• 17562 Citations
  • 70 h-Index
1982 …2019
If you made any changes in Pure, your changes will be visible here soon.

Fingerprint Dive into the research topics where Abhimanyu Garg is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 58 Similar Profiles
Lipodystrophy Medicine & Life Sciences
Congenital Generalized Lipodystrophy Medicine & Life Sciences
Type 2 Diabetes Mellitus Medicine & Life Sciences
Familial Partial Lipodystrophy Medicine & Life Sciences
Dyslipidemias Medicine & Life Sciences
Mutation Medicine & Life Sciences
Lamin Type A Medicine & Life Sciences
Adipose Tissue Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1982 2019

Efficacy of Metreleptin Treatment in Familial Partial Lipodystrophy Due to PPARG vs LMNA Pathogenic Variants

Sekizkardes, H., Cochran, E., Malandrino, N., Garg, A. & Brown, R. J., Jun 19 2019, In : Journal of Clinical Endocrinology and Metabolism. 104, 8, p. 3068-3076 9 p.

Research output: Contribution to journalArticle

Open Access
Familial Partial Lipodystrophy
Leptin
Lipodystrophy
National Institutes of Health (U.S.)
metreleptin
1 Citation (Scopus)
Infiltration
Adipocytes
Esophagus
Mutation
Muscle
3 Citations (Scopus)

Regional Body Fat Changes and Metabolic Complications in Children With Dunnigan Lipodystrophy-Causing LMNA Variants

Patni, N., Li, X., Huet, B. A., Vasandani, C., Gomez-Diaz, R. A. & Garg, A., Apr 1 2019, In : The Journal of clinical endocrinology and metabolism. 104, 4, p. 1099-1108 10 p.

Research output: Contribution to journalArticle

Lamin Type A
Lipodystrophy
Adipose Tissue
Fats
Triglycerides
Micronutrients
Type 2 Diabetes Mellitus
Diet
Food
Carbohydrates
5 Citations (Scopus)

A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation

Hussain, I., Patni, N., Ueda, M., Sorkina, E., Valerio, C. M., Cochran, E., Brown, R. J., Peeden, J., Tikhonovich, Y., Tiulpakov, A., Stender, S. R. S., Klouda, E., Tayeh, M. K., Innis, J. W., Meyer, A., Lal, P., Godoy-Matos, A. F., Teles, M. G., Adams-Huet, B., Rader, D. J. & 3 others, Hegele, R. A., Oral, E. A. & Garg, A., Mar 1 2018, In : The Journal of clinical endocrinology and metabolism. 103, 3, p. 1005-1014 10 p.

Research output: Contribution to journalArticle

Congenital Generalized Lipodystrophy
Lamin Type A
Mutation
Transplants
Progeria