Items where Author is "Radha, V"

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Number of items: 99.

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Srinivasan , S and Liju, S and Sathish, N and Siddiqui, M K and Anjana, R M and Pearson, E R and Doney, Alex S F and Mohan, V and Radha, V and Palmer, Colin N A (2023) Common and Distinct Genetic Architecture of Age at Diagnosis of Diabetes in South Indian and European Populations. Diabetes Care, 46 (8). pp. 1515-1523.

DeForest, N and Kavitha, B and Hu, S and Isaac, R and Krohn, L and Wang, M and Du, X and Saldanha, CDA and Gylys, J and Merli, E and Abagyan, R and Najmi, L and Mohan, V and Flannick, J and Peloso, G M and Gordts, PLSM and Heinz, S and Deaton, A M and Khera, A V and Olefsky, J and Radha, V and Majithia, A R (2023) Human gain-of-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of atherogenic lipoproteins. Cell Genomics, 3 (7). p. 100339.

Kavitha, B and Ranganathan, S and Gopi, S and Vetrivel, V and Hemavathy, N and Mohan, V and Radha, V (2023) Molecular characterization and re-interpretation of HNF1A variants identified in Indian MODY subjects towards precision medicine. Frontiers in Endocrinology (Lausanne), 14 (1177268).

Aarthy, R and Mourney, K A and Amutha, A and Walus, A M and Anjana, R M and Unnikrishnan, R and Jebarani, S and Venkatesan, U and Gopi, S and Radha, V and Mohan, V (2023) Prevalence, clinical features and complications of common forms of Maturity Onset Diabetes of the Young (MODY) seen at a tertiary diabetes centre in south India. Primary Care Diabetes, 17 (4). pp. 401-407.

Wall, Jeffrey D. and Sathirapongsasuti, J F and Gupta, R and Rasheed, A and Radha, V and Mohan, V (2023) South Asian medical cohorts reveal strong founder effects and high rates of homozygosity. Nature Communications, 14 (1). p. 3377.

Radha, V and Mohan, V and Rakesh, K (2022) Genetics for the pediatric endocrinologists - 1 Diagnosis of monogenic diabetes among children and adolescents. Journal of Pediatric Endocrinology and Diabete, 22 . pp. 23-30.

Sharma, R and Roy, K and Satapathy, A K and Kumar, A and Nanda, P M and Damle, N and Houghton, J A L and Flanagan, S E and Radha, V and Mohan, V and Jain, V (2022) Molecular Characterization and Management of Congenital Hyperinsulinism: A Tertiary Centre Experience. Indian Pediatrics, 59 (2). p. 105. ISSN 0019-6061

Mordi, I and Trucco, E and Syed, M G and MacGillivray, T and Nar, A and Huang, Yu and George, Gittu and Hogg, Stephen and Radha, V and Prathiba, V and Anjana, R M and Mohan, V and Palmer, C N A and Pearson, E R and Lang, C C and Doney, A S.F (2022) Prediction of Major Adverse Cardiovascular Events From Retinal, Clinical, and Genomic Data in Individuals With Type 2 Diabetes: A Population Cohort Study. Diabetes Care, 45 (3). p. 710. ISSN 0149-5992

Unnikrishnan, R and Radha, V and Mohan, V (2021) Challenges Involved in Incorporating Personalised Treatment Plan as Routine Care of Patients with Diabetes. Pharmacogenomics and Personalized Medicine, Volume 14 . p. 327. ISSN 1178-7066

Vimaleswaran, K S and Parine, N R and Bodhini, D and Jiang, J and Ramya, K and Deepa, M and Shanthi Rani, C S and Lakshmipriya, N and Sudha, V and Pradeepa, R and Anjana, R M and Mohan, V and Radha, V (2021) Circulating adiponectin mediates the association between omentin gene polymorphism and cardiometabolic health in Asian Indians. PLOS ONE, 16 (5). e0238555. ISSN 1932-6203

Aarthy, R and Aston-Mourney, K and Mikocka-Walus, A and Radha, V and Amutha, A and Anjana, R M and Unnikrishnan, Ranjit and Mohan, Viswanathan (2021) Clinical features, complications and treatment of rarer forms of maturity-onset diabetes of the young (MODY) - A review. Journal of Diabetes and its Complications, 35 (1). p. 107640. ISSN 10568727

