Publications des biobanques & CRB

BIOBANQUES fédère une centaine de Centres de Ressources Biologiques (CRBs), composés de biobanques, de tumorothèques et de centres de ressources microbiologiques (mBRCs), répartis dans toute la France et adhérant à la Charte Ethique de l'Infrastructure BIOBANQUES.

Les sites sont classés par région.

Vous pouvez effectuer une recherche par maladie ou sélectionner une région sur les colonnes de droite.


A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. International Multiple Sclerosis Genetics Consortium. Wellcome Trust Case Control Consortium 2. Damotte V et al. Genes Immun, 2014,15:126-32.

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. International Multiple Sclerosis Genetics Consortium (IMSGC). Nat Genet, 2013, 45:1353-60.

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. International Multiple Sclerosis Genetics Consortium. Brain, 2013, 136:1778-82.

Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. Lill CM et al. J Med Genet, 2013, 50:140-3.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. International Multiple Sclerosis Genetics Consortium. Wellcome Trust Case Control Consortium 2. Nature, 2011, 476:214-9.

Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility. Couturier et al. Brain, 2011, 134:693-703.

IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci. International Multiple Sclerosis Genetics Conssortium (IMSGC). Genes Immun, 2010, 11:397-405.

Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. International Multiple Sclerosis Genetics Consortium (IMSGC). Nat Genet, 2010, 42:469-70.

HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis. Cournu-Rebeix I et al. Genes Immun, 2008, 9:570-4.

A second-generation genomic screen for multiple sclerosis. Kenealy SJ et al. American-French Multiple Sclerosis Genetics Group. Am J Hum Genet, 2004, 75:1070-8.

Ag. Nat. de Sécurité Sanit. de l'Alimentation, l'Environnement et du Travail - ANSES


Biobanque cardiovasculaire Bichat

Impaired high-density lipoprotein anti-oxidant capacity in human abdominal aortic aneurysm. Delbosc S et al. Cardiovasc Res. 2013 Nov 1;100(2):307-15.

Increased metabolic activity highlighted by positron emission tomography/computed tomography in the wall of the dissected ascending aorta in a patient with Horton disease. Bruls S et al. Circ Cardiovasc Imaging. 2013 Jul;6(4):606-8.

Modifications of chromatin dynamics control Smad2 pathway activation in aneurysmal smooth muscle cells. Gomez D et al. Circ Res. 2013 Sep 13;113(7):881-90.

Smad2-dependent protease nexin-1 overexpression differentiates chronic aneurysms from acute dissections of human ascending aorta. Gomez D et al. Arterioscler Thromb Vasc Biol. 2013 Sep;33(9):2222-32.

Proteomic analysis of intraluminal thrombus highlights complement activation in human abdominal aortic aneurysms. Martinez-Pinna R et al. Arterioscler Thromb Vasc Biol. 2013 Aug;33(8):2013-20.

Identification of novel biomarkers of abdominal aortic aneurysms by 2D-DIGE and MALDI-MS from AAA-thrombus-conditioned media. Martinez-Pinna R et al. Methods Mol Biol. 2013;1000:91-101.

HDL and endothelial protection. Tran-Dinh A et al. Br J Pharmacol. 2013 Jun;169(3):493-511.

Lymphoid neogenesis in vascular chronic inflammation. Nicoletti A et al. Presse Med. 2013 Apr;42(4 Pt 2):558-60.

Biomechanical factors in the biology of aortic wall and aortic valve diseases. Back M et al. Cardiovasc Res. 2013 Jul 15;99(2):232-41.

High-density lipoprotein-based therapy reduces the hemorrhagic complications associated with tissue plasminogen activator treatment in experimental stroke. Lapergue B et al. Stroke. 2013 Mar;44(3):699-707.

Biobanque CLCC Paul Strauss

Human Papillomavirus-related tumours of the oropharynx display a lower tumour hypoxia signature. Hanns E et al. Oral Oncol, 2015, 51:848-856.

