Search Results - Talkowski, Michael

20.1 DISSECTING THE FUNCTIONAL CONSEQUENCES OF RECIPROCAL GENOMIC DISORDERS by Talkowski, Michael

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

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Lack of association between VNTR polymorphism of dopamine transporter gene (SLC6A3) and schizophrenia in a Brazilian sample by Cordeiro, Quirino, Talkowski, Michael, Wood, Joel, Ikenaga, Eliza, Vallada, Homero

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

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

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Indexcov: fast coverage quality control for whole-genome sequencing by 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 by 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 by Wang, Chen-Yu, Brand, Harrison, Shaw, Natalie D., Talkowski, Michael E., Lee, Jeannie T.

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Contribution of Copy Number Variation in Idiopathic Hypogonadotropic Hypogonadism by Stamou*, Maria, Brand*, Harrison, Lippincott, Margaret Flynn, Wong, Isaac, Plummer, Lacey, Balasubramanian, Ravikumar, Talkowski, Michael, Seminara, Stephanie Beth

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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 by 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 by 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 by 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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Molecular Analysis of a Deletion Hotspot in the NRXN1 Region Reveals the Involvement of Short Inverted Repeats in Deletion CNVs by Chen, Xiaoli, Shen, Yiping, Zhang, Feng, Chiang, Colby, Pillalamarri, Vamsee, Blumenthal, Ian, Talkowski, Michael, Wu, Bai-Lin, Gusella, James F.

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Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder by 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... by 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 by 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 by 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 by 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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Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic Hypogonadism by Stamou, Maria I, Brand, Harrison, Wang, Mei, Wong, Isaac, Lippincott, Margaret F, Plummer, Lacey, Crowley, William F, Talkowski, Michael, Seminara, Stephanie, Balasubramanian, Ravikumar

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Describing Sequencing Results of Structural Chromosome Rearrangements with a Suggested Next-Generation Cytogenetic Nomenclature by 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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