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Year Number of Results
1979 1
1982 1
1983 1
1984 4
1985 3
1986 3
1987 1
1988 4
1989 4
1990 2
1991 8
1992 2
1993 1
1995 3
1996 1
1997 4
1998 3
1999 3
2000 1
2001 6
2002 11
2003 8
2004 8
2005 6
2006 5
2007 11
2008 10
2009 14
2010 12
2011 7
2012 15
2013 18
2014 12
2015 16
2016 5
2017 11
2018 7
2019 3
2025 0

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213 results

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Page 1
Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation.
Farrell PM, White TB, Ren CL, Hempstead SE, Accurso F, Derichs N, Howenstine M, McColley SA, Rock M, Rosenfeld M, Sermet-Gaudelus I, Southern KW, Marshall BC, Sosnay PR. Farrell PM, et al. Among authors: accurso f. J Pediatr. 2017 Feb;181S:S4-S15.e1. doi: 10.1016/j.jpeds.2016.09.064. J Pediatr. 2017. PMID: 28129811 Free article.
Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.
Tabor HK, Auer PL, Jamal SM, Chong JX, Yu JH, Gordon AS, Graubert TA, O'Donnell CJ, Rich SS, Nickerson DA; NHLBI Exome Sequencing Project; Bamshad MJ. Tabor HK, et al. Am J Hum Genet. 2014 Aug 7;95(2):183-93. doi: 10.1016/j.ajhg.2014.07.006. Epub 2014 Jul 31. Am J Hum Genet. 2014. PMID: 25087612 Free PMC article.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Do R, Stitziel NO, Won HH, Jørgensen AB, Duga S, Angelica Merlini P, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL; NHLBI Exome Sequencing Project; Girelli D, Martinelli N, Farlow DN, DePristo MA, Roberts R, Stewart AF, Saleheen D, Danesh J, Epstein SE, Sivapalaratnam S, Hovingh GK, Kastelein JJ, Samani NJ, Schunkert H, Erdmann J, Shah SH, Kraus WE, Davies R, Nikpay M, Johansen CT, Wang J, Hegele RA, Hechter E, Marz W, Kleber ME, Huang J, Johnson AD, Li M, Burke GL, Gross M, Liu Y, Assimes TL, Heiss G, Lange EM, Folsom AR, Taylor HA, Olivieri O, Hamsten A, Clarke R, Reilly DF, Yin W, Rivas MA, Donnelly P, Rossouw JE, Psaty BM, Herrington DM, Wilson JG, Rich SS, Bamshad MJ, Tracy RP, Cupples LA, Rader DJ, Reilly MP, Spertus JA, Cresci S, Hartiala J, Tang WH, Hazen SL, Allayee H, Reiner AP, Carlson CS, Kooperberg C, Jackson RD, Boerwinkle E, Lander ES, Schwartz SM, Siscovick DS, McPherson R, Tybjaerg-Hansen A, Abecasis GR, Watkins H, Nickerson DA, Ardissino D, Sunyaev SR, O'Donnell CJ, Altshuler D, Gabriel S, Kathiresan S. Do R, et al. Nature. 2015 Feb 5;518(7537):102-6. doi: 10.1038/nature13917. Epub 2014 Dec 10. Nature. 2015. PMID: 25487149 Free PMC article.
Biomarkers for cystic fibrosis drug development.
Muhlebach MS, Clancy JP, Heltshe SL, Ziady A, Kelley T, Accurso F, Pilewski J, Mayer-Hamblett N, Joseloff E, Sagel SD. Muhlebach MS, et al. Among authors: accurso f. J Cyst Fibros. 2016 Nov;15(6):714-723. doi: 10.1016/j.jcf.2016.10.009. Epub 2016 Oct 27. J Cyst Fibros. 2016. PMID: 28215711 Free PMC article. Review.
Primary tracheomalacia.
Cogbill TH, Moore FA, Accurso FJ, Lilly JR. Cogbill TH, et al. Among authors: accurso fj. Ann Thorac Surg. 1983 May;35(5):538-41. doi: 10.1016/s0003-4975(10)60430-4. Ann Thorac Surg. 1983. PMID: 6847290
Seeking modifier genes in cystic fibrosis.
Accurso FJ, Sontag MK. Accurso FJ, et al. Am J Respir Crit Care Med. 2003 Feb 1;167(3):289-90. doi: 10.1164/rccm.2210006. Am J Respir Crit Care Med. 2003. PMID: 12554616 No abstract available.
Early pulmonary disease in cystic fibrosis.
Accurso FJ. Accurso FJ. Curr Opin Pulm Med. 1997 Nov;3(6):400-3. doi: 10.1097/00063198-199711000-00002. Curr Opin Pulm Med. 1997. PMID: 9391757 Review.
Newborn screening fact sheets.
Kaye CI; Committee on Genetics; Accurso F, La Franchi S, Lane PA, Hope N, Sonya P, G Bradley S, Michele A LP. Kaye CI, et al. Among authors: accurso f. Pediatrics. 2006 Sep;118(3):e934-63. doi: 10.1542/peds.2006-1783. Pediatrics. 2006. PMID: 16950973
213 results