| Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly A Kumar, SC Girimaji, SH Duvvari, MR and Blanton American Journal of Human Genetics 84, 286-290, 2009 | 304 | 2009 |
| Oncogenic microRNA-155 down-regulates tumor suppressor CDC73 and promotes oral squamous cell carcinoma cell proliferation: Implications for cancer therapeutics MI Rather, MN Nagashri, SS Swamy, A Gopinath, KS and Kumar Journal of Biological Chemistry 288, 608-618, 2013 | 147 | 2013 |
| Involvement of TSC genes and differential expression of other members of the mTOR signaling pathway in oral squamous cell carcinoma. S Chakraborty, SMA Mohiyuddin, KS Gopinath, A Kumar BMC Cancer 8, 163, 2008 | 129 | 2008 |
| Role of CYP1B1, MYOC, OPTN and OPTC genes in adult-onset primary open-angle glaucoma: Predominance of CYP1B1 mutations in Indian patients. A Kumar, MG Basavaraj, SK Gupta, I Qamar, AM Ali, V Bajaj, TK Ramesh, ... Molecular Vision 13, 13:667-676, 2007 | 129 | 2007 |
| Identification of genes associated with tumorigenesis of retinoblastoma by microarray analysis. S Chakraborty, S Khare, SK Dorairaj, VC Prabhakara, DR Prakash, ... Genomics 90, 344-353, 2007 | 124 | 2007 |
| Genetic analysis of primary microcephaly in Indian families: Novel ASPM mutations A Kumar, SH Blanton, M Babu, M Markandaya, SC Girimaji Clinical Genetics 66, 341-348, 2004 | 98 | 2004 |
| A homozygous mutation in LTBP2 causes isolated microspherophakia. A Kumar, MR Duvvari, VC Prabhakaran, JS Shetty, ... Human Genetics 128, 365-371, 2010 | 90 | 2010 |
| Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations. V Bhat, SC Girimaji, G Mohan, HR Arvinda, P Singhmar, ... Clinical Genetics 80, 532-540, 2011 | 88 | 2011 |
| Chromosomal localization and copy number of 18S+28S ribosomal RNA genes in evolutionarily diverse mosquitoes (Diptera, Culicidae) A Kumar, KS Rai Hereditas 113, 277-289, 1990 | 83 | 1990 |
| Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefevre syndrome V Selvaraju, M Markandaya, PVS Prasad, P Sathyan, G Sethuraman, ... BMC Medical Genetics 4, 5, 2003 | 77 | 2003 |
| Molecular characterization and delineation of subtle deletions in de novo “balanced” chromosomal rearrangements A Kumar, LA Becker, TW Depinet, JM Haren, CL Kurtz, NH Robin, ... Human Genetics 103, 173-178, 1998 | 67 | 1998 |
| Primary microcephaly gene MCPH1 shows signatures of tumor suppressors and is regulated by miR-27a in oral squamous cell carcinoma T Venkatesh, MN Nagashri, SS Swamy, SM Azeem Mohiyuddin, ... PLoS ONE 8, e54643, 2013 | 62 | 2013 |
| Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: Two novel mutations in SLC4A11 A Kumar, S Bhattacharjee, DR Prakash, CS Sadanand Molecular Vision 13, 39-46, 2007 | 62 | 2007 |
| Detection of deletions in de novo “balanced” chromosome rearrangements: Further evidence for their role in phenotypic abnormalities C Astbury, LA Christ, DJ Aughton, SB Cassidy, A Kumar, EE Eichler, ... Genetics In Medicine 6 (2), 81-89, 2004 | 55 | 2004 |
| microRNAs in oral cancer: Moving from bench to bed as next generation medicine W D'Souza, A Kumar Oral Oncology 111, 104916, 2020 | 51 | 2020 |
| Intraspecific variation in nuclear DNA content among world populations of a mosquito, Aedes albopictus (Skuse) A Kumar, KS Rai Theoretical and Applied Genetics 79, 748-752, 1990 | 46 | 1990 |
| Whole exome sequencing identifies a novel splice site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome. MH Shah, V Bhat, A Shetty, JS and Kumar Molecular Vision 20, 790-796, 2014 | 45 | 2014 |
| A de novo frame-shift mutation in the tuberin gene A Kumar, C Wolpert, RS Kandt, J Segal, J Pufky, AD Roses, ... Human Molecular Genetics 4, 1471-1472, 1995 | 42 | 1995 |
| A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family. N Singh, VK Bhat, A Tiwari, SG Kodaganur, SG Tontanahal, A Sarda, ... Human Molecular Genetics. 26, 1104-1114, 2017 | 41 | 2017 |
| Angelman Syndrome Protein UBE3A Interacts with Primary Microcephaly Protein ASPM, Localizes to Centrosomes and Regulates Chromosome Segregation P Singhmar, A Kumar PLoS ONE 6 (5), e20397, 2011 | 41 | 2011 |
Maheswara Rao DuvvariPostdoctoral Researcher, Johns Hopkins University School of MedicineVerified email at jhmi.edu