Allu, P K R and Kiranmayi, M and Mukherjee, S D and Chirasani, V R and Garg, R and Vishnuprabu, D and Ravikumar, S and Subramanian, L and Sahu, B S and Iyer, D R and Maghajothi, S and Sharma, S K and Ravi, M S and Khullar, M and Munirajan, A K and Gayen, J R and Senapati, S and Mullasari, A S and Mohan, V and Radha, V and Naga Prasad, S V and Mahapatra, N R (2021) Functional Gly297Ser Variant of the Physiological Dysglycemic Peptide Pancreastatin Is a Novel Risk Factor for Cardiometabolic Disorders. Diabetes, 71 (3). p. 538. ISSN 0012-1797

Allu, P K R and Kiranmayi, M and Mukherjee, S D and Chirasani, V R and Garg, R and Vishnuprabu, D and Ravi, S and Subramanian, L and Sahu, B S and Iyer, D R and Maghajothi, S and Sharma, S and Ravi, M S and Khullar, M and Munirajan, A K and Gayen, J R and Senapati, S and Mullasari, A S and Mohan, V and Radha, V and Naga Prasad, S V and Mahapatra, N R (2021) Functional Gly297Ser Variant of the Physiological Dysglycemic Peptide Pancreastatin Is a Novel Risk Factor for Cardiometabolic Disorders. Diabetes, 71 (3). p. 538. ISSN 0012-1797

Allu, Prasanna K.R. and Kiranmayi, Malapaka and Mukherjee, Sromona D. and Chirasani, Venkat R. and Garg, Richa and Vishnuprabu, Durairajpandian and Ravi, Sudesh and Subramanian, Lakshmi and Sahu, Bhavani S. and Iyer, Dhanya R. and Maghajothi, Sakthisree and Sharma, Saurabh and Ravi, Marimuthu S. and Khullar, Madhu and Munirajan, Arasambattu K. and Gayen, Jiaur R. and Senapati, Sanjib and Mullasari, Ajit S. and Mohan, V and Radha, V and Naga Prasad, Sathyamangala V. and Mahapatra, Nitish R. (2021) Functional Gly297Ser Variant of the Physiological Dysglycemic Peptide Pancreastatin Is a Novel Risk Factor for Cardiometabolic Disorders. Diabetes, 71 (3). p. 538. ISSN 0012-1797

Alsulami, S and Bodhini, D and Sudha, V and Shanthi Rani, C S and Pradeepa, R and Anjana, R M and Radha, V and Lovegrove, J A and Gayathri, R and Mohan, V and Vimaleswaran, K S (2021) Lower Dietary Intake of Plant Protein Is Associated with Genetic Risk of Diabetes-Related Traits in Urban Asian Indian Adults. Nutrients, 13 (9). p. 3064. ISSN 2072-6643

Alvarez-Silva, Camila and Kashani, Alireza and Hansen, Tue Haldor and Pinna, Nishal Kumar and Anjana, R M and Dutta, Anirban and Saxena, Shruti and Støy, Julie and Kampmann, Ulla and Nielsen, Trine and Jørgensen, Torben and Gnanaprakash, V and Gnanavadivel, R and Sukumaran, Aswath and Rani, C S S and Færch, Kristine and Radha, V and Balasubramanyam, M and Nair, Gopinath Balakrish and Das, Bhabatosh and Vestergaard, Henrik and Hansen, Torben and Mande, Sharmila Shekhar and Mohan, V and Arumugam, Manimozhiyan and Pedersen, Oluf (2021) Trans-ethnic gut microbiota signatures of type 2 diabetes in Denmark and India. Genome Medicine, 13 (1). ISSN 1756-994X

Anjana, R M and Pradeepa, R and Deepa, M and Jebarani, S and Venkatesan, U and Parvathi, S J and Balasubramanyam, M and Radha, V and Poongothai, S and Sudha, V and Shanthi Rani, C S and Ranjani, H and Amutha, A and Manickam, N and Unnikrishnan, R and Mohan, V (2020) Acceptability and Utilization of Newer Technologies and Effects on Glycemic Control in Type 2 Diabetes: Lessons Learned from Lockdown. Diabetes Technology & Therapeutics, 22 (7). p. 527. ISSN 1520-9156

Doney, Alex S F and Palmer, Colin N A and Mohan, V and Radha, V and Nar, A S and Appleby, P and Huang, Yu and Gan, Sushrima and George, Gittu and Schwartz, Russell (2020) PheGWAS: a new dimension to visualize GWAS across multiple phenotypes. Bioinformatics, 36 (8). p. 2500. ISSN 1367-4803

