Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Disease and CAPN10[original query] |
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| Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association. American journal of human genetics 2001 Dec 69 (6): 1236-44. Tsai H J, Sun G, Weeks D E, Kaushal R, Wolujewicz M, McGarvey S T, Tufa J, Viali S, Deka |
| Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus. American journal of human genetics 2002 May 70 (5): 1096-106. Fullerton Stephanie M, Bartoszewicz Angelika, Ybazeta Gustavo, Horikawa Yukio, Bell Graeme I, Kidd Kenneth K, Cox Nancy J, Hudson Richard R, Di Rienzo An |
| Haplotype combination of Calpain-10 gene polymorphism is associated with metabolic syndrome in type 2 diabetes. Diabetes research and clinical practice 2006 Sep 73 (3): 268-75. Kang Eun Seok, Nam Moonsuk, Kim Hye Joo, Kim Hyeong Jin, Myoung Sung Min, Rhee Yumie, Ahn Chul Woo, Cha Bong Soo, Lee Hyun Ch |
| Genetic prediction of future type 2 diabetes. PLoS medicine 2005 Nov 2 (12): e345. Lyssenko Valeriya, Almgren Peter, Anevski Dragi, Orho-Melander Marju, Sjögren Marketa, Saloranta Carola, Tuomi Tiinamaija, Groop Leif, |
| CAPN10 UCSNP-43, UCSNP-19 and UCSNP-63 polymorphisms and metabolic syndrome in polycystic ovary syndrome. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2007 Mar 23 (3): 173-8. Wiltgen Denusa, Furtado Lúcia, Kohek Maria B F, Spritzer Poli Ma |
| Calpain-5 gene variants are associated with diastolic blood pressure and cholesterol levels. BMC medical genetics 2007 8 (): 1. Sáez María E, Martínez-Larrad María T, Ramírez-Lorca Reposo, González-Sánchez José L, Zabena Carina, Martinez-Calatrava María J, González Alejandro, Morón Francisco J, Ruiz Agustín, Serrano-Ríos Manu |
| The CAPN10 gene is associated with insulin resistance phenotypes in the Spanish population. PloS one 2008 3 (8): e2953. Sáez María E, González-Sánchez José L, Ramírez-Lorca Reposo, Martínez-Larrad María T, Zabena Carina, González Alejandro, Morón Francisco J, Ruiz Agustín, Serrano-Ríos Manu |
| Prevalence of common disease-associated variants in Asian Indians. BMC genetics 2008 9 (1): 13. Pemberton Trevor J, Mehta Niyati U, Witonsky David, Di Rienzo Anna, Allayee Hooman, Conti David V, Patel Pragna |
| A replication study of the IRS1, CAPN10, TCF7L2, and PPARG gene polymorphisms associated with type 2 diabetes in two different populations of Mexico. Annals of human genetics 2011 Sep 75 (5): 612-20. Martínez-Gómez Laura E, Cruz Miguel, Martínez-Nava Gabriela A, Madrid-Marina Vicente, Parra Esteban, García-Mena Jaime, Espinoza-Rojo Mónica, Estrada-Velasco Barbara I, Piza-Roman Luis F, Aguilera Penelope, Burguete-García Ana |
| A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait. Journal of probability and statistics 2012 2012 . Kwon Soonil, Goodarzi Mark O, Taylor Kent D, Cui Jinrui, Chen Y-D Ida, Rotter Jerome I, Hsueh Willa, Guo Xiuqi |
| De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association. European journal of human genetics : EJHG 2013 Dec 21 (12): 1377-82. Hilger Alina, Schramm Charlotte, Pennimpede Tracie, Wittler Lars, Dworschak Gabriel C, Bartels Enrika, Engels Hartmut, Zink Alexander M, Degenhardt Franziska, Müller Annette M, Schmiedeke Eberhard, Grasshoff-Derr Sabine, Märzheuser Stefanie, Hosie Stuart, Holland-Cunz Stefan, Wijers Charlotte H W, Marcelis Carlo L M, van Rooij Iris A L M, Hildebrandt Friedhelm, Herrmann Bernhard G, Nöthen Markus M, Ludwig Michael, Reutter Heiko, Draaken Mark |
| Association of calpain-10 rs2975760 polymorphism with type 2 diabetes mellitus: a meta-analysis. International journal of clinical and experimental medicine 2014 7 (10): 3800-7. Yan Shuang-Tong, Li Chun-Lin, Tian Hui, Li Jian, Pei Yu, Liu Yu, Gong Yan-Ping, Fang Fu-Sheng, Sun Ban-R |
