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Refinado por: assunto: Genetic Variation remover
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1
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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2
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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3
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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4
Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease
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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

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5
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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6
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease
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A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease

Abul-Husn, Noura S ; Cheng, Xiping ; Li, Alexander H ; Xin, Yurong ; Schurmann, Claudia ; Stevis, Panayiotis ; Liu, Yashu ; Kozlitina, Julia ; Stender, Stefan ; Wood, G. Craig ; Stepanchick, Ann N ; Still, Matthew D ; McCarthy, Shane ; O’Dushlaine, Colm ; Packer, Jonathan S ; Balasubramanian, Suganthi ; Gosalia, Nehal ; Esopi, David ; Kim, Sun Y ; Mukherjee, Semanti ; Lopez, Alexander E ; Fuller, Erin D ; Penn, John ; Chu, Xin ; Luo, Jonathan Z ; Mirshahi, Uyenlinh L ; Carey, David J ; Still, Christopher D ; Feldman, Michael D ; Small, Aeron ; Damrauer, Scott M ; Rader, Daniel J ; Zambrowicz, Brian ; Olson, William ; Murphy, Andrew J ; Borecki, Ingrid B ; Shuldiner, Alan R ; Reid, Jeffrey G ; Overton, John D ; Yancopoulos, George D ; Hobbs, Helen H ; Cohen, Jonathan C ; Gottesman, Omri ; Teslovich, Tanya M ; Baras, Aris ; Mirshahi, Tooraj ; Gromada, Jesper ; Dewey, Frederick E

The New England journal of medicine, 2018-03, Vol.378 (12), p.1096-1106 [Periódico revisado por pares]

United States: Massachusetts Medical Society

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7
The genetic architecture of type 2 diabetes
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The genetic architecture of type 2 diabetes

Teslovich, Tanya M ; Mahajan, Anubha ; Fontanillas, Pierre ; Moutsianas, Loukas ; Rivas, Manuel A ; Rayner, N William ; Cingolani, Pablo ; Lindgren, Cecilia M ; Chen, Yuhui ; Huang, Jinyan ; Varga, Tibor V ; Green, Todd ; Fingerlin, Tasha ; Horikoshi, Momoko ; Huh, Iksoo ; Lee, Juyoung ; Lee, Selyeong ; Maxwell, Taylor J ; Yoon, Joon ; Barzilai, Nir ; Han, Bok-Ghee ; Kuulasmaa, Teemu ; Balkau, Beverley ; Giedraitis, Vilmantas ; Purcell, Shaun ; Kwak, Soo-Heon ; Afzal, Uzma ; Aguilar, David ; Cheng, Ching-Yu ; Palli, Domenico ; Fowler, Sharon P ; Freedman, Barry I ; Hicks, Pamela J ; Musani, Solomon K ; Puppala, Sobha ; Wilson, Sr, Gregory ; Surdulescu, Gabriela L ; Herder, Christian ; Doney, Alex S F ; Kinnunen, Leena ; Hakaste, Liisa ; Jørgensen, Marit E ; Justesen, Johanne Marie ; Käräjämäki, Annemari ; Lannfelt, Lars ; Narisu, Narisu ; Melander, Olle ; Milani, Lili ; Neville, Matt ; Qi, Qibin ; Rolandsson, Olov ; Stirrups, Kathleen ; Blancher, Christine ; Maguire, Jared ; Shakir, Khalid ; DePristo, Mark ; de Angelis, Martin Hrabé ; Jun, Goo ; Murphy, Jacquelyn ; Onofrio, Robert ; Thorand, Barbara ; Meisinger, Christa ; Isomaa, Bo ; Rauramaa, Rainer ; Watanabe, Richard M ; Bergman, Richard N ; Bottinger, Erwin P ; Chan, Juliana C N ; Langenberg, Claudia ; Jablonski, Kathleen A ; Lehman, Donna M ; Froguel, Philippe ; Small, Kerrin S ; Grallert, Harald ; Glaser, Benjamin ; Banks, Eric ; Gieger, Christian ; Illig, Thomas ; Buck, Gemma ; Trakalo, Joseph ; Mägi, Reedik ; Farjoun, Yossi ; Owen, Katharine R ; Gloyn, Anna L ; Tuomi, Tiinamaija ; Kooner, Jaspal Singh ; Donnelly, Peter ; Morris, Andrew D ; Hattersley, Andrew T ; Bowden, Donald W ; Laakso, Markku ; Bell, Graeme I ; Duggirala, Ravindranath ; McVean, Gilean ; Meigs, James B ; Cox, Nancy J ; Mohlke, Karen L ; Florez, Jose C ; Morris, Andrew P ; Kang, Hyun Min

