Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: ACVR1[original query] |
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The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations. Journal of medical genetics 2004 Jul 41 (7): 484-91. Howe J R, Sayed M G, Ahmed A F, Ringold J, Larsen-Haidle J, Merg A, Mitros F A, Vaccaro C A, Petersen G M, Giardiello F M, Tinley S T, Aaltonen L A, Lynch H |
Variants in the ACVR1 gene are associated with AMH levels in women with polycystic ovary syndrome. Human reproduction (Oxford, England) 2009 Jan 24 (1): 241-9. Kevenaar Marlies E, Themmen Axel P N, van Kerkwijk Anke J, Valkenburg Olivier, Uitterlinden André G, de Jong Frank H, Laven Joop S E, Visser Jenny |
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 |
Genetic variation within the hypothalamus-pituitary-ovarian axis in women with recurrent miscarriage. Human reproduction (Oxford, England) 2010 Oct 25 (10): 2664-71. Hanna Courtney W, Bretherick Karla L, Liu Chi-Chao, Stephenson Mary D, Robinson Wendy |
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 |
Common genetic variants of the BMP4, BMPR1A, BMPR1B, and ACVR1 genes, left ventricular mass, and other parameters of the heart in newborns. Genetic testing and molecular biomarkers 2012 Nov 16 (11): 1309-16. Gor?cy Iwona, Safranow Krzysztof, Dawid Gra?yna, Skonieczna-?ydecka Karolina, Kaczmarczyk Mariusz, Gor?cy Jaros?aw, Loniewska Beata, Ciechanowicz Andrz |
Genetic variation in bone morphogenetic proteins and breast cancer risk in hispanic and non-hispanic white women: The breast cancer health disparities study. International journal of cancer. Journal international du cancer 2012 Nov . Slattery ML, John EM, Torres-Mejia G, Herrick JS, Giuliano AR, Baumgartner KB, Hines LM, Wolff RK |
The phenotype and genotype of fibrodysplasia ossificans progressiva in China: a report of 72 cases. Bone 2013 Dec 57 (2): 386-91. Zhang Wei, Zhang Keqin, Song Lige, Pang Jing, Ma Hongxing, Shore Eileen M, Kaplan Frederick S, Wang Peij |
Pathway analysis of a genome-wide association study in schizophrenia. Gene 2013 Aug 525 (1): 107-15. Lee Young Ho, Kim Jae-Hoon, Song Gwan G |
Genetic variants in anti-Mullerian hormone and anti-Mullerian hormone receptor genes and breast cancer risk in Caucasians and African Americans. International journal of molecular epidemiology and genetics 2014 5 (3): 145-51. Nan Hongmei, Dorgan Joanne F, Rebbeck Timothy |
A genetic variant in microRNA target site of TGF-ß signaling pathway increases the risk of colorectal cancer in a Chinese population. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 May 35 (5): 4301-6. Gong Jing, Shen Na, Zhang Hong-Mei, Zhong Rong, Chen Wei, Miao Xiaoping, Guo An-Yu |
Spatial genomic heterogeneity in diffuse intrinsic pontine and midline high-grade glioma: implications for diagnostic biopsy and targeted therapeutics. Acta neuropathologica communications 2016 4 (1): 1. Hoffman Lindsey M, DeWire Mariko, Ryall Scott, Buczkowicz Pawel, Leach James, Miles Lili, Ramani Arun, Brudno Michael, Kumar Shiva Senthil, Drissi Rachid, Dexheimer Phillip, Salloum Ralph, Chow Lionel, Hummel Trent, Stevenson Charles, Lu Q Richard, Jones Blaise, Witte David, Aronow Bruce, Hawkins Cynthia E, Fouladi Mary |
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 |
Whole-genome sequencing identifies potential candidate genes for reproductive traits in pigs. Genomics 2019 Jan . Li Xinjian, Ye Jianwei, Han Xuelei, Qiao Ruimin, Li Xiuling, Lv Gang, Wang Kej |
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 |
Differential expression of BMP/SMAD signaling and ovarian-associated genes in the granulosa cells of FecB introgressed GMM sheep. Systems biology in reproductive medicine 2020 1 66 (3): 185-201. Kumar Satish, Rajput Pradeep Kumar, Bahire Sangharatna V, Jyotsana Basanti, Kumar Vijay, Kumar Davend |
Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations. Oral diseases 2021 Jun . Li Mary, Olotu Joy, Buxo-Martinez Carmen J, Mossey Peter A, Anand Deepti, Busch Tamara, Alade Azeez, Gowans Lord J J, Eshete Mekonen, Adeyemo Wasiu L, Naicker Thirona, Awotoye Waheed O, Gupta Sagar, Adeleke Chinyere, Bravo Valeria, Huang Siyong, Adamson Olatunbosun O, Toraño Ada M, Bello Carolina A, Soto Mairim, Soto Marilyn, Ledesma Ricardo, Marquez Myrellis, Cordero Jose F, Lopez-Del Valle Lydia M, Salcedo Maria I, Debs Natalio, Petrin Aline, Malloy Hannah, Elhadi Khalid, James Olutayo, Ogunlewe Mobolanle O, Abate Fekir, Hailu Abiye, Mohammed Ibrahim, Gravem Paul, Deribew Milliard, Gesses Mulualem, Hassan Mohaned, Pape John, Obiri-Yeboah Solomon, Arthur Fareed K N, Oti Alexander A, Donkor Peter, Marazita Mary L, Lachke Salil A, Adeyemo Adebowale A, Murray Jeffrey C, Butali Aze |
H3K27M-mutant diffuse midline gliomas should be further molecularly stratified: an integrated analysis of 669 patients. Journal of neuro-oncology 2021 11 155 (3): 225-234. Vuong Huy Gia, Le Hieu Trong, Ngo Tam N M, Fung Kar-Ming, Battiste James D, McNall-Knapp Rene, Dunn Ian |
Association of rs12997 variant in the ACVR1 gene: a member of bone morphogenic protein signaling pathway with primary open-angle glaucoma in a Saudi cohort. Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2021 1 69 (2): 402-407. Kondkar Altaf A, Azad Taif A, Sultan Tahira, 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 |
Identifying selection signatures and runs of homozygosity for spine curvature in Chinese indigenous pigs. Animal genetics 2022 5 53 (4): 513-517. Jiayuan Mo, Yujie Lu, Kuirong Chen, Siran Zhu, Wenjing Qi, Lingli Feng, Xiaoxiao Liu, Liang Liang, Ganqiu Lan, Jing Lia |
Prognostic Implication of Patient Age in H3K27M-Mutant Midline Gliomas. Frontiers in oncology 2022 4 12 858148. Vuong Huy Gia, Ngo Tam N M, Le Hieu Trong, Jea Andrew, Hrachova Maya, Battiste James, McNall-Knapp Rene, Dunn Ian |
Bioinformatics Analysis of the Genetic and Epigenetic Alterations of Bone Morphogenetic Protein Receptors in Metastatic Breast Cancer. Biochemical genetics 2023 7 . Adam Hermawan, Herwandhani Put |
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- Page last updated:Apr 22, 2024
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