Research Explorer

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Researcher

Françoise Meire

Awards & Distinctions

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 VerdinToon RosseelSascha VermeerIrina BalikovaPhilippe KestelynColombine MeunierFrançoise MeireJulie Van De VeldeOlivier VanakkerJenneke Van Den Ende et al.

2012

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness

Isabelle AudoKinga BujakowskaElise OrhanCharlotte M PoloschekSabine Defoort-DhellemmesIsabelle DrumareSusanne KohlTien D LuuOdile LecompteEberhart Zrenner et al.

A1 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

2011

Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes

Françoise MeireIsabelle DelpierreCecile BrachetFrançoise RoulezChrisitan Van NechelFanny DepasseCatherine ChristopheBjörn MentenElfride De Baere

A1 Journal Article in MOLECULAR VISION

2008

Corneal opacities in the Hallermann-Streiff syndrome

Francoise M. RoulezJosee SchuilFrançoise Meire

A1 Journal Article in OPHTHALMIC GENETICS

Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome

DIANE BEYSENSarah De JaegereDavid AmorPhilippe BouchardSophie Christin-MaitreMarc FellousPhilippe TouraineArthur W GrixRaoul HennekamFrançoise Meire et al.

A1 Journal Article in HUMAN MUTATION

2007

Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

J DESIRG MOYAO REISHN VAN REGEMORTERH DECONINCKKL DAVIDFrançoise MeireMJ ABRAMOWICZ

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

Orbital myositis in a child with linear scleroderma en coup de sabre

FM ROULEZC DANGOISSED DUFOURFrançoise Meire

A1 Journal Article in JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS

2006

Chiasmal misrouting and foveal hypoplasia without albinism

MM VAN GENDERENFCC RIEMSLAGJ SCHUILFP HOEBENJS STILMAFrançoise Meire

A1 Journal Article in BRITISH JOURNAL OF OPHTHALMOLOGY

Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosis

Suzanne YzerBart LeroyElfride De BaereThomy J de RavelMarijke N ZonneveldKrysta VoesenekUlrich KellnerJose P Martinez CirianoJan-Tjeerd HN de FaberKlaus Rohrschneider et al.

A1 Journal Article in INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

The key role of electrophysiology in the diagnosis of visually impaired children

M VAN GENDERENF RIEMSLAGF JORRITSMAF HOEBENFrançoise MeireJ STILMA

A1 Journal Article in ACTA OPHTHALMOLOGICA SCANDINAVICA

2005

Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in Blepharophimosis syndrome

DIANE BEYSENJeroen RaesBart LeroyA LucassenJRW YatesJ Clayton-SmithH IlyinaSS BrooksS Christin-MaitreMarc Fellous et al.

A1 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa

JC BOOIJRJ FLORIJNJB TEN BRINKW LOVESFrançoise MeireMJ VAN SCHOONEVELDPTVM DE JONGAAB BERGEN

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

Identification of mutations in the CRB1, RPE65, RETGC1, AIPL1, and RPGRIP1 genes in a cohort of 38 patients with juvenile retinitis pigmentosa

JC BOOIJRJ FLORIJNJB TEN BRINKW LOVESFrançoise MeireMJ VAN SCHOONEVELDPTVM DE JONGAAB BERGEN

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram

C ZEITZM VAN GENDERENJ NEIDHARDTUFO LUHMANNF HOEBENU FORSTERK WYCISKG MATYASCB HOYNGF RIEMSLAG et al.

A1 Journal Article in INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

2004

A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy

A MAUGERIFrançoise MeireCB HOYNGC VINKN VAN REGEMORTERG KARANZL YANGFPM CREMERSKaibo Zhang

A1 Journal Article in INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

Centrale en perifere neurologische toxiciteit door metronidazol

Françoise MeireBart LeroyJan De Bleecker

A2 Journal Article in TIJDSCHRIFT VOOR NEUROLOGIE EN NEUROCHIRURGIE

Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: A syndrome caused by a missense mutation in OPA1

M PAYNEZL YANGBJ KATZJEA WARNERCJ WEIGHTY ZHAOED PEARSONRL TREFTT HILLMANRJ KENNEDY et al.

