Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
82 | 4404 | 34.0 | 80% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
201 | 20439 | MELAS//MITOCHONDRIAL DNA//LEBERS HEREDITARY OPTIC NEUROPATHY |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | MELAS | Author keyword | 405 | 78% | 6% | 268 |
2 | MITOCHONDRIAL ENCEPHALOMYOPATHY | Author keyword | 189 | 79% | 3% | 122 |
3 | KEARNS SAYRE SYNDROME | Author keyword | 177 | 79% | 3% | 112 |
4 | MITOCHONDRIAL MYOPATHY | Author keyword | 149 | 54% | 4% | 190 |
5 | PEARSON SYNDROME | Author keyword | 126 | 95% | 1% | 41 |
6 | MITOCHONDRIAL DISEASE | Author keyword | 125 | 41% | 5% | 235 |
7 | LEIGH SYNDROME | Author keyword | 119 | 60% | 3% | 131 |
8 | MERRF | Author keyword | 106 | 81% | 1% | 64 |
9 | MELAS SYNDROME | Author keyword | 101 | 81% | 1% | 62 |
10 | MITOCHONDRIAL ENCEPHALOMYOPATHIES | Author keyword | 74 | 79% | 1% | 48 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | MELAS | 405 | 78% | 6% | 268 | Search MELAS | Search MELAS |
2 | MITOCHONDRIAL ENCEPHALOMYOPATHY | 189 | 79% | 3% | 122 | Search MITOCHONDRIAL+ENCEPHALOMYOPATHY | Search MITOCHONDRIAL+ENCEPHALOMYOPATHY |
3 | KEARNS SAYRE SYNDROME | 177 | 79% | 3% | 112 | Search KEARNS+SAYRE+SYNDROME | Search KEARNS+SAYRE+SYNDROME |
4 | MITOCHONDRIAL MYOPATHY | 149 | 54% | 4% | 190 | Search MITOCHONDRIAL+MYOPATHY | Search MITOCHONDRIAL+MYOPATHY |
5 | PEARSON SYNDROME | 126 | 95% | 1% | 41 | Search PEARSON+SYNDROME | Search PEARSON+SYNDROME |
6 | MITOCHONDRIAL DISEASE | 125 | 41% | 5% | 235 | Search MITOCHONDRIAL+DISEASE | Search MITOCHONDRIAL+DISEASE |
7 | LEIGH SYNDROME | 119 | 60% | 3% | 131 | Search LEIGH+SYNDROME | Search LEIGH+SYNDROME |
8 | MERRF | 106 | 81% | 1% | 64 | Search MERRF | Search MERRF |
9 | MELAS SYNDROME | 101 | 81% | 1% | 62 | Search MELAS+SYNDROME | Search MELAS+SYNDROME |
10 | MITOCHONDRIAL ENCEPHALOMYOPATHIES | 74 | 79% | 1% | 48 | Search MITOCHONDRIAL+ENCEPHALOMYOPATHIES | Search MITOCHONDRIAL+ENCEPHALOMYOPATHIES |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | STROKE LIKE EPISODES | 726 | 79% | 11% | 468 |
2 | KEARNS SAYRE SYNDROME | 714 | 70% | 13% | 593 |
3 | MELAS | 416 | 70% | 8% | 349 |
4 | RAGGED RED FIBERS | 410 | 79% | 6% | 264 |
5 | ENCEPHALOMYOPATHIES | 380 | 83% | 5% | 213 |
6 | TRANSFER RNALEUUUR GENE | 336 | 78% | 5% | 221 |
7 | ENCEPHALOMYOPATHY | 293 | 68% | 6% | 258 |
8 | LACTIC ACIDOSIS | 269 | 30% | 17% | 760 |
9 | MTDNA MUTATION | 230 | 76% | 4% | 159 |
10 | PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA | 178 | 44% | 7% | 304 |
Journals |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | MITOCHONDRION | 11 | 11% | 2% | 101 |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Mitochondrial diseases in man and mouse | 1999 | 1822 | 84 | 36% |
Mitochondrial DNA mutations in human disease | 2005 | 539 | 158 | 42% |
Mechanisms of disease: Mitochondrial respiratory-chain diseases | 2003 | 704 | 70 | 36% |
Human mitochondrial DNA: roles of inherited and somatic mutations | 2012 | 112 | 126 | 29% |
Systematic review of cardiac electrical disease in Kearns-Sayre syndrome and mitochondrial cytopathy | 2015 | 1 | 37 | 59% |
Mitochondrial DNA mutations and pathogenesis | 1997 | 273 | 162 | 77% |
Mitochondrial DNA and disease | 2012 | 71 | 98 | 40% |
Mitochondrial DNA mutations and human disease | 2010 | 102 | 238 | 49% |
Concise Reviews: Assisted Reproductive Technologies to Prevent Transmission of Mitochondrial DNA Disease | 2015 | 1 | 44 | 48% |
Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks | 2015 | 1 | 71 | 46% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | MITOCHONDRIAL GRP | 42 | 31% | 2.6% | 114 |
2 | H HOUSTON MERRITT CLIN MUSCULAR DYSTROPHY | 16 | 48% | 0.6% | 25 |
3 | WELLCOME TRUST MITOCHONDRIAL | 9 | 26% | 0.7% | 31 |
4 | NEUROL NEUROBIOL PSYCHIAT | 7 | 16% | 1.0% | 42 |
5 | NIJMEGEN MITOCHONDRIAL DISORDERS | 7 | 16% | 0.9% | 40 |
6 | ST VINCENTS MELBOURNE NEUROMUSCULAR DIAGNOST | 6 | 80% | 0.1% | 4 |
7 | UNIT GENET EPIDEMIOL MOL | 6 | 80% | 0.1% | 4 |
8 | UNIT MOL NEUROGENET | 6 | 20% | 0.6% | 27 |
9 | MENTAL RETARDAT BIRTH DEFECT | 6 | 14% | 0.9% | 39 |
10 | NEUROPEDIAT MUSCLE DISORDERS UNIT | 6 | 100% | 0.1% | 4 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000146017 | POLG//MNGIE//DEOXYRIBONUCLEOSIDE KINASE |
2 | 0.0000128142 | 4977 BP DELETION//MTDNA MUTATOR MICE//COMMON DELETION |
3 | 0.0000128138 | LEBERS HEREDITARY OPTIC NEUROPATHY//LHON//LEBER HEREDITARY OPTIC NEUROPATHY |
4 | 0.0000103124 | PONTOSUBICULAR NECROSIS//INFANTILE BILATERAL STRIATAL NECROSIS//BRAINSTEM NECROSIS |
5 | 0.0000094205 | D310//MITOCHONDRIAL MICROSATELLITE INSTABILITY//MITOCHONDRIAL HAPLOGROUPS |
6 | 0.0000092867 | DAP3//ICT1//MITOCHONDRIAL RIBOSOMAL PROTEINS |
7 | 0.0000091251 | DOUBLY UNIPARENTAL INHERITANCE//PATERNAL LEAKAGE//MITOCHONDRIAL POLARITY |
8 | 0.0000088657 | YIDC//OXA1//COX17 |
9 | 0.0000081155 | COMPLEX I//NADH UBIQUINONE OXIDOREDUCTASE//NADH UBIQUINONE OXIDOREDUCTASE |
10 | 0.0000075033 | BLUE NATIVE ELECTROPHORESIS//TMEM70//BCS1L |