Claudio Peter D'Incal (Claudio D'Incal)

ORCID

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 18

Top Venues

European journal of human genetics : EJHG

Acta neuropathologica communications

Clinical epigenetics

Cells

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

Publications

Jolien Huyghebaert, Ligia Mateiu, Ellen Elinck, Kirsten Esther Van Rossem, Bregje Christiaenssen, Claudio Peter D'Incal, Michael K McCormack, Alice Lazzarini, Geert Vandeweyer, R Frank Kooy
Identification of a DLG3 stop mutation in the MRX20 family. European journal of human genetics : EJHG 32 (3) (2024)
Claudio Peter D'Incal, Dale John Annear, Ellen Elinck, Jasper J van der Smagt, Mariëlle Alders, Alexander J M Dingemans, Ligia Mateiu, Bert B A de Vries, Wim Vanden Berghe, R Frank Kooy
Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel-Van der Aa syndrome. European journal of human genetics : EJHG (2024)
Claudio Peter D'Incal, Dale John Annear, Ellen Elinck, Jasper J van der Smagt, Mariëlle Alders, Alexander J M Dingemans, Ligia Mateiu, Bert B A de Vries, Wim Vanden Berghe, R Frank Kooy
Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel-Van der Aa syndrome. European journal of human genetics : EJHG 32 (6) (2024)
Claudio Peter D'Incal, Dale John Annear, Ellen Elinck, Jasper J van der Smagt, Mariëlle Alders, Alexander J M Dingemans, Ligia Mateiu, Bert B A de Vries, Wim Vanden Berghe, R Frank Kooy
Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel-Van der Aa syndrome. European journal of human genetics : EJHG 32 (6) (2024)
Jolien Huyghebaert, Ligia Mateiu, Ellen Elinck, Kirsten Esther Van Rossem, Bregje Christiaenssen, Claudio Peter D'Incal, Michael K McCormack, Alice Lazzarini, Geert Vandeweyer, R Frank Kooy
Identification of a DLG3 stop mutation in the MRX20 family. European journal of human genetics : EJHG 32 (3) (2024)
Claudio Peter D'Incal, Anke Van Dijck, Joe Ibrahim, Kevin De Man, Lina Bastini, Anthony Konings, Ellen Elinck, Lllana Gozes, Zlatko Marusic, Mirna Anicic, Jurica Vukovic, Nathalie Van der Aa, Ligia Mateiu, Wim Vanden Berghe, R Frank Kooy
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case. Acta neuropathologica communications 12 (1) (2024)
Jolien Huyghebaert, Ligia Mateiu, Ellen Elinck, Kirsten Esther Van Rossem, Bregje Christiaenssen, Claudio Peter D'Incal, Michael K McCormack, Alice Lazzarini, Geert Vandeweyer, R Frank Kooy
Identification of a DLG3 stop mutation in the MRX20 family. European journal of human genetics : EJHG (2024)
Claudio Peter D'Incal, Anke Van Dijck, Joe Ibrahim, Kevin De Man, Lina Bastini, Anthony Konings, Ellen Elinck, Lllana Gozes, Zlatko Marusic, Mirna Anicic, Jurica Vukovic, Nathalie Van der Aa, Ligia Mateiu, Wim Vanden Berghe, R Frank Kooy
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case. Acta neuropathologica communications 12 (1) (2024)
Jolien Huyghebaert, Ligia Mateiu, Ellen Elinck, Kirsten Esther Van Rossem, Bregje Christiaenssen, Claudio Peter D'Incal, Michael K McCormack, Alice Lazzarini, Geert Vandeweyer, R Frank Kooy
Identification of a DLG3 stop mutation in the MRX20 family. European journal of human genetics : EJHG 32 (3) (2024)
Claudio Peter D'Incal, Dale John Annear, Ellen Elinck, Jasper J van der Smagt, Mariëlle Alders, Alexander J M Dingemans, Ligia Mateiu, Bert B A de Vries, Wim Vanden Berghe, R Frank Kooy
Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel-Van der Aa syndrome. European journal of human genetics : EJHG 32 (6) (2024)
Claudio Peter D'Incal, Anke Van Dijck, Joe Ibrahim, Kevin De Man, Lina Bastini, Anthony Konings, Ellen Elinck, Lllana Gozes, Zlatko Marusic, Mirna Anicic, Jurica Vukovic, Nathalie Van der Aa, Ligia Mateiu, Wim Vanden Berghe, R Frank Kooy
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case. Acta neuropathologica communications 12 (1) (2024)
Claudio Peter D'Incal, Anke Van Dijck, Joe Ibrahim, Kevin De Man, Lina Bastini, Anthony Konings, Ellen Elinck, Lllana Gozes, Zlatko Marusic, Mirna Anicic, Jurica Vukovic, Nathalie Van der Aa, Ligia Mateiu, Wim Vanden Berghe, R Frank Kooy
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case. Acta neuropathologica communications 12 (1) (2024)
Jolien Huyghebaert, Ligia Mateiu, Ellen Elinck, Kirsten Esther Van Rossem, Bregje Christiaenssen, Claudio Peter D'Incal, Michael K McCormack, Alice Lazzarini, Geert Vandeweyer, R Frank Kooy
Identification of a DLG3 stop mutation in the MRX20 family. European journal of human genetics : EJHG 32 (3) (2024)
Claudio Peter D'Incal, Anke Van Dijck, Joe Ibrahim, Kevin De Man, Lina Bastini, Anthony Konings, Ellen Elinck, Lllana Gozes, Zlatko Marusic, Mirna Anicic, Jurica Vukovic, Nathalie Van der Aa, Ligia Mateiu, Wim Vanden Berghe, R Frank Kooy
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case. Acta neuropathologica communications 12 (1) (2024)
Claudio Peter D'Incal, Kirsten Esther Van Rossem, Kevin De Man, Anthony Konings, Anke Van Dijck, Ludovico Rizzuti, Alessandro Vitriolo, Giuseppe Testa, Illana Gozes, Wim Vanden Berghe, R Frank Kooy
Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism. Clinical epigenetics 15 (1) (2023)
Claudio Peter D'Incal, Kirsten Esther Van Rossem, Kevin De Man, Anthony Konings, Anke Van Dijck, Ludovico Rizzuti, Alessandro Vitriolo, Giuseppe Testa, Illana Gozes, Wim Vanden Berghe, R Frank Kooy
Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism. Clinical epigenetics 15 (1) (2023)
Claudio Peter D'Incal, Kirsten Esther Van Rossem, Kevin De Man, Anthony Konings, Anke Van Dijck, Ludovico Rizzuti, Alessandro Vitriolo, Giuseppe Testa, Illana Gozes, Wim Vanden Berghe, R Frank Kooy
Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism. Clinical epigenetics 15 (1) (2023)
Claudio Peter D'Incal, Jitse Broos, Thierry Torfs, R Frank Kooy, Wim Vanden Berghe
Towards Kinase Inhibitor Therapies for Fragile X Syndrome: Tweaking Twists in the Autism Spectrum Kinase Signaling Network. Cells 11 (8) (2022)

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Publication Activity (10 Years)

Top Topics

Top Venues

Claudio Peter D'Incal (Claudio D'Incal)