Onderzoeker
Basamat Almoallem Mohammed H
- Disciplines:Pediatrie en neonatologie, Moleculaire en celbiologie, Systeembiologie, Verpleegkunde, Genetica
Affiliaties
- Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf19 apr 2012 → 23 sep 2018
Publicaties
1 - 10 van 16
- Loss of function of RIMS2 causes a syndromic congenital cone-rod synaptic disease with neurodevelopmental and pancreatic involvement(2020)
Auteurs: Sabrina Mechaussier, Basamat Almoallem Mohammed H, Christina Zeitz, Kristof Van Schil, Laila Jeddawi, Alfredo Dueñas Rey, Christel Condroyer, Olivier Pelle, Michel Polak, Nathalie Boddaert, et al.
Pagina's: 859 - 871 - The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56(2020)
Auteurs: Basamat Almoallem Mohammed H, Gavin Arno, Julie De Zaeytijd, Hannah Verdin, Irina Balikova, Ingele Casteels, Thomy de Ravel, Sarah Hull, Martina Suzani, Anne Destrée, et al.
- Unraveling the molecular basis genetically heterogeneous developmental eye disorders(2017)
Auteurs: Basamat Almoallem Mohammed H
- Homozygosity mapping-guided exome sequencing in LCA patients of consanguineous origin reveals mutations in known genes and a novel candidate gene(2017)Volume: 58
Auteurs: Basamat Almoallem Mohammed H, Kristof Van Schil, Laila Jeddawi, Bart Leroy, Frauke Coppieters, Elfride De Baere
Pagina's: 1242 - 1242 - The power of homozygosity mapping-guided whole exome sequencing in a Saudi LCA population(2016)
Auteurs: Basamat Almoallem Mohammed H
Aantal pagina's: 1 - Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus(2015)
Auteurs: Basamat Almoallem Mohammed H, Miriam Bauwens, SOPHIE WALRAEDT, Patricia Delbeke, Julie De Zaeytijd, Philippe Kestelyn, Françoise Meire, Hannah Verdin, Sally Hooghe, Prasoon Kumar Thakur, et al.
Pagina's: 1701 - 1710 - Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus(2015)
Auteurs: Basamat Almoallem Mohammed H, Miriam Bauwens, SOPHIE WALRAEDT, Patricia Delbeke, Julie De Zaeytijd
Aantal pagina's: 1 - Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus(2015)Volume: 56
Auteurs: Basamat Almoallem Mohammed H, Miriam Bauwens, SOPHIE WALRAEDT, Patricia Delbeke, Julie De Zaeytijd
Aantal pagina's: 1 - Novel and known FRMD7 mutations and copy number variation in Belgian patients with X-linked idiopathic infantile nystagmus(2014)
Auteurs: Basamat Almoallem Mohammed H, Miriam Bauwens, Sophie Walraedt, Patricia Delbeke, Julie De Zaeytijd
Aantal pagina's: 1 - Novel and known FRMD7 mutations and copy number variation in Belgian patients with X-linked idiopathic infantile nystagmus(2014)
Auteurs: Basamat Almoallem Mohammed H, Miriam Bauwens, SOPHIE WALRAEDT, Patricia Delbeke, Julie De Zaeytijd
Aantal pagina's: 1