PhD Students
Name |
Year |
Research topic |
Diane Beysen |
2007 |
New insights in the molecular pathogenesis of the blepharophimosis syndrome (BPES) |
Barbara D'haene |
2010 |
The study of long-range genetic defects in human transcription factor related disorders |
Caroline Van Cauwenbergh |
2017 |
Novel genes and mechanisms underlying autosomal dominant retinitis pigmentosa and allied retinal dystrophies |
Basamat Almoallem |
2017 |
Unraveling the molecular basis of genetically heterogeneous developmental eye disorders |
Delfien Bogaert |
2017 |
Molecular diagnosis of Common Variable Immunodeficiency and related antibody disorders : an integrated immunological and genetic approach |
Master Students (2011-)
Name |
Year |
Study program |
Research topic |
Yana Novikova |
2011 |
Bioscience Engineering |
Characterization of regulatory and genic deletions of the FOXL2 locus in human developmental disorders |
Timothy Barclay |
2012 |
Medicine |
Unraveling the molecular pathogenesis of developmental glaucoma |
Elize Vantroys |
2013 |
Biomedical Sciences |
Transcriptome and identity-by-descent filtering of exome data for the identification of a novel disease gene in primary congenital glaucoma |
Liza Borms |
2013 |
Industrial Sciences: Biochemistry |
Study of the regulatory landscape of SHOX in a population of molecularly unsolved patients with LWD and ISS |
Erina De Thaye |
2014 |
Biomedical Sciences |
Niet-coderende variatie in de moleculaire pathogenese van recessieve aandoeningen: Het ABCA4 gen en de ziekte van Stargardt als model |
Ibran Mertens |
2014 |
Industrial Sciences: Biochemistry |
Mutatiescreening van FOG2 in een 46,XY DSD patiëntencohorte en identificatie van nieuwe kandidaatgenen met behulp van IBD-mapping |
Maxim Van Panteghem |
2015 |
Biomedical Sciences |
NXT-EYE: integratieve exoomsequenering voor genidentificatie in recessieve retinale dystrofieën |
Malaïka Vander Linden |
2015 |
Biomedical Sciences |
Homozygositeitsmapping en exoomsequenering voor de genetische karakterisatie van 46,XY disorders of sex development |
Santusha Prija Bihari |
2016 |
Biomedical Sciences |
NXT-DSD: Next-generation sequencing technologieën voor de genetische karakterisatie van disorders of sex development (DSD) and primaire ovariële insuffficiëntie |
Magalie De Meyer |
2016 |
Biomedical Sciences |
|
Levi Hoste |
2016 |
Medicine |
Unravelling the genetic and molecular basis of primary immune deficiencies associated with T helper 17 defects |
Gamze Kanatlar |
2016 |
Biomedical Sciences |
Identificatie en functionele karakterisatie van niet-coderende varianten in de ziekte van Stargardt |
Niels De Vriese |
2017 |
Bioscience engineering |
NXT-DSD: Next-generation sequencing technologieën voor de genetische karakterisatie van disorders of sex development |
Laurien Ruysschaert |
2017 |
Pharmaceutical Sciences |
Antisense oligonucleotide therapie in erfelijke blindheid |
Tasmien Couchement |
2017 |
Bioscience Engineering |
Functionele karakterisering van niet-coderende variaties in de ziekte van Stargardt, de meest voorkomende erfelijke netvliesaandoening. |
Julie Van De Velde |
2018 |
Industrial Sciences: Biochemistry |
Identificatie en functionele karakterisering van niet-coderende variaties van de FOXL2 regio in BPES |
Laurens Lambrechts |
2018 |
Bioscience Engineering |
Identification of a novel disease gene for autosomal recessive retinal disease using an integrated approach of homozygosity mapping and next generation sequencing in consanguineous families |
Marieke Vromman |
2018 |
Biomedical Sciences |
Antisense oligonucleotide therapy for inherited retinal disease |
Julien Derolez |
2018 |
Pharmaceutical Sciences |
Exploring the genetic heterogeneity of inherited retinal disease using next-generation sequencing strategies |
Nina Lambrechts |
2018 |
Biomedical Sciences |
Functional characterization of a novel missense mutation in the ciliopathy-associated gene CEP78 |
Bachelor Students
Name |
Year |
Study program |
Research topic |
Núria Gruartmoner Roura |
2016 |
Biotechnology |
Identification of a novel disease gene for autosomal recessive retinal blindness by combining homozygosity mapping and next-generation sequencing in consanguineous families |