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J. Lapierre · SciRah

Researcher profile · Semantic Scholar

J. Lapierre

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J. Lapierre — researcher profile on SciRah

h-index: 14
Works: 25
Citations: 415

Most-cited papers

Functional disomy of the Xq28 chromosome region
D. Sanlaville, M. Prieur, M. de Blois, D. Geneviève +11 more
2005European Journal of Human Genetics62 citations
Semantic Scholar
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
S. Brisset, G. Joly, Catherine Ozilou, J. Lapierre +6 more
2002American journal of medical genetics48 citations
Semantic Scholar
Molecular karyotyping in human constitutional cytogenetics.
D. Sanlaville, J. Lapierre, C. Turleau, A. Coquin +4 more
2005European Journal of Medical Genetics31 citations
Semantic Scholar
Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.
J. Lapierre, V. Cacheux, N. Collot, F. D. da Silva +7 more
1998Annales de Genetique31 citations
Semantic Scholar
Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study
J. Lapierre, V. Cacheux, D. Luton, N. Collot +3 more
2000Prenatal Diagnosis27 citations
Semantic Scholar
Phenotype–genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature
M. Nizon, J. Andrieux, C. Rooryck, M. de Blois +31 more
2015American Journal of Medical Genetics. Part A23 citations
Semantic Scholar
A French Approach to Test Fetuses with Ultrasound Abnormalities Using a Customized Microarray as First-Tier Genetic Test
V. Malan, J. Lapierre, M. Egloff, D. Goidin +12 more
2016Cytogenetic and Genome Research22 citations
Semantic Scholar
Altered patterns of DNA methylation on chromosomes from leukemia cell lines: identification of 5-methylcytosines by indirect immunodetection.
Mustapha Bensaada, H. Kiefer, Gérard Tachdjian, J. Lapierre +3 more
1998Cancer Genetics and Cytogenetics22 citations
Semantic Scholar
Large duplication 4q25-q34 with mild clinical effect.
H. Elghezal, H. Sendi, K. Monastiri, J. Lapierre +3 more
2004Annales de Genetique21 citations
Semantic Scholar
PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review.
Oriane Mercati, M. Abi Wardé, G. Lina-Granade, M. Rio +22 more
2020European Journal of Medical Genetics20 citations Open access
Semantic Scholar
De novo inverted duplication 9p21pter involving telomeric repeated sequences.
D. Sanlaville, C. Baumann, J. Lapierre, S. Romana +4 more
1999American journal of medical genetics20 citations
Semantic Scholar
Cytogenetic analysis from DNA by comparative genomic hybridization.
Gérard Tachdjian, A. Aboura, J. Lapierre, F. Viguié
2000Annales de Genetique19 citations
Semantic Scholar
Comparative genomic hybridization: technical development and cytogenetic aspects for routine use in clinical laboratories.
J. Lapierre, V. Cacheux, F. D. da Silva, N. Collot +3 more
1998Annales de Genetique17 citations
Semantic Scholar
17q21.31 Microdeletion: Brain Anomalies Leading to Prenatal Diagnosis
M. Egloff, F. Encha-Razavi, C. Garel, Maryse Bonnière-Darcy +8 more
2014Cytogenetic and Genome Research14 citations
Semantic Scholar
Detection of chromosomal abnormalities by comparative genomic hybridization
J. Lapierre, G. Tachdjian
2005Current Opinion in Obstetrics and Gynecology12 citations
Semantic Scholar
Formation of Nup98-containing nuclear bodies in HeLa sublines is linked to genomic rearrangements affecting chromosome 11
S. Romana, I. Radford-Weiss, J. Lapierre, V. Doye +1 more
2016Chromosoma8 citations
Semantic Scholar
[Microarray CGH: principle and use for constitutional disorders].
Damien Sanlaville, J. Lapierre, A. Coquin, C. Turleau +6 more
2005Archives de pédiatrie4 citations
Semantic Scholar
Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3
E. Martin, V. Cacheux, H. Cavé, J. Lapierre +2 more
1995Human Genetics4 citations
Semantic Scholar
CGH analysis in a cohort of 17 chromosomally normal fetuses with an increased nuchal translucency
S. Brisset, S. Romana, I. Texier, J. Lapierre +3 more
2003Prenatal Diagnosis3 citations
Semantic Scholar
Comparative Genomic Hybridization
J. Lapierre, G. Tachdjian
20013 citations
Semantic Scholar
A fertilin-derived peptide improves in vitro maturation and ploidy of human oocytes.
A. Sallem, A. Denizot, A. Ziyyat, Audrey L'Hostis +11 more
2021F&S Science2 citations Open access
Semantic Scholar
Cyclic fertilin-derived peptide stimulates in vitro human embryo development.
A. Denizot, Audrey L'Hostis, A. Sallem, Sophie Favier +17 more
2021F&S Science2 citations Open access
Semantic Scholar
A 22q13.1 duplication in mosaicism including SOX10
William Bertani-Torres, M. Serey-Gaut, Judite de Oliveira, C. Bole +9 more
2023American Journal of Medical Genetics. Part A0 citations Open access
Semantic Scholar
Formation of Nup98-containing nuclear bodies in HeLa sublines is linked to genomic rearrangements affecting chromosome 11
Serge Romana, I. Radford-Weiss, J. Lapierre, V. Doye +1 more
2015Chromosoma0 citations
Semantic Scholar
Prenatal diagnosis of a (X;X) translocation by fluorescence in situ hybridization and laser scanning image cytometry.
Gérard Tachdjian, V. Cacheux, H. Kiefer, L. Druart +4 more
1995Fetal Diagnosis and Therapy0 citations
Semantic Scholar

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S. Romana×10
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S. Romana — researcher profile on SciRah
V. Cacheux×7
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M. Vekemans×6
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C. Turleau×6
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Gérard Tachdjian

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M. de Blois — researcher profile on SciRah

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Serge Romana — researcher profile on SciRah