Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and KALRN[original query] |
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| Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking. Annals of human genetics 2009 Nov 73 (Pt 6): 551-8. Horne Benjamin D, Hauser Elizabeth R, Wang Liyong, Muhlestein Joseph B, Anderson Jeffrey L, Carlquist John F, Shah Svati H, Kraus William |
| Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients. BMC medical genetics 2012 13 (1): 48. Tsai Yu-Chun, Metzger Silke, Riess Olaf, Soehn Anne S, Nguyen Huu Ph |
| Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort. Human genetics 2013 Aug . Ward-Caviness C, Haynes C, Blach C, Dowdy E, Gregory SG, Shah SH, Horne BD, Kraus WE, Hauser ER |
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
PLoS genetics 2014 Feb 10 (2): e1004123. Medici Marco, Porcu Eleonora, Pistis Giorgio, Teumer Alexander, Brown Suzanne J, Jensen Richard A, Rawal Rajesh, Roef Greet L, Plantinga Theo S, Vermeulen Sita H, Lahti Jari, Simmonds Matthew J, Husemoen Lise Lotte N, Freathy Rachel M, Shields Beverley M, Pietzner Diana, Nagy Rebecca, Broer Linda, Chaker Layal, Korevaar Tim I M, Plia Maria Grazia, Sala Cinzia, Völker Uwe, Richards J Brent, Sweep Fred C, Gieger Christian, Corre Tanguy, Kajantie Eero, Thuesen Betina, Taes Youri E, Visser W Edward, Hattersley Andrew T, Kratzsch Jürgen, Hamilton Alexander, Li Wei, Homuth Georg, Lobina Monia, Mariotti Stefano, Soranzo Nicole, Cocca Massimiliano, Nauck Matthias, Spielhagen Christin, Ross Alec, Arnold Alice, van de Bunt Martijn, Liyanarachchi Sandya, Heier Margit, Grabe Hans Jörgen, Masciullo Corrado, Galesloot Tessel E, Lim Ee M, Reischl Eva, Leedman Peter J, Lai Sandra, Delitala Alessandro, Bremner Alexandra P, Philips David I W, Beilby John P, Mulas Antonella, Vocale Matteo, Abecasis Goncalo, Forsen Tom, James Alan, Widen Elisabeth, Hui Jennie, Prokisch Holger, Rietzschel Ernst E, Palotie Aarno, Feddema Peter, Fletcher Stephen J, Schramm Katharina, Rotter Jerome I, Kluttig Alexander, Radke Dörte, Traglia Michela, Surdulescu Gabriela L, He Huiling, Franklyn Jayne A, Tiller Daniel, Vaidya Bijay, de Meyer Tim, Jørgensen Torben, Eriksson Johan G, O'Leary Peter C, Wichmann Eric, Hermus Ad R, Psaty Bruce M, Ittermann Till, Hofman Albert, Bosi Emanuele, Schlessinger David, Wallaschofski Henri, Pirastu Nicola, Aulchenko Yurii S, de la Chapelle Albert, Netea-Maier Romana T, Gough Stephen C L, Meyer Zu Schwabedissen Henriette, Frayling Timothy M, Kaufman Jean-Marc, Linneberg Allan, Räikkönen Katri, Smit Johannes W A, Kiemeney Lambertus A, Rivadeneira Fernando, Uitterlinden André G, Walsh John P, Meisinger Christa, den Heijer Martin, Visser Theo J, Spector Timothy D, Wilson Scott G, Völzke Henry, Cappola Anne, Toniolo Daniela, Sanna Serena, Naitza Silvia, Peeters Robin |
| The association of thyroid peroxidase antibody risk loci with susceptibility to and phenotype of Graves' disease. Clinical endocrinology 2015 Oct 83 (4): 556-62. Ku? Aleksander, Szyma?ski Konrad, Peeters Robin P, Mi?kiewicz Piotr, Porcu Eleonora, Pistis Giorgio, Sanna Serena, Naitza Silvia, P?oski Rafa?, Medici Marco, Bednarczuk Toma |
