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Arnaud Lagarde

Affiliation : Hôpital de la Timone

• 5Publications (affiliation in France)
• 64Total publications
• 2938Citations
• 18h-index

ORCIDOpenAlex

Research profile

Arnaud Lagarde has 5 indexed publications (2017–2021). Their work appears mainly in “Frontiers in Genetics”, “Journal of Human Genetics” and “BMC Pediatrics”. Their most cited article, “Identification of a ERCC5 c.2333T>C (L778P) Variant in Two Tunisian Siblings With Mild Xeroderma Pigmentosum Phenotype” (2019), has been cited 15 times. 3 of these publications date from the last three years of activity. Their work is co-authored with at least 7 researchers, including institutions in Tunisia.

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Research areas

• Neuroendocrine Tumor Research Advances
• Genomics and Rare Diseases
• Genetic factors in colorectal cancer
• Ear and Head Tumors
• Colorectal Cancer Treatments and Studies

Publications (5)

• Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype
  2021 · Frontiers in Genetics · cited 4 times
• Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family
  2020 · Journal of Human Genetics · cited 4 times
• Identification of a ERCC5 c.2333T>C (L778P) Variant in Two Tunisian Siblings With Mild Xeroderma Pigmentosum Phenotype
  2019 · Frontiers in Genetics · cited 15 times
• Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome
  2018 · BMC Pediatrics · cited 4 times
• Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome
  2017 · Biology and Medicine · cited 12 times

Publication venues

• Frontiers in Genetics × 2
• Journal of Human Genetics × 1
• BMC Pediatrics × 1
• Biology and Medicine × 1

Publications per year

• 20211
• 20201
• 20191
• 20181
• 20171

Collaborations

Partner institutions : Aix-Marseille Université · Inserm · Institut Pasteur de Tunis · Tunis El Manar University · Centre de Génétique Médicale de Marseille

Co-authors’ countries : Tunisia

Co-authors

• Nicolas Lévy
• Sahar Elouej
• Annachiara De Sandre‐Giovannoli
• Valérie Delague
• Sylviane Olschwang
• Jean‐Pierre Desvignes
• Nehla Ghedira

Bibliographic data from OpenAlex (open database).