Nature (London), 2016-08, Vol.536 (7614), p.41-47 [Periódico revisado por pares]

England: Nature Publishing Group

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8
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

Scott, Laura J ; Marullo, Letizia ; Gaulton, Kyle J ; Kaakinen, Marika ; Johnson, Andrew D ; Eicher, John D ; Lee, Yeji ; Ma, Clement ; Steinthorsdottir, Valgerdur ; Thorleifsson, Gudmar ; Van Zuydam, Natalie R ; Chen, Han ; Voight, Ben F ; Grallert, Harald ; Müller-Nurasyid, Martina ; Karssen, Lennart C ; van Leeuwen, Elisabeth M ; Willems, Sara M ; Fuchsberger, Christian ; Teslovich, Tanya M ; Chanda, Pritam ; Dina, Christian ; Yengo, Loic ; Jiang, Longda ; Sparso, Thomas ; Kestler, Hans A ; Eisele, Lewin ; Strawbridge, Rona J ; Benediktsson, Rafn ; Kong, Augustine ; Sigurðsson, Gunnar ; Kerrison, Nicola D ; Luan, Jian'an ; Roden, Michael ; Thorand, Barbara ; Fox, Caroline ; Liu, Ching-Ti ; Rybin, Denis ; Tuomi, Tiinamaija ; Couper, David J ; Jørgensen, Torben ; Linneberg, Allan ; Cornelis, Marilyn C ; Hunter, David J ; Kraft, Peter ; Sun, Qi ; Perry, John R B ; Wood, Andrew R ; Zeggini, Eleftheria ; Chines, Peter S ; Stringham, Heather M ; Mühleisen, Thomas W ; Nöthen, Markus M ; Pechlivanis, Sonali ; Humphries, Steve E ; Tremoli, Elena ; Klopp, Norman ; Mӓnnistö, Satu ; Charpentier, Guillaume ; Eury, Elodie ; Gigante, Bruna ; Leander, Karin ; Bottinger, Erwin P ; Blüher, Matthias ; Kovacs, Peter ; Scapoli, Chiara ; Erbel, Raimund ; Jöckel, Karl-Heinz ; Moebus, Susanne ; de Faire, Ulf ; Hamsten, Anders ; Stumvoll, Michael ; Donnelly, Peter J ; Frayling, Timothy M ; Hattersley, Andrew T ; Salomaa, Veikko ; Pedersen, Nancy L ; Mohlke, Karen L ; Barroso, Inês ; Lannfelt, Lars ; Ingelsson, Erik ; Lind, Lars ; Lindgren, Cecilia M ; Froguel, Philippe ; Palli, Domenico ; van der Schouw, Yvonne T ; Altshuler, David ; Groop, Leif C ; van Duijn, Cornelia M ; Florez, Jose C ; Meigs, James B ; Boerwinkle, Eric ; Strauch, Konstantin ; Metspalu, Andres ; Morris, Andrew D ; Hu, Frank B ; Thorsteinsdottir, Unnur ; Dupuis, Josée ; Morris, Andrew P ; Prokopenko, Inga

Diabetes (New York, N.Y.), 2017-11, Vol.66 (11), p.2888-2902 [Periódico revisado por pares]

United States: American Diabetes Association

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9
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
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Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

