Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 34 Records) |
Query Trace: CAMK1D[original query] |
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Association of common type 2 diabetes risk gene variants and posttransplantation diabetes mellitus in renal allograft recipients in Korea. Transplantation 2009 Sep 88 (5): 693-8. Kang Eun Seok, Kim Myoung Soo, Kim Chul Hoon, Nam Chung Mo, Han Seung Jin, Hur Kyu Yeon, Ahn Chul Woo, Cha Bong Soo, Kim Soon Il, Lee Hyun Chul, Kim Yu Se |
Lack of significant effects of the type 2 diabetes susceptibility loci JAZF1, CDC123/CAMK1D, NOTCH2, ADAMTS9, THADA, and TSPAN8/LGR5 on diabetes and quantitative metabolic traits. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2010 Jan 42 (1): 14-22. Schleinitz D, Tönjes A, Böttcher Y, Dietrich K, Enigk B, Koriath M, Scholz G H, Blüher M, Zeggini E, McCarthy M I, Kovacs P, Stumvoll |
Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI. Diabetes 2010 Mar 59 (3): 751-5. Zhao Jianhua, Bradfield Jonathan P, Zhang Haitao, Annaiah Kiran, Wang Kai, Kim Cecilia E, Glessner Joseph T, Frackelton Edward C, Otieno F George, Doran James, Thomas Kelly A, Garris Maria, Hou Cuiping, Chiavacci Rosetta M, Li Mingyao, Berkowitz Robert I, Hakonarson Hakon, Grant Struan F |
Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function. Diabetes 2010 Jan 59 (1): 293-301. Simonis-Bik Annemarie M, Nijpels Giel, van Haeften Timon W, Houwing-Duistermaat Jeanine J, Boomsma Dorret I, Reiling Erwin, van Hove Els C, Diamant Michaela, Kramer Mark H H, Heine Robert J, Maassen J Antonie, Slagboom P Eline, Willemsen Gonneke, Dekker Jacqueline M, Eekhoff Elisabeth M, de Geus Eco J, 't Hart Leen |
Variant near ADAMTS9 known to associate with type 2 diabetes is related to insulin resistance in offspring of type 2 diabetes patients--EUGENE2 study. PloS one 2009 4 (9): e7236. Boesgaard Trine Welløv, Gjesing Anette Prior, Grarup Niels, Rutanen Jarno, Jansson Per-Anders, Hribal Marta Letizia, Sesti Giorgio, Fritsche Andreas, Stefan Norbert, Staiger Harald, Häring Hans, Smith Ulf, Laakso Markku, Pedersen Oluf, Hansen Torben, |
Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers. Human molecular genetics 2010 Jul 19 (14): 2886-97. Wang Xianshu, Pankratz V Shane, Fredericksen Zachary, Tarrell Robert, Karaus Mary, McGuffog Lesley, Pharaoh Paul D P, Ponder Bruce A J, Dunning Alison M, Peock Susan, Cook Margaret, Oliver Clare, Frost Debra, , Sinilnikova Olga M, Stoppa-Lyonnet Dominique, Mazoyer Sylvie, Houdayer Claude, , Hogervorst Frans B L, Hooning Maartje J, Ligtenberg Marjolijn J, , Spurdle Amanda, Chenevix-Trench Georgia, , Schmutzler Rita K, Wappenschmidt Barbara, Engel Christoph, Meindl Alfons, Domchek Susan M, Nathanson Katherine L, Rebbeck Timothy R, Singer Christian F, Gschwantler-Kaulich Daphne, Dressler Catherina, Fink Anneliese, Szabo Csilla I, Zikan Michal, Foretova Lenka, Claes Kathleen, Thomas Gilles, Hoover Robert N, Hunter David J, Chanock Stephen J, Easton Douglas F, Antoniou Antonis C, Couch Fergus |
Variations in/nearby genes coding for JAZF1, TSPAN8/LGR5 and HHEX-IDE and risk of type 2 diabetes in Han Chinese. Journal of human genetics 2010 Dec 55 (12): 810-5. Zhou Dai-zhan, Liu Yun, Zhang Di, Liu Si-min, Yu Lan, Yang Yi-feng, Zhao Teng, Chen Zhuo, Kan Meng-yuan, Zhang Zuo-feng, Feng Guo-yin, Xu He, He L |
Genetic variants at CDC123/CAMK1D and SPRY2 are associated with susceptibility to type 2 diabetes in the Japanese population. Diabetologia 2011 Dec 54 (12): 3071-7. Imamura M, Iwata M, Maegawa H, Watada H, Hirose H, Tanaka Y, Tobe K, Kaku K, Kashiwagi A, Kawamori R, Nakamura Y, Maeda |
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population. Diabetes 2012 Dec 61 (12): 3314-21. Gamboa-Meléndez Marco Alberto, Huerta-Chagoya Alicia, Moreno-Macías Hortensia, Vázquez-Cárdenas Paola, Ordóñez-Sánchez María Luisa, Rodríguez-Guillén Rosario, Riba Laura, Rodríguez-Torres Maribel, Guerra-García María Teresa, Guillén-Pineda Luz Elizabeth, Choudhry Shweta, Del Bosque-Plata Laura, Canizales-Quinteros Samuel, Pérez-Ortiz Gustavo, Escobedo-Aguirre Fernando, Parra Adalberto, Lerman-Garber Israel, Aguilar-Salinas Carlos Alberto, Tusié-Luna María Tere |
Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations. Cerebrovascular diseases (Basel, Switzerland) 2013 36 (3): 181-8. Chou S H-Y, Shulman J M, Keenan B T, Secor E A, Buchman A S, Schneider J, Bennett D A, De Jager P |
Association study of genetic variants of 17 diabetes-related genes/loci and cardiovascular risk and diabetic nephropathy in the Chinese She population. Journal of diabetes 2013 Jun 5 (2): 136-45. Chen Gang, Xu Yuan, Lin Yinghua, Lai Xiaolan, Yao Jin, Huang Baoying, Chen Zichun, Huang Huibin, Fu Xianguo, Lin Lixiang, Lai Shenghan, Wen Junpi |
Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA study. Pharmacogenomics 2014 Sep 15 (13): 1643-52. Frau Francesca, Zaninello Roberta, Salvi Erika, Ortu Maria Francesca, Braga Daniele, Velayutham Dinesh, Argiolas Giuseppe, Fresu Giovanni, Troffa Chiara, Bulla Emanuela, Bulla Patrizia, Pitzoi Silvia, Piras Daniela Antonella, Glorioso Valeria, Chittani Martina, Bernini Giampaolo, Bardini Michele, Fallo Francesco, Malatino Lorenzo, Stancanelli Benedetta, Regolisti Giuseppe, Ferri Claudio, Desideri Giovanbattista, Scioli Giuseppe Antonio, Galletti Ferruccio, Sciacqua Angela, Perticone Francesco, Degli Esposti Ezio, Sturani Alessandra, Semplicini Andrea, Veglio Franco, Mulatero Paolo, Williams Tracy A, Lanzani Chiara, Hiltunen Timo P, Kontula Kimmo, Boerwinkle Eric, Turner Stephen T, Manunta Paolo, Barlassina Cristina, Cusi Daniele, Glorioso Nico |
Diabetes susceptibility in Mayas: Evidence for the involvement of polymorphisms in HHEX, HNF4a, KCNJ11, PPAR?, CDKN2A/2B, SLC30A8, CDC123/CAMK1D, TCF7L2, ABCA1 and SLC16A11 genes. Gene 2015 Jul 565 (1): 68-75. Lara-Riegos J C, Ortiz-López M G, Peña-Espinoza B I, Montúfar-Robles I, Peña-Rico M A, Sánchez-Pozos K, Granados-Silvestre M A, Menjivar |
Identifying genetic interactions associated with late-onset Alzheimer's disease. BioData mining 2014 7 (1): 35. Floudas Charalampos S, Um Nara, Kamboh M Ilyas, Barmada Michael M, Visweswaran Shy |
The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes. PloS one 2015 10 (11): e0143607. Kong Xiaomu, Zhang Xuelian, Xing Xiaoyan, Zhang Bo, Hong Jing, Yang Wenyi |
Genetic variants associated with lean and obese type 2 diabetes in a Han Chinese population: A case-control study. Medicine 2016 Jun 95 (23): e3841. Kong Xiaomu, Xing Xiaoyan, Hong Jing, Zhang Xuelian, Yang Wenyi |
Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity. Schizophrenia research 2016 Feb . Gadelha Ary, Coleman Jonathan, Breen Gerome, Mazzoti Diego Robles, Yonamine Camila M, Pellegrino Renata, Ota Vanessa Kiyomi, Belangero Sintia Iole, Glessner Joseph, Sleiman Patrick, Hakonarson Hakon, Hayashi Mirian A F, Bressan Rodrigo |
Genetic Epidemiology of Type 2 Diabetes in Mexican Mestizos. BioMed research international 2017 2017 3937893. García-Chapa Eiralí Guadalupe, Leal-Ugarte Evelia, Peralta-Leal Valeria, Durán-González Jorge, Meza-Espinoza Juan Pab |
CDC123/CAMK1D gene rs12779790 polymorphism and rs10811661 polymorphism upstream of the CDKN2A/2B gene in women with gestational diabetes. Journal of perinatology : official journal of the California Perinatal Association 2017 Jan . Tarnowski M, Malinowski D, Safranow K, Dziedziejko V, Pawlik |
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
Nature communications 2018 07 9 (1): 2941. Xue Angli, Wu Yang, Zhu Zhihong, Zhang Futao, Kemper Kathryn E, Zheng Zhili, Yengo Loic, Lloyd-Jones Luke R, Sidorenko Julia, Wu Yeda, , McRae Allan F, Visscher Peter M, Zeng Jian, Yang Ji |
A Deep Learning Approach for Predicting Antidepressant Response in Major Depression Using Clinical and Genetic Biomarkers.
