Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
24494 | 310 | 32.3 | 70% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
0 | 4 | BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY | 4064930 |
180 | 3 | DUCHENNE MUSCULAR DYSTROPHY//DYSTROPHIN//MUSCULAR DYSTROPHY | 56784 |
1857 | 2 | TITIN//INCLUSION BODY MYOSITIS//NEMALINE MYOPATHY | 6073 |
24494 | 1 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY//PABPN1//OPMD | 310 |
Terms with highest relevance score |
rank | Term | termType | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|---|
1 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY | authKW | 6443825 | 25% | 84% | 78 |
2 | PABPN1 | authKW | 3113573 | 12% | 88% | 36 |
3 | OPMD | authKW | 1830195 | 8% | 77% | 24 |
4 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY OPMD | authKW | 895459 | 3% | 91% | 10 |
5 | OCULOPHARYNGODISTAL MYOPATHY | authKW | 506573 | 2% | 86% | 6 |
6 | OCULOPHARYNGEAL | authKW | 410418 | 2% | 83% | 5 |
7 | PABPN1 GENE | authKW | 394003 | 1% | 100% | 4 |
8 | PABP2 | authKW | 315201 | 1% | 80% | 4 |
9 | POLYA BINDING PROTEIN NUCLEAR 1 | authKW | 315201 | 1% | 80% | 4 |
10 | PABP2 GENE | authKW | 295502 | 1% | 100% | 3 |
Web of Science journal categories |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | Clinical Neurology | 2907 | 42% | 0% | 131 |
2 | Neurosciences | 777 | 30% | 0% | 94 |
3 | Genetics & Heredity | 207 | 12% | 0% | 37 |
4 | Biochemistry & Molecular Biology | 146 | 22% | 0% | 67 |
5 | Pathology | 57 | 5% | 0% | 14 |
6 | Otorhinolaryngology | 43 | 3% | 0% | 9 |
7 | Cell Biology | 43 | 8% | 0% | 25 |
8 | Ophthalmology | 28 | 3% | 0% | 10 |
9 | Biophysics | 22 | 4% | 0% | 13 |
10 | Psychiatry | 18 | 4% | 0% | 12 |
Address terms |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | BIOCHEM ORATORIUM | 98501 | 0% | 100% | 1 |
2 | CONSULTAT PATHOL NEUROMUSCULAI MYOL | 98501 | 0% | 100% | 1 |
3 | DNA KLIN DETSKE NEUROL 2 | 98501 | 0% | 100% | 1 |
4 | E SCOTLAND REG GENET | 98501 | 0% | 100% | 1 |
5 | EXCELLENCE NEUROMI | 98501 | 0% | 100% | 1 |
6 | EYE IAL | 98501 | 0% | 100% | 1 |
7 | FUNCTIONAL BIOL | 98501 | 0% | 100% | 1 |
8 | GENET MOL CHROMOSOMCNRS | 98501 | 0% | 100% | 1 |
9 | HOP NOTRE DAME CHUM NEUROGENET | 98501 | 0% | 100% | 1 |
10 | HOP PITIE SALPETRIE ERV NEUROLFEDERAT MAZARIN | 98501 | 0% | 100% | 1 |
Journals |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | NEUROMUSCULAR DISORDERS | 54297 | 12% | 2% | 36 |
2 | HUMAN MOLECULAR GENETICS | 3631 | 6% | 0% | 19 |
3 | MUSCLE & NERVE | 2338 | 4% | 0% | 13 |
4 | SKELETAL MUSCLE | 2038 | 1% | 1% | 2 |
5 | NEUROBIOLOGY OF DISEASE | 1712 | 3% | 0% | 8 |
6 | CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES | 827 | 2% | 0% | 5 |
7 | JOURNAL OF NEUROLOGY | 785 | 2% | 0% | 7 |
8 | NERVENARZT | 711 | 2% | 0% | 6 |
9 | REVUE NEUROLOGIQUE | 511 | 2% | 0% | 5 |
10 | NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY | 477 | 1% | 0% | 3 |
Author Key Words |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY | 6443825 | 25% | 84% | 78 | Search OCULOPHARYNGEAL+MUSCULAR+DYSTROPHY | Search OCULOPHARYNGEAL+MUSCULAR+DYSTROPHY |
2 | PABPN1 | 3113573 | 12% | 88% | 36 | Search PABPN1 | Search PABPN1 |
3 | OPMD | 1830195 | 8% | 77% | 24 | Search OPMD | Search OPMD |
4 | OCULOPHARYNGEAL MUSCULAR DYSTROPHY OPMD | 895459 | 3% | 91% | 10 | Search OCULOPHARYNGEAL+MUSCULAR+DYSTROPHY+OPMD | Search OCULOPHARYNGEAL+MUSCULAR+DYSTROPHY+OPMD |
