Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
991 | 10483 | 38.9 | 81% |
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 |
1302 | 1 | DYSTROPHIN//DUCHENNE MUSCULAR DYSTROPHY//BECKER MUSCULAR DYSTROPHY | 2729 |
3773 | 1 | MDX MOUSE//DUCHENNE MUSCULAR DYSTROPHY//MDX | 1912 |
6620 | 1 | CONGENITAL MUSCULAR DYSTROPHY//DYSTROGLYCAN//WALKER WARBURG SYNDROME | 1463 |
8253 | 1 | DUCHENNE MUSCULAR DYSTROPHY//DUCHENNE//MUSCULAR DYSTROPHY | 1275 |
8640 | 1 | DYSFERLIN//LIMB GIRDLE MUSCULAR DYSTROPHY//SARCOGLYCAN | 1233 |
15871 | 1 | FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY//FSHD//DUX4 | 687 |
17872 | 1 | EXON SKIPPING//MC LOCKWOOD MUSCULAR DYSTROPHY//NEUROMUSCULAR ALS | 578 |
21211 | 1 | ECHO INTENSITY//MUSCLE ULTRASOUND//MUSCLE THICKNESS | 428 |
35818 | 1 | HYPERCKEMIA//ASYMPTOMATIC CK ELEVATION//IDIOPATHIC HYPER CK EMIA | 91 |
36026 | 1 | ELECTRICAL IMPEDANCE MYOGRAPHY//NEUROMUSCULAR DIS NEUROL//HANDHELD ARRAY | 87 |
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 | DUCHENNE MUSCULAR DYSTROPHY | authKW | 2402701 | 12% | 68% | 1213 |
2 | DYSTROPHIN | authKW | 2063555 | 9% | 73% | 966 |
3 | MUSCULAR DYSTROPHY | authKW | 1362122 | 9% | 51% | 915 |
4 | NEUROMUSCULAR DISORDERS | journal | 547288 | 6% | 28% | 665 |
5 | BECKER MUSCULAR DYSTROPHY | authKW | 542507 | 2% | 87% | 215 |
6 | DYSTROGLYCAN | authKW | 533361 | 2% | 71% | 259 |
7 | CONGENITAL MUSCULAR DYSTROPHY | authKW | 519116 | 2% | 78% | 229 |
8 | MDX MOUSE | authKW | 427539 | 2% | 73% | 201 |
9 | LIMB GIRDLE MUSCULAR DYSTROPHY | authKW | 425834 | 2% | 71% | 206 |
10 | UTROPHIN | authKW | 422433 | 2% | 83% | 175 |
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 | 43674 | 29% | 1% | 3014 |
2 | Genetics & Heredity | 17237 | 18% | 0% | 1869 |
3 | Neurosciences | 14737 | 23% | 0% | 2459 |
4 | Cell Biology | 4194 | 12% | 0% | 1262 |
5 | Biochemistry & Molecular Biology | 3391 | 19% | 0% | 1978 |
6 | Medicine, Research & Experimental | 1957 | 6% | 0% | 654 |
7 | Pediatrics | 1917 | 6% | 0% | 592 |
8 | Pathology | 1487 | 4% | 0% | 425 |
9 | Physiology | 769 | 4% | 0% | 417 |
10 | Sport Sciences | 732 | 2% | 0% | 257 |
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 | DUBOWITZ NEUROMUSCULAR | 132533 | 1% | 34% | 133 |
2 | MC LOCKWOOD MUSCULAR DYSTROPHY | 92664 | 0% | 86% | 37 |
3 | NEUROMUSCULAR ALS | 60635 | 0% | 83% | 25 |
4 | MYOL | 55848 | 1% | 14% | 135 |
5 | NEUROMUSCULAR DIS | 43172 | 1% | 15% | 97 |
6 | MUSCLE BIOL UNIT | 38231 | 0% | 77% | 17 |
7 | NEUROMUSCULAR | 35099 | 1% | 8% | 149 |
8 | MOL THER Y | 31408 | 1% | 16% | 68 |
9 | NEUROMUSCULAR UNIT | 31172 | 1% | 13% | 80 |
10 | JOHN WALTON MUSCULAR DYSTROPHY | 30605 | 0% | 48% | 22 |
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 | 547288 | 6% | 28% | 665 |
2 | MUSCLE & NERVE | 98742 | 5% | 7% | 491 |
3 | SKELETAL MUSCLE | 30473 | 0% | 23% | 45 |
4 | HUMAN MOLECULAR GENETICS | 28079 | 3% | 3% | 309 |
5 | JOURNAL OF MEDICAL GENETICS | 10927 | 1% | 3% | 149 |
6 | BRAIN & DEVELOPMENT | 10603 | 1% | 3% | 116 |
7 | JOURNAL OF THE NEUROLOGICAL SCIENCES | 8160 | 2% | 2% | 171 |
8 | NEUROLOGY | 5889 | 2% | 1% | 213 |
9 | MOLECULAR THERAPY | 5646 | 1% | 2% | 84 |
10 | HUMAN GENETICS | 5143 | 1% | 2% | 121 |
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 | DUCHENNE MUSCULAR DYSTROPHY | 2402701 | 12% | 68% | 1213 | Search DUCHENNE+MUSCULAR+DYSTROPHY | Search DUCHENNE+MUSCULAR+DYSTROPHY |
