HuGE Literature Finder
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Records 1-14
Genome-wide association study of blood lipids in Indians confirms universality of established variants.
Journal of human genetics 2019 Jun 64 (6): 573-587. Bandesh Khushdeep, Prasad Gauri, Giri Anil K, Kauser Yasmeen, Upadhyay Medha, , Basu Analabha, Tandon Nikhil, Bharadwaj Dwaipay |
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The impact of low-frequency and rare variants on lipid levels.
Nature genetics 2015 Jun 47 (6): 589-97. Surakka Ida, Horikoshi Momoko, Mägi Reedik, Sarin Antti-Pekka, Mahajan Anubha, Lagou Vasiliki, Marullo Letizia, Ferreira Teresa, Miraglio Benjamin, Timonen Sanna, Kettunen Johannes, Pirinen Matti, Karjalainen Juha, Thorleifsson Gudmar, Hägg Sara, Hottenga Jouke-Jan, Isaacs Aaron, Ladenvall Claes, Beekman Marian, Esko Tõnu, Ried Janina S, Nelson Christopher P, Willenborg Christina, Gustafsson Stefan, Westra Harm-Jan, Blades Matthew, de Craen Anton J M, de Geus Eco J, Deelen Joris, Grallert Harald, Hamsten Anders, Havulinna Aki S, Hengstenberg Christian, Houwing-Duistermaat Jeanine J, Hyppönen Elina, Karssen Lennart C, Lehtimäki Terho, Lyssenko Valeriya, Magnusson Patrik K E, Mihailov Evelin, Müller-Nurasyid Martina, Mpindi John-Patrick, Pedersen Nancy L, Penninx Brenda W J H, Perola Markus, Pers Tune H, Peters Annette, Rung Johan, Smit Johannes H, Steinthorsdottir Valgerdur, Tobin Martin D, Tsernikova Natalia, van Leeuwen Elisabeth M, Viikari Jorma S, Willems Sara M, Willemsen Gonneke, Schunkert Heribert, Erdmann Jeanette, Samani Nilesh J, Kaprio Jaakko, Lind Lars, Gieger Christian, Metspalu Andres, Slagboom P Eline, Groop Leif, van Duijn Cornelia M, Eriksson Johan G, Jula Antti, Salomaa Veikko, Boomsma Dorret I, Power Christine, Raitakari Olli T, Ingelsson Erik, Järvelin Marjo-Riitta, Thorsteinsdottir Unnur, Franke Lude, Ikonen Elina, Kallioniemi Olli, Pietiäinen Vilja, Lindgren Cecilia M, Stefansson Kari, Palotie Aarno, McCarthy Mark I, Morris Andrew P, Prokopenko Inga, Ripatti Samuli, |
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Discovery of coding genetic variants influencing diabetes-related serum biomarkers and their impact on risk of type 2 diabetes.
The Journal of clinical endocrinology and metabolism 2015 Apr 100 (4): E664-71. Ahluwalia Tarunveer Singh, Allin Kristine Højgaard, Sandholt Camilla Helene, Sparsø Thomas Hempel, Jørgensen Marit Eika, Rowe Michael, Christensen Cramer, Brandslund Ivan, Lauritzen Torsten, Linneberg Allan, Husemoen Lise Lotte, Jørgensen Torben, Hansen Torben, Grarup Niels, Pedersen Ol |
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Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries.
Clinical chemistry 2015 Jan 61 (1): 231-8. Futema Marta, Shah Sonia, Cooper Jackie A, Li KaWah, Whittall Ros A, Sharifi Mahtab, Goldberg Olivia, Drogari Euridiki, Mollaki Vasiliki, Wiegman Albert, Defesche Joep, D'Agostino Maria N, D'Angelo Antonietta, Rubba Paolo, Fortunato Giuliana, Walu?-Miarka Ma?gorzata, Hegele Robert A, Aderayo Bamimore Mary, Durst Ronen, Leitersdorf Eran, Mulder Monique T, Roeters van Lennep Jeanine E, Sijbrands Eric J G, Whittaker John C, Talmud Philippa J, Humphries Steve |
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Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study.
