Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Vascular Malformations and GNAQ[original query] |
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| GNAQ Mutations in Diffuse and Solitary Choroidal Hemangiomas. Ophthalmology 2018 12 126 (5): 759-763. Francis Jasmine H, Milman Tatyana, Grossniklaus Hans, Albert Daniel, Folberg Robert, Levitin Gregory, Coupland Sarah, Catalanotti Federica, Rabady David, Kandoth Cyriac, Busam Klaus, Abramson Dav |
| Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases. Genes, chromosomes & cancer 2019 1 58 (8): 541-550. Ten Broek Roel W, Eijkelenboom Astrid, van der Vleuten Carine J M, Kamping Eveline J, Kets Marleen, Verhoeven Bas H, Grünberg Katrien, Schultze Kool Leo J, Tops Bastiaan B J, Ligtenberg Marjolijn J L, Flucke U |
| Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations. Journal of clinical medicine 2020 10 9 (11): . Paolacci Stefano, Mattassi Raul Ettore, Marceddu Giuseppe, Manara Elena, Zulian Alessandra, Guerri Giulia, De Antoni Luca, Arduino Carlo, Cavalca Daniela, Bertelli Matt |
| GNA14, GNA11, and GNAQ Mutations Are Frequent in Benign but Not Malignant Cutaneous Vascular Tumors. Frontiers in genetics 2021 5 12 663272. Jansen Philipp, Müller Hansgeorg, Lodde Georg C, Zaremba Anne, Möller Inga, Sucker Antje, Paschen Annette, Esser Stefan, Schaller Jörg, Gunzer Matthias, Standl Fabian, Bauer Sebastian, Schadendorf Dirk, Mentzel Thomas, Hadaschik Eva, Griewank Klaus |
| 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 |
| Mutational spectrum of syndromic genes in sporadic brain arteriovenous malformation. Chinese neurosurgical journal 2022 2 8 (1): 4. Wang Kun, Zhang Mingqi, Zhao Sen, Xie Zhixin, Zhang Yisen, Liu Jian, Zhang Ying, Yang Xinjian, Wu N |
| Somatic mutation spectrum of a Chinese cohort of pediatrics with vascular malformations. Orphanet journal of rare diseases 2023 9 18 (1): 261. Bin Zhang, Rui He, Zigang Xu, Yujuan Sun, Li Wei, Li Li, Yuanxiang Liu, Wu Guo, Li Song, Huijun Wang, Zhimiao Lin, Lin |
- Page last reviewed:Feb 1, 2024
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