Torthaí cuardaigh - Benjamin M. Neale
- 1 - 20 toradh as 241 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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The Future of Association Studies: Gene-Based Analysis and Replication de réir Benjamin M. Neale, Pak C. Sham
Foilsithe / Cruthaithe 2004Artigo -
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Genome-wide association studies in ADHD de réir Barbara Franke, Benjamin M. Neale, Stephen V. Faraone
Foilsithe / Cruthaithe 2009Revisão -
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Genetic research in autism spectrum disorders de réir Elise Robinson, Benjamin M. Neale, Steven E. Hyman
Foilsithe / Cruthaithe 2015Revisão -
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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia de réir Tarjinder Singh, Benjamin M. Neale, Mark J. Daly
Foilsithe / Cruthaithe 2020Pré-impressão -
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Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries de réir Siwei Chen, Benjamin M. Neale, Samuel F. Berkovic
Foilsithe / Cruthaithe 2023Pré-impressão -
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Publisher Correction: Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases de réir Marie Verbanck, Chia‐Yen Chen, Benjamin M. Neale, Ron Do
Foilsithe / Cruthaithe 2018Errata/Corrigenda -
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Whole-genome analyses of whole-brain data: working within an expanded search space de réir Sarah E. Medland, Neda Jahanshad, Benjamin M. Neale, Paul M. Thompson
Foilsithe / Cruthaithe 2014Revisão -
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Discovery of rare variants for complex phenotypes de réir Jack A. Kosmicki, Claire Churchhouse, Manuel A. Rivas, Benjamin M. Neale
Foilsithe / Cruthaithe 2016Revisão -
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The IMAGE project: methodological issues for the molecular genetic analysis of ADHD. de réir Jonna Kuntsi, Benjamin M. Neale, Wai Chen, Stephen V. Faraone, Philip Asherson
Foilsithe / Cruthaithe 2006Artigo -
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Challenges and Opportunities for Developing More Generalizable Polygenic Risk Scores de réir Ying Wang, Kristin Tsuo, Masahiro Kanai, Benjamin M. Neale, Alicia R. Martin
Foilsithe / Cruthaithe 2022Revisão -
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Incorporating family history of disease improves polygenic risk scores in diverse populations de réir Margaux L.A. Hujoel, Po‐Ru Loh, Benjamin M. Neale, Alkes L. Price
Foilsithe / Cruthaithe 2022Artigo -
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Predicting Polygenic Risk of Psychiatric Disorders de réir Alicia R. Martin, Mark J. Daly, Elise Robinson, Steven E. Hyman, Benjamin M. Neale
Foilsithe / Cruthaithe 2018Revisão -
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Phenome-wide heritability analysis of the UK Biobank de réir Tian Ge, Chia‐Yen Chen, Benjamin M. Neale, Mert R. Sabuncu, Jordan W. Smoller
Foilsithe / Cruthaithe 2017Artigo -
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A scoping review of guidelines for the use of race, ethnicity, and ancestry reveals widespread consensus but also points of ongoing disagreement de réir Madelyn Mauro, Danielle S. Allen, Bege Dauda, Santiago J. Molina, Benjamin M. Neale, Anna Lewis
Foilsithe / Cruthaithe 2022Revisão -
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Variation near complement factor I is associated with risk of advanced AMD de réir Jesen Fagerness, Julian Maller, Benjamin M. Neale, Robyn Reynolds, Mark J. Daly, Johanna M. Seddon
Foilsithe / Cruthaithe 2008Artigo -
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Clinical use of current polygenic risk scores may exacerbate health disparities de réir Alicia R. Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M. Neale, Mark J. Daly
Foilsithe / Cruthaithe 2019Revisão -
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Phenotypic extremes in rare variant study designs de réir Gina M. Peloso, Daniel J. Rader, Stacey Gabriel, Sekar Kathiresan, Mark J. Daly, Benjamin M. Neale
Foilsithe / Cruthaithe 2015Artigo -
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Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Genotype
Single-nucleotide polymorphism
Medicine
Genome-wide association study
Computational biology
Genetic association
Psychology
Psychiatry
Genome
Phenotype
Population
Computer science
Genetic architecture
Evolutionary biology
Internal medicine
Exome sequencing
Allele
Environmental health
Mathematics
Exome
Quantitative trait locus
Mutation
Neuroscience
Autism
Statistics
Heritability
Schizophrenia (object-oriented programming)