Researcher
Sara Seneca
- Keywords:Medicine
- Disciplines:Energy metabolism, Medical metabolomics, Cell physiology, Molecular diagnostics, Metabolic diseases, Genetics, Biogerontology
Affiliations
- Medical Genetics (Department)
Member
From1 Jan 2014 → Today - Reproduction and Genetics (Research group)
Member
From1 Mar 2010 → Today - Medical Genetics (Department)
Member
From1 Jan 2021 → 6 Mar 2023 - Clinical sciences (Department)
Member
From8 Apr 2019 → Today - Clinical sciences (Department)
Member
From1 Jan 2014 → 20 Oct 2022 - Department of Embryology and Genetics (Department)
Member
From1 Mar 2010 → 31 Dec 2013 - Department of Embryology and Genetics (Department)
Member
From1 Apr 2005 → 31 Dec 2010 - Department of Embryology and Genetics (Department)
Member
From1 Jan 2002 → 31 Mar 2005 - Microbiology (Research group)
Member
From1 Jul 1992 → 31 Aug 1992
Projects
1 - 2 of 2
- Development of diagnostic, biochemical and molecular methods, the prevention and the study of treatment of OXPHOS deficiency.From1 Jan 2010 → 31 Dec 2013Funding: FWO research project (including WEAVE projects)
- Research at the interface between human genetics and reproduction.From1 Jan 2009 → TodayFunding: Methusalem
Publications
1 - 10 of 63
- Sustained OMA1-mediated integrated stress response is beneficial for spastic ataxia type 5(2024)
Authors: Camilla Aurora Franchino, Martina Brughera, Valentina Baderna, Daniele De Ritis, Alessandra Rocco, Sara Seneca, Luc Régal, Paola Podini, Maurizio D'Antonio, Camilo Toro, et al.
Pages: 1043-1056 - Children born after assisted reproduction more commonly carry a mitochondrial genotype associating with low birthweight(2024)
Authors: C Spits, Joke Mertens, Florence Belva, Aafke PA van Montfoort, Marius Regin, Filippo Zambelli, Sara Seneca, Edouard Couvreu De Deckersberg, Maryse Bonduelle, H Tournaye, et al.
- EDIR(2023)
Authors: D.T. Laura Vo Ngoc, Randy Osei, Katrin Dohr, Catharina Olsen, Sara Seneca, Alexander Gheldof
- Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesis(2022)
Authors: Kah Ying Ng, Uwe Richter, Christopher B Jackson, Sara Seneca, Brendan J. Battersby
Pages: 1230-1241 - Clinical Heterogeneity in MT-ATP6 Pathogenic Variants(2022)
Authors: Sara Capiau, Joél Smet, Boel De Paepe, Yilmaz Yildiz, Mutluay Arslan, Olivier Stevens, Maxime Verschoore, Hedwig Stepman, Sara Seneca, Arnaud Vanlander
- Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the MT-ND6 gene(2021)
Authors: Justine Vandeputte, Mattias Van Heetvelde, Caroline van Cauwenbergh, Sara Seneca, Elfride De Baere, Bart P Leroy, Julie De Zaeytijd
Pages: 440-445 - Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases(2021)
Authors: Joséphine Lantoine, Anne Brysse, Vinciane Dideberg, Kathleen Claes, Sofie Symoens, Wim Coucke, Valérie Benoit, Sonia Rombout, Martine De Rijcke, Sara Seneca, et al.
- Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in TK2 gene(2020)
Authors: George K Papadimas, Efthimia Vargiami, Pinelopi Dragoumi, Rudy Van Coster, Joel Smet, Sara Seneca, Constantinos Papadopoulos, Evangelia Kararizou, Dimitrios Zafeiriou
Pages: 94-97 - Rare genetic variants potentially involved in ovarian hyperstimulation syndrome(2019)
Authors: Katrien Stouffs, Sari Daelemans, Samuel Dos Santos Ribeiro, Sara Seneca, Alexander Gheldof, Ali Sami Gürbüz, Michel De Vos, H Tournaye, C Blockeel
Pages: 491-497 - Clinical implementation of gene panel testing for lysosomal storage diseases(2019)
Authors: Alexander Gheldof, Sara Seneca, Katrien Stouffs, Willy Lissens, Anna C Jansen, Hilde Laeremans, Patrick Verloo, An-Sofie Schoonjans, Marije Meuwissen, Diana Barca, et al.