Thomas van Overeem Hansen
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Explore the profile of Thomas van Overeem Hansen including associated specialties, affiliations and a list of published articles.
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57
Citations
890
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Recent Articles
1.
Hoj A, Holm-Yildiz S, Krag T, Dejanovic D, Hansen T, Duno M, et al.
JIMD Rep
. 2025 Feb;
66(2):e12469.
PMID: 39950184
Multiple acyl-CoA dehydrogenase deficiency (MADD) is a rare inborn metabolic myopathy affecting fat and protein metabolism. Patients with late-onset MADD typically present with exercise intolerance and muscle weakness. We present...
2.
Stroomberg H, Brasso K, Blak A, Byrjalsen A, Hansen T, Roder A
Prostate Cancer Prostatic Dis
. 2025 Jan;
PMID: 39838196
Background: Men with pathogenic BRCA1/2 variants are at higher risk of prostate cancer We included men with likely pathogenic/pathogenic (LP/P) variants in BRCA1/2 in a prostate-specific antigen (PSA) screening program...
3.
Byrjalsen A, Garcia S, Borgwardt L, Wadt K, Gerdes A, Hansen T
J Gastrointest Oncol
. 2024 Nov;
15(5):2316-2322.
PMID: 39554577
Background: The occurrence of colorectal cancer (CRC) is increasing among young adults, but the etiology is still largely unknown. In addition to germline monogenetic variants also polygenic risk scores (PRS)...
4.
Beck S, Karstensen J, Bulow S, Andersen K, Hansen T, Hojen H, et al.
Am J Gastroenterol
. 2024 Oct;
PMID: 39471488
Introduction: Familial adenomatous polyposis (FAP) is caused by pathogenic variants in the APC gene. FAP is usually categorized according to phenotype: classical FAP (CFAP) and attenuated FAP (AFAP); the latter...
5.
Henriksen K, Hansen T, Wadt K, Schmiegelow K, Foss-Skiftesvik J, Stoltze U
Neurooncol Adv
. 2024 Oct;
6(1):vdae165.
PMID: 39439486
No abstract available.
6.
Byrjalsen A, Stoltze U, Lautrup C, Christensen L, Mikkelsen T, Hjalgrim L, et al.
J Med Genet
. 2024 Sep;
61(11):1023-1025.
PMID: 39317423
No abstract available.
7.
Hammer-Hansen S, Stoltze U, Bartels E, Hansen T, Byrjalsen A, Tybjaerg-Hansen A, et al.
Eur J Hum Genet
. 2024 May;
32(7):846-857.
PMID: 38740897
The care for patients with serious conditions is increasingly guided by genomic medicine, and genomic medicine may equally transform care for healthy individual if genomic population screening is implemented. This...
8.
Barington M, Bak M, Kjartansdottir K, Hansen T, Birkedal U, Ostergaard E, et al.
Am J Med Genet A
. 2024 Apr;
194(8):e63581.
PMID: 38600862
Alu elements are short, interspersed elements located throughout the genome, playing a role in human diversity, and occasionally causing genetic diseases. Here, we report a novel Alu insertion causing Mowat-Wilson...
9.
Stoltze U, Foss-Skiftesvik J, Hansen T, Rasmussen S, Karczewski K, Wadt K, et al.
Nat Commun
. 2024 Feb;
15(1):1881.
PMID: 38424437
Germline pathogenic variants associated with increased childhood mortality must be subject to natural selection. Here, we analyze publicly available germline genetic metadata from 4,574 children with cancer [11 studies; 1,083...
10.
Lord J, Oquendo C, Wai H, Douglas A, Bunyan D, Wang Y, et al.
Hum Genet
. 2024 Jan;
PMID: 38170232
Variants which disrupt splicing are a frequent cause of rare disease that have been under-ascertained clinically. Accurate and efficient methods to predict a variant's impact on splicing are needed to...