Liselot van der Laan

Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases

Jennifer Kerkhof, Cassandra Rastin, Michael A. Levy et al. · Genetics in Medicine · 2024 · 66 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

María del Rocío Pérez Baca, Eva Jacobs, Lies Vantomme et al. · The American Journal of Human Genetics · 2024 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options

Niels Vos, Lotte Kleinendorst, Liselot van der Laan et al. · European Journal of Human Genetics · 2024 · 21 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder

Kathleen Rooney, Liselot van der Laan, Slavica Trajkova et al. · Genetics in Medicine · 2023 · 20 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

DNA Methylation Signature for JARID2-Neurodevelopmental Syndrome

Eline A. Verberne, Liselot van der Laan, Sadegheh Haghshenas et al. · International Journal of Molecular Sciences · 2022 · 17 citations · Full text

Medicine, Genetics, Molecular Genetics +17