Peter Lauffer

SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling

Yuh‐Charn Lin, Marcello Niceta, Valentina Muto et al. · The American Journal of Human Genetics · 2020 · 64 citations · Full text

Developmental Anomaly, Sclerostin, Developmental Biology +9

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

Neurodevelopmental Disorders, Epigenetic Change, Genetics +12

Episignature Mapping of TRIP12 Provides Functional Insight into Clark–Baraitser Syndrome

Liselot van der Laan, Kathleen Rooney, Mariëlle Alders et al. · International Journal of Molecular Sciences · 2022 · 13 citations · Full text

Peripheral Blood DNA Methylation Signatures and Response to Tofacitinib in Moderate-to-severe Ulcerative Colitis

V Joustra, Andrew Y. F. Li Yim, Sara van Gennep et al. · Journal of Crohn s and Colitis · 2023 · 13 citations · Full text

Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles

Sadegheh Haghshenas, Hidde J. Bout, Josephine Schijns et al. · Human Genetics and Genomics Advances · 2024 · 11 citations · Full text