Manage settings
MENU
About this site
In het Nederlands
Home
Researchers
Projects
Organisations
Publications
Contact
Research Explorer
Your browser does not support JavaScript or JavaScript is not enabled. Without JavaScript some functions of this webapplication may be disabled or cause error messages. To enable JavaScript, please consult the manual of your browser or contact your system administrator.
Researcher
Françoise Meire
Profile
Projects
Publications
Activities
91
Results
2020
Exome-based panel testing as an efficient method to diagnose the highly heterogeneous ocular disorder spectrum Microphthalmia, Anophthalmia, Coloboma and Anterior Segment Dysgenesis (MAC-ASD)
Hannah Verdin
Toon Rosseel
Philippe Kestelyn
Françoise Meire
Julie Van De Velde
Olivier Vanakker
Tom Sante
Frauke Coppieters
Bart Leroy
Elfride De Baere
C3
Conference
2020
2012
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness
Bart Leroy
Elfride De Baere
Françoise Meire
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2012
2011
Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes
Françoise Meire
Björn Menten
Elfride De Baere
A1
Journal Article
in
MOLECULAR VISION
2011
2008
Corneal opacities in the Hallermann-Streiff syndrome
Françoise Meire
A1
Journal Article
in
OPHTHALMIC GENETICS
2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome
Diane Beysen
Sarah De Jaegere
Françoise Meire
Bart Leroy
Anne De Paepe
Elfride De Baere
A1
Journal Article
in
HUMAN MUTATION
2008
2007
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy
Françoise Meire
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
2007
Orbital myositis in a child with linear scleroderma en coup de sabre
Françoise Meire
A1
Journal Article
in
JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS
2007
2006
Chiasmal misrouting and foveal hypoplasia without albinism
Françoise Meire
A1
Journal Article
in
BRITISH JOURNAL OF OPHTHALMOLOGY
2006
Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosis
Bart Leroy
Elfride De Baere
Françoise Meire
A1
Journal Article
in
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
2006
The key role of electrophysiology in the diagnosis of visually impaired children
Françoise Meire
A1
Journal Article
in
ACTA OPHTHALMOLOGICA SCANDINAVICA
2006
2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in Blepharophimosis syndrome
Diane Beysen
Jeroen Raes
Bart Leroy
Françoise Meire
Ludwine Messiaen
Yves Van de Peer
Anne De Paepe
Elfride De Baere
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2005
Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa
Françoise Meire
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
2005
Identification of mutations in the CRB1, RPE65, RETGC1, AIPL1, and RPGRIP1 genes in a cohort of 38 patients with juvenile retinitis pigmentosa
Françoise Meire
C3
Conference
2005
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram
Françoise Meire
A1
Journal Article
in
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
2005
2004
A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy
Françoise Meire
A1
Journal Article
in
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
2004
Centrale en perifere neurologische toxiciteit door metronidazol
Françoise Meire
Bart Leroy
Jan De Bleecker
A2
Journal Article
in
TIJDSCHRIFT VOOR NEUROLOGIE EN NEUROCHIRURGIE
2004
Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: A syndrome caused by a missense mutation in OPA1
Françoise Meire
A1
Journal Article
in
AMERICAN JOURNAL OF OPHTHALMOLOGY
2004
Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly
Françoise Meire
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
2004
2003
Corneal deposits after the topical use of ofloxacin in two children with vernal keratoconjunctivitis
Ilse Claerhout
Philippe Kestelyn
Françoise Meire
Jean Paul Remon
Tineke Decaestecker
Jan Van Bocxlaer
A1
Journal Article
in
BRITISH JOURNAL OF OPHTHALMOLOGY
2003
FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation
Elfride De Baere
Diane Beysen
Petra De Sutter
Bart Leroy
Françoise Meire
Anne De Paepe
Ludwine Messiaen
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2003
Psammomatoid ossifyine fibroma of the ethmoid
Kristof Vandekerckhove
Françoise Meire
A4
Journal Article
in
BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE
2003
2002
Novel insights in genotype-phenotype correlations in BPES through in-depth FOXL2 mutation analysis
Elfride De Baere
Diane Beysen
Petra De Sutter
Bart Leroy
Françoise Meire
Anne De Paepe
Ludwine Messiaen
C3
Conference
2002
Symptomatic pineal cysts: clinical manifestations and management
Yves Benoit
Françoise Meire
Jacques Caemaert
A1
Journal Article
in
ACTA NEUROCHIRURGICA
2002
2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.
