AbhaRaniGuptaMDPhD

PubMed

• 10 citations
  A neurogenetic analysis of female autism.
  Allison Jack, Catherine Sullivan, Elizabeth Aylward, Susan Y. Bookheimer, Mirella Dapretto, Nadine Gaab, John D. Van Horn, Jeffrey Eilbott, Zachary Jacokes, Carinna M....> ;Brain. 2021 Jul 28
• 23 citations
  Engineering spatial-organized cardiac organoids for developmental toxicity testing.
  Plansky Hoang, Andrew Kowalczewski, Shiyang Sun, Tackla S. Winston, Adriana M. Archilla, Stephanie M. Lemus, A. Gulhan Ercan-Sencicek, Abha R. Gupta, Wenzhong Liu, Mar...> ;Stem Cell Reports. 2021 May 11
• Sex-dependent role for EPHB2 in brain development and autism-associated behavior.
  Ahlem Assali, Jennifer Y. Cho, Evgeny Tsvetkov, Abha R. Gupta, Christopher W. Cowan> ;Neuropsychopharmacology. 2021 Mar 1
• PAC1R Genotype to Phenotype Correlations in Autism Spectrum Disorder.
  Goodrich, M.,Armour, A. C.,Panchapakesan, K.,You, X.,Devaney, J.,Knoblach, S.,Sullivan, CAW.,Herrero, M. J.,Gupta, A. R.,Vaidya, C. J.,Kenworthy, L.,Corbin, J. G.> ;Autism Res. 2018 Dec 18
• Isoniazid hair concentrations in children with tuberculosis: a proof of concept study.
  Mave V, Chandanwale A, Kinikar A, Khadse S, Kagal A, Gupte N, Suryavanshi N, Nimkar S, Koli H, Khwaja S, Bharadwaj R, Joshi S, Horng H, Benet LZ, Ramachandran G, Doole...> ;Int. J. Tuberc. Lung Dis.. 2016-06-01
• No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Protein...
  Murdoch, J. D.,Gupta, A. R.,Sanders, S. J.,Walker, M. F.,Keaney, J.,Fernandez, T. V.,Murtha, M. T.,Anyanwu, S.,Ober, G. T.,Raubeson, M. J.,DiLullo, N. M.,Villa, N.,Waq...> ;PLoS Genet.. 2015 Jan 27
• Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons.
  Griesi-Oliveira, K.,Acab, A.,Gupta, A. R.,Sunaga, D. Y.,Chailangkarn, T.,Nicol, X.,Nunez, Y.,Walker, M. F.,Murdoch, J. D.,Sanders, S. J.,Fernandez, T. V.,Ji, W.,Lifton...> ;Mol. Psychiatry. 2014 Nov 12
• De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.
  Dong, S.,Walker, M. F.,Carriero, N. J.,DiCola, M.,Willsey, A. J.,Ye, A. Y.,Waqar, Z.,Gonzalez, L. E.,Overton, J. D.,Frahm, S.,Keaney, J. F.,Teran, N. A.,Dea, J.,Mandel...> ;Cell Rep. 2014 Oct 07
• Active case finding for tuberculosis among people who inject drugs on methadone treatment in Dar es Salaam, Tanzania.
  Gupta, A.,Mbwambo, J.,Mteza, I.,Shenoi, S.,Lambdin, B.,Nyandindi, C.,Doula, B. I.,Mfaume, S.,Bruce, R. D.> ;Int. J. Tuberc. Lung Dis.. 2014 Jun 07
• Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.
  Gulhan Ercan-Sencicek, A.,Jambi, S.,Franjic, D.,Nishimura, S.,Li, M.,El-Fishawy, P.,Morgan, T. M.,Sanders, S. J.,Bilguvar, K.,Suri, M.,Johnson, M. H.,Gupta, A. R.,Yuks...> ;Eur. J. Hum. Genet.. 2014 May 02
• Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
  Willsey, A. J.,Sanders, S. J.,Li, M.,Dong, S.,Tebbenkamp, A. T.,Muhle, R. A.,Reilly, S. K.,Lin, L.,Fertuzinhos, S.,Miller, J. A.,Murtha, M. T.,Bichsel, C.,Niu, W.,Cotn...> ;Cell. 2013 Nov 26
• Screening for pulmonary tuberculosis in HIV-infected individuals: AIDS Clinical Trials Group Protocol A5253.
  Swindells S, Komarow L, Tripathy S, Cain KP, MacGregor RR, Achkar JM, Gupta A, Veloso VG, Asmelash A, Omoz-Oarhe AE, Gengiah S, Lalloo U, Allen R, Shiboski C, Andersen...> ;Int. J. Tuberc. Lung Dis.. 2013-04-01
• De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
  Sanders, S. J., Murtha, M. T., Gupta, A. R., Murdoch, J. D., Raubeson, M. J., Willsey, A. J., Ercan-Sencicek, A. G., DiLullo, N. M., Parikshak, N. N., Stein, J. L., Wa...> ;Nature. 2012 May 10
• Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.
  Gupta, A. R.,Pirruccello, M.,Cheng, F.,Kang, H. J.,Fernandez, T. V.,Baskin, J. M.,Choi, M.,Liu, L.,Ercan-Sencicek, A. G.,Murdoch, J. D.,Klei, L.,Neale, B. M.,Franjic, ...> ;Mol Autism. 2014 May 27
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