Researcher profile · Semantic Scholar

H. U. Møller

h-index: 17
Works: 51
Citations: 1,743

Most-cited papers

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance
Max A. Tischfield, H. Baris, Chen Wu, G. Rudolph +45 more
2010Cell594 citations Open access
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IC3D Classification of Corneal Dystrophies—Edition 2
J. Weiss, H. U. Møller, Anthony J. Aldave, B. Seitz +12 more
2015Cornea429 citations Open access
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von Hippel-Lindau disease: Updated guideline for diagnosis and surveillance.
M. L. Binderup, M. Smerdel, Line Borgwadt, S. Beck-Nielsen +27 more
2022European Journal of Medical Genetics117 citations Open access
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Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition.
M. L. Binderup, M. Bisgaard, Vibeke Harbud, H. U. Møller +11 more
2013Danish Medical Journal63 citations
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Assignment of Granular Corneal Dystrophy Groenouw Type I (CDGG1) to Chromosome 5q
H. Eiberg, H. U. Møller, I. Berendt, J. Mohr
1994European Journal of Human Genetics50 citations
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Von Hippel-Lindau disease (vHL)
M. L. Binderup, S. Bisgaard, Vibeke Harbud, H. U. Møller +11 more
201349 citations
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Retinal hemangioblastoma: prevalence, incidence and frequency of underlying von Hippel-Lindau disease
M. L. Binderup, Anne-Sophie Stendell, Michael Galanakis, H. U. Møller +2 more
2017British Journal of Ophthalmology48 citations
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Inter‐familial variability and intra‐familial similarities of granular corneal dystrophy Groenouw type I with respect to biomicroscopical appearance and symptomatology
H. U. Møller
1989Acta ophthalmologica38 citations
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Eye features in 3 Danish patients with Multi Systemic Smooth Muscle Dysfunction Syndrome
H. U. Møller, H. Fledelius, D. Milewicz, E. Regalado +1 more
2012British Journal of Ophthalmology34 citations Open access
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Granular corneal dystrophy Groenouw type I
H. U. Møller, A. Ridgway
1990Acta ophthalmologica28 citations
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Pathology and pathomechanisms of epithelial microcystic and basement membrane abnormalities of the cornea
N. Ehlers, H. U. Møller
1988Acta ophthalmologica26 citations
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TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy
M. Whitman, B. Barry, C. Robson, F. Facio +32 more
2021Human Genetics24 citations Open access
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von Hippel-Lindau disease: Surveillance strategy for endolymphatic sac tumors
M. L. M. Poulsen, S. Gimsing, M. Kostel-janetz, H. U. Møller +3 more
2011Genetics in Medicine23 citations Open access
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Granular corneal dystrophy Groenouw type I (Grl) and Reis‐Bücklers' corneal dystrophy (R‐B) One Entity?
H. U. Møller
1989Acta ophthalmologica22 citations
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Granular corneal dystrophy Groenouw type I: Clinical aspects and treatment
H. U. Møller
1990Acta ophthalmologica20 citations
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Familial Benign Recurrent Cranial Nerve Palsies
J. G. Klee, H. U. Møller
198419 citations Open access
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Dot‐Map‐Fingerprint Dystrophy—Cogan's Microcystic Dystrophy—Normal reactions of The Corneal Epithelium?
N. Ehlers, H. U. Møller
1987Acta Ophthalmologica, Supplementum18 citations
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Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata
A. Bisgaard, Leif Normann Rasmussen, H. U. Møller, M. Kirchhoff +1 more
2007Clinical Dysmorphology17 citations
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Dystrophy: a revised definition.
M. Warburg, H. U. Møller
1989Journal of Medical Genetics17 citations Open access
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Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene
H. U. Møller, A. Ridgway
200014 citations
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An unusual presentation of Smith-Magenis syndrome with iris dysgenesis.
A. Barnicoat, H. U. Møller, R. Palmer, I. Russell-Eggitt +1 more
1996Clinical Dysmorphology14 citations
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Genetics of granular dystrophy.
A. Ridgway, H. U. Møller
1992Ophthalmology (Rochester, Minn.)14 citations Open access
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Granular corneal dystrophy Groenouw type I 115 Danish patients
H. U. Møller
1990Acta ophthalmologica14 citations
