Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
8598 | 1237 | 33.5 | 84% |
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 |
236 | 3 | ADENOSINE//NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS//ADENOSINE RECEPTORS | 48331 |
2341 | 2 | RIBONUCLEOTIDE REDUCTASE//POLG//HYDROXYUREA | 4410 |
8598 | 1 | POLG//MNGIE//DEOXYRIBONUCLEOSIDE KINASE | 1237 |
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 | POLG | authKW | 1020461 | 5% | 66% | 63 |
2 | MNGIE | authKW | 657313 | 3% | 76% | 35 |
3 | DEOXYRIBONUCLEOSIDE KINASE | authKW | 568703 | 2% | 96% | 24 |
4 | MITOCHONDRIAL DNA DEPLETION | authKW | 559984 | 3% | 69% | 33 |
5 | MITOCHONDRIAL DNA DEPLETION SYNDROME | authKW | 483605 | 2% | 85% | 23 |
6 | ALPERS SYNDROME | authKW | 467476 | 2% | 76% | 25 |
7 | MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY | authKW | 399867 | 1% | 90% | 18 |
8 | MTDNA DEPLETION | authKW | 382562 | 3% | 50% | 31 |
9 | DNA POLYMERASE GAMMA | authKW | 358276 | 2% | 48% | 30 |
10 | POLYMERASE GAMMA | authKW | 323106 | 2% | 55% | 24 |
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 | 2849 | 22% | 0% | 270 |
2 | Biochemistry & Molecular Biology | 2498 | 39% | 0% | 481 |
3 | Genetics & Heredity | 2359 | 19% | 0% | 236 |
4 | Biophysics | 276 | 6% | 0% | 80 |
5 | Neurosciences | 266 | 11% | 0% | 136 |
6 | Pediatrics | 252 | 6% | 0% | 73 |
7 | Medicine, Research & Experimental | 245 | 6% | 0% | 79 |
8 | Cell Biology | 199 | 8% | 0% | 105 |
9 | Endocrinology & Metabolism | 83 | 4% | 0% | 55 |
10 | Gastroenterology & Hepatology | 54 | 3% | 0% | 35 |
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 | SECT VET MED BIOCHEM | 274727 | 1% | 70% | 16 |
2 | VET MED CHEM | 170605 | 3% | 22% | 31 |
3 | EXPT TECHNOL MED | 143608 | 1% | 73% | 8 |
4 | UNIT MOL NEUROGENET | 83663 | 2% | 15% | 23 |
5 | LUND PROT PROD PLATFORM | 74050 | 0% | 100% | 3 |
6 | PIERFRANCO LUISA MARIANI STUDY CHILDRENS MI | 72584 | 1% | 29% | 10 |
7 | MITOCHONDRIAL GRP | 66986 | 3% | 8% | 32 |
8 | MITOCHONDRIAL DNA REPLICAT GRP | 55536 | 0% | 75% | 3 |
9 | PATOL MITOCONDRIAL | 55536 | 0% | 75% | 3 |
10 | GRP NEUROMUSCULAR MITOCHONDRIAL DIS | 49367 | 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 | NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS | 16543 | 5% | 1% | 56 |
2 | MITOCHONDRION | 15661 | 2% | 2% | 26 |
3 | NEUROMUSCULAR DISORDERS | 8187 | 2% | 1% | 28 |
4 | MOLECULAR GENETICS AND METABOLISM | 4520 | 2% | 1% | 24 |
5 | HUMAN MOLECULAR GENETICS | 2876 | 3% | 0% | 34 |
6 | ARCHIVES OF NEUROLOGY | 1778 | 2% | 0% | 22 |
7 | BRAIN | 1691 | 2% | 0% | 21 |
8 | NEUROLOGY | 1218 | 3% | 0% | 33 |
9 | JOURNAL OF INHERITED METABOLIC DISEASE | 1201 | 1% | 0% | 15 |
10 | JOURNAL OF BIOLOGICAL CHEMISTRY | 1115 | 7% | 0% | 87 |
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 | POLG | 1020461 | 5% | 66% | 63 | Search POLG | Search POLG |
2 | MNGIE | 657313 | 3% | 76% | 35 | Search MNGIE | Search MNGIE |
3 | DEOXYRIBONUCLEOSIDE KINASE | 568703 | 2% | 96% | 24 | Search DEOXYRIBONUCLEOSIDE+KINASE | Search DEOXYRIBONUCLEOSIDE+KINASE |
