Author

E. Viégas-Pèquignot

Observed names: E M Viegas-Pequignot, E Pequignot-Viegas, E V Pequignot, E V Péquignot, E VIEGASPEQUIGNOT, E Viegas-Pequignot, E Viegas-Péquignot, E. VIEGAS-PEQUIGNOT, E. Viegas-Pequignot, E. Viegas-Páquignot, E. Viegas-Péquignot, E. Viegas-P�quignot, E.V. Péquignot, Evani M. Viegas-Péquignot, Evani VIEGAS-PÉQUIGNOT, Evani Viegas Pequignot, Evani Viegas-Pequignot, Evani Viegas-Péquignot, Evani Viegas-P�quignot, Evani Viegas-péquignot, Evani Viegas‐Pequignot, Evani Viegas‐Péquignot, Viegas-Pequignot, E., Viegas-Pequignot, E.M, Viegas-Pequignot, Evani, Viegas-Péqzignot, Evani

Observed institutions: Mohammed V University, Hôpital Necker-Enfants Malades, Centre National de la Recherche Scientifique, Inserm, Commissariat à l'Énergie Atomique et aux Énergies Alternatives, Institut Gustave Roussy, Institut Necker Enfants Malades, Université Sorbonne Paris Nord, CEA Paris-Saclay - Etablissement de Fontenay-aux-roses, Institut Jacques Monod, Muséum national d'Histoire naturelle, Fondation Jérôme-Lejeune, Centre d’Immunologie de Marseille-Luminy, Université Paris Diderot, Institut Curie, University of South Alabama

OpenAlex ID: A5111911183

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

1999 · Guo-Liang Xu, Timothy H. Bestor, et al. · Nature · 1,229

LAG-3, a novel lymphocyte activation gene closely related to CD4.

1990 · F Triebel, S Jitsukawa, et al. · The Journal of Experimental Medicine · 939

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

1995 · Thomas Bourgeron, Pierre Rustin, et al. · Nature Genetics · 746

Delayed and incomplete reprogramming of chromosome methylation patterns in bovine cloned embryos

2001 · D Bourc'his, D Le Bourhis, et al. · Current Biology · 393

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

1993 · M. Jeanpierre, C. Turleau, et al. · Human Molecular Genetics · 295

A simple method for simultaneous R- or G-banding and fluorescence in situ hybridization of small single-copy genes

2008 · N. Lemieux, B. Dutrillaux, et al. · Cytogenetics and Cell Genetics · 245

Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions

2008 · Shiran Yehezkel, Yardena Segev, et al. · Human Molecular Genetics · 238

The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

2006 · S Rossignol, V Steunou, et al. · Journal of Medical Genetics · 227

High resolution R- and G-banding on the same preparation

1981 · Bernard Dutrillaux, Evani Viegas-Pequignot · Human Genetics · 206

Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment

1976 · B. Dutrillaux, J. Couturier, et al. · Chromosoma · 164

Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues

2010 · Guillaume Velasco, Florent Hubé, et al. · Proceedings of the National Academy of Sciences · 145

Tenth International Workshop on Human Gene Mapping

2008 · J.D. Tucker, M.L. Christensen, et al. · Cytogenetics and Cell Genetics · 144

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients

1994 · Pierre Miniou, Marc Jeanpierre, et al. · Human Molecular Genetics · 142

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

2004 · Y.L. Jiang, M. Rigolet, et al. · Human Mutation · 138

Mapping of single-copy DNA sequences on human chromosomes by in situ hybridization with biotinylated probes: enhancement of detection sensitivity by intensified-fluorescence digital-imaging microscopy.

1989 · E Viegas-Pequignot, B Dutrillaux, et al. · Proceedings of the National Academy of Sciences · 136

EMR1, an unusual member in the family of hormone receptors with seven transmembrane segments

1995 · Véronique Baud, Stephanie L. Chissoe, et al. · Genomics · 122

The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease.

1997 · L Bürglen, T Seroz, et al. · Europe PMC (PubMed Central) · 99

Defective B-cell-negative selection and terminal differentiation in the ICF syndrome

2003 · Carla E. Blanco-Betancourt, Anne Moncla, et al. · Blood · 91

Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization

1989 · Evani Viegas-P�quignot, Li Zhen Lin, et al. · Human Genetics · 90

Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines

1993 · Anna Almeida, Nadja Kokalj-Vokac, et al. · Human Genetics · 87

α-Satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

1997 · Pierre Miniou, Marc Jeanpierre, et al. · Human Genetics · 84

Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin

2008 · N. Kokalj-Vokac, A. Almeida, et al. · Cytogenetics and Cell Genetics · 82

Regulation of DNA methylation activity through Dnmt3L promoter methylation by Dnmt3 enzymes in embryonic development

2008 · Ye-Guang Hu, Ryutaro Hirasawa, et al. · Human Molecular Genetics · 79

Segmentation of human chromosomes induced by 5-ACR (5-azacytidine)

1976 · Evani Viegas-P�quignot, B. Dutrillaux · Human Genetics · 76

Physical mapping of human loci homologous to the chicken nov proto-oncogene.

1992 · C Martinerie, E Viegas-Pequignot, et al. · PubMed · 70

Works count: 147

Citation count: 8,301

H-index: 39

I10-index: 86