Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: TTC28[original query] |
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Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts. Human genetics 2015 Nov . Conte Federica, Oti Martin, Dixon Jill, Carels Carine E L, Rubini Michele, Zhou Huiqi |
Whole genome sequencing analysis identifies recurrent structural alterations in esophageal squamous cell carcinoma. PeerJ 2020 8 e9294. Dutta Munmee, Nakagawa Hidewaki, Kato Hiroaki, Maejima Kazuhiro, Sasagawa Shota, Nakano Kaoru, Sasaki-Oku Aya, Fujimoto Akihiro, Mateos Raúl Nicolás, Patil Ashwini, Tanaka Hiroko, Miyano Satoru, Yasuda Takushi, Nakai Kenta, Fujita Masas |
ROS1 genomic rearrangements are rare actionable drivers in microsatellite stable colorectal cancer. International journal of cancer 2022 Aug . Akhoundova Dilara, Hussung Saskia, Sivakumar Smruthy, Töpfer Antonia, Rechsteiner Markus, Kahraman Abdullah, Arnold Fabian, Angst Florian, Britschgi Christian, Zoche Martin, Moch Holger, Weber Achim, Sokol Ethan, Fritsch Ralph |
Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis. International journal of molecular sciences 2022 10 23 (19): . Horjus Julia, van Mourik-Banda Tineke, Heerings Marco A P, Hakobjan Marina, De Witte Ward, Heersema Dorothea J, Jansen Anne J, Strijbis Eva M M, de Jong Brigit A, Slettenaar Astrid E J, Zeinstra Esther M P E, Hoogervorst Erwin L J, Franke Barbara, Kruijer Wiebe, Jongen Peter J, Visser Leo J, Poelmans Gee |
Heritable Risk and Protective Genetic Components of Glaucoma Medication Non-Adherence. International journal of molecular sciences 2023 3 24 (6): . Barr Julie L, Feehan Michael, Tak Casey, Owen Leah A, Finley Robert C, Cromwell Parker A, Lillvis John H, Hicks Patrice M, Au Elizabeth, Farkas Michael H, Weiner Asher, Reynolds Andrew L, Sieminski Sandra F, Sherva Richard M, Munger Mark A, Brilliant Murray H, DeAngelis Margaret |
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