G. Johannesdottir

发表

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

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

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

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

Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus.

E. Gillanders, D. Stephan, H. Grönberg, 2000, Proceedings of the National Academy of Sciences of the United States of America.

High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriers

B. Agnarsson, R. Barkardottir, G. Eiriksdottir, 1998, Oncogene.

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 .

The BRCA1 c.4096+3A>G Variant Displays Classical Characteristics of Pathogenic BRCA1 Mutations in Hereditary Breast and Ovarian Cancers, But Still Allows Homozygous Viability

B. Agnarsson, R. Barkardottir, I. Reynisdottir, 2019, Genes.

Identification of a novel splice‐site mutation of the BRCA1 gene in two breast cancer families: Screening reveals low frequency in Icelandic breast cancer patients

A. Jonasdottir, Å. Borg, J. Bergthórsson, 1998, Human mutation.

Crisis Coordination and Communication During the 2010 Eyjafjallajökull Eruption

G. Johannesdottir, Deanne Bird, G. Gísladóttir, 2017 .

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

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

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.

Chromosome 5 imbalance mapping in breast tumors from BRCA1 and BRCA2 mutation carriers and sporadic breast tumors

Å. Borg, B. Agnarsson, R. Barkardottir, 2006, International journal of cancer.

High expression of ZNF703 independent of amplification indicates worse prognosis in patients with luminal B breast cancer

M. Ringnér, Å. Borg, O. Johannsson, 2013, Cancer medicine.

Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies

J. Kere, L. Aaltonen, P. Møller, 2006, Journal of Medical Genetics.

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.

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

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

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

D Brandeis, M Brammer, H. Stefánsson, 2017, Translational Psychiatry.

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.

Deletions on chromosome 4 in sporadic and BRCA mutated tumors and association with pathological variables.

Å. Borg, H. Olsson, B. Agnarsson, 2004, Anticancer Research.

Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families

E. Gillanders, P. Møller, Å. Borg, 2010, Breast Cancer Research.

Evidence against PALB2 involvement in Icelandic breast cancer susceptibility

E. Gillanders, B. Agnarsson, R. Barkardottir, 2008, Journal of Negative Results in Biomedicine.

People living under threat of volcanic hazard in southern Iceland: vulnerability and risk perception

G. Jóhannesdóttir, Guðrún Gísladóttir, G. Johannesdottir, 2010 .

Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer

E. Gillanders, J. Trent, J. Bergthórsson, 2000, Human Genetics.

Climate change and settlement level impacts

I. Kelman, R. McLeman, G. Johannesdottir, 2016 .