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Validation of Polymerase Chain Reaction–Based Assay to Detect Actual Number of CGG Repeats in FMR1 Gene in Indian Fragile X Syndrome Patients.
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- Journal of Child Neurology, 2017, v. 32, n. 4, p. 371, doi. 10.1177/0883073816683075
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- Article
Revisiting Schizophrenia from an Evolutionary Perspective: An Association Study of Recent Evolutionary Markers and Schizophrenia.
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- Schizophrenia Bulletin, 2021, v. 47, n. 3, p. 827, doi. 10.1093/schbul/sbaa179
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- Article
Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis.
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- Schizophrenia Bulletin, 2019, v. 45, n. 1, p. 256, doi. 10.1093/schbul/sbx196
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- Publication type:
- Article
Celiac disease-associated loci show considerable genetic overlap with neuropsychiatric diseases but with limited transethnic applicability.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01413-7
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- Article
Correlation between an intronic SNP genotype and ARL15 level in rheumatoid arthritis.
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- Journal of Genetics, 2021, v. 100, n. 1, p. 1, doi. 10.1007/s12041-021-01286-2
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- Article
Age-related gene expression alterations by SARS-CoV-2 infection contribute to poor prognosis in elderly.
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- Journal of Genetics, 2020, v. 99, n. 1, p. 1, doi. 10.1007/s12041-020-01233-7
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- Article
Genetics of ulcerative colitis: putting into perspective the incremental gains from Indian studies.
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- Journal of Genetics, 2018, v. 97, n. 5, p. 1493, doi. 10.1007/s12041-018-1015-8
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- Publication type:
- Article
Advances in the discovery of genetic risk factors for complex forms of neurodegenerative disorders: contemporary approaches, success, challenges and prospects.
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- Journal of Genetics, 2018, v. 97, n. 3, p. 625, doi. 10.1007/s12041-018-0953-5
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- Publication type:
- Article
Newborn Screening and Diagnosis of Infants with Congenital Adrenal Hyperplasia.
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- Indian Pediatrics, 2020, v. 57, n. 1, p. 49, doi. 10.1007/s13312-020-1703-3
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- Article
Association Between Neonatal Thyroid Stimulating Hormone Status and Maternal Urinary Iodine Status.
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- Indian Pediatrics, 2019, v. 56, n. 6, p. 472, doi. 10.1007/s13312-019-1571-x
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- Publication type:
- Article
An Optimal Capillary Screen Cut-off of Thyroid Stimulating Hormone for Diagnosing Congenital Hypothyroidism: Data from a Pilot Newborn Screening Program in Delhi.
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- Indian Pediatrics, 2019, v. 56, n. 4, p. 281, doi. 10.1007/s13312-019-1515-5
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- Publication type:
- Article
Effort to differentiate essential tremor plus and dystonic tremor using whole exome sequencing: an exploratory study.
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- Dystonia (2813-2106), 2024, p. 1, doi. 10.3389/dyst.2024.13181
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- Publication type:
- Article
Pre-prescription testing in psychiatry: an overview.
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- Open Journal of Psychiatry & Allied Sciences, 2022, v. 13, n. 2, p. 82, doi. 10.5958/2394-2061.2022.00014.3
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- Article
A brief summary of human molecular genetic techniques for clinical psychiatrists.
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- Open Journal of Psychiatry & Allied Sciences, 2021, v. 12, n. 1, p. 55, doi. 10.5958/2394-2061.2021.00010.0
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- Publication type:
- Article
Genetic susceptibility to Tardive Dyskinesia in chronic schizophrenia subjects: V. Association of CYP1A2 1545 C>T polymorphism.
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- Pharmacogenomics Journal, 2007, v. 7, n. 5, p. 305, doi. 10.1038/sj.tpj.6500415
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- Article
Genetic susceptibility to Tardive Dyskinesia in chronic schizophrenia subjects: I. Association of CYP1A2 gene polymorphism.
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- Pharmacogenomics Journal, 2005, v. 5, n. 1, p. 60, doi. 10.1038/sj.tpj.6500282
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- Publication type:
- Article
Genome wide study of tardive dyskinesia in schizophrenia.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01471-y
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- Publication type:
- Article
New Druggable Targets for Rheumatoid Arthritis Based on Insights From Synovial Biology.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.834247
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- Publication type:
- Article
Pharmacophore modeling and virtual screening in search of novel Bruton's tyrosine kinase inhibitors.
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- Journal of Molecular Modeling, 2019, v. 25, n. 7, p. N.PAG, doi. 10.1007/s00894-019-4047-y
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- Publication type:
- Article
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
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- Nature Genetics, 2015, v. 47, n. 9, p. 979, doi. 10.1038/ng.3359
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- Article
Human Heritable Genome Editing - Potential and Current Status for Clinical Use.
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- Asian Biotechnology & Development Review, 2021, v. 23, n. 1, p. 5
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- Article
Potential of Ayurgenomics Approach in Complex Trait Research: Leads from a Pilot Study on Rheumatoid Arthritis.
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- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045752
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- Publication type:
- Article
Limited Evidence for Parent-of-Origin Effects in Inflammatory Bowel Disease Associated Loci.
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- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045287
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- Publication type:
- Article
Caucasian and Asian Specific Rheumatoid Arthritis Risk Loci Reveal Limited Replication and Apparent Allelic Heterogeneity in North Indians.
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- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0031584
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- Publication type:
- Article
Association of regulatory variants of dopamine β-hydroxylase with cognition and tardive dyskinesia in schizophrenia subjects.
