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Louise Devisme
Affiliation : Centre Hospitalier Universitaire de Lille
- 2Publications (affiliation in France)
- 147Total publications
- 3739Citations
- 33h-index
Research profile
Louise Devisme has 2 indexed publications (2010–2014). Their work appears mainly in “European Journal of Human Genetics” and “Human Mutation”. Their most cited article, “New insights into genotype–phenotype correlation for GLI3 mutations” (2014), has been cited 126 times. Their work is co-authored with at least 12 researchers, including institutions in Tunisia.
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Create my free profile Add my publicationsResearch areas
- Fetal and Pediatric Neurological Disorders
- Prenatal Screening and Diagnostics
- Genomics and Rare Diseases
- Pregnancy and preeclampsia studies
- Neonatal Respiratory Health Research
Publications (2)
- New insights into genotype–phenotype correlation for GLI3 mutations
- High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy
Publication venues
- European Journal of Human Genetics × 1
- Human Mutation × 1
Publications per year
- 20141
- 20101
Collaborations
Partner institutions : Hôpital Necker-Enfants Malades · Assistance Publique – Hôpitaux de Paris · Inserm · Université Paris Descartes · Institut des Maladies Génétiques Imagine
Co-authors’ countries : Tunisia
Co-authors
- Muriel Holder
- Marie Gonzalès
- J. Roume
- Amale Ichkou
- Sylvie Manouvrier‐Hanu
- Férechté Encha‐Razavi
- Arnold Münnich
- Géraldine Goudefroye
- Soumaya Mougou-Zerelli
- Tania Attié‐Bitach
- Michel J. J. Vekemans
- Martine Sinico
Bibliographic data from OpenAlex (open database).
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