Gerben van der Vries

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia

Esther Nibbeling, Anna Duarri, Corien C. Verschuuren‐Bemelmans et al. · Brain · 2017 · 123 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

Birte Zurek, Kornelia Ellwanger, Lisenka E.L.M. Vissers et al. · European Journal of Human Genetics · 2021 · 103 citations · Full text

Life Sciences, Bioinformatics, Biomedical Informatics +15

Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

Carles Hernandéz-Ferrer, Davide Piscia, Enzo Cohen et al. · European Journal of Human Genetics · 2021 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics

Nicolien Hanemaaijer, Birgit Sikkema‐Raddatz, Gerben van der Vries et al. · European Journal of Human Genetics · 2011 · 71 citations · Full text

Life Sciences, Bioinformatics, Early Detection +11

Genomic aberrations in squamous cell lung carcinoma related to lymph node or distant metastasis

Mirjam C. Boelens, Klaas Kok, Pieter van der Vlies et al. · Lung Cancer · 2009 · 65 citations

Medicine, Genetics, Oncology +16