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V. Steunou · SciRah

Researcher profile · Semantic Scholar

V. Steunou

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V. Steunou — researcher profile on SciRah

h-index: 17
Works: 30
Citations: 1,786

Most-cited papers

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome
C. Gicquel, S. Rossignol, S. Cabrol, M. Houang +9 more
2005Nature Genetics516 citations
Semantic Scholar
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.
I. Netchine, S. Rossignol, M. Dufourg, S. Azzi +18 more
2007Journal of Clinical Endocrinology and Metabolism289 citations
Semantic Scholar
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.
S. Azzi, S. Rossignol, V. Steunou, T. Sas +8 more
2009Human Molecular Genetics228 citations
Semantic Scholar
The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region
S. Rossignol, V. Steunou, C. Chalas, A. Kerjean +5 more
2006Journal of Medical Genetics224 citations Open access
Semantic Scholar
Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome.
Walid Abi Habib, S. Azzi, F. Brioude, V. Steunou +13 more
2014Human Molecular Genetics67 citations
Semantic Scholar
Epigenetics, genomic imprinting and assisted reproductive technology.
Y. Le Bouc, S. Rossignol, S. Azzi, V. Steunou +2 more
2010Annales d'Endocrinologie57 citations
Semantic Scholar
Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome
S. Geoffron, Walid Abi Habib, S. Chantot-Bastaraud, B. Dubern +28 more
2018Journal of Clinical Endocrinology and Metabolism51 citations Open access
Semantic Scholar
Simultaneous Hyper‐ and Hypomethylation at Imprinted Loci in a Subset of Patients with GNAS Epimutations Underlies a Complex and Different Mechanism of Multilocus Methylation Defect in Pseudohypoparathyroidism Type 1b
S. Maupetit-Méhouas, S. Azzi, V. Steunou, Nathalie Sakakini +8 more
2013Human Mutation51 citations Open access
Semantic Scholar
Allele‐specific methylated multiplex real‐time quantitative PCR (ASMM RTQ‐PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes
S. Azzi, V. Steunou, Alexandra Rousseau, S. Rossignol +6 more
2011Human Mutation48 citations
Semantic Scholar
IGF2 Promotes Growth of Adrenocortical Carcinoma Cells, but Its Overexpression Does Not Modify Phenotypic and Molecular Features of Adrenocortical Carcinoma
M. Guillaud-Bataille, B. Ragazzon, A. de Reyniès, C. Chevalier +14 more
2014PLoS ONE46 citations Open access
Semantic Scholar
Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders
Walid Abi Habib, F. Brioude, S. Azzi, S. Rossignol +7 more
2019Science Advances40 citations Open access
Semantic Scholar
Complex Tissue‐Specific Epigenotypes in Russell–Silver Syndrome Associated with 11p15 ICR1 Hypomethylation
S. Azzi, A. Blaise, V. Steunou, M. Harbison +11 more
2014Human Mutation40 citations Open access
Semantic Scholar
Lack of alteration in GATA-1 expression in CD34+ hematopoietic progenitors from patients with idiopathic myelofibrosis.
M. Martyré, V. Steunou, M. Lebousse-Kerdiles, J. Wietzerbin
2003Blood27 citations Open access
Semantic Scholar
p95vav associates with the type I interferon (IFN) receptor and contributes to the antiproliferative effect of IFN-α in megakaryocytic cell lines
A. Micouin, J. Wietzerbin, V. Steunou, M. Martyré
2000Oncogene26 citations Open access
Semantic Scholar
Increasing knowledge in IGF1R defects: lessons from 35 new patients
É. Giabicani, M. Willems, V. Steunou, S. Chantot-Bastaraud +29 more
2019Journal of Medical Genetics25 citations Open access
Semantic Scholar
Insights from the genetic characterization of central precocious puberty associated with multiple anomalies.
A. Canton, A. Krepischi, L. Montenegro, S. Costa +16 more
2020Human Reproduction21 citations
Semantic Scholar
Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome
S. Azzi, V. Steunou, J. Tost, S. Rossignol +9 more
