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For: Strandvik B, Björck E, Fallström M, Gronowitz E, Thountzouris J, Lindblad A, Markiewicz D, Wahlström J, Tsui LC, Zielenski J. Spectrum of mutations in the CFTR gene of patients with classical and atypical forms of cystic fibrosis from southwestern Sweden: identification of 12 novel mutations. Genet Test 2001;5:235-42. [PMID: 11788090 DOI: 10.1089/10906570152742290] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 0.8] [Reference Citation Analysis]
Number Citing Articles
1 Dekkers JF, Wiegerinck CL, de Jonge HR, Bronsveld I, Janssens HM, de Winter-de Groot KM, Brandsma AM, de Jong NW, Bijvelds MJ, Scholte BJ, Nieuwenhuis EE, van den Brink S, Clevers H, van der Ent CK, Middendorp S, Beekman JM. A functional CFTR assay using primary cystic fibrosis intestinal organoids. Nat Med. 2013;19:939-945. [PMID: 23727931 DOI: 10.1038/nm.3201] [Cited by in Crossref: 548] [Cited by in F6Publishing: 505] [Article Influence: 60.9] [Reference Citation Analysis]
2 D'apice MR, Novelli G, Sangiuolo F. Diagnostic CFTR mutation analysis. Expert Opinion on Medical Diagnostics 2008;2:191-205. [DOI: 10.1517/17530059.2.2.191] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
3 Keen C, Olin AC, Edentoft A, Gronowitz E, Strandvik B. Airway nitric oxide in patients with cystic fibrosis is associated with pancreatic function, Pseudomonas infection, and polyunsaturated fatty acids. Chest 2007;131:1857-64. [PMID: 17400678 DOI: 10.1378/chest.06-2635] [Cited by in Crossref: 25] [Cited by in F6Publishing: 22] [Article Influence: 1.7] [Reference Citation Analysis]
4 Mekki C, Aissat A, Mirlesse V, Mayer Lacrosniere S, Eche E, Le Floch A, Whalen S, Prud'Homme C, Remus C, Funalot B, Castaigne V, Fanen P, de Becdelièvre A. Prenatal Ultrasound Suspicion of Cystic Fibrosis in a Multiethnic Population: Is Extensive CFTR Genotyping Needed? Genes (Basel) 2021;12:670. [PMID: 33946859 DOI: 10.3390/genes12050670] [Reference Citation Analysis]
5 Geborek A, Hjelte L. Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations. J Cyst Fibros 2011;10:187-92. [PMID: 21354377 DOI: 10.1016/j.jcf.2011.01.005] [Cited by in Crossref: 19] [Cited by in F6Publishing: 15] [Article Influence: 1.7] [Reference Citation Analysis]
6 Walsh AC, Rault G, Li Z, Scotet V, Duguépéroux I, Férec C, Roussey M, Laxova A, Farrell PM; participating CF centres of Brittany, France. Pulmonary outcome differences in U.S. and French cystic fibrosis cohorts diagnosed through newborn screening. J Cyst Fibros 2010;9:44-50. [PMID: 19926349 DOI: 10.1016/j.jcf.2009.10.004] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
7 Rohlfs EM, Zhou Z, Heim RA, Nagan N, Rosenblum LS, Flynn K, Scholl T, Akmaev VR, Sirko-Osadsa DA, Allitto BA, Sugarman EA. Cystic fibrosis carrier testing in an ethnically diverse US population. Clin Chem 2011;57:841-8. [PMID: 21474639 DOI: 10.1373/clinchem.2010.159285] [Cited by in Crossref: 54] [Cited by in F6Publishing: 47] [Article Influence: 4.9] [Reference Citation Analysis]
8 Gronowitz E, Mellström D, Strandvik B. Serum phospholipid fatty acid pattern is associated with bone mineral density in children, but not adults, with cystic fibrosis. Br J Nutr 2006;95:1159-65. [DOI: 10.1079/bjn20061778] [Cited by in Crossref: 33] [Cited by in F6Publishing: 9] [Article Influence: 2.2] [Reference Citation Analysis]
9 Mutesa L, Bours V. Diagnostic challenges of cystic fibrosis in patients of African origin. J Trop Pediatr 2009;55:281-6. [PMID: 19625487 DOI: 10.1093/tropej/fmp064] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
10 Kahre T, Teder M, Panov M, Metspalu A. Severe CF manifestation with anaemia and failure to thrive in a 394delTT homozygous patient. J Cyst Fibros 2004;3:58-60. [PMID: 15463888 DOI: 10.1016/j.jcf.2003.12.009] [Cited by in Crossref: 3] [Article Influence: 0.2] [Reference Citation Analysis]
11 Sahlberg ME, Svantesson U, Thomas EMLM, Strandvik B. Muscular Strength and Function in Patients With Cystic Fibrosis. Chest 2005;127:1587-92. [DOI: 10.1378/chest.127.5.1587] [Cited by in Crossref: 42] [Cited by in F6Publishing: 34] [Article Influence: 2.5] [Reference Citation Analysis]
12 Billet A, Elbahnsi A, Jollivet-Souchet M, Hoffmann B, Mornon JP, Callebaut I, Becq F. Functional and Pharmacological Characterization of the Rare CFTR Mutation W361R. Front Pharmacol 2020;11:295. [PMID: 32256364 DOI: 10.3389/fphar.2020.00295] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
13 Comer D, Ennis M, Mcdowell C, Beattie D, Rendall J, Hall V, Elborn J. Clinical phenotype of cystic fibrosis patients with the G551D mutation. QJM 2009;102:793-8. [DOI: 10.1093/qjmed/hcp120] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 1.5] [Reference Citation Analysis]
14 Gronowitz E, Lorentzon M, Ohlsson C, Mellström D, Strandvik B. Docosahexaenoic acid is associated with endosteal circumference in long bones in young males with cystic fibrosis. Br J Nutr 2008;99:160-7. [DOI: 10.1017/s000711450780105x] [Cited by in Crossref: 12] [Article Influence: 0.8] [Reference Citation Analysis]
15 Kiseleva A, Klimushina M, Sotnikova E, Skirko O, Divashuk M, Kurilova O, Ershova A, Khlebus E, Zharikova A, Efimova I, Pokrovskaya M, Slominsky PA, Shalnova S, Meshkov A, Drapkina O. Cystic Fibrosis Polymorphic Variants in a Russian Population. Pharmgenomics Pers Med 2020;13:679-86. [PMID: 33623413 DOI: 10.2147/PGPM.S278806] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Strandvik B, O Neal WK, Ali MA, Hammar U. Low linoleic and high docosahexaenoic acids in a severe phenotype of transgenic cystic fibrosis mice. Exp Biol Med (Maywood) 2018;243:496-503. [PMID: 29513100 DOI: 10.1177/1535370218758605] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]