Françoise Meire
Rudy Van Coster
A1
Journal Article
in
ARCHIVES OF NEUROLOGY
2001
Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis.
Françoise Meire
A1
Journal Article
in
THROMBOSIS AND HAEMOSTASIS
2001
Imaging studies in the diagnostic workup of neonatal nasal obstruction.
Bart Vanzieleghem
Marc Lemmerling
Hubert Vermeersch
Ingeborg Dhooge
Françoise Meire
Geert Mortier
Juliaan Leroy
Marc Kunnen
A1
Journal Article
in
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY
2001
Ophthalmologic and systemic features of the Alström syndrome: report of 9 cases
Françoise Meire
A4
Journal Article
in
BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE
2001
Spectrum and distribution of FOXL2 gene mutations and variants in BPES, POF and XX male patients: tentative genotype-phenotype correlation
Elfride De Baere
Bart Leroy
Geert Mortier
Françoise Meire
Anne De Paepe
Ludwine Messiaen
C3
Conference
2001
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation
Elfride De Baere
Bart Leroy
Geert Mortier
Françoise Meire
Anne De Paepe
Ludwine Messiaen
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
2001
2000
Indocyanine green angiography in Sorsby's fundus dystrophy.
Bart Lafaut
Jean Delaey
Françoise Meire
A1
Journal Article
in
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
2000
Lenticonus
Françoise Meire
A4
Journal Article
in
BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE
2000
Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.
Françoise Meire
A1
Journal Article
in
JOURNAL OF NEUROLOGY
2000
Prevalence of AIPL1 mutations in inherited retinal degenerative disease
Bart Leroy
Françoise Meire
A1
Journal Article
in
MOLECULAR GENETICS AND METABOLISM
2000
Sorsby fundus dystrophy without a mutation in the TIMP-3 gene.
Françoise Meire
A1
Journal Article
in
BRITISH JOURNAL OF OPHTHALMOLOGY
2000
Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophy.
Françoise Meire
A2
Journal Article
in
OPHTHALMIC GENETICS
2000
Use of mitomycin C and r-tPA for the management of conjunctival membrane and cataracts in a child with conjunctivitis lignosa.
Françoise Meire
Ilse Claerhout
Philippe Kestelyn
A1
Journal Article
in
BRITISH JOURNAL OF OPHTHALMOLOGY
2000
1999
Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.
Françoise Meire
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
1999
Vasoproliferative retinal tumors associated with peripheral chorioretinal scars in presumed congenital toxoplasmosis.
Françoise Meire
Jean Delaey
A1
Journal Article
in
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
1999
1998
A puzzling case: conjunctivitis lignosa ?
Françoise Meire
Michel Hanssens
Jean Delaey
A2
Journal Article
in
Bull. Soc. belge Ophtalmol.
1998
Comment on: A further observation of corneal dystrophy and perceptive deafness in two siblings.
Françoise Meire
A1
Journal Article
in
OPHTHALMIC GENETICS
1998
Isolated Norrie disease in a female caused by a balanced translocation t(X,6).
Françoise Meire
Bart Lafaut
Franki Speleman
Michel Hanssens
A2
Journal Article
in
OPHTHALMIC GENETICS
1998
Mental retardation in amaurosis congenita of Leber.
Françoise Meire
A1
Journal Article
in
NEUROPEDIATRICS
1998
Retinopathy following measles, mumps, and rubella vaccination in an immuno-incompetent girl.
