Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and WNT10A[original query] |
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| Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia. American journal of medical genetics. Part A 2013 Apr 161A (4): 671-8. Plaisancié Julie, Bailleul-Forestier Isabelle, Gaston Véronique, Vaysse Fréderic, Lacombe Didier, Holder-Espinasse Muriel, Abramowicz Marc, Coubes Christine, Plessis Ghislaine, Faivre Laurence, Demeer Bénédicte, Vincent-Delorme Catherine, Dollfus Hélène, Sigaudy Sabine, Guillén-Navarro Encarna, Verloes Alain, Jonveaux Philippe, Martin-Coignard Dominique, Colin Estelle, Bieth Eric, Calvas Patrick, Chassaing Nicol |
| WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness. Human molecular genetics 2015 Sep 24 (17): 5060-8. Cuellar-Partida Gabriel, Springelkamp Henriët, Lucas Sionne E M, Yazar Seyhan, Hewitt Alex W, Iglesias Adriana I, Montgomery Grant W, Martin Nicholas G, Pennell Craig E, van Leeuwen Elisabeth M, Verhoeven Virginie J M, Hofman Albert, Uitterlinden André G, Ramdas Wishal D, Wolfs Roger C W, Vingerling Johannes R, Brown Matthew A, Mills Richard A, Craig Jamie E, Klaver Caroline C W, van Duijn Cornelia M, Burdon Kathryn P, MacGregor Stuart, Mackey David |
| WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish. Human molecular genetics 2015 Sep 24 (18): 5069-78. Baranowska Körberg Izabella, Hofmeister Wolfgang, Markljung Ellen, Cao Jia, Nilsson Daniel, Ludwig Michael, Draaken Markus, Holmdahl Gundela, Barker Gillian, Reutter Heiko, Vukojevi? Vladana, Clementson Kockum Christina, Lundin Johanna, Lindstrand Anna, Nordenskjöld Agne |
| Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis. Human genetics 2018 7 137 (9): 689-703. Du Renqian, Dinckan Nuriye, Song Xiaofei, Coban-Akdemir Zeynep, Jhangiani Shalini N, Guven Yeliz, Aktoren Oya, Kayserili Hulya, Petty Lauren E, Muzny Donna M, Below Jennifer E, Boerwinkle Eric, Wu Nan, Gibbs Richard A, Posey Jennifer E, Lupski James R, Letra Ariadne, Uyguner Z O |
Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne.
Nature communications 2018 12 9 (1): 5075. Petridis Christos, Navarini Alexander A, Dand Nick, Saklatvala Jake, Baudry David, Duckworth Michael, Allen Michael H, Curtis Charles J, Lee Sang Hyuck, Burden A David, Layton Alison, Bataille Veronique, Pink Andrew E, , Carlavan Isabelle, Voegel Johannes J, Spector Timothy D, Trembath Richard C, McGrath John A, Smith Catherine H, Barker Jonathan N, Simpson Michael |
| Carrier screening in the Mexican Jewish community using a pan-ethnic expanded carrier screening NGS panel. Genetics in medicine : official journal of the American College of Medical Genetics 2021 12 24 (4): 821-830. Morgenstern-Kaplan Dan, Raijman-Policar Jaime, Majzner-Aronovich Sore, Aradhya Swaroop, Pineda-Alvarez Daniel E, Aguinaga Mónica, García-Vences Edna Eli |
| Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis. Journal of personalized medicine 2021 11 11 (11): . Chu Kuan-Yu, Wang Yin-Lin, Chou Yu-Ren, Chen Jung-Tsu, Wang Yi-Ping, Simmer James P, Hu Jan C-C, Wang Shih-K |
| High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of personalized medicine 2022 10 12 (10): . Tesolin Paola, Bertinetto Francesca Eleonora, Sonaglia Arianna, Cappellani Stefania, Concas Maria Pina, Morgan Anna, Ferrero Norma Maria, Zabotti Alen, Gasparini Paolo, Amoroso Antonio, Quartuccio Luca, Girotto Giorg |
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