Resultados de procura - 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 por Benjamin M. Neale, Pak C. Sham

    Publicado 2004
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  2. 2
    Genome-wide association studies in ADHD

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

    Publicado 2009
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  3. 3
    Genetic research in autism spectrum disorders

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

    Publicado 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 por Tarjinder Singh, Benjamin M. Neale, Mark J. Daly

    Publicado 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 por Siwei Chen, Benjamin M. Neale, Samuel F. Berkovic

    Publicado 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) por Benjamin M. Neale, Suzanne E. Mazzeo, Cynthia M. Bulik

    Publicado 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 por Marie Verbanck, Chia‐Yen Chen, Benjamin M. Neale, Ron Do

    Publicado 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 por Marie Verbanck, Chia‐Yen Chen, Benjamin M. Neale, Ron Do

    Publicado 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 por Sarah E. Medland, Neda Jahanshad, Benjamin M. Neale, Paul M. Thompson

    Publicado 2014
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  10. 10
    Discovery of rare variants for complex phenotypes

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

    Publicado 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. por Jonna Kuntsi, Benjamin M. Neale, Wai Chen, Stephen V. Faraone, Philip Asherson

    Publicado 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 por Ying Wang, Kristin Tsuo, Masahiro Kanai, Benjamin M. Neale, Alicia R. Martin

    Publicado 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 por Margaux L.A. Hujoel, Po‐Ru Loh, Benjamin M. Neale, Alkes L. Price

    Publicado 2022
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  14. 14
    Predicting Polygenic Risk of Psychiatric Disorders

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

    Publicado 2018
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  15. 15
    Phenome-wide heritability analysis of the UK Biobank

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

    Publicado 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 por Madelyn Mauro, Danielle S. Allen, Bege Dauda, Santiago J. Molina, Benjamin M. Neale, Anna Lewis

    Publicado 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 por Jesen Fagerness, Julian Maller, Benjamin M. Neale, Robyn Reynolds, Mark J. Daly, Johanna M. Seddon

    Publicado 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 por Alicia R. Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M. Neale, Mark J. Daly

    Publicado 2019
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  19. 19
    Phenotypic extremes in rare variant study designs

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

    Publicado 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 por Paul I. W. de Bakker, Manuel A. R. Ferreira, Xiaoming Jia, Benjamin M. Neale, Soumya Raychaudhuri, Benjamin F. Voight

    Publicado 2008
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