Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
8640 | 1233 | 40.9 | 86% |
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 |
8640 | 1 | DYSFERLIN//LIMB GIRDLE MUSCULAR DYSTROPHY//SARCOGLYCAN | 1233 |
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 | DYSFERLIN | authKW | 3117638 | 12% | 87% | 145 |
2 | LIMB GIRDLE MUSCULAR DYSTROPHY | authKW | 2077938 | 13% | 54% | 156 |
3 | SARCOGLYCAN | authKW | 1750032 | 9% | 66% | 107 |
4 | DYSFERLINOPATHY | authKW | 1213396 | 5% | 88% | 56 |
5 | MIYOSHI MYOPATHY | authKW | 1190548 | 4% | 96% | 50 |
6 | SARCOGLYCANOPATHY | authKW | 784678 | 3% | 81% | 39 |
7 | LGMD2A | authKW | 699927 | 3% | 91% | 31 |
8 | LGMD2B | authKW | 569560 | 2% | 100% | 23 |
9 | CALPAIN 3 | authKW | 518204 | 3% | 55% | 38 |
10 | CALPAINOPATHY | authKW | 340786 | 1% | 81% | 17 |
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 | 7655 | 35% | 0% | 428 |
2 | Neurosciences | 2685 | 28% | 0% | 351 |
3 | Genetics & Heredity | 1627 | 16% | 0% | 199 |
4 | Cell Biology | 1301 | 18% | 0% | 223 |
5 | Biochemistry & Molecular Biology | 514 | 21% | 0% | 255 |
6 | Pathology | 416 | 6% | 0% | 72 |
7 | Medicine, Research & Experimental | 143 | 5% | 0% | 64 |
8 | Developmental Biology | 75 | 2% | 0% | 24 |
9 | Biophysics | 51 | 3% | 0% | 43 |
10 | Anatomy & Morphology | 50 | 1% | 0% | 13 |
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 | STUDY NEUROL PATIENTS | 123817 | 0% | 100% | 5 |
2 | DIPARTIMENTO BIOMORFOL BIOTECNOL | 117982 | 1% | 53% | 9 |
3 | MEMBRANE INTEGR GRP | 74290 | 0% | 100% | 3 |
4 | NCG DIAGNOST ADVISORY SERV RARE NEUROMUSCULAR D | 74290 | 0% | 100% | 3 |
5 | PEDIAT NEUROL EXCELLENCE MED | 74290 | 0% | 100% | 3 |
6 | ORGAN PATHOPHYSIOL INTERNAL MED | 56599 | 0% | 57% | 4 |
7 | INSERM 129 | 55716 | 0% | 75% | 3 |
8 | MED NACL SIGLO XXI IMSS | 52433 | 0% | 35% | 6 |
9 | MUSCLE IMMUNOANAL UNIT | 52433 | 0% | 35% | 6 |
10 | NEUROLROY J LUCILLE A CARVER MED | 49527 | 0% | 100% | 2 |
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 | 151644 | 10% | 5% | 120 |
2 | MUSCLE & NERVE | 13395 | 5% | 1% | 62 |
3 | SKELETAL MUSCLE | 12812 | 1% | 5% | 10 |
4 | HUMAN MOLECULAR GENETICS | 6037 | 4% | 1% | 49 |
5 | NEUROLOGY INDIA | 3172 | 1% | 1% | 16 |
6 | EUROPEAN JOURNAL OF HUMAN GENETICS | 1501 | 1% | 0% | 15 |
7 | NEUROGENETICS | 1464 | 0% | 1% | 6 |
8 | JOURNAL OF MEDICAL GENETICS | 1208 | 1% | 0% | 17 |
9 | HUMAN MUTATION | 1199 | 1% | 0% | 14 |
10 | EXPERT REVIEWS IN MOLECULAR MEDICINE | 1092 | 0% | 1% | 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 | DYSFERLIN | 3117638 | 12% | 87% | 145 | Search DYSFERLIN | Search DYSFERLIN |
2 | LIMB GIRDLE MUSCULAR DYSTROPHY | 2077938 | 13% | 54% | 156 | Search LIMB+GIRDLE+MUSCULAR+DYSTROPHY | Search LIMB+GIRDLE+MUSCULAR+DYSTROPHY |
3 | SARCOGLYCAN | 1750032 | 9% | 66% | 107 | Search SARCOGLYCAN | Search SARCOGLYCAN |
