Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: CRKL[original query] |
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Genetic susceptibility on CagA-interacting molecules and gene-environment interaction with phytoestrogens: a putative risk factor for gastric cancer. PloS one 2012 7 (2): e31020. Yang Jae Jeong, Cho Lisa Y, Ko Kwang-Pil, Shin Aesun, Ma Seung Hyun, Choi Bo Youl, Han Dong Soo, Song Kyu Sang, Kim Yong Sung, Lee Jong-Young, Han Bok Ghee, Chang Soung-Hoon, Shin Hai-Rim, Kang Daehee, Yoo Keun-Young, Park Sue |
Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
High CC chemokine receptor 7 expression improves postoperative prognosis of lung adenocarcinoma patients. British journal of cancer 2013 Sep 109 (5): 1100-8. Itakura M, Terashima Y, Shingyoji M, Yokoi S, Ohira M, Kageyama H, Matui Y, Yoshida Y, Ashinuma H, Moriya Y, Tamura H, Harigaya K, Matushima K, Iizasa T, Nakagawara A, Kimura |
Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects. American journal of medical genetics. Part A 2014 Feb 164A (2): 397-406. Osoegawa Kazutoyo, Iovannisci David M, Lin Bin, Parodi Christina, Schultz Kathleen, Shaw Gary M, Lammer Edward |
High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease. American journal of medical genetics. Part A 2013 Dec 161A (12): 3087-94. Zhao Wei, Niu Guannan, Shen Botao, Zheng Yang, Gong Fangchao, Wang Xianfu, Lee Jiyun, Mulvihill John J, Chen Xiaohui, Li Shi |
Association study between genes in Reelin signaling pathway and autism identifies DAB1 as a susceptibility gene in a Chinese Han population. Progress in neuro-psychopharmacology & biological psychiatry 2013 Jul 44 226-32. Li Jun, Liu Jing, Zhao Linnan, Ma Yuanlin, Jia Meixiang, Lu Tianlan, Ruan Yanyan, Li Qizhai, Yue Weihua, Zhang Dai, Wang Lifa |
Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion. BMC medical genetics 2014 15 78. Xu Yue-Juan, Chen Sun, Zhang Jian, Fang Shao-Hai, Guo Qian-Qian, Wang Jian, Fu Qi-Hua, Li Fen, Xu Rang, Sun K |
Differential expression of CRKL and AXL genes in lung adenocarcinoma subtypes according to the epidermal growth factor receptor and anaplastic lymphoma kinase gene status. Biomedical reports 2014 Jul 2 (4): 481-489. Yu DA-Ping, Dong Yu-Jie, Zhang Hai-Qing, Wang Jing-Hui, Qu Yang, Zhou Li-Juan, Su Dan, Zhang Li-Li, Zhao Dan, Cai Yi-R |
Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Feb . Cao Ye, Li Zhihua, Rosenfeld Jill A, Pursley Amber N, Patel Ankita, Huang Jin, Wang Huilin, Chen Min, Sun Xiaofang, Leung Tak Yeung, Cheung Sau Wai, Choy Kwong W |
Expression level of CRKL and AXL combined with exon 19 deletion in EGFR and ALK status confer differential prognosis of lung adenocarcinoma subtypes. Oncology letters 2016 Nov 12 (5): 3312-3322. Cai Yi-Ran, Dong Yu-Jie, Wu Hong-Bo, Yu Da-Ping, Zhou Li-Juan, Su Dan, Zhang Li, Chen Xue-Ji |
Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans. Genes, brain, and behavior 2019 5 18 (6): e12580. Wetherill Leah, Lai Dongbing, Johnson Emma C, Anokhin Andrey, Bauer Lance, Bucholz Kathleen K, Dick Danielle M, Hariri Ahmad R, Hesselbrock Victor, Kamarajan Chella, Kramer John, Kuperman Samuel, Meyers Jacquelyn L, Nurnberger John I, Schuckit Marc, Scott Denise M, Taylor Robert E, Tischfield Jay, Porjesz Bernice, Goate Alison M, Edenberg Howard J, Foroud Tatiana, Bogdan Ryan, Agrawal Arpa |
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. American journal of human genetics 2019 12 106 (1): 26-40. Zhao Yingjie, Diacou Alexander, Johnston H Richard, Musfee Fadi I, McDonald-McGinn Donna M, McGinn Daniel, Crowley T Blaine, Repetto Gabriela M, Swillen Ann, Breckpot Jeroen, Vermeesch Joris R, Kates Wendy R, Digilio M Cristina, Unolt Marta, Marino Bruno, Pontillo Maria, Armando Marco, Di Fabio Fabio, Vicari Stefano, van den Bree Marianne, Moss Hayley, Owen Michael J, Murphy Kieran C, Murphy Clodagh M, Murphy Declan, Schoch Kelly, Shashi Vandana, Tassone Flora, Simon Tony J, Shprintzen Robert J, Campbell Linda, Philip Nicole, Heine-Suñer Damian, García-Miñaúr Sixto, Fernández Luis, , Bearden Carrie E, Vingerhoets Claudia, van Amelsvoort Therese, Eliez Stephan, Schneider Maude, Vorstman Jacob A S, Gothelf Doron, Zackai Elaine, Agopian A J, Gur Raquel E, Bassett Anne S, Emanuel Beverly S, Goldmuntz Elizabeth, Mitchell Laura E, Wang Tao, Morrow Bernice |
MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects - pilot study. The significant frequency rate of presented pathological CNV. Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia 2021 Mar . Stefekova Andrea, Capkova Pavlina, Capkova Zuzana, Curtisova Vaclava, Srovnal Josef, Mracka Enkhjargalan, Klaskova Eva, Prochazka Mart |
Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects. Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003510. Saacks Nicole A, Eales James, Spracklen Timothy F, Aldersley Thomas, Human Paul, Verryn Mark, Lawrenson John, Cupido Blanche, Comitis George, De Decker Rik, Fourie Barend, Swanson Lenise, Joachim Alexia, Brooks Andre, Ramesar Raj, Shaboodien Gasnat, Keavney Bernard D, Zühlke Liesl |
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