Peter De Rijk

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2015-2023
Publications (10 Years): 3

Top Topics

Attention Deficit Hyperactivity Disorder

Botulinum Toxin

Genome Wide Identification

Top Venues

Genome research

European journal of human genetics : EJHG

Genetics in medicine : official journal of the American College of Medical Genetics

International journal of molecular sciences

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

Publications

Claudia Theys, Joe Ibrahim, Ligia Mateiu, Archibold Mposhi, Laura García-Pupo, Tim De Pooter, Peter De Rijk, Mojca Strazisar, İkbal Agah İnce, Iuliana Vintea, Marianne G Rots, Wim Vanden Berghe
Mitochondrial GpC and CpG DNA Hypermethylation Cause Metabolic Stress-Induced Mitophagy and Cholestophagy. International journal of molecular sciences 24 (22) (2023)
Nirmal Vadgama, Alan M Pittman, Michael Simpson, Niranjanan Nirmalananthan, Robin Murray, Takeo Yoshikawa, Peter De Rijk, Elliott Rees, George Kirov, Deborah Hughes, Tomas Fitzgerald, Mark Kristiansen, Kerra Pearce, Eliza Cerveira, Qihui Zhu, Chengsheng Zhang, Charles Lee, John Hardy, Jamal Nasir
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes. European journal of human genetics : EJHG 27 (7) (2019)
Wouter De Coster, Peter De Rijk, Arne De Roeck, Tim De Pooter, Svenn D'Hert, Mojca Strazisar, Kristel Sleegers, Christine Van Broeckhoven
Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome. Genome research 29 (7) (2019)
Daliya Kancheva, Derek Atkinson, Peter De Rijk, Magdalena Zimon, Teodora Chamova, Vanyo Mitev, Ahmet Yaramis, Gian Maria Fabrizi, Haluk Topaloglu, Ivailo Tournev, Yesim Parman, Yesim Parma, Esra Battaloglu, Alejandro Estrada-Cuzcano, Albena Jordanova
Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 18 (6) (2015)