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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
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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

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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
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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

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3
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
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Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program

Klarin, Derek ; Damrauer, Scott M ; Cho, Kelly ; Sun, Yan V ; Teslovich, Tanya M ; Honerlaw, Jacqueline ; Gagnon, David R ; DuVall, Scott L ; Li, Jin ; Peloso, Gina M ; Chaffin, Mark ; Small, Aeron M ; Huang, Jie ; Tang, Hua ; Lynch, Julie A ; Ho, Yuk-Lam ; Liu, Dajiang J ; Emdin, Connor A ; Li, Alexander H ; Huffman, Jennifer E ; Lee, Jennifer S ; Natarajan, Pradeep ; Chowdhury, Rajiv ; Saleheen, Danish ; Vujkovic, Marijana ; Baras, Aris ; Pyarajan, Saiju ; Di Angelantonio, Emanuele ; Neale, Benjamin M ; Naheed, Aliya ; Khera, Amit V ; Danesh, John ; Chang, Kyong-Mi ; Abecasis, Gonçalo ; Willer, Cristen ; Dewey, Frederick E ; Carey, David J ; Concato, John ; Gaziano, J Michael ; O'Donnell, Christopher J ; Tsao, Philip S ; Kathiresan, Sekar ; Rader, Daniel J ; Wilson, Peter W F ; Assimes, Themistocles L

Nature genetics, 2018-11, Vol.50 (11), p.1514-1523 [Periódico revisado por pares]

United States: Nature Publishing Group

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4
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
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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

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5
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
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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

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6
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
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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

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7
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
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Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

Katsanis, Nicholas ; Ansley, Stephen J ; Badano, Jose L ; Blacque, Oliver E ; Hill, Josephine ; Hoskins, Bethan E ; Leitch, Carmen C ; Chul Kim, Jun ; Ross, Alison J ; Eichers, Erica R ; Teslovich, Tanya M ; Mah, Allan K ; Johnsen, Robert C ; Cavender, John C ; Alan Lewis, Richard ; Leroux, Michel R ; Beales, Philip L

Nature, 2003-10, Vol.425 (6958), p.628-633 [Periódico revisado por pares]

England: Nature Publishing Group

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8
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study
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Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study

Teslovich, Tanya M ; Kim, Daniel Seung ; Yin, Xianyong ; Stančáková, Alena ; Jackson, Anne U ; Wielscher, Matthias ; Naj, Adam ; Perry, John R B ; Huyghe, Jeroen R ; Stringham, Heather M ; Davis, James P ; Raulerson, Chelsea K ; Welch, Ryan P ; Fuchsberger, Christian ; Locke, Adam E ; Sim, Xueling ; Chines, Peter S ; Narisu, Narisu ; Kangas, Antti J ; Soininen, Pasi ; Ala-Korpela, Mika ; Gudnason, Vilmundur ; Musani, Solomon K ; Jarvelin, Marjo-Riitta ; Schellenberg, Gerard D ; Speliotes, Elizabeth K ; Kuusisto, Johanna ; Collins, Francis S ; Boehnke, Michael ; Laakso, Markku ; Mohlke, Karen L

Human molecular genetics, 2018-05, Vol.27 (9), p.1664-1674 [Periódico revisado por pares]

England: Oxford University Press

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9
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

Mercader, Josep M ; Udler, Miriam S ; Wessel, Jennifer ; Teslovich, Tanya M ; Caulkins, Lizz ; Barajas-Olmos, Francisco ; Boerwinkle, Eric ; Chen, Ling ; Contreras-Cubas, Cecilia ; Córdova, Emilio ; Correa, Adolfo ; DeFronzo, Ralph A ; Dolan, Lawrence ; Elliott, Amanda ; Floyd, James S ; Garay-Sevilla, Maria Eugenia ; García-Ortiz, Humberto ; Heard-Costa, Nancy L ; Jørgensen, Marit E ; Kang, Hyun Min ; Kelsey, Megan ; Linneberg, Allan ; Liu, Ching-Ti ; Liu, Jianjun ; Lyssenko, Valeriya ; Marcketta, Anthony ; Martínez-Hernández, Angélica ; Mayer-Davis, Elizabeth ; Morrison, Alanna C ; Ndungu, Anne ; Ng, Maggie C Y ; O'Dushlaine, Colm ; Post, Wendy S ; Vasan, Ramachandran S ; Rayner, N William ; Revilla-Monsalve, Cristina ; Santoro, Nicola ; Schurmann, Claudia ; Soberón, Xavier ; Strom, Tim M ; Thameem, Farook ; Torres, Jason M ; Vujkovic, Marijana ; Witte, Daniel R ; Atzmon, Gil ; Blangero, John ; Bonnycastle, Lori L ; Chan, Edmund ; Cheng, Ching-Yu ; Collins, Francis S ; de Vries, Paul S ; Glaser, Benjamin ; Gonzalez, Ma Elena ; Groop, Leif ; Kooner, Jaspal Singh ; Kwak, Soo Heon ; Laakso, Markku ; Nilsson, Peter ; Spector, Timothy D ; Tai, E Shyong ; Tuomilehto, Jaakko ; Wilson, James G ; Burke, Brian ; Carey, David J ; Frossard, Philippe ; Hwang, Mi Yeong ; Kim, Young Jin ; Kirchner, H Lester ; Lee, Jong-Young ; Lee, Juyoung ; Loos, Ruth J F ; Ma, Ronald C W ; Morris, Andrew D ; Palmer, Colin N A ; Pankow, James ; Rasheed, Asif ; Saleheen, Danish ; Sim, Xueling ; Small, Kerrin S ; Teo, Yik Ying ; Haiman, Christopher ; Hanis, Craig L ; Dewey, Frederick E ; Baras, Aris ; Gieger, Christian ; Meitinger, Thomas ; Lange, Leslie ; Pedersen, Oluf ; Zeitler, Philip ; Dabelea, Dana ; Abecasis, Goncalo ; Cox, Nancy J ; Sladek, Rob ; Meigs, James B ; Rotter, Jerome I ; Altshuler, David ; Burtt, Noël P ; Morris, Andrew P ; Florez, Jose C ; Boehnke, Michael

Nature (London), 2019-06, Vol.570 (7759), p.71-76 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Using GWAS Data to Identify Copy Number Variants Contributing to Common Complex Diseases
Using GWAS Data to Identify Copy Number Variants Contributing to Common Complex Diseases
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Using GWAS Data to Identify Copy Number Variants Contributing to Common Complex Diseases

Zöllner, Sebastian ; Teslovich, Tanya M.

Statistical science, 2009-11, Vol.24 (4), p.530-546 [Periódico revisado por pares]

Hayward: Institute of Mathematical Statistics

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