Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: PCSK2[original query] |
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Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population. Molecular genetics and metabolism 0 92 (1-2): 145-50. Leak Tennille S, Keene Keith L, Langefeld Carl D, Gallagher Carla J, Mychaleckyj Josyf C, Freedman Barry I, Bowden Donald W, Rich Stephen S, Sale Michèle |
Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.
BMC medical genetics 2007 8 Suppl 1 S4. O'Donnell Christopher J, Cupples L Adrienne, D'Agostino Ralph B, Fox Caroline S, Hoffmann Udo, Hwang Shih-Jen, Ingellson Erik, Liu Chunyu, Murabito Joanne M, Polak Joseph F, Wolf Philip A, Demissie Serkal |
Association of gene polymorphisms with chronic kidney disease in Japanese individuals. International journal of molecular medicine 2009 Oct 24 (4): 539-47. Yoshida Tetsuro, Kato Kimihiko, Yokoi Kiyoshi, Oguri Mitsutoshi, Watanabe Sachiro, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Aoyagi Yukitoshi, Nozawa Yoshinori, Yamada Yoshi |
Genome-wide association study of biochemical traits in Korcula Island, Croatia.
Croatian medical journal 2009 Feb 50 (1): 23-33. Zemunik Tatijana, Boban Mladen, Lauc Gordan, Jankovi? Stipan, Rotim Kresimir, Vatavuk Zoran, Benci? Goran, Dogas Zoran, Boraska Vesna, Torlak Vesela, Susac Jelena, Zobi? Ivana, Rudan Diana, Pulani? Drazen, Modun Darko, Mudni? Ivana, Gunjaca Grgo, Budimir Danijela, Hayward Caroline, Vitart Veronique, Wright Alan F, Campbell Harry, Rudan Ig |
Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals. Atherosclerosis 2009 12 210 (2): 468-73. Fujimaki Tetsuo, Kato Kimihiko, Yokoi Kiyoshi, Oguri Mitsutoshi, Yoshida Tetsuro, Watanabe Sachiro, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Aoyagi Yukitoshi, Nozawa Yoshinori, Kimura Genjiro, Yamada Yoshi |
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
Nature genetics 2010 Dec 42 (12): 1077-85. Elks Cathy E, Perry John R B, Sulem Patrick, Chasman Daniel I, Franceschini Nora, He Chunyan, Lunetta Kathryn L, Visser Jenny A, Byrne Enda M, Cousminer Diana L, Gudbjartsson Daniel F, Esko Tõnu, Feenstra Bjarke, Hottenga Jouke-Jan, Koller Daniel L, Kutalik Zoltán, Lin Peng, Mangino Massimo, Marongiu Mara, McArdle Patrick F, Smith Albert V, Stolk Lisette, van Wingerden Sophie H, Zhao Jing Hua, Albrecht Eva, Corre Tanguy, Ingelsson Erik, Hayward Caroline, Magnusson Patrik K E, Smith Erin N, Ulivi Shelia, Warrington Nicole M, Zgaga Lina, Alavere Helen, Amin Najaf, Aspelund Thor, Bandinelli Stefania, Barroso Inês, Berenson Gerald S, Bergmann Sven, Blackburn Hannah, Boerwinkle Eric, Buring Julie E, Busonero Fabio, Campbell Harry, Chanock Stephen J, Chen Wei, Cornelis Marilyn C, Couper David, Coviello Andrea D, d'Adamo Pio, de Faire Ulf, de Geus Eco J C, Deloukas Panos, Döring Angela, Smith George Davey, Easton Douglas F, Eiriksdottir Gudny, Emilsson Valur, Eriksson Johan, Ferrucci Luigi, Folsom Aaron R, Foroud