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D. Vidaud · SciRah

Researcher profile · Semantic Scholar

D. Vidaud

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D. Vidaud — researcher profile on SciRah

h-index: 47
Works: 154
Citations: 8,360

Most-cited papers

Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.
É. Pasmant, I. Laurendeau, D. Heron, M. Vidaud +2 more
2007Cancer Research657 citations Open access
Semantic Scholar
Acute portal vein thrombosis unrelated to cirrhosis: A prospective multicenter follow‐up study
A. Plessier, S. Darwish-Murad, M. Hernández-Guerra, Yann Consigny +14 more
2010Hepatology596 citations Open access
Semantic Scholar
NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype
É. Pasmant, A. Sabbagh, G. Spurlock, I. Laurendeau +20 more
2010Human Mutation251 citations Open access
Semantic Scholar
IL28B polymorphism is associated with treatment response in patients with genotype 4 chronic hepatitis C.
T. Asselah, S. De Muynck, P. Broët, J. Masliah-Planchon +15 more
2012Journal of Hepatology189 citations
Semantic Scholar
The molecular landscape of glioma in patients with Neurofibromatosis 1
F. D'Angelo, M. Ceccarelli, Tala, L. Garofano +43 more
2018Nature Medicine185 citations Open access
Semantic Scholar
Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network
A. Caye, M. Strullu, F. Guidez, B. Cassinat +29 more
2015Nature Genetics185 citations
Semantic Scholar
Liver gene expression signature of mild fibrosis in patients with chronic hepatitis C.
T. Asselah, I. Bièche, I. Laurendeau, V. Paradis +7 more
2005Gastroenterology182 citations Open access
Semantic Scholar
NF1 Molecular Characterization and Neurofibromatosis Type I Genotype–Phenotype Correlation: The French Experience
A. Sabbagh, É. Pasmant, A. Imbard, A. Luscan +10 more
2013Human Mutation177 citations
Semantic Scholar
Molecular profiling of early stage liver fibrosis in patients with chronic hepatitis C virus infection.
I. Bièche, T. Asselah, I. Laurendeau, D. Vidaud +6 more
2005Virology171 citations Open access
Semantic Scholar
Telangiectatic adenoma: An entity associated with increased body mass index and inflammation
V. Paradis, A. Champault, M. Ronot, L. Deschamps +5 more
2007Hepatology169 citations Open access
Semantic Scholar
Neurofibromatosis type 1: from genotype to phenotype
É. Pasmant, M. Vidaud, D. Vidaud, P. Wolkenstein
2012Journal of Medical Genetics159 citations Open access
Semantic Scholar
Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma.
N. Burnichon, A. Buffet, B. Parfait, E. Letouzé +10 more
2012Human Molecular Genetics151 citations
Semantic Scholar
Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1.
A. Sabbagh, É. Pasmant, I. Laurendeau, B. Parfait +8 more
2009Human Molecular Genetics146 citations Open access
Semantic Scholar
Liver fibrosis in women with chronic hepatitis C: evidence for the negative role of the menopause and steatosis and the potential benefit of hormone replacement therapy
L. Codes, T. Asselah, D. Cazals-Hatem, F. Tubach +5 more
2006Gut138 citations Open access
Semantic Scholar
Liver iron, HFE gene mutations, and hepatocellular carcinoma occurrence in patients with cirrhosis.
P. Nahon, A. Sutton, P. Rufat, M. Ziol +9 more
2008Gastroenterology134 citations Open access
Semantic Scholar
Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1.
É. Pasmant, A. Sabbagh, J. Masliah-Planchon, N. Ortonne +12 more
2011Journal of the National Cancer Institute116 citations
Semantic Scholar
Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?
É. Pasmant, B. Parfait, A. Luscan, P. Goussard +8 more
2014European Journal of Human Genetics112 citations Open access
Semantic Scholar
Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.