Cardiovascular diabetology 2014 13 (1): 77. Adams Jeremy N, Raffield Laura M, Freedman Barry I, Langefeld Carl D, Ng Maggie C Y, Carr J Jeffrey, Cox Amanda J, Bowden Donald |
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Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study.
European heart journal 2013 Apr 34 (13): 982-92. Hopewell Jemma C, Parish Sarah, Offer Alison, Link Emma, Clarke Robert, Lathrop Mark, Armitage Jane, Collins Rory, |
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Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study.
PloS one 2012 7 (4): e35651. Buyske Steven, Wu Ying, Carty Cara L, Cheng Iona, Assimes Themistocles L, Dumitrescu Logan, Hindorff Lucia A, Mitchell Sabrina, Ambite Jose Luis, Boerwinkle Eric, Buzkova Petra, Carlson Chris S, Cochran Barbara, Duggan David, Eaton Charles B, Fesinmeyer Megan D, Franceschini Nora, Haessler Jeffrey, Jenny Nancy, Kang Hyun Min, Kooperberg Charles, Lin Yi, Le Marchand Loic, Matise Tara C, Robinson Jennifer G, Rodriguez Carlos, Schumacher Fredrick R, Voight Benjamin F, Young Alicia, Manolio Teri A, Mohlke Karen L, Haiman Christopher A, Peters Ulrike, Crawford Dana C, North Kari |
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Impact of variants within seven candidate genes on statin treatment efficacy.
Physiological research / Academia Scientiarum Bohemoslovaca 2012 61 (6): 609-17. Vrablík M, Hubá?ek J A, Dlouhá D, Lánská V, Rynekrová J, Zlatohlávek L, Prusíková M, Ceška R, Adámková |
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Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies.
Journal of the American College of Cardiology 2011 Dec 58 (25): 2675-82. Qi Lu, Parast Layla, Cai Tianxi, Powers Christine, Gervino Ernest V, Hauser Thomas H, Hu Frank B, Doria Alessand |
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The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations.
Pediatric research 2011 Jun 69 (6): 538-43. Devaney Joseph M, Thompson Paul D, Visich Paul S, Saltarelli William A, Gordon Paul M, Orkunoglu-Suer E Funda, Gordish-Dressman Heather, Harmon Brennan T, Bradbury Margaret K, Panchapakesan Karuna, Khianey Rahul, Hubal Monica J, Clarkson Priscilla M, Pescatello Linda S, Zoeller Robert F, Moyna Niall M, Angelopoulos Theodore J, Kraus William E, Hoffman Eric |
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Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population.
Diabetologia 2010 Oct 53 (10): 2155-62. Fontaine-Bisson B, Renström F, Rolandsson O, , Payne F, Hallmans G, Barroso I, Franks P |
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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Fine-mapping in African Americans of 8 recently discovered genetic loci for plasma lipids: the Jackson Heart Study.
Circulation. Cardiovascular genetics 2010 Aug 3 (4): 358-64. Keebler Mary E, Deo Rahul C, Surti Aarti, Konieczkowski David, Guiducci Candace, Burtt Noel, Buxbaum Sarah G, Sarpong Daniel F, Steffes Michael W, Wilson James G, Taylor Herman A, Kathiresan Sek |
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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
American journal of human genetics 2008 Jan 82 (1): 139-49. Wallace Chris, Newhouse Stephen J, Braund Peter, Zhang Feng, Tobin Martin, Falchi Mario, Ahmadi Kourosh, Dobson Richard J, Marçano Ana Carolina B, Hajat Cother, Burton Paul, Deloukas Panagiotis, Brown Morris, Connell John M, Dominiczak Anna, Lathrop G Mark, Webster John, Farrall Martin, Spector Tim, Samani Nilesh J, Caulfield Mark J, Munroe Patricia |
- Page last reviewed:Jul 30, 2019
- Page last updated:Oct 10, 2019
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