Abhimanyu Garg

20PUBLICATIONS
22CO-AUTHORS
Medical virologyMedical infection agents (incl. prions)Medical biochemistry - lipidsGene mappingDevelopmental genetics (incl. sex determination)
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Publications (20)

|Aug 05, 2026
Emery-Dreifuss muscular dystrophy and familial partial lipodystrophy, Dunnigan variety due to heterozygous LMNA variants.

|Feb 26, 2026
Genotype-phenotype heterogeneity among patients with lipodystrophy harboring rare POLD1 variants.

Fieke W Hoff, Chao Xing, Chun-Yuan Huang

|May 28, 2025
Clinical Features, Metabolic and Autoimmune Derangements in Acquired Partial Lipodystrophy (Barraquer-Simons Syndrome).

Chatchon Kaewkrasaesin, Michael Hwang, Chandna Vasandani

|May 14, 2025
Novel and Ultrarare Heterozygous Missense LMNA Variants Causing Familial Partial Lipodystrophy.

Anum, Xilong Li, Abhimanyu Garg

|Mar 13, 2025
Efficacy and Safety of Obeticholic Acid for Treating Hepatic Steatosis in Patients With Familial Partial Lipodystrophy.

Abhimanyu Garg, Chandna Vasandani, Xilong Li

|Dec 09, 2024
Gain of Function NOTCH3 Variants Cause Familial Partial Lipodystrophy Due to Activation of Senescence Pathways.

Abhimanyu Garg, Chao Xing, Anil K Agarwal

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Frequent Collaborators

3 joint publications

Fieke W Hoff

3 joint publications

Chandna Vasandani

2 joint publications

Rebecca J Brown

1 joint publications

Anum