Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: SLIT2[original query] |
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Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.
BMC medical genetics 2007 8 Suppl 1 S2. Vasan Ramachandran S, Larson Martin G, Aragam Jayashri, Wang Thomas J, Mitchell Gary F, Kathiresan Sekar, Newton-Cheh Christopher, Vita Joseph A, Keyes Michelle J, O'Donnell Christopher J, Levy Daniel, Benjamin Emelia |
ROBO2 gene variants are associated with familial vesicoureteral reflux. Journal of the American Society of Nephrology : JASN 2008 Apr 19 (4): 825-31. Bertoli-Avella Aida M, Conte Maria Luisa, Punzo Francesca, de Graaf Bianca M, Lama Giuliana, La Manna Angela, Polito Cesare, Grassia Carolina, Nobili Bruno, Rambaldi Pier Francesco, Oostra Ben A, Perrotta Silver |
Mutations in the ROBO2 and SLIT2 genes are rare causes of familial vesico-ureteral reflux. Pediatric nephrology (Berlin, Germany) 2009 Aug 24 (8): 1501-8. Zu Shulu, Bartik Zsuzsa, Zhao Shengtian, Sillen Ulla, Nordenskjöld Agne |
Association of polymorphisms in the SLIT2 axonal guidance gene with anger in suicide attempters. Molecular psychiatry 2010 Jan 15 (1): 10-1. Sokolowski M, Wasserman J, Wasserman |
Genetic Influences on Physiological and Subjective Responses to an Aerobic Exercise Session among Sedentary Adults. Journal of cancer epidemiology 2012 2012 540563. Karoly Hollis C, Stevens Courtney J, Magnan Renee E, Harlaar Nicole, Hutchison Kent E, Bryan Angela |
Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux. Kidney international 2013 Aug 84 (2): 327-37. Dobson Mark G, Darlow John M, Hunziker Manuela, Green Andrew J, Barton David E, Puri Pr |
Genome-wide association study of the plasma triglyceride response to an n-3 polyunsaturated fatty acid supplementation.
Journal of lipid research 2014 May 55 (7): 1245-1253. Rudkowska Iwona, Guénard Frédéric, Julien Pierre, Couture Patrick, Lemieux Simone, Barbier Olivier, Calder Philip C, Minihane Anne Marie, Vohl Marie-Clau |
Whole-exome and targeted sequencing identify ROBO1 and ROBO2 mutations as progression-related drivers in myelodysplastic syndromes. Nature communications 2015 6 8806. Xu Feng, Wu Ling-Yun, Chang Chun-Kang, He Qi, Zhang Zheng, Liu Li, Shi Wen-Hui, Guo Juan, Zhu Yang, Zhao You-Shan, Gu Shu-Cheng, Fei Cheng-Ming, Wu Dong, Zhou Li-Yu, Su Ji-Ying, Song Lu-Xi, Xiao Chao, Li Xi |
High-resolution 400K oligonucleotide array comparative genomic hybridization analysis of neurofibromatosis type 1-associated cutaneous neurofibromas. Gene 2015 Mar 558 (2): 220-6. Asai Akiko, Karnan Sivasundaram, Ota Akinobu, Takahashi Miyuki, Damdindorj Lhagvasuren, Konishi Yuko, Hossain Ekhtear, Konishi Hiroyuki, Nagata Ayako, Yokoo Kazuhisa, Hosokawa Yoshita |
Candidate predisposing germline copy number variants in early onset colorectal cancer patients. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2016 Nov . Brea-Fernandez A J, Fernandez-Rozadilla C, Alvarez-Barona M, Azuara D, Ginesta M M, Clofent J, de Castro L, Gonzalez D, Andreu M, Bessa X, Llor X, Xicola R, Jover R, Castells A, Castellvi-Bel S, Capella G, Carracedo A, Ruiz-Ponte |
Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.
PLoS genetics 2019 Jun 15 (6): e1008107. Tiensuu Heli, Haapalainen Antti M, Karjalainen Minna K, Pasanen Anu, Huusko Johanna M, Marttila Riitta, Ojaniemi Marja, Muglia Louis J, Hallman Mikko, Rämet Mi |
PDL1 high expression without TP53, KEAP1 and EPHA5 mutations could better predict survival for patients with NSCLC receiving atezolizumab. Lung cancer (Amsterdam, Netherlands) 2020 Nov . Wang Haiyong, Shan Qinge, Guo Jun, Han Xiao, Zhao Chenglong, Li Huijuan, Wang Zheh |
Unique genomic features and prognostic value of COSMIC mutational signature 4 in lung adenocarcinoma and lung squamous cell carcinoma. Annals of translational medicine 2020 11 8 (18): 1176. Cai Xiuyu, Chen Zhenghe, Deng Meiling, Li Zhiyong, Wu Qianchao, Wei Jinwang, Dai Chun, Wang Guan, Luo Ch |
Whole exome sequencing and trio analysis to broaden the variant spectrum of genes in idiopathic hypogonadotropic hypogonadism. Asian journal of andrology 2020 11 23 (3): 288-293. Zhang Jian, Tang Shu-Yan, Zhu Xiao-Bin, Li Peng, Lu Jian-Qi, Cong Jiang-Shan, Wang Ling-Bo, Zhang Feng, Li Zhe |
Exome sequencing identifies SLIT2 variants in primary CNS lymphoma. British journal of haematology 2021 Jan . Kaulen Leon D, Erson-Omay E Zeynep, Henegariu Octavian, Karschnia Philipp, Huttner Anita, Günel Murat, Baehring Joachim |
SLIT2 Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic Hypogonadism. Hormone research in paediatrics 2022 7 95 (4): 384-392. Wu Jiayu, Fang Zhenghuan, Wang Xinying, Zeng Wang, Zhao Yaguang, Jiang Fang, Chen Dan-Na, Zheng Ruizhi, Li Jinchen, Men Meichao, Li Jia- |
Analyzing the key gene expression and prognostics values for acute myeloid leukemia. Translational cancer research 2022 2 9 (11): 7284-7298. Shi Lingling, Huang Yan, Huang Xunjun, Zhou Weijie, Wei Jie, Deng Donghong, Lai Yongro |
Genome-Wide Association Study Identifies ROBO2 as a Novel Susceptibility Gene for Anthracycline-Related Cardiomyopathy in Childhood Cancer Survivors.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2022 12 JCO2201527. Wang Xuexia, Singh Purnima, Zhou Liting, Sharafeldin Noha, Landier Wendy, Hageman Lindsey, Burridge Paul, Yasui Yutaka, Sapkota Yadav, Blanco Javier G, Oeffinger Kevin C, Hudson Melissa M, Chow Eric J, Armenian Saro H, Neglia Joseph P, Ritchey A Kim, Hawkins Douglas S, Ginsberg Jill P, Robison Leslie L, Armstrong Gregory T, Bhatia Smi |
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