis MC, David SP, Hinds DA, Jorgenson E, Kaprio J, Stitzel JA, Stefansson K, Thorgeirsson TE, Abecasis G, Liu DJ, Vrieze S. Show fewer authors. “Association studies of up to 1.2 million individuals yield new insights in the genetic etiology of tobacco and alcohol use.” Nature Genetics. 14 January 2019. Behavior
  • Linnér RK, Biroli P, Kong E, Meddens SFW, Wedow R. et al. Show more authors.Linnér RK, Biroli P, Kong E, Meddens SFW, Wedow R, Fontana MA, Lebreton M, Abdellaoui A, Hammerschlag AR, Nivard MG, Okbay A, Rietveld CA, Timshel PN, Tino SP, Trzaskowski M, de Vlaming R, Zünd CL, Bao Y, Buzdugan L, Caplin AH, Chen C, Eibich P, Fontanillas P, Gonzalez JR, Joshi PK, Karhunen V, Kleinman A, Levin RZ, Lill CM, Meddens GA, Muntané G, Sanchez-Roige S, van Rooij FJ, Taskesen E, Wu Y, Zhang F, 23andMe Research Team, eQTLgen Consortium, International Cannabis Consortium, Psychiatric Genomics Consortium, Social Science Genetic Association Consortium, Auton A, Boardman JD, Clark DW, Conlin A, Dolan CC, Fischbacher U, Groenen PJF, Harris KM, Hasler G, Hofman A, Ikram M, Jain S, Karlsson R, Kessler R, Kooyman M, MacKillop J, Männikkö M, Morcillo-Suarez C, McQueen MB, Schmidt KM, Smart MC, Sutter M, Thurik AR, Uitterlinden AG, White J, de Wit H, Yang J, Bertram L, Boomsma D, Esko T, Fehr E, Hinds DA, Johannesson M, Kumari M, Laibson D, Magnusson PKE, Meyer MN, Navarro A, Palmer AA, Pers TH, Posthuma D, Schunk D, Stein MB, Svento R, Tiemeier H, Timmers PRHJ, Turley P, Ursano RJ, Wagner GG, Wilson JF, Gratten J, Lee JJ, Cesarini D, Benjamin DJ, Koellinger P, Beauchamp JP. Show fewer authors. “GWAS of risk tolerance and risky behaviors in over one million individuals identify hundreds of loci and reveal shared genetic influences.” Nature Genetics. 14 January 2019. Behavior
  • Day F, Karaderi T, Jones MR, Meun C, He C. et al. Show more authors.Day F, Karaderi T, Jones MR, Meun C, He C, Drong A, Kraft P, Lin N, Huang H, Broer L, Magi R, Saxena R, Laisk T, Urbanek M, Hayes MG, Thorleitfsson G, Fernandez-Tajes J, Mahajan A, Mullin BH, Stuckey MGA, Spector TD, Wilson SG, Goodarzi MO, Davis L, Obermayer-Pietsch B, Uitterlinden AG, Anttila V, Neale BM, Jarvelin M, Fauser B, Kowalska I, Visser JA, Andersen M, Ong K, Stener-Victorin E, Ehrmann D, Legro RS, Salumets A, McCarthy MI, Morin-Papunen L, Thorsteinsdottir U, Stegansson K, the 23andMe Research Team, Styrkarsdottir U, Perry JRB, Dunaif A, Laven K, Franks S, Lindgren CM, Welt CK. Show fewer authors. “Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.” PLoS Genetics. 19 December 2018. Reproduction
  • Demontis D, Walters RK, Martin J, Mattheisen M, Als TD. et al. Show more authors.Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E, Baldursson G, Belliveau R, Bybjerg-Grauholm J, Bækvad-Hansen M, Cerrato F, Chambert K, Churchhouse C, Dumont A, Eriksson N, Gandal M, Goldstein JI, Grasby KL, Grove J, Gudmundsson OO, Hansen CS, Hauberg ME, Hollegaard MV, Howrigan DP, Huang H, Maller JB, Martin AR, Martin NG, Moran J, Pallesen J, Palmer DS, Pedersen CB, Pedersen MG, Poterba T, Poulsen JB, Ripke S, Robinson E, Satterstrom FK, Stegansson H, Stevens C, Turley P, Walters GB, Won H, Wright MJ, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium, 23andMe Research Team, Andreassen OE, Asherson P, Burton CL, Boomsma DI, Cormand B, Dalsgaard S, franke B, Gelernter J, Geschwind D, Hakonarson H, Haavik J, Kranzler HR, Kuntsi J, Langley K, Lesch K, Middeldorp C, Reif A, Rohde LA, Roussos P, Schachar R, Sklar P, Sonuga-Barke EJS, Sullivan PF, Thapar A, Tung JY, Waldman ID, Medland SE, Stefansson K, Nordentoft M, Hougaard DM, Werge T, Mors O, Mortensen PB, Daly MJ, Faraone SV, Børglum AD, Neale BM. Show fewer authors. “Discovery of the first genome-wide significant risk loci for ADHD.” Nature Genetics. 26 November 2018. Psychiatry
