Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 38 Records) |
| Query Trace: Disease and COL4A1[original query] |
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| Integrative analysis of genome-wide association studies and gene expression profiles identified candidate genes for osteoporosis in Kashin-Beck disease patients. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2015 Oct . Wen Y, Guo X, Hao J, Xiao X, Wang W, Wu C, Wang S, Yang T, Shen H, Chen X, Tan L, Tian Q, Deng H-W, Zhang |
| Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction. PLoS genetics 2016 Jul 12 (7): e1006127. Yang Wei, Ng Fu Liang, Chan Kenneth, Pu Xiangyuan, Poston Robin N, Ren Meixia, An Weiwei, Zhang Ruoxin, Wu Jingchun, Yan Shunying, Situ Haiteng, He Xinjie, Chen Yequn, Tan Xuerui, Xiao Qingzhong, Tucker Arthur T, Caulfield Mark J, Ye S |
| Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi Consortium. PloS one 2016 11 (3): e0138014. Assimes Themistocles L, Lee I-T, Juang Jyh-Ming, Guo Xiuqing, Wang Tzung-Dau, Kim Eric T, Lee Wen-Jane, Absher Devin, Chiu Yen-Feng, Hsu Chih-Cheng, Chuang Lee-Ming, Quertermous Thomas, Hsiung Chao A, Rotter Jerome I, Sheu Wayne H-H, Chen Yii-Der Ida, Taylor Kent |
| Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathy. Annals of neurology 2016 Sep . Verdura Edgard, Hervé Dominique, Bergametti Françoise, Jacquet Clémence, Morvan Typhaine, Prieto-Morin Carol, Mackowiak Alexandre, Manchon Eric, Hosseini Hassan, Cordonnier Charlotte, Girard-Buttaz Isabelle, Rosenstingl Sophie, Hagel Christian, Kuhlenbaümer Gregor, Leca-Radu Elena, Goux Didier, Fleming Lauren, Van Agtmael Tom, Chabriat Hugues, Chapon Françoise, Tournier-Lasserve Elisabe |
| Common genetic variants and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA). Atherosclerosis 2015 Dec 245 230-236. Vargas Jose D, Manichaikul Ani, Wang Xin-Qun, Rich Stephen S, Rotter Jerome I, Post Wendy S, Polak Joseph F, Budoff Matthew J, Bluemke David |
| COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls. Neurology 2017 Sep . Rannikmäe Kristiina, Sivakumaran Vhinoth, Millar Henry, Malik Rainer, Anderson Christopher D, Chong Mike, Dave Tushar, Falcone Guido J, Fernandez-Cadenas Israel, Jimenez-Conde Jordi, Lindgren Arne, Montaner Joan, O'Donnell Martin, Paré Guillaume, Radmanesh Farid, Rost Natalia S, Slowik Agnieszka, Söderholm Martin, Traylor Matthew, Pulit Sara L, Seshadri Sudha, Worrall Brad B, Woo Daniel, Markus Hugh S, Mitchell Braxton D, Dichgans Martin, Rosand Jonathan, Sudlow Cathie L M, |
| Influence of coronary artery disease and subclinical atherosclerosis related polymorphisms on the risk of atherosclerosis in rheumatoid arthritis. Scientific reports 2017 Jan 7 40303. López-Mejías Raquel, Corrales Alfonso, Vicente Esther, Robustillo-Villarino Montserrat, González-Juanatey Carlos, Llorca Javier, Genre Fernanda, Remuzgo-Martínez Sara, Dierssen-Sotos Trinidad, Miranda-Filloy José A, Huaranga Marco A Ramírez, Pina Trinitario, Blanco Ricardo, Alegre-Sancho Juan J, Raya Enrique, Mijares Verónica, Ubilla Begoña, Ferraz-Amaro Iván, Gómez-Vaquero Carmen, Balsa Alejandro, López-Longo Francisco J, Carreira Patricia, González-Álvaro Isidoro, Ocejo-Vinyals J Gonzalo, Rodríguez-Rodríguez Luis, Fernández-Gutiérrez Benjamín, Castañeda Santos, Martín Javier, González-Gay Miguel |
Association of modifiers and other genetic factors explain Marfan syndrome clinical variability.
