Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 23578 | 286 | 25.8 | 58% |
Classes in level above (level 2) |
| ID, lev. above |
Publications | Label for level above |
|---|---|---|
| 1995 | 5043 | HIRSCHSPRUNG DISEASE//INTESTINAL NEURONAL DYSPLASIA//AGANGLIONOSIS |
Terms with highest relevance score |
| Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|---|
| 1 | WAARDENBURG SYNDROME | Author keyword | 47 | 53% | 22% | 62 |
| 2 | WAARDENBURGS SYNDROME | Author keyword | 11 | 67% | 3% | 10 |
| 3 | KLEIN WAARDENBURG SYNDROME | Author keyword | 8 | 100% | 2% | 5 |
| 4 | NABLUS MASK LIKE FACIAL SYNDROME | Author keyword | 6 | 100% | 1% | 4 |
| 5 | PAX3 GENE | Author keyword | 3 | 50% | 1% | 4 |
| 6 | DYSTOPIA CANTHORUM | Author keyword | 3 | 60% | 1% | 3 |
| 7 | WS1 | Author keyword | 3 | 60% | 1% | 3 |
| 8 | BLUE IRIS | Author keyword | 2 | 67% | 1% | 2 |
| 9 | RETINAL HYPOPIGMENTATION | Author keyword | 2 | 67% | 1% | 2 |
| 10 | WAARDENBURG SYNDROME TYPE II | Author keyword | 2 | 67% | 1% | 2 |
Web of Science journal categories |
Author Key Words |
| Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
|---|---|---|---|---|---|---|---|
| 1 | WAARDENBURG SYNDROME | 47 | 53% | 22% | 62 | Search WAARDENBURG+SYNDROME | Search WAARDENBURG+SYNDROME |
| 2 | WAARDENBURGS SYNDROME | 11 | 67% | 3% | 10 | Search WAARDENBURGS+SYNDROME | Search WAARDENBURGS+SYNDROME |
| 3 | KLEIN WAARDENBURG SYNDROME | 8 | 100% | 2% | 5 | Search KLEIN+WAARDENBURG+SYNDROME | Search KLEIN+WAARDENBURG+SYNDROME |
| 4 | NABLUS MASK LIKE FACIAL SYNDROME | 6 | 100% | 1% | 4 | Search NABLUS+MASK+LIKE+FACIAL+SYNDROME | Search NABLUS+MASK+LIKE+FACIAL+SYNDROME |
| 5 | PAX3 GENE | 3 | 50% | 1% | 4 | Search PAX3+GENE | Search PAX3+GENE |
| 6 | DYSTOPIA CANTHORUM | 3 | 60% | 1% | 3 | Search DYSTOPIA+CANTHORUM | Search DYSTOPIA+CANTHORUM |
| 7 | WS1 | 3 | 60% | 1% | 3 | Search WS1 | Search WS1 |
| 8 | BLUE IRIS | 2 | 67% | 1% | 2 | Search BLUE+IRIS | Search BLUE+IRIS |
| 9 | RETINAL HYPOPIGMENTATION | 2 | 67% | 1% | 2 | Search RETINAL+HYPOPIGMENTATION | Search RETINAL+HYPOPIGMENTATION |
| 10 | WAARDENBURG SYNDROME TYPE II | 2 | 67% | 1% | 2 | Search WAARDENBURG+SYNDROME+TYPE+II | Search WAARDENBURG+SYNDROME+TYPE+II |
Key Words Plus |
| Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|
| 1 | SYNDROME WS | 26 | 100% | 4% | 11 |
| 2 | HUP2 PAIRED DOMAIN | 19 | 60% | 7% | 21 |
| 3 | PAX3 GENE | 7 | 53% | 3% | 10 |
| 4 | SPLOTCH MOUSE | 3 | 100% | 1% | 3 |
| 5 | PAX 3 | 1 | 15% | 3% | 9 |
| 6 | HIRSCHSPRUNG MEGACOLON | 1 | 100% | 1% | 2 |
| 7 | SPLOTCH | 1 | 19% | 2% | 6 |
| 8 | MITF GENE | 1 | 13% | 2% | 6 |
| 9 | SYNDROME TYPE 2 | 1 | 10% | 2% | 7 |
| 10 | ALPORT | 1 | 50% | 0% | 1 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references | % act. ref. to same field |
|---|---|---|---|---|
| Waardenburg syndrome | 1999 | 20 | 27 | 81% |
| Review and Update of Mutations Causing Waardenburg Syndrome | 2010 | 109 | 184 | 28% |
| The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature | 2009 | 10 | 9 | 33% |
| Piebaldism: an update | 2004 | 23 | 26 | 31% |
| Waardenburg Syndrome: a review of literature and case reports | 2012 | 0 | 30 | 60% |
| Waardenburg syndrome | 1999 | 2 | 20 | 50% |
| Cracking the auditory genetic code: Part II. Syndromic hereditary hearing impairment | 2000 | 5 | 108 | 19% |
| MOUSE AND HAMSTER MUTANTS AS MODELS FOR WAARDENBURG SYNDROMES IN HUMANS | 1990 | 41 | 33 | 33% |
| Syndromes and arthritis | 1997 | 3 | 47 | 2% |
| GENE-MAPPING OF OCULAR DISEASES | 1992 | 22 | 226 | 1% |
Address terms |
| Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|
| 1 | EPSTEIN S MOL OTOL | 1 | 100% | 0.7% | 2 |
| 2 | AMH | 1 | 50% | 0.3% | 1 |
| 3 | CHINESE GEN HOSP | 1 | 50% | 0.3% | 1 |
| 4 | GENET METAB CENT | 1 | 50% | 0.3% | 1 |
| 5 | MED HUMAN SCIMAHSC | 1 | 50% | 0.3% | 1 |
| 6 | SHAHID FIAZBAKHSH REHABIL COMPREHENS | 1 | 50% | 0.3% | 1 |
| 7 | DERMATOL 107 PEDIAT | 0 | 33% | 0.3% | 1 |
| 8 | ENVIRONM HLTH BIOSAFETY | 0 | 33% | 0.3% | 1 |
| 9 | ASSOC NOSTRA FAMIGLIA | 0 | 25% | 0.3% | 1 |
| 10 | CAROLINA CHILDRENS COMMUN DISORDERS PROGRAM | 0 | 25% | 0.3% | 1 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000261921 | ANIRIDIA//PAX6//PAIRED BOX |
| 2 | 0.0000142379 | HIRSCHSPRUNG DISEASE//INTESTINAL NEURONAL DYSPLASIA//AGANGLIONOSIS |
| 3 | 0.0000113217 | MELANOGENESIS//MITF//TYROSINASE |
| 4 | 0.0000082476 | SATB1//2Q DELETION//SATB2 |
| 5 | 0.0000073048 | CHOROIDEREMIA//POU3F4//DFN3 |
| 6 | 0.0000069324 | POSTERIOR NEUROPORE//NEURULATION//CURLY TAIL |
| 7 | 0.0000066824 | USHER SYNDROME//USH2A//MYO7A |
| 8 | 0.0000065695 | REVISED AMSTERDAM CRITERIA//POPULATION MEDICAL GENETICS//BOOLEAN SEARCH |
| 9 | 0.0000063511 | TRICHORHINOPHALANGEAL SYNDROME//TRPS1//TRICHO RHINO PHALANGEAL SYNDROME |
| 10 | 0.0000060760 | BLEPHAROPHIMOSIS//OHDO SYNDROME//BPES |