Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and FOXC1[original query] |
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| MYOC and FOXC1 gene analysis in primary congenital glaucoma. Molecular vision 2010 16 1996-2006. Tanwar Mukesh, Kumar Manoj, Dada Tanuj, Sihota Ramanjit, Dada Ri |
Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients.
Cancer 2012 Jun 118 (11): 2828-36. Won Hong-Hee, Lee Jeeyun, Park Joon Oh, Park Young Suk, Lim Ho Yeong, Kang Won Ki, Kim Jong-Won, Lee Soo-Youn, Park Se Ho |
| Common TGFß2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma. Molecular vision 2012 18 1526-39. Park Soo, Jamshidi Yalda, Vaideanu Daniela, Fraser Scott, Sowden Jane |
| Screening of the LTBP2 gene in a north Indian population with primary congenital glaucoma. Molecular vision 2013 19 . Mohanty K, Tanwar M, Dada R, Dada T |
| BRCA2 carriers with male breast cancer show elevated tumour methylation. BMC cancer 2017 9 17 (1): 641. Deb Siddhartha, Gorringe Kylie L, Pang Jia-Min B, Byrne David J, Takano Elena A, , Dobrovic Alexander, Fox Stephen |
| Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation. Molecular medicine reports 2018 6 18 (2): 1623-1627. Syrimis Andreas, Nicolaou Nayia, Alexandrou Angelos, Papaevripidou Ioannis, Nicolaou Michael, Loukianou Eleni, Sismani Carolina, Malas Stavros, Christophidou-Anastasiadou Violetta, Tanteles George |
| Novel PITX2 Mutations including a Mutation Causing an Unusual Ophthalmic Phenotype of Axenfeld-Rieger Syndrome. Journal of ophthalmology 2019 7 2019 5642126. Huang Liqin, Meng Yong, Guo Xiangmi |
| 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 |
| Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT). Genetics in medicine : official journal of the American College of Medical Genetics 2020 6 22 (10): 1673-1681. Wu Chen-Han Wilfred, Mann Nina, Nakayama Makiko, Connaughton Dervla M, Dai Rufeng, Kolvenbach Caroline M, Kause Franziska, Ottlewski Isabel, Wang Chunyan, Klämbt Verena, Seltzsam Steve, Lai Ethan W, Selvin Aravind, Senguttuva Prabha, Bodamer Olaf, Stein Deborah R, El Desoky Sherif, Kari Jameela A, Tasic Velibor, Bauer Stuart B, Shril Shirlee, Hildebrandt Friedhe |
| Analysis of variants in Chinese individuals with primary open-angle glaucoma using molecular inversion probe (MIP)-based panel sequencing. Molecular vision 2020 26 378-391. Liu Ting, Tang Chao, Shi Xiaolo |
| Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort. Frontiers in genetics 2022 5 13 818241. Yi Tong, Sun Hairui, Fu Yuwei, Hao Xiaoyan, Sun Lin, Zhang Ye, Han Jiancheng, Gu Xiaoyan, Liu Xiaowei, Guo Yong, Wang Xin, Zhou Xiaoxue, Zhang Siyao, Yang Qi, Fan Jiaqi, He Yih |
| First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype Association. Journal of clinical medicine 2022 1 11 (1): . Stingl Julia V, Diederich Stefan, Diel Heidi, Schuster Alexander K, Wagner Felix M, Chronopoulos Panagiotis, Aghayeva Fidan, Grehn Franz, Winter Jennifer, Schweiger Susann, Hoffmann Esther |
| Molecular mechanisms of coronary artery disease risk at the PDGFD locus. bioRxiv : the preprint server for biology 2023 2 . Kim Hyun-Jung, Cheng Paul, Travisano Stanislao, Weldy Chad, Monteiro Jo O P, Kundu Ramendra, Nguyen Trieu, Sharma Disha, Shi Huitong, Lin Yi, Liu Boxiang, Haldar Saptarsi, Jackson Simon, Quertermous Thom |
| Molecular mechanisms of coronary artery disease risk at the PDGFD locus. Nature communications 2023 2 14 (1): 847. Kim Hyun-Jung, Cheng Paul, Travisano Stanislao, Weldy Chad, Monteiro João P, Kundu Ramendra, Nguyen Trieu, Sharma Disha, Shi Huitong, Lin Yi, Liu Boxiang, Haldar Saptarsi, Jackson Simon, Quertermous Thom |
| Genetic analysis using next-generation sequencing and multiplex ligation probe amplification in Chinese aniridia patients. Orphanet journal of rare diseases 2024 10 19 (1): 394. Li Wang, Qingdan Xu, Wentao Wang, Xinghuai Sun, Yuhong Ch |
- Page last reviewed:Feb 1, 2024
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