Fibrilline 1 (French Wikipedia)
Analisys of sources in references of the Wikipedia ariticle fr.wikipedia.org/wiki/Fibrilline 1
| Site | Hosts in references | Count | Global rank | French rank |
| nih.gov | ncbi.nlm.nih.gov↓ (3) | 3 | 29 | 27 |
| sciencedirect.com | sciencedirect.com↓ (3) | 3 | 214 | 59 |
| ensembl.org | May2017.archive.ensembl.org↓ (2) | 2 | low | low |
| bmj.com | heart.bmj.com↓ (1), jmg.bmj.com↓ (1) | 2 | 639 | 242 |
| oxfordjournals.org | eurheartj.oxfordjournals.org↓ (1) | 1 | 397 | 294 |
| nature.com | nature.com↓ (1) | 1 | 137 | 91 |
| ctsnetjournals.org | jtcs.ctsnetjournals.org↓ (1) | 1 | low | low |
May2017.archive.ensembl.org
- 1. GRCh38: Ensembl release 89: ENSG00000166147 - Ensembl, May 2017
- 2. GRCm38: Ensembl release 89: ENSMUSG00000027204 - Ensembl, May 2017
eurheartj.oxfordjournals.org
- 8. 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
heart.bmj.com
- 5. Barrett PM, Topol EJ, The fibrillin-1 gene: unlocking new therapeutic pathways in cardiovascular disease, Heart, 2013;99:83-90
jmg.bmj.com
- 13. 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
jtcs.ctsnetjournals.org
- 10. 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
nature.com
- 9. 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
ncbi.nlm.nih.gov
- 3. « Publications PubMed pour l'Homme », sur National Center for Biotechnology Information, U.S. National Library of Medicine
- 4. « Publications PubMed pour la Souris », sur National Center for Biotechnology Information, U.S. National Library of Medicine
- 6. (en) Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD. MIM Number:154700 [1]
sciencedirect.com
- 7. Biery NJ, Eldadah ZA, Moore CS et al. Revised genomic organization of FBN1 and significance for regulated gene expression, Genomics, 1999;56:70–7
- 11. Lonnqvist L, Child A, Kainulainen K et al. A novel mutation of the fibrillin gene causing ectopia lentis, Genomics, 1994;19:573–6
- 12. Hayward C, Porteous ME, Brock DJ, A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly, Mol Cell Probes, 1994;8:325–7
Wikipedia Languages
- ar Arabic
- az Azerbaijani
- be Belarusian
- bg Bulgarian
- ca Catalan
- cs Czech
- da Danish
- de German
- el Greek
- en English
- eo Esperanto
- es Spanish
- et Estonian
- eu Basque
- fa Persian
- fi Finnish
- fr French
- gl Galician
- he Hebrew
- hi Hindi
- hr Croatian
- hu Hungarian
- hy Armenian
- id Indonesian
- it Italian
- ja Japanese
- ka Georgian
- kk Kazakh
- ko Korean
- la Latin
- lt Lithuanian
- ms Malay
- nl Dutch
- nn Norwegian (Nynorsk)
- no Norwegian
- pl Polish
- pt Portuguese
- ro Romanian
- ru Russian
- sh Serbo-Croatian
- simple Simple English
- sk Slovak
- sl Slovenian
- sr Serbian
- sv Swedish
- ta Tamil
- th Thai
- tr Turkish
- uk Ukrainian
- ur Urdu
- uz Uzbek
- vi Vietnamese
- vo Volapük
- zh Chinese
- zh-min-nan Min Nan
- More languages...
About the project
BestRef shows popularity and reliability scores for sources in references of Wikipedia articles in different languages. Data extraction based on complex method using Wikimedia dumps. To find the most popular and reliable sources we used information about over 200 million references of Wikipedia articles. More details...