Onderzoeker
Sarah De Jaegere
- Disciplines:Pediatrie en neonatologie, Moleculaire en celbiologie, Systeembiologie, Verpleegkunde, Genetica
Affiliaties
- Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf15 sep 2005 → 13 mei 2014 - Vakgroep Oogheelkunde (Departement)
Lid
Vanaf15 sep 2003 → 14 sep 2005
Publicaties
11 - 20 van 23
- An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients(2015)
Auteurs: Miriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, Susanne Kohl, Françoise Meire, Karin Dahan, Fanny Depasse, Sarah De Jaegere, Thomy De Ravel, Marjan De Rademaeker, et al.
Pagina's: 39 - 42 - A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease(2013)Volume: 54
Auteurs: Miriam Bauwens, Sarah De Jaegere, Barbara D'haene, Filip Pattyn
Pagina's: 3372 - 3372 - Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis(2013)Volume: 54
Auteurs: Annelot Baert, Miriam Bauwens, Sarah De Jaegere, Thomy De Ravel, Françoise Meire
Pagina's: 1313 - 1313 - Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis(2013)
Auteurs: Annelot Baert, Miriam Bauwens, Sarah De Jaegere, Thomy de Ravel, Françoise Meire
Aantal pagina's: 1 - Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis(2012)
Auteurs: Annelot Baert, Miriam Bauwens, Sarah De Jaegere, Thomy de Ravel, Françoise Meire, Nouha Abdelmoula Bouayed, Lina Florentin-Arar
Aantal pagina's: 1 - Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis(2012)
Auteurs: Annelot Baert, Miriam Bauwens, Sarah De Jaegere, Thomy de Ravel, Françoise Meire, Nouha Abdelmoula Bouayed, Lina Florentin-Arar
Aantal pagina's: 1 - Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome(2008)
Auteurs: Diane Beysen, Sarah De Jaegere, David Amor, Philippe Bouchard, Sophie Christin-Maitre, Marc Fellous, Philippe Touraine, Arthur W Grix, Raoul Hennekam, Françoise Meire, et al.
Pagina's: E205 - E219 - Exome sequencing identifies a novel RP1 mutation in a Belgian family with autosomal dominant retinitis pigmentosaVolume: 54
Auteurs: Sarah De Jaegere, Julie De Zaeytijd
Pagina's: 3355 - 3355 - Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations
Auteurs: Barbara D'haene, Françoise Meire, Ilse Claerhout, Hester Y Kroes, Astrid Plomp, Yvonne H Arens, Thomy de Ravel, Ingele Casteels, Sarah De Jaegere, Sally Hooghe, et al.
Pagina's: 324 - 333 - Exome sequencing identifies a novel RP1 mutation in a Belgian family with autosomal dominant retinitis pigmentosa
Auteurs: Sarah De Jaegere, Julie De Zaeytijd
Aantal pagina's: 1