Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
7195 | 1318 | 38.1 | 84% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
569 | 13650 | DYSTROPHIN//DUCHENNE MUSCULAR DYSTROPHY//MYOTONIC DYSTROPHY |
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 | CONGENITAL MUSCULAR DYSTROPHY | Author keyword | 196 | 66% | 14% | 182 |
2 | DYSTROGLYCAN | Author keyword | 151 | 54% | 15% | 193 |
3 | MUSCLE EYE BRAIN DISEASE | Author keyword | 130 | 97% | 3% | 36 |
4 | FUKUTIN | Author keyword | 112 | 97% | 2% | 32 |
5 | WALKER WARBURG SYNDROME | Author keyword | 105 | 82% | 5% | 62 |
6 | DYSTROGLYCANOPATHY | Author keyword | 93 | 100% | 2% | 28 |
7 | ALPHA DYSTROGLYCAN | Author keyword | 74 | 67% | 5% | 67 |
8 | MEROSIN | Author keyword | 56 | 58% | 5% | 64 |
9 | POMGNT1 | Author keyword | 52 | 87% | 2% | 26 |
10 | POMT1 | Author keyword | 48 | 100% | 1% | 17 |
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 | CONGENITAL MUSCULAR DYSTROPHY | 196 | 66% | 14% | 182 | Search CONGENITAL+MUSCULAR+DYSTROPHY | Search CONGENITAL+MUSCULAR+DYSTROPHY |
2 | DYSTROGLYCAN | 151 | 54% | 15% | 193 | Search DYSTROGLYCAN | Search DYSTROGLYCAN |
3 | MUSCLE EYE BRAIN DISEASE | 130 | 97% | 3% | 36 | Search MUSCLE+EYE+BRAIN+DISEASE | Search MUSCLE+EYE+BRAIN+DISEASE |
4 | FUKUTIN | 112 | 97% | 2% | 32 | Search FUKUTIN | Search FUKUTIN |
5 | WALKER WARBURG SYNDROME | 105 | 82% | 5% | 62 | Search WALKER+WARBURG+SYNDROME | Search WALKER+WARBURG+SYNDROME |
6 | DYSTROGLYCANOPATHY | 93 | 100% | 2% | 28 | Search DYSTROGLYCANOPATHY | Search DYSTROGLYCANOPATHY |
7 | ALPHA DYSTROGLYCAN | 74 | 67% | 5% | 67 | Search ALPHA+DYSTROGLYCAN | Search ALPHA+DYSTROGLYCAN |
8 | MEROSIN | 56 | 58% | 5% | 64 | Search MEROSIN | Search MEROSIN |
9 | POMGNT1 | 52 | 87% | 2% | 26 | Search POMGNT1 | Search POMGNT1 |
10 | POMT1 | 48 | 100% | 1% | 17 | Search POMT1 | Search POMT1 |
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 | WALKER WARBURG SYNDROME | 323 | 70% | 20% | 270 |
2 | ALPHA DYSTROGLYCAN | 239 | 51% | 25% | 332 |
3 | ABNORMAL GLYCOSYLATION | 230 | 89% | 8% | 102 |
4 | EYE BRAIN DISEASE | 173 | 76% | 9% | 122 |
5 | DEFECTIVE GLYCOSYLATION | 163 | 88% | 6% | 78 |
6 | FUKUYAMA TYPE | 141 | 75% | 8% | 102 |
7 | CONGENITAL MUSCULAR DYSTROPHY | 135 | 38% | 21% | 280 |
8 | FUKUTIN RELATED PROTEIN | 86 | 77% | 4% | 58 |
9 | LAMININ BINDING | 70 | 65% | 5% | 66 |
10 | BETA DYSTROGLYCAN | 58 | 40% | 9% | 116 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Dystroglycanopathies: coming into focus | 2011 | 71 | 44 | 89% |
Dystroglycan: from biosynthesis to pathogenesis of human disease | 2006 | 263 | 127 | 63% |
Glycobiology of alpha-dystroglycan and muscular dystrophy | 2015 | 2 | 81 | 81% |
Muscular dystrophies due to glycosylation defects | 2008 | 57 | 49 | 94% |
The O-Mannosylation Pathway: Glycosyltransferases and Proteins Implicated in Congenital Muscular Dystrophy | 2013 | 25 | 70 | 79% |
Abnormal glycosylation of dystroglycan in human genetic disease | 2009 | 37 | 118 | 92% |
Dystrophin-glycoprotein complex: Post-translational processing and dystroglycan function | 2003 | 249 | 60 | 52% |
The congenital muscular dystrophies in 2004: a century of exciting progress | 2004 | 121 | 81 | 77% |
Glyc-O-genetics of Walker-Warburg syndrome | 2005 | 57 | 59 | 81% |
Congenital muscular dystrophies involving the O-mannose pathway | 2007 | 33 | 51 | 76% |
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 | MUSCLE BIOL UNIT | 13 | 62% | 1.0% | 13 |
2 | GLYCOBIOL GRP | 12 | 40% | 1.7% | 23 |
3 | FDN AGING PROMOT HUMAN WELF | 10 | 63% | 0.8% | 10 |
4 | GENOME MEDMINATO KU | 8 | 70% | 0.5% | 7 |
5 | DUBOWITZ NEUROMUSCULAR | 8 | 15% | 3.8% | 50 |
6 | NEUROMUSCULAR BIOL DIS GRP | 6 | 58% | 0.5% | 7 |
7 | MED NUCL MAGNET ONANCE IL | 6 | 100% | 0.3% | 4 |
8 | MC LOCKWOOD MUSCULAR DYSTROPHY | 5 | 32% | 0.9% | 12 |
9 | TOKYO METROPOLITAN GERONTOL | 4 | 39% | 0.7% | 9 |
10 | NEUROL MOL BRAIN SCI | 4 | 30% | 0.9% | 12 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000191943 | RIGID SPINE SYNDROME//RIGID SPINE//EMERINOPATHY |
2 | 0.0000176786 | DYSFERLIN//MIYOSHI MYOPATHY//LIMB GIRDLE MUSCULAR DYSTROPHY |
3 | 0.0000111193 | DYSTROPHIN//BECKER MUSCULAR DYSTROPHY//DUCHENNE MUSCULAR DYSTROPHY |
4 | 0.0000105842 | MDX MICE//DUCHENNE MUSCULAR DYSTROPHY//MDX |
5 | 0.0000102288 | BETHLEM MYOPATHY//COLLAGEN VI//TYPE VI COLLAGEN |
6 | 0.0000099424 | LAMININ//BASEMENT MEMBRANE//LAMININ 5 |
7 | 0.0000069803 | UDP GALACTOSE TRANSPORTER//NUCLEOTIDE SUGAR TRANSPORTER//CMP SIALIC ACID TRANSPORTER |
8 | 0.0000057876 | AGRIN//NEUROMUSCULAR JUNCTION//ACETYLCHOLINE RECEPTORS |
9 | 0.0000057500 | LISSENCEPHALY//CORTICAL DYSPLASIA//SCHIZENCEPHALY |
10 | 0.0000057482 | CONGENITAL DISORDERS OF GLYCOSYLATION//CARBOHYDRATE DEFICIENT GLYCOPROTEIN SYNDROME//CDG |