Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
3041 | 2081 | 33.8 | 67% |
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 |
593 | 3 | JOURNAL OF THE AMERICAN LEATHER CHEMISTS ASSOCIATION//OSTEOGENESIS IMPERFECTA//JOURNAL OF THE SOCIETY OF LEATHER TECHNOLOGISTS AND CHEMISTS | 14947 |
797 | 2 | OSTEOGENESIS IMPERFECTA//EHLERS DANLOS SYNDROME//COLLAGEN | 12085 |
3041 | 1 | OSTEOGENESIS IMPERFECTA//BONE EXTRACELLULAR MATRIX BRANCH//BRUCK SYNDROME | 2081 |
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 | OSTEOGENESIS IMPERFECTA | authKW | 8015093 | 34% | 76% | 717 |
2 | BONE EXTRACELLULAR MATRIX BRANCH | address | 437541 | 2% | 76% | 39 |
3 | BRUCK SYNDROME | authKW | 223160 | 1% | 89% | 17 |
4 | COL1A2 | authKW | 210406 | 1% | 46% | 31 |
5 | COL1A1 | authKW | 197954 | 2% | 31% | 43 |
6 | BRITTLE BONE DISEASE | authKW | 194180 | 1% | 88% | 15 |
7 | HYPERPLASTIC CALLUS | authKW | 190731 | 1% | 100% | 13 |
8 | SECT CONNECT TISSUE DISORDERS | address | 165297 | 1% | 87% | 13 |
9 | OSTEOGENESIS IMPERFECTA OI | authKW | 162515 | 1% | 92% | 12 |
10 | CRTAP | authKW | 136556 | 1% | 85% | 11 |
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 | Orthopedics | 3874 | 12% | 0% | 251 |
2 | Genetics & Heredity | 3860 | 19% | 0% | 392 |
3 | Pediatrics | 3119 | 14% | 0% | 293 |
4 | Endocrinology & Metabolism | 3013 | 16% | 0% | 324 |
5 | Biochemistry & Molecular Biology | 427 | 16% | 0% | 336 |
6 | Medicine, Research & Experimental | 206 | 5% | 0% | 102 |
7 | Surgery | 202 | 8% | 0% | 157 |
8 | Otorhinolaryngology | 159 | 2% | 0% | 47 |
9 | Medicine, General & Internal | 125 | 5% | 0% | 111 |
10 | Rheumatology | 119 | 2% | 0% | 35 |
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 | BONE EXTRACELLULAR MATRIX BRANCH | 437541 | 2% | 76% | 39 |
2 | SECT CONNECT TISSUE DISORDERS | 165297 | 1% | 87% | 13 |
3 | BONE OSTEOGENESIS IMPERFECTA | 93895 | 0% | 80% | 8 |
4 | FC DONDERS NEUROSCI | 88030 | 0% | 100% | 6 |
5 | SECT PHYS BIOCHEM | 82538 | 1% | 26% | 22 |
6 | BEMB | 73358 | 0% | 100% | 5 |
7 | GENET UNIT | 55792 | 4% | 5% | 76 |
8 | HOSP UNIV LA PAZ IDIPAZ | 33004 | 0% | 38% | 6 |
9 | BGI SHENZHEN BINHAI GENOM | 29343 | 0% | 100% | 2 |
10 | CHIRURG ABT 3 | 29343 | 0% | 100% | 2 |
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 BONE AND MINERAL RESEARCH | 13691 | 4% | 1% | 79 |
2 | BONE | 10735 | 3% | 1% | 70 |
3 | CALCIFIED TISSUE INTERNATIONAL | 5051 | 2% | 1% | 41 |
4 | MATRIX | 4699 | 0% | 4% | 9 |
5 | JOURNAL OF MEDICAL GENETICS | 4623 | 2% | 1% | 43 |
6 | HUMAN MUTATION | 4473 | 2% | 1% | 35 |
7 | JOURNAL OF PEDIATRIC ORTHOPAEDICS | 4105 | 2% | 1% | 38 |
8 | AMERICAN JOURNAL OF MEDICAL GENETICS | 3031 | 2% | 0% | 43 |
9 | HUMAN GENETICS | 2599 | 2% | 0% | 38 |
10 | HORMONE RESEARCH IN PAEDIATRICS | 2540 | 1% | 1% | 12 |
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 | OSTEOGENESIS IMPERFECTA | 8015093 | 34% | 76% | 717 | Search OSTEOGENESIS+IMPERFECTA | Search OSTEOGENESIS+IMPERFECTA |
2 | BRUCK SYNDROME | 223160 | 1% | 89% | 17 | Search BRUCK+SYNDROME | Search BRUCK+SYNDROME |
