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Sandra Mercier

Affiliation : Centre National de la Recherche Scientifique · Inserm · Centre Hospitalier Universitaire de Nantes · Institut du Thorax · Nantes Université

• 3Publications (affiliation in France)
• 195Total publications
• 4798Citations
• 39h-index

ORCIDOpenAlex

Research profile

Sandra Mercier has 3 indexed publications (2014–2025). Their work appears mainly in “Clinical Genetics”, “European Journal of Human Genetics” and “Haematologica”. 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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Research areas

• Genomics and Rare Diseases
• Genetics and Neurodevelopmental Disorders
• Muscle Physiology and Disorders
• Genomic variations and chromosomal abnormalities
• Hereditary Neurological Disorders

Publications (3)

• Clinical and Neurodevelopmental Characteristics of Paralogous Gain‐of‐Function Variants at GRIA2 p.Gly792 and GRIA3 p.Gly803
  2025 · Clinical Genetics · cited 6 times
• New insights into genotype–phenotype correlation for GLI3 mutations
  2014 · European Journal of Human Genetics · cited 126 times
• Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia
  2014 · Haematologica · cited 80 times

Publication venues

• Clinical Genetics × 1
• European Journal of Human Genetics × 1
• Haematologica × 1

Publications per year

• 20251
• 20142

Collaborations

Partner institutions : Assistance Publique – Hôpitaux de Paris · Hôpital Necker-Enfants Malades · Institut des Maladies Génétiques Imagine · Sorbonne Paris Cité · Université Paris Descartes

Co-authors’ countries : Tunisia

Co-authors

• Fanny Menard
• Sophie Bayart
• Muriel Holder
• Marie Gonzalès
• Martine Sinico
• J. Roume
• Jeanne Yvonne Borg
• Catherine Vincent‐Delorme
• Géraldine Viot
• Nicole Philip
• Anne‐Lise Delezoide
• M.-F. Hurtaud-Roux

Bibliographic data from OpenAlex (open database).