Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
77 | 4605 | 34.7 | 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 |
271 | 3 | MITOCHONDRIA//MITOCHONDRIAL GENOME//MITOCHONDRIAL DNA PART A | 43930 |
381 | 2 | MITOCHONDRIA//MELAS//MITOCHONDRIAL DISEASE | 17103 |
77 | 1 | MELAS//MITOCHONDRIAL DISEASE//MITOCHONDRIAL ENCEPHALOMYOPATHY | 4605 |
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 | MELAS | authKW | 1578361 | 6% | 81% | 294 |
2 | MITOCHONDRIAL DISEASE | authKW | 1095856 | 9% | 42% | 397 |
3 | MITOCHONDRIAL ENCEPHALOMYOPATHY | authKW | 895418 | 4% | 79% | 172 |
4 | MITOCHONDRIAL MYOPATHY | authKW | 807867 | 5% | 54% | 226 |
5 | KEARNS SAYRE SYNDROME | authKW | 613023 | 2% | 80% | 115 |
6 | LEIGH SYNDROME | authKW | 586681 | 3% | 58% | 152 |
7 | MITOCHONDRIAL DISORDERS | authKW | 423486 | 3% | 46% | 138 |
8 | MELAS SYNDROME | authKW | 368502 | 1% | 86% | 65 |
9 | MERRF | authKW | 331099 | 1% | 78% | 64 |
10 | MITOCHONDRIAL CYTOPATHY | authKW | 315207 | 2% | 67% | 71 |
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 | 30292 | 36% | 0% | 1643 |
2 | Genetics & Heredity | 8990 | 19% | 0% | 888 |
3 | Pediatrics | 5009 | 12% | 0% | 560 |
4 | Neurosciences | 3514 | 18% | 0% | 832 |
5 | Endocrinology & Metabolism | 1713 | 9% | 0% | 395 |
6 | Medicine, Research & Experimental | 1458 | 8% | 0% | 356 |
7 | Pathology | 931 | 5% | 0% | 216 |
8 | Biochemistry & Molecular Biology | 458 | 13% | 0% | 595 |
9 | Biophysics | 405 | 5% | 0% | 208 |
10 | Neuroimaging | 371 | 1% | 0% | 58 |
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 | MITOCHONDRIAL GRP | 232383 | 2% | 31% | 115 |
2 | WELLCOME TRUST MITOCHONDRIAL | 89262 | 1% | 26% | 51 |
3 | H HOUSTON MERRITT CLIN MUSCULAR DYSTROPHY | 82958 | 1% | 48% | 26 |
4 | NIJMEGEN MITOCHONDRIAL DISORDERS | 47526 | 1% | 16% | 45 |
5 | NEUROL NEUROBIOL PSYCHIAT | 41510 | 1% | 15% | 41 |
6 | MENTAL RETARDAT BIRTH DEFECT | 39838 | 1% | 14% | 42 |
7 | UNIT MOL NEUROGENET | 38196 | 1% | 19% | 30 |
8 | NEUROPEDIAT MUSCLE DISORDERS UNIT | 33145 | 0% | 100% | 5 |
9 | PEDIAT NEUROL METAB | 29909 | 0% | 27% | 17 |
10 | INVEST BIOQUIM BIOL MOL | 26263 | 0% | 18% | 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 | MITOCHONDRION | 89672 | 3% | 11% | 120 |
2 | JOURNAL OF INHERITED METABOLIC DISEASE | 45172 | 4% | 4% | 176 |
3 | NEUROMUSCULAR DISORDERS | 35202 | 2% | 5% | 112 |
4 | JOURNAL OF THE NEUROLOGICAL SCIENCES | 13059 | 3% | 1% | 142 |
5 | ANNALS OF NEUROLOGY | 10715 | 2% | 1% | 113 |
6 | PEDIATRIC NEUROLOGY | 9656 | 2% | 2% | 79 |
7 | JOURNAL OF CHILD NEUROLOGY | 8627 | 2% | 2% | 80 |
8 | NEUROLOGY | 7393 | 3% | 1% | 156 |
9 | NEUROPEDIATRICS | 7136 | 1% | 2% | 47 |
10 | BRAIN & DEVELOPMENT | 5237 | 1% | 1% | 54 |
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 | MELAS | 1578361 | 6% | 81% | 294 | Search MELAS | Search MELAS |
2 | MITOCHONDRIAL DISEASE | 1095856 | 9% | 42% | 397 | Search MITOCHONDRIAL+DISEASE | Search MITOCHONDRIAL+DISEASE |
