Virginie Bernard

Virginie Bernard

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Virginie Bernard

Virginie Bernard

Publications by authors named "Virginie Bernard"

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Targeted next-generation sequencing identifies clinically relevant somatic mutations in a large cohort of inflammatory breast cancer.

Breast Cancer Res 2018 08 7;20(1):88. Epub 2018 Aug 7.

Pharmacogenomic Unit, Department of Genetics, Curie Institute, PSL Research University, 26 rue d'Ulm, 75005, Paris, France.

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http://dx.doi.org/10.1186/s13058-018-1007-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081877PMC
August 2018

Frequent Somatic Mutation in Adult Intestinal Stem Cells Drives Neoplasia and Genetic Mosaicism during Aging.

Cell Stem Cell 2015 Dec 22;17(6):663-674. Epub 2015 Oct 22.

Institut Curie, 26 rue d'Ulm, F-75248 Paris, France; CNRS UMR3215, F-75248 Paris, France; INSERM U934, F-75248 Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.stem.2015.09.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138153PMC
December 2015

Deep Sequencing Reveals Occurrence of Subclonal ALK Mutations in Neuroblastoma at Diagnosis.

Clin Cancer Res 2015 Nov 9;21(21):4913-21. Epub 2015 Jun 9.

Equipe SiRIC RTOP Recherche Translationelle en Oncologie Pédiatrique, Institut Curie, Paris, France. INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Institut Curie, Paris, France. Département de Pédiatrie, Institut Curie, Paris, France.

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http://dx.doi.org/10.1158/1078-0432.CCR-15-0423DOI Listing
November 2015

Circulating tumor DNA as a non-invasive substitute to metastasis biopsy for tumor genotyping and personalized medicine in a prospective trial across all tumor types.

Mol Oncol 2015 Apr 26;9(4):783-90. Epub 2014 Dec 26.

Circulating Cancer Biomarkers Lab, SiRIC, Translational Research Department, Institut Curie, Paris, France; Department of Medical Oncology, Institut Curie, Paris and Saint-Cloud, France; University Paris Descartes, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.molonc.2014.12.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5528781PMC
April 2015

[Treating female victims of violence in a medical-judicial unit].

Authors:
Virginie Bernard

Rev Infirm 2014 Nov(205):33-5

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November 2014

Emergence of new ALK mutations at relapse of neuroblastoma.

J Clin Oncol 2014 Sep 28;32(25):2727-34. Epub 2014 Jul 28.

Gudrun Schleiermacher, Julie Cappo, Isabelle Janoueix-Lerosey, and Olivier Delattre, L'Institut National de la Santé et de la Recherche Médicale U830, Laboratoire de Génétique et Biologie des Cancers; Gudrun Schleiermacher, Virginie Bernard, Quentin Leroy, Thomas Rio Frio, Gaelle Pierron, Eve Lapouble, and Jean Michon, Institut Curie; Michel Peuchmaur, Assistance Publique-Hôpitaux de Paris, Hôpital Universitaire Robert Debré, Service de Pathologie; Michel Peuchmaur, Université Diderot Paris 7, Sorbonne Paris-Cité, Paris; Valérie Combaret, Centre Léon-Bérard, Laboratoire de Recherche Translationnelle, Lyon, France; Niloufar Javanmardi, Anna Djos, Jonas Abrahamsson, and Tommy Martinsson, The Sahlgrenska Academy, University of Gothenburg, Sahlgrenska University Hospital, Gothenburg; Ingrid Øra, Lund University, Lund; Fredrik Hedborg, Uppsala University, and Centre for Research and Development, Uppsala University/County Council of Gävleborg, Gävle; Catarina Träger and Per Kogner, Karolinska Institute, Astrid Lindgren Children's Hospital, Stockholm; Britt-Marie Holmqvist, Linköping University Hospital, Linköping, Sweden; Frank Speleman and Bram de Wilde, Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.

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http://dx.doi.org/10.1200/JCO.2013.54.0674DOI Listing
September 2014

Learn from the best.

