Geraldine van Winckel (Géraldine Van Winckel)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 7

Top Topics

Structural Basis

Intellectual Disability

Single Molecule

Endothelial Cells

Top Venues

Scientific reports

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Ahmed El Mouatani, Geraldine van Winckel, Khaoula Zaafrane-Khachnaoui, Sandra Whalen, Amale Achaiaa, Sophie Kaltenbach, Andrea Superti-Furga, Michel Vekemans, Heidi Fodstad, Fabienne Giuliano, Tania Attie-Bitach
Homozygous GLI3 variants observed in three unrelated patients presenting with syndromic polydactyly. American journal of medical genetics. Part A 185 (12) (2021)