Françoise Meire
A1
Journal Article
in
INTERNATIONAL OPHTHALMOLOGY
1998
Subretinal fibrosis in Stargardt's disease
Jean Delaey
Françoise Meire
A2
Journal Article
in
DOCUMENTA
1998
Subretinal fibrosis in Stargardt's disease
Françoise Meire
P1
Conference
1998
The Hermansky-Pudlack syndrome
Fritz Offner
Françoise Meire
A2
Journal Article
in
Bull. Soc. Belge Ophtalmol., 267, 99-105
1998
1997
Microcephaly with chorioretinopathy: a report of two dominant families and three sporadic cases.
Françoise Meire
A2
Journal Article
in
OPHTHALMIC GENETICS
1997
The endoscopic approach for congenital nasolacrimal duct obstruction.
Koen Ingels
Philippe Kestelyn
Françoise Meire
A1
Journal Article
in
CLINICAL OTOLARYNGOLOGY
1997
1996
Cohen syndrome : the clinical symptoms and stigmata at a young age
Françoise Meire
A1
Journal Article
in
CLINICAL GENETICS
1996
Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.
Françoise Meire
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
1996
Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: A new example of the Chitty syndrome.
Rudy Van Coster
Françoise Meire
Juliaan Leroy
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1996
L'objectif de l'examen ophtalmologique chez les personnes atteintes d'un handicap auditif
Françoise Meire
[0-9]{2}
1996
Ocular manifestations in Dellemans syndrome and encephalocraniocutaneous lipomatosis. Report of three cases
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., nr. 261, pp. 65-70, 4 figg
1996
Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome.
Françoise Meire
A1
Journal Article
in
HUMAN MUTATION
1996
1995
Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.
Françoise Meire
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
1995
Congenital intranasal cyst in dacryocystocela
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., nr. 257
1995
Gene conversion between red and defective green opsin gene in blue cone monochromacy
Françoise Meire
A1
Journal Article
in
GENOMICS
1995
Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations.
Françoise Meire
Rudy Van Coster
A1
Journal Article
in
OPHTHALMIC GENETICS
1995
Ocular perforation in utero
Françoise Meire
Rafaël Van Oye
Jean Delaey
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., nr. 259, pp. 71-80, 2 figg
1995
UNILATERAL CYTOMEGALOVIRUS RETINITIS IN A PATIENT WITH IMMUNOGLOBULIN G2 DEFICIENCY.
Bart Lafaut
Frans De Baets
Françoise Meire
A1
Journal Article
in
OPHTHALMOLOGICA
1995
1994
Biometry in X-linked megalocornea: pathognomic findings.
Françoise Meire
A1
Journal Article
in
BRITISH JOURNAL OF OPHTHALMOLOGY
1994
Chromosome aberations in fibrous dysplasia
Franki Speleman
Genevieve Laureys
Françoise Meire
A1
Journal Article
in
CANCER GENETICS AND CYTOGENETICS
1994
Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON)
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., nr. 254, pp. 137-146, 6 figg
1994
DNA CARRIER DETECTION IN X-LINKED PROGRESSIVE CONE DYSTROPHY.
Françoise Meire
A1
Journal Article
in
CLINICAL GENETICS
1994
Familial exudative vitreoretinopathy.
Françoise Meire
A2
Journal Article
in
Revista Brasileira de Oftalmologia
1994
Features of mitochondrial DNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.
Françoise Meire
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
1994
Fibromuscular dysplasia of the arteries: an arterial occlusive disease with severe neurological complications at young age
Anne De Paepe
Françoise Meire
Marleen Praet
A4
Journal Article
in
Dysmorphology and genetics of cardiovascular disorders. Ed. Christos S. Bartsokas, P. Beighton, Athens, pp. 306-31 0
1994
Identification of a key recombinient which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.
Philippe Kestelyn
Monique Leys
Françoise Meire
A1
Journal Article
in
JOURNAL OF MEDICAL GENETICS
1994
Lens dislocation and optic-nerve hypoplasia in ring chromosome-21 mosaicism.
