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K Thangaraj Group`s Publications
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Title Journal Year
The promise of discovering population-specific disease-associated genes in South Asia. Nat Genet. Jul 17. doi: 10.1038/ng.3917. [Epub ahead of print]. 2017
MPV17 hepatocerebral mitochondrial DNA depletion syndrome presenting as acute flaccid paralysis - A case report. Mitochondrion. Jun 30. doi: 10.1016/j.mito.2017.06.006. [Epub ahead of print]. 2017
&sdquo;Like sugar in milk&sdquo: reconstructing the genetic history of the Parsi population. Genome Biol. 18:110. 2017
Geographical distribution of complement receptor type 1 variants and their associated disease risk. PLoS One. 2017 12(5):e0175973.2017
Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease. Neurol Genet. 2017 3(3):e149. 2017
3`-UTR SNP rs2229611 in G6PC1 affects mRNA stability, expression and Glycogen Storage Disease type-Ia risk. Clin Chim Acta. 471:46-54. 2017
Origin and spread of human mitochondrial DNA haplogroup U7. Sci Rep; 7:46044.2017
Ancient DNA Reveals Late Pleistocene Existence of Ostriches in Indian Sub-Continent. PLoS One. 12:e0164823. 2017
Reconstructing the population history of the largest tribe of India: the Dravidian speaking Gond. Eur J Hum Genet. 25:493-498. 2017
Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation. J Invest Dermatol. 137:670-677. 2017
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India. Mitochondrion 32:42-49. 2017
c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians. PLoS One. 11:e0164151.2016
The Simons Genome Diversity Project: 300 genomes from 142 diverse populations. Nature. 538: 201-206 2016
Cryptic Eimeria genotypes are common across the southern but not northern hemisphere. Int J Parasitol. Jun 282016
Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome. Clin Neurol Neurosurg. 148: 17-212016
Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India. Sci Rep. 6: 27684. 2016
Optimization of purification method and characterization of recombinant human Centrin-1. Protein Expr. Purif. 124: 48-54.2016
Reply to `Lack of replication of association of THSD7A with obesity`Int J Obes (Lond). Feb 2. doi: 10.10382016
Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis.PLoS One. 11(3):e0151510.2016
Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India. Mitochondrion. 27:1-5 2016
Genetic affinities of the Jewish populations of India. Sci Rep. 6:19166 2016
Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup. Sci Rep. 6:19157 2016
Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging. Mitochondrion. 26:81-85. 2016
Clinical, cytogenetic and molecular analysis of androgen insensitivity syndromes from south Indian cohort and detection and in-silico characterization of androgen receptor gene mutations. ClinChimActa.453:123-30. 2016
Heat shock protein 70 gene polymorphisms' influence on the electrophysiology of long QT syndrome. J Interv Card Electrophysiol. Dec 16 20152015
Genome-wide analysis correlates Ayurveda Prakriti. Sci Rep. 5:15786. 2015
The paternal ancestry of Uttarakhand does not imitate the classical caste system of India. J Hum Genet. Oct 29. 2015
Mutational analysis of SCN5A gene in long QT syndrome. Meta Gene. 6:26-35.2015
Population, genetic, and antigenic diversity of the apicomplexan Eimeria tenella and their relevance to vaccine development.Proc Natl Acad Sci (U S A), Sep 9 [Epub ahead of print]2015
Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south IndiaMitochondrion. Sep. 1 [Epub ahead of print]2015
