Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: ITGA9[original query] |
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A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy. Prenatal diagnosis 2008 Nov 28 (11): 1057-63. Ma Gwo-Chin, Liu Chin-San, Chang Shun-Ping, Yeh Kun-Tu, Ke Yu-Yuan, Chen Tze-Ho, Wang Boris Bao-Tyan, Kuo Shou-Jen, Shih Jin-Chung, Chen Mi |
A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.
Journal of human genetics 2009 Jul 54 (7): 392-7. Ng Ching Ching, Yew Poh Yin, Puah Suat Moi, Krishnan Gopala, Yap Lee Fah, Teo Soo Hwang, Lim Paul Vey Hong, Govindaraju Selvaratnam, Ratnavelu Kananathan, Sam Choon Kook, Takahashi Atsushi, Kubo Michiaki, Kamatani Naoyuki, Nakamura Yusuke, Mushiroda Tais |
Blood pressure and hypertension are associated with 7 loci in the Japanese population. Circulation 2010 Jun 121 (21): 2302-9. Takeuchi Fumihiko, Isono Masato, Katsuya Tomohiro, Yamamoto Ken, Yokota Mitsuhiro, Sugiyama Takao, Nabika Toru, Fujioka Akihiro, Ohnaka Keizo, Asano Hiroyuki, Yamori Yukio, Yamaguchi Shuhei, Kobayashi Shotai, Takayanagi Ryoichi, Ogihara Toshio, Kato Norihi |
[Association of ITGA9 gene rs189897 and rs2212020 genotypes and its haplotype with cerebral infarction]. Nan fang yi ke da xue xue bao = Journal of Southern Medical University 2011 Jun 31 (7): 1142-5. Li Xiang-min, Li Jing, Zeng Feng, Yi Ho |
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, |
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts.
Circulation. Cardiovascular genetics 2012 Dec 5 (6): 639-46. Butler Anne M, Yin Xiaoyan, Evans Daniel S, Nalls Michael A, Smith Erin N, Tanaka Toshiko, Li Guo, Buxbaum Sarah G, Whitsel Eric A, Alonso Alvaro, Arking Dan E, Benjamin Emelia J, Berenson Gerald S, Bis Josh C, Chen Wei, Deo Rajat, Ellinor Patrick T, Heckbert Susan R, Heiss Gerardo, Hsueh Wen-Chi, Keating Brendan J, Kerr Kathleen F, Li Yun, Limacher Marian C, Liu Yongmei, Lubitz Steven A, Marciante Kristin D, Mehra Reena, Meng Yan A, Newman Anne B, Newton-Cheh Christopher, North Kari E, Palmer Cameron D, Psaty Bruce M, Quibrera P Miguel, Redline Susan, Reiner Alex P, Rotter Jerome I, Schnabel Renate B, Schork Nicholas J, Singleton Andrew B, Smith J Gustav, Soliman Elsayed Z, Srinivasan Sathanur R, Zhang Zhu-ming, Zonderman Alan B, Ferrucci Luigi, Murray Sarah S, Evans Michele K, Sotoodehnia Nona, Magnani Jared W, Avery Christy |
Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Dec . Secolin R, Banzato CE, Mella LF, Santos ML, Dalgalarrondo P, Lopes-Cendes I |
Evaluation and integration of genetic signature for prediction risk of nasopharyngeal carcinoma in Southern China. BioMed research international 2014 2014 434072. Guo Xiuchan, Winkler Cheryl A, Li Ji, Guan Li, Tang Minzhong, Liao Jian, Deng Hong, de Thé Guy, Zeng Yi, O'Brien Stephen |
Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer. BMC cancer 2014 14 (1): 902. Tervasmäki Anna, Winqvist Robert, Jukkola-Vuorinen Arja, Pylkäs Kat |
New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation.
The pharmacogenomics journal 2017 Nov . Fabbri C, Tansey K E, Perlis R H, Hauser J, Henigsberg N, Maier W, Mors O, Placentino A, Rietschel M, Souery D, Breen G, Curtis C, Sang-Hyuk L, Newhouse S, Patel H, Guipponi M, Perroud N, Bondolfi G, O'Donovan M, Lewis G, Biernacka J M, Weinshilboum R M, Farmer A, Aitchison K J, Craig I, McGuffin P, Uher R, Lewis C |
PR Interval Associated Genes, Atrial Remodeling and Rhythm Outcome of Catheter Ablation of Atrial Fibrillation-A Gene-Based Analysis of GWAS Data. Frontiers in genetics 2017 8 224. Husser Daniela, Büttner Petra, Stübner Dorian, Ueberham Laura, Platonov Pyotr G, Dinov Borislav, Arya Arash, Hindricks Gerhard, Bollmann Andre |
Integrated Multiomics Approach to Identify Genetic Underpinnings of Heart Failure and Its Echocardiographic Precursors: Framingham Heart Study. Circulation. Genomic and precision medicine 2019 11 12 (12): e002489. Andersson Charlotte, Lin Honghuang, Liu Chunyu, Levy Daniel, Mitchell Gary F, Larson Martin G, Vasan Ramachandran |
Association study of hypertension susceptibility genes ITGA9, MOV10, and CACNB2 with preeclampsia in Chinese Han population. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2021 Jan 1-9. Xin Qian, Xin Gang, Li Li, Sun Wenjuan, Jiang Wen, Wang Jue, Luan Yun, Zhang Ying, Cheng Ling, Duan Shuhong, Hong Fanzhen, Ji Qinghong, Ma Weiho |
Genome-wide association study on 13?167 individuals identifies regulators of blood CD34+cell levels.
Blood 2022 1 139 (11): 1659-1669. Lopez de Lapuente Portilla Aitzkoa, Ekdahl Ludvig, Cafaro Caterina, Ali Zain, Miharada Natsumi, Thorleifsson Gudmar, Žemaitis Kristijonas, Lamarca Arrizabalaga Antton, Thodberg Malte, Pertesi Maroulio, Dhapola Parashar, Bao Erik, Niroula Abhishek, Bali Divya, Norddahl Gudmundur, Ugidos Damboriena Nerea, Sankaran Vijay G, Karlsson Göran, Thorsteinsdottir Unnur, Larsson Jonas, Stefansson Kari, Nilsson Bjö |
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