Genotoxicity evaluation of heat shock in gold fish (Carassius auratus) B Anitha, N Chandra, PM Gopinath, G Durairaj Mutation Research/Genetic Toxicology and Environmental Mutagenesis 469 (1), 1-8, 2000 | 83 | 2000 |
Molecular mechanism underlying hesperetin-induced apoptosis by in silico analysis and in prostate cancer PC-3 cells S Sambantham, M Radha, A Paramasivam, B Anandan, R Malathi, ... Asian Pacific Journal of Cancer Prevention 14 (7), 4347-4352, 2013 | 81 | 2013 |
MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India C Cyril, P Rai, N Chandra, PM Gopinath, K Satyamoorthy Indian journal of human genetics 15 (2), 60, 2009 | 53 | 2009 |
Cytogenetic evaluation of down syndrome: A review of 1020 referral cases N Chandra, C Cyril, P Lakshminarayana, P Nallasivam, A Ramesh, ... International Journal of Human Genetics 10 (1-3), 87-93, 2010 | 52 | 2010 |
Genotoxic and antigenotoxic effects of Hemidesmus indicus R. Br. root extract in cultured lymphocytes R Ananthi, N Chandra, ST Santhiya, A Ramesh Journal of ethnopharmacology 127 (2), 558-560, 2010 | 46 | 2010 |
Chromosomal abnormalities in infertile men from southern India J Suganya, SB Kujur, K Selvaraj, MS Suruli, G Haripriya, CR Samuel Journal of clinical and diagnostic research: JCDR 9 (7), GC05, 2015 | 43 | 2015 |
Chromosomal abnormalities in 979 cases of amenorrhea: A review V Kalavathi, N Chandra, GR Nambiar, J Shanker, P Sugunashankari, ... International Journal of Human Genetics 10 (1-3), 65-69, 2010 | 35 | 2010 |
Protective effect of Hemidesmus indicus R. Br. root extract against cisplatin-induced cytogenetic damage in mouse bone marrow cells R Ananthi, N Chandra, ST Santhiya Genetics and molecular biology 33, 182-185, 2010 | 27 | 2010 |
Down syndrome with tandem 21; 21 rearrangement and Ebstein's anomaly—a case report C Cyrus, E Cyril, KM Cherian, S Kulkarni, C Nallathambi International Journal of Cardiology 115 (1), E58-E60, 2007 | 20 | 2007 |
BCR-ABL Translocation in Pediatric Acute Lymphoblastic Leukemia in Southern India D Sugapriya, S Preethi, P Shanthi, N Chandra, G Jeyaraman, ... Indian Journal of Hematology and Blood Transfusion 28, 37-41, 2012 | 17 | 2012 |
Chromosomal abnormalities among children with congenital malformations R Yashwanth, N Chandra, PM Gopinath International Journal of Human Genetics 10 (1-3), 57-63, 2010 | 15 | 2010 |
Split hand/foot malformation associated with 7q21. 3 microdeletion: a case report A Sivasankaran, A Srikanth, PS Kulshreshtha, D Anuradha, JS Kadandale, ... Molecular Syndromology 6 (6), 287-296, 2016 | 11 | 2016 |
A De Novo Reciprocal t(2;18) Translocation with Regular Trisomy 21 C Cyrus, H Kaur, T Koshy, J Thankanadar, C Nallathambi Genetic Testing 11 (4), 459-462, 2007 | 11 | 2007 |
Case report-Down syndrome child with 48, XXY,+ 21 karyotype C Cyril, N Chandra, T Jegatheesan, K Chandralekha, A Ramesh, ... Indian Journal of Human Genetics 11 (1), 47-48, 2005 | 11 | 2005 |
Cytogenetic abnormalities in multiple myeloma patients at a tertiary healthcare center in India P Govindasamy, P Pandurangan, A Tarigopula, R Mani, CR Samuel Asian Pacific journal of cancer prevention: APJCP 20 (1), 235, 2019 | 10 | 2019 |
A family case of fertile human 45, X, psu dic (15; Y) males R Wimmer, W Schempp, PM Gopinath, CS Nagarajappa, N Chandra, ... Cytogenetic and Genome Research 115 (1), 94-98, 2006 | 9 | 2006 |
Balanced autosomal translocations in two women reporting recurrent miscarriage B Arumugam, CR Samuel, SS Thyagarajan Journal of Clinical and Diagnostic Research: JCDR 10 (12), GD01, 2016 | 8 | 2016 |
Y chromosome microdeletions and partial AZFc deletions in infertile men from South India J Suganya, S Kujur, K Selvaraj, M Suruli, G Haripriya, C Samuel British Journal of Medicine and Medical Research 13 (12), 1-10, 2016 | 8 | 2016 |
Ring chromosome 9 and chromosome 9p deletion syndrome in a patient Associated with developmental delay: a case report and review of the literature A Sivasankaran, MK Kanakavalli, D Anuradha, CR Samuel, LR Kandukuri Cytogenetic and Genome Research 148 (2-3), 165-173, 2016 | 7 | 2016 |
De novo 7p partial trisomy characterized by subtelomeric FISH and whole-genome array in a girl with mental retardation VO Padmalatha, KM Kulashekaran, LR Kandukuri Molecular Cytogenetics 4 (1), 1-10, 2011 | 7 | 2011 |