Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and MSX1[original query] |
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| Evaluation of two putative susceptibility loci for oral clefts in the Danish population. American journal of epidemiology 2001 May 153 (10): 1007-15. Mitchell L E, Murray J C, O'Brien S, Christensen |
| Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate. Human genetics 2002 1 110 (1): 15-20. Scapoli Luca, Martinelli Marcella, Pezzetti Furio, Carinci Francesco, Bodo Maria, Tognon Mauro, Carinci Pao |
| MSX1 polymorphism associated with risk of oral cleft in Korea: evidence from case-parent trio and case-control studies. Yonsei medical journal 2007 Feb 48 (1): 101-8. Park Jungyong, Park Beyoung Yun, Kim Hyon-Suk, Lee Jong Eun, Suh Il, Nam Chung Mo, Kang Dae Ryong, Kim Suk, Yun Ji Eun, Go Eun Na, Jee Sun Ha, Beaty Terri |
| [Transmission disequilibrium test for nonsyndromic cleft lip and palate and segment homeobox gene-1 gene]. Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology 2007 Sep 42 (9): 561-3. Wu Ping-An, Li Yun-Liang, Wu Han-Jiang, Wang Kai, Fan Guo-Zhe |
| Examination of the MSX1 gene in patients with Parkinson's disease. Acta neurologica Scandinavica 2009 Dec 120 (6): 442-4. Deng H, Zhu S H, Le W D, Yang H R, Lv H W, Xu H B, Xie W J, Jankovic |
| The c.469+46_56del mutation in the homeobox MSX1 gene--a novel risk factor in breast cancer? Cancer epidemiology 2010 Oct 34 (5): 652-5. Sliwinski Tomasz, Synowiec Ewelina, Czarny Piotr, Gomulak Paulina, Forma Ewa, Morawiec Zbigniew, Morawiec Jan, Dziki Lukasz, Wasylecka Maja, Blasiak Janu |
| Association of MSX1 799 G>T variant with nonsyndromic cleft lip/palate in South Indian adolescent patients. International journal of paediatric dentistry / the British Paedodontic Society [and] the International Association of Dentistry for Children 2012 May 22 (3): 228-31. Singh Varun P, Ramu Dine |
| Association between CDH1 and MSX1 gene polymorphisms and the risk of nonsyndromic cleft lip and/or cleft palate in a southeast Iranian population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2013 Sep 50 (5): e98-e104. Rafighdoost Hooshang, Hashemi Mohammad, Narouei Abdolreza, Eskanadri-Nasab Ebrahim, Dashti-Khadivaki Gholamali, Taheri Mohs |
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Nature genetics 2013 Jul 45 (7): 822-4. Cordell Heather J, Bentham Jamie, Topf Ana, Zelenika Diana, Heath Simon, Mamasoula Chrysovalanto, Cosgrove Catherine, Blue Gillian, Granados-Riveron Javier, Setchfield Kerry, Thornborough Chris, Breckpot Jeroen, Soemedi Rachel, Martin Ruairidh, Rahman Thahira J, Hall Darroch, van Engelen Klaartje, Moorman Antoon F M, Zwinderman Aelko H, Barnett Phil, Koopmann Tamara T, Adriaens Michiel E, Varro Andras, George Alfred L, dos Remedios Christobal, Bishopric Nanette H, Bezzina Connie R, O'Sullivan John, Gewillig Marc, Bu'Lock Frances A, Winlaw David, Bhattacharya Shoumo, Devriendt Koen, Brook J David, Mulder Barbara J M, Mital Seema, Postma Alex V, Lathrop G Mark, Farrall Martin, Goodship Judith A, Keavney Bernard |
| Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population. Medicina oral, patología oral y cirugía bucal 2013 May 18 (3): e414-20. Paranaíba Lívia-Máris-Ribeiro, de Aquino Sibele-Nascimento, Bufalino Andreia, Martelli-Júnior Hercílio, Graner Edgard, Brito Luciano-Abreu, e Passos-Bueno Maria-Rita dos Santos, Coletta Ricardo-D, Swerts Mário-Sérgio-Olivei |
| 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 |
| Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations. Journal of dental research 2016 Jul . Gowans L J J, Adeyemo W L, Eshete M, Mossey P A, Busch T, Aregbesola B, Donkor P, Arthur F K N, Bello S A, Martinez A, Li M, Augustine-Akpan E A, Deressa W, Twumasi P, Olutayo J, Deribew M, Agbenorku P, Oti A A, Braimah R, Plange-Rhule G, Gesses M, Obiri-Yeboah S, Oseni G O, Olaitan P B, Abdur-Rahman L, Abate F, Hailu T, Gravem P, Ogunlewe M O, Buxó C J, Marazita M L, Adeyemo A A, Murray J C, Butali |
| Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis. European journal of medical genetics 2016 Jun 59 (8): 377-385. Shahid Mohammad, Balto Hanan A, Al-Hammad Nouf, Joshi S, Khalil Hesham Saleh, Somily Ali Mohammed, Sinjilawi Nasr Abdul-Aziz, Al-Ghamdi Sameer, Faiyaz-Ul-Haque Muhammad, Dhillon Varinderpal |
| MSH homeobox 1 polymorphisms and the risk of non-syndromic orofacial clefts: a meta-analysis. European journal of oral sciences 2018 Apr . Gu Min, Zhang Yan, Liu Hualian, Liu Jue, Zhu Danxia, Yang |
| Association between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank. Scientific reports 2019 Nov 9 (1): 16515. Córdova-Palomera Aldo, Priest James |
| Congenital heart disease risk loci identified by genome-wide association study in European patients.
The Journal of clinical investigation 2020 Nov . Lahm Harald, Jia Meiwen, Dreßen Martina, Wirth Felix, Puluca Nazan, Gilsbach Ralf, Keavney Bernard D, Cleuziou Julie, Beck Nicole, Bondareva Olga, Dzilic Elda, Burri Melchior, König Karl C, Ziegelmüller Johannes A, Abou-Ajram Claudia, Neb Irina, Zhang Zhong, Doppler Stefanie A, Mastantuono Elisa, Lichtner Peter, Eckstein Gertrud, Hörer Jürgen, Ewert Peter, Priest James R, Hein Lutz, Lange Rüdiger, Meitinger Thomas, Cordell Heather J, Müller-Myhsok Bertram, Krane Mark |
| Unraveling the genomic basis of congenital heart disease. The Journal of clinical investigation 2021 Jan 131 (2): . Darbar Dawo |
| A single-nucleotide-polymorphism in the 5'-flanking region of MSX1 gene as a predictive marker candidate for platinum-based therapy of esophageal carcinoma. Therapeutic advances in medical oncology 2022 3 14 17588359221080580. Mori Takahiro, Ueno Kazuko, Tokunaga Katsushi, Kawai Yosuke, Matsuda Koichi, Nishida Nao, Komine Keigo, Saito Sakae, Nagasaki Masao, |
| Identification of tumour antigens and immune subtypes in the development of an anti-cancer vaccine for endometrial carcinoma. Scandinavian journal of immunology 2022 12 97 (3): e13250. Feng Jianyang, He Ho |
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