P. M. Gopinath

发表

Studies on cytotoxicity of Divine Noni , ( Noni Garcinia cambogia mix ) against human liver cancer cells ( HepG 2 Cells )

K. Satyamoorthy, J. Subramani, P. Selvam, 2013 .

Analysis of cosegregation of intragenic DNA sequence variations as markers of maternal cell contamination in prenatal diagnosis of β-thalassemia.

K. Girisha, K. Satyamoorthy, P. M. Gopinath, 2011, Translational research : the journal of laboratory and clinical medicine.

Characterization of Cat-2t, a radiation-induced dominant cataract mutation in mice.

K. Summer, P. M. Gopinath, W. Bors, 1990, Investigative ophthalmology & visual science.

Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails: Fuhrmann syndrome without WNT7A mutations.

Hitesh Shah, K. Girisha, K. Satyamoorthy, 2011, Clinical dysmorphology.

Reply to ‘Lack of replication of association of THSD7A with obesity’

K. Thangaraj, P. Kondaiah, K. Satyamoorthy, 2016, International Journal of Obesity.

Single nucleotide polymorphisms of ADRB2 gene and their association with susceptibility for Plasmodium falciparum malaria and asthma in an Indian population.

K. Satyamoorthy, P. M. Gopinath, H. Gupta, 2013, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

Genetic analysis of a group of mentally retarded children

P. M. Gopinath, A. Ramesh, B. Krishnan, 1989, Indian journal of pediatrics.

Studies on Brahma rasayana in male swiss albino mice: Chromosomal aberrations and sperm abnormalities

K. Satyamoorthy, P. M. Gopinath, K. Guruprasad, 2010, Journal of Ayurveda and integrative medicine.

Thiopurine S-methyltransferase alleles, TPMT(*)2, (*)3B and (*)3C, and genotype frequencies in an Indian population.

K. Satyamoorthy, P. M. Gopinath, S. Patra, 2009, Experimental and therapeutic medicine.

Brahmarasayana protects against Ethyl methanesulfonate or Methyl methanesulfonate induced chromosomal aberrations in mouse bone marrow cells

K. Satyamoorthy, P. M. Gopinath, K. Guruprasad, 2012, BMC Complementary and Alternative Medicine.

A novel human CRYGD mutation in a juvenile autosomal dominant cataract

K. Satyamoorthy, P. M. Gopinath, J. Graw, 2010, Molecular vision.

Effect of Amalaki rasayana on DNA damage and repair in randomized aged human individuals.

K. Satyamoorthy, P. M. Gopinath, M. B. Joshi, 2016, Journal of ethnopharmacology.

DNA methylation analysis of phenotype specific stratified Indian population

K. Thangaraj, P. Kondaiah, K. Satyamoorthy, 2015, Journal of Translational Medicine.

Determinants of Prakriti, the Human Constitution Types of Indian Traditional Medicine and its Correlation with Contemporary Science

Bhushan Patwardhan, Kapaettu Satyamoorthy, Swagata Halder, 2014, Journal of Ayurveda and integrative medicine.

Immunophenotyping of normal individuals classified on the basis of human dosha prakriti

P. Kondaiah, K. Satyamoorthy, P. M. Gopinath, 2014, Journal of Ayurveda and integrative medicine.

Homologous Robertsonian translocation (21q21q) and abortions

P. M. Gopinath, T. Sudha, 1990, Human Genetics.

A Cytogenetic Study of Couples with Miscarriages: An Experience from Manipal Referral Centre

K. Satyamoorthy, P. M. Gopinath, M. Rajasekhar, 2013 .

Cytogenetic Analysis of 1400 Referral Cases: Manipal Experience

K. Satyamoorthy, P. M. Gopinath, M. Rajasekhar, 2010 .

Chromosomal Abnormalities in 979 Cases of Amenorrhea: A Review

P. M. Gopinath, K. Marimuthu, S. T. Santhiya, 2010 .

Biochemical analysis of young rats homozygous for the cataract mutation cat.

P. M. Gopinath, W. Bors, J. Graw, 1989, Experimental eye research.

A family case of fertile human 45,X,psu dic(15;Y) males

W. Schempp, P. M. Gopinath, I. Hansmann, 2006, Cytogenetic and Genome Research.

Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family.

N. Klopp, T. Illig, P. M. Gopinath, 2006, Molecular vision.

Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis

K. Girisha, A. Dalal, K. Satyamoorthy, 2010, Annals of Hematology.

Urofacial (Ochoa) Syndrome - A Case Report

P. M. Gopinath, R. Yashwanth, N. Chandra, 2010 .

GALNS mutations in Indian patients with mucopolysaccharidosis IVA

Hitesh Shah, S. Kapoor, M. Kabra, 2014, American journal of medical genetics. Part A.

Genome-wide analysis correlates Ayurveda Prakriti

K. Thangaraj, P. Kondaiah, K. Satyamoorthy, 2015, Scientific Reports.

A novel gene THSD7A is associated with obesity

K. Thangaraj, P. Kondaiah, K. Satyamoorthy, 2015, International Journal of Obesity.

Genome-wide analysis correlates

K. Thangaraj, P. Kondaiah, K. Satyamoorthy, 2015 .

Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type

K. Girisha, K. Satyamoorthy, P. M. Gopinath, 2012, Indian journal of human genetics.

Comprehensive DNA copy number profile and BAC library construction of an Indian individual.

