Class information for:
Level 1: OCULOPHARYNGEAL MUSCULAR DYSTROPHY//PABPN1//OPMD

Basic class information

ID Publications Average number
of references
Avg. shr. active
ref. in WoS
23258 297 31.9 69%



Bar chart of Publication_year

Last years might be incomplete

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