Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
542 | 14714 | 35.7 | 73% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
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 | 5113785 | 32% | 52% | 4740 |
2 | CFTR | authKW | 979715 | 5% | 61% | 781 |
3 | JOURNAL OF CYSTIC FIBROSIS | journal | 889708 | 4% | 66% | 646 |
4 | CYST FIBROSIS | address | 529521 | 3% | 53% | 486 |
5 | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR | authKW | 527909 | 3% | 63% | 406 |
6 | PEDIATRIC PULMONOLOGY | journal | 170171 | 4% | 13% | 622 |
7 | PULMONARY EXACERBATION | authKW | 130669 | 1% | 80% | 79 |
8 | CFTR MUTATIONS | authKW | 123515 | 0% | 83% | 72 |
9 | RESPIRATORY SYSTEM | WoSSC | 121839 | 24% | 2% | 3519 |
10 | GREGORY FLEMING JAMES CYST FIBROSIS | address | 109316 | 1% | 54% | 98 |
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 | 121839 | 24% | 2% | 3519 |
2 | Pediatrics | 36169 | 18% | 1% | 2607 |
3 | Physiology | 11774 | 11% | 0% | 1555 |
4 | Critical Care Medicine | 5143 | 4% | 1% | 586 |
5 | Genetics & Heredity | 3525 | 8% | 0% | 1147 |
6 | Cell Biology | 2683 | 9% | 0% | 1308 |
7 | Medicine, General & Internal | 1701 | 7% | 0% | 980 |
8 | Gastroenterology & Hepatology | 1661 | 4% | 0% | 591 |
9 | Biochemistry & Molecular Biology | 1461 | 13% | 0% | 1900 |
10 | Medical Laboratory Technology | 1232 | 2% | 0% | 261 |
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 | 529521 | 3% | 53% | 486 |
2 | GREGORY FLEMING JAMES CYST FIBROSIS | 109316 | 1% | 54% | 98 |
3 | ADULT CYST FIBROSIS | 87270 | 1% | 57% | 74 |
4 | CF | 76832 | 1% | 48% | 78 |
5 | ADULT CYST FIBROSIS UNIT | 64609 | 0% | 57% | 55 |
6 | CYST FIBROSIS UNIT | 64560 | 0% | 47% | 67 |
7 | PEDIAT PULMONOL | 63462 | 1% | 16% | 188 |
8 | CYST FIBROSIS PULM TREATMENT | 53898 | 1% | 26% | 99 |
9 | CYST FIBROSIS CLIN | 48727 | 0% | 56% | 42 |
10 | UNIDAD FIBROSIS QUIST | 36100 | 0% | 62% | 28 |
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 | 889708 | 4% | 66% | 646 |
2 | PEDIATRIC PULMONOLOGY | 170171 | 4% | 13% | 622 |
3 | PAEDIATRIC RESPIRATORY REVIEWS | 22877 | 1% | 14% | 81 |
4 | JOURNAL OF PEDIATRICS | 13476 | 2% | 2% | 301 |
5 | AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY | 12938 | 1% | 3% | 191 |
6 | AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE | 11972 | 2% | 2% | 240 |
7 | THORAX | 11730 | 1% | 3% | 203 |
8 | AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY | 9840 | 1% | 3% | 157 |
9 | HUMAN GENETICS | 9674 | 1% | 2% | 196 |
10 | CURRENT OPINION IN PULMONARY MEDICINE | 8610 | 0% | 6% | 72 |
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 | 5113785 | 32% | 52% | 4740 | Search CYSTIC+FIBROSIS | Search CYSTIC+FIBROSIS |
2 | CFTR | 979715 | 5% | 61% | 781 | Search CFTR | Search CFTR |
