Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: EVC[original query] |
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Common variations in 4p locus are related to male completed suicide. Neuromolecular medicine 2009 11 (1): 13-9. Must Anne, Kõks Sulev, Vasar Eero, Tasa Gunnar, Lang Aavo, Maron Eduard, Väli Mari |
Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations. European journal of human genetics : EJHG 2010 Jun 18 (6): 726-32. Ingersoll Roxann G, Hetmanski Jacqueline, Park Ji-Wan, Fallin M Daniele, McIntosh Iain, Wu-Chou Yah-Huei, Chen Philip K, Yeow Vincent, Chong Samuel S, Cheah Felicia, Sull Jae Woong, Jee Sun Ha, Wang Hong, Wu Tao, Murray Tanda, Huang Shangzhi, Ye Xiaoqian, Jabs Ethylin Wang, Redett Richard, Raymond Gerald, Scott Alan F, Beaty Terri |
Integrated analysis of molecular and clinical prognostic factors in stage II/III colon cancer. Journal of the National Cancer Institute 2012 Nov 104 (21): 1635-46. Roth Arnaud D, Delorenzi Mauro, Tejpar Sabine, Yan Pu, Klingbiel Dirk, Fiocca Roberto, d'Ario Giovanni, Cisar Laura, Labianca Roberto, Cunningham David, Nordlinger Bernard, Bosman Fred, Van Cutsem Er |
Axonal guidance signaling pathway interacting with smoking in modifying the risk of pancreatic cancer: a gene- and pathway-based interaction analysis of GWAS data. Carcinogenesis 2014 May 35 (5): 1039-45. Tang Hongwei, Wei Peng, Duell Eric J, Risch Harvey A, Olson Sara H, Bueno-de-Mesquita H Bas, Gallinger Steven, Holly Elizabeth A, Petersen Gloria, Bracci Paige M, McWilliams Robert R, Jenab Mazda, Riboli Elio, Tjønneland Anne, Boutron-Ruault Marie Christine, Kaaks Rudolph, Trichopoulos Dimitrios, Panico Salvatore, Sund Malin, Peeters Petra H M, Khaw Kay-Tee, Amos Christopher I, Li Dongh |
EVC gene polymorphisms and risks of isolated hypospadias - a preliminary study. Central European journal of urology 2015 68 (2): 257-62. Kowal Andrzej, Mostowska Adrianna, Mydlak Dariusz, Eberdt-Go??bek Bo?ena, Misztal Matthew, Jagodzi?ski Pawe? P, Hozyasz Kamil |
Parkinson's disease: SNCA-, PARK2-, and LRRK2- targeting microRNAs elevated in cingulate gyrus. Parkinsonism & related disorders 2016 Sep . Tatura Roman, Kraus Theo, Giese Armin, Arzberger Thomas, Buchholz Malte, Höglinger Günter, Müller Ulri |
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome. Clinical genetics 2017 9 93 (3): 632-639. Niceta M, Margiotti K, Digilio M C, Guida V, Bruselles A, Pizzi S, Ferraris A, Memo L, Laforgia N, Dentici M L, Consoli F, Torrente I, Ruiz-Perez V L, Dallapiccola B, Marino B, De Luca A, Tartaglia |
Two novel susceptibility loci for type 2 diabetes mellitus identified by longitudinal exome-wide association studies in a Japanese population. Genomics 2017 Dec . Yasukochi Yoshiki, Sakuma Jun, Takeuchi Ichiro, Kato Kimihiko, Oguri Mitsutoshi, Fujimaki Tetsuo, Horibe Hideki, Yamada Yoshi |
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance. Frontiers in endocrinology 2021 1 11 582516. Li Lele, Gao Fenqi, Fan Lijun, Su Chang, Liang Xuejun, Gong ChunX |
Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals. Journal of medical genetics 2022 8 . Aubert-Mucca Marion, Huber Céline, Baujat Genevieve, Michot Caroline, Zarhrate Mohammed, Bras Marc, Boutaud Lucile, Malan Valérie, Attie-Bitach Tania, , Cormier-Daire Valer |
Genetic landscape of forensic DNA phenotyping markers among Mediterranean populations. Forensic science international 2023 12 354 111906. Dorra Becher, Haifa Jmel, Nadia Kheriji, Stefania Sarno, Rym Ke |
MC1R and age heteroclassification of face phenotypes in the Rio Grande do Sul population. International journal of legal medicine 2023 12 . Cássio Augusto Bettim, Alexsandro Vasconcellos da Silva, Alessandro Kahmann, Márcio Dorn, Clarice Sampaio Alho, Eduardo Avi |
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- Page last updated:Apr 22, 2024
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