Jay Tischfield

Affiliations: 
Graduate School - New Brunswick Rutgers University, New Brunswick, New Brunswick, NJ, United States 
Area:
Microbiology Biology
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"Jay Tischfield"
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Nasello C, Poppi LA, Wu J, et al. (2023) Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice. Biorxiv : the Preprint Server For Biology
Willsey J, Fernandez T, Yu D, et al. (2019) De Novo Coding Variants Are Strongly Associated with Tourette Syndrome European Neuropsychopharmacology. 29
Halikere A, Moore J, Hart R, et al. (2019) Synaptic mechanism of A118G OPRM1 Gene Variants In Human Neurons European Neuropsychopharmacology. 29: S732-S733
Edenberg H, Goate A, Liu Y, et al. (2019) Exome Sequencing and Genomic Studies To Better Understand Alcohol Dependence European Neuropsychopharmacology. 29: S731
Sun N, Nasello C, Deng L, et al. (2017) The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family. Molecular Psychiatry
Alexander J, Potamianou H, Xing J, et al. (2016) Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology. Frontiers in Neuroscience. 10: 428
Sadler B, Haller G, Edenberg H, et al. (2015) Positive Selection on Loci Associated with Drug and Alcohol Dependence. Plos One. 10: e0134393
Kapoor M, Wang JC, Wetherill L, et al. (2014) Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families. Drug and Alcohol Dependence. 142: 56-62
Chorlian DB, Rangaswamy M, Manz N, et al. (2013) Genetic and neurophysiological correlates of the age of onset of alcohol use disorders in adolescents and young adults. Behavior Genetics. 43: 386-401
Rani V, Neumann CA, Shao C, et al. (2012) Prdx1 deficiency in mice promotes tissue specific loss of heterozygosity mediated by deficiency in DNA repair and increased oxidative stress. Mutation Research. 735: 39-45
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