Rashida Anwar

Leeds, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 10 publications

Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A) cause a primary immunodeficiency disorder.

Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A) cause a primary immunodeficiency disorder.

Journal: eLife

Published: July 27, 2021

Novel Case of Tripeptidyl Peptidase 2 Deficiency Associated with Mild Clinical Phenotype.

Novel Case of Tripeptidyl Peptidase 2 Deficiency Associated with Mild Clinical Phenotype.

Journal: Journal of clinical immunology

Published: July 15, 2020

Germline TET2 loss of function causes childhood immunodeficiency and lymphoma.

Germline TET2 loss of function causes childhood immunodeficiency and lymphoma.

Journal: Blood

Published: March 17, 2020

Predicting the Occurrence of Variants in RAG1 and RAG2.

Predicting the Occurrence of Variants in RAG1 and RAG2.

Journal: Journal of clinical immunology

Published: September 25, 2018

A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype.

A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype.

Journal: Journal of clinical immunology

Published: September 05, 2018

A Case of Adult-Onset Still's Disease Caused by a Novel Splicing Mutation in TNFAIP3 Successfully Treated With Tocilizumab.

A Case of Adult-Onset Still's Disease Caused by a Novel Splicing Mutation in TNFAIP3 Successfully Treated With Tocilizumab.

Journal: Frontiers in immunology

Published: March 21, 2018

Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency.

Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency.

Journal: The Journal of allergy and clinical immunology

Published: October 18, 2017

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy.

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy.

Journal: Journal of clinical immunology

Published: May 18, 2016

An observational study on the expression levels of MDM2 and MDMX proteins, and associated effects on P53 in a series of human liposarcomas.

An observational study on the expression levels of MDM2 and MDMX proteins, and associated effects on P53 in a series of human liposarcomas.

Journal: BMC clinical pathology

Published: July 25, 2013

Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype.

Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype.

Journal: PloS one

Published: April 05, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026