The Oncogenic MicroRNA Hsa-miR-155-5p Targets the Transcription Factor ELK3 and Links It to the Hypoxia Response.Robertson ED et al. PLoS One, 2014,9:e113050.

A poor prognosis subtype of HNSCC is consistently observed across methylome, transcriptome, and miRNome analysis. Jung AC et al. Clin Cancer Res, 2013, 19:4174-84.

Identification of clinically relevant HPV-related HNSCC: in p16 should we trust? Wasylyk B et al. Oral Oncol, 2013, 49:e33-7.

DDB2: a novel regulator of NF-?B and breast tumor invasion. Ennen M et al. Cancer Res, 2013, 73:5040-52.

CD8-alpha T-Cell Infiltration in Human Papillomavirus-Related Oropharyngeal Carcinoma Correlates with Improved Patient Prognosis.Jung AC et al. Int J Cancer, 2013, 132:E26-36.

The NEDD8-conjugating pathway regulates p53-dependent cancer cell sensitivity to ionising radiations.Guihard S et al. Int J Oncol, 2012, 41:1531-40.

High-risk Human Papillomavirus-associated oropharynx squamous cell carcinoma: clinical, biological implications and therapeutical perspectives.Guihard S et al. Cancer Radiother, 2012, 16:34-43

Biological and Clinical Relevance of Transcriptionnally Active Human Papillomavirus (HPV) Infection in Oropharynx Squamous Cell Carcinoma.Jung AC et al. Int J Cancer, 2010, 126:1882-94.

Pharmacological enhancement of autophagy induced in a hepatocellular cell line by high linear energy transfer radiation.Altmeyer A et al. Anticancer Res, 2010, 30:303-10.

Biobanque de Picardie

Inactivation of viruses in platelet and plasma products using a riboflavin-and-UV-based photochemical treatment. Keil SD et al. Transfusion, 2015, 55: 1736-44

SUPPLIVER: Bioartificial supply for liver failure. Figaro S et al. IRBM, 2015, 36:101-9

Investigation of omeprazole and phenacetin first pass metabolism in humans using a microscale bioreactor and pharmacokinetic models. Bricks T et al. Biopharm Drug Dispos, 2015, 36: 275-93

Public biobanks: calculation and recovery of costs. Clement B et al. Sci Transl Med, 2014, 6:261fs45.

The French Chronic Kidney Disease-Renal Epidemiology and Information Network (CKD-REIN) cohort study. Stengel B et al. Nephrol Dial Transplant, 2014, 29:1500-7.

Permissivity of primary human hepatocytes and different hepatoma cell lines to cell culture adapted hepatitis C virus. Helle F et al. PLoS One, 2013, 8:e70809

Immunological fingerprinting method for differentiation of serum samples in research-oriented biobanks.Beaumont K et al. Clin Vaccine Immunol, 2010, 17:735-40.

Human biospecimen research: experimental protocol and quality control tools.Betsou F et al. Cancer Epidemiol Biomarkers Prev, 2009, 18:1017-25.

Long-term stability of coagulation variables: Protein S as a biomarker for preanalytical storage-related variations in human plasma. Betsou F et al. Thromb Haemost, 2009, 101:1172-5.

Procédure « standard » pour tester l’impact des variables préanalytiques sur des analyses peptidiques et protéiques et proposition de codage « standard » des procédures préanalytiques Betsou F et al. Ann Biol Clin, 2009, 67:641-9

Biobanque GH Bichat Claude Bernard

Biobanque Hopital Debré, Biobanque d'ADN

Syndrome de Floating Harbor : etude clinique et moleculaire de 19 patients. Le Goff C. et al. Abstract assises. 2014

High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters. Chaste P. et al. Molecular Autism. 2012 ; 3(5) : 2040-2392

Advances in Cohen syndrome diagnosis using Next Generation Sequencing. Tita R. et al. Abstract ESHG. 2012

Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies. Delahaye A. et al. Eur J Hum Genet. 2012;20(5):527-33

Iodine Deficiency in Northern Paris Area: Impact on Fetal Thyroid Mensuration. Luton D. et al. PLoS ONE. 2011;6(2): e14707.

