Muhammad S. Nawaz
Reykjavik, Iceland
Last Updated: 09/26/2026
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Found 13 publications
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.
Journal: Nature genetics
Published: March 09, 2023
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
Journal: Nature communications
Published: April 28, 2022
Thirty novel sequence variants impacting human intracranial volume.
Journal: Brain communications
Published: April 13, 2022
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.
Journal: Nature communications
Published: December 20, 2021
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.
Journal: Communications biology
Published: May 10, 2021
A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy.
Journal: Scientific reports
Published: August 13, 2020
Large genome-wide association study identifies three novel risk variants for restless legs syndrome.
Large genome-wide association study identifies three novel risk variants for restless legs syndrome.
Journal: Communications biology
Published: May 26, 2020
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming.
Journal: Current biology : CB
Published: December 04, 2019
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
Journal: Translational psychiatry
Published: January 17, 2019
MAP1B mutations cause intellectual disability and extensive white matter deficit.
Journal: Nature communications
Published: February 23, 2018
Rare and Common Variants Conferring Risk of Tooth Agenesis.
Journal: Journal of dental research
Published: January 25, 2018
Last Updated: 09/26/2026