skip to main content
Idioma:
Refinado por: Nome da Publicação: American Journal Of Human Genetics remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies
General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies
Material Type:
Artigo 		Adicionar ao Meu Espaço

General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies

Lee, Seunggeun ; Teslovich, Tanya M. ; Boehnke, Michael ; Lin, Xihong

American journal of human genetics, 2013-07, Vol.93 (1), p.42-53 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
2
A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

Arking, Dan E. ; Cutler, David J. ; Brune, Camille W. ; Teslovich, Tanya M. ; West, Kristen ; Ikeda, Morna ; Rea, Alexis ; Guy, Moltu ; Lin, Shin ; Cook, Edwin H. ; Chakravarti, Aravinda

American journal of human genetics, 2008-01, Vol.82 (1), p.160-164 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
3
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes

Staples, Jeffrey ; Maxwell, Evan K. ; Gosalia, Nehal ; Gonzaga-Jauregui, Claudia ; Snyder, Christopher ; Hawes, Alicia ; Penn, John ; Ulloa, Ricardo ; Bai, Xiaodong ; Lopez, Alexander E. ; Van Hout, Cristopher V. ; O’Dushlaine, Colm ; Teslovich, Tanya M. ; McCarthy, Shane E. ; Balasubramanian, Suganthi ; Kirchner, H. Lester ; Leader, Joseph B. ; Murray, Michael F. ; Ledbetter, David H. ; Shuldiner, Alan R. ; Yancoupolos, George D. ; Dewey, Frederick E. ; Carey, David J. ; Overton, John D. ; Baras, Aris ; Habegger, Lukas ; Reid, Jeffrey G.

American journal of human genetics, 2018-05, Vol.102 (5), p.874-889 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
4
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development

Nielsen, Jonas B. ; Fritsche, Lars G. ; Zhou, Wei ; Teslovich, Tanya M. ; Holmen, Oddgeir L. ; Gustafsson, Stefan ; Gabrielsen, Maiken E. ; Schmidt, Ellen M. ; Beaumont, Robin ; Wolford, Brooke N. ; Lin, Maoxuan ; Brummett, Chad M. ; Preuss, Michael H. ; Refsgaard, Lena ; Bottinger, Erwin P. ; Graham, Sarah E. ; Surakka, Ida ; Chu, Yunhan ; Skogholt, Anne Heidi ; Dalen, Håvard ; Boyle, Alan P. ; Oral, Hakan ; Herron, Todd J. ; Kitzman, Jacob ; Jalife, José ; Svendsen, Jesper H. ; Olesen, Morten S. ; Njølstad, Inger ; Løchen, Maja-Lisa ; Baras, Aris ; Gottesman, Omri ; Marcketta, Anthony ; O’Dushlaine, Colm ; Ritchie, Marylyn D. ; Wilsgaard, Tom ; Loos, Ruth J.F. ; Frayling, Timothy M. ; Boehnke, Michael ; Ingelsson, Erik ; Carey, David J. ; Dewey, Frederick E. ; Kang, Hyun M. ; Abecasis, Gonçalo R. ; Hveem, Kristian ; Willer, Cristen J.

American journal of human genetics, 2018-01, Vol.102 (1), p.103-115 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
5
A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism. Commentary
A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism. Commentary
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism. Commentary

STEPHAN, Dietrich A ; ARKING, Dan E ; COOK, Edwin H ; CHAKRAVARTI, Aravinda ; CUTLER, David J ; BRUNE, Camille W ; TESLOVICH, Tanya M ; WEST, Kristen ; IKEDA, Morna ; REA, Alexis ; GUY, Moltu ; LIN, Shin

American journal of human genetics, 2008, Vol.82 (1) [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

Texto completo disponível

Citações Citado por

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.