4 | DYSFERLINOPATHY | 1213396 | 5% | 88% | 56 | Search DYSFERLINOPATHY | Search DYSFERLINOPATHY |
5 | MIYOSHI MYOPATHY | 1190548 | 4% | 96% | 50 | Search MIYOSHI+MYOPATHY | Search MIYOSHI+MYOPATHY |
6 | SARCOGLYCANOPATHY | 784678 | 3% | 81% | 39 | Search SARCOGLYCANOPATHY | Search SARCOGLYCANOPATHY |
7 | LGMD2A | 699927 | 3% | 91% | 31 | Search LGMD2A | Search LGMD2A |
8 | LGMD2B | 569560 | 2% | 100% | 23 | Search LGMD2B | Search LGMD2B |
9 | CALPAIN 3 | 518204 | 3% | 55% | 38 | Search CALPAIN+3 | Search CALPAIN+3 |
10 | CALPAINOPATHY | 340786 | 1% | 81% | 17 | Search CALPAINOPATHY | Search CALPAINOPATHY |
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 | ANGELINI, C , FANIN, M , (2016) PROGRESS AND CHALLENGES IN DIAGNOSIS OF DYSFERLINOPATHY.MUSCLE & NERVE. VOL. 54. ISSUE 5. P. 821 -835 | 129 | 92% | 0 |
2 | ANGELINI, C , FANIN, M , (2016) PATHOGENESIS, CLINICAL FEATURES AND DIAGNOSIS OF SARCOGLYCANOPATHIES.EXPERT OPINION ON ORPHAN DRUGS. VOL. 4. ISSUE 12. P. 1239 -1251 | 128 | 84% | 0 |
3 | FANIN, M , ANGELINI, C , (2015) PROTEIN AND GENETIC DIAGNOSIS OF LIMB GIRDLE MUSCULAR DYSTROPHY TYPE 2A: THE YIELD AND THE PITFALLS.MUSCLE & NERVE. VOL. 52. ISSUE 2. P. 163 -173 | 84 | 88% | 6 |
4 | CARDENAS, AM , GONZALEZ-JAMETT, AM , CEA, LA , BEVILACQUA, JA , CAVIEDES, P , (2016) DYSFERLIN FUNCTION IN SKELETAL MUSCLE: POSSIBLE PATHOLOGICAL MECHANISMS AND THERAPEUTICAL TARGETS IN DYSFERLINOPATHIES.EXPERIMENTAL NEUROLOGY. VOL. 283. ISSUE . P. 246 -254 | 93 | 71% | 0 |
5 | HORNSEY, MA , LAVAL, SH , BARRESI, R , LOCHMULLER, H , BUSHBY, K , (2013) MUSCULAR DYSTROPHY IN DYSFERLIN-DEFICIENT MOUSE MODELS.NEUROMUSCULAR DISORDERS. VOL. 23. ISSUE 5. P. 377-387 | 80 | 66% | 7 |
6 | ANDONI, UJ , GUILLAUME, B , FRANCE, L , KARINE, N , MARTIN, K , NICOLAS, L , (2008) DYSFERLINOPATHIES.NEUROLOGY INDIA. VOL. 56. ISSUE 3. P. 289-297 | 56 | 93% | 5 |
7 | BARTHELEMY, F , WEIN, N , KRAHN, M , LEVY, N , BARTOLI, M , (2011) TRANSLATIONAL RESEARCH AND THERAPEUTIC PERSPECTIVES IN DYSFERLINOPATHIES.MOLECULAR MEDICINE. VOL. 17. ISSUE 9-10. P. 875 -882 | 64 | 70% | 16 |
8 | MAHMOOD, OA , JIANG, XM , (2014) LIMB-GIRDLE MUSCULAR DYSTROPHIES: WHERE NEXT AFTER SIX DECADES FROM THE FIRST PROPOSAL (REVIEW).MOLECULAR MEDICINE REPORTS. VOL. 9. ISSUE 5. P. 1515-1532 | 81 | 52% | 5 |
9 | BLAZEK, AD , PALEO, BJ , WEISLEDER, N , (2015) PLASMA MEMBRANE REPAIR: A CENTRAL PROCESS FOR MAINTAINING CELLULAR HOMEOSTASIS.PHYSIOLOGY. VOL. 30. ISSUE 6. P. 438 -448 | 73 | 55% | 2 |
10 | NALINI, A , POLAVARAPU, K , SUNITHA, B , KULKARNI, S , GAYATHRI, N , BHARATH, MMS , MODI, S , PREETHISH-KUMAR, V , (2015) A PROSPECTIVE STUDY ON THE IMMUNOPHENOTYPIC CHARACTERIZATION OF LIMB GIRDLE MUSCULAR DYSTROPHIES 2 IN INDIA.NEUROLOGY INDIA. VOL. 63. ISSUE 4. P. 548 -560 | 53 | 74% | 1 |
Classes with closest relation at Level 1 |