Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: PAXIP1[original query] |
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A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy. JAMA neurology 2015 Apr 72 (4): 414-22. Chen Jason A, Wang Qing, Davis-Turak Jeremy, Li Yun, Karydas Anna M, Hsu Sandy C, Sears Renee L, Chatzopoulou Doxa, Huang Alden Y, Wojta Kevin J, Klein Eric, Lee Jason, Beekly Duane L, Boxer Adam, Faber Kelley M, Haase Claudia M, Miller Josh, Poon Wayne W, Rosen Ami, Rosen Howard, Sapozhnikova Anna, Shapira Jill, Varpetian Arousiak, Foroud Tatiana M, Levenson Robert W, Levey Allan I, Kukull Walter A, Mendez Mario F, Ringman John, Chui Helena, Cotman Carl, DeCarli Charles, Miller Bruce L, Geschwind Daniel H, Coppola Giovan |
The impact of rare germline variants on human somatic mutation processes. Nature communications 2022 6 13 (1): 3724. Vali-Pour Mischan, Lehner Ben, Supek Fr |
CELSR1 Risk Alleles in Familial Bicuspid Aortic Valve and Hypoplastic Left Heart Syndrome. Circulation. Genomic and precision medicine 2022 2 15 (2): e003523. Theis Jeanne L, Niaz Talha, Sundsbak Rhianna S, Fogarty Zachary C, Bamlet William R, Hagler Donald J, Olson Timothy |
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores. Molecular genetics & genomic medicine 2022 12 e2109. Ishorst Nina, Henschel Leonie, Thieme Frederic, Drichel Dmitriy, Sivalingam Sugirthan, Mehrem Sarah L, Fechtner Ariane C, Fazaal Julia, Welzenbach Julia, Heimbach André, Maj Carlo, Borisov Oleg, Hausen Jonas, Raff Ruth, Hoischen Alexander, Dixon Michael, Rada-Iglesias Alvaro, Bartusel Michaela, Rojas-Martinez Augusto, Aldhorae Khalid, Braumann Bert, Kruse Teresa, Kirschneck Christian, Spanier Gerrit, Reutter Heiko, Nowak Stefanie, Gölz Lina, Knapp Michael, Buness Andreas, Krawitz Peter, Nöthen Markus M, Nothnagel Michael, Becker Tim, Ludwig Kerstin U, Mangold Elisabe |
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- Page last updated:Apr 16, 2024
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