Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and RBFOX1[original query] |
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Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.
JCI insight 2022 2 7 (3): . Yu Mengyao, Tcheandjieu Catherine, Georges Adrien, Xiao Ke, Tejeda Helio, Dina Christian, Le Tourneau Thierry, Fiterau Madalina, Judy Renae, Tsao Noah L, Amgalan Dulguun, Munger Chad J, Engreitz Jesse M, Damrauer Scott M, Bouatia-Naji Nabila, Priest James |
| Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.
Human molecular genetics 2013 Jul 22 (13): 2754-64. Stambolian Dwight, Wojciechowski Robert, Oexle Konrad, Pirastu Mario, Li Xiaohui, Raffel Leslie J, Cotch Mary Frances, Chew Emily Y, Klein Barbara, Klein Ronald, Wong Tien Y, Simpson Claire L, Klaver Caroline C W, van Duijn Cornelia M, Verhoeven Virginie J M, Baird Paul N, Vitart Veronique, Paterson Andrew D, Mitchell Paul, Saw Seang Mei, Fossarello Maurizio, Kazmierkiewicz Krista, Murgia Federico, Portas Laura, Schache Maria, Richardson Andrea, Xie Jing, Wang Jie Jin, Rochtchina Elena, , Viswanathan Ananth C, Hayward Caroline, Wright Alan F, Polasek Ozren, Campbell Harry, Rudan Igor, Oostra Ben A, Uitterlinden André G, Hofman Albert, Rivadeneira Fernando, Amin Najaf, Karssen Lennart C, Vingerling Johannes R, Hosseini S M, Döring Angela, Bettecken Thomas, Vatavuk Zoran, Gieger Christian, Wichmann H-Erich, Wilson James F, Fleck Brian, Foster Paul J, Topouzis Fotis, McGuffin Peter, Sim Xueling, Inouye Michael, Holliday Elizabeth G, Attia John, Scott Rodney J, Rotter Jerome I, Meitinger Thomas, Bailey-Wilson Joan |
| Analysis of colorectal cancers in British Bangladeshi identifies early onset, frequent mucinous histotype and a high prevalence of RBFOX1 deletion. Molecular cancer 2013 Jan 12 (1): 1. Sengupta N, Yau C, Sakthianandeswaren A, Mouradov D, Gibbs P, Suraweera N, Cazier JB, Polanco-Echeverry G, Ghosh A, Thaha M, Ahmed S, Feakins R, Propper D, Dorudi S, Sieber O, Silver A, Lai C |
| Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia 2013 Jan . Lal D, Trucks H, Møller RS, Hjalgrim H, Koeleman BP, de Kovel CG, Visscher F, Weber YG, Lerche H, Becker F, Schankin CJ, Neubauer BA, Surges R, Kunz WS, Zimprich F, Franke A, Illig T, Ried JS, Leu C, Nürnberg P, Sander T |
| Genetic influences on susceptibility to rheumatoid arthritis in African-Americans.
Human molecular genetics 2018 Nov . Laufer Vincent A, Tiwari Hemant K, Reynolds Richard J, Danila Maria I, Wang Jelai, Edberg Jeffrey C, Kimberly Robert P, Kottyan Leah C, Harley John B, Mikuls Ted R, Gregersen Peter K, Absher Devin M, Langefeld Carl D, Arnett Donna K, Bridges S Lou |
| Genome-wide association study identifies RBFOX1 locus influencing brain glucose metabolism.
Annals of translational medicine 2018 Nov 6 (22): 436. Kong Ling-Li, Miao Dan, Tan Lin, Liu Shu-Lei, Li Jie-Qiong, Cao Xi-Peng, Tan Lan, |
| Association Between Common Variants in RBFOX1, an RNA-Binding Protein, and Brain Amyloidosis in Early and Preclinical Alzheimer Disease.