What can we learn from old microdeletion syndromes using array-CGH screening? Mosca-Boidron A. et al. Clin Genet. 2012;82(1):41-7

VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signaling. Passemard S. et al. J Clin Invest. 2011;121(8):3072-87

Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome. Rifai L. et al. American Journal of Medical Genetics. 2010;152 A:111-117

Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series. Jaillard S. et al. Eur J Med Genet. 2010 53(2):66-75

Biobanque Hopital Ste Anne


Biobanque UREN Paris 13

Dietary patterns and risk of elevated C-reactive protein concentrations 12 years later. Julia C et al. Br J Nutr. 2013 110(4):747-54

Association between prediagnostic biomarkers of inflammation and endothelial function and cancer risk: a nested case-control study. Touvier M et al. Am J Epidemiol. 2013 1;177(1):3-13. Association between Adherence to Nutritional Guidelines, the Metabolic Syndrome and

Adiposity Markers in a French Adult General Population. Lassale C et al. PLoS One. 2013 8(10):e76349.

Profiles of organic food consumers in a large sample of French adults: results from the nutrinet-sante cohort study. Kesse-Guyot E et al. PLoS One. 2013 8(10):e76998.

Modulation of the association between plasma intercellular adhesion molecule-1and cancer risk by n-3 PUFA intake: a nested case-control study. Touvier M et al. Am J Clin Nutr, 2012, 95(4):944-50.

Pre-diagnostic levels of adiponectin and soluble vascular cell adhesion molecule-1 are associated with colorectal cancer risk. Touvier M et al. World J Gastroenterol, 2012, 18(22):2805-12.

Association between pre-diagnostic biomarkers of inflammation and endothelial function and cancer risk: a nested case-control study. Touvier M et al. Am J Epidemiol, 2013, 177(1):3-13.

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Bonnefond A et al. Nat Genet, 2012, 29,44(3):297-301.

Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits. Billings LK et al. Diabetes. 2012, 61(8): 2176-86.

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Scott RA et al. Nat Genet, 2012, 44(9) : 991-1005.



Biothèque CHU de Nîmes

Exon 7 deletion in the bcr-abl gene is frequent in chronic myeloid leukemia patients and is not correlated with resistance against imatinib. Gaillard JB et al. Mol Cancer Ther. 2010 Nov;9(11):3083-9.

Polymorphisms of human placental alkaline phosphatase are associated with in vitro fertilization success and recurrent pregnancy loss. Vatin M et al. , Am J Pathol. 2014 Feb;184(2):362-8.

Characterization of resident B cells of vascular walls in human atherosclerotic patients. Hamze M et al. J Immunol 2013;191:3006-16.

Faecal carriage of multidrug-resistant Gram-negative bacilli during a non-outbreak situation in a French university hospital. Vidal-Navarro L et al. J Antimicrob Chemother. 2010 Nov;65(11):2455-8.

Recombinant human FVIIa for reducing the need for invasive second-line therapies in severe refractory postpartum hemorrhage: a multicenter, randomized, open controlled trial. Lavigne-Lissalde G et al. J Thromb Haemost. 2015 13: 520-9

The use of preoperative routine measurement of basal serum thyrocalcitonin in candidates for thyroidectomy due to nodular thyroid disorders: results from 2733 consecutive patients. Chambon G et al. J Clin Endocrinol Metab. 2011 Jan;96(1):75-81. 

Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations. Corcia P et al. Neurology. 2012 May 8;78(19):1519-26.

Comparative incidence of pregnancy outcomes in treated obstetric antiphospholipid syndrome: the NOH-APS observational study. Bouvier S et al. Blood. 2014 Jan 16;123(3):404-13.

Comparative incidence of pregnancy outcomes in thrombophilia-positive women from the NOH-APS observational study. Bouvier S et al. Blood. 2014 Jan 16;123(3):414-21.

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