Frontiers in psychiatry 2018 9 290. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yu Younger W-Y, Yang Albert C, Tsai Shih-J |
Genetic Variants Associated With Obesity and Insulin Resistance in Hispanic Boys With Nonalcoholic Fatty Liver Disease. Journal of pediatric gastroenterology and nutrition 2018 2 66 (5): 789-796. Rausch John C, Lavine Joel E, Chalasani Naga, Guo Xiuqing, Kwon Soonil, Schwimmer Jeffrey B, Molleston Jean P, Loomba Rohit, Brunt Elizabeth M, Chen Yii-Der Ida, Goodarzi Mark O, Taylor Kent D, Yates Katherine P, Rotter Jerome I, |
Integrated genetic and epigenetic analyses uncover MSI2 association with allergic inflammation. The Journal of allergy and clinical immunology 2020 8 147 (4): 1453-1463. Kim Kyung Won, Park Sang-Cheol, Cho Hyung-Ju, Jang Haerin, Park Jaehyun, Shim Hyo Sup, Kim Eun Gyul, Kim Mi Na, Hong Jung Yeon, Kim Yoon Hee, Lee Sanghun, Weiss Scott T, Kim Chang-Hoon, Won Sungho, Sohn Myung Hy |
Backbone resonance assignments of the catalytic and regulatory domains of Ca/calmodulin-dependent protein kinase 1D. Biomolecular NMR assignments 2020 6 14 (2): 221-225. Tong Michael H G, Jeeves Mark, Rajesh Sundaresan, Ludwig Christian, Lenoir Marc, Kumar Jitendra, McClelland Darren M, Berditchevski Fedor, Hubbard Julia A, Kenyon Colin, Butterworth Sam, Knapp Stefan, Overduin Micha |
Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health.
The European respiratory journal 2020 11 57 (5): . Strausz Satu, Ruotsalainen Sanni, Ollila Hanna M, Karjalainen Juha, Kiiskinen Tuomo, Reeve Mary, Kurki Mitja, Mars Nina, Havulinna Aki S, Luonsi Elina, Mansour Aly Dina, Ahlqvist Emma, Teder-Laving Maris, Palta Priit, Groop Leif, Mägi Reedik, Mäkitie Antti, Salomaa Veikko, Bachour Adel, Tuomi Tiinamaija, , Palotie Aarno, Palotie Tuula, Ripatti Samu |
Associations of SUCNR1, GRK4, CAMK1D gene polymorphisms and the susceptibility of type 2 diabetes mellitus and essential hypertension in a northern Chinese Han population. Journal of diabetes and its complications 2020 10 35 (1): 107752. Du Bingxin, Jia Xinhui, Tian Wenqi, Yan Xueqin, Wang Ningning, Cai Defu, Li Xueyan, Zhang Hao, Jin Ming, Wu Nan, Qiu Changchun, Zhang |
Genetic Susceptibility Determines ?-Cell Function and Fasting Glycemia Trajectories Throughout Childhood: A 12-Year Cohort Study (EarlyBird 76). Diabetes care 2020 Jan . Carayol Jerome, Hosking Joanne, Pinkney Jonathan, Marquis Julien, Charpagne Aline, Metairon Sylviane, Jeffery Alison, Hager Jörg, Martin Francois-Pier |
Identification of Shared and Asian-Specific Loci for Systemic Lupus Erythematosus and Evidence for Roles of Type III Interferon Signaling and Lysosomal Function in the Disease: A Multi-Ancestral Genome-Wide Association Study.
Arthritis & rheumatology (Hoboken, N.J.) 2021 Nov . Wang Yong-Fei, Wei Wei, Tangtanatakul Pattarin, Zheng Lichuan, Lei Yao, Lin Zhiming, Qian Chengmin, Qin Xiao, Hou Fei, Zhang Xinyu, Shao Li, Satproedprai Nusara, Mahasirimongkol Surakameth, Pisitkun Prapaporn, Song Qin, Lau Yu Lung, Zhang Yan, Hirankarn Nattiya, Yang Wanli |
The Impact of ACEs on BMI: An Investigation of the Genotype-Environment Effects of BMI. Frontiers in genetics 2022 3 13 816660. Schlauch Karen A, Read Robert W, Neveux Iva, Lipp Bruce, Slonim Anthony, Grzymski Joseph |
Role of chromosomal imbalances in the pathogenesis of DSD: A retrospective analysis of 115 prenatal samples. European journal of medical genetics 2023 3 66 (6): 104748. Mary L, Fradin M, Pasquier L, Quelin C, Loget P, Le Lous M, Le Bouar G, Nivot-Adamiak S, Lokchine A, Dubourg C, Jauffret V, Nouyou B, Henry C, Launay E, Odent S, Jaillard S, Belaud-Rotureau M |
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