HuGE Literature Finder
Records 1-13
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Analysis of multiple genetic loci reveals MPDZ-NF1B rs1324183 as a putative genetic marker for keratoconus.
The British journal of ophthalmology 2018 Jul . Wang Yu Meng, Ma Li, Lu Shi Yao, Chan Tommy Chung Yan, Yam Jason C S, Tang Shu Min, Kam Ka Wai, Tam Pancy O S, Tham Clement C, Young Alvin L, Jhanji Vishal, Pang Chi Pui, Chen Li J |
Transethnic genome-wide scan identifies novel Alzheimer's disease loci.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2017 Jul 13 (7): 727-738. Jun Gyungah R, Chung Jaeyoon, Mez Jesse, Barber Robert, Beecham Gary W, Bennett David A, Buxbaum Joseph D, Byrd Goldie S, Carrasquillo Minerva M, Crane Paul K, Cruchaga Carlos, De Jager Philip, Ertekin-Taner Nilufer, Evans Denis, Fallin M Danielle, Foroud Tatiana M, Friedland Robert P, Goate Alison M, Graff-Radford Neill R, Hendrie Hugh, Hall Kathleen S, Hamilton-Nelson Kara L, Inzelberg Rivka, Kamboh M Ilyas, Kauwe John S K, Kukull Walter A, Kunkle Brian W, Kuwano Ryozo, Larson Eric B, Logue Mark W, Manly Jennifer J, Martin Eden R, Montine Thomas J, Mukherjee Shubhabrata, Naj Adam, Reiman Eric M, Reitz Christiane, Sherva Richard, St George-Hyslop Peter H, Thornton Timothy, Younkin Steven G, Vardarajan Badri N, Wang Li-San, Wendlund Jens R, Winslow Ashley R, , Haines Jonathan, Mayeux Richard, Pericak-Vance Margaret A, Schellenberg Gerard, Lunetta Kathryn L, Farrer Lindsay |
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A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder.
Molecular psychiatry 2017 Jan . Ikeda M, Takahashi A, Kamatani Y, Okahisa Y, Kunugi H, Mori N, Sasaki T, Ohmori T, Okamoto Y, Kawasaki H, Shimodera S, Kato T, Yoneda H, Yoshimura R, Iyo M, Matsuda K, Akiyama M, Ashikawa K, Kashiwase K, Tokunaga K, Kondo K, Saito T, Shimasaki A, Kawase K, Kitajima T, Matsuo K, Itokawa M, Someya T, Inada T, Hashimoto R, Inoue T, Akiyama K, Tanii H, Arai H, Kanba S, Ozaki N, Kusumi I, Yoshikawa T, Kubo M, Iwata |
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Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans.
Journal of human genetics 2016 Aug . Hellwege Jacklyn N, Palmer Nicholette D, Dimitrov Latchezar, Keaton Jacob M, Tabb Keri L, Sajuthi Satria, Taylor Kent D, Ng Maggie C Y, Speliotes Elizabeth K, Hawkins Gregory A, Long Jirong, Ida Chen Yii-Der, Lorenzo Carlos, Norris Jill M, Rotter Jerome I, Langefeld Carl D, Wagenknecht Lynne E, Bowden Donald |
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Genome-Wide Meta-Analysis of Sciatica in Finnish Population.
PloS one 2016 11 (10): e0163877. Lemmelä Susanna, Solovieva Svetlana, Shiri Rahman, Benner Christian, Heliövaara Markku, Kettunen Johannes, Anttila Verneri, Ripatti Samuli, Perola Markus, Seppälä Ilkka, Juonala Markus, Kähönen Mika, Salomaa Veikko, Viikari Jorma, Raitakari Olli T, Lehtimäki Terho, Palotie Aarno, Viikari-Juntura Eira, Husgafvel-Pursiainen Kirs |
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A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma.
