Simran Samra

5PUBLICATIONS

90CO-AUTHORS

Genetic immunologyEpigenetics (incl. genome methylation and epigenomics)Molecular targetsImmunogenetics (incl. genetic immunology)Computational physiology

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Publications (5)

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|Jun 01, 2026

Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic disease.

|Mar 14, 2026

Combined Long-Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2.

Kiana Rashidi, Bhavi P Modi, Phillip A Richmond

|Sep 19, 2025

Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic disease.

Mehul Sharma, Simran Samra, Yihui Liu

|Jul 31, 2025

ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.

Maggie P Fu, Mehul Sharma, Pariya Yousefi

|May 20, 2025

A multimorphic variant in ThPOK causes an inborn error of immunity with T cell defects and fibrosis.

Maryam Vaseghi-Shanjani, Mehul Sharma, Pariya Yousefi

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Frequent Collaborators

Stuart E Turvey

Mehul Sharma

Pariya Yousefi

Catherine M Biggs

Kate L Del Bel

Bhavi P Modi

Géraldine Blanchard-Rohner

3 joint publications

Wingfield Rehmus

3 joint publications

Liam Golding

3 joint publications

Britt I Drögemöller

Frequent Collaborators

Stuart E Turvey

Mehul Sharma

Pariya Yousefi

Catherine M Biggs