Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: GRB2[original query] |
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Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. PloS one 2011 6 (8): e23450. Moens Lotte N, De Rijk Peter, Reumers Joke, Van den Bossche Maarten J A, Glassee Wim, De Zutter Sonia, Lenaerts An-Sofie, Nordin Annelie, Nilsson Lars-Göran, Medina Castello Ignacio, Norrback Karl-Fredrik, Goossens Dirk, Van Steen Kristel, Adolfsson Rolf, Del-Favero Jurg |
Discovering genetic variants in Crohn's disease by exploring genomic regions enriched of weak association signals. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2011 Aug 43 (8): 623-31. D'Addabbo Annarita, Palmieri Orazio, Maglietta Rosalia, Latiano Anna, Mukherjee Sayan, Annese Vito, Ancona Nico |
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 |
Essential role of polymorphism of Gab1, EGFR, and EGF for the susceptibility of biliary tract cancer. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Dec 35 (12): 12497-508. Meng Ling-Q |
Role of HER2 mutations in refractory metastatic breast cancers: targeted sequencing results in patients with refractory breast cancer. Oncotarget 2015 Sep . Park Yeon Hee, Shin Hyun-Tae, Jung Hae Hyun, Choi Yoon-La, Ahn TaeJin, Park Kyunghee, Lee Aeri, Do In-Gu, Kim Ji-Yeon, Ahn Jin Seok, Park Woong-Yang, Im Young-Hyu |
Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene.
Diabetologia 2015 Oct 58 (10): 2288-97. Burdon Kathryn P, Fogarty Rhys D, Shen Weiyong, Abhary Sotoodeh, Kaidonis Georgia, Appukuttan Binoy, Hewitt Alex W, Sharma Shiwani, Daniell Mark, Essex Rohan W, Chang John H, Klebe Sonja, Lake Stewart R, Pal Bishwanath, Jenkins Alicia, Govindarjan Gowthaman, Sundaresan Periasamy, Lamoureux Ecosse L, Ramasamy Kim, Pefkianaki Maria, Hykin Philip G, Petrovsky Nikolai, Brown Matthew A, Gillies Mark C, Craig Jamie |
Hormone-related pathways and risk of breast cancer subtypes in African American women. Breast cancer research and treatment 2015 Oct . Haddad Stephen A, Lunetta Kathryn L, Ruiz-Narváez Edward A, Bensen Jeannette T, Hong Chi-Chen, Sucheston-Campbell Lara E, Yao Song, Bandera Elisa V, Rosenberg Lynn, Haiman Christopher A, Troester Melissa A, Ambrosone Christine B, Palmer Julie |
Associations of rs3740677 within GAB2 Gene with LOAD in Chinese Han Population. Molecular neurobiology 2016 Jun . Zheng Jing-Yu, Wang Hui-Fu, Wan Yu, Tan Meng-Shan, Tan Chen-Chen, Tan Lin, Zhang Wei, Zheng Zhan-Jie, Kong Ling-Li, Wang Zi-Xuan, Tan Lan, Yu Jin-T |
EGFR-GRB2 Protein Colocalization Is a Prognostic Factor Unrelated to Overall EGFR Expression or EGFR Mutation in Lung Adenocarcinoma. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2016 Nov 11 (11): 1901-1911. Toki Maria I, Carvajal-Hausdorf Daniel E, Altan Mehmet, McLaughlin Joseph, Henick Brian, Schalper Kurt A, Syrigos Konstantinos N, Rimm David |
Pri-microRNA-124 rs531564 polymorphism minor allele increases the risk of pulmonary artery hypertension by abnormally enhancing proliferation of pulmonary artery smooth muscle cells. International journal of chronic obstructive pulmonary disease 2017 12 1351-1361. Li Quanzhong, Qian Zongjie, Wang Linqi |
Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
Human molecular genetics 2017 Mar . Raffield Laura M, Louie Tin, Sofer Tamar, Jain Deepti, Ipp Eli, Taylor Kent D, Papanicolaou George J, Avilés-Santa Larissa, Lange Leslie A, Laurie Cathy C, Conomos Matthew P, Thornton Timothy A, Ida Chen Yii-Der, Qi Qibin, Cotler Scott, Thyagarajan Bharat, Schneiderman Neil, Rotter Jerome I, Reiner Alex P, Lin Henry |
Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.
