Muhammad Sulaman Nawaz

7PUBLICATIONS
49CO-AUTHORS
Condensed matter imagingGene mappingPainAboriginal and Torres Strait Islander and disabilityNeurology and neuromuscular diseases
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Publications (7)

|Apr 28, 2022
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.

Gyda Bjornsdottir, Lilja Stefansdottir, Gudmar Thorleifsson

|Mar 25, 2022
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.

Astros Th Skuladottir, Gyda Bjornsdottir, Egil Ferkingstad

|Feb 03, 2022
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.

Gyda Bjornsdottir, Lilja Stefansdottir, Gudmar Thorleifsson

|Oct 08, 2021
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.

Astros Th Skuladottir, Gyda Bjornsdottir, Muhammad Sulaman Nawaz

|Nov 26, 2020
Large genome-wide association study identifies three novel risk variants for restless legs syndrome.

Maria Didriksen, Muhammad Sulaman Nawaz, Joseph Dowsett

|Oct 19, 2019
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.

Olafur O Gudmundsson, G Bragi Walters, Andres Ingason

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