5 | OCULOPHARYNGODISTAL MYOPATHY | 506573 | 2% | 86% | 6 | Search OCULOPHARYNGODISTAL+MYOPATHY | Search OCULOPHARYNGODISTAL+MYOPATHY |
6 | OCULOPHARYNGEAL | 410418 | 2% | 83% | 5 | Search OCULOPHARYNGEAL | Search OCULOPHARYNGEAL |
7 | PABPN1 GENE | 394003 | 1% | 100% | 4 | Search PABPN1+GENE | Search PABPN1+GENE |
8 | PABP2 | 315201 | 1% | 80% | 4 | Search PABP2 | Search PABP2 |
9 | POLYA BINDING PROTEIN NUCLEAR 1 | 315201 | 1% | 80% | 4 | Search POLYA+BINDING+PROTEIN+NUCLEAR+1 | Search POLYA+BINDING+PROTEIN+NUCLEAR+1 |
10 | PABP2 GENE | 295502 | 1% | 100% | 3 | Search PABP2+GENE | Search PABP2+GENE |
Core articles |
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c: (1) Number of references referring to publications in the class. (2) Share of total number of active references referring to publications in the class. (3) Age of the article. New articles get higher score than old articles. (4) Citation rate, normalized to year. |
Rank | Reference | # ref. in cl. |
Shr. of ref. in cl. |
Citations |
---|---|---|---|---|
1 | BRAIS, B , (2009) OCULOPHARYNGEAL MUSCULAR DYSTROPHY: A POLYALANINE MYOPATHY.CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS. VOL. 9. ISSUE 1. P. 76-82 | 43 | 93% | 32 |
2 | ABU-BAKER, A , ROULEAU, GA , (2007) OCULOPHARYNGEAL MUSCULAR DYSTROPHY: RECENT ADVANCES IN THE UNDERSTANDING OF THE MOLECULAR PATHOGENIC MECHANISMS AND TREATMENT STRATEGIES.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1772. ISSUE 2. P. 173-185 | 59 | 61% | 39 |
3 | WINTER, R , LIEBOLD, J , SCHWARZ, E , (2013) THE UNRESOLVED PUZZLE WHY ALANINE EXTENSIONS CAUSE DISEASE.BIOLOGICAL CHEMISTRY. VOL. 394. ISSUE 8. P. 951-963 | 49 | 56% | 5 |
4 | BANERJEE, A , APPONI, LH , PAVLATH, GK , CORBETT, AH , (2013) PABPN1: MOLECULAR FUNCTION AND MUSCLE DISEASE.FEBS JOURNAL. VOL. 280. ISSUE 17. P. 4230-4250 | 54 | 48% | 12 |
5 | SCHRODER, JM , KLOSSOK, T , WEIS, J , (2011) OCULOPHARYNGEAL MUSCLE DYSTROPHY: FINE STRUCTURE AND MRNA EXPRESSION LEVELS OF PABPN1.CLINICAL NEUROPATHOLOGY. VOL. 30. ISSUE 3. P. 94-103 | 32 | 82% | 6 |
6 | HARISH, P , MALERBA, A , DICKSON, G , BACHTARZI, H , (2015) PROGRESS ON GENE THERAPY, CELL THERAPY, AND PHARMACOLOGICAL STRATEGIES TOWARD THE TREATMENT OF OCULOPHARYNGEAL MUSCULAR DYSTROPHY.HUMAN GENE THERAPY. VOL. 26. ISSUE 5. P. 286 -292 | 37 | 60% | 3 |
7 | RAZ, V , BUTLER-BROWNE, G , VAN ENGELEN, B , BRAIS, B , (2013) 191ST ENMC INTERNATIONAL WORKSHOP: RECENT ADVANCES IN OCULOPHARYNGEAL MUSCULAR DYSTROPHY RESEARCH: FROM BENCH TO BEDSIDE 8-10 JUNE 2012, NAARDEN, THE NETHERLANDS.NEUROMUSCULAR DISORDERS. VOL. 23. ISSUE 6. P. 516-523 | 27 | 84% | 7 |
8 | BRAIS, B , (2003) OCULOPHARYNGEAL MUSCULAR DYSTROPHY: A LATE-ONSET POLYALANINE DISEASE.CYTOGENETIC AND GENOME RESEARCH. VOL. 100. ISSUE 1-4. P. 252-260 | 43 | 67% | 44 |
9 | NADAJ-PAKLEZA, A , RICHARD, P , LUSAKOWSKA, A , GAJEWSKA, J , JAMROZIK, Z , KOSTERA-PRUSZCZYK, A , KWIECINSKI, H , KAMINSKA, A , (2009) OCULOPHARYNGEAL MUSCULAR DYSTROPHY: PHENOTYPIC AND GENOTYPIC CHARACTERISTICS OF 9 POLISH PATIENTS.NEUROLOGIA I NEUROCHIRURGIA POLSKA. VOL. 43. ISSUE 2. P. 113 -120 | 26 | 93% | 3 |
10 | RAZ, V , ROUTLEDGE, S , VENEMA, A , BUIJZE, H , VAN DER WAL, E , ANVAR, S , STRAASHEIJM, KR , KLOOSTER, R , ANTONIOU, M , VAN DER MAAREL, SM , (2011) MODELING OCULOPHARYNGEAL MUSCULAR DYSTROPHY IN MYOTUBE CULTURES REVEALS REDUCED ACCUMULATION OF SOLUBLE MUTANT PABPN1 PROTEIN.AMERICAN JOURNAL OF PATHOLOGY. VOL. 179. ISSUE 4. P. 1988-2000 | 32 | 64% | 8 |
Classes with closest relation at Level 1 |