Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 32 Records) |
| Query Trace: Disease and COL4A2[original query] |
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Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases.
Ophthalmology science 2023 5 3 (3): 100288. Tomasoni Mattia, Beyeler Michael Johannes, Vela Sofia Ortin, Mounier Ninon, Porcu Eleonora, Corre Tanguy, Krefl Daniel, Button Alexander Luke, Abouzeid Hana, Lazaros Konstantinidis, Bochud Murielle, Schlingemann Reinier, Bergin Ciara, Bergmann Sv |
| Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study. Cardiovascular diabetology 2014 13 (1): 77. Adams Jeremy N, Raffield Laura M, Freedman Barry I, Langefeld Carl D, Ng Maggie C Y, Carr J Jeffrey, Cox Amanda J, Bowden Donald |
| Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology 2015 Mar 84 (9): 918-26. Rannikmäe Kristiina, Davies Gail, Thomson Pippa A, Bevan Steve, Devan William J, Falcone Guido J, Traylor Matthew, Anderson Christopher D, Battey Thomas W K, Radmanesh Farid, Deka Ranjan, Woo Jessica G, Martin Lisa J, Jimenez-Conde Jordi, Selim Magdy, Brown Devin L, Silliman Scott L, Kidwell Chelsea S, Montaner Joan, Langefeld Carl D, Slowik Agnieszka, Hansen Björn M, Lindgren Arne G, Meschia James F, Fornage Myriam, Bis Joshua C, Debette Stéphanie, Ikram Mohammad A, Longstreth Will T, Schmidt Reinhold, Zhang Cathy R, Yang Qiong, Sharma Pankaj, Kittner Steven J, Mitchell Braxton D, Holliday Elizabeth G, Levi Christopher R, Attia John, Rothwell Peter M, Poole Deborah L, Boncoraglio Giorgio B, Psaty Bruce M, Malik Rainer, Rost Natalia, Worrall Bradford B, Dichgans Martin, Van Agtmael Tom, Woo Daniel, Markus Hugh S, Seshadri Sudha, Rosand Jonathan, Sudlow Cathie L M, , , , , |
| Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.
Neurology 2015 Dec . Traylor Matthew, Zhang Cathy R, Adib-Samii Poneh, Devan William J, Parsons Owen E, Lanfranconi Silvia, Gregory Sarah, Cloonan Lisa, Falcone Guido J, Radmanesh Farid, Fitzpatrick Kaitlin, Kanakis Allison, Barrick Thomas R, Moynihan Barry, Lewis Cathryn M, Boncoraglio Giorgio B, Lemmens Robin, Thijs Vincent, Sudlow Cathie, Wardlaw Joanna, Rothwell Peter M, Meschia James F, Worrall Bradford B, Levi Christopher, Bevan Steve, Furie Karen L, Dichgans Martin, Rosand Jonathan, Markus Hugh S, Rost Natalia, |
| 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 |
| 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 |
| Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.
Cardiovascular diabetology 2018 Apr 17 (1): 61. Charmet Romain, Duffy Seamus, Keshavarzi Sareh, Gyorgy Beata, Marre Michel, Rossing Peter, McKnight Amy Jayne, Maxwell Alexander P, Ahluwalia Tarun Veer Singh, Paterson Andrew D, Trégouët David-Alexandre, Hadjadj Sa |
| 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 |
| 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 |
| Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants.
Scientific reports 2019 Jun 9 (1): 9143. Fung Kenneth, Ramírez Julia, Warren Helen R, Aung Nay, Lee Aaron M, Tzanis Evan, Petersen Steffen E, Munroe Patricia |
| Association of COL4A2 Gene Polymorphisms with Lacunar Stroke in Xinjiang Han Populations. Journal of molecular neuroscience : MN 2019 Jun . Liang Chen, Zhang Jiyun, Liu Hai, Ma Jianhua, An Zhiwei, Xia Wen, Zhang Xiaoni |
| 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 |
| 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 |
| Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.