K. Thangaraj, K. Satyamoorthy, P. Govindaraj, 2012, Gene.

Satellite Associations in Down Syndrome

P. M. Gopinath, R. Yashwanth, N. Chandra, 2010 .

Recurrent and novel GLB1 mutations in India.

M. Kabra, S. Phadke, K. Girisha, 2015, Gene.

Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts

P. M. Gopinath, J. Graw, P. Vijayalakshmi, 2002 .

Cytogenetic Evaluation of Down Syndrome: A Review of 1020 Referral Cases

P. Nallasivam, P. M. Gopinath, A. Ramesh, 2010 .

A Cytogenetic Study of Children with Developmental Delay Mental Retardation

P. M. Gopinath, K. Satyamoorthy, M. Rajasekhar, 2011 .

MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India

K. Satyamoorthy, P. M. Gopinath, P. Rai, 2009, Indian journal of human genetics.

Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts.

P. M. Gopinath, J. Graw, P. Vijayalakshmi, 2002, Journal of medical genetics.

Multiplex ligation-dependant probe amplification study of children with idiopathic mental retardation in South India

K. Girisha, P. Sharma, P. M. Gopinath, 2013, Indian journal of human genetics.

Prevalence of Human Papillomavirus Types and Phylogenetic Analysis of HPV-16 L 1 Variants from Southern India

K. Satyamoorthy, S. Kabekkodu, Vaibhav Shukla, 2015 .

Case Report - Down syndrome child with 48,XXY,+21 karyotype

P. M. Gopinath, C. Cyrus, A. Ramesh, 2005 .

Chromosomal Abnormalities among Children with Congenital Malformations

P. M. Gopinath, R. Yashwanth, N. Chandra, 2010 .

Mitochondrial DNA variation analysis in cervical cancer.

K. Thangaraj, M. Bhat, K. Satyamoorthy, 2014, Mitochondrion.

An Uncommon Congenital Cardiovascular Malformation with Turner Syndrome – A Case Report

P. M. Gopinath, K. Cherian, A. Ramesh, 2004 .

Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 gene.

J. Adamski, P. M. Gopinath, Sharmila Anishetty, 2004, Investigative ophthalmology & visual science.

A de novo translocation of chromosomes 1 and 2 in an 18 year old boy with syndromic mental retardation.

P. M. Gopinath, J. Neetha, M. Sekhar, 2012, Genetic counseling.

Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms

M. Platzer, N. Klopp, T. Illig, 2010, Molecular vision.

Trisomy 4p and partial monosomy 18q due to paternal translocation t(4;18) (p11; q21.3)

P. M. Gopinath, G. Palka, S. Jayam, 2000, Indian journal of pediatrics.

Association of GRIN1, ABCB1, and DRD4 genes and response to antipsychotic drug treatment in schizophrenia.

R. Kukreti, K. Satyamoorthy, Meenal Gupta, 2015, Psychiatric genetics.

Genetic variation in genes involved in folate and drug metabolism in a south Indian population

K. Satyamoorthy, P. M. Gopinath, P. Rai, 2011, Indian journal of human genetics.

Upregulation of TFAM and mitochondria copy number in human lymphoblastoid cells.

K. Satyamoorthy, S. Kabekkodu, R. Rossignol, 2014, Mitochondrion.

0021-972X/06/$15.00/0 The Journal of Clinical Endocrinology & Metabolism 91(10):4028–4036 Printed in U.S.A. Copyright © 2006 by The Endocrine Society doi: 10.1210/jc.2006-0950 A Novel Human Sex-Determining Gene Linked to Xp11.21-11.23

L. Singh, K. Thangaraj, P. M. Gopinath, 2022 .

Intraindividual somatic variations in MTHFR gene polymorphisms in relation to colon cancer.

K. Satyamoorthy, P. M. Gopinath, Ravishankara Bellampalli, 2014, Pharmacogenomics.

Cytogenetic evaluation of patients with clinical spectrum of Turner syndrome

P. M. Gopinath, Rajasekhar Moka, K. Satyamoorthy, 2013, Journal of human reproductive sciences.

Reciprocal autosomal translocation t(5;14) (q32;q32) in a patient with secondary amenorrhea

P. M. Gopinath, K. Marimuthu, N. Chandra, 2007 .

Quantitative Fluorescence Polymerase Chain Reaction (QF-PCR) for Prenatal Diagnosis of Chromosomal Aneuploidies

K. Satyamoorthy, P. Kushtagi, P. M. Gopinath, 2010 .

Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms

M. Platzer, N. Klopp, T. Illig, 2010, Molecular vision.

GALNS mutations in Indian patients with mucopolysaccharidosis IVA

Hitesh Shah, S. Kapoor, M. Kabra, 2014, American journal of medical genetics. Part A.

Prevalence of human papillomavirus types and phylogenetic analysis of HPV-16 L1 variants from Southern India.

K. Satyamoorthy, S. Kabekkodu, Vaibhav Shukla, 2015, Asian Pacific journal of cancer prevention : APJCP.

Familial Robertsonian Translocation 13;21 in a Down Syndrome Patient with XYY/XY Mosaicism

K. Teena, P. M. Gopinath, C. Cyrus, 2006 .