Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: CDC42[original query] |
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GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer.
Human molecular genetics 2023 3 32 (12): 2103-2116. Koel Mariann, Võsa Urmo, Jõeloo Maarja, Läll Kristi, Gualdo Natàlia P, Laivuori Hannele, Lemmelä Susanna, , Daly Mark, Palta Priit, Mägi Reedik, Laisk Tri |
Host genetic factors and vaccine-induced immunity to HBV infection: haplotype analysis. PloS one 2010 5 (8): e12273. Ryckman Kelli K, Fielding Katherine, Hill Adrian V, Mendy Maimuna, Rayco-Solon Pura, Sirugo Giorgio, van der Sande Marianne A, Waight Pauline, Whittle Hilton C, Hall Andrew J, Williams Scott M, Hennig Branwen |
A single nucleotide polymorphism in activated Cdc42 associated tyrosine kinase 1 influences the interferon therapy in hepatitis C patients. Journal of hepatology 2011 Apr 54 (4): 629-39. Fujimoto Yoshifumi, Ochi Hidenori, Maekawa Toshiro, Abe Hiromi, Hayes C Nelson, Kumada Hiromitsu, Nakamura Yusuke, Chayama Kazua |
Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE. Human genetics 2010 1 127 (4): 421-40. Rosenfeld Jill A, Ballif Blake C, Martin Donna M, Aylsworth Arthur S, Bejjani Bassem A, Torchia Beth S, Shaffer Lisa |
Genome-wide association study of copy number variants suggests LTBP1 and FGD4 are important for alcohol drinking. PloS one 2012 7 (1): e30860. Pei Yu-Fang, Zhang Lei, Yang Tie-Lin, Han Yingying, Hai Rong, Ran Shu, Tian Qing, Shen Hui, Li Jian, Zhu Xue-Zhen, Luo Xingguang, Deng Hong-W |
Genetic variants in CDC42 and NXPH1 as susceptibility factors for constipation and diarrhoea predominant irritable bowel syndrome. Gut 2014 Jul 63 (7): 1103-11. Wouters Mira M, Lambrechts Diether, Knapp Michael, Cleynen Isabelle, Whorwell Peter, Agréus Lars, Dlugosz Aldona, Schmidt Peter Thelin, Halfvarson Jonas, Simrén Magnus, Ohlsson Bodil, Karling Pontus, Van Wanrooy Sander, Mondelaers Stéphanie, Vermeire Severine, Lindberg Greger, Spiller Robin, Dukes George, D'Amato Mauro, Boeckxstaens G |
Genome-wide association study link novel loci to endometriosis.
PloS one 2013 8 (3): e58257. Albertsen Hans M, Chettier Rakesh, Farrington Pamela, Ward Kenne |
SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility. The Journal of clinical endocrinology and metabolism 2013 May 98 (5): E973-80. He Huiling, Bronisz Agnieszka, Liyanarachchi Sandya, Nagy Rebecca, Li Wei, Huang Yungui, Akagi Keiko, Saji Motoyasu, Kula Dorota, Wojcicka Anna, Sebastian Nikhil, Wen Bernard, Puch Zbigniew, Kalemba Michal, Stachlewska Elzbieta, Czetwertynska Malgorzata, Dlugosinska Joanna, Dymecka Kinga, Ploski Rafal, Krawczyk Marek, Morrison Patrick J, Ringel Matthew D, Kloos Richard T, Jazdzewski Krystian, Symer David E, Vieland Veronica J, Ostrowski Michael, Jarz?b Barbara, de la Chapelle Albe |
Fine mapping of variants associated with endometriosis in the WNT4 region on chromosome 1p36. International journal of molecular epidemiology and genetics 2013 4 (4): 193-206. Luong Hien Tt, Painter Jodie N, Shakhbazov Konstantin, Chapman Brett, Henders Anjali K, Powell Joseph E, Nyholt Dale R, Montgomery Grant |
No association between FGD1 gene polymorphisms and intellectual developmental disability in the Qinba mountain area. Genetics and molecular research : GMR 2014 13 (1): 127-33. Li J L, Li Y J, Zhang K J, Lan L, Shi J G, Yang X, Zhang M J, Zhang F C, Gao X |
Association of Rho/Rho-kinase gene polymorphisms and expressions with obesity-related metabolic syndrome. European review for medical and pharmacological sciences 2015 May 19 (9): 1680-8. Tabur S, Oztuzcu S, Oguz E, Korkmaz H, Eroglu S, Ozkaya M, Demiryürek A |
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.