3 | MITOCHONDRIAL ENCEPHALOMYOPATHY | 895418 | 4% | 79% | 172 | Search MITOCHONDRIAL+ENCEPHALOMYOPATHY | Search MITOCHONDRIAL+ENCEPHALOMYOPATHY |
4 | MITOCHONDRIAL MYOPATHY | 807867 | 5% | 54% | 226 | Search MITOCHONDRIAL+MYOPATHY | Search MITOCHONDRIAL+MYOPATHY |
5 | KEARNS SAYRE SYNDROME | 613023 | 2% | 80% | 115 | Search KEARNS+SAYRE+SYNDROME | Search KEARNS+SAYRE+SYNDROME |
6 | LEIGH SYNDROME | 586681 | 3% | 58% | 152 | Search LEIGH+SYNDROME | Search LEIGH+SYNDROME |
7 | MITOCHONDRIAL DISORDERS | 423486 | 3% | 46% | 138 | Search MITOCHONDRIAL+DISORDERS | Search MITOCHONDRIAL+DISORDERS |
8 | MELAS SYNDROME | 368502 | 1% | 86% | 65 | Search MELAS+SYNDROME | Search MELAS+SYNDROME |
9 | MERRF | 331099 | 1% | 78% | 64 | Search MERRF | Search MERRF |
10 | MITOCHONDRIAL CYTOPATHY | 315207 | 2% | 67% | 71 | Search MITOCHONDRIAL+CYTOPATHY | Search MITOCHONDRIAL+CYTOPATHY |
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 | ZIFA, E , GIANNOULI, S , THEOTOKIS, P , STAMATIS, O , MAMURIS, Z , STATHOPOULOS, C , (2007) MITOCHONDRIAL TRNA MUTATIONS - CLINICAL AND FUNCTIONAL PERTURBATIONS.RNA BIOLOGY. VOL. 4. ISSUE 1. P. 38-66 | 224 | 78% | 29 |
2 | MURPHY, R , TURNBULL, DM , WALKER, M , HATTERSLEY, AT , (2008) CLINICAL FEATURES, DIAGNOSIS AND MANAGEMENT OF MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD) ASSOCIATED WITH THE 3243A > G MITOCHONDRIAL POINT MUTATION.DIABETIC MEDICINE. VOL. 25. ISSUE 4. P. 383 -399 | 168 | 87% | 62 |
3 | SCAGLIA, F , WONG, LJC , (2008) HUMAN MITOCHONDRIAL TRANSFER RNAS: ROLE OF PATHOGENIC MUTATION IN DISEASE.MUSCLE & NERVE. VOL. 37. ISSUE 2. P. 150-171 | 160 | 84% | 41 |
4 | SHOFFNER, JM , (2001) AN INTRODUCTION: OXIDATIVE PHOSPHORYLATION DISEASES.SEMINARS IN NEUROLOGY. VOL. 21. ISSUE 3. P. 237 -250 | 186 | 82% | 4 |
5 | FINSTERER, J , (2007) GENETIC, PATHOGENETIC, AND PHENOTYPIC IMPLICATIONS OF THE MITOCHONDRIAL A3243G TRNALEU(UUR) MUTATION.ACTA NEUROLOGICA SCANDINAVICA. VOL. 116. ISSUE 1. P. 1 -14 | 128 | 86% | 50 |
6 | MORGAN-HUGHES, JA , HANNA, MG , (1999) MITOCHONDRIAL ENCEPHALOMYOPATHIES: THE ENIGMA OF GENOTYPE VERSUS PHENOTYPE.BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS. VOL. 1410. ISSUE 2. P. 125 -145 | 156 | 85% | 33 |
7 | PULKES, T , HANNA, MG , (2001) HUMAN MITOCHONDRIAL DNA DISEASES.ADVANCED DRUG DELIVERY REVIEWS. VOL. 49. ISSUE 1-2. P. 27 -43 | 133 | 87% | 43 |
8 | FINSTERER, J , (2006) CENTRAL NERVOUS SYSTEM MANIFESTATIONS OF MITOCHONDRIAL DISORDERS.ACTA NEUROLOGICA SCANDINAVICA. VOL. 114. ISSUE 4. P. 217-238 | 140 | 65% | 75 |
9 | NARDIN, RA , JOHNS, DR , (2001) MITOCHONDRIAL DYSFUNCTION AND NEUROMUSCULAR DISEASE.MUSCLE & NERVE. VOL. 24. ISSUE 2. P. 170 -191 | 148 | 76% | 49 |
10 | SCHON, EA , BONILLA, E , DIMAURO, S , (1997) MITOCHONDRIAL DNA MUTATIONS AND PATHOGENESIS.JOURNAL OF BIOENERGETICS AND BIOMEMBRANES. VOL. 29. ISSUE 2. P. 131-149 | 125 | 77% | 284 |
Classes with closest relation at Level 1 |