Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
1681 | 2538 | 27.5 | 73% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
0 | 4 | BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY | 4064930 |
597 | 3 | CYSTIC FIBROSIS//CFTR//JOURNAL OF CYSTIC FIBROSIS | 14714 |
542 | 2 | CYSTIC FIBROSIS//CFTR//JOURNAL OF CYSTIC FIBROSIS | 14714 |
1681 | 1 | CYSTIC FIBROSIS//CFTR GENE//SWEAT TEST | 2538 |
Terms with highest relevance score |
rank | Term | termType | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|---|
1 | CYSTIC FIBROSIS | authKW | 1221507 | 38% | 11% | 962 |
2 | CFTR GENE | authKW | 571026 | 3% | 73% | 65 |
3 | SWEAT TEST | authKW | 513334 | 3% | 66% | 65 |
4 | CFTR MUTATIONS | authKW | 497733 | 2% | 69% | 60 |
5 | CFTR | authKW | 406982 | 8% | 16% | 209 |
6 | CBAVD | authKW | 369571 | 1% | 81% | 38 |
7 | IMMUNOREACTIVE TRYPSINOGEN | authKW | 316144 | 1% | 91% | 29 |
8 | CONGENITAL BILATERAL ABSENCE OF THE VAS DEFERENS | authKW | 254112 | 1% | 81% | 26 |
9 | JOURNAL OF CYSTIC FIBROSIS | journal | 212158 | 5% | 13% | 131 |
10 | SWEAT CHLORIDE | authKW | 162389 | 1% | 75% | 18 |
Web of Science journal categories |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | Genetics & Heredity | 14752 | 32% | 0% | 815 |
2 | Respiratory System | 10555 | 17% | 0% | 435 |
3 | Pediatrics | 7588 | 19% | 0% | 493 |
4 | Medical Laboratory Technology | 3074 | 6% | 0% | 152 |
5 | Andrology | 662 | 1% | 0% | 27 |
6 | Medicine, General & Internal | 631 | 9% | 0% | 225 |
7 | Medicine, Research & Experimental | 358 | 6% | 0% | 142 |
8 | Reproductive Biology | 312 | 3% | 0% | 64 |
9 | Obstetrics & Gynecology | 266 | 4% | 0% | 99 |
10 | Critical Care Medicine | 259 | 2% | 0% | 59 |
Address terms |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | CYST FIBROSIS | 146093 | 4% | 11% | 106 |
2 | SERV BIOCHIM GENET | 42176 | 1% | 18% | 20 |
3 | BAB EZZOUAR BIOL | 36088 | 0% | 100% | 3 |
4 | HAEMOGLOBINOPATHIES CYST FIBROSIS | 36088 | 0% | 100% | 3 |
5 | RECH FIBROSE KYST | 36088 | 0% | 100% | 3 |
6 | UNITED KINGDOM CYST FIBROSIS DATABASE | 36088 | 0% | 100% | 3 |
7 | VERONA CYST FIBROSIS | 36088 | 0% | 100% | 3 |
8 | SOINS MUCOVISCIDOSE | 33411 | 0% | 56% | 5 |
9 | NEW ENGLAND NEWBORN SCREENING PROGRAM | 33294 | 0% | 23% | 12 |
10 | GENET MALAD RA | 28503 | 0% | 30% | 8 |
Journals |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | JOURNAL OF CYSTIC FIBROSIS | 212158 | 5% | 13% | 131 |
2 | HUMAN GENETICS | 37117 | 6% | 2% | 157 |
3 | HUMAN MUTATION | 27830 | 4% | 2% | 96 |
4 | PEDIATRIC PULMONOLOGY | 18389 | 3% | 2% | 85 |
5 | GENETICS IN MEDICINE | 15721 | 2% | 3% | 46 |
6 | GENETIC TESTING | 12597 | 1% | 4% | 26 |
7 | JOURNAL OF MOLECULAR DIAGNOSTICS | 8226 | 1% | 2% | 28 |
8 | CLINICAL GENETICS | 7330 | 2% | 1% | 56 |
9 | JOURNAL OF MEDICAL GENETICS | 6207 | 2% | 1% | 55 |
10 | PAEDIATRIC RESPIRATORY REVIEWS | 5849 | 1% | 3% | 17 |
Author Key Words |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | CYSTIC FIBROSIS | 1221507 | 38% | 11% | 962 | Search CYSTIC+FIBROSIS | Search CYSTIC+FIBROSIS |
2 | CFTR GENE | 571026 | 3% | 73% | 65 | Search CFTR+GENE | Search CFTR+GENE |
3 | SWEAT TEST | 513334 | 3% | 66% | 65 | Search SWEAT+TEST | Search SWEAT+TEST |
4 | CFTR MUTATIONS | 497733 | 2% | 69% | 60 | Search CFTR+MUTATIONS | Search CFTR+MUTATIONS |
5 | CFTR | 406982 | 8% | 16% | 209 | Search CFTR | Search CFTR |
6 | CBAVD | 369571 | 1% | 81% | 38 | Search CBAVD | Search CBAVD |
7 | IMMUNOREACTIVE TRYPSINOGEN | 316144 | 1% | 91% | 29 | Search IMMUNOREACTIVE+TRYPSINOGEN | Search IMMUNOREACTIVE+TRYPSINOGEN |
