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Pauline Boiroux

Observed names: Boiroux, Pauline, P. Boiroux
ORCID: 0009-0002-1515-1816
Observed ORCID: 0009-0002-1515-1816
OpenAlex ID: A5035200061
Extending the phenotypes associated with TRIO gene variants in a cohort of 25 patients and review of the literature
2023 · Gabriella Gazdagh, David Hunt, et al. · American Journal of Medical Genetics Part A · 15
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Manifestations psychiatriques des maladies héréditaires du métabolisme traitables chez l’adulte
2026 · P. Boiroux, C. Demily · Encyclopédie médico-chirurgicale. Psychiatrie
The prevalence of neurodevelopmental disorders in Smith-Magenis Syndrome: a PRISMA compliant systematic review
2026 · Pauline Boiroux, Marie-Noëlle Babinet, et al. · Journal of Neurodevelopmental Disorders
The prevalence of neurodevelopmental disorders in Smith-Magenis Syndrome: a PRISMA compliant systematic review
2026 · Pauline Boiroux, Marie-Noëlle Babinet, et al. · Figshare
Additional file 1 of The prevalence of neurodevelopmental disorders in Smith-Magenis Syndrome: a PRISMA compliant systematic review
2026 · Pauline Boiroux, Marie-Noëlle Babinet, et al. · Figshare
Additional file 2 of The prevalence of neurodevelopmental disorders in Smith-Magenis Syndrome: a PRISMA compliant systematic review
2026 · Pauline Boiroux, Marie-Noëlle Babinet, et al. · Figshare
Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith–Magenis Syndrome
2026 · Albin Blanc, Christophe Nemos, et al. · American Journal of Medical Genetics Part A
Works count: 8
Citation count: 15
H-index: 1
I10-index: 1
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