Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
6620 | 1463 | 39.2 | 85% |
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 |
991 | 2 | DUCHENNE MUSCULAR DYSTROPHY//DYSTROPHIN//MUSCULAR DYSTROPHY | 10483 |
6620 | 1 | CONGENITAL MUSCULAR DYSTROPHY//DYSTROGLYCAN//WALKER WARBURG SYNDROME | 1463 |
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 | CONGENITAL MUSCULAR DYSTROPHY | authKW | 2954054 | 14% | 69% | 204 |
2 | DYSTROGLYCAN | authKW | 2303566 | 14% | 55% | 201 |
3 | WALKER WARBURG SYNDROME | authKW | 1130440 | 4% | 83% | 65 |
4 | ALPHA DYSTROGLYCAN | authKW | 1012465 | 5% | 69% | 70 |
5 | DYSTROGLYCANOPATHY | authKW | 857524 | 3% | 96% | 43 |
6 | MEROSIN | authKW | 752976 | 4% | 57% | 63 |
7 | MUSCLE EYE BRAIN DISEASE | authKW | 711775 | 2% | 95% | 36 |
8 | FUKUTIN | authKW | 610593 | 2% | 91% | 32 |
9 | FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY | authKW | 511310 | 2% | 88% | 28 |
10 | POMGNT1 | authKW | 455094 | 2% | 84% | 26 |
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 | 8172 | 33% | 0% | 483 |
2 | Neurosciences | 1933 | 23% | 0% | 334 |
3 | Genetics & Heredity | 1534 | 15% | 0% | 213 |
4 | Biochemistry & Molecular Biology | 1386 | 28% | 0% | 415 |
5 | Cell Biology | 828 | 14% | 0% | 203 |
6 | Pediatrics | 787 | 9% | 0% | 130 |
7 | Pathology | 543 | 6% | 0% | 89 |
8 | Developmental Biology | 353 | 3% | 0% | 51 |
9 | Biophysics | 94 | 4% | 0% | 59 |
10 | Mycology | 57 | 1% | 0% | 14 |
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 | MUSCLE BIOL UNIT | 213434 | 1% | 68% | 15 |
2 | GLYCOBIOL GRP | 183976 | 2% | 38% | 23 |
3 | NEUROL MOL BRAIN SCI | 137975 | 1% | 37% | 18 |
4 | DUBOWITZ NEUROMUSCULAR | 134385 | 3% | 13% | 50 |
5 | FDN AGING PROMOT HUMAN WELF | 130430 | 1% | 63% | 10 |
6 | MC LOCKWOOD MUSCULAR DYSTROPHY | 109184 | 1% | 35% | 15 |
7 | MED NUCL MAGNET ONANCE IL | 107330 | 0% | 86% | 6 |
8 | GENOME MEDMINATO KU | 102259 | 0% | 70% | 7 |
9 | TEAM MECH AGING | 78240 | 1% | 25% | 15 |
10 | NEUROMUSCULAR BIOL DIS GRP | 73038 | 0% | 50% | 7 |
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 | 99668 | 7% | 5% | 106 |
2 | BRAIN & DEVELOPMENT | 24244 | 4% | 2% | 65 |
3 | SKELETAL MUSCLE | 8742 | 1% | 5% | 9 |
4 | NEUROPEDIATRICS | 5886 | 2% | 1% | 24 |
5 | GLYCOBIOLOGY | 5720 | 2% | 1% | 28 |
6 | HUMAN MOLECULAR GENETICS | 5284 | 3% | 1% | 50 |
7 | JOURNAL OF CHILD NEUROLOGY | 2441 | 2% | 0% | 24 |
8 | ACTA NEUROPATHOLOGICA | 2026 | 2% | 0% | 24 |
9 | EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY | 1516 | 1% | 1% | 9 |
10 | OPHTHALMIC PAEDIATRICS AND GENETICS | 1363 | 0% | 1% | 5 |
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 | CONGENITAL MUSCULAR DYSTROPHY | 2954054 | 14% | 69% | 204 | Search CONGENITAL+MUSCULAR+DYSTROPHY | Search CONGENITAL+MUSCULAR+DYSTROPHY |
2 | DYSTROGLYCAN | 2303566 | 14% | 55% | 201 | Search DYSTROGLYCAN | Search DYSTROGLYCAN |
3 | WALKER WARBURG SYNDROME | 1130440 | 4% | 83% | 65 | Search WALKER+WARBURG+SYNDROME | Search WALKER+WARBURG+SYNDROME |