8 | CONGENITAL BILATERAL ABSENCE OF THE VAS DEFERENS | 254112 | 1% | 81% | 26 | Search CONGENITAL+BILATERAL+ABSENCE+OF+THE+VAS+DEFERENS | Search CONGENITAL+BILATERAL+ABSENCE+OF+THE+VAS+DEFERENS |
9 | SWEAT CHLORIDE | 162389 | 1% | 75% | 18 | Search SWEAT+CHLORIDE | Search SWEAT+CHLORIDE |
10 | NASAL POTENTIAL DIFFERENCE | 148743 | 1% | 43% | 29 | Search NASAL+POTENTIAL+DIFFERENCE | Search NASAL+POTENTIAL+DIFFERENCE |
Core articles |
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c: (1) Number of references referring to publications in the class. (2) Share of total number of active references referring to publications in the class. (3) Age of the article. New articles get higher score than old articles. (4) Citation rate, normalized to year. |
Rank | Reference | # ref. in cl. |
Shr. of ref. in cl. |
Citations |
---|---|---|---|---|
1 | CASTELLANI, C , CUPPENS, H , MACEK, M , CASSINIAN, JJ , KERERN, E , DURIE, P , TULLIS, E , ASSAEL, BM , BOMBIERI, C , BROWN, A , ET AL (2008) CONSENSUS ON THE USE AND INTERPRETATION OF CYSTIC FIBROSIS MUTATION ANALYSIS IN CLINICAL PRACTICE.JOURNAL OF CYSTIC FIBROSIS. VOL. 7. ISSUE 3. P. 179-196 | 100 | 88% | 201 |
2 | BOBADILLA, JL , MACEK, M , FINE, JP , FARRELL, PM , (2002) CYSTIC FIBROSIS: A WORLDWIDE ANALYSIS OF CFTR MUTATIONS - CORRELATION WITH INCIDENCE DATA AND APPLICATION TO SCREENING.HUMAN MUTATION. VOL. 19. ISSUE 6. P. 575 -606 | 87 | 99% | 446 |
3 | BOMBIERI, C , CLAUSTRES, M , DE BOECK, K , DERICHS, N , DODGE, J , GIRODON, E , SERMET, I , SCHWARZ, M , TZETIS, M , WILSCHANSKI, M , ET AL (2011) RECOMMENDATIONS FOR THE CLASSIFICATION OF DISEASES AS CFTR-RELATED DISORDERS.JOURNAL OF CYSTIC FIBROSIS. VOL. 10. ISSUE . P. S86-S102 | 102 | 73% | 98 |
4 | BOMBIERI, C , SEIA, M , CASTELLANI, C , (2015) GENOTYPES AND PHENOTYPES IN CYSTIC FIBROSIS AND CYSTIC FIBROSIS TRANSMEMBRANE REGULATOR-RELATED DISORDERS.SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE. VOL. 36. ISSUE 2. P. 180 -193 | 106 | 67% | 7 |
5 | FARRELL, PM , ROSENSTEIN, BJ , WHITE, TB , ACCURSO, FJ , CASTELLANI, C , CUTTING, GR , DURIE, PR , LEGRYS, VA , MASSIE, J , PARAD, RB , ET AL (2008) GUIDELINES FOR DIAGNOSIS OF CYSTIC FIBROSIS IN NEWBORNS THROUGH OLDER ADULTS: CYSTIC FIBROSIS FOUNDATION CONSENSUS REPORT.JOURNAL OF PEDIATRICS. VOL. 153. ISSUE 2. P. S4-S14 | 55 | 92% | 349 |
6 | CLAUSTRES, M , (2005) MOLECULAR PATHOLOGY OF THE CFTR LOCUS IN MALE INFERTILITY.REPRODUCTIVE BIOMEDICINE ONLINE. VOL. 10. ISSUE 1. P. 14-41 | 109 | 69% | 53 |
7 | YU, JM , CHEN, ZH , NI, Y , LI, ZX , (2012) CFTR MUTATIONS IN MEN WITH CONGENITAL BILATERAL ABSENCE OF THE VAS DEFERENS (CBAVD): A SYSTEMIC REVIEW AND META-ANALYSIS.HUMAN REPRODUCTION. VOL. 27. ISSUE 1. P. 25-35 | 61 | 88% | 33 |
8 | COMEAU, AM , ACCURSO, FJ , WHITE, TB , CAMPBELL, PW , HOFFMAN, G , PARAD, RB , WILFOND, BS , ROSENFELD, M , SONTAG, MK , MASSIE, J , ET AL (2007) GUIDELINES FOR IMPLEMENTATION OF CYSTIC FIBROSIS NEWBORN SCREENING PROGRAMS: CYSTIC FIBROSIS FOUNDATION WORKSHOP REPORT.PEDIATRICS. VOL. 119. ISSUE 2. P. E495-E518 | 62 | 94% | 50 |
9 | CASTELLANI, C , SOUTHERN, KW , BROWNLEE, K , ROELSE, JD , DUFF, A , FARRELL, M , MEHTA, A , MUNCK, A , POLLITT, R , SERMET-GAUDELUS, I , ET AL (2009) EUROPEAN BEST PRACTICE GUIDELINES FOR CYSTIC FIBROSIS NEONATAL SCREENING.JOURNAL OF CYSTIC FIBROSIS. VOL. 8. ISSUE 3. P. 153-173 | 69 | 76% | 63 |
10 | CASTELLANI, C , MASSIE, J , SONTAG, M , SOUTHERN, KW , (2016) NEWBORN SCREENING FOR CYSTIC FIBROSIS.LANCET RESPIRATORY MEDICINE. VOL. 4. ISSUE 8. P. 653 -661 | 46 | 82% | 5 |
Classes with closest relation at Level 1 |