Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and TEK[original query] |
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| Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations. Nature genetics 2009 Jan 41 (1): 118-24. Limaye Nisha, Wouters Vinciane, Uebelhoer Melanie, Tuominen Marjut, Wirkkala Riikka, Mulliken John B, Eklund Lauri, Boon Laurence M, Vikkula Miik |
| Somatic mutations in exon 17 of the TEK gene in vascular tumors and vascular malformations. Journal of vascular surgery 2011 Dec 54 (6): 1760-8. Ye Caisheng, Pan Lingxiao, Huang Yongbo, Ye Runyi, Han Anjia, Li Songqi, Li Xiaoxi, Wang Shenmi |
| Hidden risk genes with high-order intragenic epistasis in Alzheimer's disease. Journal of Alzheimer's disease : JAD 2014 41 (4): 1039-56. Sun Jiya, Song Fuhai, Wang Jiajia, Han Guangchun, Bai Zhouxian, Xie Bin, Feng Xuemei, Jia Jianping, Duan Yong, Lei Hongxi |
| Do associated auto-antibodies influence the outcome of myasthenia gravis after thymectomy? Autoimmunity 2015 Jul 1-4. Keijzers Marlies, Damoiseaux Jan, Vigneron Alain, Bodart Nicolas, Kessels Alfons, Dingemans Anne-Marie C, Hochstenbag Monique, Maessen Jos, De Baets Ma |
| Variation in the TEK gene is not associated with asthma but with allergic conjunctivitis. International journal of immunogenetics 2018 Apr . Fodor L E, Gézsi A, Gál Z, Nagy A, Kiss A, Bikov A, Szalai |
| Congenital glaucoma and CYP1B1: an old story revisited. Human genetics 2018 3 138 (8-9): 1043-1049. Alsaif Hessa S, Khan Arif O, Patel Nisha, Alkuraya Hisham, Hashem Mais, Abdulwahab Firdous, Ibrahim Niema, Aldahmesh Mohammed A, Alkuraya Fowzan |
| Identification of TIE2 as a susceptibility gene for neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. The British journal of ophthalmology 2020 Mar . Chen Zhen Ji, Ma Li, Brelen Marten E, Chen Haoyu, Tsujikawa Motokazu, Lai Timothy Y, Ho Mary, Sayanagi Kaori, Hara Chikako, Hashida Noriyasu, Tam Pancy Os, Young Alvin L, Nishida Kohji, Tham Clement C, Pang Chi Pui, Chen Li J |
| Bockenheimer disease is associated with a TEK variant. Cold Spring Harbor molecular case studies 2021 10 7 (6): . Sudduth Christopher L, Konczyk Dennis J, Smits Patrick J, Eng Whitney, Al-Ibraheemi Alyaa, Upton Joseph, Greene Arin |
| Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants. Journal of medical genetics 2022 3 60 (2): 163-173. Mussa Alessandro, Leoni Chiara, Iacoviello Matteo, Carli Diana, Ranieri Carlotta, Pantaleo Antonino, Buonuomo Paola Sabrina, Bagnulo Rosanna, Ferrero Giovanni Battista, Bartuli Andrea, Melis Daniela, Maitz Silvia, Loconte Daria Carmela, Turchiano Antonella, Piglionica Marilidia, De Luisi Annunziata, Susca Francesco Claudio, Bukvic Nenad, Forleo Cinzia, Selicorni Angelo, Zampino Giuseppe, Onesimo Roberta, Cappuccio Gerarda, Garavelli Livia, Novelli Chiara, Memo Luigi, Morando Carla, Della Monica Matteo, Accadia Maria, Capurso Martina, Piscopo Carmelo, Cereda Anna, Di Giacomo Marilena Carmela, Saletti Veronica, Spinelli Alessandro Mauro, Lastella Patrizia, Tenconi Romano, Dvorakova Veronika, Irvine Alan D, Resta Nicolet |
| Exome-based mutation screening in South African children with primary congenital glaucoma. Eye (London, England) 2022 Jan . Carstens Nadia, Goolam Saadiah, Hulley Michaella, Brandenburg Jean-Tristan, Ramsay Michele, Williams Susan Eileen Isabel |
| 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 |
| Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases. Scientific reports 2023 10 13 (1): 16769. Ishani Mhatre, Habiba Abdelhalim, William Degroat, Shreya Ashok, Bruce T Liang, Zeeshan Ahm |
| Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis. Hemoglobin 2024 4 48 (2): 101-112. Aradhana Kumari, Ganesh Chauhan, Partha Kumar Chaudhuri, Sushma Kumari, Anupa Pras |
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