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- 2020
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- Publication type:
- journal article
FMR1 haplotype analyses among Indians: a weak founder effect and other findings.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 262, doi. 10.1007/s00439-002-0872-6
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- Publication type:
- Article
Significance of an altered lncRNA landscape in schizophrenia and cognition: clues from a case–control association study.
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- European Archives of Psychiatry & Clinical Neuroscience, 2023, v. 273, n. 8, p. 1677, doi. 10.1007/s00406-023-01596-9
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- Publication type:
- Article
Evaluation of European coeliac disease risk variants in a north Indian population.
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- European Journal of Human Genetics, 2015, v. 23, n. 4, p. 530, doi. 10.1038/ejhg.2014.137
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- Publication type:
- Article
Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 418, doi. 10.1038/sj.ejhg.5201593
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- Article
FMR1 gene CGG repeat distribution among the three individual cohorts with intellectual disability, autism, and primary ovarian insufficiency from Tamil Nadu, Southern India.
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- Advanced Genetics, 2021, v. 2, n. 2, p. 1, doi. 10.1002/ggn2.10048
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- Publication type:
- Article
The Spectrum of Non-Parkinsonian Tremor: A Registry at a Tertiary Care Teaching Institute.
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- Tremor & Other Hyperkinetic Movements, 2023, v. 13, p. 1, doi. 10.5334/tohm.828
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- Publication type:
- Article
Association study identified biologically relevant receptor genes with synergistic functions in celiac disease.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50120-4
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- Article
Mutations in the α-synuclein gene in Parkinson's disease among Indians.
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- Acta Neurologica Scandinavica, 2001, v. 103, n. 2, p. 120, doi. 10.1034/j.1600-0404.2001.103002120.x
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- Article
Deciphering the landscape of lncRNA-driven ceRNA network in schizophrenia etiology.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00542-1
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- Publication type:
- Article
Shared and unique common genetic determinants between pediatric and adult celiac disease.
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- BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0211-8
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- Publication type:
- Article
Association of dopaminergic pathway gene polymorphisms with chronic renal insufficiency among Asian Indians with type-2 diabetes.
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- BMC Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2156-9-26
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- Publication type:
- Article
Evaluation of cytochrome P4502E1 polymorphisms in healthy adult Western Indians and patients with antituberculous drug-induced hepatotoxicity.
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- Indian Journal of Pharmacology, 2016, v. 48, n. 1, p. 42, doi. 10.4103/0253-7613.174519
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- Publication type:
- Article
A simple phenotypic classification for celiac disease.
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- Intestinal Research, 2018, v. 16, n. 2, p. 288, doi. 10.5217/ir.2018.16.2.288
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- Publication type:
- Article
Determination of Dopamine-β-hydroxylase Activity in Human Serum Using UHPLC-PDA Detection.
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- Neurochemical Research, 2018, v. 43, n. 12, p. 2324, doi. 10.1007/s11064-018-2653-1
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- Publication type:
- Article
Complex phenotypes in an Indian family with homozygous SCA2 mutations.
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- Annals of Neurology, 2004, v. 55, n. 1, p. 130
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- Publication type:
- Article
Microhomology-mediated endjoining repair mechanism enables rapid and effective indel generations in stem cells.
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- Journal of Biosciences, 2022, v. 47, n. 4, p. 1, doi. 10.1007/s12038-022-00307-1
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- Publication type:
- Article
Multiple allelic associations from genes involved in energy metabolism were identified in celiac disease.
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- Journal of Biosciences, 2021, v. 46, n. 3, p. 1, doi. 10.1007/s12038-021-00184-0
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- Publication type:
- Article
Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 12, p. 2078, doi. 10.1093/hmg/ddy443
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- Publication type:
- Article
Charting the Course: Towards a Comprehensive Newborn Screening Program in India.
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- International Journal of Neonatal Screening (IJNS), 2024, v. 10, n. 3, p. 43, doi. 10.3390/ijns10030043
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- Publication type:
- Article
Genetic Profiling of Genes from the Oxidative Stress Pathway Among North and South Indians.
- Published in:
- Human Biology, 2008, v. 80, n. 2, p. 161, doi. 10.3378/1534-6617(2008)80[161:GPOGFT]2.0.CO;2
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- Publication type:
- Article
Normative Genetic Profiles of RAAS Pathway Gene Polymorphisms in North Indian and South Indian Populations.
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- Human Biology, 2007, v. 79, n. 2, p. 241, doi. 10.1353/hub.2007.0033
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- Publication type:
- Article
Factors Associated with Transient Neonatal Hyperthyrotropinemia.
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- 2020
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- Publication type:
- Letter
Association of polymorphisms of CYP2C9, CYP2C19, and ABCB1, and activity of P-glycoprotein with response to anti-epileptic drugs.
- Published in:
- Journal of Postgraduate Medicine, 2014, v. 60, n. 3, p. 265, doi. 10.4103/0022-3859.138739
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- Publication type:
- Article
Deletion induced splicing in RIC3 drives nicotinic acetylcholine receptor regulation with implications for endoplasmic reticulum stress in human astrocytes.
- Published in:
- Glia, 2023, v. 71, n. 5, p. 1217, doi. 10.1002/glia.24333
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- Publication type:
- Article
Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North Indians.
- Published in:
- Alimentary Pharmacology & Therapeutics, 2007, v. 26, n. 10, p. 1325, doi. 10.1111/j.1365-2036.2007.03524.x
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- Publication type:
- Article