Omkar, P and Ravikumar, KG and Gopi, S and Raman, T and Radha, V and Mohan, V (2020) Thiamine-responsive megaloblastic anemia syndrome: A case report. Journal of Diabetology, 11 (1). p. 45. ISSN 2078-7685

Roy, K and Satapathy, A K and Houhton, J A L and Flanagan, S E and Radha, V and Mohan, V and Sharma, R and Jain, V (2019) Congenital Hyperinsulinemic Hypoglycemia and Hyperammonemia due to Pathogenic Variants in GLUD1. The Indian Journal of Pediatrics, 86 (11). p. 1051. ISSN 0019-5456

Surendran, S and Jayashri, R and Drysdale, L and Bodhini, D and Lakshmipriya, N and Shanthi Rani, C S and Sudha, V and Lovegrove, J A and Anjana, R M and Mohan, V and Radha, V and Pradeepa, R and Vimaleswaran, K S (2019) Evidence for the association between FTO gene variants and vitamin B12 concentrations in an Asian Indian population. Genes & Nutrition, 14 (1). ISSN 1555-8932

Balamurugan, K and Kavitha, B and Yang, Z and Mohan, V and Radha, V and Shyng, S L (2019) Functional characterization of activating mutations in the sulfonylurea receptor 1 ( ABCC8 ) causing neonatal diabetes mellitus in Asian Indian children. Pediatric Diabetes, 20 (4). p. 397. ISSN 1399-543X

Wall, JD and Stawiski, EW and Ratan, A and Radha, V and Mohan, V and Peeterson, AS (2019) The GenomeAsia 100K Project enables genetic discoveries across Asia. Nature, 576 (7785). p. 106. ISSN 0028-0836

Wall, Jeffrey D. and Ratan, Aakrosh and Stawiski, Eric and Wall, Jeffrey D. and Stawiski, Eric and Ratan, Aakrosh and Kim, Hie Lim and Kim, Changhoon and Gupta, Ravi and Suryamohan, Kushal and Gusareva, Elena S. and Purbojati, Rikky Wenang and Bhangale, Tushar and Stepanov, Vadim and Kharkov, Vladimir and Schrӧder, Markus S. and Ramprasad, Vedam and Tom, Jennifer and Durinck, Steffen and Bei, Qixin and Li, Jiani and Guillory, Joseph and Phalke, Samir and Basu, Analabha and Stinson, Jeremy and Nair, Sandhya and Malaichamy, Sivasankar and Biswas, Nidhan K. and Chambers, John C. and Cheng, Keith C. and George, Joyner T. and Khor, Seik Soon and Kim, Jong-Il and Cho, Belong and Menon, Ramesh and Sattibabu, Thiramsetti and Bassi, Akshi and Deshmukh, Manjari and Verma, Anjali and Gopalan, Vivek and Shin, Jong-Yeon and Pratapneni, Mahesh and Santhosh, Sam and Tokunaga, Katsushi and Md-Zain, Badrul M. and Chan, Kok Gan and Parani, Madasamy and Natarajan, Purushothaman and Hauser, Michael and Allingham, R. Rand and Santiago-Turla, Cecilia and Ghosh, Arkasubhra and Gadde, Santosh Gopi Krishna and Fuchsberger, Christian and Forer, Lukas and Shoenherr, Sebastian and Sudoyo, Herawati and Lansing, J. Stephen and Friedlaender, Jonathan and Koki, George and Cox, Murray P. and Hammer, Michael and Karafet, Tatiana and Ang, Khai C. and Mehdi, Syed Q. and Radha, V and Mohan, V and Majumder, Partha P. and Seshagiri, Sekar and Seo, Jeong-Sun and Schuster, Stephan and Peterson, Andrew S. (2019) Identification of African-Specific Admixture between Modern and Archaic Humans. The American Journal of Human Genetics, 105 (6). pp. 1254-1261. ISSN 00029297

Mohan, V and Radha, V (2019) Precision Diabetes Is Slowly Becoming a Reality. Medical Principles and Practice, 28 (1). p. 1. ISSN 1011-7571

Mohan, V and Radha, V and Nguyen, T T and Stawiski, E W and Pahuja, K B and Goldstein, L D and Tom, Jennifer and Anjana, Ranjit Mohan and Kong-Beltran, Monica and Bhangale, T and Jahnavi, S and Chandni, Radhakrishnan and Gayathri, V and George, P and Zhang, Na and Murugan, Sakthivel and Phalke, Sameer and Chaudhuri, Subhra and Gupta, Ravi and Zhang, Jingli and Santhosh, Sam and Stinson, Jeremy and Modrusan, Zora and Ramprasad, V. L. and Seshagiri, Somasekar and Peterson, Andrew S. (2018) Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India. BMC Medical Genetics, 19 (1). ISSN 1471-2350

