Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
201 | 20439 | 42.4 | 79% |
Classes in level above (level 3) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
237 | 43811 | MITOCHONDRIA//MELAS//MITOCHONDRIAL DISEASE |
Classes in level below (level 1) |
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 | 459 | 81% | 1% | 278 |
2 | MITOCHONDRIAL DNA | Journal | 390 | 59% | 2% | 441 |
3 | LEBERS HEREDITARY OPTIC NEUROPATHY | Author keyword | 389 | 90% | 1% | 172 |
4 | MITOCHONDRIAL GENOME | Author keyword | 370 | 50% | 3% | 528 |
5 | MITOCHONDRIAL DISEASE | Author keyword | 362 | 63% | 2% | 360 |
6 | LHON | Author keyword | 292 | 93% | 1% | 109 |
7 | LEIGH SYNDROME | Author keyword | 292 | 81% | 1% | 177 |
8 | MITOCHONDRIAL ENCEPHALOMYOPATHY | Author keyword | 260 | 86% | 1% | 133 |
9 | COMPLEX I | Author keyword | 248 | 48% | 2% | 374 |
10 | KEARNS SAYRE SYNDROME | Author keyword | 214 | 84% | 1% | 118 |
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 | 459 | 81% | 1% | 278 | Search MELAS | Search MELAS |
2 | LEBERS HEREDITARY OPTIC NEUROPATHY | 389 | 90% | 1% | 172 | Search LEBERS+HEREDITARY+OPTIC+NEUROPATHY | Search LEBERS+HEREDITARY+OPTIC+NEUROPATHY |
3 | MITOCHONDRIAL DNA | 380 | 22% | 8% | 1551 | Search MITOCHONDRIAL+DNA | Search MITOCHONDRIAL+DNA |
4 | MITOCHONDRIAL GENOME | 370 | 50% | 3% | 528 | Search MITOCHONDRIAL+GENOME | Search MITOCHONDRIAL+GENOME |
5 | MITOCHONDRIAL DISEASE | 362 | 63% | 2% | 360 | Search MITOCHONDRIAL+DISEASE | Search MITOCHONDRIAL+DISEASE |
6 | LHON | 292 | 93% | 1% | 109 | Search LHON | Search LHON |
7 | LEIGH SYNDROME | 292 | 81% | 1% | 177 | Search LEIGH+SYNDROME | Search LEIGH+SYNDROME |
8 | MITOCHONDRIAL ENCEPHALOMYOPATHY | 260 | 86% | 1% | 133 | Search MITOCHONDRIAL+ENCEPHALOMYOPATHY | Search MITOCHONDRIAL+ENCEPHALOMYOPATHY |
9 | COMPLEX I | 248 | 48% | 2% | 374 | Search COMPLEX+I | Search COMPLEX+I |
10 | KEARNS SAYRE SYNDROME | 214 | 84% | 1% | 118 | Search KEARNS+SAYRE+SYNDROME | Search KEARNS+SAYRE+SYNDROME |
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 | KEARNS SAYRE SYNDROME | 1207 | 82% | 3% | 697 |
2 | STROKE LIKE EPISODES | 867 | 83% | 2% | 492 |
3 | HEREDITARY OPTIC NEUROPATHY | 860 | 67% | 4% | 767 |
4 | LEIGH SYNDROME | 573 | 76% | 2% | 403 |
5 | DNA MUTATIONS | 562 | 72% | 2% | 441 |
6 | MELAS | 505 | 74% | 2% | 372 |
7 | RAGGED RED FIBERS | 492 | 83% | 1% | 278 |
8 | MTDNA MUTATION | 478 | 92% | 1% | 191 |
9 | ENCEPHALOMYOPATHIES | 466 | 88% | 1% | 224 |
10 | TRANSFER RNALEUUUR GENE | 460 | 85% | 1% | 241 |
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 | MITOCHONDRIAL DNA | 390 | 59% | 2% | 441 |
2 | MITOCHONDRION | 160 | 37% | 2% | 351 |
3 | CURRENT GENETICS | 46 | 11% | 2% | 393 |
4 | SOMATIC CELL GENETICS | 3 | 11% | 0% | 26 |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Disturbed mitochondrial dynamics and neurodegenerative disorders | 2015 | 11 | 201 | 64% |
Mitochondrial diseases in man and mouse | 1999 | 1822 | 84 | 67% |
Mitochondrial fusion and fission in cell life and death | 2010 | 355 | 129 | 83% |
Mitochondrial form and function | 2014 | 56 | 124 | 60% |
Mitochondrial Fission, Fusion, and Stress | 2012 | 312 | 42 | 50% |
Mitochondria: Dynamic organelles in disease, aging, and development | 2006 | 653 | 82 | 90% |
Fusion and Fission: Interlinked Processes Critical for Mitochondrial Health | 2012 | 156 | 135 | 81% |
Mitochondria: In Sickness and in Health | 2012 | 284 | 226 | 43% |
Functions and dysfunctions of mitochondrial dynamics | 2007 | 414 | 101 | 88% |
Insect Mitochondrial Genomics: Implications for Evolution and Phylogeny | 2014 | 35 | 129 | 68% |
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 | NIJMEGEN MITOCHONDRIAL DISORDERS | 205 | 69% | 0.9% | 176 |
2 | MITOCHONDRIAL GRP | 190 | 59% | 1.1% | 215 |
3 | WELLCOME TRUST MITOCHONDRIAL | 59 | 58% | 0.3% | 69 |
4 | ZENTRUM BIOL CHEM | 49 | 60% | 0.3% | 53 |
5 | UNIT MOL NEUROGENET | 36 | 45% | 0.3% | 60 |
6 | MOL DESIGN PHARMACEUT | 32 | 48% | 0.2% | 49 |
7 | MOL MITOCHONDRIAL MED GENET | 27 | 47% | 0.2% | 43 |
8 | MITOCHONDRIAL BIOL UNIT | 18 | 29% | 0.3% | 54 |
9 | H HOUSTON MERRITT CLIN MUSCULAR DYSTROPHY | 16 | 48% | 0.1% | 25 |
10 | MICROSCOP IMAGING | 16 | 58% | 0.1% | 18 |
Related classes at same level (level 2) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000013386 | HELSINKI BIOENERGET GRP//CYTOCHROME BC1 COMPLEX//CYTOCHROME C OXIDASE |
2 | 0.0000012079 | PERMEABILITY TRANSITION//BARTH SYNDROME//UNCOUPLING PROTEIN |
3 | 0.0000009515 | PROTEIN TRANSLOCATION//PROTEIN IMPORT//SECA |
4 | 0.0000009125 | Y CHROMOSOME//HUMAN BIOLOGY//Y STR |
5 | 0.0000008691 | PLASTID TRANSFORMATION//CYTOPLASMIC MALE STERILITY//MOLECULAR FARMING |
6 | 0.0000008626 | COENZYME Q10//UBIQUINONE//COENZYME Q |
7 | 0.0000008207 | IRISIN//FGF 21//FIBROBLAST GROWTH FACTOR 21 |
8 | 0.0000007776 | DEOXYCYTIDINE KINASE//PURINE NUCLEOSIDE PHOSPHORYLASE//NUCLEOSIDE TRANSPORT |
9 | 0.0000007223 | GJB2//CONNEXIN 26//USHER SYNDROME |
10 | 0.0000006056 | F 1 ATPASE//ATP SYNTHASE//V ATPASE |