4 | ALPHA DYSTROGLYCAN | 1012465 | 5% | 69% | 70 | Search ALPHA+DYSTROGLYCAN | Search ALPHA+DYSTROGLYCAN |
5 | DYSTROGLYCANOPATHY | 857524 | 3% | 96% | 43 | Search DYSTROGLYCANOPATHY | Search DYSTROGLYCANOPATHY |
6 | MEROSIN | 752976 | 4% | 57% | 63 | Search MEROSIN | Search MEROSIN |
7 | MUSCLE EYE BRAIN DISEASE | 711775 | 2% | 95% | 36 | Search MUSCLE+EYE+BRAIN+DISEASE | Search MUSCLE+EYE+BRAIN+DISEASE |
8 | FUKUTIN | 610593 | 2% | 91% | 32 | Search FUKUTIN | Search FUKUTIN |
9 | FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY | 511310 | 2% | 88% | 28 | Search FUKUYAMA+CONGENITAL+MUSCULAR+DYSTROPHY | Search FUKUYAMA+CONGENITAL+MUSCULAR+DYSTROPHY |
10 | POMGNT1 | 455094 | 2% | 84% | 26 | Search POMGNT1 | Search POMGNT1 |
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 | HEWITT, JE , (2009) ABNORMAL GLYCOSYLATION OF DYSTROGLYCAN IN HUMAN GENETIC DISEASE.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1792. ISSUE 9. P. 853 -861 | 109 | 92% | 42 |
2 | REED, UC , (2009) CONGENITAL MUSCULAR DYSTROPHY PART I: A REVIEW OF PHENOTYPICAL AND DIAGNOSTIC ASPECTS.ARQUIVOS DE NEURO-PSIQUIATRIA. VOL. 67. ISSUE 1. P. 144-168 | 126 | 68% | 27 |
3 | PRAISSMAN, JL , WELLS, L , (2014) MAMMALIAN O-MANNOSYLATION PATHWAY: GLYCAN STRUCTURES, ENZYMES, AND PROTEIN SUBSTRATES.BIOCHEMISTRY. VOL. 53. ISSUE 19. P. 3066 -3078 | 89 | 80% | 13 |
4 | ENDO, T , (2015) GLYCOBIOLOGY OF ALPHA-DYSTROGLYCAN AND MUSCULAR DYSTROPHY.JOURNAL OF BIOCHEMISTRY. VOL. 157. ISSUE 1. P. 1 -12 | 69 | 85% | 18 |
5 | YOSHIDA-MORIGUCHI, T , CAMPBELL, KP , (2015) MATRIGLYCAN: A NOVEL POLYSACCHARIDE THAT LINKS DYSTROGLYCAN TO THE BASEMENT MEMBRANE.GLYCOBIOLOGY. VOL. 25. ISSUE 7. P. 702 -713 | 83 | 72% | 15 |
6 | REED, UC , (2009) CONGENITAL MUSCULAR DYSTROPHY PART II: A REVIEW OF PATHOGENESIS AND THERAPEUTIC PERSPECTIVES.ARQUIVOS DE NEURO-PSIQUIATRIA. VOL. 67. ISSUE 2A. P. 343 -362 | 112 | 63% | 16 |
7 | KANAGAWA, M , KOBAYASHI, K , TAJIRI, M , MANYA, H , KUGA, A , YAMAGUCHI, Y , AKASAKA-MANYA, K , FURUKAWA, J , MIZUNO, M , KAWAKAMI, H , ET AL (2016) IDENTIFICATION OF A POST-TRANSLATIONAL MODIFICATION WITH RIBITOL-PHOSPHATE AND ITS DEFECT IN MUSCULAR DYSTROPHY.CELL REPORTS. VOL. 14. ISSUE 9. P. 2209 -2223 | 36 | 88% | 15 |
8 | BARRESI, R , CAMPBELL, KP , (2006) DYSTROGLYCAN: FROM BIOSYNTHESIS TO PATHOGENESIS OF HUMAN DISEASE.JOURNAL OF CELL SCIENCE. VOL. 119. ISSUE 2. P. 199-207 | 80 | 63% | 291 |
9 | KANAGAWA, M , (2014) DYSTROGLYCAN GLYCOSYLATION AND ITS INVOLVEMENT IN MUSCULAR DYSTROPHY.TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY. VOL. 26. ISSUE 149. P. 41 -57 | 72 | 85% | 0 |
10 | NAKAMURA, N , LYALIN, D , PANIN, VM , (2010) PROTEIN O-MANNOSYLATION IN ANIMAL DEVELOPMENT AND PHYSIOLOGY: FROM HUMAN DISORDERS TO DROSOPHILA PHENOTYPES.SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY. VOL. 21. ISSUE 6. P. 622-630 | 74 | 86% | 16 |
Classes with closest relation at Level 1 |