Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
24377 | 263 | 23.5 | 61% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
2775 | 2622 | CHARGE SYNDROME//CHOANAL ATRESIA//NAGER SYNDROME |
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 | FRASER SYNDROME | Author keyword | 77 | 82% | 17% | 45 |
2 | CRYPTOPHTHALMOS | Author keyword | 50 | 88% | 9% | 23 |
3 | FRAS1 | Author keyword | 44 | 100% | 6% | 16 |
4 | FREM | Author keyword | 12 | 86% | 2% | 6 |
5 | FREM2 | Author keyword | 9 | 83% | 2% | 5 |
6 | ABLEPHARON MACROSTOMIA SYNDROME | Author keyword | 8 | 100% | 2% | 5 |
7 | BARBER SAY SYNDROME | Author keyword | 8 | 100% | 2% | 5 |
8 | CRYPTOPHTHALMOS SYNDROME | Author keyword | 8 | 100% | 2% | 5 |
9 | FREM1 | Author keyword | 8 | 100% | 2% | 5 |
10 | MOTA SYNDROME | Author keyword | 6 | 100% | 2% | 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 | FRASER SYNDROME | 77 | 82% | 17% | 45 | Search FRASER+SYNDROME | Search FRASER+SYNDROME |
2 | CRYPTOPHTHALMOS | 50 | 88% | 9% | 23 | Search CRYPTOPHTHALMOS | Search CRYPTOPHTHALMOS |
3 | FRAS1 | 44 | 100% | 6% | 16 | Search FRAS1 | Search FRAS1 |
4 | FREM | 12 | 86% | 2% | 6 | Search FREM | Search FREM |
5 | FREM2 | 9 | 83% | 2% | 5 | Search FREM2 | Search FREM2 |
6 | ABLEPHARON MACROSTOMIA SYNDROME | 8 | 100% | 2% | 5 | Search ABLEPHARON+MACROSTOMIA+SYNDROME | Search ABLEPHARON+MACROSTOMIA+SYNDROME |
7 | BARBER SAY SYNDROME | 8 | 100% | 2% | 5 | Search BARBER+SAY+SYNDROME | Search BARBER+SAY+SYNDROME |
8 | CRYPTOPHTHALMOS SYNDROME | 8 | 100% | 2% | 5 | Search CRYPTOPHTHALMOS+SYNDROME | Search CRYPTOPHTHALMOS+SYNDROME |
9 | FREM1 | 8 | 100% | 2% | 5 | Search FREM1 | Search FREM1 |
10 | MOTA SYNDROME | 6 | 100% | 2% | 4 | Search MOTA+SYNDROME | Search MOTA+SYNDROME |
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 | CRYPTOPHTHALMOS | 71 | 80% | 17% | 44 |
2 | MYELENCEPHALIC BLEBS | 30 | 100% | 5% | 12 |
3 | SYNDACTYLY SYNDROME | 27 | 92% | 4% | 11 |
4 | BLEBBED PHENOTYPE | 26 | 67% | 9% | 24 |
5 | ATROPHIC SKIN | 13 | 80% | 3% | 8 |
6 | FRASER SYNDROME | 11 | 36% | 10% | 25 |
7 | MOTA SYNDROME | 11 | 100% | 2% | 6 |
8 | SUBLAMINA DENSA | 8 | 100% | 2% | 5 |
9 | MOUSE MYELENCEPHALIC BLEBS | 7 | 64% | 3% | 7 |
10 | BILATERAL RENAL AGENESIS | 7 | 53% | 3% | 9 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes | 2002 | 84 | 65 | 74% |
The role of Fras1/Frem proteins in the structure and function of basement membrane | 2011 | 14 | 52 | 52% |
Fraser syndrome: A new case report with review of the literature | 2008 | 2 | 4 | 100% |
Let's stick together: The role of the Fras1 and Frem proteins in epidermal adhesion | 2007 | 20 | 38 | 47% |
FRASER SYNDROME (CRYPTOPHTHALMOS-SYNDACTYLY SYNDROME) - A REVIEW OF 11 CASES WITH POSTMORTEM FINDINGS | 1988 | 42 | 5 | 100% |
Prenatal detection of Fraser syndrome without cryptophthalmos: case report and review of the literature | 2001 | 16 | 24 | 71% |
THE CLINICAL SPECTRUM OF THE FRASER SYNDROME - REPORT OF 3 NEW CASES AND REVIEW | 1987 | 41 | 6 | 100% |
The genetics of Fraser syndrome and the blebs mouse mutants | 2005 | 36 | 37 | 41% |
Congenital Upper Eyelid Coloboma: Embryologic, Nomenclatorial, Nosologic, Etiologic, Pathogenetic, Epidemiologic, Clinical, and Management Perspectives | 2015 | 0 | 107 | 52% |
ISOLATED AND SYNDROMIC CRYPTOPHTHALMOS | 1986 | 82 | 17 | 47% |
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 | OCULOPLAST ORBIT UNIT | 1 | 50% | 0.4% | 1 |
2 | OCULOPLAST RECONSTRUCT LACRIMAL ORBITAL SERV | 1 | 50% | 0.4% | 1 |
3 | OPHTHALMOL CLIN 4V2 OPHTHALMOL | 1 | 50% | 0.4% | 1 |
4 | PERINATAL GENET PROGRAM | 1 | 50% | 0.4% | 1 |
5 | SECT GENET METABOL | 1 | 50% | 0.4% | 1 |
6 | SETOR UVEITES | 1 | 50% | 0.4% | 1 |
7 | SYDNEY SW GENET SERV | 1 | 50% | 0.4% | 1 |
8 | UNIT PEDIAT DEV GENET EYE DIS | 1 | 50% | 0.4% | 1 |
9 | SEKIGUCHI BIOMATRIX SIGNALING PROJECT | 1 | 15% | 1.5% | 4 |
10 | CUTANEOUS DEV BIOL | 0 | 33% | 0.4% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000140479 | EYELID RECONSTRUCTION//POSTERIOR LAMELLA//UPPER EYELID RECONSTRUCTION |
2 | 0.0000135530 | FRONTONASAL DYSPLASIA//PROBOSCIS LATERALIS//CRANIOFRONTONASAL DYSPLASIA |
3 | 0.0000079997 | GRHL2//GRAINYHEAD//GRAINY HEAD |
4 | 0.0000068108 | POSTERIOR NEUROPORE//NEURULATION//CURLY TAIL |
5 | 0.0000066049 | NAGER SYNDROME//ACROFACIAL DYSOSTOSIS//GOLDENHAR SYNDROME |
6 | 0.0000063500 | FETAL FACE//FETAL PALATE//HDLIVE |
7 | 0.0000062356 | TRISOMY 18//TRISOMY 13//PATAU SYNDROME |
8 | 0.0000060685 | ACCESSORY SCROTUM//CONGENITAL HYPERTRICHOSIS//CANTU SYNDROME |
9 | 0.0000059510 | BLEPHAROPHIMOSIS//OHDO SYNDROME//BPES |
10 | 0.0000056318 | SACROCOCCYGEAL TERATOMA//EPIGNATHUS//CERVICAL TERATOMA |