| Rb suppresses human cone-precursor-derived retinoblastoma tumours XL Xu, HP Singh, L Wang, DL Qi, BK Poulos, DH Abramson, SC Jhanwar, ... Nature 514 (7522), 385-388, 2014 | 220 | 2014 |
| Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration JS Friedman, B Chang, C Kannabiran, C Chakarova, HP Singh, S Jalali, ... The American Journal of Human Genetics 79 (6), 1059-1070, 2006 | 149 | 2006 |
| Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth S Seo, HP Singh, PM Lacal, A Sasman, A Fatima, T Liu, KM Schultz, ... Proceedings of the National Academy of Sciences 109 (6), 2015-2020, 2012 | 112 | 2012 |
| Global patterns in human mitochondrial DNA and Y-chromosome variation caused by spatial instability of the local cultural processes V Kumar, BT Langstieh, KV Madhavi, VM Naidu, HP Singh, S Biswas, ... PLoS Genetics 2 (4), e53, 2006 | 73 | 2006 |
| Developmental stage-specific proliferation and retinoblastoma genesis in RB-deficient human but not mouse cone precursors HP Singh, S Wang, K Stachelek, S Lee, MW Reid, ME Thornton, CM Craft, ... Proceedings of the National Academy of Sciences 115 (40), E9391-E9400, 2018 | 68 | 2018 |
| Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening HP Singh, S Jalali, R Narayanan, C Kannabiran Investigative ophthalmology & visual science 50 (9), 4065-4071, 2009 | 68 | 2009 |
| ABO blood groups in gastrointestinal tract (GIT) and breast carcinoma patients K Guleria, HP Singh, H Kaur, V Sambyal The Anthropologist 7 (3), 189-192, 2005 | 54 | 2005 |
| Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa C Kannabiran, H Singh, N Sahini, S Jalali, G Mohan Molecular Vision 18, 1165, 2012 | 48 | 2012 |
| Homozygous null mutations in the ABCA4 gene in two families with autosomal recessive retinal dystrophy HP Singh, S Jalali, JF Hejtmancik, C Kannabiran American journal of ophthalmology 141 (5), 906-913, 2006 | 19 | 2006 |
| Non-random chromosomal aberrations in peripheral blood leucocytes of gastrointestinal tract and breast cancer patients K Guleria, HP Singh, J Singh, H Kaur, V Sambyal International Journal of Human Genetics 5 (3), 205-211, 2005 | 16 | 2005 |
| Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23 C Kannabiran, HP Singh, S Jalali Human genetics 131, 717-723, 2012 | 8 | 2012 |
| Anthropological perspective of the single nucleotide polymorphisms in the NPY and DRD2 genes among the socio-economically stratified populations of Andhra Pradesh, India BM Reddy, ANS Reddy, T Nagaraja, L Bhaskar, HP Singh, VM Naidu, ... International Journal of Human Genetics 7 (4), 277-284, 2007 | 4 | 2007 |
| Fox transcription factors in corneal angiogenesis KM Schultz, A Sasman, S Seo, HP Singh, PM Lacal, A Fatima, L Ting, ... Angiogenesis 16 (1), 249-250, 2013 | 1 | 2013 |
| Abstract LB-39: Human cone precursor-derived retinoblastoma tumors XL Xu, HP Singh, L Wang, D Qi, BK Poulos, DH Abramson, SC Jhanwar, ... Cancer Research 74 (19_Supplement), LB-39-LB-39, 2014 | | 2014 |
| Additional complexities in Axenfeld-Rieger Syndrome-implications for pediatric glaucoma OJ Lehmann, M Asai-Coakwell, H Singh, E Strachan Investigative Ophthalmology & Visual Science 55 (13), 3797-3797, 2014 | | 2014 |
| Reply to Chakrabarti et al.: Corneal angiogenesis in patients with null FOXC1 variants S Seo, HP Singh, PM Lacal, A Sasman, A Fatima, T Liu, KM Schultz, ... Proceedings of the National Academy of Sciences 109 (24), E1510-E1510, 2012 | | 2012 |