2 | DYSTROPHIN | 2063555 | 9% | 73% | 966 | Search DYSTROPHIN | Search DYSTROPHIN |
3 | MUSCULAR DYSTROPHY | 1362122 | 9% | 51% | 915 | Search MUSCULAR+DYSTROPHY | Search MUSCULAR+DYSTROPHY |
4 | BECKER MUSCULAR DYSTROPHY | 542507 | 2% | 87% | 215 | Search BECKER+MUSCULAR+DYSTROPHY | Search BECKER+MUSCULAR+DYSTROPHY |
5 | DYSTROGLYCAN | 533361 | 2% | 71% | 259 | Search DYSTROGLYCAN | Search DYSTROGLYCAN |
6 | CONGENITAL MUSCULAR DYSTROPHY | 519116 | 2% | 78% | 229 | Search CONGENITAL+MUSCULAR+DYSTROPHY | Search CONGENITAL+MUSCULAR+DYSTROPHY |
7 | MDX MOUSE | 427539 | 2% | 73% | 201 | Search MDX+MOUSE | Search MDX+MOUSE |
8 | LIMB GIRDLE MUSCULAR DYSTROPHY | 425834 | 2% | 71% | 206 | Search LIMB+GIRDLE+MUSCULAR+DYSTROPHY | Search LIMB+GIRDLE+MUSCULAR+DYSTROPHY |
9 | UTROPHIN | 422433 | 2% | 83% | 175 | Search UTROPHIN | Search UTROPHIN |
10 | DYSFERLIN | 381764 | 1% | 89% | 148 | Search DYSFERLIN | Search DYSFERLIN |
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 | BLAKE, DJ , WEIR, A , NEWEY, SE , DAVIES, KE , (2002) FUNCTION AND GENETICS OF DYSTROPHIN AND DYSTROPHIN-RELATED PROTEINS IN MUSCLE.PHYSIOLOGICAL REVIEWS. VOL. 82. ISSUE 2. P. 291-329 | 361 | 76% | 581 |
2 | MCGREEVY, JW , HAKIM, CH , MCINTOSH, MA , DUAN, DS , (2015) ANIMAL MODELS OF DUCHENNE MUSCULAR DYSTROPHY: FROM BASIC MECHANISMS TO GENE THERAPY.DISEASE MODELS & MECHANISMS. VOL. 8. ISSUE 3. P. 195 -213 | 246 | 78% | 30 |
3 | ALLEN, DG , WHITEHEAD, NP , FROEHNER, SC , (2016) ABSENCE OF DYSTROPHIN DISRUPTS SKELETAL MUSCLE SIGNALING: ROLES OF CA2+, REACTIVE OXYGEN SPECIES, AND NITRIC OXIDE IN THE DEVELOPMENT OF MUSCULAR DYSTROPHY.PHYSIOLOGICAL REVIEWS. VOL. 96. ISSUE 1. P. 253 -305 | 294 | 58% | 7 |
4 | ERVASTI, JM , SONNEMANN, KJ , (2008) BIOLOGY OF THE STRIATED MUSCLE DYSTROPHIN-GLYCOPROTEIN COMPLEX.INTERNATIONAL REVIEW OF CYTOLOGY: A SURVEY OF CELL BIOLOGY, VOL 265. VOL. 265. ISSUE . P. 191-+ | 230 | 81% | 65 |
5 | FAIRCLOUGH, RJ , PERKINS, KJ , DAVIES, KE , (2012) PHARMACOLOGICALLY TARGETING THE PRIMARY DEFECT AND DOWNSTREAM PATHOLOGY IN DUCHENNE MUSCULAR DYSTROPHY.CURRENT GENE THERAPY. VOL. 12. ISSUE 3. P. 206 -244 | 297 | 56% | 20 |
6 | GUIRAUD, S , AARTSMA-RUS, A , VIEIRA, NM , DAVIES, KE , VAN OMMEN, GJB , KUNKEL, LM , (2015) THE PATHOGENESIS AND THERAPY OF MUSCULAR DYSTROPHIES.ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 16. VOL. 16. ISSUE . P. 281 -+ | 178 | 76% | 11 |
7 | KORNEGAY, JN , SPURNEY, CF , NGHIEM, PP , BRINKMEYER-LANGFORD, CL , HOFFMAN, EP , NAGARAJU, K , (2014) PHARMACOLOGIC MANAGEMENT OF DUCHENNE MUSCULAR DYSTROPHY: TARGET IDENTIFICATION AND PRECLINICAL TRIALS.ILAR JOURNAL. VOL. 55. ISSUE 1. P. 119 -149 | 215 | 68% | 10 |
8 | MOSQUEIRA, M , ZEIGER, U , FORDERER, M , BRINKMEIER, H , FINK, RHA , (2013) CARDIAC AND RESPIRATORY DYSFUNCTION IN DUCHENNE MUSCULAR DYSTROPHY AND THE ROLE OF SECOND MESSENGERS.MEDICINAL RESEARCH REVIEWS. VOL. 33. ISSUE 5. P. 1174-1213 | 205 | 64% | 16 |
9 | MUNTONI, F , TORELLI, S , FERLINI, A , (2003) DYSTROPHIN AND MUTATIONS: ONE GENE, SEVERAL PROTEINS, MULTIPLE PHENOTYPES.LANCET NEUROLOGY. VOL. 2. ISSUE 12. P. 731-740 | 134 | 97% | 310 |
10 | ANGELINI, C , FANIN, M , (2016) PATHOGENESIS, CLINICAL FEATURES AND DIAGNOSIS OF SARCOGLYCANOPATHIES.EXPERT OPINION ON ORPHAN DRUGS. VOL. 4. ISSUE 12. P. 1239 -1251 | 141 | 93% | 0 |
Classes with closest relation at Level 2 |