Tatiana, Garcia Melissa, Gasparini Paolo, Geller Frank, Gieger Christian, , Gudnason Vilmundur, Hall Per, Hankinson Susan E, Ferreli Liana, Heath Andrew C, Hernandez Dena G, Hofman Albert, Hu Frank B, Illig Thomas, Järvelin Marjo-Riitta, Johnson Andrew D, Karasik David, Khaw Kay-Tee, Kiel Douglas P, Kilpeläinen Tuomas O, Kolcic Ivana, Kraft Peter, Launer Lenore J, Laven Joop S E, Li Shengxu, Liu Jianjun, Levy Daniel, Martin Nicholas G, McArdle Wendy L, Melbye Mads, Mooser Vincent, Murray Jeffrey C, Murray Sarah S, Nalls Michael A, Navarro Pau, Nelis Mari, Ness Andrew R, Northstone Kate, Oostra Ben A, Peacock Munro, Palmer Lyle J, Palotie Aarno, Paré Guillaume, Parker Alex N, Pedersen Nancy L, Peltonen Leena, Pennell Craig E, Pharoah Paul, Polasek Ozren, Plump Andrew S, Pouta Anneli, Porcu Eleonora, Rafnar Thorunn, Rice John P, Ring Susan M, Rivadeneira Fernando, Rudan Igor, Sala Cinzia, Salomaa Veikko, Sanna Serena, Schlessinger David, Schork Nicholas J, Scuteri Angelo, Segrè Ayellet V, Shuldiner Alan R, Soranzo Nicole, Sovio Ulla, Srinivasan Sathanur R, Strachan David P, Tammesoo Mar-Liis, Tikkanen Emmi, Toniolo Daniela, Tsui Kim, Tryggvadottir Laufey, Tyrer Jonathon, Uda Manuela, van Dam Rob M, van Meurs Joyce B J, Vollenweider Peter, Waeber Gerard, Wareham Nicholas J, Waterworth Dawn M, Weedon Michael N, Wichmann H Erich, Willemsen Gonneke, Wilson James F, Wright Alan F, Young Lauren, Zhai Guangju, Zhuang Wei Vivian, Bierut Laura J, Boomsma Dorret I, Boyd Heather A, Crisponi Laura, Demerath Ellen W, van Duijn Cornelia M, Econs Michael J, Harris Tamara B, Hunter David J, Loos Ruth J F, Metspalu Andres, Montgomery Grant W, Ridker Paul M, Spector Tim D, Streeten Elizabeth A, Stefansson Kari, Thorsteinsdottir Unnur, Uitterlinden André G, Widen Elisabeth, Murabito Joanne M, Ong Ken K, Murray An |
Association of type 2 diabetes susceptibility genes (TCF7L2, SLC30A8, PCSK1 and PCSK2) and proinsulin conversion in a Chinese population. Molecular biology reports 2012 Jan 39 (1): 17-23. Zheng Xiaoya, Ren Wei, Zhang Suhua, Liu Jingjing, Li Sufang, Li Jinchao, Yang Ping, He Jun, Su Shaochu, Li Pi |
Effect of a common variant of the PCSK2 gene on reduced insulin secretion. Diabetologia 2012 Dec 55 (12): 3245-51. Jonsson A, Isomaa B, Tuomi T, Eriksson J G, Groop L, Lyssenko |
A high-density genome-wide association screen of sporadic ALS in US veterans.
PloS one 2012 7 (3): e32768. Kwee Lydia Coulter, Liu Yutao, Haynes Carol, Gibson Jason R, Stone Annjanette, Schichman Steven A, Kamel Freya, Nelson Lorene M, Topol Barbara, Van den Eeden Stephen K, Tanner Caroline M, Cudkowicz Merit E, Grasso Daniela L, Lawson Robert, Muralidhar Sumitra, Oddone Eugene Z, Schmidt Silke, Hauser Michael |
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
PloS one 2012 7 (12): 12. Comuzzie AG, Cole SA, Laston SL, Voruganti VS, Haack K, Gibbs RA, Butte NF |
A genome-wide association meta-analysis of preschool internalizing problems.