Human reproduction (Oxford, England) 2017 04 32 (4): 780-793. Uimari Outi, Rahmioglu Nilufer, Nyholt Dale R, Vincent Katy, Missmer Stacey A, Becker Christian, Morris Andrew P, Montgomery Grant W, Zondervan Krina |
Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. Journal of affective disorders 2018 03 228 20-25. Mühleisen Thomas W, Reinbold Céline S, Forstner Andreas J, Abramova Lilia I, Alda Martin, Babadjanova Gulja, Bauer Michael, Brennan Paul, Chuchalin Alexander, Cruceanu Cristiana, Czerski Piotr M, Degenhardt Franziska, Fischer Sascha B, Fullerton Janice M, Gordon Scott D, Grigoroiu-Serbanescu Maria, Grof Paul, Hauser Joanna, Hautzinger Martin, Herms Stefan, Hoffmann Per, Kammerer-Ciernioch Jutta, Khusnutdinova Elza, Kogevinas Manolis, Krasnov Valery, Lacour André, Laprise Catherine, Leber Markus, Lissowska Jolanta, Lucae Susanne, Maaser Anna, Maier Wolfgang, Martin Nicholas G, Mattheisen Manuel, Mayoral Fermin, McKay James D, Medland Sarah E, Mitchell Philip B, Moebus Susanne, Montgomery Grant W, Müller-Myhsok Bertram, Oruc Lilijana, Pantelejeva Galina, Pfennig Andrea, Pojskic Lejla, Polonikov Alexey, Reif Andreas, Rivas Fabio, Rouleau Guy A, Schenk Lorena M, Schofield Peter R, Schwarz Markus, Streit Fabian, Strohmaier Jana, Szeszenia-Dabrowska Neonila, Tiganov Alexander S, Treutlein Jens, Turecki Gustavo, Vedder Helmut, Witt Stephanie H, Schulze Thomas G, Rietschel Marcella, Nöthen Markus M, Cichon Sv |
Genome-wide association study meta-analysis identifies five new loci for systemic lupus erythematosus.
Arthritis research & therapy 2018 May 20 (1): 100. Julià Antonio, López-Longo Francisco Javier, Pérez Venegas José J, Bonàs-Guarch Silvia, Olivé Àlex, Andreu José Luís, Aguirre-Zamorano Mª Ángeles, Vela Paloma, Nolla Joan M, de la Fuente José Luís Marenco, Zea Antonio, Pego-Reigosa José María, Freire Mercedes, Díez Elvira, Rodríguez-Almaraz Esther, Carreira Patricia, Blanco Ricardo, Taboada Víctor Martínez, López-Lasanta María, Corbeto Mireia López, Mercader Josep M, Torrents David, Absher Devin, Marsal Sara, Fernández-Nebro Anton |
Rs7219 Regulates the Expression of GRB2 by Affecting miR-1288-Mediated Inhibition and Contributes to the Risk of Schizophrenia in the Chinese Han Population. Cellular and molecular neurobiology 2019 Jan 39 (1): 137-147. Yang Jialei, Guo Xiaojing, Zhu Lulu, Huang Jiao, Long Jianxiong, Chen Qiang, Pan Runde, Chen Zhaoxia, Wu Xulong, Su |
Evaluation of genetic susceptibility between systemic lupus erythematosus and GRB2 gene. Scientific reports 2019 Jul 9 (1): 10335. Xu Meifeng, Liu Yan, Li Xiaoli, Cheng Chuantao, Liu Yale, Dong Wei, Du Shaoyi, Xiao Shengxia |
Prognostic effect of VEGF gene variants in metastatic non-small-cell lung cancer patients. Angiogenesis 2019 Apr . Sullivan Ivana, Riera Pau, Andrés Marta, Altés Albert, Majem Margarita, Blanco Remei, Capdevila Laia, Barba Andrés, Barnadas Agustí, Salazar Julia |
The Germline Variants rs61757955 and rs34988193 Are Predictive of Survival in Lower Grade Glioma Patients. Molecular cancer research : MCR 2019 1 17 (5): 1075-1086. Chatrath Ajay, Kiran Manjari, Kumar Pankaj, Ratan Aakrosh, Dutta Anind |
The SLAMF3 rs509749 polymorphism correlates with malignant potential in multiple myeloma. Experimental hematology 2020 Aug . Ishibashi Mariko, Sunakawa-Kii Mika, Kaito Yuta, Kinoshita Ryosuke, Asayama Toshio, Kuribayashi Yasuko, Inokuchi Koiti, Morita Rimpei, Tamura Hide |
