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A novel stop-loss mutation in NKX2-2 gene as a cause of neonatal diabetes mellitus: molecular characterization and structural analysis.
- Published in:
- Acta Diabetologica, 2024, v. 61, n. 2, p. 189, doi. 10.1007/s00592-023-02192-y
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- Publication type:
- Article
Precision Diabetes Is Slowly Becoming a Reality.
- Published in:
- 2019
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- Publication type:
- journal article
Lack of association of PTPN1 gene polymorphisms with type 2 diabetes in south Indians.
- Published in:
- Journal of Genetics, 2011, v. 90, n. 2, p. 323, doi. 10.1007/s12041-011-0060-3
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- Publication type:
- Article
WFS1 Gene–associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India.
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- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 5, p. 1328, doi. 10.1210/clinem/dgac002
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- Publication type:
- Article
Molecular Characterization and Management of Congenital Hyperinsulinism: A Tertiary Centre Experience.
- Published in:
- Indian Pediatrics, 2022, v. 59, n. 2, p. 105, doi. 10.1007/s13312-022-2438-0
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- Publication type:
- Article
Diabetes Mellitus Due to Wolfram Syndrome Type 1 (DIDMOAD).
- Published in:
- 2021
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- Publication type:
- Letter
Clinical and molecular characterization of children with neonatal diabetes mellitus at a tertiary care center in northern India.
- Published in:
- Indian Pediatrics, 2017, v. 54, n. 6, p. 467, doi. 10.1007/s13312-017-1049-7
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- Publication type:
- Article
Challenges Involved in Incorporating Personalised Treatment Plan as Routine Care of Patients with Diabetes.
- Published in:
- Pharmacogenomics & Personalized Medicine, 2021, v. 14, p. 327, doi. 10.2147/PGPM.S271582
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- Publication type:
- Article
Trans-ethnic gut microbiota signatures of type 2 diabetes in Denmark and India.
- Published in:
- Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-021-00856-4
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- Publication type:
- Article
Trans-ethnic gut microbial signatures of prediabetic subjects from India and Denmark.
- Published in:
- Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-021-00851-9
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- Publication type:
- Article
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.
- Published in:
- Nature Genetics, 2011, v. 43, n. 10, p. 984, doi. 10.1038/ng.921
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- Publication type:
- Article
Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India.
- Published in:
- BMC Medical Genetics, 2018, v. 19, p. 1, doi. 10.1186/s12881-018-0528-6
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- Publication type:
- Article
Multifaceted genome-wide study identifies novel regulatory loci in SLC22A11 and ZNF45 for body mass index in Indians.
- Published in:
- Molecular Genetics & Genomics, 2020, v. 295, n. 4, p. 1013, doi. 10.1007/s00438-020-01678-6
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- Publication type:
- Article
Association of recently identified type 2 diabetes gene variants with Gestational Diabetes in Asian Indian population.
- Published in:
- Molecular Genetics & Genomics, 2017, v. 292, n. 3, p. 585, doi. 10.1007/s00438-017-1292-6
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- Publication type:
- Article
Correction to: Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function.
- Published in:
- 2022
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- Publication type:
- Correction Notice
Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function.
- Published in:
- Diabetologia, 2022, v. 65, n. 6, p. 973, doi. 10.1007/s00125-022-05671-z
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- Publication type:
- Article
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38766-1
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- Publication type:
- Article
H syndrome: A rare case with homozygous mutation in SLC29A3 gene.
- Published in:
- Indian Journal of Paediatric Dermatology, 2020, v. 21, n. 4, p. 354, doi. 10.4103/ijpd.IJPD_58_20
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- Publication type:
- Article
Common Variants of Inflammatory Cytokine Genes Are Associated with Risk of Nephropathy in Type 2 Diabetesamong Asian Indians.
- Published in:
- PLoS ONE, 2009, v. 4, n. 4, p. 1, doi. 10.1371/journal.pone.0005168
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- Publication type:
- Article
Polymorphisms in the Fatty Acid-Binding Protein 2 and Apolipoprotein C-III Genes Are Associated with the Metabolic Syndrome and Dyslipidemia in a South Indian Population.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 3, p. 1705, doi. 10.1210/jc.2004-1338
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- Publication type:
- Article
A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians.
