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Ludwine Messiaen | Researchclopedia

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Ludwine Messiaen

University of Alabama at Birmingham ORCID

279

Works

10,926

Citations

55

h-index

139

i10-index

Research Topics

Neurofibromatosis and Schwannoma Cases Chromatin Remodeling and Cancer Genomic variations and chromosomal abnormalities

Affiliations

Brigham and Women's Hospital2012–2012

Harvard University2012–2012

University of Alabama2004–2021

Chinese Academy of Medical Sciences & Peking Union Medical College1987–1987

University of Washington2015–2015

Top Works

Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

Eric Legius,Ludwine Messiaen,et al.

2021716 citations

Neuroblastoma Research and Treatments

Sarcoma Diagnosis and Treatment

Exhaustive mutation analysis of theNF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects

Ludwine Messiaen,Tom Callens,et al.

2000497 citations

Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype

Hilde Brems,Magdalena Chmara,et al.

2007471 citations

An Absence of Cutaneous Neurofibromas Associated with a 3-bp Inframe Deletion in Exon 17 of the NF1 Gene (c.2970-2972 delAAT): Evidence of a Clinically Significant NF1 Genotype-Phenotype Correlation

Meena Upadhyaya,Susan Huson,et al.

2006360 citations

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

Arkadiusz Piotrowski,Jing Xie,et al.

2013319 citations

Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation

Scott R. Plotkin,Ludwine Messiaen,et al.

2022256 citations

Elucidating Distinct Roles for <i>NF1</i> in Melanomagenesis

Ophélia Maertens,Bryan W. Johnson,et al.

2012245 citations

FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation

Elfride De Baere,Diane Beysen,et al.

2003241 citations

Mutations of <i>VMD2</i> Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC)

Jill Yardley,Bart P. Leroy,et al.

2004226 citations