Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
22416 | 325 | 21.2 | 68% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
3033 | 1997 | HYPERTROPHIC OSTEOARTHROPATHY//SECKEL SYNDROME//PACHYDERMOPERIOSTOSIS |
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 | SECKEL SYNDROME | Author keyword | 95 | 82% | 17% | 55 |
2 | FLOATING HARBOR SYNDROME | Author keyword | 91 | 94% | 10% | 32 |
3 | MOPD II | Author keyword | 21 | 90% | 3% | 9 |
4 | FILIPPI SYNDROME | Author keyword | 17 | 100% | 2% | 8 |
5 | PRIMORDIAL DWARFISM | Author keyword | 11 | 65% | 3% | 11 |
6 | MEIER GORLIN SYNDROME | Author keyword | 11 | 78% | 2% | 7 |
7 | MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM | Author keyword | 8 | 100% | 2% | 5 |
8 | MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM TYPE II | Author keyword | 8 | 100% | 2% | 5 |
9 | HUMAN DNA DAMAGE PONSE DISORDERS GRP | Address | 7 | 50% | 3% | 10 |
10 | PRENATAL GROWTH RETARDATION | Author keyword | 6 | 80% | 1% | 4 |
Web of Science journal categories |
Author Key Words |
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 | SECKEL SYNDROME | 28 | 39% | 17% | 56 |
2 | PRIMORDIAL DWARFISM | 24 | 53% | 10% | 32 |
3 | MOPD II | 23 | 100% | 3% | 10 |
4 | BIRD HEADED DWARFISM | 21 | 90% | 3% | 9 |
5 | STATURE TYPE II | 21 | 90% | 3% | 9 |
6 | II MOPD II | 17 | 79% | 3% | 11 |
7 | PCNT GENE | 15 | 88% | 2% | 7 |
8 | CEPHALIC PRIMORDIAL DWARFISM | 13 | 71% | 3% | 10 |
9 | PCNT | 11 | 100% | 2% | 6 |
10 | SHORT STATURE SYNDROME | 10 | 73% | 2% | 8 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: Report of four cases and review of the literature | 1998 | 23 | 12 | 100% |
Microcephalic osteodysplastic primordial dwarfism type II: Report of three cases and review | 1998 | 21 | 14 | 100% |
Filippi syndrome: A specific MCA/MR complex within the spectrum of so called "craniodigital syndromes". Report of an additional patient with a peculiar mpp and review of the literature | 2002 | 3 | 13 | 100% |
Meier-Gorlin syndrome | 2015 | 0 | 21 | 86% |
The ''bird headed'' dwarfism or Seckel syndrome. Does it really exist? | 1996 | 5 | 14 | 100% |
Investigating microcephaly | 2013 | 5 | 25 | 28% |
Congenital microcephaly | 2014 | 4 | 112 | 15% |
Mechanisms and pathways of growth failure in primordial dwarfism | 2011 | 42 | 122 | 18% |
Intrauterine programming of ageing | 2010 | 9 | 32 | 16% |
Human DNA damage response and repair deficiency syndromes: Linking genomic instability and cell cycle checkpoint proficiency | 2009 | 36 | 158 | 10% |
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 | HUMAN DNA DAMAGE PONSE DISORDERS GRP | 7 | 50% | 3.1% | 10 |
2 | HGU | 2 | 67% | 0.6% | 2 |
3 | DOUBLE STRAND BREAK REPAIR | 1 | 100% | 0.6% | 2 |
4 | HUMAN GENET 836 | 1 | 40% | 0.6% | 2 |
5 | SARAH M CHARLES E SEAY MUSCULOSKELETAL | 1 | 16% | 1.5% | 5 |
6 | CINCINNATI GROWTH DISORDERS | 1 | 50% | 0.3% | 1 |
7 | HUMAN CLIN GENET CHKG | 1 | 50% | 0.3% | 1 |
8 | IMAGINE GENET | 1 | 50% | 0.3% | 1 |
9 | JUVENILE EDUC | 1 | 50% | 0.3% | 1 |
10 | MED GENET FOETOPATHOL | 1 | 50% | 0.3% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000254825 | ASPM//MCPH1//WDR62 |
2 | 0.0000141187 | HOMO FLORESIENSIS//LIANG BUA//ARCHAEOL STUDIES PROGRAM |
3 | 0.0000135685 | PACHYDERMODACTYLY//DIGITAL FIBROMATOSIS//ATROPHIA MACULOSA VARIOLIFORMIS CUTIS |
4 | 0.0000090515 | CEREBRO COSTO MANDIBULAR SYNDROME//MALPUECH SYNDROME//MICHELS SYNDROME |
5 | 0.0000082249 | HYDRANENCEPHALY//FOWLER SYNDROME//FLVCR2 |
6 | 0.0000066452 | WIEDEMANN RAUTENSTRAUCH SYNDROME//NEONATAL PROGEROID SYNDROME//HALLERMANN STREIFF SYNDROME |
7 | 0.0000060058 | DUBOWITZ SYNDROME//CERVICAL SPINE ABNORMALITIES//CHEM S MINAMI KU |
8 | 0.0000057897 | CENTROSOME//CENTRIOLE//CENTRIN |
9 | 0.0000053482 | COHEN SYNDROME//COH1//VPS13B |
10 | 0.0000052282 | RUBINSTEIN TAYBI SYNDROME//CORNEAL KELOID//TRISOMY 16Q |