Radha, V and Ramya, B and Gopi, S and Kavitha, B and Preetika, S and Thai, K and Unnikrishnan, R and Mohan, V and Gupta, P K (2018) Successful transition to sulphonylurea therapy from insulin in a child with permanent neonatal diabetes due to a KCNJ11 gene mutation. Journal of Diabetology, 9 (2). p. 65. ISSN 2078-7685

Jain, V and Satapathy, A and Yadav, J and Sharma, R and Radha, V and Mohan, V and De Franco, E and Ellard, S (2017) Clinical and Molecular Characterization of Children with Neonatal Diabetes Mellitus at a Tertiary Care Center in Northern India. INDIAN PEDIATRICS, 54 . p. 467.

Radha, V and Mohan, V (2017) Genetic basis of monogenic diabetes. Current Science , 113 (7). p. 1277.

Ayyappa, K A and Shatwan, I and Bodhini, D and Bramwell, L R and Ramya, K and Sudha, V and Anjana, R M and Lovegrove, J A and Mohan, V and Radha, V and Vimaleswaran, K S (2017) High fat diet modifies the association of lipoprotein lipase gene polymorphism with high density lipoprotein cholesterol in an Asian Indian population. Nutrition & Metabolism, 14 (1). ISSN 1743-7075

Kiranmayi, M and Chirasani, V R and Allu, P K R and Subramanian, L and Martelli, E E and Sahu, B S and Vishnuprabu, D and Kumaragurubaran, R and Sharma, S K and Bodhini, D and Dixit, M and Munirajan, A K and Khullar, M and Radha, V and Mohan, V and Mullasari, A S and Naga Prasad, S V and Senapati, S and Mahapatra, N R (2016) Catestatin Gly364Ser Variant Alters Systemic Blood Pressure and the Risk for Hypertension in Human Populations via Endothelial Nitric Oxide Pathway. Hypertension, 68 (2). p. 334. ISSN 0194-911X

Radha, V and Mohan, V (2016) Genetics in diabetes: Type 2 diabetes and related trait. Indian Journal of Medical Research, 143 (6). p. 838. ISSN 0971-5916

Radha, V and Kanthimathi, S and Anjana, R M and Mohan, V (2016) Genetics of gestational diabetes mellitus. Journal Of Pakistan Medical Association . s11.

Kanthimathi, S and Liju, S and Laasya, D and Anjana, R M and Mohan, V and Radha, V (2016) Hexokinase Domain Containing 1 (HKDC1) Gene Variants and their Association with Gestational Diabetes Mellitus in a South Indian Population. Annals of Human Genetics, 80 (4). p. 241. ISSN 00034800

Kanthimathi, S and Chidambaram, M and Liju, S and Bhavadharini, B and Bodhini, D and Prakash, V G and Amutha, A and Bhavatharini, A and Anjana, R M and Mohan, V and Radha, V (2015) Identification of Genetic Variants of Gestational Diabetes in South Indians. Diabetes Technology & Therapeutics, 17 (7). p. 462. ISSN 1520-9156

Radha, V and Bodhini, D and Narayani, N and Mohan, V (2014) Association study of the ABCC8 gene variants with type 2 diabetes in south Indians. Indian Journal of Human Genetics, 20 (1). p. 37. ISSN 0971-6866

Jahnavi, S and Poovazhagi, V and Kanthimathi, S and Gayathri, V and Mohan, V and Radha, V (2014) EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome. Pediatric diabetes, 15 (4). pp. 313-8. ISSN 1399-5448

Radha, V and Mohan, V (2014) Genetics fo Type 2 Diabetes. RSSDI TEXTBOOK OF DIABETES MELLITUS .

