Eva Pipiras - Concepedia

Author

Eva Pipiras

Hôpital Jean-Verdier

Also Known As

E PIPIRAS, E Pipiras, E. PIpiras, E. Pipiras, Eva Pipiras, Madan-Khetarpal, Suneeta, Pipiras, E.

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Hôpital Jean-Verdier Inserm Assistance Publique – Hôpitaux de Paris Hôpital Robert-Debré Université Paris Cité

About

Eva Pipiras is an author at Hôpital Jean-Verdier specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	15	1.1K
2	Public Health	2	2	57
3	Social Sciences	2	2	141
4	Health Sciences	1	1	41
5	Biology	1	1	67

Eva Pipiras

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Expression of Fragile Sites Triggers Intrachromosomal Mammalian Gene Amplification and Sets Boundaries to Early Amplicons Arnaud Coquelle, Eva Pipiras, Franck Toledo, Cell ChromatinGenome InstabilityDevelopmental BiologyGenetic DisorderGenetics	1997	394
Interstitial deletions and intrachromosomal amplification initiated from a double-strand break targeted to a mammalian chromosome Eva Pipiras The EMBO Journal ChromatinGenome InstabilityMammalian ChromosomeDouble-strand BreakCytogenetics	1998	117
Haploinsufficiency of<i>SOX5</i>at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features Allen N. Lamb, Jill A. Rosenfeld, Nicholas J. Neill, Human Mutation Brain DevelopmentGeneticsLanguage DevelopmentGenomic MechanismAtypical Language Development	2012	101
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations Laïla El Khattabi, Solveig Heide, Jean‐Hubert Caberg, Journal of Medical Genetics	2018	93
<i>WWOX</i>-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation Cyril Mignot, Laëtitia Lambert, Laurent Pasquier, Journal of Medical Genetics	2014	79
Structural chromosomal mosaicism and prenatal diagnosis Eva Pipiras, Céline Dupont, Sandra Chantot‐Bastaraud, Prenatal Diagnosis	2004	74
First cryptic balanced reciprocal translocation mosaicism and familial transmission Céline Dupont, Andrée Delahaye‐Duriez, Lydie Bürglen, American Journal of Medical Genetics Part A	2008	72
Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1 Laïla El Khattabi, Fabien Guimiot, Eva Pipiras, European Journal of Human Genetics BiologyLinkage DisequilibriumGenetic DisorderMedicineGenetics	2014	67
Pre‐ and postnatal phenotype of 6p25 deletions involving the <i>FOXC1</i> gene Andrée Delahaye‐Duriez, Suonavy Khung‐Savatovsky, Azzedine Aboura, American Journal of Medical Genetics Part A Dandy-walker Malformation SpectrumFoxc1 DeletionGeneticsPathologyMolecular Genetics	2012	67
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes Justine Besseau-Ayasse, C. Violle-Poirsier, Anne Bazin, Prenatal Diagnosis	2014	59

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