Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
20822 | 444 | 28.9 | 61% |
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 |
584 | 3 | POMPE DISEASE//PIN1//CYCLOPHILIN | 15652 |
1662 | 2 | POMPE DISEASE//GLYCOGEN STORAGE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II | 6857 |
20822 | 1 | MCARDLES DISEASE//MYOPHOSPHORYLASE//GLYCOGENOSIS TYPE V | 444 |
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 | MCARDLES DISEASE | authKW | 6333956 | 25% | 84% | 109 |
2 | MYOPHOSPHORYLASE | authKW | 2296319 | 8% | 90% | 37 |
3 | GLYCOGENOSIS TYPE V | authKW | 1650537 | 5% | 100% | 24 |
4 | MYOPHOSPHORYLASE DEFICIENCY | authKW | 1299299 | 5% | 82% | 23 |
5 | PYGM | authKW | 898624 | 3% | 93% | 14 |
6 | GLYCOGEN STORAGE DISEASE TYPE V | authKW | 774832 | 3% | 87% | 13 |
7 | MYOPHOSPHORYLASE GENE | authKW | 412634 | 1% | 100% | 6 |
8 | PATOL MITOCONDRIAL NEUROMUSCULAR | address | 298999 | 2% | 43% | 10 |
9 | GLYCOGEN STORAGE DISEASE V | authKW | 275090 | 1% | 100% | 4 |
10 | MCARDLE | authKW | 275090 | 1% | 100% | 4 |
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 | 5742 | 49% | 0% | 219 |
2 | Neurosciences | 1272 | 32% | 0% | 143 |
3 | Sport Sciences | 374 | 7% | 0% | 32 |
4 | Medicine, General & Internal | 262 | 13% | 0% | 56 |
5 | Genetics & Heredity | 152 | 9% | 0% | 40 |
6 | CYTOLOGY & HISTOLOGY | 77 | 1% | 0% | 3 |
7 | Medicine, Research & Experimental | 71 | 6% | 0% | 26 |
8 | Physiology | 66 | 5% | 0% | 23 |
9 | Endocrinology & Metabolism | 31 | 5% | 0% | 20 |
10 | Pediatrics | 29 | 4% | 0% | 17 |
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 | PATOL MITOCONDRIAL NEUROMUSCULAR | 298999 | 2% | 43% | 10 |
2 | MITOCHONDRIAL PATHOL NEUROMUSCULAR DISORDERS LA | 206317 | 1% | 100% | 3 |
3 | INVEST BIOQUIM BIOL MOL CIBBIM | 157191 | 1% | 57% | 4 |
4 | NEUROMUSCULAR MITOCHONDRIAL PATHOL | 137545 | 0% | 100% | 2 |
5 | H HOUSTON MERRITT CLIN MUSCULAR DYSTROPHY | 127340 | 2% | 19% | 10 |
6 | ENFERMEDADES MITOCONDRIALES NEUROMUSCULA | 123788 | 1% | 60% | 3 |
7 | INVEST BIOQUIM BIOL MOL | 95243 | 3% | 11% | 13 |
8 | MEDEA SCI | 91695 | 0% | 67% | 2 |
9 | NEUROMUSCULAR UNITSECT 3342 | 91695 | 0% | 67% | 2 |
10 | TRANSLAT NEUROMUSCULAR DIS | 91695 | 0% | 67% | 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 | 35811 | 8% | 1% | 35 |
2 | MUSCLE & NERVE | 17144 | 9% | 1% | 42 |
3 | NEUROLOGY | 3951 | 8% | 0% | 35 |
4 | EXERCISE AND SPORT SCIENCES REVIEWS/SERIES | 2454 | 0% | 4% | 1 |
5 | EUROPEAN JOURNAL OF BASIC AND APPLIED HISTOCHEMISTRY | 2370 | 0% | 3% | 1 |
6 | NEUROLOGIC CLINICS | 1912 | 2% | 0% | 7 |
7 | MOLECULAR GENETICS AND METABOLISM | 1398 | 2% | 0% | 8 |
8 | JOURNAL OF THE NEUROLOGICAL SCIENCES | 1317 | 3% | 0% | 14 |
9 | ARCHIVES OF NEUROLOGY | 1029 | 2% | 0% | 10 |
10 | TRANSACTIONS OF THE AMERICAN NEUROLOGICAL ASSOCIATION | 927 | 0% | 1% | 1 |
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 | MCARDLES DISEASE | 6333956 | 25% | 84% | 109 | Search MCARDLES+DISEASE | Search MCARDLES+DISEASE |
2 | MYOPHOSPHORYLASE | 2296319 | 8% | 90% | 37 | Search MYOPHOSPHORYLASE | Search MYOPHOSPHORYLASE |
3 | GLYCOGENOSIS TYPE V | 1650537 | 5% | 100% | 24 | Search GLYCOGENOSIS+TYPE+V | Search GLYCOGENOSIS+TYPE+V |
4 | MYOPHOSPHORYLASE DEFICIENCY | 1299299 | 5% | 82% | 23 | Search MYOPHOSPHORYLASE+DEFICIENCY | Search MYOPHOSPHORYLASE+DEFICIENCY |
