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Acid suppression does not change respiratory symptoms in children with asthma and gastro-oesophageal reflux disease

Archives of disease in childhood, 2005-09, Vol.90 (9), p.956-960

2005

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

Natural hazards and earth system sciences, 2010-02, Vol.10 (2), p.407-420

2010

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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

Journal of medical genetics, 2006-11, Vol.43 (11), p.856-862

2006

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

American journal of human genetics, 1996-04, Vol.58 (4), p.749-756

1996

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

Translational psychiatry, 2017-04, Vol.7 (4), p.e1109-e1109

2017

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

Cancer research (Chicago, Ill.), 1996-08, Vol.56 (16), p.3663-3665

1996

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

Cancer research (Chicago, Ill.), 1995-11, Vol.55 (21), p.4830-4832

1995

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Mortality among masons in Iceland

British Journal of Industrial Medicine, 1986-08, Vol.43 (8), p.522-525

1986

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Mortality and Cancer Incidence among Marine Engineers and Machinists in Iceland

Scandinavian Journal of Work, Environment ＆ Health, 1988-06, Vol.14 (3), p.197-200

1988

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Gastroesophageal reflux disease in children: Association between symptoms and pH monitoring

Scandinavian journal of gastroenterology, 2005-06, Vol.40 (6), p.636-640

2005

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Deletions on Chromosome 4 in Sporadic and BRCA Mutated Tumors and Association with Pathological Variables

Anticancer research, 2004-09, Vol.24 (5A), p.2681-2687

2004

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Chromosome 17q-Linkage Seems to be Infrequent in Icelandic Families at Risk of Breast Cancer

Acta oncologica, 1995, Vol.34 (5), p.657-662

1995

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P0997 PH‐MONITORING AND SYMPTOMS OF GASTROESOPHAGEAL REFLUX IN 7–16 YEAR OLD CHILDREN

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (S1), p.S436-S436

2004

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P1010 SYMPTOMS OF GASTROESOPHAGEAL REFLUX ARE PREVALENT IN CHILDHOOD ASTHMA

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (S1), p.S441-S442

2004

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P1010 SYMPTOMS OF GASTROESOPHAGEAL REFLUX ARE PREVALENT IN CHILDHOOD ASTHMA

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (Supplement 1), p.S441-S442

2004

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P0997 PH-MONITORING AND SYMPTOMS OF GASTROESOPHAGEAL REFLUX IN 7???16 YEAR OLD CHILDREN

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (Supplement 1), p.S436

2004

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

Human genetics, 2000-10, Vol.107 (4), p.372-375

2000

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

Oncogene, 1998-01, Vol.16 (1), p.21-26

1998

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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

Human mutation, 1998, Vol.11 (S1), p.S195-S197

1998

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

Cancer research (Chicago, Ill.), 1998-10, Vol.58 (19), p.4421-4425

1998

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OMEPRAZOLE AND ASTHMA OUTCOME IN CHILDREN WITH ASTHMA AND GASTROESOPHAGEAL REFLUX DISEASE: A RANDOMISED CONTROL TRIAL

Journal of pediatric gastroenterology and nutrition, 2005-05, Vol.40 (5), p.659-659

2005

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OMEPRAZOLE AND ASTHMA OUTCOME IN CHILDREN WITH ASTHMA AND GASTROESOPHAGEAL REFLUX DISEASE: A RANDOMISED CONTROL TRIAL: PG4‐14

Journal of pediatric gastroenterology and nutrition, 2005-05, Vol.40 (5), p.659-659

2005

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OMEPRAZOLE AND ASTHMA OUTCOME IN CHILDREN WITH ASTHMA AND GASTROESOPHAGEAL REFLUX DISEASE: A RANDOMISED CONTROL TRIAL: PG4-14

Journal of pediatric gastroenterology and nutrition, 2005-05, Vol.40 (5), p.659

2005

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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

Human mutation, 1998, Vol.Suppl 1, p.S195-S197

1998

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

European journal of cancer (1990), 1998-12, Vol.34 (13), p.2076-2081

1998

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Acid suppression does not change respiratory symptoms in children with asthma and gastro-oesophageal reflux disease

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

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

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

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

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

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

Mortality among masons in Iceland

Mortality and Cancer Incidence among Marine Engineers and Machinists in Iceland

Gastroesophageal reflux disease in children: Association between symptoms and pH monitoring

Deletions on Chromosome 4 in Sporadic and BRCA Mutated Tumors and Association with Pathological Variables

Chromosome 17q-Linkage Seems to be Infrequent in Icelandic Families at Risk of Breast Cancer

P0997 PH‐MONITORING AND SYMPTOMS OF GASTROESOPHAGEAL REFLUX IN 7–16 YEAR OLD CHILDREN

P1010 SYMPTOMS OF GASTROESOPHAGEAL REFLUX ARE PREVALENT IN CHILDHOOD ASTHMA

P1010 SYMPTOMS OF GASTROESOPHAGEAL REFLUX ARE PREVALENT IN CHILDHOOD ASTHMA

P0997 PH-MONITORING AND SYMPTOMS OF GASTROESOPHAGEAL REFLUX IN 7???16 YEAR OLD CHILDREN

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

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

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

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

OMEPRAZOLE AND ASTHMA OUTCOME IN CHILDREN WITH ASTHMA AND GASTROESOPHAGEAL REFLUX DISEASE: A RANDOMISED CONTROL TRIAL

OMEPRAZOLE AND ASTHMA OUTCOME IN CHILDREN WITH ASTHMA AND GASTROESOPHAGEAL REFLUX DISEASE: A RANDOMISED CONTROL TRIAL: PG4‐14

OMEPRAZOLE AND ASTHMA OUTCOME IN CHILDREN WITH ASTHMA AND GASTROESOPHAGEAL REFLUX DISEASE: A RANDOMISED CONTROL TRIAL: PG4-14

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

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

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