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Hardeep Singh

Title(s)Assistant Professor of Research Ophthalmology
Address4640 West Sunset Boulevard
Off Campus
Los Angeles CA 90027
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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. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. 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. Li Z, Qi DL, Singh HP, Zou Y, Shen B, Cobrinik D. PMID: 30643022.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimalsCells
    2. 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. Singh HP, Wang S, Stachelek K, Lee S, Reid MW, Thornton ME, Craft CM, Grubbs BH, Cobrinik D. PMID: 30213853.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
    3. Rb suppresses human cone-precursor-derived retinoblastoma tumours. Nature. 2014 Oct 16; 514(7522):385-8. Xu XL, Singh HP, Wang L, Qi DL, Poulos BK, Abramson DH, Jhanwar SC, Cobrinik D. PMID: 25252974.
      View in: PubMed   Mentions: 46     Fields:    Translation:HumansCells
    4. Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa. Mol Vis. 2012; 18:1165-74. Kannabiran C, Singh H, Sahini N, Jalali S, Mohan G. PMID: 22605927.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    5. 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. Seo S, Singh HP, Lacal PM, Sasman A, Fatima A, Liu T, Schultz KM, Losordo DW, Lehmann OJ, Kume T. PMID: 22171010.
      View in: PubMed   Mentions: 32     Fields:    Translation:AnimalsCells
    6. Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23. Hum Genet. 2012 May; 131(5):717-23. Kannabiran C, Singh HP, Jalali S. PMID: 22083234.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    7. Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening. Invest Ophthalmol Vis Sci. 2009 Sep; 50(9):4065-71. Singh HP, Jalali S, Narayanan R, Kannabiran C. PMID: 19339744.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    8. 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. 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. PMID: 17186464.
      View in: PubMed   Mentions: 55     Fields:    Translation:HumansAnimalsCells
    9. 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. Kumar V, Langstieh BT, Madhavi KV, Naidu VM, Singh HP, Biswas S, Thangaraj K, Singh L, Reddy BM. PMID: 16617372.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    10. Homozygous null mutations in the ABCA4 gene in two families with autosomal recessive retinal dystrophy. Am J Ophthalmol. 2006 May; 141(5):906-13. Singh HP, Jalali S, Hejtmancik JF, Kannabiran C. PMID: 16546111.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
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