Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
11241 | 997 | 45.9 | 86% |
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 |
11241 | 1 | CYSTIC FIBROSIS//INFECT CYST FIBROSIS UNIT//ANTI INFLAMMATORY AGENTS ADMINISTRATION DOSAGE ADVERSE EFFECTS | 997 |
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 | 472497 | 38% | 4% | 375 |
2 | INFECT CYST FIBROSIS UNIT | address | 146387 | 1% | 34% | 14 |
3 | ANTI INFLAMMATORY AGENTS ADMINISTRATION DOSAGE ADVERSE EFFECTS | authKW | 69998 | 0% | 57% | 4 |
4 | U719 | address | 63798 | 1% | 42% | 5 |
5 | JOURNAL OF CYSTIC FIBROSIS | journal | 63718 | 5% | 5% | 45 |
6 | AIRWAY SURFACE DEHYDRATION | authKW | 61251 | 0% | 100% | 2 |
7 | HEAD OUT SPIROMETRY | authKW | 61251 | 0% | 100% | 2 |
8 | LUNG INFLAMMATION MOUSE MODEL | authKW | 61251 | 0% | 100% | 2 |
9 | PEDIAT UNIT B TRAMBUSTI | address | 61251 | 0% | 100% | 2 |
10 | RESPIRATORY TRACT DISEASES DRUG THERAPY ETIOLOGY | authKW | 61251 | 0% | 100% | 2 |
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 | Respiratory System | 27655 | 43% | 0% | 431 |
2 | Critical Care Medicine | 1406 | 8% | 0% | 76 |
3 | Immunology | 1306 | 19% | 0% | 186 |
4 | Cell Biology | 1288 | 20% | 0% | 197 |
5 | Physiology | 758 | 10% | 0% | 103 |
6 | Pediatrics | 659 | 10% | 0% | 97 |
7 | Biochemistry & Molecular Biology | 347 | 19% | 0% | 193 |
8 | Allergy | 149 | 2% | 0% | 20 |
9 | Medicine, Research & Experimental | 142 | 6% | 0% | 56 |
10 | Infectious Diseases | 133 | 4% | 0% | 42 |
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 | INFECT CYST FIBROSIS UNIT | 146387 | 1% | 34% | 14 |
2 | U719 | 63798 | 1% | 42% | 5 |
3 | PEDIAT UNIT B TRAMBUSTI | 61251 | 0% | 100% | 2 |
4 | RIFERIMENTO FIBROSI CIST REG LAZIO | 61251 | 0% | 100% | 2 |
5 | UMR S719 | 55124 | 0% | 60% | 3 |
6 | COCHRANE CYST FIBROSIS GENET DISORDERS REVIEW G | 45936 | 0% | 50% | 3 |
7 | TRANSLAT PULMONOL | 45924 | 1% | 17% | 9 |
8 | U514 | 43543 | 1% | 18% | 8 |
9 | CYST FIBROSIS | 40535 | 4% | 4% | 35 |
10 | EXPT TREATMENT CYST FIBROSIS | 36741 | 1% | 20% | 6 |
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 | 63718 | 5% | 5% | 45 |
2 | AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY | 23998 | 6% | 1% | 63 |
3 | AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY | 15602 | 5% | 1% | 54 |
4 | PEDIATRIC PULMONOLOGY | 11451 | 4% | 1% | 42 |
5 | AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE | 10985 | 6% | 1% | 59 |
6 | RESPIRATORY RESEARCH | 3837 | 2% | 1% | 15 |
7 | EUROPEAN RESPIRATORY JOURNAL | 2803 | 3% | 0% | 29 |
8 | JOURNAL OF INNATE IMMUNITY | 2339 | 1% | 1% | 6 |
9 | THORAX | 1222 | 2% | 0% | 17 |
10 | MEDIATORS OF INFLAMMATION | 1184 | 1% | 0% | 11 |
Author Key Words |
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 | HARTL, D , GAGGAR, A , BRUSCIA, E , HECTOR, A , MARCOS, V , JUNG, A , GREENE, C , MCELVANEY, G , MALL, M , DORING, G , (2012) INNATE IMMUNITY IN CYSTIC FIBROSIS LUNG DISEASE.JOURNAL OF CYSTIC FIBROSIS. VOL. 11. ISSUE 5. P. 363 -382 | 99 | 42% | 77 |
2 | CANTIN, AM , HARTL, D , KONSTAN, MW , CHMIEL, JF , (2015) INFLAMMATION IN CYSTIC FIBROSIS LUNG DISEASE: PATHOGENESIS AND THERAPY.JOURNAL OF CYSTIC FIBROSIS. VOL. 14. ISSUE 4. P. 419 -430 | 67 | 50% | 35 |
3 | NICHOLS, DP , CHMIEL, JF , (2015) INFLAMMATION AND ITS GENESIS IN CYSTIC FIBROSIS.PEDIATRIC PULMONOLOGY. VOL. 50. ISSUE . P. S39 -S56 | 83 | 44% | 6 |
4 | BRUSCIA, EM , BONFIELD, TL , (2016) CYSTIC FIBROSIS LUNG IMMUNITY: THE ROSE OF THE MACROPHAGE.JOURNAL OF INNATE IMMUNITY. VOL. 8. ISSUE 6. P. 550 -563 | 52 | 54% | 2 |
5 | COHEN, TS , PRINCE, A , (2012) CYSTIC FIBROSIS: A MUCOSAL IMMUNODEFICIENCY SYNDROME.NATURE MEDICINE. VOL. 18. ISSUE 4. P. 509 -519 | 58 | 33% | 159 |
6 | JACQUOT, J , TABARY, O , LE ROUZIC, P , CLEMENT, A , (2008) AIRWAY EPITHELIAL CELL INFLAMMATORY SIGNALLING IN CYSTIC FIBROSIS.INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY. VOL. 40. ISSUE 9. P. 1703-1715 | 57 | 48% | 59 |
7 | BARTLETT, JA , RAMACHANDRAN, S , WOHLFORD-LENANE, CL , BARKER, CK , PEZZULO, AA , ZABNER, J , WELSH, MJ , MEYERHOLZ, DK , STOLTZ, DA , MCCRAY, PB , (2016) NEWBORN CYSTIC FIBROSIS PIGS HAVE A BLUNTED EARLY RESPONSE TO AN INFLAMMATORY STIMULUS.AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE. VOL. 194. ISSUE 7. P. 845 -854 | 33 | 61% | 3 |
8 | BRUSCIA, EM , BONFIELD, TL , (2016) INNATE AND ADAPTIVE IMMUNITY IN CYSTIC FIBROSIS.CLINICS IN CHEST MEDICINE. VOL. 37. ISSUE 1. P. 17 -+ | 55 | 41% | 1 |
9 | LAVAL, J , RALHAN, A , HARTL, D , (2016) NEUTROPHILS IN CYSTIC FIBROSIS.BIOLOGICAL CHEMISTRY. VOL. 397. ISSUE 6. P. 485 -496 | 51 | 46% | 0 |
10 | RATNER, D , MUELLER, C , (2012) IMMUNE RESPONSES IN CYSTIC FIBROSIS ARE THEY INTRINSICALLY DEFECTIVE?.AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY. VOL. 46. ISSUE 6. P. 715-722 | 45 | 50% | 25 |
Classes with closest relation at Level 1 |