Viðar Ö Eðvarðsson (Vidar O Edvardsson)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 6

Top Topics

Dna Methylation

Urinary Incontinence

Top Venues

The Journal of urology

European journal of human genetics : EJHG

Pediatric nephrology (Berlin, Germany)

This page only lists publications with an associated author ORCID identifier.

Publications

Anders Breinbjerg, Cecilie Siggaard Jørgensen, G Bragi Walters, Jakob Grove, Thomas Damm Als, Konstantinos Kamperis, Lilja Stéfansdóttir, Janne P Thirstrup, Britt Borg, Clara Albiñana, Bjarni Johann Vilhjalmsson, Viðar Ö Eðvarðsson, Hreinn Stefánsson, Preben Bo Mortensen, Esben Agerbo, Thomas M Werge, Anders Dupont Børglum, Ditte Demontis, Kári Stefánsson, Søren Rittig, Jane Hvarregaard Christensen
Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study. The Journal of urology (2024)
Anders Breinbjerg, Cecilie Siggaard Jørgensen, G Bragi Walters, Jakob Grove, Thomas Damm Als, Konstantinos Kamperis, Lilja Stéfansdóttir, Janne P Thirstrup, Britt Borg, Clara Albiñana, Bjarni Johann Vilhjalmsson, Viðar Ö Eðvarðsson, Hreinn Stefánsson, Preben Bo Mortensen, Esben Agerbo, Thomas M Werge, Anders Dupont Børglum, Ditte Demontis, Kári Stefánsson, Søren Rittig, Jane Hvarregaard Christensen
Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study. The Journal of urology (2024)
Anders Breinbjerg, Cecilie Siggaard Jørgensen, G Bragi Walters, Jakob Grove, Thomas Damm Als, Konstantinos Kamperis, Lilja Stéfansdóttir, Janne P Thirstrup, Britt Borg, Clara Albiñana, Bjarni Johann Vilhjalmsson, Viðar Ö Eðvarðsson, Hreinn Stefánsson, Preben Bo Mortensen, Esben Agerbo, Thomas M Werge, Anders Dupont Børglum, Ditte Demontis, Kári Stefánsson, Søren Rittig, Jane Hvarregaard Christensen
Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study. The Journal of urology (2024)
Hrafnhildur L Runolfsdottir, John Andrew Sayer, Olafur S Indridason, Viðar Ö Eðvarðsson, Brynjar O Jensson, Gudny Anna Arnadottir, Sigurjon A Gudjonsson, Run Fridriksdottir, Hildigunnur Katrinardottir, Daniel Gudbjartsson, Unnur Thorsteinsdottir, Patrick Sulem, Kari Stefansson, Runolfur Palsson
Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency. European journal of human genetics : EJHG 29 (7) (2021)
Solborg E Ingvarsdottir, Olafur Skuli Indridason, Runolfur Palsson, Viðar Ö Eðvarðsson
Stone recurrence among childhood kidney stone formers: results of a nationwide study in Iceland. Urolithiasis 48 (5) (2020)
Hrafnhildur Linnet Runolfsdottir, Runolfur Palsson, Inger MSch Agustsdottir, Olafur S Indridason, Viðar Ö Eðvarðsson
Long-term renal outcomes of APRT deficiency presenting in childhood. Pediatric nephrology (Berlin, Germany) 34 (3) (2018)