|Cryptic Eimeria genotypes are common across the southern but not northern hemisphere.
||Int J Parasitol. Jun 28||2016|
|Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.
||Clin Neurol Neurosurg. 148: 17-21||2016|
|Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.
||Sci Rep. 6: 27684.
|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: 10.1038||2016|
|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.
|Genetic affinities of the Jewish populations of India.
||Sci Rep. 6:19166
|Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup.
||Sci Rep. 6:19157
|Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging.
|Clinical, cytogenetic and molecular analysis of androgen insensitivity syndromes from south Indian cohort and detection and in-silico characterization of androgen receptor gene mutations.
|Heat shock protein 70 gene polymorphisms' influence on the electrophysiology of long QT syndrome.
||J Interv Card Electrophysiol. Dec 16 2015||2015|
|Genome-wide analysis correlates Ayurveda Prakriti.
||Sci Rep. 5:15786.
|The paternal ancestry of Uttarakhand does not imitate the classical caste system of India.
||J Hum Genet. Oct 29.
|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 India||Mitochondrion. Sep. 1 [Epub ahead of print]||2015|
|Mannose-binding Lectin (MBL) as a susceptible host factor influencing Indian Visceral Leishmaniasis.||Parasitol Int. 64:591-596||2015|
|A novel gene THSD7A is associated with obesity||Int 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. 13:151||2015|
|IL10 Variant g.5311A Is Associated with Visceral Leishmaniasis in Indian Population.||PLoS One. 10:e0124559||2015|
|Mitochondrial disorders: Challenges in diagnosis & treatment.||Indian J Med Res. 141:13-26||2015|
|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.
|Mechanistic Heterogeneity in Contractile Properties of α-Tropomyosin (TPM1) Mutants Associated with Inherited Cardiomyopathies.||J Biol Chem. 290: 7003-7015||2015|
|c. 620C> T mutation in GATA4 is associated with congenital heart disease in South India||BMC Med. Genet. 16 (1): 7||2015|
|M235T Polymorphism in the AGT Gene and A/G Substitution in the REN Gene Correlate with End-Stage Renal Disease.||Nephron. 129:104-108||2015|
|SRD5A2 Gene Polymorphisms and the Risk of Benign Prostatic Hyperplasia but not Prostate Cancer.||Asian Pac J Cancer Prev. 16: 1033-1036||2015|
|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 21||2015|
|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. 75:1177-1181||2014|
|Mitochondrial Myopathy, Cardiomyopathy, and Pontine Signal Changes in an Adult Patient With Isolated Complex II Deficiency.
||J. Clin. Neuromuscul. Dis. 16:69-73||2014|
|Determinants of prakriti, the human constitution types of Indian traditional medicine and its correlation with contemporary science.||J. Ayurveda Integr. Med. 5:167-75||2014|
|Ancient human genomes suggest three ancestral populations for present-day Europeans||Nature 513: 409||2014|
|Reduced prevalence of placental malaria in primiparae with blood group O
||Malar J. 13: 289||2014|
|Genetics of male infertility: Indian scenario
||Mol Cytogenet. 21: 7 (Suppl.)||2014|
|Mitochondria in health and disease.
||Mitochondrion 16: 1||2014|
|Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G.||PLoS One. 9(7):e102763||2014|
|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):e101451||2014|
|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. 87:20130478||2014|
|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
|Relic excavated in western India is probably of Georgian Queen Ketevan.||Mitochondrion. 14:1-6||2014|
|MBL2 variations and malaria susceptibility in Indian populations.||Infect Immun. 82:52-61||2014|
|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. 16:49-54||2013|
|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.
||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:e75979||2013|
|Genetic Structure of Tibeto-Burman Populations of Bangladesh: Evaluating the Gene Flow along the sides of Bay-of-Bengal||PLoS One. 8(10):e75064.||2013|
|Androgen Receptor CAG Repeats Length Polymorphism and the Risk of Polycystic Ovarian Syndrome (PCOS)||PLoS One. 8(10):e75709||2013|
|Variations in ncRNA gene LOC284889 and MIF-794CATT repeats are associated with malaria susceptibility in Indian populations.||Malar J. Sep 25;12(1):345
|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):559-565||2013|
|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 India||Ann 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. 19:1282-1289||2013|
|Haplogroup heterogeneity of LHON patients carrying m.14484T>C mutation in India||Invest. Ophthalmol. Vis. Sci. May 14 [Epub ahead of print]||2013|
|The "Double Panda" Sign in Leigh Disease||J 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 Populations||Eur Addict Res. 19(6): 307-313||2013|
|Mitochondrial DNA variations in myelodysplastic syndrome||Ann Hematol. Mar 9. [Epub ahead of print]||2013|
|Mitochondrial DNA variations in Madras motor neuron disease||Mitochondrion. Feb 15 [Epub ahead of print]||2013|
|Genetic evidence of TAP1 gene variant as a susceptibility factor in Indian leprosy patients||Hum 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: S1567-1348||2013|
|Mitochondrial DNA variations in ova and blastocyst: Implications in assisted reproduction.
||Mitochondrion. Jan 15. doi:pii: S1567-7249||2013|
|Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities||Cell 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:e48477||2012|
|IL-4 Haplotype -590T, -34T and Intron-3 VNTR R2 Is Associated with Reduced Malaria Risk among Ancestral Indian Tribal Populations||PLoS One. 7(10):e48136||2012|
|Complex genetic origin of Indian populations and its implications||J Biosci. Nov;37(5):911-9||2012|
|Genomic view on the peopling of India||Investig 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 India||Am J Addict. 21: 343-347||2012|
|Genetic and functional evaluation of the role of DLL1 in susceptibility to visceral leishmaniasis in India.||Inf. Genet. Evol. 24 April
|Comprehensive DNA copy number profile and BAC library construction of an
Indian individual||Gene (21 March)||2012|
|Genetic affinities of the central Indian tribal populations.||PLoS One. 7: e32546||2012|
|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 Amplification||Intl J Hum Sci 9 (1), 102-109||2012|
|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. 16:138-41||2012|
|Genetic and functional evaluation of the role of CXCR1 and CXCR2 in susceptibility to visceral leishmaniasis in north-east India||BMC 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. 89:731-44||2011|
|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:e24792||2011|
|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. 56:1343-1345||2011|
|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. 24:617-622||2010|
|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: 487-493||2009|
|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. 9:11||2008|
|Allelic variation and haplotype structure of the Dopamine receptor gene DRD2 in 9 Indian populations.||Genet. Testing 12:153-160||2008|
|Maternal footprints of southeast Asians in north India.||Hum. Heredity. 28:66:1-9||2008|
|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: e1141||2007|
|CA repeat and RsaI polymorphisms in ERß gene are not associated with infertility in Indian men.||Intl. J. Androl. 30:1-7||2007|
|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: 47||2007|
|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. 51:998-1005||2006|
|Genetic affinities among the lower caste and tribal groups of India: inference from Y chromosome and Mitochonfrial DNA.||BMC Genetics 7: 42||2006|
|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|