Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
23258 | 297 | 31.9 | 69% |
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 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY | Author keyword | 113 | 79% | 24% | 72 |
2 | PABPN1 | Author keyword | 70 | 87% | 11% | 34 |
3 | OPMD | Author keyword | 40 | 82% | 8% | 23 |
4 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY OPMD | Author keyword | 24 | 91% | 3% | 10 |
5 | OCULOPHARYNGODISTAL MYOPATHY | Author keyword | 11 | 100% | 2% | 6 |
6 | PABP2 | Author keyword | 6 | 80% | 1% | 4 |
7 | OCULOPHARYNGEAL | Author keyword | 6 | 71% | 2% | 5 |
8 | PABPN1 GENE | Author keyword | 6 | 100% | 1% | 4 |
9 | POLYA BINDING PROTEIN NUCLEAR 1 | Author keyword | 6 | 100% | 1% | 4 |
10 | PABP2 GENE | Author keyword | 3 | 100% | 1% | 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 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY | 113 | 79% | 24% | 72 | Search OCULOPHARYNGEAL+MUSCULAR+DYSTROPHY | Search OCULOPHARYNGEAL+MUSCULAR+DYSTROPHY |
2 | PABPN1 | 70 | 87% | 11% | 34 | Search PABPN1 | Search PABPN1 |
3 | OPMD | 40 | 82% | 8% | 23 | Search OPMD | Search OPMD |
4 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY OPMD | 24 | 91% | 3% | 10 | Search OCULOPHARYNGEAL+MUSCULAR+DYSTROPHY+OPMD | Search OCULOPHARYNGEAL+MUSCULAR+DYSTROPHY+OPMD |
5 | OCULOPHARYNGODISTAL MYOPATHY | 11 | 100% | 2% | 6 | Search OCULOPHARYNGODISTAL+MYOPATHY | Search OCULOPHARYNGODISTAL+MYOPATHY |
6 | PABP2 | 6 | 80% | 1% | 4 | Search PABP2 | Search PABP2 |
7 | OCULOPHARYNGEAL | 6 | 71% | 2% | 5 | Search OCULOPHARYNGEAL | Search OCULOPHARYNGEAL |
8 | PABPN1 GENE | 6 | 100% | 1% | 4 | Search PABPN1+GENE | Search PABPN1+GENE |
9 | POLYA BINDING PROTEIN NUCLEAR 1 | 6 | 100% | 1% | 4 | Search POLYA+BINDING+PROTEIN+NUCLEAR+1 | Search POLYA+BINDING+PROTEIN+NUCLEAR+1 |
10 | PABP2 GENE | 3 | 100% | 1% | 3 | Search PABP2+GENE | Search PABP2+GENE |
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 | PABPN1 | 35 | 89% | 5% | 16 |
2 | REDUCE AGGREGATE FORMATION | 27 | 92% | 4% | 11 |
3 | PABP2 GENE | 23 | 79% | 5% | 15 |
4 | NUCLEAR INCLUSIONS | 23 | 33% | 19% | 56 |
5 | CHROMOSOME 14Q112 Q13 | 22 | 81% | 4% | 13 |
6 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY | 17 | 27% | 18% | 52 |
7 | DISTAL SPREAD | 6 | 80% | 1% | 4 |
8 | NEUROGENIC INVOLVEMENT | 6 | 80% | 1% | 4 |
9 | POLYALANINE EXPANSION MUTANT | 6 | 80% | 1% | 4 |
10 | BUKHARA JEWS | 6 | 100% | 1% | 4 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Oculopharyngeal muscular dystrophy: A polyalanine myopathy | 2009 | 29 | 46 | 93% |
Oculopharyngeal muscular dystrophy: Recent advances in the understanding of the molecular pathogenic mechanisms and treatment strategies | 2007 | 36 | 96 | 60% |
PABPN1: molecular function and muscle disease | 2013 | 9 | 113 | 49% |
Molecular mechanisms underlying polyalanine diseases | 2009 | 32 | 85 | 33% |
Oculopharyngeal muscular dystrophy - An underdiagnosed disease in China? Report a China-born Chinese with PABPN1 mutation and epidemiology review of the literature | 2012 | 1 | 14 | 100% |
Oculopharyngeal muscular dystrophy as a paradigm for muscle aging | 2014 | 2 | 51 | 49% |
The unresolved puzzle why alanine extensions cause disease | 2013 | 3 | 88 | 55% |
Alanine tracts: the expanding story of human illness and trinucleotide repeats | 2004 | 144 | 48 | 19% |
NEUROPATHIC FINDINGS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - A REPORT OF 7 CASES AND A REVIEW OF THE LITERATURE | 1993 | 19 | 12 | 83% |
Progress on Gene Therapy, Cell Therapy, and Pharmacological Strategies Toward the Treatment of Oculopharyngeal Muscular Dystrophy | 2015 | 0 | 62 | 60% |
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 | EQUIPE ACCUEIL 4059 | 1 | 40% | 0.7% | 2 |
2 | MRNA REGULAT DEV | 1 | 33% | 0.7% | 2 |
3 | BIOMED UNIT ASSOCIATED | 1 | 50% | 0.3% | 1 |
4 | CHUMHOP NOTRE DAME | 1 | 50% | 0.3% | 1 |
5 | ETUD MALAD CERVEAU | 1 | 50% | 0.3% | 1 |
6 | MED MOL GENETGENE EXP S THER Y GRP | 1 | 50% | 0.3% | 1 |
7 | MED UNIT IMMUNOL INFECT DIS | 1 | 50% | 0.3% | 1 |
8 | NEUROL ADV BIOMED SCI | 1 | 50% | 0.3% | 1 |
9 | NEUROL NEUROSCI MICROBIOL | 1 | 50% | 0.3% | 1 |
10 | UNIDAD ESOFAGO GASTR | 1 | 50% | 0.3% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000111593 | POLYADENYLATION//ALTERNATIVE POLYADENYLATION//POLYA POLYMERASE |
2 | 0.0000099645 | POLYA BINDING PROTEIN//POLY A BINDING PROTEIN//PABP |
3 | 0.0000098679 | DYSFERLIN//MIYOSHI MYOPATHY//LIMB GIRDLE MUSCULAR DYSTROPHY |
4 | 0.0000098632 | ZENKERS DIVERTICULUM//EPIPHRENIC DIVERTICULUM//ZENKER DIVERTICULUM |
5 | 0.0000093677 | NEURONAL INTRANUCLEAR INCLUSION DISEASE//INTRANUCLEAR INCLUSION BODY DISEASE//NEURONAL INTRANUCLEAR HYALINE INCLUSION DISEASE |
6 | 0.0000091367 | BLEPHAROPHIMOSIS//OHDO SYNDROME//BPES |
7 | 0.0000065182 | HUMAN MUSCLE DEVELOPMENT//UNITE PEDAG RECH MED//HUMAN MUSCLE CULTURE |
8 | 0.0000064658 | HUNTINGTIN//POLYGLUTAMINE//HUNTINGTONS DISEASE |
9 | 0.0000061426 | CONGENITAL CENTRAL HYPOVENTILATION SYNDROME//PHOX2B//PHOX2B GENE |
10 | 0.0000056246 | SYNPOLYDACTYLY//RADIAL LONGITUDINAL DEFICIENCY//HAND FOOT GENITAL SYNDROME |