Hasil Pencarian - 23 and Me Research Team

Perbaiki Hasil
  1. 1
    Further validation of the THINC‐it tool and extension of the normative data set in a study of n = 10.019 typical controls

    Further validation of the THINC‐it tool and extension of the normative data set in a study of n = 10.019 typical controls oleh Maria Dalby, Peter Annas, 23andMe Research Team, John E. Harrison

    Diterbitkan 2022-12-01
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  2. 2
    The association of clinical phenotypes to known AD/FTD genetic risk loci and their inter-relationship.

    The association of clinical phenotypes to known AD/FTD genetic risk loci and their inter-relationship. oleh Qingqin S Li, Chao Tian, 23andMe Research Team, David Hinds, Guy R Seabrook

    Diterbitkan 2020-01-01
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  3. 3
    The genetic architecture of pneumonia susceptibility implicates mucin biology and a relationship with psychiatric illness

    The genetic architecture of pneumonia susceptibility implicates mucin biology and a relationship with psychiatric illness oleh William R. Reay, Michael P. Geaghan, 23andMe Research Team, Murray J. Cairns

    Diterbitkan 2022-06-01
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  4. 4
    Using a polygenic score in a family design to understand genetic influences on musicality

    Using a polygenic score in a family design to understand genetic influences on musicality oleh Laura W. Wesseldijk, Abdel Abdellaoui, Reyna L. Gordon, 23andMe Research Team, Fredrik Ullén, Miriam A. Mosing

    Diterbitkan 2022-08-01
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  5. 5
    Validity of the cold pressor test and pain sensitivity questionnaire via online self-administration.

    Validity of the cold pressor test and pain sensitivity questionnaire via online self-administration. oleh Matthew H McIntyre, 23andMe Research Team, Achim Kless, Peter Hein, Mark Field, Joyce Y Tung

    Diterbitkan 2020-01-01
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  6. 6
    Transcriptome-wide association study identifies new susceptibility genes and pathways for depression

    Transcriptome-wide association study identifies new susceptibility genes and pathways for depression oleh Xiaoyan Li, Xi Su, Jiewei Liu, Huijuan Li, Ming Li, the 23andMe Research Team, Wenqiang Li, Xiong-Jian Luo

    Diterbitkan 2021-05-01
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  7. 7
    Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma

    Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma oleh Hélène Choquet, Chen Jiang, Jie Yin, Yuhree Kim, Thomas J. Hoffmann, 23andMe Research Team, Eric Jorgenson, Maryam M. Asgari

    Diterbitkan 2024-01-01
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  8. 8
    Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets

    Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets oleh Carla Márquez-Luna, Steven Gazal, Po-Ru Loh, Samuel S. Kim, Nicholas Furlotte, Adam Auton, 23andMe Research Team, Alkes L. Price

    Diterbitkan 2021-10-01
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  9. 9
    A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

    A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine oleh Yanjun Guo, Pamela M. Rist, Iyas Daghlas, Franco Giulianini, The International Headache Genetics Consortium, The 23andMe Research Team, Tobias Kurth, Daniel I. Chasman

    Diterbitkan 2020-07-01
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  10. 10
    Analysis of rare Parkinson’s disease variants in millions of people

    Analysis of rare Parkinson’s disease variants in millions of people oleh Vanessa Pitz, Mary B. Makarious, Sara Bandres-Ciga, Hirotaka Iwaki, 23andMe Research Team, Andrew B. Singleton, Mike Nalls, Karl Heilbron, Cornelis Blauwendraat

    Diterbitkan 2024-01-01
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  11. 11
    Disease risk scores for skin cancers

    Disease risk scores for skin cancers oleh Pierre Fontanillas, Babak Alipanahi, Nicholas A. Furlotte, Michaela Johnson, Catherine H. Wilson, 23andMe Research Team, Steven J. Pitts, Robert Gentleman, Adam Auton

    Diterbitkan 2021-01-01
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  12. 12
    A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort

    A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort oleh Karen A. Schlauch, Robert W. Read, Vincent C. Lombardi, Gai Elhanan, William J. Metcalf, Anthony D. Slonim, the 23andMe Research Team, Joseph J. Grzymski

    Diterbitkan 2020-02-01
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  13. 13
    Gene expression imputation identifies candidate genes and susceptibility loci associated with cutaneous squamous cell carcinoma

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

    Diterbitkan 2018-10-01
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  14. 14
    A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma

    A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma oleh Mathias Seviiri, Matthew H. Law, Jue-Sheng Ong, Puya Gharahkhani, Pierre Fontanillas, The 23andMe Research Team, Catherine M. Olsen, David C. Whiteman, Stuart MacGregor

    Diterbitkan 2022-12-01
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  15. 15
    Genome-wide association analysis and replication in 810,625 individuals with varicose veins

    Genome-wide association analysis and replication in 810,625 individuals with varicose veins oleh Waheed-Ul-Rahman Ahmed, Sam Kleeman, Michael Ng, Wei Wang, Adam Auton, 23andMe Research Team, Regent Lee, Ashok Handa, Krina T. Zondervan, Akira Wiberg, Dominic Furniss

    Diterbitkan 2022-06-01
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  16. 16
    Fox Insight collects online, longitudinal patient-reported outcomes and genetic data on Parkinson’s disease

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

    Diterbitkan 2020-02-01
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  17. 17
    An ensemble penalized regression method for multi-ancestry polygenic risk prediction

    An ensemble penalized regression method for multi-ancestry polygenic risk prediction oleh Jingning Zhang, Jianan Zhan, Jin Jin, Cheng Ma, Ruzhang Zhao, Jared O’Connell, Yunxuan Jiang, 23andMe Research Team, Bertram L. Koelsch, Haoyu Zhang, Nilanjan Chatterjee

    Diterbitkan 2024-04-01
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  18. 18
    Distinct clinical phenotypes for Crohn’s disease derived from patient surveys

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

    Diterbitkan 2021-04-01
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  19. 19
    Genetic prediction of impulse control disorders in Parkinson's disease

    Genetic prediction of impulse control disorders in Parkinson's disease oleh Daniel Weintraub, Marijan Posavi, Pierre Fontanillas, Thomas F. Tropea, Eugenia Mamikonyan, Eunran Suh, John Q. Trojanowski, Paul Cannon, Vivianna M. Van Deerlin, 23andMe Research Team, Alice S. Chen‐Plotkin

    Diterbitkan 2022-07-01
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  20. 20
    Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure

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

    Diterbitkan 2020-02-01
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