Michael E. Talkowski, Ph.D.

2008 University of Pittsburgh, Pittsburgh, PA, United States 
Genetics, Epidemiology, Neuroscience Biology
"Michael Talkowski"


Sign in to add mentor
Vishwajit L. Nimgaonkar grad student 2008 University of Pittsburgh
 (The dopaminergic network and genetic susceptibility to schizophrenia.)
BETA: Related 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.

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
See more...