Journal of the American Academy of Child and Adolescent Psychiatry 2014 Jun 53 (6): 667-676.e7. Benke Kelly S, Nivard Michel G, Velders Fleur P, Walters Raymond K, Pappa Irene, Scheet Paul A, Xiao Xiangjun, Ehli Erik A, Palmer Lyle J, Whitehouse Andrew J O, Verhulst Frank C, Jaddoe Vincent W, Rivadeneira Fernando, Groen-Blokhuis Maria M, van Beijsterveldt Catharina E M, Davies Gareth E, Hudziak James J, Lubke Gitta H, Boomsma Dorret I, Pennell Craig E, Tiemeier Henning, Middeldorp Christel M, |
Quantitative candidate gene association studies of metabolic traits in Han Chinese type 2 diabetes patients. Genetics and molecular research : GMR 2015 14 (4): 15471-81. Wei F J, Cai C Y, Yu P, Lv J, Ling C, Shi W T, Jiao H X, Chang B C, Yang F H, Tian Y, Li M S, Wang Y H, Zou L, Shi J M, Chen L M, Li W |
Genetic polymorphisms of PCSK2 are associated with glucose homeostasis and progression to type 2 diabetes in a Chinese population. Scientific reports 2015 5 14380. Chang Tien-Jyun, Chiu Yen-Feng, Sheu Wayne H-H, Shih Kuang-Chung, Hwu Chii-Min, Quertermous Thomas, Jou Yuh-Shan, Kuo Shan-Shan, Chang Yi-Cheng, Chuang Lee-Mi |
MC1R variants affect the expression of melanocortin and melanogenic genes and the association between melanocortin genes and coloration. Molecular ecology 2016 Sep . San-Jose Luis M, Ducrest Anne-Lyse, Ducret Valérie, Simon Céline, Richter Hannes, Wakamatsu Kazumasa, Roulin Alexand |
Functional analysis of PCSK2 coding variants: A founder effect in the Old Order Amish population. Diabetes research and clinical practice 2017 Jul 131 82-90. Winters Alexandra, Ramos-Molina Bruno, Jarvela Timothy S, Yerges-Armstrong Laura, Pollin Toni I, Lindberg Ir |
Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy.
BMC medical genetics 2018 May 19 (1): 71. Graham Patricia S, Kaidonis Georgia, Abhary Sotoodeh, Gillies Mark C, Daniell Mark, Essex Rohan W, Chang John H, Lake Stewart R, Pal Bishwanath, Jenkins Alicia J, Hewitt Alex W, Lamoureux Ecosse L, Hykin Philip G, Petrovsky Nikolai, Brown Matthew A, Craig Jamie E, Burdon Kathryn |
Heterozygous rare genetic variants in non-syndromic early-onset obesity. International journal of obesity (2005) 2019 3 44 (4): 830-841. Serra-Juhé Clara, Martos-Moreno Gabriel Á, Bou de Pieri Francesc, Flores Raquel, Chowen Julie A, Pérez-Jurado Luis A, Argente Jes |
Common variants in genes involved in islet amyloid polypeptide (IAPP) processing and the degradation pathway are associated with T2DM risk: A Chinese population study. Diabetes research and clinical practice 2022 Feb 185 109235. Xu Jie, Jin Li, Chen Jie, Zhang Rong, Zhang Hong, Li Yangyang, Peng Danfeng, Gu Yunjuan, Wheeler Michael B, Hu Che |
Association of common variants of TCF7L2 and PCSK2 with gestational diabetes mellitus in West Bengal, India. Nucleosides, nucleotides & nucleic acids 2023 8 1-18. Jayita Basu, Ruchira Mukherjee, Pooja Sahu, Chhanda Datta, Subhankar Chowdhury, Debasmita Mandal, Amlan Gho |
Susceptibility of PCSK2 Polymorphism to Hirschsprung Disease in Southern Chinese Children. Clinical and experimental gastroenterology 2023 5 16 59-64. Bingtong Wang, Wenlin Fang, Dingjiang Qin, Qiuming He, Chaoting L |
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- Page last updated:Apr 22, 2024
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