Jack Reilly

Years Active: 2023-2024
Publications (10 Years): 2

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

Publications

Camilla Sarli, Liselot van der Laan, Jack Reilly, Slavica Trajkova, Diana Carli, Alfredo Brusco, Michael A Levy, Raissa Relator, Jennifer Kerkhof, Haley McConkey, Matthew L Tedder, Cindy D Skinner, Mariëlle Alders, Peter Henneman, Raoul C M Hennekam, Claudia Ciaccio, Stefano D'Arrigo, Antonio Vitobello, Laurence Olivier-Faivre, Sacha Weber, Aline Vincent-Devulder, Laurence Perrin, Alexia Bourgois, Toshiyuki Yamamoto, Kay Metcalfe, Marcella Zollino, Usha Kini, Daniela Oliveira, Sergio B Sousa, Denise Williams, Gerarda Cappuccio, Bekim Sadikovic, Nicola Brunetti-Pierri
Blepharophimosis with intellectual disability and Helsmoortel-Van Der Aa Syndrome share episignature and phenotype. American journal of medical genetics. Part C, Seminars in medical genetics (2024)
Niels Vos, Jack Reilly, Mariet W Elting, Philippe M Campeau, David Coman, Zornitza Stark, Tiong Yang Tan, David J Amor, Simran Kaur, Miya StJohn, Angela T Morgan, Benjamin A Kamien, Chirag Patel, Matthew L Tedder, Giuseppe Merla, Paolo Prontera, Marco Castori, Kai Muru, Felicity Collins, John Christodoulou, Janine Smith, Bruria Ben Zeev, Alessandra Murgia, Emanuela Leonardi, Natacha Esber, Antonio Martinez-Monseny, Didac Casas-Alba, Matthew Wallis, Marcel M A M Mannens, Michael A Levy, Raissa Relator, Marielle Alders, Bekim Sadikovic
DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with KAT6A / KAT6B variants. Epigenomics (2023)

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