JAMA neurology 2020 Jun . Raghavan Neha S, Dumitrescu Logan, Mormino Elizabeth, Mahoney Emily R, Lee Annie J, Gao Yizhe, Bilgel Murat, Goldstein David, Harrison Theresa, Engelman Corinne D, Saykin Andrew J, Whelan Christopher D, Liu Jimmy Z, Jagust William, Albert Marilyn, Johnson Sterling C, Yang Hyun-Sik, Johnson Keith, Aisen Paul, Resnick Susan M, Sperling Reisa, De Jager Philip L, Schneider Julie, Bennett David A, Schrag Matthew, Vardarajan Badri, Hohman Timothy J, Mayeux Richard, |
| Telomerase Reverse Transcriptase Promoter Mutations Identify a Genomically Defined and Highly Aggressive Human Pleural Mesothelioma Subgroup. Clinical cancer research : an official journal of the American Association for Cancer Research 2020 Apr . Pirker Christine, Bilecz Agnes, Grusch Michael, Mohr Thomas, Heidenreich Barbara, Laszlo Viktoria, Stockhammer Paul, Lötsch-Gojo Daniela, Gojo Johannes, Gabler Lisa, Spiegl-Kreinecker Sabine, Doeme Balazs, Steindl Ariane, Klikovits Thomas, Hoda Mir Alireza, Jakopovic Marko, Samarzija Miroslav, Mohorcic Katja, Kern Izidor, Kiesel Barbara, Brcic Luka, Oberndorfer Felicitas, Müllauer Leonhard, Klepetko Walter, Schmidt Wolfgang M, Kumar Rajiv, Hegedus Balazs, Berger Walt |
| Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.
JAMA neurology 2020 10 78 (1): 102-113. Kunkle Brian W, Schmidt Michael, Klein Hans-Ulrich, Naj Adam C, Hamilton-Nelson Kara L, Larson Eric B, Evans Denis A, De Jager Phil L, Crane Paul K, Buxbaum Joe D, Ertekin-Taner Nilufer, Barnes Lisa L, Fallin M Daniele, Manly Jennifer J, Go Rodney C P, Obisesan Thomas O, Kamboh M Ilyas, Bennett David A, Hall Kathleen S, Goate Alison M, Foroud Tatiana M, Martin Eden R, Wang Li-Sao, Byrd Goldie S, Farrer Lindsay A, Haines Jonathan L, Schellenberg Gerard D, Mayeux Richard, Pericak-Vance Margaret A, Reitz Christiane, , Graff-Radford Neill R, Martinez Izri, Ayodele Temitope, Logue Mark W, Cantwell Laura B, Jean-Francois Melissa, Kuzma Amanda B, Adams L D, Vance Jeffery M, Cuccaro Michael L, Chung Jaeyoon, Mez Jesse, Lunetta Kathryn L, Jun Gyungah R, Lopez Oscar L, Hendrie Hugh C, Reiman Eric M, Kowall Neil W, Leverenz James B, Small Scott A, Levey Allan I, Golde Todd E, Saykin Andrew J, Starks Takiyah D, Albert Marilyn S, Hyman Bradley T, Petersen Ronald C, Sano Mary, Wisniewski Thomas, Vassar Robert, Kaye Jeffrey A, Henderson Victor W, DeCarli Charles, LaFerla Frank M, Brewer James B, Miller Bruce L, Swerdlow Russell H, Van Eldik Linda J, Paulson Henry L, Trojanowski John Q, Chui Helena C, Rosenberg Roger N, Craft Suzanne, Grabowski Thomas J, Asthana Sanjay, Morris John C, Strittmatter Stephen M, Kukull Walter |
| Causal influences of neuroticism on mental health and cardiovascular disease. Human genetics 2021 May . Zhang Fuquan, Baranova Ancha, Zhou Chao, Cao Hongbao, Chen Jiu, Zhang Xiangrong, Xu Mingqi |
| Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. EBioMedicine 2022 10 85 104290. Clark Lorraine N, Gao Yizhe, Wang Gao T, Hernandez Nora, Ashley-Koch Allison, Jankovic Joseph, Ottman Ruth, Leal Suzanne M, Rodriguez Sandra M Barral, Louis Elan |
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