5 | PYGM | 898624 | 3% | 93% | 14 | Search PYGM | Search PYGM |
6 | GLYCOGEN STORAGE DISEASE TYPE V | 774832 | 3% | 87% | 13 | Search GLYCOGEN+STORAGE+DISEASE+TYPE+V | Search GLYCOGEN+STORAGE+DISEASE+TYPE+V |
7 | MYOPHOSPHORYLASE GENE | 412634 | 1% | 100% | 6 | Search MYOPHOSPHORYLASE+GENE | Search MYOPHOSPHORYLASE+GENE |
8 | GLYCOGEN STORAGE DISEASE V | 275090 | 1% | 100% | 4 | Search GLYCOGEN+STORAGE+DISEASE+V | Search GLYCOGEN+STORAGE+DISEASE+V |
9 | MCARDLE | 275090 | 1% | 100% | 4 | Search MCARDLE | Search MCARDLE |
10 | MUSCLE PHOSPHORYLASE | 275090 | 1% | 100% | 4 | Search MUSCLE+PHOSPHORYLASE | Search MUSCLE+PHOSPHORYLASE |
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 | NOGALES-GADEA, G , BRULL, A , SANTALLA, A , ANDREU, AL , ARENAS, J , MARTIN, MA , LUCIA, A , DE LUNA, N , PINOS, T , (2015) MCARDLE DISEASE: UPDATE OF REPORTED MUTATIONS AND POLYMORPHISMS IN THE PYGM GENE.HUMAN MUTATION. VOL. 36. ISSUE 7. P. 669 -678 | 76 | 82% | 3 |
2 | MIGOCKA-PATRZALEK, M , KOSIERADZKA, A , LEWANDOWSKI, D , POSYNIAK, E , DUBINSKA-MAGIERA, M , DACZEWSKA, M , (2015) MCARDLE DISEASE: PATHOGENESIS AND THERAPY PERSPECTIVES.POSTEPY BIOLOGII KOMORKI. VOL. 42. ISSUE 3. P. 431 -443 | 59 | 91% | 0 |
3 | NOGALES-GADEA, G , SANTALLA, A , BRULL, A , DE LUNA, N , LUCIA, A , PINOS, T , (2015) THE PATHOGENOMICS OF MCARDLE DISEASE-GENES, ENZYMES, MODELS, AND THERAPEUTIC IMPLICATIONS.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 38. ISSUE 2. P. 221 -230 | 52 | 78% | 2 |
4 | LUCIA, A , NOGALES-GADEA, G , PEREZ, M , MARTIN, MA , ANDREU, AL , ARENAS, J , (2008) MCARDLE DISEASE: WHAT DO NEUROLOGISTS NEED TO KNOW?.NATURE CLINICAL PRACTICE NEUROLOGY. VOL. 4. ISSUE 10. P. 568-577 | 46 | 90% | 35 |
5 | NOGALES-GADEA, G , ARENAS, J , ANDREU, AL , (2007) MOLECULAR GENETICS OF MCARDLE'S DISEASE.CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS. VOL. 7. ISSUE 1. P. 84-92 | 48 | 92% | 8 |
6 | SANTALLA, A , NOGALES-GADEA, G , ORTENBLAD, N , BRULL, A , DE LUNA, N , PINOS, T , LUCIA, A , (2014) MCARDLE DISEASE: A UNIQUE STUDY MODEL IN SPORTS MEDICINE.SPORTS MEDICINE. VOL. 44. ISSUE 11. P. 1531 -1544 | 58 | 51% | 0 |
7 | NOGALES-GADEA, G , SANTALLA, A , BALLESTER-LOPEZ, A , ARENAS, J , MARTIN, MA , GODFREY, R , PINOS, T , PINTOS-MORELL, G , COLL-CANTI, J , LUCIA, A , (2016) EXERCISE AND PREEXERCISE NUTRITION AS TREATMENT FOR MCARDLE DISEASE.MEDICINE AND SCIENCE IN SPORTS AND EXERCISE. VOL. 48. ISSUE 4. P. 673 -679 | 30 | 83% | 1 |
8 | QUINLIVAN, R , MARTINUZZI, A , SCHOSER, B , (2014) PHARMACOLOGICAL AND NUTRITIONAL TREATMENT FOR MCARDLE DISEASE (GLYCOGEN STORAGE DISEASE TYPE V).COCHRANE DATABASE OF SYSTEMATIC REVIEWS. VOL. . ISSUE 11. P. - | 32 | 84% | 1 |
9 | RUBIO, JC , GARCIA-CONSUEGRA, I , NOGALES-GADEA, G , BLAZQUEZ, A , CABELLO, A , LUCIA, A , ANDREU, AL , ARENAS, J , MARTIN, MA , (2007) A PROPOSED MOLECULAR DIAGNOSTIC FLOWCHART FOR MYOPHOSPHORYLASE DEFICIENCY (MCARDLE DISEASE) IN BLOOD SAMPLES FROM SPANISH PATIENTS.HUMAN MUTATION. VOL. 28. ISSUE 2. P. - | 26 | 96% | 13 |
10 | VIEITEZ, I , TEIJEIRA, S , FERNANDEZ, JM , SAN MILLAN, B , MIRANDA, S , ORTOLANO, S , LOUIS, S , LAFORET, P , NAVARRO, C , (2011) MOLECULAR AND CLINICAL STUDY OF MCARDLE'S DISEASE IN A COHORT OF 123 EUROPEAN PATIENTS. IDENTIFICATION OF 20 NOVEL MUTATIONS.NEUROMUSCULAR DISORDERS. VOL. 21. ISSUE 12. P. 817-823 | 23 | 92% | 12 |
Classes with closest relation at Level 1 |