Sign In

Login

Password

Forgot Password ? Sign Up

MORM syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "MORM syndrome" in English language version.

refsWebsite
Global rank English rank
7nih.gov
4th place
4th place
4doi.org
2nd place
2nd place
3omim.org
4,380th place
4,305th place
2semanticscholar.org
11th place
8th place
1dur.ac.uk
3,728th place
2,318th place
1ulb.ac.be
low place
low place
1aoa.org
low place
low place
1biologists.org
3,870th place
3,434th place

aoa.org

  • "Visual Acuity". American Optometric Association. Retrieved 3 December 2015.

biologists.org

jcs.biologists.org

doi.org

  • Hampshire, D. J.; Ayub, M.; Springell, K.; Roberts, E.; Jafri, H.; Rashid, Y.; Bond, J.; Riley, J. H.; Woods, C. G. (May 2006). "MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34" (PDF). European Journal of Human Genetics. 14 (5): 543–548. doi:10.1038/sj.ejhg.5201577. PMID 16493448. S2CID 20931689.
  • Jacoby M, Cox JJ, Gayral S, et al. (September 2009). "INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse" (PDF). Nat. Genet. 41 (9): 1027–31. doi:10.1038/ng.427. PMID 19668215. S2CID 5249668.
  • Romero-Corral, Abel; Caples, Sean; Lopez-Jimenez, Francisco; Somers, Virend (2010). "Interactions Between Obesity and Obstructive Sleep Apnea". Chest. 137 (3): 711–719. doi:10.1378/chest.09-0360. PMC 3021364. PMID 20202954.
  • Plotnikova, Olga; Seo, Seongjin; Cottle, Denny; Conduit, Sarah; Hakim, Sandra; Dyson, Jennifer; Mitchell, Christina; Smyth, Ian (2015). "INPP5E interacts with AURKA, linking phosphoinositide signaling to primary cilium stability" (PDF). Journal of Cell Science. 128 (2): 364–372. doi:10.1242/jcs.161323. PMC 4294778. PMID 25395580. Retrieved 15 October 2015.

dur.ac.uk

dro.dur.ac.uk

  • Hampshire, D. J.; Ayub, M.; Springell, K.; Roberts, E.; Jafri, H.; Rashid, Y.; Bond, J.; Riley, J. H.; Woods, C. G. (May 2006). "MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34" (PDF). European Journal of Human Genetics. 14 (5): 543–548. doi:10.1038/sj.ejhg.5201577. PMID 16493448. S2CID 20931689.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Hampshire, D. J.; Ayub, M.; Springell, K.; Roberts, E.; Jafri, H.; Rashid, Y.; Bond, J.; Riley, J. H.; Woods, C. G. (May 2006). "MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34" (PDF). European Journal of Human Genetics. 14 (5): 543–548. doi:10.1038/sj.ejhg.5201577. PMID 16493448. S2CID 20931689.
  • Jacoby M, Cox JJ, Gayral S, et al. (September 2009). "INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse" (PDF). Nat. Genet. 41 (9): 1027–31. doi:10.1038/ng.427. PMID 19668215. S2CID 5249668.
  • Romero-Corral, Abel; Caples, Sean; Lopez-Jimenez, Francisco; Somers, Virend (2010). "Interactions Between Obesity and Obstructive Sleep Apnea". Chest. 137 (3): 711–719. doi:10.1378/chest.09-0360. PMC 3021364. PMID 20202954.
  • Plotnikova, Olga; Seo, Seongjin; Cottle, Denny; Conduit, Sarah; Hakim, Sandra; Dyson, Jennifer; Mitchell, Christina; Smyth, Ian (2015). "INPP5E interacts with AURKA, linking phosphoinositide signaling to primary cilium stability" (PDF). Journal of Cell Science. 128 (2): 364–372. doi:10.1242/jcs.161323. PMC 4294778. PMID 25395580. Retrieved 15 October 2015.

ncbi.nlm.nih.gov

omim.org

semanticscholar.org

api.semanticscholar.org

  • Hampshire, D. J.; Ayub, M.; Springell, K.; Roberts, E.; Jafri, H.; Rashid, Y.; Bond, J.; Riley, J. H.; Woods, C. G. (May 2006). "MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34" (PDF). European Journal of Human Genetics. 14 (5): 543–548. doi:10.1038/sj.ejhg.5201577. PMID 16493448. S2CID 20931689.
  • Jacoby M, Cox JJ, Gayral S, et al. (September 2009). "INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse" (PDF). Nat. Genet. 41 (9): 1027–31. doi:10.1038/ng.427. PMID 19668215. S2CID 5249668.

ulb.ac.be

dipot.ulb.ac.be