Gerald Sulem
Reykjavik, Iceland
Last Updated: 09/26/2026
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Found 9 publications
Sequence variants associating with urinary biomarkers.
Journal: Human molecular genetics
Published: September 06, 2018
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis.
Journal: Nature genetics
Published: February 14, 2018
A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease.
Journal: Nature communications
Published: January 29, 2018
Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
Journal: Nature genetics
Published: July 28, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters.
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters.
Journal: BMC medical genetics
Published: June 20, 2017
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA.
Journal: BMC medical genetics
Published: March 10, 2017
Epigenetic and genetic components of height regulation.
Journal: Nature communications
Published: April 28, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Journal: Nature communications
Published: June 15, 2015
Showing 1-9 of 9
Last Updated: 09/26/2026