European journal of human genetics : EJHG 2018 12 26 (12): 1759-1772. Aubart Melodie, Gazal Steven, Arnaud Pauline, Benarroch Louise, Gross Marie-Sylvie, Buratti Julien, Boland Anne, Meyer Vincent, Zouali Habib, Hanna Nadine, Milleron Olivier, Stheneur Chantal, Bourgeron Thomas, Desguerre Isabelle, Jacob Marie-Paule, Gouya Laurent, Génin Emmanuelle, Deleuze Jean-François, Jondeau Guillaume, Boileau Catheri |
| A role for collagen type IV in cardiovascular disease? American journal of physiology. Heart and circulatory physiology 2018 Sep 315 (3): H610-H625. Steffensen L B, Rasmussen L |
| Association of COL4A1 (rs605143, rs565470) and CD14 (rs2569190) genes polymorphism with coronary artery disease. Molecular and cellular biochemistry 2018 Jan . Raza Syed Tasleem, Abbas Shania, Eba Ale, Karim Fazal, Wani Irshad Ahmad, Rizvi Saliha, Zaidi Alina, Mahdi Farza |
| Genome-wide association study of cerebral small vessel disease reveals established and novel loci.
Brain : a journal of neurology 2019 Oct 142 (10): 3176-3189. Chung Jaeyoon, Marini Sandro, Pera Joanna, Norrving Bo, Jimenez-Conde Jordi, Roquer Jaume, Fernandez-Cadenas Israel, Tirschwell David L, Selim Magdy, Brown Devin L, Silliman Scott L, Worrall Bradford B, Meschia James F, Demel Stacie, Greenberg Steven M, Slowik Agnieszka, Lindgren Arne, Schmidt Reinhold, Traylor Matthew, Sargurupremraj Muralidharan, Tiedt Steffen, Malik Rainer, Debette Stéphanie, Dichgans Martin, Langefeld Carl D, Woo Daniel, Rosand Jonathan, Anderson Christopher |
| COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans. Human genetics 2019 6 138 (10): 1105-1115. Kitzler Thomas M, Schneider Ronen, Kohl Stefan, Kolvenbach Caroline M, Connaughton Dervla M, Dai Rufeng, Mann Nina, Nakayama Makiko, Majmundar Amar J, Wu Chen-Han W, Kari Jameela A, El Desoky Sherif M, Senguttuvan Prabha, Bogdanovic Radovan, Stajic Natasa, Valivullah Zaheer, Lek Monkol, Mane Shrikant, Lifton Richard P, Tasic Velibor, Shril Shirlee, Hildebrandt Friedhe |
| Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects. Brain : a journal of neurology 2019 3 142 (4): 1009-1023. Mishra Aniket, Chauhan Ganesh, Violleau Marie-Helene, Vojinovic Dina, Jian Xueqiu, Bis Joshua C, Li Shuo, Saba Yasaman, Grenier-Boley Benjamin, Yang Qiong, Bartz Traci M, Hofer Edith, Soumaré Aïcha, Peng Fen, Duperron Marie-Gabrielle, Foglio Mario, Mosley Thomas H, Schmidt Reinhold, Psaty Bruce M, Launer Lenore J, Boerwinkle Eric, Zhu Yicheng, Mazoyer Bernard, Lathrop Mark, Bellenguez Celine, Van Duijn Cornelia M, Ikram M Arfan, Schmidt Helena, Longstreth W T, Fornage Myriam, Seshadri Sudha, Joutel Anne, Tzourio Christophe, Debette Stephan |
| Targeted resequencing identifies genes with recurrent variation in cerebral palsy. NPJ genomic medicine 2019 4 27. van Eyk C L, Corbett M A, Frank M S B, Webber D L, Newman M, Berry J G, Harper K, Haines B P, McMichael G, Woenig J A, MacLennan A H, Gecz |
| How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study. Neurology 2019 11 93 (22): e2007-e2020. Tan Rhea Y Y, Traylor Matthew, Megy Karyn, Duarte Daniel, Deevi Sri V V, Shamardina Olga, Mapeta Rutendo P, , Ouwehand Willem H, Gräf Stefan, Downes Kate, Markus Hugh |
| A Novel COL4A2 Mutation Associated with Recurrent Strokes. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2020 9 29 (10): 105156. McHugh Daryl C, Esenwa Charl |
| 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 |
| The role of vascular dementia associated genes in patients with Alzheimer's disease: A large case-control study in the Chinese population. CNS neuroscience & therapeutics 2021 Sep . Xiao Xuewen, Guo Lina, Liao Xinxin, Zhou Yafang, Zhang Weiwei, Zhou Lu, Wang Xin, Liu Xixi, Liu Hui, Xu Tianyan, Zhu Yuan, Yang Qijie, Hao Xiaoli, Liu Yingzi, Wang Junling, Li Jinchen, Jiao Bin, Shen |
