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Papers authored by Le Meur N

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MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations.

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Le Meur N, Holder-Espinasse M, Jaillard S, Goldenberg A, Joriot S, Amati-Bonneau P, Guichet A, Barth M, Charollais A, Journel H, Auvin S, Boucher C, Kerckaert JP, David V, Manouvrier-Hanu S, Saugier-Veber P,

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Journal of medical genetics 47(1):22-9, 2010 Jan - Who cited this? | PubMed ID: 19592390 | Fulltext

Modeling synthetic lethality.

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Le Meur N and Gentleman R

Genome biology 9(9):R135, 2008 Sep 12 - Who cited this? | PubMed ID: 18789146 | Fulltext

Using flowViz to visualize flow cytometry data.

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Sarkar D, Le Meur N, and Gentleman R

Bioinformatics (Oxford, England) 24(6):878, 2008 Mar 15 - Who cited this? | PubMed ID: 18245128 | Fulltext

M@IA: a modular open-source application for microarray workflow and integrative datamining.

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Le Béchec A, Zindy P, Sierocinski T, Petritis D, Bihouée A, Le Meur N, Léger J, and Théret N

In silico biology 8(1):63, 2008 - Who cited this? | PubMed ID: 18430991 | Fulltext

Data quality assessment of ungated flow cytometry data in high throughput experiments.

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Le Meur N, Rossini A, Gasparetto M, Smith C, Brinkman RR, and Gentleman R

Cytometry. Part A : the journal of the International Society for Analytical Cytology 71(6):393-403, 2007 Jun - Who cited this? | PubMed ID: 17366638 | Fulltext

Contrasting gene expression profiles in two canine models of atrial fibrillation.

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Cardin S, Libby E, Pelletier P, Le Bouter S, Shiroshita-Takeshita A, Le Meur N, Léger J, Demolombe S, Ponton A, Glass L, and Nattel S

Circulation research 100(3):425, 2007 Feb 16 - Who cited this? | PubMed ID: 17234964 | Fulltext

Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation.

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Saugier-Veber P, Goldenberg A, Drouin-Garraud V, de La Rochebrochard C, Layet V, Drouot N, Le Meur N, Gilbert-Du-Ssardier B, Joly-Hélas G, Moirot H, Rossi A, Tosi M, and Frébourg T

European journal of human genetics : EJHG 14(9):1009, 2006 Sep - Who cited this? | PubMed ID: 16773131 | Fulltext

Transcriptome profiling uncovers metabolic and regulatory processes occurring during the transition from desiccation-sensitive to desiccation-tolerant stages in Medicago truncatula seeds.

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Buitink J, Leger JJ, Guisle I, Vu BL, Wuillème S, Lamirault G, Le Bars A, Le Meur N, Becker A, Küster H, and Leprince O

The Plant journal : for cell and molecular biology 47(5):735, 2006 Sep - Who cited this? | PubMed ID: 16923015 | Fulltext

Characterization of the expression of the hypoxia-induced genes neuritin, TXNIP and IGFBP3 in cancer.

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Le Jan S, Le Meur N, Cazes A, Philippe J, Le Cunff M, Léger J, Corvol P, and Germain S

FEBS letters 580(14):3395-400, 2006 Jun 12 - Who cited this? | PubMed ID: 16723126 | Fulltext

Hepatocyte iron loading capacity is associated with differentiation and repression of motility in the HepaRG cell line.

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Troadec MB, Glaise D, Lamirault G, Le Cunff M, Guérin E, Le Meur N, Détivaud L, Zindy P, Leroyer P, Guisle I, Duval H, Gripon P, Théret N, Boudjema K, Guguen-Guillouzo C, Brissot P,

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Genomics 87(1):93, 2006 Jan - Who cited this? | PubMed ID: 16325370 | Fulltext

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.

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Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerrière A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, and Campion D

Nature genetics 38(1):24, 2006 Jan - Who cited this? | PubMed ID: 16369530 | Fulltext

Gene expression profile associated with chronic atrial fibrillation and underlying valvular heart disease in man.

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Lamirault G, Gaborit N, Le Meur N, Chevalier C, Lande G, Demolombe S, Escande D, Nattel S, Léger JJ, and Steenman M

Journal of molecular and cellular cardiology 40(1):173-84, 2006 Jan - Who cited this? | PubMed ID: 16242148 | Fulltext

Cellular gene expression survey of PseudoRabies Virus (PRV) infected Human Embryonic Kidney cells (HEK-293).

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Blanchard Y, Le Meur N, Le Cunff M, Blanchard P, Léger J, and Jestin A

Veterinary research 37(5):705-23, 2006 - Who cited this? | PubMed ID: 16820135 | Fulltext

Data standards for flow cytometry.

