skip to main content
Idioma:
Resultados 1 2 3 4 next page
Refinado por: assunto: Genetics & Heredity 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
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study
Material Type:
Artigo 		Adicionar ao Meu Espaço

Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study

Davis, James P ; Huyghe, Jeroen R ; Locke, Adam E ; Jackson, Anne U ; Sim, Xueling ; Stringham, Heather M ; Teslovich, Tanya M ; Welch, Ryan P ; Fuchsberger, Christian ; Narisu, Narisu ; Chines, Peter S ; Kangas, Antti J ; Soininen, Pasi ; Ala-Korpela, Mika ; Kuusisto, Johanna ; Collins, Francis S ; Laakso, Markku ; Boehnke, Michael ; Mohlke, Karen L Loos, Ruth J. F.

PLoS genetics, 2017-10, Vol.13 (10), p.e1007079-e1007079 [Periódico revisado por pares]

United States: Public Library of Science

Texto completo disponível

Citações Citado por
4
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits
Material Type:
Artigo 		Adicionar ao Meu Espaço

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

Voight, Benjamin F ; Kang, Hyun Min ; Ding, Jun ; Palmer, Cameron D ; Sidore, Carlo ; Chines, Peter S ; Burtt, Noël P ; Fuchsberger, Christian ; Li, Yanming ; Erdmann, Jeanette ; Frayling, Timothy M ; Heid, Iris M ; Jackson, Anne U ; Johnson, Toby ; Kilpeläinen, Tuomas O ; Lindgren, Cecilia M ; Morris, Andrew P ; Prokopenko, Inga ; Randall, Joshua C ; Saxena, Richa ; Soranzo, Nicole ; Speliotes, Elizabeth K ; Teslovich, Tanya M ; Wheeler, Eleanor ; Maguire, Jared ; Parkin, Melissa ; Potter, Simon ; Rayner, N William ; Robertson, Neil ; Stirrups, Kathleen ; Winckler, Wendy ; Sanna, Serena ; Mulas, Antonella ; Nagaraja, Ramaiah ; Cucca, Francesco ; Barroso, Inês ; Deloukas, Panos ; Loos, Ruth J F ; Kathiresan, Sekar ; Munroe, Patricia B ; Newton-Cheh, Christopher ; Pfeufer, Arne ; Samani, Nilesh J ; Schunkert, Heribert ; Hirschhorn, Joel N ; Altshuler, David ; McCarthy, Mark I ; Abecasis, Gonçalo R ; Boehnke, Michael Gibson, Greg

PLoS genetics, 2012-08, Vol.8 (8), p.e1002793-e1002793 [Periódico revisado por pares]

United States: Public Library of Science

Texto completo disponível

Citações Citado por
5
Population bottlenecks as a potential major shaping force of human genome architecture
Population bottlenecks as a potential major shaping force of human genome architecture
Material Type:
Artigo 		Adicionar ao Meu Espaço

Population bottlenecks as a potential major shaping force of human genome architecture

Gherman, Adrian ; Chen, Peter E ; Teslovich, Tanya M ; Stankiewicz, Pawel ; Withers, Marjorie ; Kashuk, Carl S ; Chakravarti, Aravinda ; Lupski, James R ; Cutler, David J ; Katsanis, Nicholas Trask, Barbara J

PLoS genetics, 2007-07, Vol.3 (7), p.e119-e119 [Periódico revisado por pares]

United States: Public Library of Science

Texto completo disponível

Citações Citado por
6
Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration
Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration
Material Type:
Artigo 		Adicionar ao Meu Espaço

Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration

Kwong, Alan ; Zawistowski, Matthew ; Fritsche, Lars G ; Zhan, Xiaowei ; Bragg-Gresham, Jennifer ; Branham, Kari E ; Advani, Jayshree ; Othman, Mohammad ; Ratnapriya, Rinki ; Teslovich, Tanya M ; Stambolian, Dwight ; Chew, Emily Y ; Abecasis, Gonçalo R ; Swaroop, Anand

Human molecular genetics, 2024-02, Vol.33 (4), p.374-385 [Periódico revisado por pares]

England: Oxford University Press

Texto completo disponível

Citações Citado por
7
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion
Material Type:
Artigo 		Adicionar ao Meu Espaço

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

Huyghe, Jeroen R ; Jackson, Anne U ; Fogarty, Marie P ; Buchkovich, Martin L ; Stančáková, Alena ; Stringham, Heather M ; Sim, Xueling ; Yang, Lingyao ; Fuchsberger, Christian ; Cederberg, Henna ; Chines, Peter S ; Teslovich, Tanya M ; Romm, Jane M ; Ling, Hua ; McMullen, Ivy ; Ingersoll, Roxann ; Pugh, Elizabeth W ; Doheny, Kimberly F ; Neale, Benjamin M ; Daly, Mark J ; Kuusisto, Johanna ; Scott, Laura J ; Kang, Hyun Min ; Collins, Francis S ; Abecasis, Gonçalo R ; Watanabe, Richard M ; Boehnke, Michael ; Laakso, Markku ; Mohlke, Karen L

Nature genetics, 2013-02, Vol.45 (2), p.197-201 [Periódico revisado por pares]

United States: Nature Publishing Group

Texto completo disponível

Citações Citado por
8
The centrosome in human genetic disease
The centrosome in human genetic disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

The centrosome in human genetic disease

Katsanis, Nicholas ; Badano, Jose L ; Teslovich, Tanya M

Nature reviews. Genetics, 2005-03, Vol.6 (3), p.194-205 [Periódico revisado por pares]

London: Nature Publishing Group

Texto completo disponível

Citações Citado por
9
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
10
Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease
Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease

Peloso, Gina M ; Nomura, Akihiro ; Khera, Amit V ; Chaffin, Mark ; Won, Hong-Hee ; Ardissino, Diego ; Danesh, John ; Schunkert, Heribert ; Wilson, James G ; Samani, Nilesh ; Erdmann, Jeanette ; McPherson, Ruth ; Watkins, Hugh ; Saleheen, Danish ; McCarthy, Shane ; Teslovich, Tanya M ; Leader, Joseph B ; Lester Kirchner, H ; Marrugat, Jaume ; Nohara, Atsushi ; Kawashiri, Masa-Aki ; Tada, Hayato ; Dewey, Frederick E ; Carey, David J ; Baras, Aris ; Kathiresan, Sekar

Circulation. Cardiovascular genetics, 2019-05, Vol.12 (5), p.e002376-e002376 [Periódico revisado por pares]

United States: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Data de Publicação 

De até
Refinar
  1. Antes de2005  (3)
  2. 2005Até2007  (5)
  3. 2008Até2011  (5)
  4. 2012Até2015  (15)
  5. Após 2015  (10)
  6. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.