Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 30243 | 140 | 23.5 | 66% |
Classes in level above (level 2) |
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 | KBG SYNDROME | Author keyword | 53 | 95% | 13% | 18 |
| 2 | AARSKOG SCOTT SYNDROME | Author keyword | 44 | 100% | 11% | 16 |
| 3 | FACIOGENITAL DYSPLASIA | Author keyword | 14 | 100% | 5% | 7 |
| 4 | FGD1 GENE | Author keyword | 14 | 100% | 5% | 7 |
| 5 | ANKRD11 | Author keyword | 12 | 75% | 6% | 9 |
| 6 | FGD1 | Author keyword | 12 | 75% | 6% | 9 |
| 7 | AARSKOG SYNDROME | Author keyword | 11 | 65% | 8% | 11 |
| 8 | MACRODONTIA | Author keyword | 6 | 50% | 6% | 8 |
| 9 | UOC MOL MED | Address | 6 | 100% | 3% | 4 |
| 10 | FRABIN | Author keyword | 3 | 57% | 3% | 4 |
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 | KBG SYNDROME | 53 | 95% | 13% | 18 | Search KBG+SYNDROME | Search KBG+SYNDROME |
| 2 | AARSKOG SCOTT SYNDROME | 44 | 100% | 11% | 16 | Search AARSKOG+SCOTT+SYNDROME | Search AARSKOG+SCOTT+SYNDROME |
| 3 | FACIOGENITAL DYSPLASIA | 14 | 100% | 5% | 7 | Search FACIOGENITAL+DYSPLASIA | Search FACIOGENITAL+DYSPLASIA |
| 4 | FGD1 GENE | 14 | 100% | 5% | 7 | Search FGD1+GENE | Search FGD1+GENE |
| 5 | ANKRD11 | 12 | 75% | 6% | 9 | Search ANKRD11 | Search ANKRD11 |
| 6 | FGD1 | 12 | 75% | 6% | 9 | Search FGD1 | Search FGD1 |
| 7 | AARSKOG SYNDROME | 11 | 65% | 8% | 11 | Search AARSKOG+SYNDROME | Search AARSKOG+SYNDROME |
| 8 | MACRODONTIA | 6 | 50% | 6% | 8 | Search MACRODONTIA | Search MACRODONTIA |
| 9 | FRABIN | 3 | 57% | 3% | 4 | Search FRABIN | Search FRABIN |
| 10 | 16Q243 MICRODELETION | 2 | 67% | 1% | 2 | Search 16Q243+MICRODELETION | Search 16Q243+MICRODELETION |
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 | FACIOGENITAL DYSPLASIA FGD1 | 13 | 80% | 6% | 8 |
| 2 | FACIOGENITAL DYSPLASIA | 11 | 54% | 10% | 14 |
| 3 | DIGITAL GENITAL SYNDROME | 8 | 100% | 4% | 5 |
| 4 | AARSKOG SCOTT SYNDROME | 4 | 42% | 6% | 8 |
| 5 | FGD1 GENE | 4 | 56% | 4% | 5 |
| 6 | AARSKOG SYNDROME | 4 | 44% | 5% | 7 |
| 7 | FGD1 | 3 | 57% | 3% | 4 |
| 8 | KBG SYNDROME | 3 | 50% | 3% | 4 |
| 9 | FRABIN | 2 | 40% | 3% | 4 |
| 10 | CRANIOFACIAL DYSMORPHISM | 2 | 27% | 4% | 6 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
|---|---|---|---|---|
| KBG syndrome: Report of twins, neurological characteristics, and delineation of diagnostic criteria | 2007 | 20 | 9 | 100% |
| KBG syndrome | 2006 | 12 | 9 | 100% |
| KBG syndrome: review of the literature and findings of 5 affected patients | 2009 | 2 | 8 | 88% |
| Frabin and other related Cdc42-specific guanine nucleotide exchange factors couple the actin cytoskeleton with the plasma membrane | 2008 | 17 | 43 | 35% |
| A CASE OF AARSKOG SYNDROME WITH A REVIEW OF JAPANESE LITERATURE | 1982 | 1 | 5 | 100% |
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 | UOC MOL MED | 6 | 100% | 2.9% | 4 |
| 2 | JCR PHARMACEUT CO LTDNISHI KU | 1 | 50% | 1.4% | 2 |
| 3 | DISCIPLINES GENET MED | 0 | 20% | 1.4% | 2 |
| 4 | PEDIAT NEUROL PSYCHIAT UNIT | 0 | 33% | 0.7% | 1 |
| 5 | RADIOL BIOMOL IMAGING | 0 | 33% | 0.7% | 1 |
| 6 | HUMAN GENET CYTOGENET | 0 | 25% | 0.7% | 1 |
| 7 | SEZ CARDIOCHIRURG | 0 | 25% | 0.7% | 1 |
| 8 | CRC ONCOGENE SIGNAL TRANSDUCT GRP | 0 | 20% | 0.7% | 1 |
| 9 | MOTHERCARE UNIT CLIN GENET | 0 | 20% | 0.7% | 1 |
| 10 | RIC DISABIL MENTALE MOTORIA | 0 | 20% | 0.7% | 1 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000139377 | X LINKED MENTAL RETARDATION//XLMR//PQBP1 |
| 2 | 0.0000113822 | TIAM1//RHOB//RHOGDI2 |
| 3 | 0.0000099342 | PODOSOMES//INVADOPODIA//CORTACTIN |
| 4 | 0.0000087406 | DOOR SYNDROME//KIRNERS DEFORMITY//COFFIN SIRIS SYNDROME |
| 5 | 0.0000077985 | KABUKI SYNDROME//KABUKI MAKE UP SYNDROME//NIIKAWA KUROKI SYNDROME |
| 6 | 0.0000077661 | VAV//VAV1//VAV3 |
| 7 | 0.0000068966 | FRONTONASAL DYSPLASIA//PROBOSCIS LATERALIS//CRANIOFRONTONASAL DYSPLASIA |
| 8 | 0.0000067767 | REVISED AMSTERDAM CRITERIA//POPULATION MEDICAL GENETICS//BOOLEAN SEARCH |
| 9 | 0.0000067275 | BREATHLESS//TRACHEALESS//TRACHEAL SYSTEM |
| 10 | 0.0000064979 | NECTIN//TSLC1//AFADIN |