Mannose-binding Lectin (MBL) as a susceptible host factor influencing Indian Visceral Leishmaniasis.Parasitol Int. 64:591-5962015
A novel gene THSD7A is associated with obesityInt J Obes. Aug 4. [Epub ahead of print]2015
Mitochondrial Biology: From Molecules to Disease Symposium Mitochondrion. Jul 22 [Epub ahead of print]2015
Correlation of Interleukin-6 levels and lectins during Schistosoma haematobium infection. Cytokine. May 14 [Epub ahead of print]2015
Propagation of pure fetal and maternal mesenchymal stromal cells from terminal chorionic villi of human term placenta.Nat. Sci Rep. 5:10054.2015
Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 Gene.Neuropediatrics. May 14.2015
Association of Ficolin-2 Serum Levels and FCN2 Genetic Variants with Indian Visceral Leishmaniasis.PLoS One. 10:e0125940.2015
DNA methylation analysis of phenotype specific stratified Indian population.J Transl Med. 13:1512015
IL10 Variant g.5311A Is Associated with Visceral Leishmaniasis in Indian Population.PLoS One. 10:e01245592015
Mitochondrial disorders: Challenges in diagnosis & treatment.Indian J Med Res. 141:13-262015
MTHFR 677C>T Polymorphism and the Risk of Breast Cancer: Evidence from an Original Study and Pooled Data for 28031 Cases and 31880 Controls. PLoS One. 10:e0120654. 2015
Mechanistic Heterogeneity in Contractile Properties of α-Tropomyosin (TPM1) Mutants Associated with Inherited Cardiomyopathies.J Biol Chem. 290: 7003-70152015
c. 620C> T mutation in GATA4 is associated with congenital heart disease in South IndiaBMC Med. Genet. 16 (1): 72015
M235T Polymorphism in the AGT Gene and A/G Substitution in the REN Gene Correlate with End-Stage Renal Disease.Nephron. 129:104-1082015
SRD5A2 Gene Polymorphisms and the Risk of Benign Prostatic Hyperplasia but not Prostate Cancer.Asian Pac J Cancer Prev. 16: 1033-10362015
Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.DNA Cell Biol. Jan 212015
A novel insertion-induced frameshift mutation of the androgen receptor gene in a patient with primary amenorrhea.Meta Gene. 2:11-15. 2014
Analysis of genetic variants in the IL4 promoter and VNTR loci in Indian patients with Visceral Leishmaniasis. Hum. Immunol. 75:1177-11812014
Mitochondrial Myopathy, Cardiomyopathy, and Pontine Signal Changes in an Adult Patient With Isolated Complex II Deficiency. J. Clin. Neuromuscul. Dis. 16:69-732014
Determinants of prakriti, the human constitution types of Indian traditional medicine and its correlation with contemporary science.J. Ayurveda Integr. Med. 5:167-752014
Ancient human genomes suggest three ancestral populations for present-day EuropeansNature 513: 4092014
Reduced prevalence of placental malaria in primiparae with blood group O Malar J. 13: 2892014
Genetics of male infertility: Indian scenario Mol Cytogenet. 21: 7 (Suppl.)2014
Mitochondria in health and disease. Mitochondrion 16: 12014
Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G.PLoS One. 9(7):e1027632014
A Novel Arginine to Tryptophan (R144W) Mutation in Troponin T (cTnT) Gene in an Indian Multigenerational Family with Dilated Cardiomyopathy (FDCM)PLoS One. 9(7):e1014512014
A novel androgen receptor gene mutation in a patient with congenital adrenal hyperplasia associated with penoscrotal hypospadias.Transl Res. (May 6)2014
RAF1 mutations in childhood-onset dilated cardiomyopathy.Nature Genetics (April 28)2014
Unravelling the distinct strains of Tharu ancestry.Eur. J. Hum. Genet. (March 26)2014
Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndrome.Br J Radiol. 87:201304782014
Novel mutations in ATPase 8, ND1 and ND5 genes associated with peripheral neuropathy of diabetes.Diabetes Res Clin Pract. (Jan 5)2014
A novel insertion-induced frameshift mutation of the androgen receptor gene in a patient with primary amenorrhea Meta Gene 2, 11-15 2014
Relic excavated in western India is probably of Georgian Queen Ketevan.Mitochondrion. 14:1-62014
MBL2 variations and malaria susceptibility in Indian populations.Infect Immun. 82:52-612014
SRD5A2 gene polymorphisms affect the risk of breast cancer.Breast. Dec 20.2013
Analysis of microsatellite polymorphisms in South Indian patients with non syndromic cleft lip and palate. Balkan J Med Genet. 16:49-542013
Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations. Brain Dev. (Nov 18)2013
The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent. PLoS Genet. 9(11):e1003912.2013
Mitochondrial DNA variations associated with hypertrophic cardiomyopathy. Link Mitochondrion. (Nov 9)2013
Strong Impact of TGF-β1 Gene Polymorphisms on Breast Cancer Risk in Indian Women: A Case-Control and Population-Based Study.PLoS One 8:e759792013
Genetic Structure of Tibeto-Burman Populations of Bangladesh: Evaluating the Gene Flow along the sides of Bay-of-BengalPLoS One. 8(10):e75064.2013
Androgen Receptor CAG Repeats Length Polymorphism and the Risk of Polycystic Ovarian Syndrome (PCOS)PLoS One. 8(10):e757092013
Variations in ncRNA gene LOC284889 and MIF-794CATT repeats are associated with malaria susceptibility in Indian populations.Malar J. Sep 25;12(1):345 2013
L712V mutation in the androgen receptor gene causes complete androgen insensitivity syndrome due to severe loss of androgen function.Steroids Sep 18 [Epub ahead of print]2013
LRRK2 and RIPK2 Variants in the NOD 2-Mediated Signaling Pathway Are Associated with Susceptibility to Mycobacterium leprae in Indian Populations.PLoS One. Aug 28;8(8):e73103.2013
A mitochondrial DNA variant 10398G>A in breast cancer among South Indians: An original study with meta-analysis.Mitochondrion Aug 29;13(6):559-5652013
Association of progesterone receptor gene polymorphism with male infertility and clinical outcome of ICSI.J Assist Reprod Genet.(2013 Aug 11)2013
Genetic Evidence for Recent Population Mixture in India.Am J Hum Genet.(2013 Aug 7)2013
Variation at diabetes- and obesity-associated loci may mirror neutral patterns of human population diversity and diabetes prevalence in IndiaAnn Hum Genet. Jul 1 [Epub ahead of print]2013
Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy.Mol Vis. 19:1282-12892013
Haplogroup heterogeneity of LHON patients carrying m.14484T>C mutation in IndiaInvest. Ophthalmol. Vis. Sci. May 14 [Epub ahead of print]2013
The "Double Panda" Sign in Leigh DiseaseJ Child Neurol. Apr 18. [Epub ahead of print]2013
Association between Neuropeptide Y Gene Polymorphisms and Alcohol Dependence: A Case-Control Study in Two Independent PopulationsEur Addict Res. 19(6): 307-3132013
Mitochondrial DNA variations in myelodysplastic syndromeAnn Hematol. Mar 9. [Epub ahead of print]2013
Mitochondrial DNA variations in Madras motor neuron diseaseMitochondrion. Feb 15 [Epub ahead of print]2013
Genetic evidence of TAP1 gene variant as a susceptibility factor in Indian leprosy patientsHum Immunol. Feb 5 [Epub ahead of print]2013
A rare non-synonymous c.102C>G SNP in the IFNB1 gene might be a risk factor for cerebral malaria in Indian populations.Infect Genet Evol. Jan 16. doi:pii: S1567-13482013