Scientific reports 2015 5 10442. Al-Tassan Nada A, Whiffin Nicola, Hosking Fay J, Palles Claire, Farrington Susan M, Dobbins Sara E, Harris Rebecca, Gorman Maggie, Tenesa Albert, Meyer Brian F, Wakil Salma M, Kinnersley Ben, Campbell Harry, Martin Lynn, Smith Christopher G, Idziaszczyk Shelley, Barclay Ella, Maughan Timothy S, Kaplan Richard, Kerr Rachel, Kerr David, Buchannan Daniel D, Ko Win Aung, Hopper John, Jenkins Mark, Lindor Noralane M, Newcomb Polly A, Gallinger Steve, Conti David, Schumacher Fred, Casey Graham, Dunlop Malcolm G, Tomlinson Ian P, Cheadle Jeremy P, Houlston Richard |
Low Gene Dosage of Cdc42 Is Not Associated with Protein Dysfunction in Patients with Colorectal Cancer. DNA and cell biology 2016 Aug . González-Quiroz Matías, Calderón Ximena, Oyarzún Ingrid, Hoepfner Claudia, Azócar Andrés, Aguirre Adam, Álvarez Karin, Quera Rodrigo, López-Köstner Francisco, Meléndez Jai |
A comprehensive genome-wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variants. International journal of cancer 2016 Jun . Vaysse Amaury, Fang Shenying, Brossard Myriam, Wei Qingyi, Chen Wei V, Mohamdi Hamida, Vincent-Fetita Lynda, Margaritte-Jeannin Patricia, Lavielle Nolwenn, Maubec Eve, Lathrop Mark, Avril Marie-Françoise, Amos Christopher I, Lee Jeffrey E, Demenais Floren |
Intensified vmPFC surveillance over PTSS under perturbed microRNA-608/AChE interaction. Translational psychiatry 2016 6 e801. Lin T, Simchovitz A, Shenhar-Tsarfaty S, Vaisvaser S, Admon R, Hanin G, Hanan M, Kliper E, Bar-Haim Y, Shomron N, Fernandez G, Lubin G, Fruchter E, Hendler T, Soreq |
Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. Human molecular genetics 2017 (22): 5046-5058. Powell Joseph E, Fung Jenny N, Shakhbazov Konstantin, Sapkota Yadav, Cloonan Nicole, Hemani Gibran, Hillman Kristine M, Kaufmann Susanne, Luong Hien T, Bowdler Lisa, Painter Jodie N, Holdsworth-Carson Sarah J, Visscher Peter M, Dinger Marcel E, Healey Martin, Nyholt Dale R, French Juliet D, Edwards Stacey L, Rogers Peter A W, Montgomery Grant |
Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function. Human molecular genetics 2017 10 26 (20): 4011-4027. Lee Mei-Chin, Shei William, Chan Anita S, Chua Boon-Tin, Goh Shuang-Ru, Chong Yaan-Fun, Hilmy Maryam H, Nongpiur Monisha E, Baskaran Mani, Khor Chiea-Chuen, Aung Tin, Hunziker Walter, Vithana Eranga |
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
Nature communications 2018 Sep 9 (1): 3636. Rafnar Thorunn, Gunnarsson Bjarni, Stefansson Olafur A, Sulem Patrick, Ingason Andres, Frigge Michael L, Stefansdottir Lilja, Sigurdsson Jon K, Tragante Vinicius, Steinthorsdottir Valgerdur, Styrkarsdottir Unnur, Stacey Simon N, Gudmundsson Julius, Arnadottir Gudny A, Oddsson Asmundur, Zink Florian, Halldorsson Gisli, Sveinbjornsson Gardar, Kristjansson Ragnar P, Davidsson Olafur B, Salvarsdottir Anna, Thoroddsen Asgeir, Helgadottir Elisabet A, Kristjansdottir Katrin, Ingthorsson Orri, Gudmundsson Valur, Geirsson Reynir T, Arnadottir Ragnheidur, Gudbjartsson Daniel F, Masson Gisli, Asselbergs Folkert W, Jonasson Jon G, Olafsson Karl, Thorsteinsdottir Unnur, Halldorsson Bjarni V, Thorleifsson Gudmar, Stefansson Ka |
Regulation of thymocyte trafficking by Tagap, a GAP domain protein linked to human autoimmunity. Science signaling 2018 Jun 11 (534): . Duke-Cohan Jonathan S, Ishikawa Yuki, Yoshizawa Akihiro, Choi Young-Il, Lee Chin-Nien, Acuto Oreste, Kissler Stephan, Reinherz Ellis |
Genetics of endometriosis: State of the art on genetic risk factors for endometriosis. Best practice & research. Clinical obstetrics & gynaecology 2018 3 50 61-71. Fung Jenny N, Montgomery Grant |
A miR-18a binding-site polymorphism in CDC42 3'UTR affects CDC42 mRNA expression in placentas and is associated with litter size in pigs. Mammalian genome : official journal of the International Mammalian Genome Society 2018 12 30 (1-2): 34-41. Liu Ruize, Deng Dadong, Liu Xiangdong, Xiao Yujing, Huang Ji, Wang Feiyu, Li Xinyun, Yu M |
A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.
