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A case report of an atypical severe case of skin picking disorder managed by a multidisciplinary team

BMC psychiatry, 2024-03, Vol.24 (1), p.238-238, Article 238

2024

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Atypical Neuropsychiatric Presentation of FTD-ALS Caused by a Pathogenic Repeat Expansion in C9orf72: A Case Report

Journal of geriatric psychiatry and neurology, 2024-03, Vol.37 (2), p.157-162

2024

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Germline mutations in MAP3K6 are associated with familial gastric cancer

PLoS genetics, 2014-10, Vol.10 (10), p.e1004669-e1004669

2014

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Individual consent in cluster randomised trials for non-pharmaceutical interventions: going beyond the Ottawa statement

Critical public health, 2024-12, Vol.34 (1), p.1-9

2024

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Focused chemical genomics using zebrafish xenotransplantation as a pre-clinical therapeutic platform for T-cell acute lymphoblastic leukemia

Haematologica (Roma), 2015-01, Vol.100 (1), p.70-76

2015

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Letter to the editor regarding "Covid-19 transmission in fitness centers in Norway - a randomized trial"

BMC public health, 2022-12, Vol.22 (1), p.2433-2433, Article 2433

2022

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Stroke survival and the impact of geographic proximity to family members: A population-based cohort study

Social science & medicine (1982), 2022-09, Vol.309, p.115252-115252, Article 115252

2022

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Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations

JAMA ophthalmology, 2014-12, Vol.132 (12), p.1393

2014

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Geographical variation in cardiovascular disease mortality in Norway: The role of life course socioeconomic position and parental health

Health & place, 2023-09, Vol.83, p.103095-103095, Article 103095

2023

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Feeding Practices and Dietary Diversity in the First Year of Life: PreventADALL, a Scandinavian Randomized Controlled Trial and Birth Cohort Study

The Journal of nutrition, 2023-08, Vol.153 (8), p.2463-2471

2023

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Associations between having breakfast and reading literacy achievement among Nordic primary school students

Education Inquiry, 2024-04, Vol.ahead-of-print (ahead-of-print), p.1-13

2024

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Adherence to a healthy and potentially sustainable Nordic diet is associated with child development in The Norwegian Mother, Father and Child Cohort Study (MoBa)

Nutrition journal, 2022-07, Vol.21 (1), p.1-46, Article 46

2022

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The yeast oxysterol binding protein Kes1 maintains sphingolipid levels

PloS one, 2013-04, Vol.8 (4), p.e60485-e60485

2013

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Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome

Nature genetics, 2011-04, Vol.43 (4), p.360-364

2011

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Evaluation of Skin Prick Test Reading Time at 10 versus 15 min in Young Infants

International archives of allergy and immunology, 2022-08, Vol.183 (8), p.824-834

2022

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Localization of lipid raft proteins to the plasma membrane is a major function of the phospholipid transfer protein Sec14

PloS one, 2013-01, Vol.8 (1), p.e55388

2013

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Fetal thoracic circumference in mid‐pregnancy and infant lung function

Pediatric pulmonology, 2023-01, Vol.58 (1), p.35-45

2023

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Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia

Pediatric blood & cancer, 2016-07, Vol.63 (7), p.1307-1309

2016

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Lipid Binding Requirements for Oxysterol-binding Protein Kes1 Inhibition of Autophagy and Endosome-trans-Golgi Trafficking Pathways

The Journal of biological chemistry, 2010-10, Vol.285 (44), p.33875-33884

2010

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Polygenic risk score-analysis of thromboembolism in patients with acute lymphoblastic leukemia

Thrombosis research, 2020-12, Vol.196, p.15-20

2020

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Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort

European journal of endocrinology, 2018-12, Vol.179 (6), p.363-372

2018

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Genetic counselling for the prevention of mental health consequences of cannabis use: A randomized controlled trial‐within‐cohort

Early intervention in psychiatry, 2021-10, Vol.15 (5), p.1306-1314

2021

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Postmenopausal osteoporosis is a musculoskeletal disease with a common genetic trait which responds to strength training: a translational intervention study

Therapeutic advances in musculoskeletal disease, 2020, Vol.12, p.1759720X20929443-1759720X20929443

2020

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Infant lung function and maternal physical activity in the first half of pregnancy

ERJ open research, 2022-10, Vol.8 (4), p.172

2022

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A case report of an atypical severe case of skin picking disorder managed by a multidisciplinary team

Atypical Neuropsychiatric Presentation of FTD-ALS Caused by a Pathogenic Repeat Expansion in C9orf72: A Case Report

Germline mutations in MAP3K6 are associated with familial gastric cancer

Individual consent in cluster randomised trials for non-pharmaceutical interventions: going beyond the Ottawa statement

Focused chemical genomics using zebrafish xenotransplantation as a pre-clinical therapeutic platform for T-cell acute lymphoblastic leukemia

Letter to the editor regarding "Covid-19 transmission in fitness centers in Norway - a randomized trial"

Stroke survival and the impact of geographic proximity to family members: A population-based cohort study

Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations

Geographical variation in cardiovascular disease mortality in Norway: The role of life course socioeconomic position and parental health

Feeding Practices and Dietary Diversity in the First Year of Life: PreventADALL, a Scandinavian Randomized Controlled Trial and Birth Cohort Study

Associations between having breakfast and reading literacy achievement among Nordic primary school students

Adherence to a healthy and potentially sustainable Nordic diet is associated with child development in The Norwegian Mother, Father and Child Cohort Study (MoBa)

A multicenter randomized trial for quality of life evaluation by non-invasive intelligent tools during post-curative treatment follow-up for head and neck cancer: Clinical study protocol

The yeast oxysterol binding protein Kes1 maintains sphingolipid levels

Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome

Evaluation of Skin Prick Test Reading Time at 10 versus 15 min in Young Infants

Localization of lipid raft proteins to the plasma membrane is a major function of the phospholipid transfer protein Sec14

Fetal thoracic circumference in mid‐pregnancy and infant lung function

Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia

Lipid Binding Requirements for Oxysterol-binding Protein Kes1 Inhibition of Autophagy and Endosome-trans-Golgi Trafficking Pathways

Polygenic risk score-analysis of thromboembolism in patients with acute lymphoblastic leukemia

Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort

Genetic counselling for the prevention of mental health consequences of cannabis use: A randomized controlled trial‐within‐cohort

Postmenopausal osteoporosis is a musculoskeletal disease with a common genetic trait which responds to strength training: a translational intervention study

Infant lung function and maternal physical activity in the first half of pregnancy

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