Sahra Bodo, C. Colas, O. Buhard, A. Collura +46 more
2015Gastroenterology94 citations Open access
Semantic Scholar
SPiP: Splicing Prediction Pipeline, a machine learning tool for massive detection of exonic and intronic variant effects on mRNA splicing
R. Leman, B. Parfait, D. Vidaud, E. Girodon +32 more
2022Human Mutation89 citations Open access
Semantic Scholar
Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion
T. De Raedt, M. Stephens, I. Heyns, H. Brems +10 more
2006Nature Genetics87 citations
Semantic Scholar
Genetic polymorphisms in antioxidant enzymes modulate hepatic iron accumulation and hepatocellular carcinoma development in patients with alcohol-induced cirrhosis.
A. Sutton, P. Nahon, D. Pessayre, P. Rufat +9 more
2006Cancer Research80 citations Open access
Semantic Scholar
Molecular profiling of malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1, based on large-scale real-time RT-PCR
P. Lévy, D. Vidaud, K. Leroy, I. Laurendeau +6 more
2004Molecular Cancer73 citations Open access
Semantic Scholar
High predictive value of early viral kinetics in retreatment with peginterferon and ribavirin of chronic hepatitis C patients non-responders to standard combination therapy.
R. Moucari, M. Ripault, V. Oulés, M. Martinot-Peignoux +8 more
2007Journal of Hepatology59 citations
Semantic Scholar
Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis
Camille Louvrier, É. Pasmant, A. Briand-Suleau, Joëlle Cohen +11 more
2018Neuro-Oncology58 citations Open access
Semantic Scholar
Confirmation of mutation landscape of NF1‐associated malignant peripheral nerve sheath tumors
Pierre Sohier, A. Luscan, A. Lloyd, K. Ashelford +6 more
2017Genes, Chromosomes and Cancer58 citations
Semantic Scholar
Extrahepatic Portal Venous System Thrombosis in Recurrent Acute and Chronic Alcoholic Pancreatitis Is Caused by Local Inflammation and Not Thrombophilia
V. Rebours, L. Boudaoud, M. Vullierme, D. Vidaud +6 more
2012American Journal of Gastroenterology57 citations
Semantic Scholar
First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis
É. Pasmant, P. Goussard, L. Baranes, I. Laurendeau +9 more
2011European Journal of Human Genetics55 citations Open access
Semantic Scholar
Microarray-Based Identification of Tenascin C and Tenascin XB, Genes Possibly Involved in Tumorigenesis Associated with Neurofibromatosis Type 1
P. Lévy, H. Ripoche, I. Laurendeau, V. Lazar +10 more
2007Clinical Cancer Research54 citations
Semantic Scholar
MicroRNAome profiling in benign and malignant neurofibromatosis type 1-associated nerve sheath tumors: evidences of PTEN pathway alterations in early NF1 tumorigenesis
J. Masliah-Planchon, É. Pasmant, A. Luscan, I. Laurendeau +12 more
2013BMC Genomics53 citations Open access
Semantic Scholar
SETD2 and DNMT3A screen in the Sotos-like syndrome French cohort
C. Tlemsani, A. Luscan, N. Leulliot, E. Bieth +20 more
2016Journal of Medical Genetics52 citations
Semantic Scholar
Identification of Genes Potentially Involved in the Increased Risk of Malignancy in NF1-Microdeleted Patients
É. Pasmant, J. Masliah-Planchon, P. Lévy, I. Laurendeau +8 more
2011Molecular Medicine49 citations Open access
Semantic Scholar
Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patients
V. Piddubnyak, P. Rigou, L. Michel, J. Rain +6 more
2007Cell Death and Differentiation40 citations
Semantic Scholar
Molecular Profiles of Neurofibromatosis Type 1-Associated Plexiform Neurofibromas
P. Lévy, I. Bièche, K. Leroy, B. Parfait +5 more
2004Clinical Cancer Research39 citations
Semantic Scholar
Moyamoya syndrome in children with neurofibromatosis type 1: Italian–French experience
C. Santoro, F. Di Rocco, M. Kossorotoff, M. Zérah +15 more
2017American Journal of Medical Genetics. Part A38 citations
Semantic Scholar
