Found: 117
Select item for more details and to access through your institution.
TEX13B is essential for metabolic reprogramming during germ cell differentiation.
- Published in:
- Human Reproduction, 2024, v. 39, n. 7, p. 1390, doi. 10.1093/humrep/deae094
- By:
- Publication type:
- Article
Genetic Affinities and Adaptation of the South-West Coast Populations of India.
- Published in:
- Genome Biology & Evolution, 2023, v. 15, n. 12, p. 1, doi. 10.1093/gbe/evad225
- By:
- Publication type:
- Article
Novel MYBPC3 Mutations in Indian Population with Cardiomyopathies.
- Published in:
- Pharmacogenomics & Personalized Medicine, 2023, v. 16, p. 883, doi. 10.2147/PGPM.S407179
- By:
- Publication type:
- Article
Signatures of high altitude adaptation in Tibeto‐Burman tribes of the Darjeeling Hill Region.
- Published in:
- American Journal of Human Biology, 2023, v. 35, n. 5, p. 1, doi. 10.1002/ajhb.23858
- By:
- Publication type:
- Article
Deciphering the West Eurasian Genetic Footprints in Ancient South India.
- Published in:
- Genes, 2023, v. 14, n. 5, p. 963, doi. 10.3390/genes14050963
- By:
- Publication type:
- Article
Exome sequencing and functional analyses revealed CETN1 variants leads to impaired cell division and male fertility.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 4, p. 533, doi. 10.1093/hmg/ddac216
- By:
- Publication type:
- Article
The matrilineal ancestry of Nepali populations.
- Published in:
- Human Genetics, 2023, v. 142, n. 2, p. 167, doi. 10.1007/s00439-022-02488-z
- By:
- Publication type:
- Article
Pinpointing the Geographic Origin of 165-Year-Old Human Skeletal Remains Found in Punjab, India: Evidence From Mitochondrial DNA and Stable Isotope Analysis.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.813934
- By:
- Publication type:
- Article
High-altitude adaptation: Role of genetic and epigenetic factors.
- Published in:
- Journal of Biosciences, 2021, v. 46, n. 4, p. 1, doi. 10.1007/s12038-021-00228-5
- By:
- Publication type:
- Article
Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from India.
- Published in:
- Journal of Molecular Neuroscience, 2021, v. 71, n. 11, p. 2219, doi. 10.1007/s12031-020-01765-8
- By:
- Publication type:
- Article
Novel FCN2 Variants and Haplotypes are Associated with Rheumatic Heart Disease.
- Published in:
- DNA & Cell Biology, 2021, v. 40, n. 10, p. 1338, doi. 10.1089/dna.2021.0478
- By:
- Publication type:
- Article
Dissecting the genetic history of the Roman Catholic populations of West Coast India.
- Published in:
- Human Genetics, 2021, v. 140, n. 10, p. 1487, doi. 10.1007/s00439-021-02346-4
- By:
- Publication type:
- Article
Mitochondrial Genetic Heterogeneity in Leber's Hereditary Optic Neuropathy: Original Study with Meta-Analysis.
- Published in:
- Genes, 2021, v. 12, n. 9, p. 1300, doi. 10.3390/genes12091300
- By:
- Publication type:
- Article
Publisher Correction: The major genetic risk factor for severe COVID‑19 does not show any association among South Asian populations.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Mutations in the desert hedgehog (DHH) gene in the disorders of sexual differentiation and male infertility.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 7, p. 1871, doi. 10.1007/s10815-021-02140-1
- By:
- Publication type:
- Article
The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91711-4
- By:
- Publication type:
- Article
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
- Published in:
- Journal of Neurology, 2021, v. 268, n. 6, p. 2192, doi. 10.1007/s00415-020-10390-9
- By:
- Publication type:
- Article
Heterogeneity in Hematological Parameters of High and Low Altitude Tibetan Populations.
- Published in:
- Journal of Blood Medicine, 2021, v. 12, p. 287, doi. 10.2147/JBM.S294564
- By:
- Publication type:
- Article
CYP2C9 Variations and Their Pharmacogenetic Implications Among Diverse South Asian Populations.
- Published in:
- Pharmacogenomics & Personalized Medicine, 2021, v. 14, p. 135, doi. 10.2147/PGPM.S272015
- By:
- Publication type:
- Article
Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures.
- Published in:
- Journal of Molecular Neuroscience, 2020, v. 70, n. 12, p. 1962, doi. 10.1007/s12031-020-01595-8
- By:
- Publication type:
- Article
Correction to: Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
A Distinct Phylogenetic Cluster of Indian Severe Acute Respiratory Syndrome Coronavirus 2 Isolates.
- Published in:
- Open Forum Infectious Diseases, 2020, v. 7, n. 11, p. 1, doi. 10.1093/ofid/ofaa434
- By:
- Publication type:
- Article
Novel homozygous FAN1 mutation in a familial case of karyomegalic interstitial nephritis.
