Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: FSTL5[original query] |
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Genome-wide host-pathogen analyses reveal genetic interaction points in tuberculosis disease.
Nature communications 2023 2 14 (1): 549. Phelan Jody, Gomez-Gonzalez Paula Josefina, Andreu Nuria, Omae Yosuke, Toyo-Oka Licht, Yanai Hideki, Miyahara Reiko, Nedsuwan Supalert, de Sessions Paola Florez, Campino Susana, Sallah Neneh, Parkhill Julian, Smittipat Nat, Palittapongarnpim Prasit, Mushiroda Taisei, Kubo Michiaki, Tokunaga Katsushi, Mahasirimongkol Surakameth, Hibberd Martin L, Clark Taane |
New genetic associations in thiopurine-related bone marrow toxicity among inflammatory bowel disease patients. Pharmacogenomics 2013 Apr 14 (6): 631-40. Zabala William, Cruz Raquel, Barreiro-de Acosta Manuel, Chaparro María, Panes Julián, Echarri Ana, Esteve Maria, Carpio Daniel, Andreu Montserrat, García-Planella Esther, Domenech Eugeni, Carracedo Angel, Gisbert Javier P, Barros Francisco, |
A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study.
Carcinogenesis 2014 Nov 35 (11): 2512-9. Schmit Stephanie L, Schumacher Fredrick R, Edlund Christopher K, Conti David V, Raskin Leon, Lejbkowicz Flavio, Pinchev Mila, Rennert Hedy S, Jenkins Mark A, Hopper John L, Buchanan Daniel D, Lindor Noralane M, Le Marchand Loic, Gallinger Steven, Haile Robert W, Newcomb Polly A, Huang Shu-Chen, Rennert Gad, Casey Graham, Gruber Stephen |
Severity of Mitral Valve Degeneration Is Associated with Chromosome 15 Loci in Whippet Dogs. PloS one 2015 10 (10): e0141234. Stern Joshua A, Hsue Weihow, Song Kun-Ho, Ontiveros Eric S, Luis Fuentes Virginia, Stepien Rebecca |
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia. Psychiatry research 2017 1 258 598-599. Gardella Rita, Sacchetti Emilio, Legati Andrea, Magri Chiara, Traversa Michele, Gennarelli Massi |
A logical relationship for schizophrenia, bipolar, and major depressive disorder. Part 4: Evidence from chromosome 4 high-density association screen. The Journal of comparative neurology 2019 Feb 527 (2): 392-405. Tang Jian, Chen Xing, Cai Bin, Chen Ga |
Genetic loci for alcohol-related life events and substance-induced affective symptoms: indexing the "dark side" of addiction. Translational psychiatry 2019 Feb 9 (1): 71. Peng Qian, Bizon Chris, Gizer Ian R, Wilhelmsen Kirk C, Ehlers Cindy |
Metabolite Genome-Wide Association Study for Indoleamine 2,3-Dioxygenase Activity Associated with Chronic Kidney Disease. Genes 2021 12 12 (12): . Kim Hye-Rim, Jin Hyun-Seok, Eom Yong-B |
Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits.
HGG advances 2021 Jan 2 (1): . Sun Daokun, Richard Melissa, Musani Solomon K, Sung Yun Ju, Winkler Thomas W, Schwander Karen, Chai Jin Fang, Guo Xiuqing, Kilpeläinen Tuomas O, Vojinovic Dina, Aschard Hugues, Bartz Traci M, Bielak Lawrence F, Brown Michael R, Chitrala Kumaraswamy, Hartwig Fernando P, Horimoto Andrea R V R, Liu Yongmei, Manning Alisa K, Noordam Raymond, Smith Albert V, Harris Sarah E, Kühnel Brigitte, Lyytikäinen Leo-Pekka, Nolte Ilja M, Rauramaa Rainer, van der Most Peter J, Wang Rujia, Ware Erin B, Weiss Stefan, Wen Wanqing, Yanek Lisa R, Arking Dan E, Arnett Donna K, Barac Ana, Boerwinkle Eric, Broeckel Ulrich, Chakravarti Aravinda, Chen Yii-Der Ida, Cupples L Adrienne, Davigulus Martha L, de Las Fuentes Lisa, de Mutsert Renée, de Vries Paul S, Delaney Joseph A C, Roux Ana V Diez, Dörr Marcus, Faul Jessica D, Fretts Amanda M, Gallo Linda C, Grabe Hans Jörgen, Gu C Charles, Harris Tamara B, Hartman Catharina C A, Heikkinen Sami, Ikram M Arfan, Isasi Carmen, Johnson W Craig, Jonas Jost Bruno, Kaplan Robert C, Komulainen Pirjo, Krieger Jose E, Levy Daniel, , Liu Jianjun, Lohman Kurt, Luik Annemarie I, Martin Lisa W, Meitinger Thomas, Milaneschi Yuri, O'Connell Jeff R, Palmas Walter R, Peters Annette, Peyser Patricia A, Pulkki-Råback Laura, Raffel Leslie J, Reiner Alex P, Rice Kenneth, Robinson Jennifer G, Rosendaal Frits R, Schmidt Carsten Oliver, Schreiner Pamela J, Schwettmann Lars, Shikany James M, Shu Xiao-Ou, Sidney Stephen, Sims Mario, Smith Jennifer A, Sotoodehnia Nona, Strauch Konstantin, Tai E Shyong, Taylor Kent, Uitterlinden André G, van Duijn Cornelia M, Waldenberger Melanie, Wee Hwee-Lin, Wei Wen-Bin, Wilson Gregory, Xuan Deng, Yao Jie, Zeng Donglin, Zhao Wei, Zhu Xiaofeng, Zonderman Alan B, Becker Diane M, Deary Ian J, Gieger Christian, Lakka Timo A, Lehtimäki Terho, North Kari E, Oldehinkel Albertine J, Penninx Brenda W J H, Snieder Harold, Wang Ya-Xing, Weir David R, Zheng Wei, Evans Michele K, Gauderman W James, Gudnason Vilmundur, Horta Bernardo L, Liu Ching-Ti, Mook-Kanamori Dennis O, Morrison Alanna C, Pereira Alexandre C, Psaty Bruce M, Amin Najaf, Fox Ervin R, Kooperberg Charles, Sim Xueling, Bierut Laura, Rotter Jerome I, Kardia Sharon L R, Franceschini Nora, Rao Dabeeru C, Fornage Myri |
Colorectal cancer-associated SNP rs17042479 is involved in the regulation of NAF1 promoter activity. PloS one 2022 17 (9): e0274033. Olsson Josephine B, Gugerel Marietta B, Jessen Stine B, Jørgensen Jannie, Gögenur Ismail, Hansen Camilla, Kirkeby Lene T, Olsen Jørgen, Pedersen Ole B V, Vestlev Peter M, Dahlgaard Katja, Troelsen Jesper |
Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development. Human genetics 2022 11 . Safizadeh Shabestari Seyed Ali, Nassir Nasna, Sopariwala Samana, Karimov Islam, Tambi Richa, Zehra Binte, Kosaji Noor, Akter Hosneara, Berdiev Bakhrom K, Uddin Mohamm |
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- Page last updated:Apr 22, 2024
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