Mitochondrial DNA variations in ova and blastocyst: Implications in assisted reproduction. Mitochondrion. Jan 15. doi:pii: S1567-72492013
Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain AbnormalitiesCell Rep. Dec 12 [Epub ahead of print]2012
The phylogeography of Y-chromosome haplogroup H1a1a-M82 reveals the likely Indian origin of the European Romani populations.PLoS One 7:e484772012
IL-4 Haplotype -590T, -34T and Intron-3 VNTR R2 Is Associated with Reduced Malaria Risk among Ancestral Indian Tribal PopulationsPLoS One. 7(10):e481362012
Complex genetic origin of Indian populations and its implicationsJ Biosci. Nov;37(5):911-92012
Genomic view on the peopling of IndiaInvestig Genet. Oct 1;3(1):20. [Epub ahead of print]2012
Novel mutations in calcium/calmodulin-dependent protein kinase IV (CAMK4) gene in infertile men.Int J Androl. Aug 17 [Epub ahead of print]2012
High prevalence of Arginine to Glutamine Substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians.BMC Med Genet. Aug 10;13(1):69. [Epub ahead of print]2012
Association of SNP41, SNP56 and a novel SNP in PDE4D gene with stroke and its subtypes.Gene. Jul 3. [Epub ahead of print]2012
Dopamine Transporter (DAT1) VNTR Polymorphism and Alcoholism in Two Culturally Different Populations of South IndiaAm J Addict. 21: 343-3472012
Genetic and functional evaluation of the role of DLL1 in susceptibility to visceral leishmaniasis in India.Inf. Genet. Evol. 24 April 2012
Comprehensive DNA copy number profile and BAC library construction of an Indian individualGene (21 March)2012
Genetic affinities of the central Indian tribal populations.PLoS One. 7: e325462012
Complete Androgen Insensitivity Syndrome Despite Partial Loss of Androgen Function Due to L712V Mutation in the Androgen Receptor Gene.J Androl. Feb 23. [Epub ahead of print]2012
Standardization of PCR conditions for an Ancient DNA AmplificationIntl J Hum Sci 9 (1), 102-1092012
Resistance/response molecular signature for oral tongue squamous cell carcinoma.Dis Markers. 32: 51-64.2012
EPHX1 Gene Polymorphisms in Alcohol Dependence and their Distribution among the Indian Populations.Am J Drug Alcohol Abuse. 2012 Jan 19. [Epub ahead of print]2012
Herders of Indian and European cattle share their predominant allele for lactase persistence.Mol Biol Evol. 29: 249-60.2012
Molecular Basis of β-Thalassemia in Karnataka, India.Genet Test Mol Biomarkers. 16:138-412012
Genetic and functional evaluation of the role of CXCR1 and CXCR2 in susceptibility to visceral leishmaniasis in north-east IndiaBMC Med Genet. Dec 15; 12:162.2011
Shared and unique components of human population structure and genome-wide signals of positive selection in South Asia.Am J Hum Genet. 89:731-442011
Cardiac Troponin T (TNNT2) mutations are less prevalent in Indian hypertrophic cardiomyopathy patients.DNA Cell Biol. (in press).2011
Cellular model of Warburg effect identifies tumor promoting function of UCP2 in breast cancer and its suppression by genipin.PLoS One 6:e247922011
Analysis of mitochondrial genome revealed a rare 50bp deletion and substitutions in a family with hypertension.Mitochondrion. Jul 20. [Epub ahead of print].2011
Indian Siddis: African Descendants with Indian Admixture.Am J Hum Genet. 89: 154-161.2011
No evidence for association between SLC11A1 and visceral leishmaniasis in India.BMC Med Genet. 12:71.2011
Contribution of muscle biopsy and genetics to the diagnosis of chronic progressive external opthalmoplegia of mitochondrial origin.J Clin Neurosci. 18:535-538.2011
