Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Disease and COL3A1[original query] |
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| Genetic variability in the extracellular matrix as a determinant of cardiovascular risk: association of type III collagen COL3A1 polymorphisms with coronary artery disease. Blood 2002 Aug 100 (4): 1220-3. Muckian Clare, Fitzgerald Anthony, O'Neill Anne, O'Byrne Anna, Fitzgerald Desmond J, Shields Denis |
| Analysis of the COL3A1 gene in patients with spontaneous cervical artery dissections. Journal of neurology 2002 Jul 249 (7): 862-6. von Pein Florian, Välkkilä Merja, Schwarz Ralf, Morcher Marion, Klima Bernhard, Grau Armin, Ala-Kokko Leena, Hausser Ingrid, Brandt Tobias, Grond-Ginsbach Casp |
| Genetic analysis of polymorphisms in biologically relevant candidate genes in patients with abdominal aortic aneurysms. Journal of vascular surgery 2005 Jun 41 (6): 1036-42. Ogata Toru, Shibamura Hidenori, Tromp Gerard, Sinha Moumita, Goddard Katrina A B, Sakalihasan Natzi, Limet Raymond, MacKean Gerald L, Arthur Claudette, Sueda Taijiro, Land Susan, Kuivaniemi Hele |
| Collagen type III alpha I is a gastro-oesophageal reflux disease susceptibility gene and a male risk factor for hiatus hernia. Gut 2009 Aug 58 (8): 1063-9. Asling B, Jirholt J, Hammond P, Knutsson M, Walentinsson A, Davidson G, Agreus L, Lehmann A, Lagerström-Fermer |
| The relationship between COL3A1 exon 31 polymorphism and pelvic organ prolapse. The Journal of urology 2009 Mar 181 (3): 1213-6. Jeon Myung Jae, Chung Sue Min, Choi Jong Rak, Jung Hyun Joo, Kim Sei Kwang, Bai Sang Wo |
| Copy number variation in patients with cervical artery dissection. European journal of human genetics : EJHG 2012 Dec 20 (12): 1295-9. Grond-Ginsbach Caspar, Chen Bowang, Pjontek Rastislav, Wiest Tina, Jiang Yanxiang, Burwinkel Barbara, Tchatchou Sandrine, Krawczak Michael, Schreiber Stefan, Brandt Tobias, Kloss Manja, Arnold Marie-Luise, Hemminki Kari, Lichy Christoph, Lyrer Philippe A, Hausser Ingrid, Engelter Stefan |
| Variants of COL3A1 are associated with the risk of stroke recurrence and prognosis in the Chinese population: a prospective study. Journal of molecular neuroscience : MN 2014 Jun 53 (2): 196-203. Lv Wenfei, Lin Yahui, Song Weihua, Sun Kai, Yu Hui, Zhang Yinhui, Zhang Channa, Li Liang, Suo Miaomiao, Hui Rutai, Chen Jingzh |
| Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD). Journal of human genetics 2018 Aug . Wang Kun, Zhao Sen, Zhang Qianqian, Yuan Jian, Liu Jiaqi, Ding Xinghuan, Song Xiaofei, Lin Jiachen, Du Renqian, Zhou Yangzhong, Sugimoto Michihiko, Chen Weisheng, Yuan Bo, Liu Jian, Yan Zihui, Liu Bowen, Zhang Yisen, Li Xiaoxin, Niu Yuchen, Long Bo, Shen Yiping, Zhang Shuyang, Abe Kuniya, Su Jianzhong, Wu Zhihong, Wu Nan, Liu Pengfei, Yang Xinjian, |
| A Variant of COL3A1 (rs3134646) Is Associated With Risk of Developing Diverticulosis in White Men. Diseases of the colon and rectum 2018 Mar . Reichert Matthias Christian, Kupcinskas Juozas, Krawczyk Marcin, Jüngst Christoph, Casper Markus, Grünhage Frank, Appenrodt Beate, Zimmer Vincent, Weber Susanne Nicole, Tamelis Algimantas, Lukosiene Jaune Ieva, Pauziene Neringa, Kiudelis Gediminas, Jonaitis Laimas, Schramm Christoph, Goeser Tobias, Schulz Antje, Malinowski Maciej, Glanemann Matthias, Kupcinskas Limas, Lammert Fra |
| Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection. Circulation. Genomic and precision medicine 2019 6 12 (6): e002476. Wolford Brooke N, Hornsby Whitney E, Guo Dongchuan, Zhou Wei, Lin Maoxuan, Farhat Linda, McNamara Jennifer, Driscoll Anisa, Wu Xiaoting, Schmidt Ellen M, Norton Elizabeth L, Mathis Michael R, Ganesh Santhi K, Douville Nicholas J, Brummett Chad M, Kitzman Jacob, Chen Y Eugene, Kim Karen, Deeb G Michael, Patel Himanshu, Eagle Kim A, Milewicz Dianna M, J Willer Cristen, Yang |
| Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jan . Renner Sina, Schüler Helke, Alawi Malik, Kolbe Verena, Rybczynski Meike, Woitschach Rixa, Sheikhzadeh Sara, Stark Veronika C, Olfe Jakob, Roser Elke, Seggewies Friederike Sophia, Mahlmann Adrian, Hempel Maja, Hartmann Melanie J, Hillebrand Mathias, Wieczorek Dagmar, Volk Alexander Erich, Kloth Katja, Koch-Hogrebe Margarete, Abou Jamra Rami, Mitter Diana, Altmüller Janine, Wey-Fabrizius Alexandra, Petersen Christine, Rau Isabella, Borck Guntram, Kubisch Christian, Mir Thomas S, von Kodolitsch Yskert, Kutsche Kerstin, Rosenberger Geo |