A1 Journal Article in AMERICAN JOURNAL OF OPHTHALMOLOGY

Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly

RR RICHARDSOND DONNAIFrançoise MeireMJ DIXON

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

2003

Corneal deposits after the topical use of ofloxacin in two children with vernal keratoconjunctivitis

Ilse ClaerhoutPhilippe KestelynFrançoise MeireJean Paul RemonTineke DecaesteckerJan Van Bocxlaer

A1 Journal Article in BRITISH JOURNAL OF OPHTHALMOLOGY

FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

Elfride De BaereDIANE BEYSENChristine OleyBirgit LorenzJulie CocquetPetra De SutterKoen DevriendtMichael DixonMarc FellousJean-Pierre Fryns et al.

A1 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

Psammomatoid ossifyine fibroma of the ethmoid

Kristof VandekerckhoveK Van Den AbeeleCaroline Van den broeckeK VerstraeteFrançoise Meire

A4 Journal Article in BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE

2002

Novel insights in genotype-phenotype correlations in BPES through in-depth FOXL2 mutation analysis

Elfride De BaereDIANE BEYSENC OLEYPetra De SutterA GARZAC JONSRUDP KOIVISTOBart LeroyB LORENZFrançoise Meire et al.

Symptomatic pineal cysts: clinical manifestations and management

G MichielsenYves BenoitE BaertFrançoise MeireJacques Caemaert

A1 Journal Article in ACTA NEUROCHIRURGICA

2001

A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.

S SENECAH VERHELSTL DE MEIRLEIRFrançoise MeireC GROOTEW LISSENSRudy Van Coster

A1 Journal Article in ARCHIVES OF NEUROLOGY

Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis.

V SCHUSTERP ZEITLERS SEREGARDU OZCELIKD ANADOLL LUCHTMAN-JONESFrançoise MeireAM MINGERSC SCHAMBECKHW KRETH

A1 Journal Article in THROMBOSIS AND HAEMOSTASIS

Imaging studies in the diagnostic workup of neonatal nasal obstruction.

Bart VanzieleghemMarc LemmerlingHubert VermeerschP GOVAERTIngeborg DhoogeFrançoise MeireGeert MortierJuliaan LeroyMarc Kunnen

A1 Journal Article in JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY

Ophthalmologic and systemic features of the Alström syndrome: report of 9 cases

K Van Den AbeeleM CraenJ SchuilFrançoise Meire

A4 Journal Article in BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE

Spectrum and distribution of FOXL2 gene mutations and variants in BPES, POF and XX male patients: tentative genotype-phenotype correlation

Elfride De BaereM DIXONK SMALLE JABSBart LeroyK DEVRIENDTY GILLEROTGeert MortierFrançoise MeireL VAN MALDERGEM et al.

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation

Elfride De BaereMichael J DixonKent W SmallEthylin W JabsBart LeroyKoenraad DevriendtYves GillerotGeert MortierFrançoise MeireLioinel Van Maldergem et al.

A1 Journal Article in HUMAN MOLECULAR GENETICS

2000

Indocyanine green angiography in Sorsby's fundus dystrophy.

Bart LafautE DE BACKERT KOHNOJean DelaeyFrançoise Meire

A1 Journal Article in GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

K JacobsFrançoise Meire

A4 Journal Article in BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE

Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.

L VANOPDENBOSCHB DUBOISMB D'HOOGHEFrançoise MeireH CARTON

A1 Journal Article in JOURNAL OF NEUROLOGY

Prevalence of AIPL1 mutations in inherited retinal degenerative disease

Melanie M SohockiIsabelle PerraultBart LeroyAnnette M PayneSharola DharmarajShomi S BhattacharyaJosseline KaplanIrene H MaumeneeRobert KoenekoopFrançoise Meire et al.

A1 Journal Article in MOLECULAR GENETICS AND METABOLISM

Sorsby fundus dystrophy without a mutation in the TIMP-3 gene.

JJM ASSINKE DE BACKERJB TEN BRINKT KOHNOPTVM DE JONGAAB BERGENFrançoise Meire

A1 Journal Article in BRITISH JOURNAL OF OPHTHALMOLOGY

Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophy.

