Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
21781 | 348 | 25.0 | 64% |
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 | LERI WEILL DYSCHONDROSTEOSIS | Author keyword | 107 | 97% | 9% | 31 |
2 | SHOX | Author keyword | 59 | 69% | 14% | 50 |
3 | MADELUNGS DEFORMITY | Author keyword | 32 | 85% | 5% | 17 |
4 | SHOX GENE | Author keyword | 27 | 74% | 6% | 20 |
5 | MADELUNG DEFORMITY | Author keyword | 25 | 75% | 5% | 18 |
6 | LERI WEILL SYNDROME | Author keyword | 19 | 76% | 4% | 13 |
7 | LANGER MESOMELIC DYSPLASIA | Author keyword | 18 | 89% | 2% | 8 |
8 | DYSCHONDROSTEOSIS | Author keyword | 17 | 75% | 3% | 12 |
9 | MESOMELIC DYSPLASIA | Author keyword | 14 | 65% | 4% | 13 |
10 | SHOX DEFICIENCY | Author keyword | 9 | 83% | 1% | 5 |
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 | LERI WEILL DYSCHONDROSTEOSIS | 107 | 97% | 9% | 31 | Search LERI+WEILL+DYSCHONDROSTEOSIS | Search LERI+WEILL+DYSCHONDROSTEOSIS |
2 | SHOX | 59 | 69% | 14% | 50 | Search SHOX | Search SHOX |
3 | MADELUNGS DEFORMITY | 32 | 85% | 5% | 17 | Search MADELUNGS+DEFORMITY | Search MADELUNGS+DEFORMITY |
4 | SHOX GENE | 27 | 74% | 6% | 20 | Search SHOX+GENE | Search SHOX+GENE |
5 | MADELUNG DEFORMITY | 25 | 75% | 5% | 18 | Search MADELUNG+DEFORMITY | Search MADELUNG+DEFORMITY |
6 | LERI WEILL SYNDROME | 19 | 76% | 4% | 13 | Search LERI+WEILL+SYNDROME | Search LERI+WEILL+SYNDROME |
7 | LANGER MESOMELIC DYSPLASIA | 18 | 89% | 2% | 8 | Search LANGER+MESOMELIC+DYSPLASIA | Search LANGER+MESOMELIC+DYSPLASIA |
8 | DYSCHONDROSTEOSIS | 17 | 75% | 3% | 12 | Search DYSCHONDROSTEOSIS | Search DYSCHONDROSTEOSIS |
9 | MESOMELIC DYSPLASIA | 14 | 65% | 4% | 13 | Search MESOMELIC+DYSPLASIA | Search MESOMELIC+DYSPLASIA |
10 | SHOX DEFICIENCY | 9 | 83% | 1% | 5 | Search SHOX+DEFICIENCY | Search SHOX+DEFICIENCY |
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 | LERI WEILL DYSCHONDROSTEOSIS | 67 | 71% | 16% | 54 |
2 | DYSCHONDROSTEOSIS | 52 | 65% | 14% | 50 |
3 | HOMEOBOX GENE SHOX | 36 | 71% | 8% | 29 |
4 | LANGER MESOMELIC DYSPLASIA | 33 | 100% | 4% | 13 |
5 | LERI WEILL SYNDROME | 30 | 68% | 8% | 27 |
6 | GENE SHOX | 25 | 70% | 6% | 21 |
7 | SHORT STATURE HOMEOBOX | 24 | 91% | 3% | 10 |
8 | LERI WEILL | 13 | 80% | 2% | 8 |
9 | TURNER SYNDROME | 12 | 10% | 31% | 108 |
10 | PAR1 DELETION | 11 | 100% | 2% | 6 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Short Stature due to SHOX Deficiency: Genotype, Phenotype, and Therapy | 2011 | 51 | 38 | 89% |
Madelung Deformity | 2013 | 2 | 24 | 83% |
SHOX haploinsufficiency and overdosage: impact of gonadal function status | 2001 | 56 | 21 | 52% |
The pseudoautosomal regions, SHOX and disease | 2006 | 59 | 46 | 39% |
MADELUNG'S DEFORMITY: A REVIEW | 2010 | 1 | 8 | 75% |
SHOX: Growth, Leri-Weill and Turner syndromes | 2000 | 34 | 32 | 41% |
Diagnosis of Lung Cancer by SHOX2 Gene Methylation Assay | 2015 | 0 | 39 | 36% |
Use of the MLPA Assay in the Molecular Diagnosis of Gene Copy Number Alterations in Human Genetic Diseases | 2012 | 27 | 152 | 8% |
Turner syndrome with gonadal dysgenesis and tall stature - A case report | 2007 | 0 | 12 | 42% |
Genetic Evaluation of Short Stature | 2014 | 0 | 88 | 14% |
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 | ROYAL CHILDRENS HOSP FDN | 2 | 67% | 0.6% | 2 |
2 | CHCG DIAGNOST GENOME ANAL | 1 | 100% | 0.6% | 2 |
3 | DIPARTIMENTO PEDIAT GINECOL | 1 | 100% | 0.6% | 2 |
4 | MED MOL GENET INGEMM | 1 | 22% | 1.1% | 4 |
5 | INVEST BIOMED ENFERMEDADES RARAS CIBERER | 1 | 33% | 0.6% | 2 |
6 | HOSP CLINDISCIPLINA ENDOCRINOL MED | 1 | 50% | 0.3% | 1 |
7 | IT CONSULTING | 1 | 50% | 0.3% | 1 |
8 | MATER SERV | 1 | 50% | 0.3% | 1 |
9 | ORTHOPED TRAUMATOL HAND SURG MICROSURG | 1 | 50% | 0.3% | 1 |
10 | PRACOVISTE KUTNA HORA | 1 | 50% | 0.3% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000171011 | TURNER SYNDROME//TURNERS SYNDROME//ULLRICH TURNER SYNDROME |
2 | 0.0000166883 | MIXED GONADAL DYSGENESIS//GONADOBLASTOMA//RING Y CHROMOSOME |
3 | 0.0000144527 | WEISMANN NETTER STUHL SYNDROME//GLOMERULOCYSTIC KIDNEY//GLOMERULOCYSTIC KIDNEY DISEASE |
4 | 0.0000108134 | 47 XYY MALES//TAURODONTISM//MANDIBULAR PROGNATHISM |
5 | 0.0000103023 | ZFAT//CENT ADV MOL MED//ZBTB38 GENE |
6 | 0.0000102138 | ACHONDROPLASIA//HYPOCHONDROPLASIA//THANATOPHORIC DYSPLASIA |
7 | 0.0000079512 | BRACHYDACTYLY TYPE C//PROXIMAL SYMPHALANGISM//GDF 5 |
8 | 0.0000076101 | PREMATURE OVARIAN FAILURE//PRIMARY OVARIAN INSUFFICIENCY//AUTOIMMUNE OOPHORITIS |
9 | 0.0000069450 | SYNPOLYDACTYLY//RADIAL LONGITUDINAL DEFICIENCY//HAND FOOT GENITAL SYNDROME |
10 | 0.0000061629 | CONGENITAL RADIOULNAR SYNOSTOSIS//RADIOULNAR SYNOSTOSIS//CONGENITAL RADIO ULNAR SYNOSTOSIS |