Výsledky vyhledávání - Talkowski, Michael E

Dopamine Genes and Schizophrenia: Case Closed or Evidence Pending? Autor 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 Autor Talkowski, Michael E, Chowdari, KV, Lewis, David A, Nimgaonkar, Vishwajit L

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

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Indexcov: fast coverage quality control for whole-genome sequencing Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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... Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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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