| The Kalirin Gene rs9289231 Polymorphism as a Novel Predisposing Marker for Coronary Artery Disease. Laboratory medicine 2014 45 (4): 302-6. Boroumand Mohammadali, Ziaee Shayan, Zarghami Nosratollah, Anvari Maryam Sotudeh, Cheraghi Sara, Abbasi Seyed Hesameddin, Jalali Arash, Pourgholi Lei |
| KALRN Rare and Common Variants and Susceptibility to Ischemic Stroke in Chinese Han Population. Neuromolecular medicine 2015 Sep 17 (3): 241-50. Dang Meizheng, Wang Zhenzhen, Zhang Ruyou, Li Xiaoying, Peng Yanqing, Han Xuesong, Sun Litao, Tian Jiaw |
| Association of KALRN, ADIPOQ, and FTO gene polymorphism in type 2 diabetic patients with coronary artery disease: possible predisposing markers. Coronary artery disease 2016 May . Mofarrah Mohsen, Ziaee Shayan, Pilehvar-Soltanahmadi Yones, Zarghami Faraz, Boroumand Mohammadali, Zarghami Nosratoll |
| A novel relationship for schizophrenia, bipolar and major depressive disorder Part 3: Evidence from chromosome 3 high density association screen. The Journal of comparative neurology 2017 Aug . Chen Xing, Long Feng, Cai Bin, Chen Xiaohong, Chen Ga |
| G908R NOD2 variant in a family with sarcoidosis. Respiratory research 2018 3 19 (1): 44. Besnard Valérie, Calender Alain, Bouvry Diane, Pacheco Yves, Chapelon-Abric Catherine, Jeny Florence, Nunes Hilario, Planès Carole, Valeyre Dominiq |
| Association between Serum Kalirin Levels and the KALRN gene rs9289231 Polymorphism in Early-Onset Coronary Artery Disease. The journal of Tehran Heart Center 2018 11 13 (2): 58-64. Shafiei Afsaneh, Pilehvar-Soltanahmadi Younes, Ziaee Shayan, Mofarrah Mohsen, Zarghami Nosratoll |
| Association of an IRF3 putative functional uORF variant with resistance to Brucella infection: A candidate gene based analysis of InDel polymorphisms in goats. Cytokine 2018 11 115 109-115. Rossi Ursula A, Hasenauer Flavia C, Caffaro María E, Raschia Maria A, Maurizio Estefania, Cortez Hector S, Neumann Roberto D, Poli Mario A, Rossetti Carlos |
| Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population.
EBioMedicine 2020 Jul 57 102840. Shi Xiu-Yu, Wang Geng, Li Ting, Li Zhixiu, Leo Paul, Liu Zhisheng, Wu Gefei, Zhu Hongmin, Zhang Yuqin, Li Dong, Gao Li, Yang Liu, Wang Wei, Liao Jianxiang, Wang Jiwen, Zhou Shuizhen, Wang Hua, Li Xiaojing, Gao Jingyun, Zhang Li, Shu Xiaomei, Li Dan, Li Yan, Chen Chunhong, Zhang Xiuju, Partida Gabriel Cuellar, Lundberg Mischa, Reutens David, Bartlett Perry, Brown Matthew A, Zou Li-Ping, Xu Hu |
| Genome-Wide Association Meta-Analysis of Single-Nucleotide Polymorphisms and Symptomatic Venous Thromboembolism during Therapy for Acute Lymphoblastic Leukemia and Lymphoma in Caucasian Children.
Cancers 2020 May 12 (5): . Mateos Marion K, Tulstrup Morten, Quinn Michael Cj, Tuckuviene Ruta, Marshall Glenn M, Gupta Ramneek, Mayoh Chelsea, Wolthers Benjamin O, Barbaro Pasquale M, Ruud Ellen, Sutton Rosemary, Huttunen Pasi, Revesz Tamas, Trakymiene Sonata S, Barbaric Draga, Tedgård Ulf, Giles Jodie E, Alvaro Frank, Jonsson Olafur G, Mechinaud Françoise, Saks Kadri, Catchpoole Daniel, Kotecha Rishi S, Dalla-Pozza Luciano, Chenevix-Trench Georgia, Trahair Toby N, MacGregor Stuart, Schmiegelow Kje |
| Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing. Human genomics 2022 09 16 (1): 36. Chen Shasha, Jin Qinchun, Hou Shiqiang, Li Mingfei, Zhang Yuan, Guan Lihua, Pan Wenzhi, Ge Junbo, Zhou Dax |
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