Kanthimathi, S and Jahnavi, S and Balamurugan, K and Ranjani, H and Sonya, J and Goswami, S and Chowdhury, S and Mohan, V and Radha, V (2014) Glucokinase Gene Mutations (MODY 2) in Asian Indians. Diabetes Technology & Therapeutics, 16 (3). p. 180. ISSN 1520-9156

Kanthimathi, S and Balamurugan, K and Mohan, V and Shanthirani, C S and Gayathri, V and Radha, V (2014) Identification and Molecular Characterization ofHNF1BGene Mutations in Indian Diabetic Patients with Renal Abnormalities. Annals of Human Genetics, 79 (1). p. 10. ISSN 00034800

Jahnavi, S and Poovazhagi, V and Kanthimathi, S and Balamurugan, K and Bodhini, D and Yadav, J and Jain, V and Khadgawat, R and Sikdar, M and Bhavatharini, A and Das, A K and Kaur, T and Mohan, V and Radha, V (2014) NovelABCC8(SUR1) Gene Mutations in Asian Indian Children with Congenital Hyperinsulinemic Hypoglycemia. Annals of Human Genetics, 78 (5). p. 311. ISSN 00034800

Radha, V and Mohan, V (2014) Predictive value of genomics in the screening of type 2 diabetes: limitations and current status. Advances in Genomics and Genetics . p. 45. ISSN 1179-9870

Ayyappa, K A and Ghosh, S and Mohan, V and Radha, V (2013) Association of Hepatic Lipase Gene Polymorphisms with Hypertriglyceridemia and Low High-Density Lipoprotein-Cholesterol Levels Among South Indian Subjects Without Diabetes. Diabetes Technology & Therapeutics, 15 (6). p. 503. ISSN 1520-9156

Poovazhagi, V and Shanthirani, S and Jahnavi, S and Radha, V and Mohan, V (2013) Berardinelli Seip congenital lipodystrophy presenting with neonatal diabetes mellitus due to a mutation in the AGPAT2 gene. International Journal of Diabetes in Developing Countries, 33 (1). p. 66. ISSN 0973-3930

Jahnavi, S and Poovazhagi, V and Mohan, V and Bodhini, D and Raghupathy, P and Amutha, A and Suresh Kumar, P and Adhikari, P and Shriraam, M and Kaur, T and Das, A K and Molnes, J and Njolstad, P R and Unnikrishnan, R and Radha, V (2013) Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children. Clinical genetics, 83 (5). pp. 439-45. ISSN 1399-0004

Poovazhagi, V and Sangaralingam, T and Senniappan, S and Jahnavi, S and Radha, V and Mohan, V (2013) Clinical Presentation and Long Term Outcome of 40 children with Infantile Onset Diabetes Mellitus in South India. Indian pediatrics . ISSN 0974-7559

Ramya, K and Ayyappa, K A and Ghosh, S and Mohan, V and Radha, V (2013) Genetic association of ADIPOQ gene variants with type 2 diabetes, obesity and serum adiponectin levels in south Indian population. Gene, 532 (2). p. 253. ISSN 03781119

Saxena, R and Saleheen, Danish and Been, L F and Garavito, M L and Braun, T and Bjonnes, A and Young, R and Ho, W K and Rasheed, A and Frossard, Philippe and Sim, Xueling and Hassanali, Neelam and Radha, V and Chidambaram, M and Liju, S and Rees, S D and Ng, D P K and Wong, T Y and Yamauchi, T and Hara, K and Tanaka, Y and Hirose, H and McCarthy, M I and Morris, A P and Basit, Abdul and Barnett, A H and Katulanda, P and Matthews, D R and Mohan, V and Wander, G S and Singh, J R and Mehra, N K and Ralhan, S and Kamboh, M I and Mulvihill, J J and Maegawa, H and Tobe, K and Maeda, S and Cho, Y S and Tai, E S and Kelly, M A and Chambers, J C and Kooner, J S and Kadowaki, T and Deloukas, P and Rader, D J and Danesh, J and Sanghera, D K (2013) Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India. Diabetes, 62 (5). p. 1746. ISSN 0012-1797

Atray, A and Jahnavi, S and Thai, K and Hiremath, P and Anjana, R M and Unnikrishnan, R and Mohan, V and Radha, V (2013) Rabson Mendenhall Syndrome; a case report. Journal of Diabetology, 2 (4). pp. 1-5.