4 | MITOCHONDRIAL DNA DEPLETION | 559984 | 3% | 69% | 33 | Search MITOCHONDRIAL+DNA+DEPLETION | Search MITOCHONDRIAL+DNA+DEPLETION |
5 | MITOCHONDRIAL DNA DEPLETION SYNDROME | 483605 | 2% | 85% | 23 | Search MITOCHONDRIAL+DNA+DEPLETION+SYNDROME | Search MITOCHONDRIAL+DNA+DEPLETION+SYNDROME |
6 | ALPERS SYNDROME | 467476 | 2% | 76% | 25 | Search ALPERS+SYNDROME | Search ALPERS+SYNDROME |
7 | MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY | 399867 | 1% | 90% | 18 | Search MITOCHONDRIAL+NEUROGASTROINTESTINAL+ENCEPHALOMYOPATHY | Search MITOCHONDRIAL+NEUROGASTROINTESTINAL+ENCEPHALOMYOPATHY |
8 | MTDNA DEPLETION | 382562 | 3% | 50% | 31 | Search MTDNA+DEPLETION | Search MTDNA+DEPLETION |
9 | DNA POLYMERASE GAMMA | 358276 | 2% | 48% | 30 | Search DNA+POLYMERASE+GAMMA | Search DNA+POLYMERASE+GAMMA |
10 | POLYMERASE GAMMA | 323106 | 2% | 55% | 24 | Search POLYMERASE+GAMMA | Search POLYMERASE+GAMMA |
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 | EL-HATTAB, A , SCAGLIA, F , (2013) MITOCHONDRIAL DNA DEPLETION SYNDROMES: REVIEW AND UPDATES OF GENETIC BASIS, MANIFESTATIONS, AND THERAPEUTIC OPTIONS.NEUROTHERAPEUTICS. VOL. 10. ISSUE 2. P. 186-198 | 102 | 84% | 46 |
2 | COPELAND, WC , (2012) DEFECTS IN MITOCHONDRIAL DNA REPLICATION AND HUMAN DISEASE.CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY. VOL. 47. ISSUE 1. P. 64 -74 | 92 | 90% | 69 |
3 | SUOMALAINEN, A , ISOHANNI, P , (2010) MITOCHONDRIAL DNA DEPLETION SYNDROMES - MANY GENES, COMMON MECHANISMS.NEUROMUSCULAR DISORDERS. VOL. 20. ISSUE 7. P. 429 -437 | 73 | 91% | 71 |
4 | FINSTERER, J , AHTING, U , (2013) MITOCHONDRIAL DEPLETION SYNDROMES IN CHILDREN AND ADULTS.CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES. VOL. 40. ISSUE 5. P. 635-644 | 80 | 90% | 6 |
5 | COPELAND, WC , (2008) INHERITED MITOCHONDRIAL DISEASES OF DNA REPLICATION.ANNUAL REVIEW OF MEDICINE. VOL. 59. ISSUE . P. 131-146 | 65 | 82% | 137 |
6 | COPELAND, WC , (2014) DEFECTS OF MITOCHONDRIAL DNA REPLICATION.JOURNAL OF CHILD NEUROLOGY. VOL. 29. ISSUE 9. P. 1216 -1224 | 61 | 81% | 6 |
7 | SUN, R , WANG, LY , (2014) THYMIDINE KINASE 2 ENZYME KINETICS ELUCIDATE THE MECHANISM OF THYMIDINE-INDUCED MITOCHONDRIAL DNA DEPLETION.BIOCHEMISTRY. VOL. 53. ISSUE 39. P. 6142 -6150 | 59 | 88% | 1 |
8 | STUMPF, JD , SANETO, RP , COPELAND, WC , (2013) CLINICAL AND MOLECULAR FEATURES OF POLG-RELATED MITOCHONDRIAL DISEASE.COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY. VOL. 5. ISSUE 4. P. - | 65 | 76% | 12 |
9 | LIBERNINI, L , LUPIS, C , MASTRANGELO, M , CARROZZO, R , SANTORELLI, FM , INGHILLERI, M , LEUZZI, V , (2012) MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY: NOVEL PATHOGENIC MUTATIONS IN THYMIDINE PHOSPHORYLASE GENE IN TWO ITALIAN BROTHERS.NEUROPEDIATRICS. VOL. 43. ISSUE 4. P. 201-208 | 54 | 98% | 4 |
10 | ANAGNOSTOU, ME , NG, YS , TAYLOR, RW , MCFARLAND, R , (2016) EPILEPSY DUE TO MUTATIONS IN THE MITOCHONDRIAL POLYMERASE GAMMA (POLG) GENE: A CLINICAL AND MOLECULAR GENETIC REVIEW.EPILEPSIA. VOL. 57. ISSUE 10. P. 1531 -1545 | 57 | 85% | 0 |
Classes with closest relation at Level 1 |