  • Walters RK, Adams MJ, Adkins AE, Aliev F, Bacanu S. et al. Show more authors.Walters RK, Adams MJ, Adkins AE, Aliev F, Bacanu S, Batzler A, Bertelsen S, Biernacka J, Bigdeli TB, Chen L, Clark T, Chou Y, Degenhardt F, Docherty AR, Fontanillas P, Foo J, Fox L, Frank J, Giegling I, Gordon S, Hack L, Hartz S, Heilmann-Heimbach S, Herms S, Hodgkinson C, Hoffmann P, Hottenga J, Kennedy MA, Alanne-Kinnunen M, Knote B, Lahti J, Lahti-Pulkkinen M, Ligthart L, Loukola A, Maher BS, Mbarek H, McIntosh AM, McQueen MB, Milaneschi Y, Palviainen T, Pearson J, Peterson R, Polimanti R, Ripatti S, Ryu E, Saccone N, Salvatore J, Sanchez-Roige S, Schwandt M, Sherva R, Streit F, Strohmaier J, Thomas N, Wang J, Webb BT, Wedow R, Wetherill L, Wills AG, 23andMe Research Team, Boardman J, Chen D, Choi D, Copeland WE, Culverhouse RC, Dahmen N, Degenhardt L, Domingue BW, Elson SL, Frye M, Gäbel W, Ising M, Johnson EC, Keyes M, Kiefer F, Kramer J, Kuperman S, Lucae S, Lynskey MT, Maier W, Mann K, Männistö, McClintick JN, Meyers JL, Müller-Myhsok B, Nurnberger JI, Palotie A, Preuss U, Räikkönen K, Reynolds MD, Ridinger M, Scherbaum N, Shuckit M, Soyka M, Treutlein J, Witt S, Wodarz N, Zill P, Adkins D, Boden JM, Boomsma D, Bierut LJ, Brown SA, Bucholz KK, Chicho S, Costello EJ, de Wit H, Diazgranados N, Dick DM, Eriksson JG, Farrer LA, Foroud TM, Gillespie NA, Goate AA, Goldman D, Grucza RA, Hancock DB, Harris KM, Heath AC, Hesselbrock V, Hewitt JK, Hopfer C, Horwood J, Iacono W, Johnson EO, Kaprio JA, Karpyak V, Kendler KS, Kranzler HR, Krauter K, Lichtenstein P, Lind PA, McGue M, MacKillop J, Madden PAF, Maes H, Magnusson P, Martin NG, Medland SE, Montgomery GW, Nelson EC, Nöthen M, Palmer AA, Pedersen NL, Penninx BWJH, Porjesz B, Rice JP, Rietschel M, Riley BP, Rose R, Rujescu D, Shen P, Silberg J, Stallings MC, Tarter RE, Vanyukov MM, Vrieze S, Wall TL, Whitfield JB, Zhao H, Neale BM, Gelernter J, Edenberg HJ, Agrawal A. Show fewer authors. “Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders.” Nature Neuroscience. 26 November 2018. Behavior
  • Orlova E, Yeh A, Shi M, Firek B, Ranganathan S. et al. Show more authors.Orlova E, Yeh A, Shi M, Firek B, Ranganathan S, 23andMe Research Team, Whitcomb DC, Finegold DN, Ferrel RE, Barmada MM, Marazita ML, Hinds DA, Shaffer JR, Morowitz MJ Show fewer authors. “Genetic association and differential expression of PITX2 with acute appendicitis.” Human Genetics. 3 November 2018. Immunity
  • Sanchez-Roige S, Palmer AA, Fontanillas P, Elson S, 23andMe Research Team. et al. Show more authors.Sanchez-Roige S, Palmer AA, Fontanillas P, Elson S, 23andMe Research Team, Substance Use Disorder Working Group of the Psychiatric Genomics Consortium, Adams MJ, Howard DM, Edenberg HJ, Davies G, Crist RC, Deary I, McIntosh AM, Clarke TK Show fewer authors. “Meta-analysis GWAS of the Alcohol Use Disorder Identification Test (AUDIT) in two population based cohorts (N=141,958).” American Journal of Psychiatry. 19 October 2018. [bioRxiv] Behavior Psychiatry