Bodhini, D and Sandhiya, M and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V and Radha, V (2012) Association of His1085HisINSRGene Polymorphism with Type 2 Diabetes in South Indians. Diabetes Technology & Therapeutics, 14 (8). p. 696. ISSN 1520-9156

Anuradha, S and Radha, V and Mohan, V (2011) Association of novel variants in the hepatocyte nuclear factor 4A gene with maturity onset diabetes of the young and early onset type 2 diabetes. Clinical Genetics, 80 (6). pp. 541-549. ISSN 00099163

Bodhini, D and Radha, V and Mohan, V (2011) Association study of IRS1 gene polymorphisms with type 2 diabetes in south Indians. Diabetes technology & therapeutics, 13 (7). pp. 767-72. ISSN 1557-8593

Ramya, K and Radha, V and Ghosh, S and Majumder, P P and Mohan, V (2011) Genetic Variations in theFTOGene Are Associated with Type 2 Diabetes and Obesity in South Indians (CURES-79). Diabetes Technology & Therapeutics, 13 (1). pp. 33-42. ISSN 1520-9156

Kooner, J S and Saleheen, Danish and Sim, Xueling and Sehmi, Joban and Zhang, Weihua and Frossard, Philippe and Been, Latonya F and Chia, Kee-Seng and Dimas, Antigone S and Hassanali, Neelam and Jafar, Tazeen and Jowett, Jeremy B M and Li, Xinzhong and Radha, V and Rees, Simon D and Takeuchi, Fumihiko and Young, Robin and Aung, Tin and Basit, Abdul and Chidambaram, M and Das, Debashish and Grundberg, Elin and Hedman, Å K and Hydrie, Z I and Islam, M and Khor, Chiea-Chuen and Kowlessur, S and Kristensen, M M and Liju, S and Lim, Wei-Yen and Matthews, D R and Liu, J and Morris, A P and Nica, A C and Pinidiyapathirage, J M and Prokopenko, I and Rasheed, A and Samuel, M and Shah, N and Shera, A S and Small, K S and Suo, C and Wickremasinghe, A R and Wong, T Y and Yang, M and Zhang, F and Abecasis, G R and Barnett, A H and Caulfield, M and Deloukas, P and Frayling, T M and Froguel, P and Kato, N and Katulanda, P and Kelly, M A and Liang, J and Mohan, V and Sanghera, D K and Scott, J and Seielstad, M and Zimmet, P Z and Elliott, P and Teo, Y Y and McCarthy, M I and Danesh, J and Tai, E S and Chambers, J C (2011) Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nature Genetics, 43 (10). p. 984. ISSN 1061-4036

Bodhini, D and Radha, V and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V (2011) GLUT4Gene Polymorphisms and Their Association with Type 2 Diabetes in South Indians. Diabetes Technology & Therapeutics, 13 (9). p. 913. ISSN 1520-9156

Bodhini, D and Radha, V and Ghosh, S and Majumder, P P and Mohan, V (2011) Lack of association of PTPN1 gene polymorphisms with type 2 diabetes in south Indians. Journal of genetics, 90 (2). pp. 323-6. ISSN 0973-7731

Mohan, V and Goldhaber-Fiebert, J D and Radha, V and Gokulakrishnan, K (2011) Screening with OGTT alone or in combination with the Indian diabetes risk score or genotyping of TCF7L2 to detect undiagnosed type 2 diabetes in Asian Indians. The Indian journal of medical research, 133 (3). pp. 294-9. ISSN 0971-5916

Vimaleswaran, K S and Radha, V and Ghosh, S and Majumder, P P and Sathyanarayana Rao, M R and Mohan, V (2011) Uncoupling Protein 2and3Gene Polymorphisms and Their Association with Type 2 Diabetes in Asian Indians. Diabetes Technology & Therapeutics, 13 (1). pp. 19-25. ISSN 1520-9156

Bodhini, D and Radha, V and Ghosh, S and Sanapala, K R and Majumder, P P and Rao, M R S and Mohan, V (2010) Association of calpain 10 gene polymorphisms with type 2 diabetes mellitus in Southern Indians. Metabolism . ISSN 00260495 (In Press)

Anuradha, S and Radha, V and Mohan, V (2010) Association of novel variants in the hepatocyte nuclear factor 4A gene with maturity onset diabetes of the young and early onset type 2 diabetes. Clinical Genetics . no. ISSN 00099163 (In Press)

Gayathri, S B and Radha, V and Vimaleswaran, K S and Mohan, V (2010) Association of thePPARGC1AGene Polymorphism With Diabetic Nephropathy in an Asian Indian Population (CURES-41). Metabolic Syndrome and Related Disorders, 8 (2). p. 119. ISSN 1540-4196

Vimaleswaran, K S and Radha, V and Jayapriya, M G and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V (2010) Evidence for an association with type 2 diabetes mellitus at the PPARG locus in a South Indian population. Metabolism, 59 (4). pp. 457-62. ISSN 00260495