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Early treatment of granular dystrophy (Groenouw type I)
H. U. Møller, N. Ehlers
1985Acta ophthalmologica13 citations
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Recessively inherited, simple optic atrophy--does it exist?
H. U. Møller
1992Ophthalmic Paediatrics and Genetics9 citations
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Excessive myopia and glaucoma.
H. U. Møller
1948Acta ophthalmologica9 citations
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Corneal deposits associated with flecainide.
H. U. Møller, K. Thygesen, P. Kruit
1991British medical journal7 citations Open access
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Prevalence of corneal dystrophies in the United States: estimates from claims data.
H. U. Møller, L. Sunde
2013Investigative Ophthalmology and Visual Science5 citations
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Is Tadpole Pupil in an Adolescent Girl Caused by Denervation Hypersensitivity?
J. Hansen, H. U. Møller
2017Neuropediatrics4 citations
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Linkage relations of the locus for granular corneal dystrophy Groenouw type I with 35 polymorphic systems
H. U. Møller, H. Eiberg, T. Kruse
1989Acta ophthalmologica4 citations
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Diagnosis of tumours in anterior and middle cranial fossae.
M. Bardram, H. U. Møller
1952Acta ophthalmologica4 citations
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FAMILIAL ANGIOMATOSIS RETINÆ ET CEREBELLI — LINDAU'S DISEASE
H. U. Møller
20092 citations
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Groenouw's Granular Corneal Dystrophy I
H. U. Møller
19872 citations
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[Corneal erosions aggravated by local anesthetic eye-drops].
H. U. Møller, N. Ahrendt
1983Ugeskrift for læger2 citations
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[Diagnosis, monitoring and treatment of tuberous sclerosis complex].
M. Reinhard, L. Sunde, M. Madsen, B. N. Andersen +15 more
2019Ugeskrift for læger1 citations
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The Corneal Dystrophies-Does the Literature Clarify or Confuse?
J. Weiss, H. U. Møller, W. Lisch
2018American journal of ophthalmology-glaucoma1 citations
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DARK VISION IN GLAUCOMA
H. U. Møller
20091 citations
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[Follow-up study of patients after eye enucleation].
H. U. Møller
1983Ugeskrift for læger1 citations
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[Applicability of nebacetin in ophthalmology].
B. Lawaetz, H. U. Møller, G. Österberg
1953Ugeskrift for læger1 citations
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Therapeutic value of nebacetin in ophthalmology.
B. Lawaetz, H. U. Møller, G. Osterberg
1953American journal of ophthalmology-glaucoma1 citations
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[Idiopathic intracranial hypertension is a rare cause of headache in children].
A. Viuff, J. Hansen, H. U. Møller
2013Ugeskrift for læger0 citations
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Vibeke Harbud, The Danish association for von Hippel-Lindau patients and their relatives
M. L. Binderup, M. Bisgaard, Vibeke Harbud, H. U. Møller +9 more
20130 citations
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Genotype of lattice corneal dystrophy (R124C mutation in TGFBI) in a patient presenting with features of Avellino corneal dystrophy.
W. Lisch, H. U. Møller
2011Cornea0 citations
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[Von Hippel-Lindau disease--a multidisciplinary, underdiagnosed condition].
H. U. Møller
1999Ugeskrift for læger0 citations
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In honour of Mette Warburg
H. Jensen, H. U. Møller
19960 citations
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[Von Hippel-Lindau disease. A condition requiring multidisciplinary efforts].
H. U. Møller, P. Frimodt-Møller, J. Haase, U. Dyreborg
1986Ugeskrift for læger0 citations
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[Occlusion of the central retinal artery with scintigraphic demonstration of the source of emboli in the aorta].
H. U. Møller, D. Marushak, J. Rasmussen, K. Schmidt
1983Ugeskrift for læger0 citations
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[Iatrogenic tarsorrhaphy with cyanoacrylate].
H. U. Møller, D. Marushak
1983Ugeskrift for læger0 citations
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About Farvesans Survey
H. U. Møller
19470 citations
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TRANSACTIONS OF THE OPHTHALMOLOGICAL SOCIETY OF COPENHAGEN
H. U. Møller
19300 citations
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S. Gimsing

×4

U. Knigge×4

L. Bøgeskov×4

P. Bagi×4

M. Bisgaard×4

C. Thomsen×4

W. Lisch×3

T. van Overeem Hansen×3