Author

Kristján Norland

Mayo ClinicORCID 0009-0009-3418-119XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 2

Signature Assays, Organisms & Methods

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Approach:statistical model· 4 Research Focus:GWAS / association mapping· 3 Organism:human· 3 Assay:GWAS summary statistics· 2 Assay:whole-genome sequencing· 2 Research Focus:imputation· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Iftikhar J. KulloiD· 3 shared Daniel J. SchaidiD· 2 shared Jie NaiD· 2 shared Johanna L. SmithiD· 2 shared Abram Bunya KamizaiD· 1 shared Adebowale AdeyemoiD· 1 shared Agnar HelgasoniD· 1 shared Alicia Huerta· 1 shared

Activity by Year

2022-2024 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Iftikhar J. KulloORCID

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Author profile →

4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 5, 2024

Comparative Performance of Polygenic Risk Scores for Atherosclerotic Cardiovascular Disease Subtypes in the All of Us Research Program

Johanna L. Smith, Kristján Norland, Marwan E. Hamed…·Iftikhar J. Kullo

This study evaluates polygenic risk scores (PRS) for ASCVD subtypes across diverse ancestry groups, finding that multi-ancestry and multi-trait PRS perform best, with CHD and AAA scores outperforming IS and PAD.

DOI 10.1101/2024.11.05.24316750

humanwhole-genome sequencing

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Genetic & Genomic MedicineJournal of the American College of CardiologyPeer-reviewedNov 1, 2024

Joint Association of Polygenic Risk and Social Determinants of Health with Coronary Heart Disease in the United States

Kristján Norland, Daniel J. Schaid, Mohammadreza Naderian…·Iftikhar J. Kullo

The paper assesses the joint impact of polygenic risk and social determinants of health on coronary heart disease in the US using the All of Us dataset.

21 citationstop 1%

humanGWAS summary statistics

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GeneticsBioinformaticsPeer-reviewedMar 13, 2024

Admix-kit: An Integrated Toolkit and Pipeline for Genetic Analyses of Admixed Populations

Kangcheng Hou, Stephanie M. Gogarten, Joohyun Kim…·Minxian Wang

Admix-kit provides tools for genetic analysis of admixed populations, enabling simulation, association testing, and polygenic scoring.

23 citationstop 3%

GWAS summary statisticsstatistical model

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GeneticsNaturePeer-reviewedJul 20, 2022

The sequences of 150,119 genomes in the UK biobank

Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore…·Kāri Stefánsson

The paper analyzes whole genome sequences of 150,119 UK Biobank individuals, identifying variants and associations with traits, and provides a haplotype reference panel for imputation.

448 citationstop 1%

humanwhole-genome sequencing

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