J. Gudmundsson

发表

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24

D. Gudbjartsson, A. Sigurdsson, T. Blondal, 2007, Nature Genetics.

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

Kevin M. Bradley, D. Gudbjartsson, A. Sigurdsson, 2008, Nature Genetics.

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer

D. Gudbjartsson, L. Kiemeney, J. Gulcher, 2007, Nature Genetics.

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

A. Sigurdsson, L. Kiemeney, J. Gulcher, 2008, Nature Genetics.

High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients.

D. Easton, Å. Borg, O. Johannsson, 1996, Cancer research.

Identification of the breast cancer susceptibility gene BRCA2

D. Bentley, A. Ashworth, S. Seal, 1995, Nature.

GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer

M. Daly, L. Kiemeney, K. Stefánsson, 2020, Nature Communications.

Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.

Paolo Vineis, Simonetta Guarrera, Giuseppe Matullo, 2014, Human molecular genetics.

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.

Kari Stefansson, Florian Zink, Gisli Masson, 2017, Blood.

A common variant associated with prostate cancer in European and African populations

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2006, Nature Genetics.

High Prevalence of the 999 del 5 Mutation in Icelandic Breast and Ovarian Cancer Patients 1

D. Easton, Å. Borg, J. Gudmundsson, 2006 .

Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes

D. Gudbjartsson, A. Sigurdsson, T. Blondal, 2007, Nature Genetics.

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

Tony Fletcher, Paolo Vineis, Simonetta Guarrera, 2008, Nature Genetics.

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility

Kari Stefansson, Brian T Helfand, William J Catalona, 2009, Nature Genetics.

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

Kari Stefansson, Brian T Helfand, Gudmar Thorleifsson, 2012, Nature Genetics.

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

Daniel F. Gudbjartsson, Kari Stefansson, Gudmar Thorleifsson, 2008, Nature.

Estimating robustness of the tileShuffle method with repeated probes

D. Gudbjartsson, A. Sigurdsson, K. Stefánsson, 2014, 1403.3028.

A Method for Detecting Long Non-Coding RNAs with Tiled RNA Expression Microarrays

D. Gudbjartsson, A. Sigurdsson, K. Stefánsson, 2014, PloS one.

Genome-wide association study yields variants at 20 p 12 . 2 that associate with urinary bladder cancer

Katja, Gerald, Anne, 2014 .

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2020, Communications Biology.

The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland

J. Gulcher, U. Thorsteinsdóttir, A. Kong, 2006, PLoS medicine.

Identification of the breast cancer susceptibility gene BRCA2

Julian Peto, Peter Devilee, Rosalind Eeles, 1996, Nature.

Frequent Occurrence of BRCA 2 Linkage in Icelandic Breast Cancer Families and Segregation of a Common BRCA 2 Haplotype

J. Gudmundsson, J. Bergthórsson, R. Barkardottir, 2007 .

L. Kiemeney, L. Joosten, M. Netea, 2012 .

The effect of the ATG16L1 Thr300Ala polymorphism on susceptibility and outcome of patients with epithelial cell-derived thyroid carcinoma.

L. Kiemeney, L. Joosten, M. Netea, 2012, Endocrine-related cancer.

A common variant at 8q24.21 is associated with renal cell cancer

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2013, Nature Communications.

Inherited risk of prostate cancer.

L. Kiemeney, J. Gudmundsson, T. Rafner, 2007 .

Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2016, Human molecular genetics.

Loss of heterozygosity on chromosome 9 in human breast cancer: Association with clinical variables and genetic changes at other chromosome regions

A. Sigurdsson, J. Gudmundsson, J. Bergthórsson, 1995, International journal of cancer.

Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations.

J. Gudmundsson, R. Barkardottir, G. Eiriksdottir, 1995, British Journal of Cancer.

Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13.

J. Gudmundsson, R. Barkardottir, G. Johannesdottir, 1995, Cancer research.

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

Bjarni V. Halldórsson, A. Ingason, B. Halldórsson, 2018, Nature Communications.

Loss of heterozygosity at chromosome 7q in human breast cancer: association with clinical variables.

A. Sigurdsson, Á. Kristjánsson, J. Gudmundsson, 1997, Anticancer research.

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

D. Gudbjartsson, A. Sigurdsson, Á. Jónasdóttir, 2008, Nature Genetics.

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

Paolo Vineis, Simonetta Guarrera, Giuseppe Matullo, 2010, Nature Genetics.

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

Paolo Vineis, Giuseppe Matullo, Kari Stefansson, 2009, Nature Genetics.

Loss-of-function variants in ATM confer risk of gastric cancer

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2015, Nature Genetics.

Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus

Clement Adebamowo, Olufunmilayo I. Olopade, Robert Johansson, 2010, PLoS genetics.

Mutations in BRIP1 confer high risk of ovarian cancer

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2011, Nature Genetics.

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

Hannes P. Eggertsson, B. Halldórsson, D. Gudbjartsson, 2020, Communications Biology.

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

D. Gudbjartsson, Á. Jónasdóttir, L. Kiemeney, 2009, Nature Genetics.

Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin

A. Uitterlinden, D. Gudbjartsson, A. Sigurdsson, 2018, Journal of the National Cancer Institute.

Mapping loss of heterozygosity at chromosome 13q: loss at 13q12-q13 is associated with breast tumour progression and poor prognosis.

J. Gudmundsson, B. Agnarsson, R. Barkardottir, 1998, European journal of cancer.

Cross-cancer genome-wide association analysis of lung, ovary, breast, prostate and colon cancer identifies a novel cancer locus at 1q22

Stacey, Ali Amin Al Olama, Nilanjan, 2015 .

