[Psychosocial aspects of presymptomatic testing for genetic diseases]

Renal manifestations of tuberous sclerosis complex: patients' and parents' knowledge and routines for renal follow-up - a questionnaire study.

BMC nephrology·2018

Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1.

Clinical genetics·2015

15q11.2 microdeletion - seven new patients with delayed development and/or behavioural problems.

European journal of medical genetics·2010

Low frequency of VHL germline mutations in Norwegian patients presenting with isolated central nervous system hemangioblastomas--a population-based study.

Acta neurologica Scandinavica·2009

Somatic mutations of KIT in familial testicular germ cell tumours.

British journal of cancer·2004

The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer.

European journal of cancer (Oxford, England : 1990)·2003

Perspectives on the use of coercion in highly specialised rehabilitation: a focus group study.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2026

Occupational injuries treated at Oslo A&E - a prospective study.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2026

Cross-reactivity in cashew nut allergy.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2026

Correction: Shared and condition-associated gut microbiota alterations in older adults with depression and constipation: evidence from the American Gut Project.

Frontiers in microbiology·2026

Clinically altered brain activity may not look like aged brain activity: Implications for brain-age modeling and biomarker strategies.

Alzheimer's & dementia (New York, N. Y.)·2026

Research progress and application prospects of multi-omics integration strategies in precision risk stratification of type 1 diabetes mellitus.

Frontiers in immunology·2026

Investigating the causal impact of gut microbiota on periodontitis based on Mendelian randomization, bulk transcriptomics, and single-cell transcriptomics.

Frontiers in cell and developmental biology·2026

Partitioned blood pressure polygenic risk reveals differential genetic effects of tissue-specific enhancers and their interactions on cardiovascular disease.

Research square·2026

Enhanced chromatin compaction is associated with de novo expression of a nuclear microprotein, global loss of H3 acetylation and local transcriptional changes in retinal rod photoreceptors.

Research square·2026

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[Psychosocial aspects of presymptomatic testing for genetic diseases]

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Renal manifestations of tuberous sclerosis complex: patients' and parents' knowledge and routines for renal follow-up - a questionnaire study.

Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1.

15q11.2 microdeletion - seven new patients with delayed development and/or behavioural problems.

Low frequency of VHL germline mutations in Norwegian patients presenting with isolated central nervous system hemangioblastomas--a population-based study.

Somatic mutations of KIT in familial testicular germ cell tumours.

The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer.

Perspectives on the use of coercion in highly specialised rehabilitation: a focus group study.

Occupational injuries treated at Oslo A&E - a prospective study.

Cross-reactivity in cashew nut allergy.

Correction: Shared and condition-associated gut microbiota alterations in older adults with depression and constipation: evidence from the American Gut Project.

Clinically altered brain activity may not look like aged brain activity: Implications for brain-age modeling and biomarker strategies.

Research progress and application prospects of multi-omics integration strategies in precision risk stratification of type 1 diabetes mellitus.

Investigating the causal impact of gut microbiota on periodontitis based on Mendelian randomization, bulk transcriptomics, and single-cell transcriptomics.

Partitioned blood pressure polygenic risk reveals differential genetic effects of tissue-specific enhancers and their interactions on cardiovascular disease.

Enhanced chromatin compaction is associated with de novo expression of a nuclear microprotein, global loss of H3 acetylation and local transcriptional changes in retinal rod photoreceptors.

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