Anil K. Agarwal - Concepedia

Author

Anil K. Agarwal

The University of Texas Southwestern Medical Center ORCID

Also Known As

A Agarwal, A K Agarwal, A. Agarwal, A. K. AGARWAL, A. K. Agarwal, A.K. Agarwal, ANIL KUMAR AGARWAL, Agarwal, A., Agarwal, Anil Kumar, Anil Agarwal

173

Publications

9.5K

Citations

H-Index

139

Concepts

All Affiliations

The University of Texas Southwestern Medical Center Southwestern Medical Center Pediatrics and Genetics Population Council

About

Anil K. Agarwal is an author at The University of Texas Southwestern Medical Center specializing in medicine, biochemistry, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	36	4K
2	Health Sciences	8	8	528
3	Engineering	4	4	147
4	Education	1	1	22
5	Language Studies	1	1	16

Anil K. Agarwal

Publications

7.6K

Citations

H-Index

Page 1

	Year	Citations
Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase Tomoatsu Mune, Fraser M. Rogerson, Heli Nikkilä, Nature Genetics HypertensionSodium HomeostasisMedicinePhysiologyKidney Isozyme	1995	623
The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology Kimberly M. Szymanski, Derk D. Binns, René Bartz, Proceedings of the National Academy of Sciences Proteinlipid InteractionGeneticsMolecular GeneticsYeast SeipinProtein Folding	2007	612
AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34 Anil K. Agarwal, Elif Arioǧlu, Salomé de Almeida, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseCongenital Generalized Lipodystrophy	2002	516
Cloning and Expression of Rat cDNA Encoding Corticosteroid 11β-Dehydrogenase Anil K. Agarwal, Carl Monder, Benjamin Eckstein, Journal of Biological Chemistry GeneticsGlucocorticoidCellular PhysiologyOxidative StressNodg Gene	1989	452
Seipin is required for converting nascent to mature lipid droplets Huajin Wang, Michel Becuwe, Benjamin E. Housden, eLife	2016	392
Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia Anil K. Agarwal Human Molecular Genetics	2003	390
PSMB8 Encoding the β5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome Anil K. Agarwal, Chao Xing, George Demartino, The American Journal of Human Genetics Panniculitis-induced Lipodystrophy SyndromeProtein FunctionDisease MechanismMedicineNatural Sciences	2010	327
A Novel Heterozygous Mutation in Peroxisome Proliferator-Activated Receptor-γ Gene in a Patient with Familial Partial Lipodystrophy Anil K. Agarwal, Abhimanyu Garg The Journal of Clinical Endocrinology & Metabolism	2002	267
Phenotypic and Genetic Heterogeneity in Congenital Generalized Lipodystrophy Anil K. Agarwal, Vinaya Simha, Elif A Oral, The Journal of Clinical Endocrinology & Metabolism	2003	242
Molecular Mechanisms of Hepatic Steatosis and Insulin Resistance in the AGPAT2-Deficient Mouse Model of Congenital Generalized Lipodystrophy Vı́ctor Cortés, David E. Curtis, Suja Sukumaran, Cell Metabolism Insulin ResistanceObesityMetabolic SyndromeAgpat2-deficient Mouse ModelMetabolic Disorder	2009	223

Page 1