Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
26684 | 248 | 21.1 | 56% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
7 | 4 | INFECTIOUS DISEASES//MICROBIOLOGY//VIROLOGY | 1353914 |
443 | 3 | PERIODONTITIS//PERIODONTAL DISEASE//JOURNAL OF CLINICAL PERIODONTOLOGY | 26437 |
3478 | 2 | JOURNAL OF VETERINARY DENTISTRY//CAFFEY DISEASE//RAINE SYNDROME | 1477 |
26684 | 1 | CAFFEY DISEASE//RAINE SYNDROME//FAM20C | 248 |
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 | CAFFEY DISEASE | authKW | 2991964 | 11% | 90% | 27 |
2 | RAINE SYNDROME | authKW | 1994643 | 7% | 90% | 18 |
3 | FAM20C | authKW | 1370440 | 6% | 70% | 16 |
4 | INFANTILE CORTICAL HYPEROSTOSIS | authKW | 1266439 | 5% | 86% | 12 |
5 | HYPERTROPHIC OSTEODYSTROPHY | authKW | 1064159 | 4% | 79% | 11 |
6 | METAPHYSEAL OSTEOPATHY | authKW | 615632 | 2% | 100% | 5 |
7 | CORTICAL HYPEROSTOSIS | authKW | 502760 | 3% | 58% | 7 |
8 | CRANIOMANDIBULAR OSTEOPATHY | authKW | 328334 | 2% | 67% | 4 |
9 | HYPEROSTOSIS CORTICAL CONGENITAL | authKW | 246253 | 1% | 100% | 2 |
10 | FAM20A | authKW | 184686 | 1% | 50% | 3 |
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 | Veterinary Sciences | 2300 | 34% | 0% | 85 |
2 | Pediatrics | 582 | 17% | 0% | 43 |
3 | Genetics & Heredity | 364 | 17% | 0% | 42 |
4 | Radiology, Nuclear Medicine & Medical Imaging | 78 | 8% | 0% | 20 |
5 | Dentistry, Oral Surgery & Medicine | 74 | 5% | 0% | 12 |
6 | Orthopedics | 61 | 5% | 0% | 12 |
7 | Obstetrics & Gynecology | 22 | 4% | 0% | 9 |
8 | Medicine, General & Internal | 14 | 5% | 0% | 13 |
9 | Pathology | 14 | 3% | 0% | 7 |
10 | Endocrinology & Metabolism | 9 | 4% | 0% | 9 |
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 | CHURCHILL HOSP OXFORD | 123126 | 0% | 100% | 1 |
2 | GENET MEDEQUIPE AVENIREA3949 | 123126 | 0% | 100% | 1 |
3 | KLIN GYNAKOL GEBURTSHILFE WERPUNKT GEBURTSHI | 123126 | 0% | 100% | 1 |
4 | REFERENCE MALAD RA MALAD OSSEUSES CONSTITU | 123126 | 0% | 100% | 1 |
5 | UNIV HOSP BRASILIA DENT | 123126 | 0% | 100% | 1 |
6 | CRANIO IAL DIAG | 102245 | 3% | 12% | 7 |
7 | LONGJIANG OLAR | 82082 | 1% | 33% | 2 |
8 | ECHOG MED FOETALE | 61562 | 0% | 50% | 1 |
9 | IMAGING CHILD ABUSE NEGLECT | 61562 | 0% | 50% | 1 |
10 | MOTHERCARE CLIN GENET | 61562 | 0% | 50% | 1 |
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 | KLEINTIERPRAXIS | 8260 | 4% | 1% | 11 |
2 | CLINICAL DYSMORPHOLOGY | 3967 | 2% | 1% | 6 |
3 | ARCHIVES FRANCAISES DE PEDIATRIE | 2432 | 2% | 0% | 6 |
4 | INTERNATIONAL JOURNAL OF ORAL SCIENCE | 1827 | 1% | 1% | 2 |
5 | MEDECINE NUCLEAIRE | 1557 | 0% | 1% | 1 |
6 | CANADIAN VETERINARY JOURNAL-REVUE VETERINAIRE CANADIENNE | 1539 | 3% | 0% | 7 |
7 | VETERINARY AND COMPARATIVE ORTHOPAEDICS AND TRAUMATOLOGY | 1512 | 2% | 0% | 4 |
8 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 1036 | 3% | 0% | 7 |
9 | JOURNAL OF THE AMERICAN ANIMAL HOSPITAL ASSOCIATION | 988 | 2% | 0% | 5 |
10 | CLINICAL GENETICS | 862 | 2% | 0% | 6 |
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 | CAFFEY DISEASE | 2991964 | 11% | 90% | 27 | Search CAFFEY+DISEASE | Search CAFFEY+DISEASE |
2 | RAINE SYNDROME | 1994643 | 7% | 90% | 18 | Search RAINE+SYNDROME | Search RAINE+SYNDROME |
3 | FAM20C | 1370440 | 6% | 70% | 16 | Search FAM20C | Search FAM20C |
4 | INFANTILE CORTICAL HYPEROSTOSIS | 1266439 | 5% | 86% | 12 | Search INFANTILE+CORTICAL+HYPEROSTOSIS | Search INFANTILE+CORTICAL+HYPEROSTOSIS |
5 | HYPERTROPHIC OSTEODYSTROPHY | 1064159 | 4% | 79% | 11 | Search HYPERTROPHIC+OSTEODYSTROPHY | Search HYPERTROPHIC+OSTEODYSTROPHY |
