Patrick Sulem
Reykjavik, Iceland
Last Updated: 09/26/2026
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Found 229 publications
Resistant Hypertension Variants Link to Hyperaldosteronism and Potassium Levels.
Journal: Hypertension (Dallas, Tex. : 1979)
Published: July 09, 2026
Congenital insensitivity to pain caused by a novel SCN9A-genotype
Journal: Laeknabladid
Published: May 27, 2026
WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.
Journal: Clinical genetics
Published: January 06, 2026
Sequence Diversity Lost in Early Pregnancy.
Journal: Obstetrical & gynecological survey
Published: November 25, 2025
Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.
Journal: American journal of medical genetics. Part A
Published: October 14, 2025
The genetic architecture of fibromyalgia across 2.5 million individuals.
Journal: medRxiv : the preprint server for health sciences
Published: September 26, 2025
The genetic architecture of fibromyalgia across 2.5 million individuals.
Journal: Nature medicine
Published: September 18, 2025
Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication.
Journal: Biological psychiatry global open science
Published: August 19, 2025
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.
Journal: Nature genetics
Published: June 02, 2025
A novel spliceosomopathy caused by de novo SF3B3 variants.
Journal: Genome medicine
Published: April 26, 2025
Last Updated: 09/26/2026