Human Genome Epidemiology Literature Finder
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Records 1 - 28 (of 28 Records) |
| Query Trace: Disease and BMP4[original query] |
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| Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance. American journal of human genetics 2007 Oct 81 (4): 799-807. Milet Jacqueline, Dehais Valerie, Bourgain Catherine, Jouanolle Anne Marie, Mosser Annick, Perrin Michele, Morcet Jeff, Brissot Pierre, David Veronique, Deugnier Yves, Mosser Je |
| Investigation of the association of BMP gene variants with nephropathy in Type 1 diabetes mellitus. Diabetic medicine : a journal of the British Diabetic Association 2010 Jun 27 (6): 624-30. McKnight A J, Pettigrew K A, Patterson C C, Kilner J, Sadlier D M, Maxwell A P, |
| Mutation -538 T/C in bone morphogenetic protein 4 do not increase the risk in sickle-cell disease with orthopedic complications but strongly associated with increased LDH and uric acid level in Indian patients from Chhattisgarh and Jharkhand states. Clinica chimica acta; international journal of clinical chemistry 2010 May 411 (9-10): 664-70. Abhishek Kumar, Sohail Mohammad, Kumar Ritesh, Patra P K, Choudhary S |
| Evaluation of germline BMP4 mutation as a cause of colorectal cancer. Human mutation 2011 Jan 32 (1): E1928-38. Lubbe Steven J, Pittman Alan M, Matijssen Cornelis, Twiss Philip, Olver Bianca, Lloyd Amy, Qureshi Mobshra, Brown Nathan, Nye Emma, Stamp Gordon, Blagg Julian, Houlston Richard |
| Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma. Molecular vision 2009 15 . Zhang Xiaohui, Li Shiqiang, Xiao Xueshan, Jia Xiaoyun, Wang Panfeng, Shen Huangxuan, Guo Xiangming, Zhang Qingjio |
| Mutation screening of BMP4 and Id2 genes in Chinese patients with congenital ureteropelvic junction obstruction. European journal of pediatrics 2012 Mar 171 (3): 451-6. He Jun Li, Liu Jun Hong, Liu Feng, Tan Ping, Lin Tao, Li Xu Lia |
| Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. PLoS genetics 2011 Jun 7 (6): e1002105. Tomlinson Ian P M, Carvajal-Carmona Luis G, Dobbins Sara E, Tenesa Albert, Jones Angela M, Howarth Kimberley, Palles Claire, Broderick Peter, Jaeger Emma E M, Farrington Susan, Lewis Annabelle, Prendergast James G D, Pittman Alan M, Theodoratou Evropi, Olver Bianca, Walker Marion, Penegar Steven, Barclay Ella, Whiffin Nicola, Martin Lynn, Ballereau Stephane, Lloyd Amy, Gorman Maggie, Lubbe Steven, , , , Howie Bryan, Marchini Jonathan, Ruiz-Ponte Clara, Fernandez-Rozadilla Ceres, Castells Antoni, Carracedo Angel, Castellvi-Bel Sergi, Duggan David, Conti David, Cazier Jean-Baptiste, Campbell Harry, Sieber Oliver, Lipton Lara, Gibbs Peter, Martin Nicholas G, Montgomery Grant W, Young Joanne, Baird Paul N, Gallinger Steven, Newcomb Polly, Hopper John, Jenkins Mark A, Aaltonen Lauri A, Kerr David J, Cheadle Jeremy, Pharoah Paul, Casey Graham, Houlston Richard S, Dunlop Malcolm |
| Genetic variation in the transforming growth factor-ß signaling pathway and survival after diagnosis with colon and rectal cancer. Cancer 2011 Sep 117 (18): 4175-83. Slattery Martha L, Lundgreen Abbie, Herrick Jennifer S, Wolff Roger K, Caan Bette |