Françoise MeireMM VAN GENDERENK LEMMENSMH ENS-DOKKUM

A2 Journal Article in OPHTHALMIC GENETICS

Use of mitomycin C and r-tPA for the management of conjunctival membrane and cataracts in a child with conjunctivitis lignosa.

Françoise MeireIlse ClaerhoutPhilippe Kestelyn

A1 Journal Article in BRITISH JOURNAL OF OPHTHALMOLOGY

1999

Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.

I HANSONA CHURCHILLJ LOVER AXTONT MOOREM CLARKEFrançoise MeireV VAN HEYNINGEN

A1 Journal Article in HUMAN MOLECULAR GENETICS

Vasoproliferative retinal tumors associated with peripheral chorioretinal scars in presumed congenital toxoplasmosis.

BA LAFUATFrançoise MeireAM LEYSG DRALANDSJean Delaey

A1 Journal Article in GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

1998

A puzzling case: conjunctivitis lignosa ?

C DEMEULEMEESTERFrançoise MeireMichel HanssensJean Delaey

A2 Journal Article in Bull. Soc. belge Ophtalmol.

Comment on: A further observation of corneal dystrophy and perceptive deafness in two siblings.

Françoise MeireV PANTELISJ SCHUIL

A1 Journal Article in OPHTHALMIC GENETICS

Genetics in ophthalmology

Françoise Meire

A4 Journal Article in BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE

Isolated Norrie disease in a female caused by a balanced translocation t(X,6).

Françoise MeireBart LafautFranki SpelemanMichel Hanssens

A2 Journal Article in OPHTHALMIC GENETICS

Mental retardation in amaurosis congenita of Leber.

J SCHUILFrançoise MeireJW DELLEMAN

A1 Journal Article in NEUROPEDIATRICS

Retinopathy following measles, mumps, and rubella vaccination in an immuno-incompetent girl.

J SCHUILEM VAN DE PUTTECM ZWAANFD KOOLEFrançoise Meire

A1 Journal Article in INTERNATIONAL OPHTHALMOLOGY

Subretinal fibrosis in Stargardt's disease

Jean DE LAEYFrançoise Meire

Subretinal fibrosis in Stargardt's disease

Jean DelaeyFrançoise Meire

A2 Journal Article in DOCUMENTA

The Hermansky-Pudlack syndrome

A BRANDTFritz OffnerJ QUATACKERJ PHILIPPEFrançoise Meire

A2 Journal Article in Bull. Soc. Belge Ophtalmol., 267, 99-105

1997

Microcephaly with chorioretinopathy: a report of two dominant families and three sporadic cases.

MM VAN GENDERENJ SCHUILFrançoise Meire

A2 Journal Article in OPHTHALMIC GENETICS

The endoscopic approach for congenital nasolacrimal duct obstruction.

Koen IngelsPhilippe KestelynFrançoise MeireG INGELSR VANWEISSENBRUCH

A1 Journal Article in CLINICAL OTOLARYNGOLOGY

1996

Cohen syndrome : the clinical symptoms and stigmata at a young age

Jean-Pierre FrynsEric LegiusKoen DevriendtFrançoise MeireLieve StandaertEmiel BatenHerman Van den Berghe

A1 Journal Article in CLINICAL GENETICS

Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.

AAB BERGENJB TENBRINKF RIEMSLAGEJM SCHUURMANFrançoise MeireM TIJMESPTVM DEJONG

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: A new example of the Chitty syndrome.

SG VANDAELERudy Van CosterFrançoise MeireAM SMETSJuliaan Leroy

A1 Journal Article in AMERICAN JOURNAL OF MEDICAL GENETICS

L'objectif de l'examen ophtalmologique chez les personnes atteintes d'un handicap auditif

Françoise Meire

Ocular manifestations in Dellemans syndrome and encephalocraniocutaneous lipomatosis. Report of three cases

G NARBAYFrançoise MeireA VERLOESI CASTEELSE DE VOS

A2 Journal Article in Bull. Soc. belge Ophtalmol., nr. 261, pp. 65-70, 4 figg

Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome.

S FUCHSD VANDEPOLU BEUDTU KELLNERFrançoise MeireW BERGERA GAL

A1 Journal Article in HUMAN MUTATION

1995

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

G VANCAMPMN VANTHIENENI HANDIGB VANROYVS RAOA MILUNSKYAP READCT BALDWINLA FARRERM BONDUELLE et al.

