Siddaramappa J. Patil

Bengaluru, KA, India

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 74 publications

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

Journal: Journal of human immunity

Published: April 15, 2026

Isolation and complete genome analysis of Porcine Parvovirus 1 from swine with reproductive failure in southern India.

Isolation and complete genome analysis of Porcine Parvovirus 1 from swine with reproductive failure in southern India.

Journal: Archives of microbiology

Published: November 07, 2025

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

Journal: medRxiv : the preprint server for health sciences

Published: September 19, 2025

Isolation and complete genome analysis of porcine circovirus-1 associated with reproductive failurein swine: foremost study in India.

Isolation and complete genome analysis of porcine circovirus-1 associated with reproductive failurein swine: foremost study in India.

Journal: Archives of microbiology

Published: July 30, 2025

Spatial Modeling of Anthrax Risk in India's Agro-Climatic Zones: A Future Perspective.

Spatial Modeling of Anthrax Risk in India's Agro-Climatic Zones: A Future Perspective.

Journal: Acta tropica

Published: July 18, 2025

Exploring the diagnostic utility of recombinant low molecular weight cystic fluid proteins, Ag2 and Ag2V1, for serosurveillance of porcine cysticercosis.

Exploring the diagnostic utility of recombinant low molecular weight cystic fluid proteins, Ag2 and Ag2V1, for serosurveillance of porcine cysticercosis.

Journal: Experimental parasitology

Published: July 02, 2025

Tetralogy of Fallot and craniosynostosis - differential manifestation in a familial case of CHDED syndrome caused by novel pathogenic PRKD1 variant.

Tetralogy of Fallot and craniosynostosis - differential manifestation in a familial case of CHDED syndrome caused by novel pathogenic PRKD1 variant.

Journal: Journal of human genetics

Published: May 28, 2025

Development of an enzyme immunoassay employing low molecular weight recombinant Ag1 and Ag1V1 proteins of cystic fluid for the serodiagnosis of porcine cysticercosis.

Development of an enzyme immunoassay employing low molecular weight recombinant Ag1 and Ag1V1 proteins of cystic fluid for the serodiagnosis of porcine cysticercosis.

Journal: Veterinary parasitology

Published: March 14, 2025

Gene expression meta-analysis identifies novel pathways of the avian influenza virus disease.

Gene expression meta-analysis identifies novel pathways of the avian influenza virus disease.

Journal: Journal of biomolecular structure & dynamics

Published: November 27, 2024

Identification of molecular and cellular infection response biomarkers associated with anthrax infection through comparative analysis of gene expression data.

Identification of molecular and cellular infection response biomarkers associated with anthrax infection through comparative analysis of gene expression data.

Journal: Computers in biology and medicine

Published: July 25, 2024

Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population.

Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population.

Journal: American journal of medical genetics. Part A

Published: July 06, 2024

Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia.

Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia.

Journal: European journal of human genetics : EJHG

Published: July 01, 2024

Showing 1-12 of 74

Last Updated: 09/26/2026