Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and PCSK1[original query] |
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Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
Diabetes 2011 Oct 60 (10): 2624-34. Strawbridge Rona J, Dupuis Josée, Prokopenko Inga, Barker Adam, Ahlqvist Emma, Rybin Denis, Petrie John R, Travers Mary E, Bouatia-Naji Nabila, Dimas Antigone S, Nica Alexandra, Wheeler Eleanor, Chen Han, Voight Benjamin F, Taneera Jalal, Kanoni Stavroula, Peden John F, Turrini Fabiola, Gustafsson Stefan, Zabena Carina, Almgren Peter, Barker David J P, Barnes Daniel, Dennison Elaine M, Eriksson Johan G, Eriksson Per, Eury Elodie, Folkersen Lasse, Fox Caroline S, Frayling Timothy M, Goel Anuj, Gu Harvest F, Horikoshi Momoko, Isomaa Bo, Jackson Anne U, Jameson Karen A, Kajantie Eero, Kerr-Conte Julie, Kuulasmaa Teemu, Kuusisto Johanna, Loos Ruth J F, Luan Jian'an, Makrilakis Konstantinos, Manning Alisa K, Martínez-Larrad María Teresa, Narisu Narisu, Nastase Mannila Maria, Ohrvik John, Osmond Clive, Pascoe Laura, Payne Felicity, Sayer Avan A, Sennblad Bengt, Silveira Angela, Stancáková Alena, Stirrups Kathy, Swift Amy J, Syvänen Ann-Christine, Tuomi Tiinamaija, van 't Hooft Ferdinand M, Walker Mark, Weedon Michael N, Xie Weijia, Zethelius Björn, , , , , , Ongen Halit, Mälarstig Anders, Hopewell Jemma C, Saleheen Danish, Chambers John, Parish Sarah, Danesh John, Kooner Jaspal, Ostenson Claes-Göran, Lind Lars, Cooper Cyrus C, Serrano-Ríos Manuel, Ferrannini Ele, Forsen Tom J, Clarke Robert, Franzosi Maria Grazia, Seedorf Udo, Watkins Hugh, Froguel Philippe, Johnson Paul, Deloukas Panos, Collins Francis S, Laakso Markku, Dermitzakis Emmanouil T, Boehnke Michael, McCarthy Mark I, Wareham Nicholas J, Groop Leif, Pattou François, Gloyn Anna L, Dedoussis George V, Lyssenko Valeriya, Meigs James B, Barroso Inês, Watanabe Richard M, Ingelsson Erik, Langenberg Claudia, Hamsten Anders, Florez Jose |
| A genetic variant in the seed region of miR-4513 shows pleiotropic effects on lipid and glucose homeostasis, blood pressure, and coronary artery disease. Human mutation 2014 Dec 35 (12): 1524-31. Ghanbari Mohsen, de Vries Paul S, de Looper Hans, Peters Marjolein J, Schurmann Claudia, Yaghootkar Hanieh, Dörr Marcus, Frayling Timothy M, Uitterlinden Andre G, Hofman Albert, van Meurs Joyce B J, Erkeland Stefan J, Franco Oscar H, Dehghan Abb |
| Genetic variants in PCSK1 gene are associated with the risk of coronary artery disease in type 2 diabetes in a Chinese Han population: a case control study. PloS one 2014 9 (1): e87168. Wei Xiaowei, Ma Xiaowei, Lu Ran, Bai Ge, Zhang Jianwei, Deng Ruifen, Gu Nan, Feng Nan, Guo Xiaoh |
| Implication of genetic variants in overweight and obesity susceptibility among the young Arab population of the United Arab Emirates. Gene 2020 Feb 739 144509. El Hajj Chehadeh Sarah, Osman Wael, Nazar Suna, Jerman Laila, Alghafri Ameera, Sajwani Ali, Alawlaqi Mohamed, AlObeidli Mohamed, Jelinek Herbert F, AlAnouti Fatme, Khalaf Kinda, Alsafar Habi |
| Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease. Nature communications 2020 Feb 11 (1): 995. Serra Eva Gonçalves, Schwerd Tobias, Moutsianas Loukas, Cavounidis Athena, Fachal Laura, Pandey Sumeet, Kammermeier Jochen, Croft Nicholas M, Posovszky Carsten, Rodrigues Astor, Russell Richard K, Barakat Farah, Auth Marcus K H, Heuschkel Robert, Zilbauer Matthias, Fyderek Krzysztof, Braegger Christian, Travis Simon P, Satsangi Jack, Parkes Miles, Thapar Nikhil, Ferry Helen, Matte Julie C, Gilmour Kimberly C, Wedrychowicz Andrzej, Sullivan Peter, Moore Carmel, Sambrook Jennifer, Ouwehand Willem, Roberts David, Danesh John, Baeumler Toni A, Fulga Tudor A, Carrami Eli M, Ahmed Ahmed, Wilson Rachel, Barrett Jeffrey C, Elkadri Abdul, Griffiths Anne M, , , , , , , Snapper Scott B, Shah Neil, Muise Aleixo M, Wilson David C, Uhlig Holm H, Anderson Carl |
| Heterozygous Genetic Variants in Autosomal Recessive Genes of the Leptin-Melanocortin Signalling Pathway Are Associated With the Development of Childhood Obesity. Frontiers in endocrinology 2022 13 832911. Šket Robert, Kotnik Primož, Bizjan Barbara Jenko, Kocen Valentina, Mlinari? Matej, Tesovnik Tine, Debeljak Maruša, Battelino Tadej, Kova? Jern |
| The Spectrum of Genetic Variants Associated with the Development of Monogenic Obesity in Qatar. Obesity facts 2022 1 15 (3): 357-365. AbouHashem Nadien, Zaied Roan E, Al-Shafai Kholoud, Nofal Mariam, Syed Najeeb, Al-Shafai Masha |
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