Home › Researcher directory › Laurent Daniel

Laurent Daniel

Affiliation : Inserm · Assistance Publique Hôpitaux de Marseille · Hôpital de la Conception · Hôpital de la Timone

• 4Publications (affiliation in France)
• 330Total publications
• 7317Citations
• 46h-index

ORCIDOpenAlex

Research profile

Laurent Daniel has 4 indexed publications (1999–2022). Their work appears mainly in “Journal of the American Society of Nephrology”, “Our Dermatology Online” and “La Revue de Médecine Interne”. Their most cited article, “A Homozygous Missense Mutation in the Ciliary Gene TTC21B Causes Familial FSGS” (2014), has been cited 119 times. Their work is co-authored with at least 12 researchers, including institutions in Tunisia, Switzerland, Morocco.

Is this you? Get your research seen

Create your free DzCademia profile and add your articles: they will show up more easily on Google and in AI assistants like ChatGPT, so more people can read and cite your work.

Create my free profile Add my publications

Research areas

• Renal Diseases and Glomerulopathies
• Vasculitis and related conditions
• Renal Transplantation Outcomes and Treatments
• Systemic Lupus Erythematosus Research
• Renal cell carcinoma treatment

Publications (4)

• Metastasis of a widespread malignant melanoma in the bladder and the upper urinary tract: A case report
  2022 · Our Dermatology Online · cited 1 times
• A Homozygous Missense Mutation in the Ciliary Gene TTC21B Causes Familial FSGS
  2014 · Journal of the American Society of Nephrology · cited 119 times
• Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios
  2006 · Journal of the American Society of Nephrology · cited 103 times
• Adénopathies pseudotumorales, mode exceptionnel de révélation de l'amylose systémique
  1999 · La Revue de Médecine Interne · cited 5 times

Publication venues

• Journal of the American Society of Nephrology × 2
• Our Dermatology Online × 1
• La Revue de Médecine Interne × 1

Publications per year

• 20221
• 20141
• 20061
• 19991

Collaborations

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

Co-authors’ countries : Tunisia · Switzerland · Morocco

Co-authors

• Marie-Claire Gübler
• Thomas Jacob Neuhaus
• Mireille Lacoste
• Jean Marie Gasc
• Marie Gonzalès
• Tahya Sellami
• Marie‐Noelle Péraldi
• Laure‐Hélène Noël
• Anne‐Lise Delezoide
• Pierre L. Corvol
• Liliane Guicharnaud
• Emilie Filhol

Bibliographic data from OpenAlex (open database).