Abha R. Gupta, Ph.D.
Affiliations: | University of Pennsylvania, Philadelphia, PA, United States |
Area:
Ocular Gene TherapyGoogle:
"Abha Gupta"Parents
Sign in to add mentorMatthew W. State | grad student | UCSF (Neurotree) | ||
Jean Bennett | grad student | 2000 | Penn | |
(Generation of an animal model for macular degeneration.) |
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Publications
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Fernandez TV, Williams ZP, Kline T, et al. (2023) Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene. Plos One. 18: e0291978 |
Enriquez KD, Gupta AR, Hoffman EJ. (2021) Signaling Pathways and Sex Differential Processes in Autism Spectrum Disorder. Frontiers in Psychiatry. 12: 716673 |
Assali A, Cho JY, Tsvetkov E, et al. (2021) Sex-dependent role for EPHB2 in brain development and autism-associated behavior. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology |
Herrero MJ, Velmeshev D, Hernandez-Pineda D, et al. (2020) Identification of amygdala-expressed genes associated with autism spectrum disorder. Molecular Autism. 11: 39 |
Cappi C, Oliphant ME, Péter Z, et al. (2019) De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. Biological Psychiatry |
Goodrich M, Armour AC, Panchapakesan K, et al. (2018) PAC1R Genotype to Phenotype Correlations in Autism Spectrum Disorder. Autism Research : Official Journal of the International Society For Autism Research |
Gupta AR, Westphal A, Yang DY, et al. (2017) Neurogenetic analysis of childhood disintegrative disorder. Molecular Autism. 8: 19 |
Murdoch JD, Gupta AR, Sanders SJ, et al. (2015) No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins. Plos Genetics. 11: e1004852 |
Ercan-Sencicek AG, Jambi S, Franjic D, et al. (2015) Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. European Journal of Human Genetics : Ejhg. 23: 165-72 |
Griesi-Oliveira K, Acab A, Gupta AR, et al. (2014) Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons. Molecular Psychiatry |