- Published in:
- Indian Journal of Nephrology, 2020, v. 30, n. 4, p. 283, doi. 10.4103/ijn.IJN_278_19
- By:
- Publication type:
- Article
Ancient mtDNA from the extinct Indian cheetah supports unexpectedly deep divergence from African cheetahs.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-60751-7
- By:
- Publication type:
- Article
swarupkchakrabarti@gmail.com.
- Published in:
- Journal of Stem Cells, 2019, v. 14, n. 3, p. 161
- By:
- Publication type:
- Article
Novel NR5A1 Pathogenic Variants Cause Phenotypic Heterogeneity in 46,XY Disorders of Sex Development.
- Published in:
- Sexual Development, 2019, v. 13, n. 4, p. 178, doi. 10.1159/000505527
- By:
- Publication type:
- Article
Early Indians: The Story of Our Ancestors and Where We Came From.
- Published in:
- 2019
- By:
- Publication type:
- Book Review
The peopling of Lakshadweep Archipelago.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-43384-3
- By:
- Publication type:
- Article
High frequencies of Non Allelic Homologous Recombination (NAHR) events at the AZF loci and male infertility risk in Indian men.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-42690-0
- By:
- Publication type:
- Article
Retinoblastoma discordance in families with twins.
- Published in:
- 2019
- By:
- Publication type:
- case study
SNPs in ERCC1, ERCC2, and XRCC1 genes of the DNA repair pathway and risk of male infertility in the Asian populations: association study, meta-analysis, and trial sequential analysis.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 1, p. 79, doi. 10.1007/s10815-018-1339-6
- By:
- Publication type:
- Article
A Complete Absence of Missense Mutation in Myosin Regulatory and Essential Light Chain Genes of South Indian Hypertrophic and Dilated Cardiomyopathies.
- Published in:
- Cardiology, 2018, v. 141, n. 3, p. 156, doi. 10.1159/000495027
- By:
- Publication type:
- Article
The influences of genes, the environment, and social factors on the evolution of skin color diversity in India.
- Published in:
- American Journal of Human Biology, 2018, v. 30, n. 5, p. N.PAG, doi. 10.1002/ajhb.23170
- By:
- Publication type:
- Article
Geographical distribution of complement receptor type 1 variants and their associated disease risk.
- Published in:
- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0175973
- By:
- Publication type:
- Article
Ancient DNA Reveals Late Pleistocene Existence of Ostriches in Indian Sub-Continent.
- Published in:
- PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0164823
- By:
- Publication type:
- Article
c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.
- Published in:
- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164151
- By:
- Publication type:
- Article
Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.
- Published in:
- Scientific Reports, 2016, p. 27684, doi. 10.1038/srep27684
- By:
- Publication type:
- Article
Corrigendum: Genetic affinities of the Jewish populations of India.
- Published in:
- Scientific Reports, 2016, p. 26421, doi. 10.1038/srep26421
- By:
- Publication type:
- Article
Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis.
- Published in:
- PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0151510
- By:
- Publication type:
- Article
Heat shock protein 70 gene polymorphisms' influence on the electrophysiology of long QT syndrome.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup.
- Published in:
- Scientific Reports, 2016, p. 19157, doi. 10.1038/srep19157
- By:
- Publication type:
- Article
Genetic affinities of the Jewish populations of India.
- Published in:
- Scientific Reports, 2016, p. 19166, doi. 10.1038/srep19166
- By:
- Publication type:
- Article
Vocal cord palsy in a case of chronic progressive external ophthalmoplegia.
- Published in:
- 2015
- By:
- Publication type:
- Letter to the Editor
Palatal Tremor in POLG-Associated Ataxia.
- Published in:
- Movement Disorders Clinical Practice, 2015, v. 2, n. 3, p. 318, doi. 10.1002/mdc3.12195
- By:
- Publication type:
- Article
Propagation of pure fetal and maternal mesenchymal stromal cells from terminal chorionic villi of human term placenta.
- Published in:
- Scientific Reports, 2015, p. 10054, doi. 10.1038/srep10054
- By:
- Publication type:
- Article
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.
- Published in:
- DNA & Cell Biology, 2015, v. 34, n. 5, p. 350, doi. 10.1089/dna.2014.2650
- By:
- Publication type:
- Article
IL10 Variant g.5311A Is Associated with Visceral Leishmaniasis in Indian Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0124559
- By:
- Publication type:
- Article
Association of Ficolin-2 Serum Levels and FCN2 Genetic Variants with Indian Visceral Leishmaniasis.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125940
- By:
- Publication type:
- Article
MTHFR 677C>T Polymorphism and the Risk of Breast Cancer: Evidence from an Original Study and Pooled Data for 28031 Cases and 31880 Controls.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0120654
- By:
- Publication type:
- Article
c.620C>T mutation in GATA4 is associated with congenital heart disease in South India.
- Published in:
- BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0152-7
- By:
- Publication type:
- Article