Michael E. Talkowski, Ph.D.
Affiliations: | 2008 | University of Pittsburgh, Pittsburgh, PA, United States |
Area:
Genetics, Epidemiology, Neuroscience BiologyGoogle:
"Michael Talkowski"Parents
Sign in to add mentor| Vishwajit L. Nimgaonkar | grad student | 2008 | University of Pittsburgh | |
| (The dopaminergic network and genetic susceptibility to schizophrenia.) | ||||
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Publications
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| Macakova M, Bohuslavova B, Vochozkova P, et al. (2016) Mutated Huntingtin Causes Testicular Pathology in Transgenic Minipig Boars. Neuro-Degenerative Diseases |
| Tai DJ, Ragavendran A, Manavalan P, et al. (2016) Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR. Nature Neuroscience |
| Mukherjee K, Ishii K, Pillalamarri V, et al. (2016) Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis. Human Molecular Genetics |
| Sanders SJ, He X, Willsey AJ, et al. (2015) Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron. 87: 1215-1233 |
| Durst R, Sauls K, Peal DS, et al. (2015) Mutations in DCHS1 cause mitral valve prolapse. Nature |
| Turner TN, Sharma K, Oh EC, et al. (2015) Loss of δ-catenin function in severe autism. Nature. 520: 51-6 |
| Biagioli M, Ferrari F, Mendenhall EM, et al. (2015) Htt CAG repeat expansion confers pleiotropic gains of mutant huntingtin function in chromatin regulation. Human Molecular Genetics. 24: 2442-57 |
| Macera MJ, Sobrino A, Levy B, et al. (2015) Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing. Prenatal Diagnosis. 35: 299-301 |
| Brand H, Collins RL, Hanscom C, et al. (2015) Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation American Journal of Human Genetics. 97: 170-176 |
| Migliavacca E, Golzio C, Männik K, et al. (2015) A potential contributory role for ciliary dysfunction in the 16p11.2 600 kb BP4-BP5 pathology American Journal of Human Genetics. 96: 784-796 |