2014Journal of Medical Genetics20 citations
Semantic Scholar
Altered transcription of the stem cell leukemia gene in myelofibrosis with myeloid metaplasia
V. Steunou, M. Le Bousse-Kerdilès, A. Colin-Micouin, Denis Clay +2 more
2003Leukemia10 citations
Semantic Scholar
Lack of interferon‐α‐induced tyrosine phosphorylation of Vav proto‐oncogene in patients with myelofibrosis with myeloid metaplasia
A. Micouin, V. Steunou, J. Wietzerbin, M. Martyré
20003 citations Open access
Semantic Scholar
PEDIATRIC SEXUAL DIFFERENTIATION, PUBERTY, AND BONE BIOLOGY Investigation of Imprinting Defects in MKRN3 and DLK1 in Children with Idiopathic Central Precocious Puberty Through Specific DNA Methylation Analysis
V. Steunou
20200 citations
Semantic Scholar
Increasing Knowledge in IGF1R Defects: Lessons from 20 New Patients
É. Giabicani, M. Willems, V. Steunou, S. Chantot-Bastaraud +4 more
20190 citations
Semantic Scholar
Investigation of Imprinting Alterations in MKRN3 and DLK1 in a Cohort of Girls with Central Precocious Puberty Through Specific DNA Methylation Analysis
A. Canton, V. Steunou, V. Brito, Sobrier Marie Laure +5 more
20190 citations
Semantic Scholar
Silver Russell and Beckwith-Wiedemann Syndromes: Mosaic Distribution of Epigenetic Anomalies
Aurélie Pham, É. Giabicani, V. Steunou, I. Netchine +1 more
20180 citations
Semantic Scholar
PO4-9: Complex tissue-specific epigenotypes in Russell Silver syndrome with 11p15 ICR1 hypomethylation: major consequences for the diagnosis
S. Azzi, A. Blaise, V. Steunou, N. Thibaud +2 more
20140 citations
Semantic Scholar
Le phénomène d’héritage comme construction d’une architecture signifiante en Navarre
V. Steunou
20130 citations
Semantic Scholar
Simultaneous gain and loss of methylation at imprinted loci in a subset of patients with pseudohypoparathyroidism type 1b and GNAS epimutations
S. Maupetit-Méhouas, S. Azzi, V. Steunou, C. Reynès +4 more
20120 citations
Semantic Scholar
P-18 Russell-Silver Syndrome: clinical scoring system and molecular investigations on a large series of patients
I. Netchine, S. Rossignol, S. Azzi, F. Danton +6 more
20080 citations
Semantic Scholar
P-17 Heterogeneous clinical presentation in patients with yet-unreported type 1 IGF receptor molecular defects
S. Azzi, Nathalie Thibaud, J. Ricort, P. Souchon +10 more
20080 citations
Semantic Scholar
P-83 Study of two IGF-1R gene expression variants
V. Steunou, S. Azzi, S. Rossignol, I. Netchine +1 more
20080 citations
Semantic Scholar
Lack of interferon-alpha-induced tyrosine phosphorylation of Vav proto-oncogene in patients with myelofibrosis with myeloid metaplasia.
A. Micouin, V. Steunou, J. Wietzerbin, M. Martyré
2000British Journal of Haematology0 citations
Semantic Scholar

Frequent co-authors

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I. Netchine×21
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I. Netchine — researcher profile on SciRah
S. Rossignol×16
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S. Rossignol — researcher profile on SciRah
Y. Le Bouc×16
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Y. Le Bouc — researcher profile on SciRah
S. Azzi×16
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S. Azzi — researcher profile on SciRah

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N. Thibaud — researcher profile on SciRah

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C. Gicquel — researcher profile on SciRah

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F. Brioude — researcher profile on SciRah

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F. Danton — researcher profile on SciRah

Walid Abi Habib×5

Marilyne Le Jule×5

É. Giabicani×5

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É. Giabicani — researcher profile on SciRah

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S. Cabrol — researcher profile on SciRah