Françoise Meire
A1
Journal Article
in
ANNALES DE GENETIQUE
1994
Megalocornea: clinical and genetic-aspects
Françoise Meire
A1
Journal Article
in
DOCUMENTA OPHTHALMOLOGICA
1994
Ocular anomalies in an unbalanced translocation between chromosomes 7 and 8
Bart Leroy
Franki Speleman
Michel Hanssens
Françoise Meire
A4
Journal Article
in
BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE
1994
Pseudoglioma: a clinico-pathological report
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge Ophtalmol, nr. 255, pp. 99-105, 5 figg
1994
X-linked progressive cone dystrophy.
Françoise Meire
Monique Leys
A1
Journal Article
in
BRITISH JOURNAL OF OPHTHALMOLOGY
1994
1993
ADDITIONAL EVIDENCE FOR A GENE LOCUS FOR PROGRESSIVE CONE DYSTROPHY WITH LATE ROD INVOLVEMENT IN XP21.1-P11.3.
Françoise Meire
A1
Journal Article
in
GENOMICS
1993
Congenital ectropion uveae with glaucoma
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., nr. 249, pp. 131-137, 3 figg
1993
HETEROGENEITY VERSUS VARIABILITY IN MEGALOCORNEA-MENTAL RETARDATION (MMR) SYNDROMES - REPORT OF NEW CASES AND DELINEATION OF 4 PROBABLE TYPES.
Françoise Meire
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1993
Osteoporosis-pseudoglioma syndrome
Anne De Paepe
Juliaan Leroy
Lieve Nuytinck
Françoise Meire
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
1993
Treatment of long term complications of toxoplasma chorioretinal scars
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., nr. 248, pp. 59
1993
1992
Autosomal dominant congenital miosis with megalocornea.
Françoise Meire
A1
Journal Article
in
OPHTHALMIC PAEDIATRICS AND GENETICS
1992
Leber's hereditary optic neuropathy. Clinical and molecular genetic aspects. Preliminary results in our families
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge ophtalmol., 243
1992
1991
DNA variants: A third allele of the Pstl RFLP at DXS94
Françoise Meire
A2
Journal Article
in
HUMAN GENETICS
1991
Hereditary ectopia lentis
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., 241
1991
Ocular manifestations of congenital Marfan syndrome with contractures.
Françoise Meire
A2
Journal Article
in
OPHTHALMIC PAEDIATRICS AND GENETICS
1991
Optic atrophy as a complication of neonatal alloimmune thrombocytopenia
Françoise Meire
Johanna Van Egmond
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., 241
1991
PERSISTING CHLOROQUINE-INDUCED MYASTHENIA.
Jan De Bleecker
Jacques De Reuck
Jozef Quatacker
Françoise Meire
A1
Journal Article
in
ACTA CLINICA BELGICA
1991
Retinal manifestations in fibromuscular dysplasia
Françoise Meire
Jean Delaey
A2
Journal Article
in
Eur. J. Ophthalmol., 1
1991
The Hallerman-Strciff syndrome
Françoise Meire
A2
Journal Article
in
Bull. Soc. belge Ophtalmol., 241
1991
X-linked megalocomea. Ocular findings and linkage analysis.
Françoise Meire
A2
Journal Article
in
OPHTHALMIC PAEDIATRICS AND GENETICS
1991
Genetics in Ophthalmology. Bull. Soc. belge Ophtalmol., nr. 269, 1998, pp. 3-244.
Françoise Meire
A2
Journal Article
Optic nerve hypoplasia. Ophthalmol., nr. 105,1998, pp. 4-5.
Françoise Meire
[0-9]{2}
Visusstoornissen. Kindergeneeskunde. Ed. Van den Brande J., Heymans H., Monnens L. Elsevier/Brugge, 1998, pp. 727-744.
Françoise Meire
[0-9]{2}