Ohcanbohtosat - Talkowski, Michael E

Dopamine Genes and Schizophrenia: Case Closed or Evidence Pending? Dahkki Talkowski, Michael E., Bamne, Mikhil, Mansour, Hader, Nimgaonkar, Vishwajit L.

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Can RGS4 Polymorphisms Be Viewed as Credible Risk Factors for Schizophrenia? A Critical Review of the Evidence Dahkki Talkowski, Michael E, Chowdari, KV, Lewis, David A, Nimgaonkar, Vishwajit L

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Mechanisms for Structural Variation in the Human Genome Dahkki Currall, Benjamin B., Chiang, C., Talkowski, Michael E., Morton, Cynthia C.

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Indexcov: fast coverage quality control for whole-genome sequencing Dahkki Pedersen, Brent S, Collins, Ryan L, Talkowski, Michael E, Quinlan, Aaron R

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Functional Analysis of Upstream Common Polymorphisms of the Dopamine Transporter Gene Dahkki Bamne, Mikhil N., Talkowski, Michael E., Chowdari, Kodavali V., Nimgaonkar, Vishwajit L.

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Role of the Chromosome Architectural Factor SMCHD1 in X-Chromosome Inactivation, Gene Regulation, and Disease in Humans Dahkki Wang, Chen-Yu, Brand, Harrison, Shaw, Natalie D., Talkowski, Michael E., Lee, Jeannie T.

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Low incidence of off-target mutations in individual CRISPR-Cas9 and TALEN targeted human stem cell clones detected by whole-genome sequencing Dahkki Veres, Adrian, Gosis, Bridget S., Ding, Qiurong, Collins, Ryan, Ragavendran, Ashok, Brand, Harrison, Erdin, Serkan, Talkowski, Michael E., Musunuru, Kiran

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Linkage Disequilibrium Patterns and Functional Analysis of RGS4 Polymorphisms in Relation to Schizophrenia Dahkki Chowdari, Kodavali V., Bamne, Mikhil, Wood, Joel, Talkowski, Michael E., Mirnics, Karoly, Levitt, Pat, Lewis, David A., Nimgaonkar, Vishwajit L.

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Systematic Association Studies of Mitochondrial DNA Variations in Schizophrenia: Focus on the ND5 Gene Dahkki Bamne, Mikhil N., Talkowski, Michael E., Moraes, Carlos T., Manuck, Stephen B., Ferrell, Robert E., Chowdari, Kodavali V., Nimgaonkar, Vishwajit L.

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Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder Dahkki Bahl, Samira, Chiang, Colby, Beauchamp, Roberta L, Neale, Benjamin M, Daly, Mark J, Gusella, James F, Talkowski, Michael E, Ramesh, Vijaya

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Developmental Variability in Autism Across 17 000 Autistic Individuals and 4000 Siblings Without an Autism Diagnosis: Comparisons by Cohort, Intellectual Disability, Genetic Etiolo... Dahkki Kuo, Susan S., van der Merwe, Celia, Fu, Jack M., Carey, Caitlin E., Talkowski, Michael E., Bishop, Somer L., Robinson, Elise B.

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RGS4 Polymorphisms Associated With Variability of Cognitive Performance in a Family-Based Schizophrenia Sample Dahkki Prasad, Konasale M., Almasy, Laura, Gur, Ruben C., Gur, Raquel E., Pogue-Geile, Michael, Chowdari, Kodavali V., Talkowski, Michael E., Nimgaonkar, Vishwajit L.

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An eMERGE Clinical Center at Partners Personalized Medicine Dahkki Smoller, Jordan W., Karlson, Elizabeth W., Green, Robert C., Kathiresan, Sekar, MacArthur, Daniel G., Talkowski, Michael E., Murphy, Shawn N., Weiss, Scott T.

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Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin Dahkki Zepeda-Mendoza, Cinthya J., Bardon, Alexandra, Kammin, Tammy, Harris, David J., Cox, Helen, Redin, Claire, Ordulu, Zehra, Talkowski, Michael E., Morton, Cynthia C.

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Describing Sequencing Results of Structural Chromosome Rearrangements with a Suggested Next-Generation Cytogenetic Nomenclature Dahkki Ordulu, Zehra, Wong, Kristen E., Currall, Benjamin B., Ivanov, Andrew R., Pereira, Shahrin, Althari, Sara, Gusella, James F., Talkowski, Michael E., Morton, Cynthia C.

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A Novel Microduplication of ARID1B: Clinical, Genetic and Proteomic Findings Dahkki Seabra, Catarina M., Szoko, Nicholas, Erdin, Serkan, Ragavendran, Ashok, Stortchevoi, Alexei, Maciel, Patrícia, Lundberg, Kathleen, Schlatzer, Daniela, Smith, Janice, Talkowski, Michael E., Gusella, James F., Natowicz, Marvin R.

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16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro Dahkki Sundberg, Maria, Pinson, Hannah, Smith, Richard S., Winden, Kellen D., Venugopal, Pooja, Tai, Derek J. C., Gusella, James F., Talkowski, Michael E., Walsh, Christopher A., Tegmark, Max, Sahin, Mustafa

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Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem Cells Dahkki Keen, Kim L, Petersen, Andrew J, Figueroa, Alexander G, Fordyce, Benjamin I, Shin, Jaeweon, Yadav, Rachita, Erdin, Serkan, Pearce, Robert A, Talkowski, Michael E, Bhattacharyya, Anita, Terasawa, Ei

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Genetic Associations between Neuregulin-1 SNPs and Neurocognitive Function in Multigenerational, Multiplex Schizophrenia Families Dahkki Yokley, Jessica L., Prasad, Konasale M., Chowdari, Kodavali V., Talkowski, Michael E., Wood, Joel, Gur, Ruben C., Gur, Raquel E., Almasy, Laura, Nimgaonkar, Vishwajit L., Pogue-Geile, Michael F.

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KCTD13 is a major driver of mirrored neuroanatomical phenotypes associated with the 16p11.2 CNV Dahkki Golzio, Christelle, Willer, Jason, Talkowski, Michael E, Oh, Edwin C, Taniguchi, Yu, Jacquemont, Sébastien, Reymond, Alexandre, Sun, Mei, Sawa, Akira, Gusella, James F, Kamiya, Atsushi, Beckmann, Jacques S, Katsanis, Nicholas

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