Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and GRB2[original query] |
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| Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy. Clinical endocrinology 2007 Nov 67 (5): 663-7. Syed A A, Simmonds M J, Brand O J, Franklyn J A, Gough S C L, Heward J |
| GAB2 is not associated with late-onset Alzheimer's disease in Japanese. European journal of human genetics : EJHG 2009 May 17 (5): 682-6. Miyashita Akinori, Arai Hiroyuki, Asada Takashi, Imagawa Masaki, Shoji Mikio, Higuchi Susumu, Urakami Katsuya, Toyabe Shinichi, Akazawa Kohei, Kanazawa Ichiro, Ihara Yasuo, Kuwano Ryo |
| 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 variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass. International journal of obesity (2005) 2012 Feb 36 (2): 201-6. Cummings N, Shields K A, Curran J E, Bozaoglu K, Trevaskis J, Gluschenko K, Cai G, Comuzzie A G, Dyer T D, Walder K R, Zimmet P, Collier G R, Blangero J, Jowett J B |
| 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 |
| 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 |
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 |
| 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 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 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 |
| 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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