Search Results - Noël P. Burtt
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1
Association of Blood Lipids With Common DNA Sequence Variants at 19 Genetic Loci in the Multiethnic United States National Health and Nutrition Examination Survey III by Mary Keebler, Christopher Sanders, Aarti Surti, Candace Guiducci, Noël P. Burtt, Sekar Kathiresan
Published 2009Revisão -
2
Functional Investigations of <i>HNF1A</i> Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population by Laeya A. Najmi, Ingvild Aukrust, Jason Flannick, Janne Molnes, Noël P. Burtt, Anders Molven, Leif Groop, David Altshuler, Stefan Johansson, Lise Bjørkhaug, Pål R. Njølstad
Published 2016Artigo -
3
Polymorphisms Associated with Cholesterol and Risk of Cardiovascular Events by Sekar Kathiresan, Olle Melander, Dragi Anevski, Candace Guiducci, Noël P. Burtt, Charlotta Roos, Joel N. Hirschhorn, Göran Berglund, Bo Hedblad, Leif Groop, David Altshuler, Christopher Newton‐Cheh, Marju Orho‐Melander
Published 2008Artigo -
4
Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease by Richa Saxena, Paul I.W. de Bakker, Karyn Singer, Vamsi K. Mootha, Noël P. Burtt, Joel N. Hirschhorn, Daniel Gaudet, Bo Isomaa, Mark J. Daly, Leif Groop, Kristin Ardlie, David Altshuler
Published 2006Artigo -
5
Genomewide Linkage Analysis of Stature in Multiple Populations Reveals Several Regions with Evidence of Linkage to Adult Height by Joel N. Hirschhorn, Cecilia M. Lindgren, Mark J. Daly, Andrew Kirby, S. F. Schaffner, Noël P. Burtt, David Altshuler, Alex Parker, John D. Rioux, Jill Platko, Daniel Gaudet, Thomas J. Hudson, Leif Groop, Eric S. Lander
Published 2001Artigo -
6
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction by Jessica Shea, Vineeta Agarwala, Anthony Philippakis, Jared Maguire, Eric Banks, Mark A. DePristo, Brian Thomson, Candace Guiducci, Robert C. Onofrio, Sekar Kathiresan, Stacey Gabriel, Noël P. Burtt, Mark J. Daly, Leif Groop, David Altshuler
Published 2011Artigo -
7
Association of Common Variation in the <i>HNF1α</i> Gene Region With Risk of Type 2 Diabetes by Wendy Winckler, Noël P. Burtt, Johan Holmkvist, Camilla Cervin, Paul I.W. de Bakker, Maria Sun, Peter Almgren, Jaakko Tuomilehto, Daniel Gaudet, Thomas J. Hudson, Kristin Ardlie, Mark J. Daly, Joel N. Hirschhorn, David Altshuler, Leif Groop
Published 2005Artigo -
8
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study by Sekar Kathiresan, Alisa K. Manning, Serkalem Demissie, Ralph B. D’Agostino, Aarti Surti, Candace Guiducci, Lauren Gianniny, Noël P. Burtt, Olle Melander, Marju Orho‐Melander, Donna K. Arnett, Gina M. Peloso, José M. Ordovás, L. Adrienne Cupples
Published 2007Artigo -
9
Association Testing in 9,000 People Fails to Confirm the Association of the Insulin Receptor Substrate-1 G972R Polymorphism With Type 2 Diabetes by José C. Florez, Marketa Sjögren, Noël P. Burtt, Marju Orho‐Melander, Steve Schayer, Maria Sun, Peter Almgren, Ulf Lindblad, Jaakko Tuomilehto, Daniel Gaudet, Thomas J. Hudson, Mark J. Daly, Kristin Ardlie, Joel N. Hirschhorn, David Altshuler, Leif Groop
Published 2004Artigo -
10
Cerebrovascular Disease Knowledge Portal by Katherine Crawford, Cristina Gallego-Fábrega, Christina Kourkoulis, Laura Miyares, Sandro Marini, Jason Flannick, Noël P. Burtt, Marcin von Grotthuss, Benjamin Alexander, Maria C. Costanzo, Neil Vaishnav, Rainer Malik, Jennifer L. Hall, Michael Chong, Jonathan Rosand, Guido J. Falcone
Published 2018Revisão -
11
Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs by Seong Kyu Han, Michelle Mcnulty, Christopher J. Benway, Pei Wen, Anya Greenberg, Ana C. Onuchic-Whitford, Dongkeun Jang, Jason Flannick, Noël P. Burtt, Parker C. Wilson, Benjamin D. Humphreys, Xiaoquan Wen, Zhe Han, Dongwon Lee, Matthew G. Sampson
Published 2023Artigo -
12