Frequent EGFR Positivity and Overexpression in High-Grade Areas of Human MPNSTs
Séverine Tabone-Eglinger, R. Bahleda, J. Côté, P. Terrier +9 more
2008Sarcoma37 citations Open access
Semantic Scholar
Severe Phenotype in Patients with Large Deletions of NF1
Laurence Pacot, D. Vidaud, A. Sabbagh, I. Laurendeau +46 more
2021Cancers34 citations Open access
Semantic Scholar
Characterization of a 7.6-Mb germline deletion encompassing the NF1 locus and about a hundred genes in an NF1 contiguous gene syndrome patient
É. Pasmant, Aurélie de Saint-Trivier, I. Laurendeau, A. Dieux-Coeslier +4 more
2008European Journal of Human Genetics32 citations
Semantic Scholar
Non-invasive prenatal diagnosis of paternally inherited disorders from maternal plasma: detection of NF1 and CFTR mutations using droplet digital PCR
Aurélia Gruber, M. Pacault, L. El Khattabi, Nicolas Vaucouleur +13 more
2018Clinical Chemistry and Laboratory Medicine31 citations
Semantic Scholar
Epithelial-to-Mesenchymal Transition and Oncogenic Ras Expression in Resistance to the Protein Kinase Cβ Inhibitor Enzastaurin in Colon Cancer Cells
M. Serova, Lucile Astorgues-Xerri, I. Bièche, S. Albert +9 more
2010Molecular Cancer Therapeutics31 citations Open access
Semantic Scholar
Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya Angiopathy
L. Grangeon, S. Guey, J. Schwitalla, F. Bergametti +9 more
2019Stroke30 citations Open access
Semantic Scholar
Significant gene expression differences in histologically “Normal” liver biopsies: Implications for control tissue
T. Asselah, I. Bièche, I. Laurendeau, M. Martinot-Peignoux +6 more
2008Hepatology27 citations Open access
Semantic Scholar
Technical Advance Detection and Characterization of NF1 Microdeletions by Custom High Resolution Array CGH
É. Pasmant, A. Sabbagh, J. Masliah-Planchon, I. Laurendeau +4 more
200926 citations
Semantic Scholar
NF1 single and multi-exons copy number variations in neurofibromatosis type 1
A. Imbard, É. Pasmant, A. Sabbagh, A. Luscan +11 more
2015Journal of Human Genetics19 citations
Semantic Scholar
NF1 mutations identify molecular and clinical subtypes of lung adenocarcinomas
C. Tlemsani, N. Pécuchet, Aurélia Gruber, I. Laurendeau +19 more
2019Cancer Medicine17 citations Open access
Semantic Scholar
Prothrombin Saint‐Denis: a natural variant with a point mutation resulting in Asp to Glu substitution at position 552 in prothrombin
Stanislas Rouy, D. Vidaud, J. Alessandri, M. Dautzenberg +3 more
2006British Journal of Haematology17 citations
Semantic Scholar
Increase in type II collagen turnover after iron depletion in patients with hereditary haemochromatosis.
P. Richette, C. Eymard, M. Deberg, D. Vidaud +5 more
2010Rheumatology16 citations Open access
Semantic Scholar
Global proteomic analysis of microdissected cirrhotic nodules reveals significant biomarkers associated with clonal expansion
N. Guedj, D. Dargère, F. Degos, J. Janneau +4 more
2006Laboratory Investigation16 citations Open access
Semantic Scholar
FAS promoter polymorphisms correlate with activity grade in hepatitis C patients
D. McIlroy, I. Theodorou, V. Ratziu, D. Vidaud +3 more
2005European Journal of Gastroenterology and Hepathology16 citations
Semantic Scholar
Differential Expression of CCN1/CYR61, CCN3/NOV, CCN4/WISP1, and CCN5/WISP2 in Neurofibromatosis Type 1 Tumorigenesis
É. Pasmant, N. Ortonne, L. Rittié, I. Laurendeau +11 more
2010Journal of Neuropathology and Experimental Neurology15 citations
Semantic Scholar
Neurofibromatosis 1: Analysis of the demand for prenatal diagnosis in a French cohort of 361 patients
D. Farhi, S. Bastuji-Garin, K. Khosrotehrani, D. Vidaud +3 more
2008American Journal of Medical Genetics. Part A15 citations
Semantic Scholar

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