Follow
Chandra R Samuel
Chandra R Samuel
Associate Professor [Retd.]
Verified email at unom.ac.in - Homepage
Title
Cited by
Cited by
Year
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
832000
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
812013
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
532009
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
522010
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
462010
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
432015
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
352010
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
272010
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
202007
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
172012
Chromosomal abnormalities among children with congenital malformations
R Yashwanth, N Chandra, PM Gopinath
International Journal of Human Genetics 10 (1-3), 57-63, 2010
152010
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
112016
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
112007
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
112005
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
102019
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
92006
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
82016
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
82016
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
72016
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
72011
The system can't perform the operation now. Try again later.
Articles 1–20