Maurice A. M. Van Steensel
Researcher Next ID · RN-036879
Researcher · Biochemistry, Genetics and Molecular Biology
Agency for Science, Technology and Research
Singapore, Singapore
- Works count
- 647
- Citation count
- 10,907
- H-index
- 55
- i10-index
- 160
Research interests
Publications
Framework nucleic acids as programmable carrier for transdermal drug delivery
Nature Communications · 2019 · https://doi.org/10.1038/s41467-019-09029-9
Homeostasis of the sebaceous gland and mechanisms of acne pathogenesis
British Journal of Dermatology · 2019 · https://doi.org/10.1111/bjd.17981
Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14
The American Journal of Human Genetics · 2012 · https://doi.org/10.1016/j.ajhg.2012.05.010
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies
Human Molecular Genetics · 2011 · https://doi.org/10.1093/hmg/ddr344
Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families
British Journal of Cancer · 2011 · https://doi.org/10.1038/bjc.2011.463
Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009
Journal of the American Academy of Dermatology · 2010 · https://doi.org/10.1016/j.jaad.2009.11.020
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
Nature Genetics · 2009 · https://doi.org/10.1038/ng.276
Birt-Hogg-Dubé syndrome: diagnosis and management
The Lancet Oncology · 2009 · https://doi.org/10.1016/s1470-2045(09)70188-3
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema
Nature Genetics · 2007 · https://doi.org/10.1038/ng2020
Clinical and Pathological Features of Pachyonychia Congenita
Journal of Investigative Dermatology Symposium Proceedings · 2005 · https://doi.org/10.1111/j.1087-0024.2005.10202.x
Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia
The American Journal of Human Genetics · 2003 · https://doi.org/10.1086/375614
A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
Journal of Investigative Dermatology · 2002 · https://doi.org/10.1046/j.1523-1747.2002.01735.x
Current projects
No projects listed.