- Published in:
- Human Genetics, 2008, v. 123, n. 6, p. 599, doi. 10.1007/s00439-008-0506-8
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- Publication type:
- Article
Molecular characterization and re-interpretation of HNF1A variants identified in Indian MODY subjects towards precision medicine.
- Published in:
- Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1177268
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- Publication type:
- Article
Circulating adiponectin mediates the association between omentin gene polymorphism and cardiometabolic health in Asian Indians.
- Published in:
- PLoS ONE, 2021, v. 16, n. 5, p. 1, doi. 10.1371/journal.pone.0238555
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- Publication type:
- Article
Clinical Profile and Outcome of Infantile Onset Diabetes Mellitus in Southern India.
- Published in:
- Indian Pediatrics, 2013, v. 50, n. 8, p. 759, doi. 10.1007/s13312-013-0219-5
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- Publication type:
- Article
Persistent Hyperinsulinemic Hypoglycemia in Infancy-A Case Report.
- Published in:
- Journal of Nepal Paediatric Society, 2021, v. 41, n. 1, p. 107, doi. 10.3126/jnps.v41i1.30806
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- Publication type:
- Article
Identification and Molecular Characterization of HNF1B Gene Mutations in Indian Diabetic Patients with Renal Abnormalities.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12093
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- Publication type:
- Article
Novel ABCC8 ( SUR1) Gene Mutations in Asian Indian Children with Congenital Hyperinsulinemic Hypoglycemia.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 5, p. 311, doi. 10.1111/ahg.12070
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- Publication type:
- Article
Genetics of gestational diabetes mellitus.
- Published in:
- Journal of the Pakistan Medical Association, 2016, v. 66, p. S-11
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- Publication type:
- Article
Role of Genetic Polymorphism Peroxisome Proliferator-Activated Receptor-γ2 Pro12Ala on Ethnic Susceptibility to Diabetes in South-Asian and Caucasian Subjects.
- Published in:
- Diabetes Care, 2006, v. 29, n. 5, p. 1046, doi. 10.2337/dc05-1473
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- Publication type:
- Article
A prevalent amino acid polymorphism at codon 98 (Ala98Val) of the hepatocyte nuclear factor-1alpha is associated with maturity-onset diabetes of the young and younger age at onset of type 2 diabetes in Asian Indians.
- Published in:
- 2005
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- Publication type:
- journal article
A Prevalent Amino Acid Polymorphism at Codon 98 (Ala98Val) of the Hepatocyte Nuclear Factor-1α Is Associated With Maturity-Onset Diabetes of the Young and Younger Age at Onset of Type 2 Diabetes in Asian Indians.
- Published in:
- Diabetes Care, 2005, v. 28, n. 10, p. 2430, doi. 10.2337/diacare.28.10.2430
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- Publication type:
- Article
Study of Association of Vitamin D Receptor Gene Polymorphisms with Diabetic Nephropathy.
- Published in:
- Journal of Diabetology: Official Journal of Diabetes in Asia Study Group, 2024, v. 15, n. 2, p. 222, doi. 10.4103/jod.jod_34_24
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- Publication type:
- Article
Association of rs11643718 SLC12A3 and rs741301 ELMO1 Variants with Diabetic Nephropathy in South Indian Population.
- Published in:
- Annals of Human Genetics, 2016, v. 80, n. 6, p. 336, doi. 10.1111/ahg.12174
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- Publication type:
- Article
Hexokinase Domain Containing 1 ( HKDC1) Gene Variants and their Association with Gestational Diabetes Mellitus in a South Indian Population.
- Published in:
- Annals of Human Genetics, 2016, v. 80, n. 4, p. 241, doi. 10.1111/ahg.12155
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- Publication type:
- Article
Association of TCF7L2 Polymorphism with Diabetic Nephropathy in the South Indian Population.
