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MONOGENIC DIABETES
REGISTRY OF INDIA

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  Monogenic Diabetes Publications
 
  1. Patil O, Ravikumar KG, Gopi S, Raman T, Radha V, Mohan V. Thiamine-Responsive Megaloblastic Anemia syndrome: A case Report. Journal of Diabetology, 2019, DOJ: 10.4103/jod.jod_51_18.

  2. Roy K, Satapathy AK, Houhton JAL, Flanagan SE, Radha V, Mohan V, Sharma R, Jain V.Congenital Hyperinsulinemic Hypoglycemia and Hyperammonemia due to Pathogenic Variants in GLUD1.Indian J Pediatr. 2019 May 22. doi: 10.1007/s12098-019-02980-x.

  3. Balamurugan K, Kavitha B, Yang Z, Mohan V, Radha V, Shyng SL (2019) Functional characterization of activating mutations in the sulfonylurea receptor 1 (ABCC8) causing neonatal diabetes mellitus in Asian Indian children. Pediatr Diabetes. 20(4):397-407. doi: 10.1111/pedi.12843.

  4. Mohan V, Radha V, Nguyen TT, Stawiski EW, Pahuja KB, Goldstein LD, Tom J, Anjana RM, Kong-Beltran M, Bhangale T, Jahnavi S, Chandni R, Gayathri V, et al. Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India. BMC Med Genet. 2018, 19(1):22. doi: 10.1186/s12881-018-0528-6.

  5. Radha V, Ramya B,  Gopi S, Kavitha B, Preetika S, Kalpana T, Unnikrishnan R, Mohan V, Gupta PK. Successful transition to sulphonylurea therapy from insulin in a child with permanent neonatal diabetes due to a KCNJ11 gene mutation. J. of Diabetology, 2018, 9:65-7.

  6. Radha V, Mohan V. Genetic basis of monogenic diabetes. Current Science, 2017, 113(7), 1277-1286.
  7. Mukherjee S, Rastogi A, Radha V, Gopi S, Mohan V, Bhansali A. An infant with diabetes mellitus: Is it always T1DM? Diabetes Res Clin Pract.2017, 125:62-64.

  8. Jain V, Satapathy A, Yadav J, Sharma R, Radha V, Mohan V, De Franco E, Ellard S. Clinical and Molecular Characterization of Children with Neonatal Diabetes Mellitus at a Tertiary Care Center in Northern India. Indian Pediatr. 2017, 15;54(6):467-471.

  9. Balamurugan K, Bjørkhaug L, Mahajan S, Kanthimathi S, Njølstad PR, Srinivasan N, Mohan V, Radha V. Structure - Function studies of HNF1A (MODY3) gene mutations in South Indian patients with monogenic diabetes. Clin Genet. 2016, 90(6):486-495.. doi: 10.1111/cge.12757.

  10. Kanthimathi S, Balamurugan K, Shanthi Rani CS, Gayathri V, Mohan V, Radha V. Identification and Functional Characterization of Hepatocyte Nuclear Factor -1B (MODY 5) Gene Mutations in Indian Diabetic Patients with Renal Abnormalities, Annals of Human Genetics, 2015, 79(1):10-9.

  11. Radha V, Kanthimathi S, Mohan V. What is New in Genomics of Maturity-onset Diabetes of the Young and Neonatal Diabetes in India?  (Chapter 81) RSSDI Annual Conference Update-2015.

  12. Radha V, Bodhini D, Kanthimathi S, Mohan V. Genomics of diabetes in clinical care today (Chapter 13). Advances in Diabetes-Novel Insight (Sridhar R, ed), Jaypee Brothers Medical Publishers Private Limited, 2015, Page 150-171.

  13. Kanthimathi S, Jahnavi S, Balamurugan K, Ranjani H,  Sonya J,  Goswami S,  Chowdhury S,  Mohan V, Radha V. Glucokinase gene mutations (mody2) in Asian Indians. Diabetes Technol Ther. 2014, 16(3):180-185.

  14. Jahnavi S, Poovazhagi V, Kanthimathi S, Balamurugan K, Bodhini D,  Jaivinder Y, Vandana J, Khadgawat R, Jevalikar G, Mahuya S, Bhavatharini A, Dass AK, Kaur T, Mohan V, Radha V. Novel ABCC8 (SUR1) gene mutations in Asian Indian children with Congenital hyperinsulinemic hypoglycemia. Annals of Human Genetics,2014, 78: 311–319.

  15. Varadarajan P, Ananthanarayanan K, Mirna K, Suresh J, Venkatesan R, Mohan V. Clinical Profile and Outcome of Persistent Hyperinsulinemic Hypoglycemia of Infancy. Pediatric Oncall, 2013: 50(8):759-63.

  16. Jahnavi S, Poovazhagi V, Mohan V, Radha V. Neonatal Diabetes and Hyperinsulinemia: The Indian experience. Journal of Neonatology, 2013, 27(2):15-23.

