Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Hemorrhage and COL4A1[original query] |
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| COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage. Annals of neurology 2012 Apr 71 (4): 470-7. Weng Yi-Chinn, Sonni Akshata, Labelle-Dumais Cassandre, de Leau Michelle, Kauffman W Berkeley, Jeanne Marion, Biffi Alessandro, Greenberg Steven M, Rosand Jonathan, Gould Douglas |
| 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, , , , , |
| 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, |
| Genetic Variations of COL4A1 Gene and Intracerebral Hemorrhage Outcome: A Cohort Study in a Chinese Han Population. World neurosurgery 2018 Feb . Xia Chao, Lin Sen, Yang Jie, He Sha, Li Hao, Liu Ming, You Ch |
| Genetic Variations of the COL4A1 Gene and Intracerebral Hemorrhage Risk: A Case-Control Study in a Chinese Han Population. World neurosurgery 2018 Jan . Lin Sen, Xia Chao, He Sha, Yang Jie, Li Hao, Zheng Jun, Liu Ming, You Ch |
| Rare Missense Functional Variants at COL4A1 and COL4A2 in Sporadic Intracerebral Hemorrhage. Neurology 2021 5 97 (3): e236-47. Chung Jaeyoon, Hamilton Graham, Kim Minsup, Marini Sandro, Montgomery Bailey, Henry Jonathan, Cho Art E, Brown Devin L, Worrall Bradford B, Meschia James F, Silliman Scott L, Selim Magdy, Tirschwell David L, Kidwell Chelsea S, Kissela Brett, Greenberg Steven M, Viswanathan Anand, Goldstein Joshua N, Langefeld Carl D, Rannikmae Kristiina, Sudlow Catherine Lm, Samarasekera Neshika, Rodrigues Mark, Al-Shahi Salman Rustam, Prendergast James G D, Harris Sarah E, Deary Ian, Woo Daniel, Rosand Jonathan, Van Agtmael Tom, Anderson Christopher |
| Monogenic Causes of Apparently Idiopathic Perinatal Intracranial Hemorrhage. Annals of neurology 2021 2 89 (4): 813-822. Hausman-Kedem Moran, Malinger Gustavo, Modai Shira, Kushner Steven A, Shiran Shelly I, Ben-Sira Liat, Roth Jonathan, Constantini Shlomi, Fattal-Valevski Aviva, Ben-Shachar Sh |
| 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 |
| Rare and Common Variants in COL4A1 in Chinese Patients With Intracerebral Hemorrhage. Frontiers in neurology 2022 6 13 827165. Liu Xiaolu, Yang Qiong, Tang Lu, He Ji, Tian Danyang, Wang Baojun, Xie Lihong, Li Changbao, Fan Dongshe |
| COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage. Prenatal diagnosis 2022 2 42 (5): 601-610. Coste Thibault, Vincent-Delorme Catherine, Stichelbout Morgane, Devisme Louise, Gelot Antoinette, Deryabin Igor, Pelluard Fanny, Aloui Chaker, Leutenegger Anne-Louise, Jouannic Jean-Marie, Héron Delphine, Gould Douglas B, Tournier-Lasserve Elisabe |
| Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity. Prenatal diagnosis 2025 1 . Thibault Coste, Chaker Aloui, Justine Chanclud, Eléonore Blondiaux, Jelena Martinovic, Tania Attie-Bitach, Florence Petit, Delphine Héron, Alexandre G de Brevern, Ragousandirane Radjasandirane, Michaelle Corpechot, Hélène Morel, Rachel Petermann, Anne-Louise Leutenegger, Elisabeth Tournier-Lasser |
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