Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 15115 | 661 | 33.9 | 76% |
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 | NANCE HORAN SYNDROME | Author keyword | 24 | 91% | 2% | 10 |
| 2 | AUTOSOMAL DOMINANT CONGENITAL CATARACT | Author keyword | 9 | 83% | 1% | 5 |
| 3 | GJA8 | Author keyword | 8 | 100% | 1% | 5 |
| 4 | CONGENITAL HEREDITARY DISORDERS | Address | 6 | 100% | 1% | 4 |
| 5 | CRYGD | Author keyword | 6 | 100% | 1% | 4 |
| 6 | CRYAA | Author keyword | 5 | 60% | 1% | 6 |
| 7 | CONGENITAL CATARACT | Author keyword | 5 | 15% | 5% | 31 |
| 8 | CONGENITAL NUCLEAR CATARACT | Author keyword | 4 | 75% | 0% | 3 |
| 9 | OPHTHALM ANAT PHYSIOL | Address | 4 | 75% | 0% | 3 |
| 10 | PAEDIAT OPHTHALMOL CLIN | Address | 4 | 75% | 0% | 3 |
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 | NANCE HORAN SYNDROME | 24 | 91% | 2% | 10 | Search NANCE+HORAN+SYNDROME | Search NANCE+HORAN+SYNDROME |
| 2 | AUTOSOMAL DOMINANT CONGENITAL CATARACT | 9 | 83% | 1% | 5 | Search AUTOSOMAL+DOMINANT+CONGENITAL+CATARACT | Search AUTOSOMAL+DOMINANT+CONGENITAL+CATARACT |
| 3 | GJA8 | 8 | 100% | 1% | 5 | Search GJA8 | Search GJA8 |
| 4 | CRYGD | 6 | 100% | 1% | 4 | Search CRYGD | Search CRYGD |
| 5 | CRYAA | 5 | 60% | 1% | 6 | Search CRYAA | Search CRYAA |
| 6 | CONGENITAL CATARACT | 5 | 15% | 5% | 31 | Search CONGENITAL+CATARACT | Search CONGENITAL+CATARACT |
| 7 | CONGENITAL NUCLEAR CATARACT | 4 | 75% | 0% | 3 | Search CONGENITAL+NUCLEAR+CATARACT | Search CONGENITAL+NUCLEAR+CATARACT |
| 8 | HSF4 | 3 | 39% | 1% | 7 | Search HSF4 | Search HSF4 |
| 9 | NHS GENE | 3 | 100% | 0% | 3 | Search NHS+GENE | Search NHS+GENE |
| 10 | INHERITED CATARACT | 3 | 60% | 0% | 3 | Search INHERITED+CATARACT | Search INHERITED+CATARACT |
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 | ZONULAR PULVERULENT CATARACT | 85 | 79% | 8% | 54 |
| 2 | INHERITED CATARACT | 41 | 87% | 3% | 20 |
| 3 | AUTOSOMAL DOMINANT CATARACT | 40 | 64% | 6% | 39 |
| 4 | X LINKED CATARACT | 37 | 100% | 2% | 14 |
| 5 | DOMINANT CONGENITAL CATARACT | 35 | 56% | 7% | 43 |
| 6 | D CRYSTALLIN GENE | 33 | 100% | 2% | 13 |
| 7 | CRYBB2 | 31 | 82% | 3% | 18 |
| 8 | CONGENITAL CATARACT | 29 | 29% | 13% | 86 |
| 9 | CRYAA | 28 | 69% | 4% | 24 |
| 10 | POSTERIOR POLAR CATARACT | 24 | 53% | 5% | 31 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references | % act. ref. to same field |
|---|---|---|---|---|
| Molecular genetics of congenital nuclear cataract | 2014 | 4 | 52 | 90% |
| Congenital cataracts and their molecular genetics | 2008 | 144 | 150 | 75% |
| Molecular characteristics of inherited congenital cataracts | 2010 | 27 | 214 | 65% |
| Genetics of crystallins: Cataract and beyond | 2009 | 108 | 182 | 36% |
| Molecular genetic basis of inherited cataract and associated phenotypes | 2004 | 127 | 80 | 64% |
| The genetic and molecular basis of congenital cataract | 2011 | 15 | 32 | 66% |
| Clinical and experimental advances in congenital and paediatric cataracts | 2011 | 29 | 104 | 38% |
| Genetics of human cataract | 2013 | 18 | 33 | 27% |
| Connexin mutants and cataracts | 2013 | 10 | 125 | 38% |
| The human crystallin gene families | 2012 | 11 | 85 | 42% |
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 | CONGENITAL HEREDITARY DISORDERS | 6 | 100% | 0.6% | 4 |
| 2 | OPHTHALM ANAT PHYSIOL | 4 | 75% | 0.5% | 3 |
| 3 | PAEDIAT OPHTHALMOL CLIN | 4 | 75% | 0.5% | 3 |
| 4 | OGVFB | 2 | 33% | 0.9% | 6 |
| 5 | DANEK GARTENER HUMAN GENET | 2 | 67% | 0.3% | 2 |
| 6 | ROCKY MTN LIONS EYE | 2 | 67% | 0.3% | 2 |
| 7 | UCSF JOINT PROGRAM BIOENGN | 2 | 67% | 0.3% | 2 |
| 8 | SECT OPHTHALM MOL GENET | 2 | 50% | 0.5% | 3 |
| 9 | MOGS | 1 | 100% | 0.3% | 2 |
| 10 | GENET DISORDERS | 1 | 13% | 1.4% | 9 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000226583 | LENS//LENS DEVELOPMENT//CP49 |
| 2 | 0.0000216831 | ALPHA CRYSTALLIN//SMALL HEAT SHOCK PROTEIN//ALPHA B CRYSTALLIN |
| 3 | 0.0000186922 | CHILDHOOD BLINDNESS//CONGENITAL CATARACT//MILES PEDIAT OPHTHALMOL |
| 4 | 0.0000109037 | MARINESCO SJOGREN SYNDROME//MICRO SYNDROME//WARBURG MICRO SYNDROME |
| 5 | 0.0000103842 | NANOPHTHALMOS//ANOPHTHALMIA//MICROPHTHALMIA |
| 6 | 0.0000103084 | ANIRIDIA//PAX6//PAIRED BOX |
| 7 | 0.0000095196 | ZETA CRYSTALLIN//CAMEL LENS//PIG3 |
| 8 | 0.0000088404 | AXENFELD RIEGER SYNDROME//PETERS ANOMALY//FOXC1 |
| 9 | 0.0000077883 | SPECIFIC LOCUS MUTATIONS//DOUBLING DOSE//SPECIFIC LOCUS TEST |
| 10 | 0.0000073101 | MEMBRANOUS CATARACT//GOLFBALL APPEARANCE//GOLFBALL STRUCTURE |