| Epistasis of polymorphisms related to the articular cartilage extracellular matrix in knee osteoarthritis: Analysis-based multifactor dimensionality reduction. Genetics and molecular biology 2020 43 (2): e20180349. Fernández-Torres Javier, Martínez-Nava Gabriela Angélica, Zamudio-Cuevas Yessica, Lozada Carlos, Garrido-Rodríguez Daniela, Martínez-Flores Kari |
| Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups. Stroke 2020 Feb STROKEAHA119028840. Grami Nickrooz, Chong Michael, Lali Ricky, Mohammadi-Shemirani Pedrum, Henshall David E, Rannikmäe Kristiina, Paré Guillau |
| Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing. Circulation. Genomic and precision medicine 2020 10 13 (6): e003030. Carss Keren J, Baranowska Anna A, Armisen Javier, Webb Tom R, Hamby Stephen E, Premawardhana Diluka, Al-Hussaini Abtehale, Wood Alice, Wang Quanli, Deevi Sri V V, Vitsios Dimitrios, Lewis Samuel H, Kotecha Deevia, Bouatia-Naji Nabila, Hesselson Stephanie, Iismaa Siiri E, Tarr Ingrid, McGrath-Cadell Lucy, Muller David W, Dunwoodie Sally L, Fatkin Diane, Graham Robert M, Giannoulatou Eleni, Samani Nilesh J, Petrovski Slavé, Haefliger Carolina, Adlam Dav |
| 99-Case Study of Sporadic Aortic Dissection by Whole Exome Sequencing Indicated Novel Disease-Associated Genes and Variants in Chinese Population. BioMed research international 2020 2020 7857043. Wang Zanxin, Zhuang Xianmian, Chen Bailang, Wen Junmin, Peng Fang, Liu Xiling, Wei Minx |
| Mutational Profile of Malignant Pleural Mesothelioma (MPM) in the Phase II RAMES Study. Cancers 2020 10 12 (10): . Pagano Maria, Ceresoli Luca Giovanni, Zucali Paolo Andrea, Pasello Giulia, Garassino Marina, Grosso Federica, Tiseo Marcello, Soto Parra Hector, Zanelli Francesca, Cappuzzo Federico, Grossi Francesco, De Marinis Filippo, Pedrazzoli Paolo, Gnoni Roberta, Bonelli Candida, Torricelli Federica, Ciarrocchi Alessia, Normanno Nicola, Pinto Carmi |
| Genome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucoma. BMC genomics 2021 Aug 22 (1): 590. Lo Faro Valeria, Ten Brink Jacoline B, Snieder Harold, Jansonius Nomdo M, Bergen Arthur |
| Novel variants identified in a three?generation family with concomitant exotropia. Experimental and therapeutic medicine 2022 10 24 (5): 688. Li Jiaxun, Ma Yishi, Zhou Wentao, Lyu Wenchao, Wang Liming, Mao Song, Li Jin, Shi Xuefe |
| Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility. American journal of medical genetics. Part A 2022 Jan . Murad Andrea M, Hill Hannah L, Wang Yu, Ghannam Michael, Yang Min-Lee, Pugh Norma L, Asch Federico M, Hornsby Whitney, Driscoll Anisa, McNamara Jennifer, Willer Cristen J, Regalado Ellen S, , , Milewicz Dianna M, Eagle Kim A, Ganesh Santhi |
| The Associations of Single Nucleotide Polymorphisms of the COL3A1, COL6A5, and COL8A1 Genes with Atopic Dermatitis. Journal of personalized medicine 2023 4 13 (4): . Krzysztof Szalus, Weronika Zysk, Jolanta Gle?, Monika Zab?otna, Roman J Nowicki, Magdalena Trzeci |
| Re-evaluation of a Fibrillin-1 Gene Variant of Uncertain Significance Using the ClinGen Guidelines. Annals of laboratory medicine 2023 10 . Seo Wan Kim, Boyeon Kim, Yoonjung Kim, Kyung-A L |
| Association Between Cardiac Size, Systolic Function, and Complications in Vascular Ehlers-Danlos Syndrome. Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes 2024 9 8465371241278523. Aly Fawzy, William Warnica, Kate Hanneman, Rachel M Wald, Erwin Oechslin, Paaladinesh Thavendiranathan, Gauri R Kar |
| Identification of differentially expressed genes to predict the risk of heart failure in older patients with hypertrophic cardiomyopathy. Aging 2024 7 16 . Hao Dong, Chufan Yin, Dongping Xiao, Yong Ta |
| Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients. Circulation. Genomic and precision medicine 2024 4 e003978. Serwet Demirdas, Lisa M van den Bersselaar, Rosan Lechner, Jessica Bos, Suzanne I M Alsters, Marieke J H Baars, Annette F Baas, Özlem Baysal, Saskia N van der Crabben, Eelco Dulfer, Noor A A Giesbertz, Apollonia T J M Helderman-van den Enden, Yvonne Hilhorst-Hofstee, Marlies J E Kempers, Fenne L Komdeur, Bart Loeys, Daniëlle Majoor-Krakauer, Charlotte W Ockeloen, Eline Overwater, Peter J van Tintelen, Marsha Voorendt, Vivian de Waard, Alessandra Maugeri, Hennie T Brüggenwirth, Ingrid M B H van de Laar, Arjan C Houweli |
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