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Spidlen J, Gentleman RC, Haaland PD, Langille M, Le Meur N, Ochs MF, Schmitt C, Smith CA, Treister AS, and Brinkman RR

Omics : a journal of integrative biology 10(2):209-14, 2006 - Who cited this? | PubMed ID: 16901228 | Fulltext

Profiling dendritic cell maturation with dedicated microarrays.

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McIlroy D, Tanguy-Royer S, Le Meur N, Guisle I, Royer PJ, Léger J, Meflah K, and Grégoire M

Journal of leukocyte biology 78(3):794-803, 2005 Sep - Who cited this? | PubMed ID: 15961579 | Fulltext

Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation.

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Gaborit N, Steenman M, Lamirault G, Le Meur N, Le Bouter S, Lande G, Léger J, Charpentier F, Christ T, Dobrev D, Escande D, Nattel S, and Demolombe S

Circulation 112(4):471-81, 2005 Jul 26 - Who cited this? | PubMed ID: 16027256 | Fulltext

Molecular characterization of a 14q deletion in a boy with features of Holt-Oram syndrome.

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Le Meur N, Goldenberg A, Michel-Adde C, Drouin-Garraud V, Blaysat G, Marret S, Amara SA, Moirot H, Joly-Hélas G, Mace B, Kleinfinger P, Saugier-Veber P, Frébourg T, and Rossi A

American journal of medical genetics. Part A 134(4):439-42, 2005 May 1 - Who cited this? | PubMed ID: 15810003 | Fulltext

Distinct molecular portraits of human failing hearts identified by dedicated cDNA microarrays.

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Steenman M, Lamirault G, Le Meur N, Le Cunff M, Escande D, and Léger JJ

European journal of heart failure : journal of the Working Group on Heart Failure of the European Society of Cardiology 7(2):157-65, 2005 Mar 2 - Who cited this? | PubMed ID: 15701461 | Fulltext

Gene expression profiling in human cardiovascular disease.

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Steenman M, Lamirault G, Le Meur N, and Léger JJ

Clinical chemistry and laboratory medicine : CCLM / FESCC 43(7):696-701, 2005 - Who cited this? | PubMed ID: 16207127 | Fulltext

DNA chip technology in cardiovascular research.

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Lamirault G, Steenman M, Le Meur N, Demolombe S, Trochu JN, and Léger JJ

Archives des maladies du coeur et des vaisseaux 97(12):1251-5, 2004 Dec - Who cited this? | PubMed ID: 15669368 | Fulltext

Inactivation of the RRB1-Pescadillo pathway involved in ribosome biogenesis induces chromosomal instability.

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Killian A, Le Meur N, Sesboüé R, Bourguignon J, Bougeard G, Gautherot J, Bastard C, Frébourg T, and Flaman JM

Oncogene 23(53):8597-602, 2004 Nov 11 - Who cited this? | PubMed ID: 15467761 | Fulltext

Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome.

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Le Meur N, Martin C, Saugier-Veber P, Joly G, Lemoine F, Moirot H, Rossi A, Bachy B, Cabot A, Joly P, and Frébourg T

European journal of human genetics : EJHG 12(5):415, 2004 May - Who cited this? | PubMed ID: 14970844 | Fulltext

Transcriptome variations in human CaCo-2 cells: a model for enterocyte differentiation and its link to iron absorption.

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Bédrine-Ferran H, Le Meur N, Gicquel I, Le Cunff M, Soriano N, Guisle I, Mottier S, Monnier A, Teusan R, Fergelot P, Le Gall JY, Léger J, and Mosser J

Genomics 83(5):772-89, 2004 May - Who cited this? | PubMed ID: 15081108 | Fulltext

A dynamic, web-accessible resource to process raw microarray scan data into consolidated gene expression values: importance of replication.

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Le Meur N, Lamirault G, Bihouée A, Steenman M, Bédrine-Ferran H, Teusan R, Ramstein G, and Léger JJ

Nucleic acids research 32(18):5349-58, 2004 - Who cited this? | PubMed ID: 15475389 | Fulltext

Identification of novel L1CAM mutations using fluorescence-assisted mismatch analysis.

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Saugier-Veber P, Martin C, Le Meur N, Lyonnet S, Munnich A, David A, Hénocq A, Héron D, Jonveaux P, Odent S, Manouvrier S, Moncla A, Morichon N, Philip N, Satge D, Tosi M,

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Human mutation 12(4):259-66, 1998 - Who cited this? | PubMed ID: 9744477 | Fulltext

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