L A Larsen
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Explore the profile of L A Larsen including associated specialties, affiliations and a list of published articles.
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40
Citations
373
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Recent Articles
1.
Kjaersgaard Andersen R, Clemmensen S, Larsen L, Hjelmborg J, Odum N, Jemec G, et al.
Br J Dermatol
. 2021 Jul;
186(1):78-85.
PMID: 34289077
Background: Hidradenitis suppurativa (HS) is a recurrent inflammatory skin disease that, apart from rare causative loss-of-function mutations, has a widely unknown genetic aetiology. Objectives: To estimate the relative importance of...
2.
Koefoed K, Skat-Rordam J, Andersen P, Warzecha C, Pye M, Andersen T, et al.
Sci Rep
. 2018 Jun;
8(1):9542.
PMID: 29934521
Smad ubiquitin regulatory factor 1 (SMURF1) is a HECT-type E3 ubiquitin ligase that plays a critical role in vertebrate development by regulating planar cell polarity (PCP) signaling and convergent extension...
3.
Joergensen T, Christensen K, Lindholt J, Larsen L, Green A, Houlind K
Eur J Vasc Endovasc Surg
. 2016 Apr;
52(1):41-6.
PMID: 27107486
Objective: First degree relatives of patients with abdominal aortic aneurysm (AAA) have an increased risk of developing AAA; however, despite intensive investigation, the specific genetic factors involved in the development...
4.
Andersen P, Larsen L, Fowler Jr V, Stegger M, Skov R, Christensen K
Eur J Clin Microbiol Infect Dis
. 2013 May;
32(10):1321-6.
PMID: 23657294
Staphylococcus aureus is a human commensal bacterium found in the nasal cavity and other body sites. Identifying risk factors for S. aureus nasal carriage is of interest, as nasal carriage...
5.
Brudzewsky D, Pedersen A, Claesson M, Gad M, Kristensen N, Lage K, et al.
Scand J Immunol
. 2009 Jun;
69(5):437-46.
PMID: 19508375
Inflammatory bowel disease (IBD) is a multifactorial disorder with an unknown aetiology. The aim of this study is to employ a murine model of IBD to identify pathways and genes,...
6.
Erdogan F, Larsen L, Zhang L, Tumer Z, Tommerup N, Chen W, et al.
J Med Genet
. 2008 Aug;
45(11):704-9.
PMID: 18713793
Background: Congenital heart disease (CHD) is the most common birth defect and affects nearly 1% of newborns. The aetiology of CHD is largely unknown and only a small percentage can...
7.
Buysse K, Crepel A, Menten B, Pattyn F, Antonacci F, Veltman J, et al.
J Med Genet
. 2008 Jul;
45(10):672-8.
PMID: 18628311
Background: Recent molecular studies of breakpoints of recurrent chromosome rearrangements revealed the role of genomic architecture in their formation. In particular, segmental duplications representing blocks of >1 kb with >90%...
8.
Erdogan F, Belloso J, Gabau E, Ajbro K, Guitart M, Ropers H, et al.
Eur J Med Genet
. 2007 Nov;
51(1):81-6.
PMID: 17998172
In this study we report a female patient with an interstitial duplication of a region (10q22-q23) which is rarely reported in the literature. We fine mapped the aberration with array...
9.
Tumer Z, Henriksen A, Bache I, Brixen K, Kalscheuer V, Kalschauer V, et al.
Am J Med Genet A
. 2005 May;
135(3):339-41.
PMID: 15887263
No abstract available.
10.
Boonen S, Stahl D, Kreiborg S, Rosenberg T, Kalscheuer V, Larsen L, et al.
Am J Med Genet A
. 2005 Feb;
132A(3):324-8.
PMID: 15690381
Basal cell nevus syndrome (Gorlin syndrome) is an autosomal dominant disorder characterized by the presence of multiple basal cell carcinomas (BCC), odontogenic keratocysts, palmoplantar pits, and calcification in the falx...