Set-Based Rare Variant Expression Quantitative Trait Loci in Blood and Brain from Alzheimer Disease Study Participants. Genes 2021 Mar 12 (3): . Patel Devanshi, Zhang Xiaoling, Farrell John J, Lunetta Kathryn L, Farrer Lindsay |
Genomic alterations associated with mutational signatures, DNA damage repair and chromatin remodeling pathways in cervical carcinoma. NPJ genomic medicine 2021 Oct 6 (1): 82. Halle Mari K, Sundaresan Aishwarya, Zhang Jianqing, Pedamallu Chandra Sekhar, Srinivasasainagendra Vinodh, Blair Jessica, Brooke Dewey, Bertelsen Bjørn I, Woie Kathrine, Shrestha Sadeep, Tiwari Hemant, Wong Yick Fu, Krakstad Camilla, Ojesina Akinyemi |
Association of GAB2 with Quality of Life and Negative Emotions in Patients with Gastric Cancer after Postoperative Comprehensive Care. Evidence-based complementary and alternative medicine : eCAM 2022 2022 1732214. Zhuang Juping, Yu Jiejie, Yang Yanc |
Identification of Grb2-associated binding protein 3 expression to predict clinical outcomes and immunotherapeutic responses in lung adenocarcinoma. Journal of biochemical and molecular toxicology 2022 7 36 (10): e23166. Wang Ning, Zhou Xue, Wang Xue, Zhu Xiaow |
In-Silico and In-Vitro Analysis of Human SOS1 Protein Causing Noonan Syndrome - A Novel Approach to Explore the Molecular Pathways. Current genomics 2022 4 22 (7): 526-540. Sigamani Vinoth, Rajasingh Sheeja, Gurusamy Narasimman, Panda Arunima, Rajasingh Johns |
Shared genetic loci for body fat storage and adipocyte lipolysis in humans. Scientific reports 2022 3 12 (1): 3666. Kulyté Agné, Lundbäck Veroniqa, Arner Peter, Strawbridge Rona J, Dahlman Ingr |
High expression of GRB2 associated binding protein 3 mRNA predicts positive prognosis in melanoma. Melanoma research 2022 12 33 (1): 27-37. Li Chunting, Ye Zhenzhen, Wang Yimeng, Wang Guanyu, Zhang Qian, Zhang Chunl |
Association of GAB1 gene with asthma susceptibility and the efficacy of inhaled corticosteroids in children. BMC pulmonary medicine 2023 12 23 (1): 493. Yuxuan Zhang, Jun Liu, Yanjie Zhi, Xuan You, Bing W |
Identification of Novel Genetic Risk Factors for Focal Segmental Glomerulosclerosis in Children: Results From the Chronic Kidney Disease in Children (CKiD) Cohort.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2023 1 . Durand Axelle, Winkler Cheryl A, Vince Nicolas, Douillard Venceslas, Geffard Estelle, Binns-Roemer Elizabeth, Ng Derek K, Gourraud Pierre-Antoine, Reidy Kimberley, Warady Bradley, Furth Susan, Kopp Jeffrey B, Kaskel Frederick J, Limou Soph |
Identification of a Single Nucleotide Polymorphism of Vitamin D Receptor (VDR) and Vitamin D Binding Protein (VDBP) Gene and Its Dysregulated Pathway Through VDR-VDBP Interaction Network Analysis in Vitamin D-Deficient Infertile Females. Cureus 2024 4 16 (3): e55602. Zil E Rubab, Sumaira Naz, Mussarat Ashraf, Saba Shahid, Rehana Rehm |
Bioinformatic analysis reveals the clinical value of SASH3 in survival prognosis and immune infiltration of acute myelocytic leukemia (AML). American journal of translational research 2024 1 15 (12): 6858-6866. Yufei Li, Lin Wang, Xueyuan Jia, Yanru Yang, Zhengqi Q |
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- Page last updated:Apr 16, 2024
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