Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: KCNH7[original query] |
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IFIH1-GCA-KCNH7 locus: influence on multiple sclerosis risk. European journal of human genetics : EJHG 2008 Jul 16 (7): 861-4. Martínez Alfonso, Santiago José Luis, Cénit M Carmen, de Las Heras Virginia, de la Calle Hermenegildo, Fernández-Arquero Miguel, Arroyo Rafael, de la Concha Emilio G, Urcelay Ele |
IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients. European journal of human genetics : EJHG 2009 Jun 17 (6): 844-7. Couturier Nicolas, Gourraud Pierre-Antoine, Cournu-Rebeix Isabelle, Gout Claire, Bucciarelli Florence, Edan Gilles, Babron Marie-Claude, Clerget-Darpoux Françoise, Clanet Michel, Fontaine Bertrand, Brassat Dav |
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
PLoS genetics 2012 8 (2): e1002490. Demirkan Ay?e, van Duijn Cornelia M, Ugocsai Peter, Isaacs Aaron, Pramstaller Peter P, Liebisch Gerhard, Wilson James F, Johansson Åsa, Rudan Igor, Aulchenko Yurii S, Kirichenko Anatoly V, Janssens A Cecile J W, Jansen Ritsert C, Gnewuch Carsten, Domingues Francisco S, Pattaro Cristian, Wild Sarah H, Jonasson Inger, Polasek Ozren, Zorkoltseva Irina V, Hofman Albert, Karssen Lennart C, Struchalin Maksim, Floyd James, Igl Wilmar, Biloglav Zrinka, Broer Linda, Pfeufer Arne, Pichler Irene, Campbell Susan, Zaboli Ghazal, Kolcic Ivana, Rivadeneira Fernando, Huffman Jennifer, Hastie Nicholas D, Uitterlinden Andre, Franke Lude, Franklin Christopher S, Vitart Veronique, , Nelson Christopher P, Preuss Michael, , Bis Joshua C, O'Donnell Christopher J, Franceschini Nora, , Witteman Jacqueline C M, Axenovich Tatiana, Oostra Ben A, Meitinger Thomas, Hicks Andrew A, Hayward Caroline, Wright Alan F, Gyllensten Ulf, Campbell Harry, Schmitz Gerd, |
A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder. Human molecular genetics 2014 Dec 23 (23): 6395-406. Strauss Kevin A, Markx Sander, Georgi Benjamin, Paul Steven M, Jinks Robert N, Hoshi Toshinori, McDonald Ann, First Michael B, Liu Wencheng, Benkert Abigail R, Heaps Adam D, Tian Yutao, Chakravarti Aravinda, Bucan Maja, Puffenberger Erik |
Identification of novel loci for bipolar I disorder in a multi-stage genome-wide association study. Progress in neuro-psychopharmacology & biological psychiatry 2014 Jun 51 58-64. Kuo P H, Chuang L C, Liu J R, Liu C M, Huang M C, Lin S K, Sunny Sun H, Hsieh M H, Hung H, Lu R |
Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Molecular autism 2015 6 43. Griswold Anthony J, Dueker Nicole D, Van Booven Derek, Rantus Joseph A, Jaworski James M, Slifer Susan H, Schmidt Michael A, Hulme William, Konidari Ioanna, Whitehead Patrice L, Cuccaro Michael L, Martin Eden R, Haines Jonathan L, Gilbert John R, Hussman John P, Pericak-Vance Margaret |
Somatic mutations in ZFHX4 gene are associated with poor overall survival of Chinese esophageal squamous cell carcinoma patients. Scientific reports 2017 Jul 7 (1): 4951. Qing Tao, Zhu Sibo, Suo Chen, Zhang Lei, Zheng Yuanting, Shi Lemi |
Association Study of KCNH7 Polymorphisms and Individual Responses to Risperidone Treatment in Schizophrenia. Frontiers in psychiatry 2019 9 10 633. Wang Xueping, Su Yi, Yan Hao, Huang Zhuo, Huang Yu, Yue Weih |
Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis.
PLoS medicine 2020 06 17 (6): e1003132. Dapas Matthew, Lin Frederick T J, Nadkarni Girish N, Sisk Ryan, Legro Richard S, Urbanek Margrit, Hayes M Geoffrey, Dunaif Andr |
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- Page last updated:Apr 22, 2024
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