Class information for:
Level 1: CYSTIC FIBROSIS//CFTR GENE//CBAVD

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
1676 2460 26.8 72%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
660 12667 CYSTIC FIBROSIS//CFTR//JOURNAL OF CYSTIC FIBROSIS

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 CYSTIC FIBROSIS Author keyword 99 10% 37% 899
2 CFTR GENE Author keyword 62 67% 2% 56
3 CBAVD Author keyword 60 80% 2% 37
4 IMMUNOREACTIVE TRYPSINOGEN Author keyword 59 90% 1% 26
5 SWEAT TEST Author keyword 57 70% 2% 47
6 CFTR MUTATIONS Author keyword 52 68% 2% 45
7 CONGENITAL BILATERAL ABSENCE OF THE VAS DEFERENS Author keyword 40 79% 1% 26
8 CFTR Author keyword 34 16% 8% 194
9 SWEAT CHLORIDE Author keyword 23 76% 1% 16
10 JOURNAL OF CYSTIC FIBROSIS Journal 18 14% 5% 115

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 CYSTIC FIBROSIS 99 10% 37% 899 Search CYSTIC+FIBROSIS Search CYSTIC+FIBROSIS
2 CFTR GENE 62 67% 2% 56 Search CFTR+GENE Search CFTR+GENE
3 CBAVD 60 80% 2% 37 Search CBAVD Search CBAVD
4 IMMUNOREACTIVE TRYPSINOGEN 59 90% 1% 26 Search IMMUNOREACTIVE+TRYPSINOGEN Search IMMUNOREACTIVE+TRYPSINOGEN
5 SWEAT TEST 57 70% 2% 47 Search SWEAT+TEST Search SWEAT+TEST
6 CFTR MUTATIONS 52 68% 2% 45 Search CFTR+MUTATIONS Search CFTR+MUTATIONS
7 CONGENITAL BILATERAL ABSENCE OF THE VAS DEFERENS 40 79% 1% 26 Search CONGENITAL+BILATERAL+ABSENCE+OF+THE+VAS+DEFERENS Search CONGENITAL+BILATERAL+ABSENCE+OF+THE+VAS+DEFERENS
8 CFTR 34 16% 8% 194 Search CFTR Search CFTR
9 SWEAT CHLORIDE 23 76% 1% 16 Search SWEAT+CHLORIDE Search SWEAT+CHLORIDE
10 NASAL POTENTIAL DIFFERENCE 16 43% 1% 28 Search NASAL+POTENTIAL+DIFFERENCE Search NASAL+POTENTIAL+DIFFERENCE

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 CFTR GENE 161 51% 9% 226
2 IMMUNOREACTIVE TRYPSINOGEN 137 92% 2% 55
3 DISSEMINATED BRONCHIECTASIS 82 81% 2% 50
4 REGULATOR CFTR GENE 67 71% 2% 54
5 CONGENITAL BILATERAL ABSENCE 67 46% 4% 107
6 CFTR MUTATIONS 58 66% 2% 54
7 DELTA F508 41 36% 4% 92
8 PARTIAL PENETRANCE 40 76% 1% 28
9 VAS DEFERENS 37 14% 10% 239
10 CYSTIC FIBROSIS GENE 32 14% 8% 208

Journals


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 JOURNAL OF CYSTIC FIBROSIS 18 14% 5% 115

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Cystic fibrosis: A worldwide analysis of CFTR mutations - Correlation with incidence data and application to screening 2002 391 88 99%
Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice 2008 165 114 87%
Cystic fibrosis genetics: from molecular understanding to clinical application 2015 5 138 34%
Cystic fibrosis: terminology and diagnostic algorithms 2006 103 33 82%
CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis 2012 21 69 88%
Novel personalized therapies for cystic fibrosis: treating the basic defect in all patients 2015 4 95 36%
Genotype and phenotype in cystic fibrosis 2000 195 91 75%
Cystic fibrosis 2009 286 144 16%
Guidelines for the performance of the sweat test for the diagnosis of cystic fibrosis 2007 35 6 100%
The phenotypic consequences of CFTR mutations 2003 149 69 59%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 CYST FIBROSIS 12 12% 3.9% 95
2 SERV BIOCHIM GENET 5 19% 0.9% 21
3 SOINS MUCOVISCIDOSE 4 56% 0.2% 5
4 BAB EZZOUAR BIOL 3 100% 0.1% 3
5 PEDIAT BAMBINO GESU BASILICATA 3 100% 0.1% 3
6 RECH FIBROSE KYST 3 100% 0.1% 3
7 UNITED KINGDOM CYST FIBROSIS DATABASE 3 100% 0.1% 3
8 CYST FIBROSIS UNIT 3 13% 0.7% 18
9 PEDIAT CYST FIBROSIS 2 44% 0.2% 4
10 STOCKHOLM CF 2 32% 0.2% 6

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000205592 MICROVILLAR ENZYMES//BRI BAS PROGRAM//CLIN MOLEC MED
2 0.0000168037 HUMAN MOL GENET PROGRAM//BAK FOONG PILL//EPITHELIAL CELL BIOL
3 0.0000144117 NEWBORN SCREENING//CARRIER TESTING//CARRIER SCREENING
4 0.0000137883 CFTR//CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR//GREGORY FLEMING JAMES CYST FIBROSIS
5 0.0000123976 DISTAL INTESTINAL OBSTRUCTION SYNDROME//FIBROSING COLONOPATHY//MECONIUM ILEUS EQUIVALENT
6 0.0000119244 REG PAEDIAT CF UNIT//ADOLESCENTS AND ADULTS//ADULT CYST FIBROSIS UNIT
7 0.0000115995 CYSTIC FIBROSIS PARANASAL SINUSES//NASAL POLYPS COMPLICATIONS DRUG THERAPY//SINUS DEVELOPMENT
8 0.0000107664 CYSTIC FIBROSIS RELATED DIABETES//CYSTIC FIBROSIS RELATED DIABETES CFRD//JOURNAL OF CYSTIC FIBROSIS
9 0.0000105835 JOURNAL OF CYSTIC FIBROSIS//INHALED TOBRAMYCIN//PULMONARY EXACERBATION
10 0.0000105460 PSEUDO BARTTER//HYPOELECTROLYTEMIA//HYPOCHLOREMIC METABOLIC ALKALOSIS