Samiha S. Shaikh
Cambridge, ENG, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Letter: Further nuanced data on the role of P2RX7 SNPs in chronic pain states.
Journal: The journal of pain
Published: July 09, 2024
Midfacial toddler excoriation syndrome (MiTES): case series, diagnostic criteria and evidence for a pathogenic mechanism.
Journal: The British journal of dermatology
Published: November 15, 2023
Evidence of a genetic background predisposing to complex regional pain syndrome type 1.
Journal: Journal of medical genetics
Published: February 23, 2023
Phenotypic manifestation of α-synuclein strains derived from Parkinson's disease and multiple system atrophy in human dopaminergic neurons.
Journal: Nature communications
Published: April 22, 2020
A third HSAN5 mutation disrupts the nerve growth factor furin cleavage site.
Journal: Molecular pain
Published: October 10, 2018
Before progressing from "exomes" to "genomes"… don't forget splicing variants.
Journal: European journal of human genetics : EJHG
Published: October 16, 2017
A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV).
Journal: Human mutation
Published: April 29, 2016
Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception.
Journal: Nature genetics
Published: July 30, 2015
A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development.
Journal: Brain : a journal of neurology
Published: January 09, 2015
Transcriptional regulator PRDM12 is essential for human pain perception.
Journal: Nature genetics
Published: September 29, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026