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

Congenital intranasal cyst in dacryocystocela

E DE BACKERK INGELSP VAN CAUWENBERGEFrançoise Meire

A2 Journal Article in Bull. Soc. belge Ophtalmol., nr. 257

Gene conversion between red and defective green opsin gene in blue cone monochromacy

E ReyniersMN VanthienenFrançoise MeireK BoulleK DevriesPhilippe KestelijnPJ Willems

A1 Journal Article in GENOMICS

Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations.

Françoise MeireRudy Van CosterP COCHAUXB OBERMAIERKUSSERC CANDAELEJJ MARTIN

A1 Journal Article in OPHTHALMIC GENETICS

Ocular perforation in utero

A GOBERTG VEREECKENFrançoise MeireRafaël Van OyeJean Delaey

A2 Journal Article in Bull. Soc. belge Ophtalmol., nr. 259, pp. 71-80, 2 figg

UNILATERAL CYTOMEGALOVIRUS RETINITIS IN A PATIENT WITH IMMUNOGLOBULIN G2 DEFICIENCY.

Bart LafautRNG VIANNAFrans De BaetsFrançoise Meire

A1 Journal Article in OPHTHALMOLOGICA

1994

Biometry in X-linked megalocornea: pathognomic findings.

Françoise MeireJW DELLEMAN

A1 Journal Article in BRITISH JOURNAL OF OPHTHALMOLOGY

Chromosome aberations in fibrous dysplasia

P DalcinR SciotFranki SpelemanI SamsonGenevieve LaureysC De PotterFrançoise MeireB Van DammeH Van Den Berghe

A1 Journal Article in CANCER GENETICS AND CYTOGENETICS

Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON)

Françoise MeireP COCHAUXC CANDAELEC BROUX

A2 Journal Article in Bull. Soc. belge Ophtalmol., nr. 254, pp. 137-146, 6 figg

DNA CARRIER DETECTION IN X-LINKED PROGRESSIVE CONE DYSTROPHY.

AAB BERGENFrançoise MeireEJM SCHUURMANJW DELLEMAN

A1 Journal Article in CLINICAL GENETICS

Familial exudative vitreoretinopathy.

R VIANNAS SEROPFrançoise Meire

A2 Journal Article in Revista Brasileira de Oftalmologia

Features of mitochondrial DNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

B OBERMAIERKUSSERB LORENZS SCHUBRINGA PAPROTTAK ZERREST MEITINGERFrançoise MeireP COCHAUXA BLANKENAGELG KOMMERELL et al.

A1 Journal Article in AMERICAN JOURNAL OF HUMAN GENETICS

Fibromuscular dysplasia of the arteries: an arterial occlusive disease with severe neurological complications at young age

MN VAN THIENENAnne De PaepeFrançoise MeireP PARIZELE VAN MARCKMarleen PraetJG LEROJ DUMON

A4 Journal Article in Dysmorphology and genetics of cardiovascular disorders. Ed. Christos S. Bartsokas, P. Beighton, Athens, pp. 306-31 0

Identification of a key recombinient which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.

AAB BERGENPhilippe KestelynMonique LeysFrançoise Meire

A1 Journal Article in JOURNAL OF MEDICAL GENETICS

Lens dislocation and optic-nerve hypoplasia in ring chromosome-21 mosaicism.

Françoise MeireJP FRYNS

A1 Journal Article in ANNALES DE GENETIQUE

Megalocornea: clinical and genetic-aspects

Françoise Meire

A1 Journal Article in DOCUMENTA OPHTHALMOLOGICA

Ocular anomalies in an unbalanced translocation between chromosomes 7 and 8

G VereeckenBart LeroyFranki SpelemanMichel HanssensFrançoise Meire

A4 Journal Article in BULLETIN DE LA SOCIETE BELGE D'OPHTALMOLOGIE

Pseudoglioma: a clinico-pathological report

M HANSSENSFrançoise Meire

A2 Journal Article in Bull. Soc. belge Ophtalmol, nr. 255, pp. 99-105, 5 figg

X-linked progressive cone dystrophy.