Vimaleswaran, K S and Radha, V and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V (2010) A Haplotype at theUCP1Gene Locus Contributes to Genetic Risk for Type 2 Diabetes in Asian Indians (CURES-72). Metabolic Syndrome and Related Disorders, 8 (1). p. 63. ISSN 1540-4196

Chidambaram, M and Radha, V and Mohan, V (2010) Replication of recently described type 2 diabetes gene variants in a South Indian population. Metabolism, 59 (12). p. 1760. ISSN 00260495

Gayathri, S B and Radha, V and Vimaleswaran, K S and Mohan, V (2009) Association of thePPARGC1AGene Polymorphism With Diabetic Nephropathy in an Asian Indian Population (CURES-41). Metabolic Syndrome and Related Disorders . pp. 1-8. ISSN 1540-4196 (In Press)

Vimaleswaran, K S and Radha, V and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V (2009) A Haplotype at theUCP1Gene Locus Contributes to Genetic Risk for Type 2 Diabetes in Asian Indians (CURES-72). Metabolic Syndrome and Related Disorders, 8 (1). pp. 49-54. ISSN 1540-4196

Radha, V and Ek, J and Anuradha, S and Hansen, T and Pedersen, O and Mohan, V (2009) Identification of novel variants in the hepatocyte nuclear factor-1alpha gene in South Indian patients with maturity onset diabetes of young. The Journal of clinical endocrinology and metabolism, 94 (6). pp. 1959-65. ISSN 1945-7197

Vimaleswaran, K S and Radha, V and Ramya, K and Babu, H N S and Savitha, N and Roopa, V and Monalisa, D and Deepa, R and Ghosh, S and Majumder, P P and Rao, M R and Mohan, V (2008) A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics, 123 (6). pp. 599-605. ISSN 0340-6717

Bodhini, D and Radha, V and Dhar, M and NIarayani, N and Mohan, V (2007) The rs12255372(G/T) and rs7903146(C/T) polymorphisms of the TCF7L2 gene are associated with type 2 diabetes mellitus in Asian Indians. Metabolism, 56 (9). pp. 1174-78. ISSN 00260495

Vimaleswaran, K S and Radha, V and Deepa, R and Mohan, V (2007) Absence of Association of Metabolic Syndrome with PPARGC1A, PPARG and UCP1 Gene Polymorphisms in Asian Indians. Metabolic Syndrome and Related Disorders, 5 (2). pp. 153-62. ISSN 1540-4196

Radha, V and Vimaleswaran, K S and Ayyappa, K A and Mohan, V (2007) Association of lipoprotein lipase gene polymorphisms with obesity and type 2 diabetes in an Asian Indian population. International Journal of Obesity, 31 (6). pp. 913-8. ISSN 0307-0565

Bodhini, D and Radha, V and Deepa, R and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V (2007) The G1057D polymorphism of IRS-2 gene and its relationship with obesity in conferring susceptibility to type 2 diabetes in Asian Indians. International journal of obesity (2005), 31 (1). pp. 97-102. ISSN 0307-0565

Mohan, V and Sudha, V and Radhika, G and Radha, V and Rema, M and Deepa, R (2007) Gene-environment interactions and the diabetes epidemic in India. Forum of nutrition, 60 . pp. 118-26. ISSN 1660-0347

Radha, V and Mohan, V (2007) Genetic predisposition to type 2 diabetes among Asian Indians. The Indian journal of medical research, 125 (3). pp. 259-74. ISSN 0971-5916

Radha, V and Vimaleswaran, K S and Babu, S and Deepa, R and Anjana, M and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V (2007) Lack of association between serum adiponectin levels and the Pro12Ala polymorphism in Asian Indians. Diabetic Medicine, 24 (4). pp. 398-402. ISSN 07423071

Ramprasad, S and Radha, V and Mathias, R A and Majumder, P P and Rao, M R S and Rema, M (2007) Rage gene promoter polymorphisms and diabetic retinopathy in a clinic-based population from South India. Eye, 21 (3). pp. 395-401. ISSN 0950-222X

Vimaleswaran, K S and Radha, V and Anjana, M and Deepa, R and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V (2007) Thr394Thr polymorphism of PPARGC1A gene is associated with Type 2 diabetes and total body fat in Asian Indians. International Journal of Obesity, 31 (3). p. 563. ISSN 0307-0565

Radha, V and Mohan, V and Vidya, R and Ashok, A and Deepa, R and Mathias, R A (2006) Association of Lipoprotein Lipase Hind III and Ser 447 Ter Polymorphisms With Dyslipidemia in Asian Indians. The American Journal of Cardiology, 97 (9). p. 1337. ISSN 00029149

