Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: FMN1[original query] |
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Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk. Nature genetics 2008 Jan 40 (1): 26-8. Jaeger Emma, Webb Emily, Howarth Kimberley, Carvajal-Carmona Luis, Rowan Andrew, Broderick Peter, Walther Axel, Spain Sarah, Pittman Alan, Kemp Zoe, Sullivan Kate, Heinimann Karl, Lubbe Steven, Domingo Enric, Barclay Ella, Martin Lynn, Gorman Maggie, Chandler Ian, Vijayakrishnan Jayaram, Wood Wendy, Papaemmanuil Elli, Penegar Steven, Qureshi Mobshra, , Farrington Susan, Tenesa Albert, Cazier Jean-Baptiste, Kerr David, Gray Richard, Peto Julian, Dunlop Malcolm, Campbell Harry, Thomas Huw, Houlston Richard, Tomlinson I |
Microsatellite scan identifies new candidate genes for susceptibility to alcoholic chronic pancreatitis in Japanese patients. Disease markers 2008 25 (3): 175-80. Kitahara Kei, Kawa Shigeyuki, Katsuyama Yoshihiko, Umemura Takeji, Ozaki Yayoi, Takayama Mari, Arakura Norikazu, Ota Mas |
[A study of the single nucleotide polymorphism in seven genes (GHR, IGFBP3, IGFR1, IRS1, FMN1, ANXA2, TaGLN) in ethnic Russians and in patients with prostate cancer]. Molekuliarnaia genetika, mikrobiologiia i virusologiia 2010 (2): 34-7. Lisitskaia K V, Krakhmaleva I N, Shishkin S |
An association study revealed substantial effects of dominance, epistasis and substance dependence co-morbidity on alcohol dependence symptom count.
Addiction biology 2016 May . Chen Gang, Zhang Futao, Xue Wenda, Wu Ruyan, Xu Haiming, Wang Kesheng, Zhu J |
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways. PloS one 2017 12 (8): e0182778. Giacopuzzi Edoardo, Gennarelli Massimo, Minelli Alessandra, Gardella Rita, Valsecchi Paolo, Traversa Michele, Bonvicini Cristian, Vita Antonio, Sacchetti Emilio, Magri Chia |
GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma.
Experimental eye research 2017 Dec . Zagajewska Katarzyna, Pi?tkowska Magdalena, Goryca Krzysztof, Ba?abas Aneta, Kluska Anna, Paziewska Agnieszka, Po?piech Ewelina, Grabska-Liberek Iwona, Hennig Ewa |
Genome-wide association study identifies new loci for albuminuria in the Japanese population.
Clinical and experimental nephrology 2020 Apr . Okuda Hiroshi, Okamoto Koji, Abe Michiaki, Ishizawa Kota, Makino Satoshi, Tanabe Osamu, Sugawara Junichi, Hozawa Atsushi, Tanno Kozo, Sasaki Makoto, Tamiya Gen, Yamamoto Masayuki, Ito Sadayoshi, Ishii Tadas |
Associations between genetic variants of KIF5B, FMN1, and MGAT3 in the cadherin pathway and pancreatic cancer risk. Cancer medicine 2020 Nov . Zhao Lingling, Liu Hongliang, Luo Sheng, Moorman Patricia G, Walsh Kyle M, Li Wei, Wei Qing |
COVID-19 in pediatrics: Genetic susceptibility.
Frontiers in genetics 2022 9 13 928466. Glessner Joseph T, Chang Xiao, Mentch Frank, Qu Huiqi, Abrams Debra J, Thomas Alexandria, Sleiman Patrick M A, Hakonarson Hak |
A genetic locus within the FMN1/GREM1 gene region interacts with body mass index in colorectal cancer risk. Cancer research 2023 5 . Elom K Aglago, Andre E Kim, Yi Lin, Conghui Qu, Marina Evangelou, Yu Ren, John Morrison, Demetrius Albanes, Volker Arndt, Elizabeth L Barry, James W Baurley, Sonja I Berndt, Stephanie A Bien, D Timothy Bishop, Emmanouil Bouras, Hermann Brenner, Daniel D Buchanan, Arif Budiarto, Robert Carreras-Torres, Graham Casey, Tjeng Wawan Cenggoro, Andrew T Chan, Jenny Chang-Claude, Xuechen Chen, David V Conti, Matthew Devall, Virginia Díez-Obrero, Niki Dimou, David Drew, Jane C Figueiredo, Steven Gallinger, Graham G Giles, Stephen B Gruber, Andrea Gsur, Marc J Gunter, Heather Hampel, Sophia Harlid, Akihisa Hidaka, Tabitha A Harrison, Michael Hoffmeister, Jeroen R Huyghe, Mark A Jenkins, Kristina Jordahl, Amit D Joshi, Eric S Kawaguchi, Temitope O Keku, Anshul Kundaje, Susanna C Larsson, Loic Le Marchand, Juan Pablo Lewinger, Li Li, Brigid M Lynch, Bharuno Mahesworo, Marko Mandic, Mireia Obón-Santacana, Victor Moreno, Neil Murphy, Hongmei Nan, Rami Nassir, Polly A Newcomb, Shuji Ogino, Jennifer Ose, Rish K Pai, Julie R Palmer, Nikos Papadimitriou, Bens Pardamean, Anita R Peoples, Elizabeth A Platz, John D Potter, Ross L Prentice, Gad Rennert, Edward Ruiz-Narvaez, Lori C Sakoda, Peter C Scacheri, Stephanie L Schmit, Robert E Schoen, Anna Shcherbina, Martha L Slattery, Mariana C Stern, Yu-Ru Su, Catherine M Tangen, Stephen N Thibodeau, Duncan C Thomas, Yu Tian, Cornelia M Ulrich, Fränzel J B van Duijnhoven, Bethany Van Guelpen, Kala Visvanathan, Pavel Vodicka, Jun Wang, Emily White, Alicja Wolk, Michael O Woods, Anna H Wu, Natalia Zemlianskaia, Li Hsu, W James Gauderman, Ulrike Peters, Konstantinos K Tsilidis, Peter T Campbe |
The association of five polymorphisms with diabetic retinopathy in a Chinese population. Ophthalmic genetics 2023 4 1-6. Li Huan, Ning Meizhen, Li Qinyun, Wang Ting, Li Wei, Xiao Jialing, Wang Liang, Wang Kaifang, Zou Rong, Hao Fang, Yu Man, Shi Yi, Lei Chuntao, Wang Ziyang, Yang Zhenglin, Xu Huijuan, Gong |
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- Page last updated:Apr 22, 2024
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