| Association of Caucasian-identified variants with colorectal cancer risk in Singapore Chinese. PloS one 2012 7 (8): e42407. Thean Lai Fun, Li Hui Hua, Teo Yik Ying, Koh Woon-Puay, Yuan Jian-Min, Teoh Mei Lin, Koh Poh Koon, Tang Choong Leong, Cheah Peh Ye |
| Common TGFß2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma. Molecular vision 2012 18 1526-39. Park Soo, Jamshidi Yalda, Vaideanu Daniela, Fraser Scott, Sowden Jane |
| Gene-gene interactions in APOL1-associated nephropathy. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2014 Mar 29 (3): 587-94. Divers Jasmin, Palmer Nicholette D, Lu Lingyi, Langefeld Carl D, Rocco Michael V, Hicks Pamela J, Murea Mariana, Ma Lijun, Bowden Donald W, Freedman Barry |
| Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract. Jornal de pediatria 0 90 (1): 58-64. Reis Geisilaine Soares dos, Simões E Silva Ana Cristina, Freitas Izabella Silva, Heilbuth Thiago Ramos, Marco Luiz Armando de, Oliveira Eduardo Araújo, Miranda Débora Marqu |
| Genetic risk score for nonsyndromic cleft lip with or without cleft palate for a Chilean population. Genetic counseling (Geneva, Switzerland) 2014 25 (2): 143-9. Blanco R, Colombo A, Suazo |
| Common variations in BMP4 confer genetic susceptibility to sporadic congenital heart disease in a Han Chinese population. Pediatric cardiology 2014 Dec 35 (8): 1442-7. Qian Bo, Mo Ran, Da Min, Peng Wei, Hu Yuanli, Mo Xumi |
| BMP4 and FGF3 haplotypes increase the risk of tendinopathy in volleyball athletes. Journal of science and medicine in sport / Sports Medicine Australia 2015 Mar 18 (2): 150-5. Salles José Inácio, Amaral Marcus Vinícius, Aguiar Diego Pinheiro, Lira Daisy Anne, Quinelato Valquiria, Bonato Letícia Ladeira, Duarte Maria Eugenia Leite, Vieira Alexandre Rezende, Casado Priscila Ladei |
| Genetic association analysis in a clinically and histologically confirmed otosclerosis population confirms association with the TGFB1 gene but suggests an association of the RELN gene with a clinically indistinguishable otosclerosis-like phenotype. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2014 Jul 35 (6): 1058-64. Sommen Manou, Van Camp Guy, Liktor Balázs, Csomor Péter, Fransen Erik, Sziklai István, Schrauwen Isabelle, Karosi Tam |
| A Candidate-Pathway Approach to Identify Gene-Environment Interactions: Analyses of Colon Cancer Risk and Survival. Journal of the National Cancer Institute 2015 Sep 107 (9): . Sharafeldin Noha, Slattery Martha L, Liu Qi, Franco-Villalobos Conrado, Caan Bette J, Potter John D, Yasui Yuta |
| Association of single nucleotide polymorphisms in AXIN2, BMP4, and IRF6 with Non-Syndromic Cleft Lip with or without Cleft Palate in a sample of the southeast Iranian population. Journal of applied oral science : revista FOB 0 25 (6): 650-656. Rafighdoost Houshang, Hashemi Mohammad, Danesh Hiva, Bizhani Fatemeh, Bahari Gholamreza, Taheri Mohs |
| Involvement of the bone morphogenic protein/SMAD signaling pathway in the etiology of congenital anomalies of the kidney and urinary tract accompanied by cryptorchidism. BMC urology 2017 12 17 (1): 112. Mizuno Kentaro, Nakane Akihiro, Nishio Hidenori, Moritoki Yoshinobu, Kamisawa Hideyuki, Kurokawa Satoshi, Kato Taiki, Ando Ryosuke, Maruyama Tetsuji, Yasui Takahiro, Hayashi Yuta |