Vimaleswaran, K S and Radha, V and Anjana, M and Deepa, R and Ghosh, S and Majumder, P P and Rao, M R S and Mohan, V (2006) Effect of polymorphisms in the PPARGC1A gene on body fat in Asian Indians. International Journal of Obesity, 30 (6). p. 884. ISSN 0307-0565

Vimaleswaran, K S and Radha, V and Mohan, V (2006) Thr54 allele carriers of the Ala54Thr variant of FABP2 gene have associations with metabolic syndrome and hypertriglyceridemia in urban South Indians. Metabolism, 55 (9). pp. 1222-6. ISSN 00260495

Mohan, V and Balasubramanyam, M and Radha, V (2005) Genomics and Proteomics of Type 2 Diabetes in Indians. The Journal of the Association of Physicians of India, 53 (6). pp. 507-509.

Abate, Nicola and Chandalia, M and Satija, P and Adams-Huet, B and Grundy, S M and Sandeep, S and Radha, V and Deepa, R and Mohan, V (2005) ENPP1/PC-1 K121Q polymorphism and genetic susceptibility to type 2 diabetes. Diabetes, 54 (4). pp. 1207-13. ISSN 0012-1797

Mohan, V and Deepa, R and Pradeepa, R and Vimaleswaran, K S and Mohan, A and Velmurugan, K and Radha, V (2005) Association of low adiponectin levels with the metabolic syndrome?the Chennai Urban Rural Epidemiology Study (CURES-4). Metabolism, 54 (4). pp. 476-81. ISSN 00260495

Vimaleswaran, K S and Radha, V and Ghosh, S and Majumder, P P and Deepa, R and Babu, H N S and Rao, M R S and Mohan, V (2005) Peroxisome proliferator-activated receptor-gamma co-activator-1alpha (PGC-1alpha) gene polymorphisms and their relationship to Type 2 diabetes in Asian Indians. Diabetic Medicine, 22 (11). pp. 1516-21. ISSN 0742-3071

Anuradha, S and Radha, V and Deepa, R and Hansen, T and Carstensen, B and Pedersen, O and Mohan, V (2005) 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. Diabetes care, 28 (10). pp. 2430-5. ISSN 0149-5992

Guettier, J M and Georgopoulos, A and Tsai, M Y and Radha, V and Shanthirani, C S and Deepa, R and Gross, M D and Gundu , Rao and Mohan, V (2004) 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. Journal of Clinical Endocrinology & Metabolism, 90 (3). pp. 1705-11. ISSN 0021-972X

Radha, V and Vimaleswaran, K S and Deepa, R and Mohan, V (2003) The genetics of diabetes mellitus. The Indian journal of medical research, 117 . pp. 225-38. ISSN 0971-5916

Radha, V and Rema, M and Mohan, V (2002) Genes and diabetic retinopathy. Indian journal of ophthalmology, 50 (1). pp. 5-11. ISSN 0301-4738

Book Section

Radha, V and Mohan, V (2021) Genomics of Type 2 Diabetes Mellitus and Monogenic Forms of Diabetes. In: Current Trends in Diabetes Focus on South Assians. JAYPEE Brothers, pp. 161-177. ISBN 9789390020171

Radha, V and Mohan, V (2020) Maturity onset Diabetes of the Young. In: RSSDI Textbook of Diabetes Mellitus. JAYPEE Brothers, New Delhi, pp. 169-178. ISBN 9789352702268

Ramya, B and Lovelena , M and Radha, V and Unnikrishnan, R and Mohan, V (2018) Werner Syndrome: A Case Report. In: Diabetes : Clinical Case Series - II. Jaypee Brothers Medical Publishers, p. 153.

Radha, V and Kanthimathi, S and Mohan, V (2015) What is New in Genomic of Maturity-onset Diabetes of the Young and Neonatal Diabetes in India? In: RSSDI Update 2015. Jaypee, New Delhi, pp. 26-32. ISBN 9789352500512

Radha, V and Mohan, V (2008) Genetics of Diabetes – An Overview. In: RSSDI Textbook of Diabetes Mellitus. RSSDI, pp. 367-376.

Radha, V and Mohan, V (2008) Studies on Genetics of diabetes in Ethnic Indians. In: RSSDI Textbook of Diabetes Mellitus. RSSDI, pp. 403-412.

This list was generated on Fri Apr 19 21:45:22 2024 IST.