Genetic variants associated with platelet count are predictive of human disease and physiological markers

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2021, Communications Biology.

New basal cell carcinoma susceptibility loci

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2015, Nature Communications.

FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease

D. Gudbjartsson, A. Sigurdsson, U. Thorsteinsdóttir, 2020, Nature.

High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutation.

A. Sigurdsson, J. Gudmundsson, B. Agnarsson, 1998, Cancer research.

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.

D. Gudbjartsson, T. Thorgeirsson, L. Kiemeney, 2011, Cancer research.

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

Kari Stefansson, Wei Li, Jon Hrafnkelsson, 2009, Nature Genetics.

Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.

Steven Gallinger, Peter Kraft, Nazneen Rahman, 2016, Cancer research.

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

Bjarni V. Halldórsson, A. Ingason, B. Halldórsson, 2018, Nature Communications.

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

Kari Stefansson, Brian T Helfand, Torben Hansen, 2011, Nature Genetics.

A genome-wide association study yields five novel thyroid cancer risk loci

Sandya Liyanarachchi, Kari Stefansson, Gudmar Thorleifsson, 2017, Nature Communications.

Prostate Cancer in Special Populations

K. Stefánsson, W. Foulkes, J. Gudmundsson, 2010 .

Chromosome 17q-linkage seems to be infrequent in Icelandic families at risk of breast cancer.

A. Jonasdottir, J. Gudmundsson, R. Barkardottir, 1995, Acta oncologica.

Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2018, Nature Genetics.

Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk

Hannes P. Eggertsson, Pall I. Olason, Bjarni V. Halldórsson, 2021, Cancer Research.

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood

D. Gudbjartsson, T. Thorgeirsson, U. Thorsteinsdóttir, 2019, Cancer Epidemiology, Biomarkers & Prevention.

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma

D. Gudbjartsson, Á. Jónasdóttir, U. Thorsteinsdóttir, 2014, Human molecular genetics.

New common variants affecting susceptibility to basal cell carcinoma

D. Gudbjartsson, A. Sigurdsson, T. Blondal, 2009, Nature Genetics.

Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Nature Communications.

A common variant at 8 q 24 . 21 is associated with renal cell cancer

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2017 .

Discovery of common variants associated with low TSH levels and thyroid cancer risk

Kari Stefansson, Gudmar Thorleifsson, Jon Hrafnkelsson, 2012, Nature Genetics.

Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype.

J. Gudmundsson, R. Barkardottir, G. Johannesdottir, 1996, American journal of human genetics.

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

Paolo Vineis, Abbas Ghaderi, Simonetta Guarrera, 2011, Human molecular genetics.

Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2010, Science Translational Medicine.

Assessing thyroid cancer risk using polygenic risk scores

L. Kiemeney, K. Stefánsson, G. Thorleifsson, 2020, Proceedings of the National Academy of Sciences.

Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysis

K. Stefánsson, J. Morrison, P. Sulem, 2009, Cancer Epidemiology, Biomarkers & Prevention.

Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2018, Nature Genetics.

European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables

M. Beckmann, A. Børresen-Dale, D. Birnbaum, 1999, British Journal of Cancer.

National Cancer Institute Prostate Cancer Genetics Workshop.

J. Witte, N. Camp, S. Chanock, 2011, Cancer research.

The effect of SNPs on expression levels in Nimblegen RNA expression microarrays

Gunnar Stefansson, Asgeir Sigurdsson, Kári Stefánsson, 2015, Int. J. Data Min. Bioinform..

Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non‐polyposis colon cancer trait

J. Gudmundsson, J. Bergthórsson, A. Arason, 1995, Clinical genetics.

Mapping of chromosome-3 alterations in human breast-cancer using microsatellite PCR markers - correlation with clinical-variables.

J. Gudmundsson, R. Barkardottir, G. Eiriksdottir, 1995, International journal of oncology.

Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study

H. Stefánsson, E. Sigurdsson, D. Gudbjartsson, 2023, Communications medicine.

Evaluation of Association of HNF1B Variants with Diverse Cancers: Collaborative Analysis of Data from 19 Genome-Wide Association Studies

J. Murabito, M. McCarthy, E. Zeggini, 2010, PloS one.

Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Nature Communications.

The effect of the ATG16L1 Thr300Ala polymorphism on susceptibility and outcome of patients with epithelial cell-derived thyroid carcinoma.

L. Kiemeney, L. Joosten, M. Netea, 2012, Endocrine-related cancer.

Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis

D. Gudbjartsson, T. Thorgeirsson, U. Thorsteinsdóttir, 2023, Nature Genetics.

Actionable Genotypes and Their Association with Life Span in Iceland.

Gudmundur A. Thorisson, Hannes P. Eggertsson, H. Stefánsson, 2023, The New England journal of medicine.

Evaluation of Association of HNF1B Variants with Diverse Cancers: Collaborative Analysis of Data from 19 Genome-Wide Association Studies

Aleksandar, Manal M. Hassan, Shannon M. Lynch, 2010, PloS one.

Variants with Diverse Cancers : Collaborative Analysis of Data from 19 Genome-Wide Association Studies

J. Murabito, E. Zeggini, D. Gudbjartsson, 2010 .

Evaluation of Association of HNF 1 B Variants with Diverse Cancers : Collaborative Analysis of Data from 19 Genome-Wide Association Studies

J. Murabito, E. Zeggini, D. Gudbjartsson, 2010 .

Loss-of-function variants in ATM confer risk of gastric cancer

D. Gudbjartsson, A. Sigurdsson, A. Jonasdottir, 2015, Nature Genetics.