Françoise MeireAAB BERGENA DEROUCKMonique LeysJW DELLEMAN

A1 Journal Article in BRITISH JOURNAL OF OPHTHALMOLOGY

1993

ADDITIONAL EVIDENCE FOR A GENE LOCUS FOR PROGRESSIVE CONE DYSTROPHY WITH LATE ROD INVOLVEMENT IN XP21.1-P11.3.

AAB BERGENFrançoise MeireJ TENBRINKEJM SCHUURMANGJB VANOMMENJW DELLEMAN

A1 Journal Article in GENOMICS

Congenital ectropion uveae with glaucoma

C CANDAELEA LEFEBVREFrançoise MeireP KESTELYN

A2 Journal Article in Bull. Soc. belge Ophtalmol., nr. 249, pp. 131-137, 3 figg

HETEROGENEITY VERSUS VARIABILITY IN MEGALOCORNEA-MENTAL RETARDATION (MMR) SYNDROMES - REPORT OF NEW CASES AND DELINEATION OF 4 PROBABLE TYPES.

A VERLOESH JOURNELC ELMERJP MISSONM LEMERRERJ KAPLANL VANMALDERGEMH DECONINCKFrançoise Meire

A1 Journal Article in AMERICAN JOURNAL OF MEDICAL GENETICS

Osteoporosis-pseudoglioma syndrome

Anne De PaepeJuliaan LeroyLieve NuytinckFrançoise MeireJan Capoen

A1 Journal Article in AMERICAN JOURNAL OF MEDICAL GENETICS

Treatment of long term complications of toxoplasma chorioretinal scars

K BUYSI CASTEELSR VIANNAL DRALANDSA LEYSFrançoise MeireL MIS SOTTEN

A2 Journal Article in Bull. Soc. belge Ophtalmol., nr. 248, pp. 59

1992

Autosomal dominant congenital miosis with megalocornea.

Françoise MeireJW DELLEMAN

A1 Journal Article in OPHTHALMIC PAEDIATRICS AND GENETICS

Leber's hereditary optic neuropathy. Clinical and molecular genetic aspects. Preliminary results in our families

E VAN CAELENBERGHEFrançoise MeireC BROUXG VASSARTP CO-CHAUX

A2 Journal Article in Bull. Soc. belge ophtalmol., 243

1991

DNA variants: A third allele of the Pstl RFLP at DXS94

M OEHLERE SCHWINGERFrançoise MeireA GAL

A2 Journal Article in HUMAN GENETICS

Hereditary ectopia lentis

Françoise Meire

A2 Journal Article in Bull. Soc. belge Ophtalmol., 241

Ocular manifestations of congenital Marfan syndrome with contractures.

Françoise MeireJ DELLEMANE BLEEKER-WAGEMAKERS

A2 Journal Article in OPHTHALMIC PAEDIATRICS AND GENETICS

Optic atrophy as a complication of neonatal alloimmune thrombocytopenia

C ELEWAUTFrançoise MeireR VAN COSTERJohanna Van Egmond

A2 Journal Article in Bull. Soc. belge Ophtalmol., 241

PERSISTING CHLOROQUINE-INDUCED MYASTHENIA.

Jan De BleeckerJacques De ReuckJozef QuatackerFrançoise Meire

A1 Journal Article in ACTA CLINICA BELGICA

Retinal manifestations in fibromuscular dysplasia

Françoise MeireJean DelaeyM VAN THIENENL SCHUDDINCK

A2 Journal Article in Eur. J. Ophthalmol., 1

The Hallerman-Strciff syndrome

G DE WILDEFrançoise Meire

A2 Journal Article in Bull. Soc. belge Ophtalmol., 241

X-linked megalocomea. Ocular findings and linkage analysis.

Françoise MeireE BLEEKER-WAGEMAKERSM OEHLERA GALJ DELLEMAN

A2 Journal Article in OPHTHALMIC PAEDIATRICS AND GENETICS

Optic nerve hypoplasia. Ophthalmol., nr. 105,1998, pp. 4-5.

Françoise Meire

Visusstoornissen. Kindergeneeskunde. Ed. Van den Brande J., Heymans H., Monnens L. Elsevier/Brugge, 1998, pp. 727-744.

Françoise Meire