Jonathan Baets

Publication Activity (10 Years)

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

Top Topics

Pseudomonas Aeruginosa

Saccharomyces Cerevisiae

Dna Damage Response

Top Venues

Brain communications

medRxiv : the preprint server for health sciences

Acta neurologica Belgica

Life science alliance

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

Publications

Wouter Steyaert, Lydia Sagath, German Demidov, Vicente A Yépez, Anna Esteve-Codina, Julien Gagneur, Kornelia Ellwanger, Ronny Derks, Janneke M Weiss, Amber den Ouden, Simone van den Heuvel, Hilde Swinkels, Nick Zomer, Marloes Steehouwer, Luke O'Gorman, Galuh Astuti, Kornelia Neveling, Rebecca Schüle, Jishu Xu, Matthis Synofzik, Danique Beijer, Holger Hengel, Ludger Schöls, Kristl G Claeys, Jonathan Baets, Liedewei Van de Vondel, Alessandra Ferlini, Rita Selvatici, Heba Morsy, Marwa Saeed Abd Elmaksoud, Volker Straub, Juliane Müller, Veronica Pini, Luke Perry, Anna Sarkozy, Irina T Zaharieva, Francesco Muntoni, Enrico Bugiardini, Kiran Polavarapu, Rita Horvath, Evan Reid, Hanns Lochmüller, Marco Spinazzi, Marco Savarese, null null, null null, null null, null null, Leslie Matalonga, Steven Laurie, Han G Brunner, Holm Graessner, Sergi Beltran, Stephan Ossowski, Lisenka E L M Vissers, Christian Gilissen, Alexander Hoischen
Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing. medRxiv : the preprint server for health sciences (2024)
Danique Beijer, Sheila Marte, Jiaxin C Li, Willem De Ridder, Jessie Z Chen, Abigail L D Tadenev, Kathy E Miers, Tine Deconinck, Richard Macdonell, Wilson Marques, Peter De Jonghe, Samia L Pratt, Rebecca Meyer-Schuman, Stephan Zuchner, Anthony Antonellis, Robert W Burgess, Jonathan Baets
Dominant NARS1 mutations causing axonal Charcot-Marie-Tooth disease expand NARS1 -associated diseases. Brain communications 6 (2) (2024)
Danique Beijer, Sheila Marte, Jiaxin C Li, Willem De Ridder, Jessie Z Chen, Abigail L D Tadenev, Kathy E Miers, Tine Deconinck, Richard Macdonell, Wilson Marques, Peter De Jonghe, Samia L Pratt, Rebecca Meyer-Schuman, Stephan Zuchner, Anthony Antonellis, Robert W Burgess, Jonathan Baets
Dominant NARS1 mutations causing axonal Charcot-Marie-Tooth disease expand NARS1 -associated diseases. Brain communications 6 (2) (2024)
Danique Beijer, Sheila Marte, Jiaxin C Li, Willem De Ridder, Jessie Z Chen, Abigail L D Tadenev, Kathy E Miers, Tine Deconinck, Richard Macdonell, Wilson Marques, Peter De Jonghe, Samia L Pratt, Rebecca Meyer-Schuman, Stephan Zuchner, Anthony Antonellis, Robert W Burgess, Jonathan Baets
Dominant NARS1 mutations causing axonal Charcot-Marie-Tooth disease expand NARS1 -associated diseases. Brain communications 6 (2) (2024)
Danique Beijer, Sheila Marte, Jiaxin C Li, Willem De Ridder, Jessie Z Chen, Abigail L D Tadenev, Kathy E Miers, Tine Deconinck, Richard Macdonell, Wilson Marques, Peter De Jonghe, Samia L Pratt, Rebecca Meyer-Schuman, Stephan Zuchner, Anthony Antonellis, Robert W Burgess, Jonathan Baets
Dominant NARS1 mutations causing axonal Charcot-Marie-Tooth disease expand NARS1 -associated diseases. Brain communications 6 (2) (2024)
Jan L De Bleecker, Kristl G Claeys, Stéphanie Delstanche, Vinciane Van Parys, Jonathan Baets, Sébastien Tilleux, Gauthier Remiche
A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium. Acta neurologica Belgica (2023)
Danique Beijer, Thomas Agnew, Johannes Gregor Matthias Rack, Evgeniia A Prokhorova, Tine Deconinck, Berten Ceulemans, Stojan Peric, Vedrana Milic Rasic, Peter De Jonghe, Ivan Ahel, Jonathan Baets
Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response. Life science alliance 4 (11) (2021)