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202 results
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Direct-access genetic testing: the view from Europe.
Kricka LJ, Fortina P, Mai Y, Patrinos GP. Kricka LJ, et al. Among authors: fortina p. Nat Rev Genet. 2011 Sep 13;12(10):670. doi: 10.1038/nrg3073. Nat Rev Genet. 2011. PMID: 21915107 No abstract available.
Clinical exome performance for reporting secondary genetic findings.
Park JY, Clark P, Londin E, Sponziello M, Kricka LJ, Fortina P. Park JY, et al. Among authors: fortina p. Clin Chem. 2015 Jan;61(1):213-20. doi: 10.1373/clinchem.2014.231456. Epub 2014 Nov 20. Clin Chem. 2015. PMID: 25414276 Free PMC article.
Molecular diagnostics: hurdles for clinical implementation.
Fortina P, Surrey S, Kricka LJ. Fortina P, et al. Trends Mol Med. 2002 Jun;8(6):264-6. doi: 10.1016/s1471-4914(02)02331-6. Trends Mol Med. 2002. PMID: 12067610
Concordance study of 3 direct-to-consumer genetic-testing services.
Imai K, Kricka LJ, Fortina P. Imai K, et al. Among authors: fortina p. Clin Chem. 2011 Mar;57(3):518-21. doi: 10.1373/clinchem.2010.158220. Epub 2010 Dec 15. Clin Chem. 2011. PMID: 21159896
Cyclin D1 induction of Dicer governs microRNA processing and expression in breast cancer.
Yu Z, Wang L, Wang C, Ju X, Wang M, Chen K, Loro E, Li Z, Zhang Y, Wu K, Casimiro MC, Gormley M, Ertel A, Fortina P, Chen Y, Tozeren A, Liu Z, Pestell RG. Yu Z, et al. Among authors: fortina p. Nat Commun. 2013;4:2812. doi: 10.1038/ncomms3812. Nat Commun. 2013. PMID: 24287487 Free PMC article.
Current perspectives in protein array technology.
Kricka LJ, Master SR, Joos TO, Fortina P. Kricka LJ, et al. Among authors: fortina p. Ann Clin Biochem. 2006 Nov;43(Pt 6):457-67. doi: 10.1258/000456306778904731. Ann Clin Biochem. 2006. PMID: 17132276 Review.
Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss.
Bason L, Dudley T, Lewis K, Shah U, Potsic W, Ferraris A, Fortina P, Rappaport E, Krantz ID. Bason L, et al. Among authors: fortina p. Clin Genet. 2002 Jun;61(6):459-64. doi: 10.1034/j.1399-0004.2002.610611.x. Clin Genet. 2002. PMID: 12121355
Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: clinical observations and genetic analysis.
Kobayashi M, Kaplan BS, Bellah RD, Sartore M, Rappaport E, Steele MW, Mansfield E, Gasparini P, Surrey S, Fortina P. Kobayashi M, et al. Among authors: fortina p. Am J Med Genet. 1995 Nov 6;59(2):218-24. doi: 10.1002/ajmg.1320590219. Am J Med Genet. 1995. PMID: 8588589
Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: effects of imprinting.
Ming JE, Blagowidow N, Knoll JH, Rollings L, Fortina P, McDonald-McGinn DM, Spinner NB, Zackai EH. Ming JE, et al. Among authors: fortina p. Am J Med Genet. 2000 May 1;92(1):19-24. doi: 10.1002/(sici)1096-8628(20000501)92:1<19::aid-ajmg4>3.0.co;2-#. Am J Med Genet. 2000. PMID: 10797418
Parallel molecular genetic analysis.
McKenzie SE, Mansfield E, Rappaport E, Surrey S, Fortina P. McKenzie SE, et al. Among authors: fortina p. Eur J Hum Genet. 1998 Sep-Oct;6(5):417-29. doi: 10.1038/sj.ejhg.5200218. Eur J Hum Genet. 1998. PMID: 9801865 Review.
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