The association of clinical phenotypes to known AD/FTD genetic risk loci and their inter-relationship.

by Qingqin S Li, Chao Tian, 23andMe Research Team, David Hinds, Guy R Seabrook
Published 2020-01-01

Validity of the cold pressor test and pain sensitivity questionnaire via online self-administration.

by Matthew H McIntyre, 23andMe Research Team, Achim Kless, Peter Hein, Mark Field, Joyce Y Tung
Published 2020-01-01

Transcriptome-wide association study identifies new susceptibility genes and pathways for depression

by Xiaoyan Li, Xi Su, Jiewei Liu, Huijuan Li, Ming Li, the 23andMe Research Team, Wenqiang Li, Xiong-Jian Luo
Published 2021-05-01

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

by Yanjun Guo, Pamela M. Rist, Iyas Daghlas, Franco Giulianini, The International Headache Genetics Consortium, The 23andMe Research Team, Tobias Kurth, Daniel I. Chasman
Published 2020-07-01

Disease risk scores for skin cancers

by Pierre Fontanillas, Babak Alipanahi, Nicholas A. Furlotte, Michaela Johnson, Catherine H. Wilson, 23andMe Research Team, Steven J. Pitts, Robert Gentleman, Adam Auton
Published 2021-01-01

A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort

by Karen A. Schlauch, Robert W. Read, Vincent C. Lombardi, Gai Elhanan, William J. Metcalf, Anthony D. Slonim, the 23andMe Research Team, Joseph J. Grzymski
Published 2020-02-01

Gene expression imputation identifies candidate genes and susceptibility loci associated with cutaneous squamous cell carcinoma

by Nilah M. Ioannidis, Wei Wang, Nicholas A. Furlotte, David A. Hinds, 23andMe Research Team, Carlos D. Bustamante, Eric Jorgenson, Maryam M. Asgari, Alice S. Whittemore
Published 2018-10-01

Fox Insight collects online, longitudinal patient-reported outcomes and genetic data on Parkinson’s disease

by Luba Smolensky, Ninad Amondikar, Karen Crawford, Scott Neu, Catherine M. Kopil, Margaret Daeschler, Lindsey Riley, 23andMe Research Team, Ethan Brown, Arthur W. Toga, Caroline Tanner
Published 2020-02-01

Distinct clinical phenotypes for Crohn’s disease derived from patient surveys

by Tianyun Liu, Lichy Han, Mera Tilley, Lovisa Afzelius, Mateusz Maciejewski, Scott Jelinsky, Chao Tian, Matthew McIntyre, the 23andMe Research Team, Nan Bing, Kenneth Hung, Russ B. Altman
Published 2021-04-01

Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure

by Marios Arvanitis, Emmanouil Tampakakis, Yanxiao Zhang, Wei Wang, Adam Auton, 23andMe Research Team, Diptavo Dutta, Stephanie Glavaris, Ali Keramati, Nilanjan Chatterjee, Neil C. Chi, Bing Ren, Wendy S. Post, Alexis Battle
Published 2020-02-01

Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum

by Marlena S. Fejzo, Olga V. Sazonova, J. Fah Sathirapongsasuti, Ingileif B. Hallgrímsdóttir, Vladimir Vacic, Kimber W. MacGibbon, Frederic P. Schoenberg, Nicholas Mancuso, Dennis J. Slamon, Patrick M. Mullin, 23andMe Research Team
Published 2018-03-01

A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects

by Hélène Choquet, Ronald B. Melles, Deepti Anand, Jie Yin, Gabriel Cuellar-Partida, Wei Wang, 23andMe Research Team, Thomas J. Hoffmann, K. Saidas Nair, Pirro G. Hysi, Salil A. Lachke, Eric Jorgenson
Published 2021-06-01

Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity

by Emmanuel O. Adewuyi, Yadav Sapkota, International Endogene Consortium (IEC), 23andMe Research Team, International Headache Genetics Consortium (IHGC), Asa Auta, Kosuke Yoshihara, Mette Nyegaard, Lyn R. Griffiths, Grant W. Montgomery, Daniel I. Chasman, Dale R. Nyholt
Published 2020-02-01

Genetic determinants of daytime napping and effects on cardiometabolic health

by Hassan S. Dashti, Iyas Daghlas, Jacqueline M. Lane, Yunru Huang, Miriam S. Udler, Heming Wang, Hanna M. Ollila, Samuel E. Jones, Jaegil Kim, Andrew R. Wood, 23andMe Research Team, Michael N. Weedon, Stella Aslibekyan, Marta Garaulet, Richa Saxena
Published 2021-02-01

Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan

by Ben Hollis, Felix R. Day, Alexander S. Busch, Deborah J. Thompson, Ana Luiza G. Soares, Paul R. H. J. Timmers, Alex Kwong, Doug F. Easton, Peter K. Joshi, Nicholas J. Timpson, The PRACTICAL Consortium, 23andMe Research Team, Ken K. Ong, John R. B. Perry
Published 2020-03-01

Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci

by Tom Dudding, Simon Haworth, Penelope A. Lind, J. Fah Sathirapongsasuti, 23andMe Research Team, Joyce Y. Tung, Ruth Mitchell, Lucía Colodro-Conde, Sarah E. Medland, Scott Gordon, Benjamin Elsworth, Lavinia Paternoster, Paul W. Franks, Steven J. Thomas, Nicholas G. Martin, Nicholas J. Timpson
Published 2019-03-01

FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression

by Kia Joo Puan, Boris San Luis, Nurhashikin Yusof, Dilip Kumar, Anand Kumar Andiappan, Wendy Lee, Samanta Cajic, Dragana Vuckovic, Jing De Chan, Tobias Döllner, Han Wei Hou, Yunxuan Jiang, Chao Tian, the 23andMe Research Team, Erdmann Rapp, Michael Poidinger, De Yun Wang, Nicole Soranzo, Bernett Lee, Olaf Rötzschke
Published 2021-07-01

Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

by Jiyuan An, Puya Gharahkhani, Matthew H. Law, Jue-Sheng Ong, Xikun Han, Catherine M. Olsen, Rachel E. Neale, John Lai, Tom L. Vaughan, Ines Gockel, René Thieme, Anne C. Böhmer, Janusz Jankowski, Rebecca C. Fitzgerald, Johannes Schumacher, Claire Palles, BEACON, 23andMe Research Team, David C. Whiteman, Stuart MacGregor
Published 2019-09-01

Author Correction: Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases

by Jiyuan An, Puya Gharahkhani, Matthew H. Law, Jue-Sheng Ong, Xikun Han, Catherine M. Olsen, Rachel E. Neale, John Lai, Tom L. Vaughan, Ines Gockel, René Thieme, Anne C. Böhmer, Janusz Jankowski, Rebecca C. Fitzgerald, Johannes Schumacher, Claire Palles, BEACON, 23andMe Research Team, David C. Whiteman, Stuart MacGregor
Published 2019-12-01