6 | METAPHYSEAL OSTEOPATHY | 615632 | 2% | 100% | 5 | Search METAPHYSEAL+OSTEOPATHY | Search METAPHYSEAL+OSTEOPATHY |
7 | CORTICAL HYPEROSTOSIS | 502760 | 3% | 58% | 7 | Search CORTICAL+HYPEROSTOSIS | Search CORTICAL+HYPEROSTOSIS |
8 | CRANIOMANDIBULAR OSTEOPATHY | 328334 | 2% | 67% | 4 | Search CRANIOMANDIBULAR+OSTEOPATHY | Search CRANIOMANDIBULAR+OSTEOPATHY |
9 | HYPEROSTOSIS CORTICAL CONGENITAL | 246253 | 1% | 100% | 2 | Search HYPEROSTOSIS+CORTICAL+CONGENITAL | Search HYPEROSTOSIS+CORTICAL+CONGENITAL |
10 | FAM20A | 184686 | 1% | 50% | 3 | Search FAM20A | Search FAM20A |
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 | ACEVEDO, AC , POULTER, JA , ALVES, PG , DE LIMA, CL , CASTRO, LC , YAMAGUTI, PM , PAULA, LM , PARRY, DA , LOGAN, CV , SMITH, CEL , ET AL (2015) VARIABILITY OF SYSTEMIC AND ORO-DENTAL PHENOTYPE IN TWO FAMILIES WITH NON-LETHAL RAINE SYNDROME WITH FAM20C MUTATIONS.BMC MEDICAL GENETICS. VOL. 16. ISSUE . P. - | 31 | 70% | 7 |
2 | FAUNDES, V , CASTILLO-TAUCHER, S , GONZALEZ-HORMAZABAL, P , CHANDLER, K , CROSBY, A , CHIOZA, B , (2014) RAINE SYNDROME: AN OVERVIEW.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 57. ISSUE 9. P. 536 -542 | 26 | 84% | 5 |
3 | KAMOUN-GOLDRAT, A , LE MERRER, M , (2008) INFANTILE CORTICAL HYPEROSTOSIS (CAFFEY DISEASE): A REVIEW.JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY. VOL. 66. ISSUE 10. P. 2145-2150 | 23 | 96% | 15 |
4 | ABABNEH, FK , ALSWAID, A , YOUSSEF, T , AL AZZAWI, M , CROSBY, A , ALBALWI, MA , (2013) HEREDITARY DELETION OF THE ENTIRE FAM20C GENE IN A PATIENT WITH RAINE SYNDROME.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 161. ISSUE 12. P. 3155-3160 | 18 | 100% | 11 |
5 | SHANDILYA, R , GADRE, KS , SHARMA, J , JOSHI, P , (2013) INFANTILE CORTICAL HYPEROSTOSIS (CAFFEY DISEASE): A CASE REPORT AND REVIEW OF THE LITERATURE-WHERE ARE WE AFTER 70 YEARS?.JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY. VOL. 71. ISSUE 7. P. 1195-1201 | 18 | 95% | 3 |
6 | SEIDAHMED, MZ , ALAZAMI, AM , ABDELBASIT, OB , AL HUSSEIN, K , MIQDAD, AM , ABU-SA'DA, O , MUSTAFA, T , BAHJAT, S , ALKURAYA, FS , (2015) REPORT OF A CASE OF RAINE SYNDROME AND LITERATURE REVIEW.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 167. ISSUE 10. P. 2394 -2398 | 16 | 100% | 2 |
7 | KITAOKA, T , MIYOSHI, Y , NAMBA, N , MIURA, K , KUBOTA, T , OHATA, Y , FUJIWARA, M , TAKAGI, M , HASEGAWA, T , JUPPNER, H , ET AL (2014) TWO JAPANESE FAMILIAL CASES OF CAFFEY DISEASE WITH AND WITHOUT THE COMMON COL1A1 MUTATION AND NORMAL BONE DENSITY, AND REVIEW OF THE LITERATURE.EUROPEAN JOURNAL OF PEDIATRICS. VOL. 173. ISSUE 6. P. 799-804 | 14 | 82% | 2 |
8 | CERRUTI-MAINARDI, P , VENTURI, G , SPUNTON, M , FAVARON, E , ZIGNANI, M , PROVERA, S , DALLAPICCOLA, B , (2011) INFANTILE CORTICAL HYPEROSTOSIS AND COL1A1 MUTATION IN FOUR GENERATIONS.EUROPEAN JOURNAL OF PEDIATRICS. VOL. 170. ISSUE 11. P. 1385-1390 | 12 | 100% | 3 |
9 | KOCHAR, GS , CHOUDHARY, A , GADODIA, A , GUPTA, N , SIMPSON, MA , CROSBY, AH , KABRA, M , (2010) RAINE SYNDROME: A CLINICAL, RADIOGRAPHIC AND GENETIC INVESTIGATION OF A CASE FROM THE INDIAN SUBCONTINENT.CLINICAL DYSMORPHOLOGY. VOL. 19. ISSUE 3. P. 153 -156 | 12 | 100% | 5 |
10 | SIMPSON, MA , SCHEUERLE, A , HURST, J , PATTON, MA , STEWART, H , CROSBY, AH , (2009) MUTATIONS IN FAM20C ALSO IDENTIFIED IN NON-LETHAL OSTEOSCLEROTIC BONE DYSPLASIA.CLINICAL GENETICS. VOL. 75. ISSUE 3. P. 271 -276 | 12 | 92% | 39 |
Classes with closest relation at Level 1 |