3 | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR | 527909 | 3% | 63% | 406 | Search CYSTIC+FIBROSIS+TRANSMEMBRANE+CONDUCTANCE+REGULATOR | Search CYSTIC+FIBROSIS+TRANSMEMBRANE+CONDUCTANCE+REGULATOR |
4 | PULMONARY EXACERBATION | 130669 | 1% | 80% | 79 | Search PULMONARY+EXACERBATION | Search PULMONARY+EXACERBATION |
5 | CFTR MUTATIONS | 123515 | 0% | 83% | 72 | Search CFTR+MUTATIONS | Search CFTR+MUTATIONS |
6 | CYSTIC FIBROSIS RELATED DIABETES | 108357 | 0% | 93% | 56 | Search CYSTIC+FIBROSIS+RELATED+DIABETES | Search CYSTIC+FIBROSIS+RELATED+DIABETES |
7 | CFTR GENE | 104540 | 0% | 75% | 67 | Search CFTR+GENE | Search CFTR+GENE |
8 | SWEAT TEST | 99665 | 0% | 70% | 69 | Search SWEAT+TEST | Search SWEAT+TEST |
9 | IVACAFTOR | 80333 | 0% | 82% | 47 | Search IVACAFTOR | Search IVACAFTOR |
10 | CHLORIDE CHANNEL | 77304 | 1% | 17% | 220 | Search CHLORIDE+CHANNEL | Search CHLORIDE+CHANNEL |
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 | TURCK, D , BRAEGGER, CP , COLOMBO, C , DECLERCQ, D , MORTON, A , PANCHEVA, R , ROBBERECHT, E , STERN, M , STRANDVIK, B , WOLFE, S , ET AL (2016) ESPEN-ESPGHAN-ECFS GUIDELINES ON NUTRITION CARE FOR INFANTS, CHILDREN, AND ADULTS WITH CYSTIC FIBROSIS.CLINICAL NUTRITION. VOL. 35. ISSUE 3. P. 557 -577 | 163 | 85% | 6 |
2 | CUTTING, GR , (2015) CYSTIC FIBROSIS GENETICS: FROM MOLECULAR UNDERSTANDING TO CLINICAL APPLICATION.NATURE REVIEWS GENETICS. VOL. 16. ISSUE 1. P. 45 -56 | 115 | 83% | 66 |
3 | GIBSON, RL , BURNS, JL , RAMSEY, BW , (2003) PATHOPHYSIOLOGY AND MANAGEMENT OF PULMONARY INFECTIONS IN CYSTIC FIBROSIS.AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE. VOL. 168. ISSUE 8. P. 918-951 | 224 | 52% | 793 |
4 | RATJEN, F , BELL, SC , ROWE, SM , GOSS, CH , QUITTNER, AL , BUSH, A , (2015) CYSTIC FIBROSIS.NATURE REVIEWS DISEASE PRIMERS. VOL. 1. ISSUE . P. - | 184 | 72% | 6 |
5 | CALLEBAUT, I , HOFFMANN, B , LEHN, P , MORNON, JP , (2017) MOLECULAR MODELLING AND MOLECULAR DYNAMICS OF CFTR.CELLULAR AND MOLECULAR LIFE SCIENCES. VOL. 74. ISSUE 1. P. 3 -22 | 164 | 83% | 0 |
6 | RIORDAN, JR , (2008) CFTR FUNCTION AND PROSPECTS FOR THERAPY.ANNUAL REVIEW OF BIOCHEMISTRY. VOL. 77. ISSUE . P. 701-726 | 133 | 77% | 280 |
7 | VEIT, G , AVRAMESCU, RG , CHIANG, AN , HOUCK, SA , CAI, ZW , PETERS, KW , HONG, JS , POLLARD, HB , GUGGINO, WB , BALCH, WE , ET AL (2016) FROM CFTR BIOLOGY TOWARD COMBINATORIAL PHARMACOTHERAPY: EXPANDED CLASSIFICATION OF CYSTIC FIBROSIS MUTATIONS.MOLECULAR BIOLOGY OF THE CELL. VOL. 27. ISSUE 3. P. 424 -433 | 77 | 91% | 14 |
8 | ELBORN, JS , (2016) CYSTIC FIBROSIS.LANCET. VOL. 388. ISSUE 10059. P. 2519 -2531 | 97 | 82% | 9 |
9 | LOPES-PACHECO, M , (2016) CFTR MODULATORS: SHEDDING LIGHT ON PRECISION MEDICINE FOR CYSTIC FIBROSIS.FRONTIERS IN PHARMACOLOGY. VOL. 7. ISSUE . P. - | 158 | 80% | 0 |
10 | 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 | 117 | 84% | 98 |
Classes with closest relation at Level 2 |