Common Single Nucleotide Polymorphisms in <i>TCF7L2</i> Are Reproducibly Associated With Type 2 Diabetes and Reduce the Insulin Response to Glucose in Nondiabetic Individuals by Richa Saxena, Lauren Gianniny, Noël P. Burtt, Valeriya Lyssenko, Candace Giuducci, Marketa Sjögren, José C. Florez, Peter Almgren, Bo Isomaa, Marju Orho‐Melander, Ulf Lindblad, Mark J. Daly, Jaakko Tuomilehto, Joel N. Hirschhorn, Kristin Ardlie, Leif Groop, David Altshuler
Published 2006Artigo -
13
5′ Flanking Variants of Resistin Are Associated With Obesity by James C. Engert, Marie‐Claude Vohl, Scott M. Williams, Pierre Lepage, Jorge Loredo‐Osti, Janet Faith, Carole Doré, Yannick Renaud, Noël P. Burtt, Amélie Villeneuve, Joel N. Hirschhorn, David Altshuler, Leif Groop, Jean‐Pierre Després, Daniel Gaudet, Thomas J. Hudson
Published 2002Artigo -
14
An effector index to predict target genes at GWAS loci by Vincenzo Forgetta, Lai Jiang, Nicholas A. Vulpescu, Megan S. Hogan, Siyuan Chen, John Morris, Stepan Grinek, Christian Benner, Dongkeun Jang, Quy Hoang, Noël P. Burtt, Jason Flannick, Mark I. McCarthy, Eric B. Fauman, Celia M.T. Greenwood, Matthew T. Maurano, J. Brent Richards
Published 2022Artigo -
15
The Lipid Droplet Knowledge Portal: A resource for systematic analyses of lipid droplet biology by Niklas Mejhert, Katlyn R. Gabriel, Scott Frendo‐Cumbo, Natalie Krahmer, Jiunn Song, Leena Kuruvilla, Chandramohan Chitraju, Sebastian Boland, Dongkeun Jang, Marcin von Grotthuss, Maria C. Costanzo, Mikael Rydén, James A. Olzmann, Jason Flannick, Noël P. Burtt, Robert V. Farese, Tobias C. Walther
Published 2022Artigo -
16
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency by Sarah E. Calvo, Elena J. Tucker, Alison G. Compton, Denise M. Kirby, Gabriel Crawford, Noël P. Burtt, Manuel A. Rivas, Candace Guiducci, Damien L. Bruno, Olga Goldberger, Michelle C Redman, Esko Wiltshire, Callum Wilson, David Altshuler, Stacey B. Gabriel, Mark J. Daly, David R. Thorburn, Vamsi K. Mootha
Published 2010Artigo -
17
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus by Robert Graham, Chris Cotsapas, Leela Davies, Rachel Hackett, Christopher J. Lessard, Joanlise M Leon, Noël P. Burtt, Candace Guiducci, Melissa Parkin, Casey Gates, Robert M. Plenge, Timothy W. Behrens, Joan Wither, John D. Rioux, Paul R. Fortin, Deborah Cunninghame Graham, Andrew Wong, Timothy J. Vyse, Mark J. Daly, David Altshuler, Kathy L. Moser, Patrick M. Gaffney
Published 2008Artigo -
18
The Neurodegenerative Disease Knowledge Portal by Allison A. Dilliott, Maria C. Costanzo, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Bradford Casey, Quy Hoang, Hirotaka Iwaki, Dongkeun Jang, Jonggeol Jeffrey Kim, Hampton L. Leonard, Kristin Levine, Mary B. Makarious, Trang Thi Huyen Nguyen, Guy A. Rouleau, Andrew Singleton, Patrick Smadbeck, Justin Solle, Dan Vitale, Mike A. Nalls, Jason Flannick, Noël P. Burtt, Sali M.K. Farhan
Published 2025Revisão -
19
Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction by Diego Ardissino, Carlo Berzuini, Piera Angelica Merlini, Pier Mannuccio Mannucci, Aarti Surti, Noël P. Burtt, Benjamin F. Voight, Marco Tubaro, Flora Peyvandi, M. Spreafico, Patrizia Celli, Daniela Lina, Maria Francesca Notarangelo, Maurizio Ferrario, Raffaela Fetiveau, Giorgio Casari, Michele Galli, Flavio Ribichini, Marco Rossi, Francesco Bernardi, Nicola Marziliano, Pietro Zonzin, Francesco Mauri, Alberto Piazza, Luisa Foco, Luisa Bernardinelli, David Altshuler, Sekar Kathiresan
Published 2011Artigo -
20
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans by Sekar Kathiresan, Olle Melander, Candace Guiducci, Aarti Surti, Noël P. Burtt, Mark J. Rieder, Gregory M. Cooper, Charlotta Roos, Benjamin F. Voight, Aki S. Havulinna, Björn Wahlstrand, Thomas Hedner, Dolores Corella, E Shyong Tai, José M. Ordovás, Göran Berglund, Erkki Vartiainen, Jari Lahti, Bo Hedblad, Marja‐Riitta Taskinen, Christopher Newton‐Cheh, Veikko Salomaa, Leena Peltonen, Leif Groop, David Altshuler, Marju Orho‐Melander
Published 2008Revisão
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