Výsledky vyhledávání - Noël P. Burtt

Upřesnit hledání
  1. 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

    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 Autor Mary Keebler, Christopher Sanders, Aarti Surti, Candace Guiducci, Noël P. Burtt, Sekar Kathiresan

    Vydáno 2009
    Získat plný text Získat plný text
    Revisão
    Přidat do oblíbených
    Uloženo v:
  2. 2
    Functional Investigations of <i>HNF1A</i> Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population

    Functional Investigations of <i>HNF1A</i> Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population Autor 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

    Vydáno 2016
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  3. 3
    Polymorphisms Associated with Cholesterol and Risk of Cardiovascular Events

    Polymorphisms Associated with Cholesterol and Risk of Cardiovascular Events Autor 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

    Vydáno 2008
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  4. 4
    Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease

    Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease Autor 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

    Vydáno 2006
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  5. 5
    Genomewide Linkage Analysis of Stature in Multiple Populations Reveals Several Regions with Evidence of Linkage to Adult Height

    Genomewide Linkage Analysis of Stature in Multiple Populations Reveals Several Regions with Evidence of Linkage to Adult Height Autor 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

    Vydáno 2001
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  6. 6
    Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction

    Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction Autor 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

    Vydáno 2011
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  7. 7
    Association of Common Variation in the <i>HNF1α</i> Gene Region With Risk of Type 2 Diabetes

    Association of Common Variation in the <i>HNF1α</i> Gene Region With Risk of Type 2 Diabetes Autor 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

    Vydáno 2005
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  8. 8
    A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study

    A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study Autor 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

    Vydáno 2007
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  9. 9
    Association Testing in 9,000 People Fails to Confirm the Association of the Insulin Receptor Substrate-1 G972R Polymorphism With Type 2 Diabetes

    Association Testing in 9,000 People Fails to Confirm the Association of the Insulin Receptor Substrate-1 G972R Polymorphism With Type 2 Diabetes Autor 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

    Vydáno 2004
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  10. 10
    Cerebrovascular Disease Knowledge Portal

    Cerebrovascular Disease Knowledge Portal Autor 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

    Vydáno 2018
    Získat plný text Získat plný text
    Revisão
    Přidat do oblíbených
    Uloženo v:
  11. 11
    Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs

    Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs Autor 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

    Vydáno 2023
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  12. 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

    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 Autor 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

    Vydáno 2006
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  13. 13
    5′ Flanking Variants of Resistin Are Associated With Obesity

    5′ Flanking Variants of Resistin Are Associated With Obesity Autor 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

    Vydáno 2002
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  14. 14
    An effector index to predict target genes at GWAS loci

    An effector index to predict target genes at GWAS loci Autor 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

    Vydáno 2022
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  15. 15
    The Lipid Droplet Knowledge Portal: A resource for systematic analyses of lipid droplet biology

    The Lipid Droplet Knowledge Portal: A resource for systematic analyses of lipid droplet biology Autor 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

    Vydáno 2022
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  16. 16
    High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency

    High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency Autor 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

    Vydáno 2010
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  17. 17
    Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus

    Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Autor 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

    Vydáno 2008
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  18. 18
    The Neurodegenerative Disease Knowledge Portal

    The Neurodegenerative Disease Knowledge Portal Autor 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

    Vydáno 2025
    Získat plný text
    Revisão
    Přidat do oblíbených
    Uloženo v:
  19. 19
    Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction

    Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction Autor 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

    Vydáno 2011
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  20. 20
    Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

    Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans Autor 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

    Vydáno 2008
    Získat plný text
    Revisão
    Přidat do oblíbených
    Uloženo v:

Vyhledávací nástroje: