Hanne Jensen
Overview
Explore the profile of Hanne Jensen including associated specialties, affiliations and a list of published articles.
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Articles
62
Citations
657
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Recent Articles
1.
Duelund N, Nisted I, Frederiksen I, Jorgensen M, Heegaard S, Jensen H
Int J Circumpolar Health
. 2024 Sep;
83(1):2403221.
PMID: 39283053
Vision screening during childhood is vital for the early detection and treatment of visual impairment that may significantly impact a child's development and quality of life. This nationwide cross-sectional study...
2.
Duelund N, Nisted I, Jorgensen M, Heegaard S, Jensen H
Acta Ophthalmol
. 2024 Jul;
103(2):162-170.
PMID: 39004821
Purpose: To estimate the prevalence of amblyopia and refractive errors among 6-year-old children in Greenland and to assess the impact of incorporating autorefraction, stereoacuity and near visual acuity testing into...
3.
Kessel L, Jensen H, Larsen A, Rosenberg T, Nissen K
Acta Ophthalmol
. 2024 Apr;
102(7):790-796.
PMID: 38662528
Purpose: The aim of the study was to describe the temporal changes in causes and prevalence of childhood visual impairment in Denmark based on the National Danish Registry of Children...
4.
Christensen L, Jensen H, Kristensen S, Goldinger M, Gjedsted J, Christensen S, et al.
Dan Med J
. 2021 Aug;
68(8).
PMID: 34356015
Introduction: Patients in intensive care units (ICUs) have treatment limited or withdrawn if further treatment is considered futile. This multicentre prospective observational study was part of a European study of...
5.
Jespersgaard C, Bertelsen M, Arif F, Gellert-Kristensen H, Fang M, Jensen H, et al.
Genes (Basel)
. 2020 Dec;
11(12).
PMID: 33353011
Bi-allelic pathogenic variants in cause retinitis pigmentosa (RP). Since deletions of more than one exon have been reported repeatedly for , CNV (copy number variation) analysis of next-generation sequencing (NGS)...
6.
Jespersgaard C, Hey A, Ilginis T, Duelund Hjortshoj T, Fang M, Bertelsen M, et al.
Invest Ophthalmol Vis Sci
. 2020 Feb;
61(2):29.
PMID: 32084271
Purpose: Cone-rod dystrophy (CRD) is a rare hereditary eye disorder that causes progressive degeneration of cone and rod photoreceptors. More than 30 genes, including RAB28, have been associated with CRD;...
7.
Al-Bakri M, Sander B, Bach-Holm D, Larsen D, Jensen H, Kessel L
Acta Ophthalmol
. 2019 Mar;
97(8):778-783.
PMID: 30860655
Background: Children with cataract require frequent monitoring to detect complications, adjust refractive correction and treat amblyopia. This is time consuming for the families. The aim of the study was to...
8.
Jespersgaard C, Fang M, Bertelsen M, Dang X, Jensen H, Chen Y, et al.
Sci Rep
. 2019 Feb;
9(1):1219.
PMID: 30718709
Inherited retinal diseases (IRDs) are a common cause of visual impairment. IRD covers a set of genetically highly heterogeneous disorders with more than 150 genes associated with one or more...
9.
Silva R, Arno G, Cipriani V, Pontikos N, Defoort-Dhellemmes S, Kalhoro A, et al.
Hum Mutat
. 2019 Feb;
40(5):578-587.
PMID: 30710461
The autosomal dominant progressive bifocal chorioretinal atrophy (PBCRA) disease locus has been mapped to chromosome 6q14-16.2 that overlaps the North Carolina macular dystrophy (NCMD) locus MCDR1. NCMD is a nonprogressive...
10.
Xu L, Jensen H, Johnston J, Di Maria E, Kloth K, Cristea I, et al.
Am J Hum Genet
. 2018 Nov;
103(6):976-983.
PMID: 30449416
We have investigated a distinct disorder with progressive corneal neovascularization, keloid formation, chronic skin ulcers, wasting of subcutaneous tissue, flexion contractures of the fingers, and acro-osteolysis. In six affected individuals...