Cancer discovery 2015 Sep 5 (9): 920-31. Mirabello Lisa, Koster Roelof, Moriarity Branden S, Spector Logan G, Meltzer Paul S, Gary Joy, Machiela Mitchell J, Pankratz Nathan, Panagiotou Orestis A, Largaespada David, Wang Zhaoming, Gastier-Foster Julie M, Gorlick Richard, Khanna Chand, de Toledo Silvia Regina Caminada, Petrilli Antonio S, Patiño-Garcia Ana, Sierrasesúmaga Luis, Lecanda Fernando, Andrulis Irene L, Wunder Jay S, Gokgoz Nalan, Serra Massimo, Hattinger Claudia, Picci Piero, Scotlandi Katia, Flanagan Adrienne M, Tirabosco Roberto, Amary Maria Fernanda, Halai Dina, Ballinger Mandy L, Thomas David M, Davis Sean, Barkauskas Donald A, Marina Neyssa, Helman Lee, Otto George M, Becklin Kelsie L, Wolf Natalie K, Weg Madison T, Tucker Margaret, Wacholder Sholom, Fraumeni Joseph F, Caporaso Neil E, Boland Joseph F, Hicks Belynda D, Vogt Aurelie, Burdett Laurie, Yeager Meredith, Hoover Robert N, Chanock Stephen J, Savage Sharon |
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The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotype.
The Journal of allergy and clinical immunology 2014 Sep 134 (3): 576-582.e1. Dizier Marie-Hélène, Margaritte-Jeannin Patricia, Madore Anne-Marie, Moffatt Miriam, Brossard Myriam, Lavielle Nolwenn, Sarnowski Chloé, Just Jocelyne, Cookson William, Lathrop Mark, Laprise Catherine, Bouzigon Emmanuelle, Demenais Floren |
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A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.
Journal of affective disorders 2013 Feb 145 (2): 200-7. Lee Heon-Jeong, Woo Hyun Goo, Greenwood Tiffany A, Kripke Daniel F, Kelsoe John |
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Inhibition of AHR transcription by NF1C is affected by a single-nucleotide polymorphism, and is involved in suppression of human uterine endometrial cancer.
Oncogene 2012 Dec . Li D, Takao T, Tsunematsu R, Morokuma S, Fukushima K, Kobayashi H, Saito T, Furue M, Wake N, Asanoma K |
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Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features.
Journal of human genetics 2012 Mar 57 (3): 207-11. Yoneda Yuriko, Saitsu Hirotomo, Touyama Mayumi, Makita Yoshio, Miyamoto Akie, Hamada Keisuke, Kurotaki Naohiro, Tomita Hiroaki, Nishiyama Kiyomi, Tsurusaki Yoshinori, Doi Hiroshi, Miyake Noriko, Ogata Kazuhiro, Naritomi Kenji, Matsumoto Naomic |
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Suggestive evidence of associations between liver X receptor ? polymorphisms with type 2 diabetes mellitus and obesity in three cohort studies: HUNT2 (Norway), MONICA (France) and HELENA (Europe).
BMC medical genetics 2010 11 144. Solaas Karianne, Legry Vanessa, Retterstol Kjetil, Berg Paul R, Holven Kirsten B, Ferrières Jean, Amouyel Philippe, Lien Sigbjorn, Romeo Javier, Valtueña Jara, Widhalm Kurt, Ruiz Jonatan R, Dallongeville Jean, Tonstad Serena, Rootwelt Helge, Halvorsen Bente, Nenseter Marit S, Birkeland Kare I, Thorsby Per M, Meirhaeghe Aline, Nebb Hilde |
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[Studies on the genetic pathogenesis of myasthenia gravis caused by CTLA-4 gene polymorphism].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2004 Dec 21 (6): 574-8. Mao Hai-ting, Wang Xiong-biao, Zhang Ling, Gu Hong-t |
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Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Molecular medicine (Cambridge, Mass.) 0 16 (7-8): 247-53. Rose Jed E, Behm Frédérique M, Drgon Tomas, Johnson Catherine, Uhl George |
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- Page last updated:Feb 20, 2020
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