Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
10779 | 967 | 29.7 | 66% |
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 | NEMALINE MYOPATHY | Author keyword | 199 | 82% | 12% | 117 |
2 | CONGENITAL MYOPATHY | Author keyword | 95 | 56% | 12% | 115 |
3 | CENTRONUCLEAR MYOPATHY | Author keyword | 83 | 76% | 6% | 59 |
4 | MYOTUBULAR MYOPATHY | Author keyword | 71 | 77% | 5% | 49 |
5 | X LINKED MYOTUBULAR MYOPATHY | Author keyword | 50 | 88% | 2% | 23 |
6 | MTM1 | Author keyword | 50 | 86% | 3% | 25 |
7 | DNM2 | Author keyword | 44 | 100% | 2% | 16 |
8 | NEMALINE ROD MYOPATHY | Author keyword | 44 | 88% | 2% | 21 |
9 | ACTA1 | Author keyword | 42 | 83% | 2% | 24 |
10 | CONGENITAL MYOPATHIES | Author keyword | 33 | 66% | 3% | 31 |
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 | NEMALINE MYOPATHY | 199 | 82% | 12% | 117 | Search NEMALINE+MYOPATHY | Search NEMALINE+MYOPATHY |
2 | CONGENITAL MYOPATHY | 95 | 56% | 12% | 115 | Search CONGENITAL+MYOPATHY | Search CONGENITAL+MYOPATHY |
3 | CENTRONUCLEAR MYOPATHY | 83 | 76% | 6% | 59 | Search CENTRONUCLEAR+MYOPATHY | Search CENTRONUCLEAR+MYOPATHY |
4 | MYOTUBULAR MYOPATHY | 71 | 77% | 5% | 49 | Search MYOTUBULAR+MYOPATHY | Search MYOTUBULAR+MYOPATHY |
5 | X LINKED MYOTUBULAR MYOPATHY | 50 | 88% | 2% | 23 | Search X+LINKED+MYOTUBULAR+MYOPATHY | Search X+LINKED+MYOTUBULAR+MYOPATHY |
6 | MTM1 | 50 | 86% | 3% | 25 | Search MTM1 | Search MTM1 |
7 | DNM2 | 44 | 100% | 2% | 16 | Search DNM2 | Search DNM2 |
8 | NEMALINE ROD MYOPATHY | 44 | 88% | 2% | 21 | Search NEMALINE+ROD+MYOPATHY | Search NEMALINE+ROD+MYOPATHY |
9 | ACTA1 | 42 | 83% | 2% | 24 | Search ACTA1 | Search ACTA1 |
10 | CONGENITAL MYOPATHIES | 33 | 66% | 3% | 31 | Search CONGENITAL+MYOPATHIES | Search CONGENITAL+MYOPATHIES |
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 | FIBER TYPE DISPROPORTION | 81 | 73% | 6% | 61 |
2 | CENTRONUCLEAR MYOPATHY | 60 | 59% | 7% | 68 |
3 | NEMALINE MYOPATHY | 59 | 45% | 10% | 97 |
4 | INTRANUCLEAR RODS | 56 | 100% | 2% | 19 |
5 | HYALINE BODY MYOPATHY | 51 | 91% | 2% | 21 |
6 | ACTA1 | 44 | 100% | 2% | 16 |
7 | LINKED MYOTUBULAR MYOPATHY | 44 | 58% | 5% | 51 |
8 | CENTRAL NUCLEI | 42 | 94% | 2% | 15 |
9 | DYNAMIN 2 | 40 | 76% | 3% | 28 |
10 | CONGENITAL MYOPATHY | 39 | 41% | 8% | 73 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Centronuclear myopathies: A widening concept | 2010 | 73 | 8 | 100% |
Centronuclear (myotubular) myopathy | 2008 | 77 | 127 | 74% |
Skeletal muscle alpha-actin diseases (actinopathies): pathology and mechanisms | 2013 | 16 | 67 | 78% |
Nemaline Myopathies | 2011 | 29 | 62 | 74% |
Myosinopathies: pathology and mechanisms | 2013 | 23 | 79 | 42% |
Centronuclear Myopathies | 2011 | 26 | 33 | 76% |
Nemaline myopathy: current concepts | 1997 | 88 | 59 | 83% |
Myopathies associated with beta-tropomyosin mutations | 2012 | 16 | 54 | 69% |
Congenital Myopathies: An Update | 2012 | 19 | 90 | 60% |
What's new in congenital myopathies? | 2008 | 30 | 58 | 74% |
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 | MANTON ORPHAN DIS PROGRAM GENOM | 23 | 100% | 1.0% | 10 |
2 | MANTON ORPHAN DIS GENET | 21 | 85% | 1.1% | 11 |
3 | GENET GENOMMANTON ORPHAN DIS | 13 | 80% | 0.8% | 8 |
4 | INMR | 7 | 67% | 0.6% | 6 |
5 | DIAGNOST GENET | 6 | 21% | 2.6% | 25 |
6 | TRANSLAT MED NEUROGENET | 5 | 38% | 1.1% | 11 |
7 | UNITE MORPHOL NEUROMUSCULAIRE | 5 | 35% | 1.1% | 11 |
8 | CHAIRE GENET HUMAINE | 4 | 25% | 1.6% | 15 |
9 | EA3949 | 3 | 57% | 0.4% | 4 |
10 | FOLKHALSAN MED GENET | 3 | 100% | 0.3% | 3 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000180444 | RIGID SPINE SYNDROME//RIGID SPINE//EMERINOPATHY |
2 | 0.0000144824 | MYOFIBRILLAR MYOPATHY//DESMINOPATHY//PLECTIN |
3 | 0.0000096483 | TITIN//CONNECTIN//OBSCURIN |
4 | 0.0000095282 | ELECTRICAL IMPEDANCE MYOGRAPHY//MUSCLE ULTRASOUND//CENTRAL HYPOTONIA |
5 | 0.0000092743 | ARTHROGRYPOSIS//NEU LAXOVA SYNDROME//AMYOPLASIA |
6 | 0.0000082864 | MALIGNANT HYPERTHERMIA//IN VITRO CONTRACTURE TEST//HYPERTHERMIA MALIGNANT |
7 | 0.0000072102 | DYSFERLIN//MIYOSHI MYOPATHY//LIMB GIRDLE MUSCULAR DYSTROPHY |
8 | 0.0000067688 | DYNAMIN//F BAR DOMAIN//AMPHIPHYSIN |
9 | 0.0000067190 | TROPOMODULIN//TROPOMYOSIN//LEIOMODIN |
10 | 0.0000064122 | CONGENITAL MYASTHENIC SYNDROME//CONGENITAL MYASTHENIC SYNDROMES//TUBULAR AGGREGATES |