Identification of the source of ivory idol by DNA analysis.J.Forensic Science. 56:1343-13452011
Mitochondrial dysfunction and genetic heterogeneity in chronic periodontitis.Mitochondrion. 11:504-512.2011
Mitochondrial DNA variations associated with recurrent pregnancy loss among Indian women.Mitochondrion. 11:450-456.2011
Novel alleles of HLA-DQ and -DR loci show association with recurrent miscarriages among South Indian women.Hum Reprod. 26:765-774.2011
. Role of 14-bp insertion/deletion polymorphism in HLA-G among Indian women with recurrent spontaneous abortions.Tissue Antigens. 77:131-135.2011
Establishing the identity of the massacred tigress in a case of wildlife crime.J. Forensic Sci. 5: 74-75.2011
CAG repeat length polymorphism in the androgen receptor gene and breast cancer risk: data on Indian women and survey from the world.Breast Cancer Res Treat. 127:751-760.2011
Population Genetic Structure in Indian Austroasiatic speakers: The Role of Landscape Barriers and Sex-specific Admixture.Mol. Biol. Evol. 28: 1013-1024.2011
G708E Mutation in the Androgen Receptor Results in Complete Loss of Androgen Function.J. Androl. 32:193-198.2011
Haplotypes on 9p21 Modify the Risk for Coronary Artery Disease Among Indians.DNA Cell Biol. 30:105-110.2011
The TNP1 haplotype - GCG is associated with azoospermia.Intl. J Androl. 34:173-182.2011
Role of ethnic variations in TNF-a and TNF-ß polymorphisms and risk of breast cancer in India. Breast Cancer Res. Treat. 126:739-747.2011
A novel Arg615Ser mutation of androgen receptor DNA-binding domain in three 46,XY sisters with complete androgen insensitivity syndrome and bilateral inguinal hernia.Fertil. Steril. 95:804.e19-21.2011
The Influence of Natural Barriers in Shaping the Genetic Structure of Maharashtra Populations. PLoS One 5: e15283.2010
Population-based case-control study of DRD2 gene polymorphisms and alcoholism.J. Addict. Dis. 29: 475-480.2010
C601S mutation in the androgen receptor results in partial loss of androgen function.J. Stroid Biochem. Mol. Biol. 122: 359-363.2010
HLA-G polymorphism patterns show lack of detectable association with recurrent spontaneous abortion.Tissue Antigens 76:216-222.2010
Androgen receptor CAG repeat polymorphism and epigenetic influence among the south Indian women with Polycystic Ovary Syndrome.PLoS One. 5:e12401.2010
Neuropeptide Y gene polymorphisms are not associated with obesity in a South Indian population.Eur. J. Clin. Nutr. 4: 868-872.2010
Genetic Polymorphisms of 15 Autosomal STR Loci in three Isolated Tribal Populations of Bangladesh.Forensic Sci. Intl. Genet. 4:265-226.2010
Mitochondrial DNA haplogroup 'R' is associated with Noonan syndrome of south India. Mitochondrion 10: 166-173.2010
Traces of sub-Saharan and Middle Eastern Lineages in Indian Muslim Populations.Eur J Hum Genet 18: 354-363.2010
Role of Progesterone Receptor polymorphisms in the Recurrent Spontaneous Abortions: Indian case.PLoS One 5:e8712.2010
R659X mutation in the MLH1 gene in hereditary non-polyposis colorectal cancer (HNPCC) in an Indian extended family.Ind. J. Med. 131:64-70.2010
Neuropeptide Y gene functional polymorphism influences susceptibility to hypertension in Indian population.J. Hum. Hyperten. 24:617-6222010
Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a.Eur. J. Hum. Genet. 18: 479-484.2009
The latitude wise prevalence of the CCR5- d32-HIV resistance allele in India.Bal. J. Med. Genet. 12: 3-13.2009
Dopamine transporter (DAT1) VNTR polymorphism in twelve Indian populations.Neurol. Sci. 30: 487-4932009
