Researcher
Hannah Verdin
- Disciplines:Medical genomics, Molecular diagnostics, Genetics, Developmental genetics, Genome structure and regulation, Clinical genetics and molecular diagnostics
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → 31 May 2020 - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 2009 → 30 Sep 2018
Projects
1 - 3 of 3
- Dissection of the cis-regulatory landscape of FOXL2From1 Jan 2016 → 31 Dec 2018Funding: FWO research project (including WEAVE projects)
- Dissection of the cis-regulatory landscape of FOXL2 in development and diseaseFrom1 Oct 2014 → 31 May 2020Funding: FWO fellowships, BOF - Other initiatives
- Functional study of long-range genetic defects in human developmental disorders.From1 Oct 2009 → 30 Sep 2013Funding: FWO fellowships, BOF - Other initiatives
Publications
1 - 10 of 49
- A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing(2023)
Authors: Nolwenn Jean-Marçais, Estrella López-Martín, Maria Antonietta Mencarelli, Sébastien Moutton, Rolph Pfundt, Hana Safraou, Christel Thauvin-Robinet, Julien Thevenon, Frédéric Tran Mau-Them, Bert B.A. de Vries, et al.
- Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders(2023)
Authors: Nika Schuermans, Hannah Verdin, Jody Ghijsels, Madeleine Hellemans, Elke Debackere, Elke Bogaert, Sofie Symoens, Leslie Naesens, Elien Lecomte, David Crosiers, et al.
- Twist exome capture allows for lower average sequence coverage in clinical exome sequencing(2023)
Authors: Burcu Yaldiz, Erdi Kucuk, Juliet Hampstead, Tom Hofste, Rolph Pfundt, Jordi Corominas Galbany, Tuula Rinne, Helger G. Yntema, Alexander Hoischen, Marcel Nelen, et al.
- Endocrine outcome and seminal parameters in young adult men born with hypospadias : a cross-sectional cohort study(2022)
Authors: Lloyd Tack, Anne-Françoise Spinoit, Piet Hoebeke, Stefan Riedl, Alexander Springer, Ursula Tonnhofer, Manuela Hiess, Julia Weninger, Ahmed Mahmoud, Kelly Tilleman, et al.
- Blepharophimosis, ptosis, and epicanthus inversus syndrome(2022)
Authors: Hannah Verdin, Charlotte Matton
- Marked hypotonia : an additional feature of ANO3-related movement disorder(2022)
Authors: Arnout Bruggeman, Nika Schuermans, Hannah Verdin, Bart Dermaut
- Expanding the clinical spectrum and management of traboulsi syndrome : report on two siblings homozygous for a novel pathogenic variant in ASPH(2021)
Authors: Tom Van Hoorde, Fanny Nerinckx, Elke kreps, Dimitri Roels, Philippe Huyghe, Hannah Verdin, Irina Balikova
Pages: 493 - 499 - Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer(2020)
Authors: Kezhi Yan, Justine Rousseau, Keren Machol, Laura A. Cross, Katherine E. Agre, Cynthia Forster Gibson, Anne Goverde, Kendra L. Engleman, Hannah Verdin, Elfride De Baere, et al.
- Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicism(2020)
Authors: Elise Pozza, Hannah Verdin, Hilde Deconinck, Annelies Dheedene, Irina Balikova
- The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56(2020)
Authors: 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.