Arteriosclerosis, thrombosis, and vascular biology 2019 Dec 39 (12): 2542-2552. Veluchamy Abirami, Ballerini Lucia, Vitart Veronique, Schraut Katharina E, Kirin Mirna, Campbell Harry, Joshi Peter K, Relan Devanjali, Harris Sarah, Brown Ellie, Vaidya Suraj S, Dhillon Baljean, Zhou Kaixin, Pearson Ewan R, Hayward Caroline, Polasek Ozren, Deary Ian J, MacGillivray Thomas, Wilson James F, Trucco Emanuele, Palmer Colin N A, Doney Alexander S |
| 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 |
| Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke. Stroke 2020 3 51 (4): 1056-1063. Ilinca Andreea, Martinez-Majander Nicolas, Samuelsson Sofie, Piccinelli Paul, Truvé Katarina, Cole John, Kittner Steven, Soller Maria, Kristoffersson Ulf, Tatlisumak Turgut, Puschmann Andreas, Putaala Jukka, Lindgren Ar |
| 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 |
| HIF2? supports pro-metastatic behavior in pheochromocytomas/paragangliomas. Endocrine-related cancer 2020 10 27 (11): 625-640. Bechmann Nicole, Moskopp Mats Leif, Ullrich Martin, Calsina Bruna, Wallace Pål William, Richter Susan, Friedemann Markus, Langton Katharina, Fliedner Stephanie M J, Timmers Henri J L M, Nölting Svenja, Beuschlein Felix, Fassnacht Martin, Prejbisz Aleksander, Pacak Karel, Ghayee Hans K, Bornstein Stefan R, Dieterich Peter, Pietzsch Jens, Wielockx Ben, Robledo Mercedes, Qin Nan, Eisenhofer Grae |
| 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 |
| A Study of Associations Between rs9349379 (PHACTR1), rs2891168 (CDKN2B-AS), rs11838776 (COL4A2) and rs4880 (SOD2) Polymorphic Variants and Coronary Artery Disease in Iranian Population. Biochemical genetics 2021 Jun . Yari Abolfazl, Saleh-Gohari Nasrollah, Mirzaee Moghaddameh, Hashemi Fatemeh, Saeidi Kolso |
| Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
The Lancet. Neurology 2021 (5): 351-361. Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K, Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J, Griessenauer Christoph J, Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P, Lindgren Arne, Meschia James F, Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D, Kittner Steven J, Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M, Anderson Christopher D, Wardlaw Joanna, Lewis Cathryn M, Markus Hugh S, , , , |
| 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 |
| 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 |
| 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 |
| PECAM1, COL4A2, PHACTR1, and LMOD1 Gene Polymorphisms in Patients with Unstable Angina. Journal of clinical medicine 2022 Jan 11 (2): . Kosi?ski Krzysztof, Malinowski Damian, Safranow Krzysztof, Dziedziejko Violetta, Pawlik Andrz |
| 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, |
| Association of COL4A2 indel polymorphism with the development of stomach adenocarcinoma in Chinese populations. Nucleosides, nucleotides & nucleic acids 2024 9 1-12. Huihai Shi, Jialin Ma, Jing Wang, Jiale Luo, Mengyue Ji, Ting Xu, Yingxiao Shen, Chunxiao Zh |
| Identification of Genetic Loci Associated With Intracerebral Hemorrhage Using a Multitrait Analysis Approach. Neurology 2024 9 103 (8): e209666. Elena Muiño, Jara Carcel-Marquez, Laia Llucià-Carol, Cristina Gallego-Fabrega, Natalia Cullell, Miquel Lledós, Jesús M Martín-Campos, Paula Villatoro-González, Alba Sierra-Marcos, Victoria Ros-Castelló, Ana Aguilera-Simón, Joan Marti-Fabregas, Israel Fernandez-Caden |
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