Venu Pullabhatla
Kidlington, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 11 publications
Clinical and analytical validation of an 82-gene comprehensive genome-profiling panel for identifying and interpreting variants responsible for inherited retinal dystrophies.
Journal: PloS one
Published: February 20, 2024
The Th1 cell regulatory circuitry is largely conserved between human and mouse.
Journal: Life science alliance
Published: March 24, 2021
Phase I/II open-label trial of intravenous allogeneic mesenchymal stromal cell therapy in adults with recessive dystrophic epidermolysis bullosa.
Journal: Journal of the American Academy of Dermatology
Published: July 02, 2019
De novo mutations implicate novel genes in systemic lupus erythematosus.
Journal: Human molecular genetics
Published: September 12, 2017
Candidate driver genes involved in genome maintenance and DNA repair in Sézary syndrome.
Journal: Blood
Published: February 11, 2016
Role of retinoic acid in the stability of the T-helper-type 1 lineage and implications for autoimmunity.
Journal: Lancet (London, England)
Published: August 28, 2015
Intraindividual genome expression analysis reveals a specific molecular signature of psoriasis and eczema.
Journal: Science translational medicine
Published: July 11, 2014
An in-depth characterization of the major psoriasis susceptibility locus identifies candidate susceptibility alleles within an HLA-C enhancer element.
Journal: PloS one
Published: April 24, 2013
Rare pathogenic variants in IL36RN underlie a spectrum of psoriasis-associated pustular phenotypes.
Journal: The Journal of investigative dermatology
Published: January 11, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026