  17. Jahnavi S, Poovazhagi V, Mohan V, Bodhini D, Raghupathy P, Amutha A, Kumar PS, Adhikari P, Shriraam M, Tanvir K, Das A, Molnes J, Njolstad P, Unnikrishnan R, Radha V. Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children. Clin Genet. 2013, 83: 439-445.

  18. Jahnavi S, Poovazhagi V, Kanthimathi S, Gayathri V, Mohan V, Radha V. EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott Rallison syndrome. Pediatric Diabetes, 2013,  15(4):313-318.

  19. Poovazhagi V, Sangaralingam T, Senniappan S, Jahnavi S, Radha V, Mohan V. Clinical Presentation and Long Term Outcome of 40 children with Infantile Onset Diabetes Mellitus in South India. Indian Pediatrics, February 05, 2013 [E-Pub ahead of print].

  20. Atray A, Jahnavi S,  Thai K, Hiremath P, Anjana RM, Unnikrishnan R, Mohan V, Radha V. Rabson Mendenhall Syndrome; a case report. Journal of Diabetology, 2:4.

  21. Poovazhagi V, Shanthi S, Jahnavi S, Radha V, Mohan V. Berardinelli Seip congenital lipodystrophy presenting with neonatal diabetes mellitus due to a mutation in the AGPAT2 gene. Int J Diabetes Dev Ctries. 2012, DOI 10.1007/s13410-012-0099-6.

  22. Mohan V. Type 2 diabetes can also be multigenerational like MODY. International Journal of Diabetes in Developing Countries. 2011;31: 125 – 127.

  23. Anuradha S, Radha V, Mohan V. Association of novel variants in the hepatocyte nuclear factor 4A gene with maturity onset diabetes of the young and early onset type 2 diabetes. Clin Genet. 2010, 80:541-549.

  24. Radha V, Ek J, Anuradha S, Hansen T,Pedersen O, Mohan V. Identification of novel variants in the hepatocyte nuclear factor 1 alpha gene  in South Indian patients with maturity onset diabetes of young. J Clin Endocrine & Metabolism, 2009, 94(6), 1959-1965.

  25. Mohan V, Ami Ritesh Sanghvi. Monogenic Forms of Diabetes Mellitus and Maturity Onset Diabetes of Young (MODY).  In: RSSDI Textbook of Diabetes Mellitus. 2nd edition.  Tripathy BB, Chandalia HB, Das AK, Rao PV, Madhu SV, Mohan V, RSSDI, 2008;p.393-402.

  26. Anuradha S, Radha V, Deepa R, Hansen T, Carstensen B, Pederson O, Mohan V.A prevalent amino acid polymorphism at Codon 98 (Ala98Val) of the Hepatocyte Nuclear Factor-1A is associated with maturity onset diabetes of the young and younger age at onset of Type 2 diabetes in Asian Indians.  Diabetes Care 2005, 28; 2430-2435.

  27. Premalatha G, Rema M, Mohan V. MODY- Maturity onset diabetes of youth – Monogenic diabetes mellitus.  In: RSSDI Textbook of Diabetes Mellitus.  Ahuja MMS, Tripathy BB, Sam G.P.Moses, Chandalia HB,  Das AK, Rao PV, Madhu SV.  Research Society for the study of Diabetes in India, Hyderabad. 2002;p.163-167.

  28. McCarthy MI, Hitchins M, Hitman GA, Cassell P, Hawrami K, Morton N, Mohan V, Ramachandran A,  Snehalatha C, Viswanathan M.  Positive association in the absence of linkage suggests a minor role for the glucokinase in the pathogenesis type 2 (non insulin dependent) diabetes mellitus amongst South Indians. Diabetologia. 1993;36:633-641.

  29. Hitman GA, Kambo PK, Viswanathan M, Mohan V.  An analysis of amplified insulin gene products in diabetics of Indian origin.  Journal of Medical Genetics. 1991;28:97-100.

  30. Mohan V, Ramachandran A, Snehalatha C, Viswanathan M.  Maturity onset diabetes of the young in Asian Indians. In: Proceedings of the German Society for Internal Medicine (Ed), Pfieffer EF, Bergmann Veriag JF, Munchen, 1988;p.505-509.

  31. Mohan V, Sharp PS, Aber VR, Mather HM,  Kohner EM.  Insulin resistance in maturity onset diabetes of the young.  Diabetes and Metabolism.  1987;13:193-197.

  32. Mohan V, Snehalatha C, Ramachandran A, Viswanathan M.  Abnormalities in insulin secretion in healthy offspring of Indian patients with maturity onset diabetes of the young.  Diabetes Care.  1986;9:53.

  33. Mohan V, Snehalatha C, Ramachandran A, Jayashree R, Viswanathan M.  C-peptide responses to glucose load in maturity onset diabetes of the young (MODY). Diabetes Care. 1985;8:69-72.

  34. Mohan V, Ramachandran A, Snehalatha C, Rema M, Bharani G, Viswanathan M.  High prevalence of maturity onset diabetes of the young (MODY) among Indians.  Diabetes Care.   1985;8:374-374.
 
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