Arama Sonuçları - Benjamin M. Neale

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  1. 1
    The Future of Association Studies: Gene-Based Analysis and Replication

    The Future of Association Studies: Gene-Based Analysis and Replication Yazar: Benjamin M. Neale, Pak C. Sham

    Baskı/Yayın Bilgisi 2004
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  2. 2
    Genome-wide association studies in ADHD

    Genome-wide association studies in ADHD Yazar: Barbara Franke, Benjamin M. Neale, Stephen V. Faraone

    Baskı/Yayın Bilgisi 2009
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  3. 3
    Genetic research in autism spectrum disorders

    Genetic research in autism spectrum disorders Yazar: Elise Robinson, Benjamin M. Neale, Steven E. Hyman

    Baskı/Yayın Bilgisi 2015
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  4. 4
    Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

    Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia Yazar: Tarjinder Singh, Benjamin M. Neale, Mark J. Daly

    Baskı/Yayın Bilgisi 2020
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  5. 5
    Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries

    Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries Yazar: Siwei Chen, Benjamin M. Neale, Samuel F. Berkovic

    Baskı/Yayın Bilgisi 2023
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  6. 6
    A Twin Study of Dietary Restraint, Disinhibition and Hunger: An Examination of the Eating Inventory (Three Factor Eating Questionnaire)

    A Twin Study of Dietary Restraint, Disinhibition and Hunger: An Examination of the Eating Inventory (Three Factor Eating Questionnaire) Yazar: Benjamin M. Neale, Suzanne E. Mazzeo, Cynthia M. Bulik

    Baskı/Yayın Bilgisi 2003
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  7. 7
    Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases

    Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases Yazar: Marie Verbanck, Chia‐Yen Chen, Benjamin M. Neale, Ron Do

    Baskı/Yayın Bilgisi 2018
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  8. 8
    Publisher Correction: Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases

    Publisher Correction: Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases Yazar: Marie Verbanck, Chia‐Yen Chen, Benjamin M. Neale, Ron Do

    Baskı/Yayın Bilgisi 2018
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  9. 9
    Whole-genome analyses of whole-brain data: working within an expanded search space

    Whole-genome analyses of whole-brain data: working within an expanded search space Yazar: Sarah E. Medland, Neda Jahanshad, Benjamin M. Neale, Paul M. Thompson

    Baskı/Yayın Bilgisi 2014
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  10. 10
    Discovery of rare variants for complex phenotypes

    Discovery of rare variants for complex phenotypes Yazar: Jack A. Kosmicki, Claire Churchhouse, Manuel A. Rivas, Benjamin M. Neale

    Baskı/Yayın Bilgisi 2016
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  11. 11
    The IMAGE project: methodological issues for the molecular genetic analysis of ADHD.

    The IMAGE project: methodological issues for the molecular genetic analysis of ADHD. Yazar: Jonna Kuntsi, Benjamin M. Neale, Wai Chen, Stephen V. Faraone, Philip Asherson

    Baskı/Yayın Bilgisi 2006
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  12. 12
    Challenges and Opportunities for Developing More Generalizable Polygenic Risk Scores

    Challenges and Opportunities for Developing More Generalizable Polygenic Risk Scores Yazar: Ying Wang, Kristin Tsuo, Masahiro Kanai, Benjamin M. Neale, Alicia R. Martin

    Baskı/Yayın Bilgisi 2022
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  13. 13
    Incorporating family history of disease improves polygenic risk scores in diverse populations

    Incorporating family history of disease improves polygenic risk scores in diverse populations Yazar: Margaux L.A. Hujoel, Po‐Ru Loh, Benjamin M. Neale, Alkes L. Price

    Baskı/Yayın Bilgisi 2022
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  14. 14
    Predicting Polygenic Risk of Psychiatric Disorders

    Predicting Polygenic Risk of Psychiatric Disorders Yazar: Alicia R. Martin, Mark J. Daly, Elise Robinson, Steven E. Hyman, Benjamin M. Neale

    Baskı/Yayın Bilgisi 2018
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  15. 15
    Phenome-wide heritability analysis of the UK Biobank

    Phenome-wide heritability analysis of the UK Biobank Yazar: Tian Ge, Chia‐Yen Chen, Benjamin M. Neale, Mert R. Sabuncu, Jordan W. Smoller

    Baskı/Yayın Bilgisi 2017
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  16. 16
    A scoping review of guidelines for the use of race, ethnicity, and ancestry reveals widespread consensus but also points of ongoing disagreement

    A scoping review of guidelines for the use of race, ethnicity, and ancestry reveals widespread consensus but also points of ongoing disagreement Yazar: Madelyn Mauro, Danielle S. Allen, Bege Dauda, Santiago J. Molina, Benjamin M. Neale, Anna Lewis

    Baskı/Yayın Bilgisi 2022
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  17. 17
    Variation near complement factor I is associated with risk of advanced AMD

    Variation near complement factor I is associated with risk of advanced AMD Yazar: Jesen Fagerness, Julian Maller, Benjamin M. Neale, Robyn Reynolds, Mark J. Daly, Johanna M. Seddon

    Baskı/Yayın Bilgisi 2008
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  18. 18
    Clinical use of current polygenic risk scores may exacerbate health disparities

    Clinical use of current polygenic risk scores may exacerbate health disparities Yazar: Alicia R. Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M. Neale, Mark J. Daly

    Baskı/Yayın Bilgisi 2019
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  19. 19
    Phenotypic extremes in rare variant study designs

    Phenotypic extremes in rare variant study designs Yazar: Gina M. Peloso, Daniel J. Rader, Stacey Gabriel, Sekar Kathiresan, Mark J. Daly, Benjamin M. Neale

    Baskı/Yayın Bilgisi 2015
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  20. 20
    Practical aspects of imputation-driven meta-analysis of genome-wide association studies

    Practical aspects of imputation-driven meta-analysis of genome-wide association studies Yazar: Paul I. W. de Bakker, Manuel A. R. Ferreira, Xiaoming Jia, Benjamin M. Neale, Soumya Raychaudhuri, Benjamin F. Voight

    Baskı/Yayın Bilgisi 2008
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