| Are COL4A1 and COL4A2 gene polymorphisms associated with cerebral palsy? Turkish journal of physical medicine and rehabilitation 2021 Jun 67 (2): 242-249. Güvener Orhan, Sezgin Melek, Tezol Özlem, Barlas ?brahim Ömer, Özdemir Asena Ayça, Kan?k Emine Ar |
| Genome-wide identification of Chiari malformation type I associated candidate genes and chromosomal variations. Turkish journal of biology = Turk biyoloji dergisi 2020 44 (6): 449-456. Av?ar Timuçin, Çali? ?eyma, Yilmaz Baran, Dem?rc? Otluo?lu Gülden, Holyavk?n Can, KiliÇ Türk |
| Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2022 Aug . Coste T, Aloui C, Petit F, Moutton S, Devisme L, Wells C F, Leboucq N, Verpillat P, Yvert M, Rivier F, Tournier-Lasserve |
| Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants. Neurology. Genetics 2022 8 8 (5): e200015. Ferguson Amy Christina, Thrippleton Sophie, Henshall David, Whittaker Ed, Conway Bryan, MacLeod Malcolm, Malik Rainer, Rawlik Konrad, Tenesa Albert, Sudlow Cathie, Rannikmae Kristii |
| A Genome-Wide Association Study on Abdominal Adiposity-Related Traits in Adult Korean Men. Obesity facts 2022 4 15 (4): 590-599. Kim Hyun-Jin, Son Ho-Young, Sung Joohon, Yun Jae Moon, Kwon Hyuktae, Cho Belong, Kim Jong-Il, Park Jin- |
| Genetic Study of Cerebral Small Vessel Disease in Chinese Han Population. Frontiers in neurology 2022 4 13 829438. Wang Yunchao, Shi Changhe, Li Yusheng, Yu Wenkai, Wei Sen, Fan Yu, Mao Chengyuan, Yang Zhihua, Yu Lulu, Zhao Zichen, Li Shanshan, Gao Yuan, Xu Yumi |
| Genetic analysis reveals novel variants for vascular cognitive impairment. Acta neurologica Scandinavica 2022 3 146 (1): 42-50. Mönkäre Saana, Kuuluvainen Liina, Schleutker Johanna, Bras Jose, Roine Susanna, Pöyhönen Minna, Guerreiro Rita, Myllykangas Lii |
| The genetic and phenotypic spectra of adult genetic leukoencephalopathies in a cohort of 309 patients. Brain : a journal of neurology 2022 11 . Wu Chujun, Wang Mengwen, Wang Xingao, Li Wei, Li Shaowu, Chen Bin, Niu Songtao, Tai Hongfei, Pan Hua, Zhang Zaiqia |
| High frequency of HTRA1 AND ABCC6 mutations in Japanese patients with adult-onset cerebral small vessel disease. Journal of neurology, neurosurgery, and psychiatry 2022 10 94 (1): 74-81. Uemura Masahiro, Hatano Yuya, Nozaki Hiroaki, Ando Shoichiro, Kondo Hajime, Hanazono Akira, Iwanaga Akira, Murota Hiroyuki, Osakada Yosuke, Osaki Masato, Kanazawa Masato, Kanai Mitsuyasu, Shibata Yoko, Saika Reiko, Miyatake Tadashi, Aizawa Hitoshi, Ikeuchi Takeshi, Tomimoto Hidekazu, Mizuta Ikuko, Mizuno Toshiki, Ishihara Tomohiko, Onodera Osa |
| Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis. American journal of medical genetics. Part A 2022 Sep . Kumar Runjun D, Meng Linyan, Liu Pengfei, Miyake Christina Y, Worley Kim C, Bi Weimin, Lalani Seema |
| Genotypic Analysis of COL4A1 Gene in Diabetic Nephropathy and Type 2 Diabetes Mellitus Patients: A Comparative Genetic Study. DNA and cell biology 2023 8 . Neha Shukla, Shivani Kumari, Poornima Verma, Atar Singh Kushwah, Monisha Banarjee, S N Sankhwar, Aneesh Srivastava, M S Ansari, Naveen Kumar Gaut |
| Rare neurovascular genetic and imaging markers across neurodegenerative diseases. Alzheimer's & dementia : the journal of the Alzheimer's Association 2023 6 . Allison A Dilliott, Stephanie A Berberian, Kelly M Sunderland, Malcolm A Binns, Julia Zimmer, Miracle Ozzoude, Christopher J M Scott, Fuqiang Gao, Anthony E Lang, David P Breen, Maria C Tartaglia, Brian Tan, Richard H Swartz, Ekaterina Rogaeva, Michael Borrie, Elizabeth Finger, Corinne E Fischer, Andrew Frank, Morris Freedman, Sanjeev Kumar, Stephen Pasternak, Bruce G Pollock, Tarek K Rajji, David F Tang-Wai, Agessandro Abrahao, John Turnbull, Lorne Zinman, Leanne Casaubon, Dar Dowlatshahi, Ayman Hassan, Jennifer Mandzia, Demetrios Sahlas, Gustavo Saposnik, David Grimes, Connie Marras, Thomas Steeves, Mario Masellis, Sali M K Farhan, Robert Bartha, Sean Symons, Robert A Hegele, Sandra E Black, Joel Ramirez, |
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