Frontiers in genetics 2019 10 511. Edwards Todd L, Giri Ayush, Hellwege Jacklyn N, Hartmann Katherine E, Stewart Elizabeth A, Jeff Janina M, Bray Michael J, Pendergrass Sarah A, Torstenson Eric S, Keaton Jacob M, Jones Sarah H, Gogoi Radhika P, Kuivaniemi Helena, Jackson Kathryn L, Kho Abel N, Kullo Iftikhar J, McCarty Catherine A, Im Hae Kyung, Pacheco Jennifer A, Pathak Jyotishman, Williams Marc S, Tromp Gerard, Kenny Eimear E, Peissig Peggy L, Denny Joshua C, Roden Dan M, Velez Edwards Digna |
Elevated MMP9 expression in breast cancer is a predictor of shorter patient survival. Breast cancer research and treatment 2020 5 182 (2): 267-282. Joseph Chitra, Alsaleem Mansour, Orah Nnamdi, Narasimha Pavan L, Miligy Islam M, Kurozumi Sasagu, Ellis Ian O, Mongan Nigel P, Green Andrew R, Rakha Emad |
Associations between pancreatic expression quantitative traits and risk of pancreatic ductal adenocarcinoma.
Carcinogenesis 2021 Jul . Pistoni Laura, Gentiluomo Manuel, Lu Ye, López de Maturana Evangelina, Hlavac Viktor, Vanella Giuseppe, Darvasi Erika, Milanetto Anna Caterina, Oliverius Martin, Vashist Yogesh, Di Leo Milena, Mohelnikova-Duchonova Beatrice, Talar-Wojnarowska Renata, Gheorghe Cristian, Petrone Maria Chiara, Strobel Oliver, Arcidiacono Paolo Giorgio, Vodickova Ludmila, Szentesi Andrea, Capurso Gabriele, Gajdán László, Malleo Giuseppe, Theodoropoulos George E, Basso Daniela, Soucek Pavel, Brenner Hermann, Lawlor Rita T, Morelli Luca, Ivanauskas Audrius, , Kauffmann Emanuele Federico, Macauda Angelica, Gazouli Maria, Archibugi Livia, Nentwich Michael, Love?ek Martin, Cavestro Giulia Martina, Vodicka Pavel, Landi Stefano, Tavano Francesca, Sperti Cosimo, Hackert Thilo, Kupcinskas Juozas, Pezzilli Raffaele, Andriulli Angelo, Pollina Luca, Kreivenaite Edita, Gioffreda Domenica, Jamroziak Krzysztof, Hegyi Péter, Izbicki Jakob R, Testoni Sabrina Gloria Giulia, Zuppardo Raffaella Alessia, Bozzato Dania, Neoptolemos John P, Malats Núria, Canzian Federico, Campa Danie |
Polymorphism of rs6426749 at 1p36.12 is associated with the risk of osteoarthritis in Taiwanese female population. Journal of the Chinese Medical Association : JCMA 2021 Mar . Tsai Dung-Jang, Tai Ming-Cheng, Kao Chung-Cheng, Chen Wei-Teing, Wu Li-Wei, Chiu Chih-Chien, Tu Ming-Yu, Chen Yi-Chou, Wu Chia-Chun, Su Sui-Lu |
Estrogen receptor alpha and NFATc1 bind to a bone mineral density-associated SNP to repress WNT5B in osteoblasts. American journal of human genetics 2021 12 109 (1): 97-115. Suthon Sarocha, Lin Jianjian, Perkins Rachel S, Crockarell John R, Miranda-Carboni Gustavo A, Krum Susan |
MiR-608 overexpression in idiopathic pulmonary fibrosis (IPF). BMC pulmonary medicine 2021 Jan 21 (1): 1. Epstein Shochet Gali, Israeli-Shani Lilach, Kains Isabelle, Wand Ori, Shitrit Dav |
Mutations at the C-terminus of CDC42 cause distinct hematopoietic and autoinflammatory disorders. The Journal of allergy and clinical immunology 2022 2 150 (1): 223-228. Coppola Simona, Insalaco Antonella, Zara Erika, Di Rocco Martina, Marafon Denise Pires, Spadaro Francesca, Pannone Luca, Farina Luciapia, Pasquini Luca, Martinelli Simone, De Benedetti Fabrizio, Tartaglia Mar |
Rho GTPase gene expression and breast cancer risk: a Mendelian randomization analysis. Scientific reports 2022 01 12 (1): 1463. Kazmi Nabila, Robinson Tim, Zheng Jie, Kar Siddhartha, Martin Richard M, Ridley Anne |
Human ARHGEF9 intellectual disability syndrome is phenocopied by a mutation that disrupts collybistin binding to the GABA Molecular psychiatry 2022 Feb . Hines Dustin J, Contreras April, Garcia Betsua, Barker Jeffrey S, Boren Austin J, Moufawad El Achkar Christelle, Moss Stephen J, Hines Rochelle |
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- Page last updated:Apr 22, 2024
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