Dopamine Genes and Schizophrenia: Case Closed or Evidence Pending?

door Talkowski, Michael E., Bamne, Mikhil, Mansour, Hader, Nimgaonkar, Vishwajit L.
Gepubliceerd in 2007

Can RGS4 Polymorphisms Be Viewed as Credible Risk Factors for Schizophrenia? A Critical Review of the Evidence

door Talkowski, Michael E, Chowdari, KV, Lewis, David A, Nimgaonkar, Vishwajit L
Gepubliceerd in 2006

Mechanisms for Structural Variation in the Human Genome

door Currall, Benjamin B., Chiang, C., Talkowski, Michael E., Morton, Cynthia C.
Gepubliceerd in 2013

Indexcov: fast coverage quality control for whole-genome sequencing

door Pedersen, Brent S, Collins, Ryan L, Talkowski, Michael E, Quinlan, Aaron R
Gepubliceerd in Gigascience (2017)

Functional Analysis of Upstream Common Polymorphisms of the Dopamine Transporter Gene

door Bamne, Mikhil N., Talkowski, Michael E., Chowdari, Kodavali V., Nimgaonkar, Vishwajit L.
Gepubliceerd in 2010

Role of the Chromosome Architectural Factor SMCHD1 in X-Chromosome Inactivation, Gene Regulation, and Disease in Humans

door Wang, Chen-Yu, Brand, Harrison, Shaw, Natalie D., Talkowski, Michael E., Lee, Jeannie T.
Gepubliceerd in Genetics (2019)

Low incidence of off-target mutations in individual CRISPR-Cas9 and TALEN targeted human stem cell clones detected by whole-genome sequencing

door Veres, Adrian, Gosis, Bridget S., Ding, Qiurong, Collins, Ryan, Ragavendran, Ashok, Brand, Harrison, Erdin, Serkan, Talkowski, Michael E., Musunuru, Kiran
Gepubliceerd in 2014

Linkage Disequilibrium Patterns and Functional Analysis of RGS4 Polymorphisms in Relation to Schizophrenia

door Chowdari, Kodavali V., Bamne, Mikhil, Wood, Joel, Talkowski, Michael E., Mirnics, Karoly, Levitt, Pat, Lewis, David A., Nimgaonkar, Vishwajit L.
Gepubliceerd in 2008

Systematic Association Studies of Mitochondrial DNA Variations in Schizophrenia: Focus on the ND5 Gene

door Bamne, Mikhil N., Talkowski, Michael E., Moraes, Carlos T., Manuck, Stephen B., Ferrell, Robert E., Chowdari, Kodavali V., Nimgaonkar, Vishwajit L.
Gepubliceerd in 2008

Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder

door Bahl, Samira, Chiang, Colby, Beauchamp, Roberta L, Neale, Benjamin M, Daly, Mark J, Gusella, James F, Talkowski, Michael E, Ramesh, Vijaya
Gepubliceerd in 2013

RGS4 Polymorphisms Associated With Variability of Cognitive Performance in a Family-Based Schizophrenia Sample

door Prasad, Konasale M., Almasy, Laura, Gur, Ruben C., Gur, Raquel E., Pogue-Geile, Michael, Chowdari, Kodavali V., Talkowski, Michael E., Nimgaonkar, Vishwajit L.
Gepubliceerd in 2010

An eMERGE Clinical Center at Partners Personalized Medicine

door Smoller, Jordan W., Karlson, Elizabeth W., Green, Robert C., Kathiresan, Sekar, MacArthur, Daniel G., Talkowski, Michael E., Murphy, Shawn N., Weiss, Scott T.
Gepubliceerd in J Pers Med (2016)

Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin

door Zepeda-Mendoza, Cinthya J., Bardon, Alexandra, Kammin, Tammy, Harris, David J., Cox, Helen, Redin, Claire, Ordulu, Zehra, Talkowski, Michael E., Morton, Cynthia C.
Gepubliceerd in Eur J Hum Genet (2018)

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

door Ordulu, Zehra, Wong, Kristen E., Currall, Benjamin B., Ivanov, Andrew R., Pereira, Shahrin, Althari, Sara, Gusella, James F., Talkowski, Michael E., Morton, Cynthia C.
Gepubliceerd in 2014

A Novel Microduplication of ARID1B: Clinical, Genetic and Proteomic Findings

door 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.
Gepubliceerd in Am J Med Genet A (2017)

16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro

door 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
Gepubliceerd in Nat Commun (2021)

Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem Cells

door 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
Gepubliceerd in Endocrinology (2021)

Genetic Associations between Neuregulin-1 SNPs and Neurocognitive Function in Multigenerational, Multiplex Schizophrenia Families

door 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.
Gepubliceerd in 2012

KCTD13 is a major driver of mirrored neuroanatomical phenotypes associated with the 16p11.2 CNV

door 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
Gepubliceerd in 2012

SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility

door Schilit, Samantha L.P., Menon, Shreya, Friedrich, Corinna, Kammin, Tammy, Wilch, Ellen, Hanscom, Carrie, Jiang, Sizun, Kliesch, Sabine, Talkowski, Michael E., Tüttelmann, Frank, MacQueen, Amy J., Morton, Cynthia C.
Gepubliceerd in Am J Hum Genet (2020)