Zanoni, Paolo ; Khetarpal, Sumeet A. ; Larach, Daniel B. ; Hancock-Cerutti, William F. ; Millar, John S. ; Cuchel, Marina ; DerOhannessian, Stephanie ; Kontush, Anatol ; Surendran, Praveen ; Saleheen, Danish ; Trompet, Stella ; Jukema, J. Wouter ; De Craen, Anton ; Deloukas, Panos ; Sattar, Naveed ; Ford, Ian ; Packard, Chris ; Majumder, Abdullah al Shafi ; Alam, Dewan S. ; Di Angelantonio, Emanuele ; Abecasis, Goncalo ; Chowdhury, Rajiv ; Erdmann, Jeanette ; Nordestgaard, Børge G. ; Nielsen, Sune F. ; Tybjærg-Hansen, Anne ; Schmidt, Ruth Frikke ; Kuulasmaa, Kari ; Liu, Dajiang J. ; Perola, Markus ; Blankenberg, Stefan ; Salomaa, Veikko ; Männistö, Satu ; Amouyel, Philippe ; Arveiler, Dominique ; Ferrieres, Jean ; Müller-Nurasyid, Martina ; Ferrario, Marco ; Kee, Frank ; Willer, Cristen J. ; Samani, Nilesh ; Schunkert, Heribert ; Butterworth, Adam S. ; Howson, Joanna M. M. ; Peloso, Gina M. ; Stitziel, Nathan O. ; Danesh, John ; Kathiresan, Sekar ; Rader, Daniel J.

Science (American Association for the Advancement of Science), 2016-03, Vol.351 (6278), p.1166-1171 [Periódico revisado por pares]

United States: American Association for the Advancement of Science

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10
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

Zhao, Wei ; Robertson, Neil R ; Kitajima, Hidetoshi ; Taliun, Daniel ; Jensen, Richard A ; Lohman, Kurt K ; Flannick, Jason ; Grarup, Niels ; Trubetskoy, Vassily Vladimirovich ; Müller-Nurasyid, Martina ; Li-Gao, Ruifang ; Smith, Albert Vernon ; Ligthart, Symen ; Malerba, Giovanni ; Demirkan, Ayse ; Tajes, Juan Fernandez ; Preuss, Michael ; Graff, Marielisa ; Highland, Heather M ; Justice, Anne E ; Liu, Dajiang J ; Peloso, Gina Marie ; Afaq, Saima ; Afzal, Shoaib ; Almgren, Peter ; Amin, Najaf ; Bang, Lia B ; Brody, Jennifer A ; Canouil, Mickaël ; Chen, Yii-Der Ida ; Christensen, Cramer ; Eastwood, Sophie V ; Gambaro, Giovanni ; Grove, Megan L ; Hackinger, Sophie ; Tybjærg-Hansen, Anne ; Jäger, Susanne ; Jørgensen, Marit E ; Jørgensen, Torben ; Käräjämäki, Annemari ; Kovacs, Peter ; Kronenberg, Florian ; Lin, Keng-Hung ; Liu, Ching-Ti ; Loh, Marie ; Mamakou, Vasiliki ; McKean-Cowdin, Roberta ; Neville, Matt ; Nielsen, Sune F ; Ntalla, Ioanna ; Rice, Kenneth ; Rode, Line ; Rolandsson, Olov ; Selvin, Elizabeth ; Small, Kerrin S ; Surendran, Praveen ; Thorand, Barbara ; Thorleifsson, Gudmar ; Varbo, Anette ; Yengo, Loïc ; Young, Robin ; Boeing, Heiner ; Boerwinkle, Eric ; Dedoussis, George ; Dehghan, Abbas ; Florez, Jose C ; Frossard, Philippe ; Kuusisto, Johanna ; Launer, Lenore J ; Moitry, Marie ; Perola, Markus ; Rasheed, Asif ; Rosendaal, Frits R ; Rosengren, Anders H ; Sladek, Rob ; Smith, Blair H ; Varma, Rohit ; Willer, Cristen J ; Dupuis, Josée ; Franks, Paul W ; Groop, Leif ; Hansen, Torben ; Hattersley, Andrew T ; Ingelsson, Erik ; Karpe, Fredrik ; Kooner, Jaspal Singh ; Laakso, Markku ; Lind, Lars ; Liu, Yongmei ; Loos, Ruth J F ; Mook-Kanamori, Dennis ; Palmer, Colin N A ; Pankow, James S ; Rauramaa, Rainer ; Sattar, Naveed ; Soranzo, Nicole ; Stumvoll, Michael ; Barroso, Inês ; Saleheen, Danish ; Rotter, Jerome I

Nature genetics, 2018-04, Vol.50 (4), p.559-571 [Periódico revisado por pares]

United States: Nature Publishing Group

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