Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and ACVR1[original query] |
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| Sequencing of TGF-beta pathway genes in familial cases of intracranial aneurysm. Stroke; a journal of cerebral circulation 2009 May 40 (5): 1604-11. Santiago-Sim Teresa, Mathew-Joseph Sumy, Pannu Hariyadarshi, Milewicz Dianna M, Seidman Christine E, Seidman J G, Kim Dong |
| Identification of genes for bone mineral density variation by computational disease gene identification strategy. Journal of bone and mineral metabolism 2011 Nov 29 (6): 709-16. Li Gloria H Y, Deng Hong-Wen, Kung Annie W C, Huang Qing-Ya |
| Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns. Genome medicine 2017 Oct 9 (1): 95. Li Alexander H, Hanchard Neil A, Furthner Dieter, Fernbach Susan, Azamian Mahshid, Nicosia Annarita, Rosenfeld Jill, Muzny Donna, D'Alessandro Lisa C A, Morris Shaine, Jhangiani Shalini, Parekh Dhaval R, Franklin Wayne J, Lewin Mark, Towbin Jeffrey A, Penny Daniel J, Fraser Charles D, Martin James F, Eng Christine, Lupski James R, Gibbs Richard A, Boerwinkle Eric, Belmont John |
| Peripheral Blood Mononuclear Cell Immunophenotyping in Fibrodysplasia Ossificans Progressiva Patients: Evidence for Monocyte DNAM1 Up-regulation. Cytometry. Part B, Clinical cytometry 2017 10 94 (4): 613-622. Del Zotto Genny, Antonini Francesca, Azzari Irma, Ortolani Claudio, Tripodi Gino, Giacopelli Francesca, Cappato Serena, Moretta Lorenzo, Ravazzolo Roberto, Bocciardi Rena |
| Genetic variants in anti-Müllerian hormone-related genes and breast cancer risk: results from the AMBER consortium. Breast cancer research and treatment 2020 9 185 (2): 469-478. Nichols Hazel B, Graff Mariaelisa, Bensen Jeannette T, Lunetta Kathryn L, O'Brien Katie M, Troester Melissa A, Williams Lindsay A, Young Kristin, Hong Chi-Chen, Yao Song, Haiman Christopher A, Ruiz-Narváez Edward A, Ambrosone Christine B, Palmer Julie R, Olshan Andrew |
| Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin. BMC medical genetics 2020 Jul 21 (1): 145. Kondkar Altaf A, Sultan Tahira, Azad Taif A, Osman Essam A, Almobarak Faisal A, Al-Obeidan Saleh |
| A Targeted Next-Generation Sequencing Panel to Genotype Gliomas. Life (Basel, Switzerland) 2022 Jun 12 (7): . Guarnaccia Maria, Guarnaccia Laura, La Cognata Valentina, Navone Stefania Elena, Campanella Rolando, Ampollini Antonella, Locatelli Marco, Miozzo Monica, Marfia Giovanni, Cavallaro Sebastia |
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