| Pancreatic Pericytes Support ß-Cell Function in a Tcf7l2-Dependent Manner. Diabetes 2018 03 67 (3): 437-447. Sakhneny Lina, Rachi Eleonor, Epshtein Alona, Guez Helen C, Wald-Altman Shane, Lisnyansky Michal, Khalifa-Malka Laura, Hazan Adina, Baer Daria, Priel Avi, Weil Miguel, Landsman Lim |
| Clinical and biological significance of adamantinomatous craniopharyngioma with CTNNB1 mutation. Journal of neurosurgery 2018 Jul 1-10. Hara Takuma, Akutsu Hiroyoshi, Takano Shingo, Kino Hiroyoshi, Ishikawa Eiichi, Tanaka Shuho, Miyamoto Hidetaka, Sakamoto Noriaki, Hattori Keiichiro, Sakata-Yanagimoto Mamiko, Chiba Shigeru, Hiyama Takashi, Masumoto Tomohiko, Matsumura Aki |
| Nomograms incorporating genetic variants in BMP/Smad4/Hamp pathway to predict disease outcomes after definitive radiotherapy for non-small cell lung cancer. Cancer medicine 2018 May . Yang Ju, Xu Ting, Gomez Daniel R, Yuan Xianglin, Nguyen Quynh-Nhu, Jeter Melenda, Song Yipeng, Komaki Ritsuko, Hu Ye, Hahn Stephen M, Liao Zhongxi |
| Genetic investigation of ocular developmental genes in 52 patients with anophthalmia/microphthalmia. Ophthalmic genetics 2018 Feb 1-9. Vidya Nair Gopinathan, Rajkumar Sankaranarayanan, Vasavada Abhay |
| ECCR1 and NFKB2 Polymorphisms as Potential Biomarkers of Non-small Cell Lung Cancer in a Polish Population. Anticancer research 2019 Jun 39 (6): 3269-3272. Chaszczewska-Markowska Monika, Kosacka Monika, Chryplewicz Agnieszka, Dy?a Tomasz, Brzecka Anna, Bogunia-Kubik Katarzy |
| Common Genetic Variants on Bone Morphogenetic Protein Receptor Type IB (BMPR1B) Gene Are Predictive for Carotid Intima-Media Thickness. Circulation journal : official journal of the Japanese Circulation Society 2019 2 83 (4): 749-756. Wu Yih-Jer, Lee Yi-Nan, Wu Tzu-Wei, Chou Chao-Liang, Wang Li- |
| Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders. The Journal of clinical endocrinology and metabolism 2021 Mar . Vishnopolska Sebastian Alexis, Mercogliano Maria Florencia, Camilletti Maria Andrea, Mortensen Amanda Helen, Braslavsky Debora, Keselman Ana, Bergadá Ignacio, Olivieri Federico, Miranda Lucas, Marino Roxana, Ramírez Pablo, Pérez Garrido Natalia, Patiño Mejia Helen, Ciaccio Marta, Di Palma Maria Isabel, Belgorosky Alicia, Martí Marcelo Adrian, Kitzman Jacob Otto, Camper Sally Ann, Pérez-Millán Maria In |
Whole exome sequence analysis in 51?624 participants identifies novel genes and variants associated with refractive error and myopia.
Human molecular genetics 2022 1 31 (11): 1909-1919. Guggenheim Jeremy A, Clark Rosie, Cui Jiangtian, Terry Louise, Patasova Karina, Haarman Annechien E G, Musolf Anthony M, Verhoeven Virginie J M, Klaver Caroline C W, Bailey-Wilson Joan E, Hysi Pirro G, Williams Cathy, , |
| Investigation of the Role of BMP2 and -4 in ASD, VSD and Complex Congenital Heart Disease. Diagnostics (Basel, Switzerland) 2023 8 13 (16): . Dimitrios Bobos, Giannoula Soufla, Dimitrios C Angouras, Ioannis Lekakis, Sotirios Georgopoulos, Euthemia Melissa |
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