Isaac Scott Walton (Isaac S Walton)

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 6

Top Topics

Transforming Growth Factor

Amyotrophic Lateral Sclerosis

Top Venues

Journal of medical genetics

Journal of anatomy

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

Publications

Isaac Scott Walton, Emma McCann, Astrid Weber, Jenny E V Morton, Peter Noons, Louise C Wilson, Rosanna C Ching, Deirdre Cilliers, David Johnson, Julie M Phipps, Deborah J Shears, Gregory P L Thomas, Steven A Wall, Stephen R F Twigg, Andrew O M Wilkie
Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non-syndromic sagittal and metopic craniosynostosis. Journal of anatomy (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics 61 (4) (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics 61 (4) (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics 61 (4) (2024)
Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Mania De Praeter, Helen Lord, Christopher Mark Watson, David T Bonthron, Lut Van Laer, Andrew O M Wilkie, Bart L Loeys
Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of medical genetics 61 (4) (2024)