Frits A. Beemer

Identification of the familial cylindromatosis tumour-suppressor gene

Graham R. Bignell, William Warren, Sheila Seal et al. · Nature Genetics · 2000 · 672 citations

Medicine, Genetics, Oncology +10

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

Marie‐José H. van den Boogaard, M. Dorland, Frits A. Beemer et al. · Nature Genetics · 2000 · 587 citations

Dentistry, Craniofacial Biology, Orthodontics +16

Clinical Screening as Compared with DNA Analysis in Families with Multiple Endocrine Neoplasia Type 2A

Cornelis J.M. Lips, Rudy M. Landsvater, Jo W.M. Höppener et al. · New England Journal of Medicine · 1994 · 455 citations

Medicine, Genetics, Molecular Genetics +17

p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation

Hans van Bokhoven, Ben C.J. Hamel, Mike Bamshad et al. · The American Journal of Human Genetics · 2001 · 378 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy

Claire Navarro, Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard et al. · Human Molecular Genetics · 2004 · 368 citations · Full text

Medicine, Genetics, Molecular Genetics +17