Publications 2022

Strømsvik N, Olsson P, Gravdehaug B, Lurås H, Schlichting E, Jørgensen K, Wangensteen T, Vamre T, Heramb C, Mæhle L, Grindedal EM (2022)
"It was an important part of my treatment": a qualitative study of Norwegian breast Cancer patients' experiences with mainstreamed genetic testing
Hered Cancer Clin Pract, 20 (1), 6
DOI 10.1186/s13053-022-00212-6, PubMed 35123550

Publications 2020

Grindedal EM, Jørgensen K, Olsson P, Gravdehaug B, Lurås H, Schlichting E, Vamre T, Wangensteen T, Heramb C, Mæhle L (2020)
Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway
Fam Cancer, 19 (2), 133-142
DOI 10.1007/s10689-020-00160-x, PubMed 32002722

Publications 2019

Malt EA, Juhasz K, Frengen A, Wangensteen T, Emilsen NM, Hansen B, Agafonov O, Nilsen HL (2019)
Neuropsychiatric phenotype in relation to gene variants in the hemizygous allele in 3q29 deletion carriers: A case series
Mol Genet Genomic Med, 7 (9), e889
DOI 10.1002/mgg3.889, PubMed 31347308

Wangensteen T, Felde CN, Ahmed D, Mæhle L, Ariansen SL (2019)
Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations
Hered Cancer Clin Pract, 17, 14
DOI 10.1186/s13053-019-0113-9, PubMed 31143303

Publications 2018

Heramb C, Wangensteen T, Grindedal EM, Ariansen SL, Lothe S, Heimdal KR, Mæhle L (2018)
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway
Hered Cancer Clin Pract, 16, 3
DOI 10.1186/s13053-017-0085-6, PubMed 29339979

Publications 2013

Wangensteen T, Retterstøl L, Rødningen OK, Hjelmesaeth J, Aukrust P, Halvorsen B (2013)
De novo 19p13.2 microdeletion encompassing the insulin receptor and resistin genes in a patient with obesity and learning disability
Am J Med Genet A, 161A (6), 1480-6
DOI 10.1002/ajmg.a.35927, PubMed 23637016

Publications 2011

Wangensteen T (2011)
Genetic predisposition to obesity: studies of monogenic and complex obesity genes
In Series of dissertations submitted to the Faculty of Medicine, University of Oslo, Unipub, Oslo, no. 1084, 1 b. (flere pag.)
BIBSYS 111580269, ISBN 978-82-8264-122-7

Publications 2010

Wangensteen T, Akselsen H, Holmen J, Undlien D, Retterstøl L (2010)
A common haplotype in NAPEPLD is associated with severe obesity in a Norwegian population-based cohort (the HUNT study)
Obesity (Silver Spring), 19 (3), 612-7
DOI 10.1038/oby.2010.219, PubMed 20885390

Wangensteen T, Egeland T, Akselsen H, Holmen J, Undlien D, Retterstøl L (2010)
FTO genotype and weight gain in obese and normal weight adults from a Norwegian population based cohort (the HUNT study)
Exp Clin Endocrinol Diabetes, 118 (9), 649-52
DOI 10.1055/s-0030-1249636, PubMed 20373279

Publications 2009

Coccia M, Brooks SP, Webb TR, Christodoulou K, Wozniak IO, Murday V, Balicki M, Yee HA, Wangensteen T, Riise R, Saggar AK, Park SM, Kanuga N, Francis PJ, Maher ER, Moore AT, Russell-Eggitt IM, Hardcastle AJ (2009)
X-linked cataract and Nance-Horan syndrome are allelic disorders
Hum Mol Genet, 18 (14), 2643-55
DOI 10.1093/hmg/ddp206, PubMed 19414485

Kolsgaard ML, Wangensteen T, Brunborg C, Joner G, Holven KB, Halvorsen B, Aukrust P, Tonstad S (2009)
Elevated visfatin levels in overweight and obese children and adolescents with metabolic syndrome
Scand J Clin Lab Invest, 69 (8), 858-64
DOI 10.3109/00365510903348677, PubMed 19929281

Wangensteen T, Kolsgaard ML, Mattingsdal M, Joner G, Tonstad S, Undlien D, Retterstol L (2009)
Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway
Exp Clin Endocrinol Diabetes, 117 (6), 266-73
DOI 10.1055/s-0028-1102942, PubMed 19301229

Publications 2008

Kimber W, Peelman F, Prieur X, Wangensteen T, O'Rahilly S, Tavernier J, Farooqi IS (2008)
Functional characterization of naturally occurring pathogenic mutations in the human leptin receptor
Endocrinology, 149 (12), 6043-52
DOI 10.1210/en.2008-0544, PubMed 18703626

Kolsgaard ML, Andersen LF, Tonstad S, Brunborg C, Wangensteen T, Joner G (2008)
Ethnic differences in metabolic syndrome among overweight and obese children and adolescents: the Oslo Adiposity Intervention Study
Acta Paediatr, 97 (11), 1557-63
DOI 10.1111/j.1651-2227.2008.00955.x, PubMed 18657125

Publications 2007

Farooqi IS, Wangensteen T, Collins S, Kimber W, Matarese G, Keogh JM, Lank E, Bottomley B, Lopez-Fernandez J, Ferraz-Amaro I, Dattani MT, Ercan O, Myhre AG, Retterstol L, Stanhope R, Edge JA, McKenzie S, Lessan N, Ghodsi M, De Rosa V, Perna F, Fontana S, Barroso I, Undlien DE, O'Rahilly S (2007)
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor
N Engl J Med, 356 (3), 237-47
DOI 10.1056/NEJMoa063988, PubMed 17229951

Publications 2005

Haas C, Wangensteen T, Giezendanner N, Kratzer A, Bär W (2005)
Y-chromosome STR haplotypes in a population sample from Switzerland (Zurich area)
Forensic Sci Int, 158 (2-3), 213-8
DOI 10.1016/j.forsciint.2005.04.036, PubMed 15964729

Wangensteen T, Undlien D, Tonstad S, Retterstøl L (2005)
[Genetic causes of obesity]
Tidsskr Nor Laegeforen, 125 (22), 3090-3
PubMed 16299561

Publications 2003

Wangensteen T, Nordal G, Hem E, Børdahl PE (2003)
[A watershed in Norwegian obstetrics]
Tidsskr Nor Laegeforen, 123 (24), 3549-52
PubMed 14691497