Reconstructing Indian Population History.Nature. 461: 489-494.2009
Longer CAG repeat length in Androgen Receptor gene is associated with premature ovarian failure.Hum. Reprod. 24:3230-5.2009
Deep rooting in-situ expansion of mtDNA haplogroup R8 in South Asia.PLoS ONE 4: e6545.2009
APOB gene signal peptide deletion polymorphism is not associated with infertility in Indian men.J. Androl. 30:734-8.2009
Estrogen receptor gene mutations in Indian infertile men.Mol. Hum. Reprod. 15:513-20.2009
Longer (TA)n Repeat but not A49T and V89L Polymorphisms in SRD5A2 Gene May Confer Prostate Cancer Risk in South Indian Men. J. Androl. 30:703-10.2009
Diverse genetic origin of Indian Muslims: evidence from autosomal STR loci.J Hum Genet. 54: 340-348.2009
Transmission of hepatitis C virus infection from asymptomatic mother to child in southern India.Int J Infect Dis. 13:e399-400.2009
A common Cardiac Myosin Binding Protein C variant associated with cardiomyopathies in South Asia.Nat. Genet. 41 187- 191.2009
Genetic heterogeneity in the Indian stocks of seahorse (Hippocampus kuda and Hippocampus trimaculatus) inferred from mtDNA cytochrome b gene.Hydrobiol. 621: 213 - 221.2009
Ala 586 Asp mutation in androgen receptor disrupts transactivation function without affecting androgen binding.Fertil Steril. 91:933.e23-8.2009
Phylogeography of mtDNA haplogroup R7 in the Indian peninsula.BMC Evol. Biol. 4;8:227.2008
Novel variants in UBE2B gene and idiopathic male infertility.J. Androl. 29:564-571.2008
CAG repeat variation in the mtDNA polymerase g (POLG) is not associated with oligoasthenozoospermia.Intl. J. Androl. 32:647-655.2008
Mitochondrial DNA Variation and Substructure among the Tribal Populations of Andhra Pradesh, India.Ann. Hum. Biol. 20:683-692.2008
Reduced CAG repeats length in androgen receptor gene is associated with violent criminal behavior. Intl.J. Legal Med. 22:367-372.2008
Transmission of "a" determinant variants of Hepatitis B virus in immunized babies to HBsAg carrier mothers.Jpn. J. Infect. Dis. 61: 73-76.2008
Microsatellite-based phylogeny of Indian domestic goats.BMC Genet. 9:112008
Allelic variation and haplotype structure of the Dopamine receptor gene DRD2 in 9 Indian populations.Genet. Testing 12:153-1602008
Maternal footprints of southeast Asians in north India.Hum. Heredity. 28:66:1-92008
Androgen insensitivity syndrome: Do trinucleotide repeats in androgen receptor gene have any Role?Asian J. Androl. 10:616-624.2008
. Allelic variation in the NPY gene in 14 Indian populations.J. Hum. Genet. 52:592-598.2007
Austro-Asiatic Tribes of Northeast India Provide Hitherto Missing Genetic Link between South and Southeast Asia.PLoS ONE 2: e11412007
CA repeat and RsaI polymorphisms in ERß gene are not associated with infertility in Indian men.Intl. J. Androl. 30:1-72007
L859F Mutation in androgen receptor gene results in complete loss of androgen binding to the receptor.J. Androl. 28:772-776.2007
Y-chromosomal insights into the genetic impact of the caste system in India.Hum Genet. 121:137-144.2007
Is there an inter-relationship between prostate specific antigen, kallikrein-2 and androgen receptor gene polymorphisms with risk of prostate cancer in north Indian population? Steroids 72:335-341.2007
Single Nucleotide Polymorphisms in Alcohol Dehydrogenase (ADH) genes among Some Indian populations.Am. J. Hum. Biol. 19:338-344.2007
Phenotypic heterogeneity of mutations in androgen receptor gene.Asian J. Androl. 9:147-179.2007