- Published in:
- Annals of Human Genetics, 2015, v. 79, n. 5, p. 373, doi. 10.1111/ahg.12122
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- Publication type:
- Article
Evidence for the association between FTO gene variants and vitamin B12 concentrations in an Asian Indian population.
- Published in:
- Genes & Nutrition, 2019, v. 14, n. 1, p. N.PAG, doi. 10.1186/s12263-019-0649-3
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- Publication type:
- Article
Maternally inherited diabetes and deafness (MIDD)—a series of case reports.
- Published in:
- International Journal of Diabetes in Developing Countries, 2023, v. 43, n. 4, p. 583, doi. 10.1007/s13410-022-01156-2
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- Publication type:
- Article
Genetic Risk Factors in Drug‐Induced Liver Injury Due to Isoniazid‐Containing Antituberculosis Drug Regimens.
- Published in:
- Clinical Pharmacology & Therapeutics, 2021, v. 109, n. 4, p. 1125, doi. 10.1002/cpt.2100
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- Publication type:
- Article
Interaction between FTO gene variants and lifestyle factors on metabolic traits in an Asian Indian population.
- Published in:
- Nutrition & Metabolism, 2016, v. 13, p. 1, doi. 10.1186/s12986-016-0098-6
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- Publication type:
- Article
GCK Gene Screening and Association of GCK Variants With Gestational Diabetes in North Indian Population.
- Published in:
- Clinical Medicine Insights: Endocrinology & Diabetes, 2018, n. 11, p. 1, doi. 10.1177/1179551418806896
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- Publication type:
- Article
TCF7L2 Gene Polymorphisms Are Associated with Maturity Onset Diabetes of Young (MODY) and Early-Onset Type 2 Diabetes in Asian Indians.
- Published in:
- Diabetes, 2007, v. 56, p. A301
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- Publication type:
- Article
ENPP1/PC-1 K121Q polymorphism and genetic susceptibility to type 2 diabetes.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Genotype‐phenotype correlation of K<sub>ATP</sub> channel gene defects causing permanent neonatal diabetes in Indian patients.
- Published in:
- Pediatric Diabetes, 2021, v. 22, n. 1, p. 82, doi. 10.1111/pedi.13109
- By:
- Publication type:
- Article
Functional characterization of activating mutations in the sulfonylurea receptor 1 (ABCC8) causing neonatal diabetes mellitus in Asian Indian children.
- Published in:
- Pediatric Diabetes, 2019, v. 20, n. 4, p. 397, doi. 10.1111/pedi.12843
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- Publication type:
- Article
EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome.
- Published in:
- Pediatric Diabetes, 2014, v. 15, n. 4, p. 313, doi. 10.1111/pedi.12089
- By:
- Publication type:
- Article
Congenital Hyperinsulinemic Hypoglycemia and Hyperammonemia due to Pathogenic Variants in GLUD1.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Replication of genome-wide association signals in Asian Indians with early-onset type 2 diabetes.
- Published in:
- Acta Diabetologica, 2016, v. 53, n. 6, p. 915, doi. 10.1007/s00592-016-0889-2
- By:
- Publication type:
- Article
Genetics for the pediatric endocrinologists – 1.
- Published in:
- Journal of Pediatric Endocrinology & Diabetes, 2022, v. 2, n. 1, p. 1, doi. 10.25259/JPED_6_2022
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- Publication type:
- Article
Exploring lipodystrophy gene expression in adipocytes: unveiling insights into the pathogenesis of insulin resistance, type 2 diabetes, and clustering diseases (metabolic syndrome) in Asian Indians.
- Published in:
- Frontiers in Endocrinology, 2024, p. 1, doi. 10.3389/fendo.2024.1468824
- By:
- Publication type:
- Article
Common and Distinct Genetic Architecture of Age at Diagnosis of Diabetes in South Indian and European Populations.
- Published in:
- Diabetes Care, 2023, v. 46, n. 8, p. 1515, doi. 10.2337/dc23-0243
- By:
- Publication type:
- Article