Fibrilline 1 (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fibrilline 1" in French language version.

refsWebsite

Global rank French rank

4^th place

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3sciencedirect.com

149^th place

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1,626^th place

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1,226^th place

347^th place

1oxfordjournals.org

1,389^th place

508^th place

234^th place

147^th place

1ctsnetjournals.org

low place

low place

bmj.com

heart.bmj.com

Barrett PM, Topol EJ, The fibrillin-1 gene: unlocking new therapeutic pathways in cardiovascular disease, Heart, 2013;99:83-90

jmg.bmj.com

Faivre L, Gorlin RJ, Wirtz MK et al. In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome, J Med Genet, 2003;40:34–6

ctsnetjournals.org

jtcs.ctsnetjournals.org

Fedak PW, de Sa MP, Verma S et al. Vascular matrix remodeling in patients with bicuspid aortic valve malformations: implications for aortic dilatation, J Thorac Cardiovasc Surg, 2003;126:797–806

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000166147 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000027204 - Ensembl, May 2017

nature.com

Lemaire SA, McDonald ML, Guo DC et al. Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1, Nat Genet, 2011;43:996–1000

nih.gov

ncbi.nlm.nih.gov

« Publications PubMed pour l'Homme », sur National Center for Biotechnology Information, U.S. National Library of Medicine
« Publications PubMed pour la Souris », sur National Center for Biotechnology Information, U.S. National Library of Medicine
(en) Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD. MIM Number:154700 [1]

oxfordjournals.org

eurheartj.oxfordjournals.org

Detaint D, Faivre L, Collod-Beroud G et al. Cardiovascular manifestations in men and women carrying a FBN1 mutation, Eur Heart J, 2010;31:2223–9

sciencedirect.com

Biery NJ, Eldadah ZA, Moore CS et al. Revised genomic organization of FBN1 and significance for regulated gene expression, Genomics, 1999;56:70–7
Lonnqvist L, Child A, Kainulainen K et al. A novel mutation of the fibrillin gene causing ectopia lentis, Genomics, 1994;19:573–6
Hayward C, Porteous ME, Brock DJ, A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly, Mol Cell Probes, 1994;8:325–7