A novel BRCA1 mutation in an Indian family with hereditary breast/ovarian cancer.Breast Cancer Res. Treat. 101:3-6.2007
Nonprogressive juvenile-onset spinal muscular atrophy: A clinico-radiological and CAG repeat study of androgen receptor gene.J Neurol Sci. 252:24-28.2007
Independent origin of 185delAG BRCA1 mutation in an Indian family.Neoplasma 54:51-56.2007
Novel mitochondrial DNA mutations implicated in Noonan syndrome.Intl. J. Cardiol. 120:284-285.2007
Y-chromosome evidence suggests a common paternal heritage of Austro-Asiatic populations.BMC Evol. Biol.7: 472007
Autosomal STR data on the enigmatic Andaman islanders. Forensic Sci. Intl. 169:247-251.2007
Y-chromosome STR haplotypes in two endogamous tribal populations of Karnataka, India. J. Forensic Sci. 52: 751-753.2007
A novel human sex-determining gene linked to Xp11.21-11.23.J. Clin. Endo. Metabol. 91:4028-36.2006
In situ origin of deep rooting lineages of mitochondrial Macrohaplogroup 'M' in India.BMC Genomics. 7: 151- 2006
Response to Comment "Reconstructing the Origin of Andaman Islanders".Science, 311:407.2006
Male infertility: No Evidence of Involvement of Androgen Receptor Gene among Indian Men.J. Androl. 27: 102-105.2006
A novel missense mutation C11994T in the mitochondrial ND4 gene as a cause of low sperm motility in the Indian subcontinent.Fert. Sterl. 86:1783-1785.2006
Novel mitochondrial mutation in ND4 gene associated with Leigh Syndrome. Acta Neurol.Scan. 114:350-353.2006
GGN repeat length and GGN/CAG haplotype variations in the androgen receptor gene and prostate cancer risk in south Indian Men.J. Hum. Genet. 51:998-10052006
Genetic affinities among the lower caste and tribal groups of India: inference from Y chromosome and Mitochonfrial DNA.BMC Genetics 7: 422006
A Simple and Inexpensive Molecular Method for Sexing and Identification of the Forensic Samples of Elephant Origin. J. Forensic Sci 51:805-807.2006
No association of androgen receptor GGN repeat length polymorphism with infertility in Indian Men.J. Androl. 27:785-789.2006
Genetic Profile of Nine Autosomal STR Loci among Halakki and Kunabhi populations of Karnataka, India.J. Forensic Sci. 51: 190-192.2006
Genetic profile of nine STR loci among Goud and Padmashali populations of Andhra Pradesh, India. Forensic Sci Intl 157: 201-205.2006
Global patterns in Human mtDNA Versus Y-chromosome Variation Caused by Spatial Instability of the Local Cultural Processes.PLoS Genet. 2: e53; 0420-0424.2006
South Indian men with reduced CAG repeat length in the androgen receptor gene have increased risk of prostate cancer.J. Hum. Genet. 52: 254-257.2006
Novel mitochondrial DNA mutations in a rare variety of hypertrophic cardiomyopathy.Intl. J. Cardiol. 109: 432-433.2006
Clinical and genetic uniqueness in an individual with MELAS.Am. J. Med. Genet (B). 141B: 440-444.2006
Asian and Non-Asian Origins of Mon-Khmer and Mundari Speaking Austro-Asiatic populations of India.Am. J. Hum. Biol. 18: 461-469.2006
A to G transitions at 260, 386 and 437 in DAZL gene are not associated with spermatogenic failure in Indian population.Intl. J. Androl. 29:510-514.2006
Unique origin of Andaman islanders: insight from autosomal loci.J. Hum. Genet. 51:800-804.2006
A novel androgen receptor mutation resulting in complete androgen insensitivity syndrome and bilateral Leydig cell hyperplasia.J. Androl. 27:510-516.2006
SRY negative 46,XX male with normal genitals, complete masculinization and infertility. Mol. Hum. Rep. 12: 341-346.2006
उपयोगी संपर्क संबंधित संपर्क परिसर
कापीराइट 2010 सीसीएमबी,उप्पल रोड,हैदराबाद 500007, तेलंगाना