Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 54 Records) |
Query Trace: 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 |
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 |
Genetic polymorphisms in collagen-related genes are associated with pelvic organ prolapse. Menopause (New York, N.Y.) 2019 Oct . Li Lei, Sun Zhijing, Chen Juan, Zhang Ye, Shi Honghui, Zhu L |
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 |
Genomic analysis of 21 patients with corneal neuralgia after refractive surgery. Pain reports 0 5 (4): e826. Yuan Jun-Hui, Schulman Betsy R, Effraim Philip R, Sulayman Dib-Hajj, Jacobs Deborah S, Waxman Stephen |
Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesions. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2020 6 57 (5): 783-789. Maurice P, Guilbaud L, Garel J, Mine M, Dugas A, Friszer S, Maisonneuve E, Moutard M-L, Coste T, Héron D, Tournier-Lasserve E, Garel C, Jouannic J |
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 |
Replication of Top Loci From COL4A1/2 Associated With White Matter Hyperintensity Burden in Patients With Ischemic Stroke. Stroke 2020 11 51 (12): 3751-3755. Li Jiang, Abedi Vida, , Zand Ramin, Griessenauer Christoph |
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 |
Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of familial pancreatic cancer patients. Clinical genetics 2021 7 100 (5): 551-562. Tan Ming, Brusgaard Klaus, Gerdes Anne-Marie, Mortensen Michael Bau, Detlefsen Sönke, Schaffalitzky de Muckadell Ove B, Joergensen Maiken Thyreg |
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 |
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 |
KLK3 SNP-SNP interactions for prediction of prostate cancer aggressiveness. Scientific reports 2021 4 11 (1): 9264. Lin Hui-Yi, Huang Po-Yu, Cheng Chia-Ho, Tung Heng-Yuan, Fang Zhide, Berglund Anders E, Chen Ann, French-Kwawu Jennifer, Harris Darian, Pow-Sang Julio, Yamoah Kosj, Cleveland John L, Awasthi Shivanshu, Rounbehler Robert J, Gerke Travis, Dhillon Jasreman, Eeles Rosalind, Kote-Jarai Zsofia, Muir Kenneth, , Schleutker Johanna, Pashayan Nora, , Neal David E, Nielsen Sune F, Nordestgaard Børge G, Gronberg Henrik, Wiklund Fredrik, Giles Graham G, Haiman Christopher A, Travis Ruth C, Stanford Janet L, Kibel Adam S, Cybulski Cezary, Khaw Kay-Tee, Maier Christiane, Thibodeau Stephen N, Teixeira Manuel R, Cannon-Albright Lisa, Brenner Hermann, Kaneva Radka, Pandha Hardev, , Srinivasan Srilakshmi, Clements Judith, Batra Jyotsna, Park Jong |
Coexistence of RASA1 and COL4A2 variants caused pial arteriovenous fistula (AVF) in a patient with capillary malformation-arteriovenous malformation. Clinical neurology and neurosurgery 2021 4 204 106612. Kumai Tadashi, Sadato Akiyo, Kurahashi Hiroki, Kato Takema, Adachi Kazuhide, Hirose Yuic |
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, , , , |
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 |
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- |
Association of Circulating Cathepsin B Levels With Blood Pressure and Aortic Dilation. Frontiers in cardiovascular medicine 2022 4 9 762468. Chai Tianci, Tian Mengyue, Yang Xiaojie, Qiu Zhihuang, Lin Xinjian, Chen Liangw |
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 |
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 |
A novel prognostic signature based on N7-methylguanosine-related long non-coding RNAs in breast cancer. Frontiers in genetics 2022 10 13 1030275. Huang Zhidong, Lou Kaixin, Liu Ho |
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, |
Cold-induced vasodilation response in a Japanese cohort: insights from cold-water immersion and genome-wide association studies.
Journal of physiological anthropology 2023 3 42 (1): 2. Yasukochi Yoshiki, Sera Toshihiro, Kohno Taiki, Nakashima Yusuke, Uesugi Musashi, Kudo Susu |
Whole genome sequencing versus chromosomal microarray analysis in prenatal diagnosis. American journal of obstetrics and gynecology 2023 3 . Hu Ping, Zhang Qinxin, Cheng Qing, Luo Chunyu, Zhang Cuiping, Zhou Ran, Meng Lulu, Huang Mingtao, Wang Yuguo, Wang Yan, Qiao Fengchang, Xu Zhengfe |
Association of the COL4A2 Gene Polymorphisms with Primary Intracerebral Hemorrhage Risk and Outcome in Chinese Han Population. Molecular neurobiology 2024 4 . Huan Wang, Yuyi Zhu, Lukai Zheng, Mingxi Chen, Zilong Hao, Rui Guo, Ling Feng, Deren Wa |
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- Page last updated:Apr 29, 2024
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