| A mouse model for hereditary hemorrhagic telangiectasia (HHT) type 2 S Srinivasan, MA Hanes, T Dickens, MEM Porteous, SP Oh, LP Hale, ... Human molecular genetics 12 (5), 473-482, 2003 | 219 | 2003 |
| Modulation of the baboon (Papio anubis) uterine endometrium by chorionic gonadotrophin during the period of uterine receptivity AT Fazleabas, KM Donnelly, S Srinivasan, JD Fortman, JB Miller Proceedings of the National Academy of Sciences 96 (5), 2543-2548, 1999 | 199 | 1999 |
| Vascular morphogenesis: tales of two syndromes DA Marchuk, S Srinivasan, TL Squire, JS Zawistowski Human molecular genetics 12 (suppl_1), R97-R112, 2003 | 188 | 2003 |
| The promise of discovering population-specific disease-associated genes in South Asia N Nakatsuka, P Moorjani, N Rai, B Sarkar, A Tandon, N Patterson, ... Nature genetics 49 (9), 1403-1407, 2017 | 149 | 2017 |
| Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations NW Plummer, CJ Gallione, S Srinivasan, JS Zawistowski, DN Louis, ... The American journal of pathology 165 (5), 1509-1518, 2004 | 128 | 2004 |
| Neuronal expression of the Ccm2 gene in a new mouse model of cerebral cavernous malformations NW Plummer, TL Squire, S Srinivasan, E Huang, JS Zawistowski, ... Mammalian genome 17, 119-128, 2006 | 74 | 2006 |
| Implantation in the baboon: endometrial responses AT Fazleabas, JJ Kim, S Srinivasan, KM Donnelly, A Brudney, RC Jaffe Seminars in reproductive endocrinology 17 (03), 257-265, 1999 | 70 | 1999 |
| Deficits in Reproduction and Pro-Gonadotropin-Releasing Hormone Processing in Male Cpefat Mice S Srinivasan, DO Bunch, Y Feng, RM Rodriguiz, M Li, RL Ravenell, ... Endocrinology 145 (4), 2023-2034, 2004 | 47 | 2004 |
| Organization for rare diseases India (ORDI)–Addressing the challenges and opportunities for the Indian rare diseases' community HK Rajasimha, PB Shirol, P Ramamoorthy, M Hegde, S Barde, ... Genetics research 96, e009, 2014 | 43 | 2014 |
| Neonatal Co‐Infection with Helicobacter Species Markedly Accelerates the Development of Inflammation‐Associated Colonic Neoplasia in IL‐10−/–Mice LP Hale, D Perera, MR Gottfried, L Maggio‐Price, S Srinivasan, ... Helicobacter 12 (6), 598-604, 2007 | 31 | 2007 |
| Pro-GnRH processing WC Wetsel, S Srinivasan Progress in brain research 141, 221-241, 2002 | 31 | 2002 |
| Mutations in ARSB in MPS VI patients in India J Mathew, SM Jagadeesh, M Bhat, SU Kumar, S Thiyagarajan, ... Molecular genetics and metabolism reports 4, 53-61, 2015 | 20 | 2015 |
| The promise of disease gene discovery in South Asia N Nakatsuka, P Moorjani, N Rai, B Sarkar, A Tandon, N Patterson, ... bioRxiv, 047035, 2016 | 3 | 2016 |
| Identification of Missense Mutation Pro77Arg As A Founder Mutation in Morquio-A Syndrome in Indian Gujarati Patel Ethnicity JJ Sheth, R Bhavsar, A Nair, C Patel, P Naik, M Shah, M Chaudhary, ... | | 2020 |
| 49 ENG, ACVRL1, SMAD4, and Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome) S SRINIVASAN, JN BERG, DA MARCHUK Epstein's Inborn Errors of Development: The Molecular Basis of Clinical …, 2016 | | 2016 |
| Investigation of TGF-beta plasma levels as a modifier of the phenotype of hereditary hemorrhagic telangiectasia TL Squire, S Srinivasan, RJ Akhurst, HM Arthur, DA Marchuk American Journal of Human Genetics: Annual Meeting of the American Society …, 2003 | | 2003 |
| A murine model for hereditary hemorrhagic telangiectasia type 2. S Srinivasan, T Dickens, LP Hale, DA Marchuk AMERICAN JOURNAL OF HUMAN GENETICS 71 (4), 542-542, 2002 | | 2002 |
Edward Mitchell (Mitch) EddyEmeritus Investigator, RDBL, NIEHS, NIHVerified email at niehs.nih.gov