3 | COL1A2 | 210406 | 1% | 46% | 31 | Search COL1A2 | Search COL1A2 |
4 | COL1A1 | 197954 | 2% | 31% | 43 | Search COL1A1 | Search COL1A1 |
5 | BRITTLE BONE DISEASE | 194180 | 1% | 88% | 15 | Search BRITTLE+BONE+DISEASE | Search BRITTLE+BONE+DISEASE |
6 | HYPERPLASTIC CALLUS | 190731 | 1% | 100% | 13 | Search HYPERPLASTIC+CALLUS | Search HYPERPLASTIC+CALLUS |
7 | OSTEOGENESIS IMPERFECTA OI | 162515 | 1% | 92% | 12 | Search OSTEOGENESIS+IMPERFECTA+OI | Search OSTEOGENESIS+IMPERFECTA+OI |
8 | CRTAP | 136556 | 1% | 85% | 11 | Search CRTAP | Search CRTAP |
9 | IDIOPATHIC JUVENILE OSTEOPOROSIS | 118838 | 0% | 90% | 9 | Search IDIOPATHIC+JUVENILE+OSTEOPOROSIS | Search IDIOPATHIC+JUVENILE+OSTEOPOROSIS |
10 | OSTEOGENESIS IMPERFECT | 118838 | 0% | 90% | 9 | Search OSTEOGENESIS+IMPERFECT | Search OSTEOGENESIS+IMPERFECT |
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 | FORLINO, A , MARINI, JC , (2016) OSTEOGENESIS IMPERFECTA.LANCET. VOL. 387. ISSUE 10028. P. 1657 -1671 | 95 | 75% | 32 |
2 | FORLINO, A , CABRAL, WA , BARNES, AM , MARINI, JC , (2011) NEW PERSPECTIVES ON OSTEOGENESIS IMPERFECTA.NATURE REVIEWS ENDOCRINOLOGY. VOL. 7. ISSUE 9. P. 540 -557 | 144 | 76% | 170 |
3 | TREJO, P , RAUCH, F , (2016) OSTEOGENESIS IMPERFECTA IN CHILDREN AND ADOLESCENTS-NEW DEVELOPMENTS IN DIAGNOSIS AND TREATMENT.OSTEOPOROSIS INTERNATIONAL. VOL. 27. ISSUE 12. P. 3427 -3437 | 83 | 91% | 1 |
4 | MAROM, R , LEE, YC , GRAFE, I , LEE, B , (2016) PHARMACOLOGICAL AND BIOLOGICAL THERAPEUTIC STRATEGIES FOR OSTEOGENESIS IMPERFECTA.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 172. ISSUE 4. P. 367 -383 | 111 | 66% | 0 |
5 | RAUCH, F , GLORIEUX, FH , (2004) OSTEOGENESIS IMPERFECTA.LANCET. VOL. 363. ISSUE 9418. P. 1377-1385 | 81 | 70% | 466 |
6 | VAN DIJK, FS , SILLENCE, DO , (2014) OSTEOGENESIS IMPERFECTA: CLINICAL DIAGNOSIS, NOMENCLATURE AND SEVERITY ASSESSMENT.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 164. ISSUE 6. P. 1470 -1481 | 47 | 94% | 70 |
7 | MONTI, E , MOTTES, M , FRASCHINI, P , BRUNELLI, P , FORLINO, A , VENTURI, G , DORO, F , PERLINI, S , CAVARZERE, P , ANTONIAZZI, F , (2010) CURRENT AND EMERGING TREATMENTS FOR THE MANAGEMENT OF OSTEOGENESIS IMPERFECTA.THERAPEUTICS AND CLINICAL RISK MANAGEMENT. VOL. 6. ISSUE . P. 367 -381 | 88 | 77% | 22 |
8 | PRIMORAC, D , ROWE, DW , MOTTES, M , BARISIC, I , ANTICEVIC, D , MIRANDOLA, S , LIRA, MG , KALAJZIC, I , KUSEC, V , GLORIEUX, FH , (2001) OSTEOGENESIS IMPERFECTA AT THE BEGINNING OF BONE AND JOINT DECADE.CROATIAN MEDICAL JOURNAL. VOL. 42. ISSUE 4. P. 393 -415 | 113 | 75% | 27 |
9 | BESIO, R , FORLINO, A , (2015) TREATMENT OPTIONS FOR OSTEOGENESIS IMPERFECTA.EXPERT OPINION ON ORPHAN DRUGS. VOL. 3. ISSUE 2. P. 165 -181 | 79 | 73% | 1 |
10 | ROHRBACH, M , GIUNTA, C , (2012) RECESSIVE OSTEOGENESIS IMPERFECTA: CLINICAL, RADIOLOGICAL, AND MOLECULAR FINDINGS.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 160C. ISSUE 3. P. 175-189 | 72 | 76% | 19 |
Classes with closest relation at Level 1 |