| Gene-gene and gene-environment interactions in the etiology of type 2 diabetes mellitus in the population of Hyderabad, India. Meta gene 2015 Sep 5 9-20. Uma Jyothi Kommoju, Reddy Battini Moh |
| [Association analysis of SNP-63 and indel-19 variant in the calpain-10 gene with polycystic ovary syndrome in women of reproductive age]. Cirugía y cirujanos 0 83 (1): 35-42. Flores-Martínez Silvia Esperanza, Castro-Martínez Anna Gabriela, López-Quintero Andrés, García-Zapién Alejandra Guadalupe, Torres-Rodríguez Ruth Noemí, Sánchez-Corona Jo |
| [SNP-19 genotypic variants of CAPN10 gene and its relation to diabetes mellitus type 2 in a population of Ciudad Juarez, Mexico]. Nutrición hospitalaria 2015 31 (2): 744-50. Loya Méndez Yolanda, Reyes Leal Gilberto, Sánchez González Adriana, Portillo Reyes Verónica, Reyes Ruvalcaba David, Bojórquez Rangel Guiller |
| 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 |
| The SNP43 (G/A) polymorphism in CAPN10 gene confers an increased risk of cognitive impairment in cerebral small vessel disease. Journal of clinical laboratory analysis 2018 Jul e22615. Wu Kai, Cai Yi |
| Association analysis of calpain 10 gene variants/haplotypes with gestational diabetes mellitus among Mexican women. Cellular and molecular biology (Noisy-le-Grand, France) 2018 Feb 64 (3): 81-86. Castro-Martínez Anna Gabriela, Sánchez-Corona José, Vázquez-Vargas Adriana Patricia, García-Zapién Alejandra Guadalupe, López-Quintero Andres, Villalpando-Velazco Héctor Javier, Flores-Martínez Silvia Esperan |
| Blood-based analysis of type-2 diabetes mellitus susceptibility genes identifies specific transcript variants with deregulated expression and association with disease risk. Scientific reports 2019 Feb 9 (1): 1512. Christodoulou Maria-Ioanna, Avgeris Margaritis, Kokkinopoulou Ioanna, Maratou Eirini, Mitrou Panayota, Kontos Christos K, Pappas Efthimios, Boutati Eleni, Scorilas Andreas, Fragoulis Emmanuel |
| [Genetic analysis of a case with 2q37 microdeletion syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 12 39 (1): 81-84. Lian Xiaohui, Zhang Xiao, Huang Mingyan, Lin Juan, Zeng Ji |
| Large-scale rare variant burden testing in Parkinson's disease. Brain : a journal of neurology 2023 6 . Mary B Makarious, Julie Lake, Vanessa Pitz, Allen Ye Fu, Joseph L Guidubaldi, Caroline Warly Solsberg, Sara Bandres-Ciga, Hampton L Leonard, Jonggeol Jeffrey Kim, Kimberley J Billingsley, Francis P Grenn, Pilar Alvarez Jerez, Chelsea Alvarado, Hirotaka Iwaki, Michael Ta, Dan Vitale, Dena Hernandez, Ali Torkamani, Mina Ryten, John Hardy, , Sonja W Scholz, Bryan J Traynor, Clifton L Dalgard, Debra J Ehrlich, Toshiko Tanaka, Luigi Ferrucci, Thomas G Beach, Geidy E Serrano, Raquel Real, Huw R Morris, Jinhui Ding, J Raphael Gibbs, Andrew B Singleton, Mike A Nalls, Tushar Bhangale, Cornelis Blauwendra |
| Association of CAPN10 gene (rs3842570) polymorphism with the type 2 diabetes mellitus among the population of Noakhali region in Bangladesh: a case-control study. Genomics & informatics 2023 10 21 (3): e33. Munia Sultana, Md Mafizul Islam, Md Murad Hossain, Md Anisur Rahman, Shuvo Chandra Das, Dhirendra Nath Barman, Farhana Siddiqi Mitu, Shipan Das Gup |
| Whole Exome Sequencing Revealed Paternal Inheritance of Obesity-related Genetic Variants in a Family with an Exclusively Breastfed Infant. Journal of clinical research in pediatric endocrinology 2024 6 . Hazal Banu Olgun Celebioglu, Ayse Pinar Ozturk, Sukran Poyrazoglu, Feyza Nur Tunc |
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