Chuanhua Fu

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

Arkadiusz Piotrowski, Jing Xie, Ying F Liu et al. · Nature Genetics · 2013 · 322 citations

Life Sciences, Genetics, Molecular Genetics +15

Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)

Ludwine M. Messiaen, J. Vogt, Kathrin Bengesser et al. · Human Mutation · 2010 · 117 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Decoding NF1 Intragenic Copy-Number Variations

Meng-Chang Hsiao, Arkadiusz Piotrowski, Tom Callens et al. · The American Journal of Human Genetics · 2015 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Identification of recurrent type-2<i>NF1</i>microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder

J. Vogt, Kathrin Bengesser, Kathleen Claes et al. · Human Mutation · 2012 · 28 citations

Life Sciences, Genetics, Molecular Genetics +17

Identification of <i>SPRED1</i> deletions using RT‐PCR, multiplex ligation‐dependent probe amplification and quantitative PCR

Emily Spencer, Julia Davis, Fady M. Mikhail et al. · American Journal of Medical Genetics Part A · 2011 · 19 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16