Scott Smemo, Ph.D.
Affiliations: | Columbia University, New York, NY |
Area:
Retinal degeneration, Genome editing, Gene therapy, iPS cellsGoogle:
"Scott Smemo"Mean distance: 19.27 (cluster 28) | S | N | B | C | P |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Yang J, Bassuk AG, Merl-Pham J, et al. (2016) Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumors. Human Molecular Genetics |
| van den Boogaard M, Smemo S, Burnicka-Turek O, et al. (2014) A common genetic variant within SCN10A modulates cardiac SCN5A expression. The Journal of Clinical Investigation. 124: 1844-52 |
| Arnolds DE, Liu F, Fahrenbach JP, et al. (2012) TBX5 drives Scn5a expression to regulate cardiac conduction system function. The Journal of Clinical Investigation. 122: 2509-18 |
| Smemo S, Campos LC, Moskowitz IP, et al. (2012) Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease. Human Molecular Genetics. 21: 3255-63 |
| Shen T, Aneas I, Sakabe N, et al. (2011) Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function. The Journal of Clinical Investigation. 121: 4640-54 |
| Wahrle SE, Shah AR, Fagan AM, et al. (2007) Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms. Molecular Neurodegeneration. 2: 7 |
| Nowotny P, Simcock X, Bertelsen S, et al. (2007) Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 469-74 |
| Smemo S, Borevitz JO. (2007) Redundancy in genotyping arrays. Plos One. 2: e287 |
| Li Y, Grupe A, Rowland C, et al. (2006) DAPK1 variants are associated with Alzheimer's disease and allele-specific expression. Human Molecular Genetics. 15: 2560-8 |
| Grupe A, Li Y, Rowland C, et al. (2006) A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. American Journal of Human Genetics. 78: 78-88 |