Mark Nellist

Years Active: 2019-2022
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Hannie C W Douben, Mark Nellist, Leontine van Unen, Peter Elfferich, Esmee Kasteleijn, Marianne Hoogeveen-Westerveld, Jesse Louwen, Monique van Veghel-Plandsoen, Walter de Valk, Jasper J Saris, Femke Hendriks, Esther Korpershoek, Lies H Hoefsloot, Margreethe van Vliet, Yolande van Bever, Ingrid M B H van de Laar, Emmelien Aten, Augusta M A Lachmeijer, Walter Taal, Lisa van den Bersselaar, Juliette Schuurmans, Rianne Oostenbrink, Rick van Minkelen, Yvette van Ierland, Tjakko J van Ham
High-yield identification of pathogenic NF1 variants by skin fibroblast transcriptome screening after apparently normal diagnostic DNA testing. Human mutation (2022)
Luiz G Dufner Almeida, Santoesha Nanhoe, Andrea Zonta, Mitra Hosseinzadeh, Regina Kom-Gortat, Peter Elfferich, Gerben Schaaf, Annegien Kenter, Daniel Kümmel, Nicola Migone, Sue Povey, Rosemary Ekong, Mark Nellist
Comparison of the functional and structural characteristics of rare TSC2 variants with clinical and genetic findings. Human mutation 41 (4) (2019)

Mark Nellist.css-eqlu8i{font-size:small;padding-left:4px;}