General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies
Lee, Seunggeun, Teslovich, Tanya M., Boehnke, Michael, Lin, Xihong
Published in American journal of human genetics (11.07.2013)
Published in American journal of human genetics (11.07.2013)
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LocusZoom: regional visualization of genome-wide association scan results
Pruim, Randall J., Welch, Ryan P., Sanna, Serena, Teslovich, Tanya M., Chines, Peter S., Gliedt, Terry P., Boehnke, Michael, Abecasis, Gonçalo R., Willer, Cristen J.
Published in Bioinformatics (15.09.2010)
Published in Bioinformatics (15.09.2010)
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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
Published in PLoS genetics (01.08.2012)
Published in PLoS genetics (01.08.2012)
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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
Published in PLoS genetics (30.10.2017)
Published in PLoS genetics (30.10.2017)
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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
Published in American journal of human genetics (01.01.2008)
Published in American journal of human genetics (01.01.2008)
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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
Published in Human molecular genetics (01.02.2024)
Published in Human molecular genetics (01.02.2024)
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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.
Published in American journal of human genetics (03.05.2018)
Published in American journal of human genetics (03.05.2018)
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Chronic CD4+ T-Cell Activation and Depletion in Human Immunodeficiency Virus Type 1 Infection: Type I Interferon-Mediated Disruption of T-Cell Dynamics
SEDAGHAT, Ahmad R, GERMAN, Jennifer, TESLOVICH, Tanya M, COFRANCESCO, Joseph, JIE, Chunfa C, CONOVER TALBOT, C, SILICIANO, Robert F
Published in Journal of Virology (01.02.2008)
Published in Journal of Virology (01.02.2008)
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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
Published in Circulation. Cardiovascular genetics (01.05.2019)
Published in Circulation. Cardiovascular genetics (01.05.2019)
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Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus
Mahajan, Anubha, Sim, Xueling, Ng, Hui Jin, Manning, Alisa, Rivas, Manuel A, Highland, Heather M, Locke, Adam E, Grarup, Niels, Im, Hae Kyung, Cingolani, Pablo, Flannick, Jason, Fontanillas, Pierre, Fuchsberger, Christian, Gaulton, Kyle J, Teslovich, Tanya M, Rayner, N William, Robertson, Neil R, Beer, Nicola L, Rundle, Jana K, Bork-Jensen, Jette, Ladenvall, Claes, Blancher, Christine, Buck, David, Buck, Gemma, Burtt, Noël P, Gabriel, Stacey, Gjesing, Anette P, Groves, Christopher J, Hollensted, Mette, Huyghe, Jeroen R, Jackson, Anne U, Jun, Goo, Justesen, Johanne Marie, Mangino, Massimo, Murphy, Jacquelyn, Neville, Matt, Onofrio, Robert, Small, Kerrin S, Stringham, Heather M, Syvänen, Ann-Christine, Trakalo, Joseph, Abecasis, Goncalo, Bell, Graeme I, Blangero, John, Cox, Nancy J, Duggirala, Ravindranath, Hanis, Craig L, Seielstad, Mark, Wilson, James G, Christensen, Cramer, Brandslund, Ivan, Rauramaa, Rainer, Surdulescu, Gabriela L, Doney, Alex S F, Lannfelt, Lars, Linneberg, Allan, Isomaa, Bo, Tuomi, Tiinamaija, Jørgensen, Marit E, Jørgensen, Torben, Kuusisto, Johanna, Uusitupa, Matti, Salomaa, Veikko, Spector, Timothy D, Morris, Andrew D, Palmer, Colin N A, Collins, Francis S, Mohlke, Karen L, Bergman, Richard N, Ingelsson, Erik, Lind, Lars, Tuomilehto, Jaakko, Hansen, Torben, Watanabe, Richard M, Prokopenko, Inga, Dupuis, Josee, Karpe, Fredrik, Groop, Leif, Laakso, Markku, Pedersen, Oluf, Florez, Jose C, Morris, Andrew P, Altshuler, David, Meigs, James B, Boehnke, Michael, McCarthy, Mark I, Lindgren, Cecilia M, Gloyn, Anna L
Published in PLoS genetics (01.01.2015)
Published in PLoS genetics (01.01.2015)
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The centrosome in human genetic disease
Katsanis, Nicholas, Badano, Jose L, Teslovich, Tanya M
Published in Nature reviews. Genetics (01.03.2005)
Published in Nature reviews. Genetics (01.03.2005)
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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.
Published in Nature genetics (01.11.2018)
Published in Nature genetics (01.11.2018)
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Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci
Service, Susan K, Teslovich, Tanya M, Fuchsberger, Christian, Ramensky, Vasily, Yajnik, Pranav, Koboldt, Daniel C, Larson, David E, Zhang, Qunyuan, Lin, Ling, Welch, Ryan, Ding, Li, McLellan, Michael D, O'Laughlin, Michele, Fronick, Catrina, Fulton, Lucinda L, Magrini, Vincent, Swift, Amy, Elliott, Paul, Jarvelin, Marjo-Riitta, Kaakinen, Marika, McCarthy, Mark I, Peltonen, Leena, Pouta, Anneli, Bonnycastle, Lori L, Collins, Francis S, Narisu, Narisu, Stringham, Heather M, Tuomilehto, Jaakko, Ripatti, Samuli, Fulton, Robert S, Sabatti, Chiara, Wilson, Richard K, Boehnke, Michael, Freimer, Nelson B
Published in PLoS genetics (01.01.2014)
Published in PLoS genetics (01.01.2014)
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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
Published in Human molecular genetics (01.05.2018)
Published in Human molecular genetics (01.05.2018)
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Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene
Li, Jin Billy, Gerdes, Jantje M, Haycraft, Courtney J, Fan, Yanli, Teslovich, Tanya M, May-Simera, Helen, Li, Haitao, Blacque, Oliver E, Li, Linya, Leitch, Carmen C, Lewis, Richard Allan, Green, Jane S, Parfrey, Patrick S, Leroux, Michel R, Davidson, William S, Beales, Philip L, Guay-Woodford, Lisa M, Yoder, Bradley K, Stormo, Gary D, Katsanis, Nicholas, Dutcher, Susan K
Published in Cell (14.05.2004)
Published in Cell (14.05.2004)
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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
Published in PLoS genetics (01.07.2007)
Published in PLoS genetics (01.07.2007)
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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
Published in Nature genetics (01.02.2013)
Published in Nature genetics (01.02.2013)
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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
Published in Nature (09.10.2003)
Published in Nature (09.10.2003)
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A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment
RENDTORFF, Nanna D, MEI ZHU, FRIDERICI, Karen H, STEPHAN, Dietrich A, TRANEBJAERG, Lisbeth, FAGERHEIM, Toril, ANTAL, Torben L, JONES, Marypat, TESLOVICH, Tanya M, GILLANDERS, Elizabeth M, BARMADA, Michael, TEIG, Erik, TRENT, Jeffrey M
Published in European journal of human genetics : EJHG (01.10.2006)
Published in European journal of human genetics : EJHG (01.10.2006)
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