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Hardeep Singh

Title(s)Assistant Professor of Research Ophthalmology
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    Collapse Biography 
    Collapse Education and Training
    Children's Hospital Los Angeles, Los Angeles, USAPost Doc06/2019Retinoblastoma Development
    University of Alberta, Edmonton, CanadaPost Doc08/2011Retinal Development
    L. V. Prasad Eye Institute, Hyderabad, IndiaPhD2010Genetics of Retinal Dystrophies

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Li Z, Qi DL, Singh HP, Zou Y, Shen B, Cobrinik D. A novel thyroid hormone receptor isoform, TRß2-46, promotes SKP2 expression and retinoblastoma cell proliferation. J Biol Chem. 2019 02 22; 294(8):2961-2969. PMID: 30643022.
      View in: PubMed
    2. Singh HP, Wang S, Stachelek K, Lee S, Reid MW, Thornton ME, Craft CM, Grubbs BH, Cobrinik D. Developmental stage-specific proliferation and retinoblastoma genesis in RB-deficient human but not mouse cone precursors. Proc Natl Acad Sci U S A. 2018 10 02; 115(40):E9391-E9400. PMID: 30213853.
      View in: PubMed
    3. Xu XL, Singh HP, Wang L, Qi DL, Poulos BK, Abramson DH, Jhanwar SC, Cobrinik D. Rb suppresses human cone-precursor-derived retinoblastoma tumours. Nature. 2014 Oct 16; 514(7522):385-8. PMID: 25252974.
      View in: PubMed
    4. Kannabiran C, Singh H, Sahini N, Jalali S, Mohan G. Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa. Mol Vis. 2012; 18:1165-74. PMID: 22605927.
      View in: PubMed
    5. Seo S, Singh HP, Lacal PM, Sasman A, Fatima A, Liu T, Schultz KM, Losordo DW, Lehmann OJ, Kume T. Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth. Proc Natl Acad Sci U S A. 2012 Feb 07; 109(6):2015-20. PMID: 22171010.
      View in: PubMed
    6. Kannabiran C, Singh HP, Jalali S. Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23. Hum Genet. 2012 May; 131(5):717-23. PMID: 22083234.
      View in: PubMed
    7. Singh HP, Jalali S, Narayanan R, Kannabiran C. Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening. Invest Ophthalmol Vis Sci. 2009 Sep; 50(9):4065-71. PMID: 19339744.
      View in: PubMed
    8. Friedman JS, Chang B, Kannabiran C, Chakarova C, Singh HP, Jalali S, Hawes NL, Branham K, Othman M, Filippova E, Thompson DA, Webster AR, Andréasson S, Jacobson SG, Bhattacharya SS, Heckenlively JR, Swaroop A. Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration. Am J Hum Genet. 2006 Dec; 79(6):1059-70. PMID: 17186464.
      View in: PubMed
    9. Kumar V, Langstieh BT, Madhavi KV, Naidu VM, Singh HP, Biswas S, Thangaraj K, Singh L, Reddy BM. Global patterns in human mitochondrial DNA and Y-chromosome variation caused by spatial instability of the local cultural processes. PLoS Genet. 2006 Apr; 2(4):e53. PMID: 16617372.
      View in: PubMed
    10. Singh HP, Jalali S, Hejtmancik JF, Kannabiran C. Homozygous null mutations in the ABCA4 gene in two families with autosomal recessive retinal dystrophy. Am J Ophthalmol. 2006 May; 141(5):906-13. PMID: 16546111.
      View in: PubMed