PLoS Comput Biol 2014 May 29;10(5):e1003645. Epub 2014 May 29.

Computational Cancer Biology, Netherlands Cancer Institute, Amsterdam, Netherlands.

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http://dx.doi.org/10.1371/journal.pcbi.1003645DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038457PMC
May 2014

Mitochondrial carbonic anhydrase VA deficiency resulting from CA5A alterations presents with hyperammonemia in early childhood.

Am J Hum Genet 2014 Mar 13;94(3):453-61. Epub 2014 Feb 13.

Division of Biochemical Diseases, BC Children's Hospital, University of British Columbia, Vancouver, BC V6H 3V4, Canada; Department of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, BC V6H 3V4, Canada; Treatable Intellectual Disability Endeavour in British Columbia, BC Children's Hospital, University of British Columbia, Vancouver, BC V5Z 4H4, Canada.

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http://dx.doi.org/10.1016/j.ajhg.2014.01.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951944PMC
March 2014

Explain bioinformatics to your grandmother!

PLoS Comput Biol 2013 Oct 31;9(10):e1003305. Epub 2013 Oct 31.

Next Generation Sequencing Platform - ICGex, Curie Institute, Paris, France.

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http://dx.doi.org/10.1371/journal.pcbi.1003305DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814846PMC
October 2013

Identification of cis-regulatory sequence variations in individual genome sequences.

Genome Med 2011 Oct 10;3(10):65. Epub 2011 Oct 10.

Centre for Molecular Medicine and Therapeutics at the Child and Family Research Institute, Department of Medical Genetics, University of British Columbia, 950 West 28th Avenue, Vancouver, BC V5Z 4H4, Canada.

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http://dx.doi.org/10.1186/gm281DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239227PMC
October 2011

Improved detection of motifs with preferential location in promoters.

Genome 2010 Sep;53(9):739-52

Unité de Recherche en Génomique Végétale (URGV), UMR INRA 1165 - CNRS 8114 - UEVE, 91057 Evry CEDEX, France.

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http://dx.doi.org/10.1139/g10-042DOI Listing
September 2010

TC-motifs at the TATA-box expected position in plant genes: a novel class of motifs involved in the transcription regulation.

BMC Genomics 2010 Mar 12;11:166. Epub 2010 Mar 12.

Unité de Recherche en Génomique Végétale (URGV), UMR INRA 1165-CNRS 8114-UEVE, 2 Rue Gaston Crémieux, 91057 Evry Cedex, France.

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http://www-urgv.versailles.inra.fr/pub/20222994_TC-motifs-at
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http://www.biomedcentral.com/1471-2164/11/166
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http://dx.doi.org/10.1186/1471-2164-11-166DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2842252PMC
March 2010

Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation.

Eur J Med Genet 2007 May-Jun;50(3):200-8. Epub 2007 Feb 20.

Laboratoire de Génétique, Service de Génétique Moléculaire et Clinique, Bâtiment 7, Hôpital Edouard Herriot, Lyon, France.

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http://dx.doi.org/10.1016/j.ejmg.2007.02.001DOI Listing
July 2007

A computed method for noninvasive MRI assessment of pulmonary arterial hypertension.

J Appl Physiol (1985) 2004 Feb 29;96(2):463-8. Epub 2003 Aug 29.

Service de Médecine Nucléaire, Hôpital du Haut-Lévêque, 33604 Pessac, France.

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http://dx.doi.org/10.1152/japplphysiol.00292.2003DOI Listing
February 2004

The -308 G/A tumor necrosis factor-alpha gene dimorphism: a risk factor for unstable angina.

Clin Chem Lab Med 2003 Apr;41(4):511-6

Institut Fédératif de Recherche no 4 Heart-Lung-Vessel-Thrombosis, Institut National de la Santé et de la Recherche Médicale (U441), Pessac, France.

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http://dx.doi.org/10.1515/CCLM.2003.077DOI Listing
April 2003