  • Diogo D, Tian C, Franklin C, Alanne-Kinnunen M, March M. et al. Show more authors.Diogo D, Tian C, Franklin C, Alanne-Kinnunen M, March M, Spencer C, Vangjeli C, Weale M, Mattsson H, Elina K, Sleiman P, Reilly D, McElwee J, Maranville J, Chatterjee A, Bhandari A, 23andMe Research Team, Reeve M, Hutz J, Bing N, John S, MacArthur D, Salomaa V, Ripatti S, Hakonarson H, Daly M, Palotie A, Hinds D, Donnelly P, Fox C, Day-Williams A, Plenge R, Runz H. Show fewer authors. “Phenome-wide association studies across large ‘real-world data’ population cohorts support drug target validation.” Nature Communications. 16 October 2018. Methods
  • Ioannidis NM, Wang W, Fulotte NA, Hinds DA, 23andMe Research Team. et al. Show more authors.Ioannidis NM, Wang W, Fulotte NA, Hinds DA, 23andMe Research Team, Bustamante CD, Jorgenson E, Asgari MM, Whittemore AS. Show fewer authors. “Gene expression imputation identifies candidate genes and susceptibility loci associated with risk of cutaneous squamous cell carcinoma.” Nature Communications. 15 October 2018. Cancer
  • Trajanoska K, Morris JA, Oei L, Zheng H, Evans DM. et al. Show more authors.Trajanoska K, Morris JA, Oei L, Zheng H, Evans DM, Kiel DP, Ohlsson C, Richards JB, Rivadeneira F, the 23andMe Research Team. Show fewer authors. “Assessment of the genetic and clinical determinants of fracture risk: genome wide association and Mendelian randomisation study.” British Medical Journal. 29 August 2018. Musculoskeletal
  • Winslow AR, Hyde GL, Wilk JB, Eriksson N, Cannon P. et al. Show more authors.Winslow AR, Hyde GL, Wilk JB, Eriksson N, Cannon P, Miller MR, Hirst WD. Show fewer authors. “Self-report data as a tool for subtype identification in genetically-defined Parkinson’s Disease.” Scientific Reports. 28 August 2018. Neurology
  • Pasman JA, Verweij KJH, Gerring Z, Stringer S, Sanchez-Roige S. et al. Show more authors.Pasman JA, Verweij KJH, Gerring Z, Stringer S, Sanchez-Roige S, Treur JL, Abdellaoui A, Nivard MG, Baselmans BML, Ong J, Ip HF, van der Zee MD, Bartels M, Day JF, Fontanillas P, Elson SL, the 23andMe Research Team, de Wit H, Davis LK, MacKillop J, International Cannabis Consortium, Derringer JL, Branje SJT, Hartman CA, Heath AC, van Lier PAC, Madden PAF, Magi R, Meeus W, Montgomery GW, Oldehinkel AJ, Pausova Z, Ramos-Quiroga JA, Paus T, Ribases M, Kaprio J, Boks MPM, Bell JT, Spector TD, Gelernter J, Boomsma DI, Martin NG, MacGregor S, Perry JRB, Palmer AA, Posthuma D, Manuafo MR, Gillespie NA, Derks EM, Vink JM. Show fewer authors. “GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia.” Nature Neuroscience. 27 August 2018. Behavior
  • Jones HJ, Heron J, Hammerton G, Stochl J, Jones PB. et al. Show more authors.Jones HJ, Heron J, Hammerton G, Stochl J, Jones PB, Cannon M, Smith GD, Holmans P, Lewis G, Linden DEJ, O'Donovan MC, Owen MJ, Walters J, Zammit S, 23andMe Research Team. Show fewer authors. “Investigating the genetic architecture of general and specific psychopathology in adolescence.” Translational Psychiatry. 8 August 2018. Psychiatry
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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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