Michael Edward Talkowski, Ph.D.
This page shows the publications co-authored by Michael Talkowski and Rachita Yadav.
New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders. Curr Opin Genet Dev. 2020 12; 65:195-206.
Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly. Cell. 2018 02 22; 172(5):897-909.e21.
Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin. Am J Hum Genet. 2021 11 04; 108(11):2145-2158.
Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem Cells. Endocrinology. 2021 09 01; 162(9).
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nat Genet. 2018 04 26; 50(5):727-736.
Ectopic expression of RAD52 and dn53BP1 improves homology-directed repair during CRISPR-Cas9 genome editing. Nat Biomed Eng. 2017 11; 1(11):878-888.
The connection strength for co-authors is the sum of the scores for each of their shared publications.
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