Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 5468 | 1553 | 41.1 | 77% |
Classes in level above (level 2) |
| ID, lev. above |
Publications | Label for level above |
|---|---|---|
| 295 | 18105 | FANCONI ANEMIA//ATAXIA TELANGIECTASIA//WERNER SYNDROME |
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 | ATAXIA TELANGIECTASIA | Author keyword | 338 | 62% | 22% | 347 |
| 2 | ATM GENE | Author keyword | 39 | 80% | 2% | 24 |
| 3 | ATAXIA TELEANGIECTASIA | Author keyword | 24 | 91% | 1% | 10 |
| 4 | ATAXIA TELANGIECTASIA CLIN | Address | 21 | 90% | 1% | 9 |
| 5 | ATAXIA TELANGIECTASIA MUTATED | Author keyword | 10 | 29% | 2% | 28 |
| 6 | ATM MUTATIONS | Author keyword | 8 | 75% | 0% | 6 |
| 7 | LOUIS BAR SYNDROME | Author keyword | 8 | 100% | 0% | 5 |
| 8 | DNA REPAIR GRP | Address | 7 | 53% | 1% | 10 |
| 9 | A T | Author keyword | 6 | 71% | 0% | 5 |
| 10 | ATAXIA TELANGIECTASIA MUTATED GENE | Author keyword | 5 | 60% | 0% | 6 |
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 | ATAXIA TELANGIECTASIA | 338 | 62% | 22% | 347 | Search ATAXIA+TELANGIECTASIA | Search ATAXIA+TELANGIECTASIA |
| 2 | ATM GENE | 39 | 80% | 2% | 24 | Search ATM+GENE | Search ATM+GENE |
| 3 | ATAXIA TELEANGIECTASIA | 24 | 91% | 1% | 10 | Search ATAXIA+TELEANGIECTASIA | Search ATAXIA+TELEANGIECTASIA |
| 4 | ATAXIA TELANGIECTASIA MUTATED | 10 | 29% | 2% | 28 | Search ATAXIA+TELANGIECTASIA+MUTATED | Search ATAXIA+TELANGIECTASIA+MUTATED |
| 5 | ATM MUTATIONS | 8 | 75% | 0% | 6 | Search ATM+MUTATIONS | Search ATM+MUTATIONS |
| 6 | LOUIS BAR SYNDROME | 8 | 100% | 0% | 5 | Search LOUIS+BAR+SYNDROME | Search LOUIS+BAR+SYNDROME |
| 7 | A T | 6 | 71% | 0% | 5 | Search A+T | Search A+T |
| 8 | ATAXIA TELANGIECTASIA MUTATED GENE | 5 | 60% | 0% | 6 | Search ATAXIA+TELANGIECTASIA+MUTATED+GENE | Search ATAXIA+TELANGIECTASIA+MUTATED+GENE |
| 9 | ATM KINASE | 4 | 33% | 1% | 9 | Search ATM+KINASE | Search ATM+KINASE |
| 10 | ATAXIA TELANGIECTASIA HETEROZYGOSIS | 3 | 100% | 0% | 3 | Search ATAXIA+TELANGIECTASIA+HETEROZYGOSIS | Search ATAXIA+TELANGIECTASIA+HETEROZYGOSIS |
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 | ATAXIA TELANGIECTASIA GENE | 55 | 32% | 9% | 142 |
| 2 | ATAXIA TELANGIECTASIA HETEROZYGOTES | 44 | 65% | 3% | 42 |
| 3 | WITHOUT TELANGIECTASIA | 31 | 92% | 1% | 12 |
| 4 | ATM GENE | 29 | 34% | 5% | 71 |
| 5 | 11Q22 23 | 27 | 92% | 1% | 11 |
| 6 | ATM DEFICIENT MICE | 20 | 33% | 3% | 49 |
| 7 | 5762INS137 | 17 | 100% | 1% | 8 |
| 8 | ATAXIA TELANGIECTASIA CELLS | 13 | 24% | 3% | 47 |
| 9 | CYCLE CHECKPOINT PATHWAY | 11 | 28% | 2% | 34 |
| 10 | ATAXIA TELANGIECTASIA LOCUS | 11 | 69% | 1% | 9 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references | % act. ref. to same field |
|---|---|---|---|---|
| Ataxia-telangiectasia: from a rare disorder to a paradigm for cell signalling and cancer | 2008 | 395 | 107 | 29% |
| The ATM protein kinase and cellular redox signaling: beyond the DNA damage response | 2012 | 88 | 91 | 42% |
| Pathogenesis of ataxia-telangiectasia: the next generation of ATM functions | 2013 | 30 | 118 | 42% |
| ATM and breast cancer susceptibility | 2006 | 66 | 59 | 83% |
| Ataxia-telangiectasia, an evolving phenotype | 2004 | 205 | 47 | 68% |
| ATM and related protein kinases: Safeguarding genome integrity | 2003 | 1559 | 161 | 14% |
| The many substrates and functions of ATM | 2000 | 455 | 101 | 31% |
| Cancer risk in ATM heterozygotes: A model of phenotypic and mechanistic differences between missense and truncating mutations | 1999 | 121 | 28 | 86% |
| The genetic defect in ataxia-telangiectasia | 1997 | 364 | 126 | 55% |
| ATM signaling and genornic stability in response to DNA damage | 2005 | 127 | 76 | 41% |
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 | ATAXIA TELANGIECTASIA CLIN | 21 | 90% | 0.6% | 9 |
| 2 | DNA REPAIR GRP | 7 | 53% | 0.6% | 10 |
| 3 | GENET ANAL COMMON DIS | 5 | 60% | 0.4% | 6 |
| 4 | EUDOWOOD PEDIAT ALLERGY IMMUNOL | 3 | 57% | 0.3% | 4 |
| 5 | ONCOL 5216 | 3 | 100% | 0.2% | 3 |
| 6 | ORAL DIAG ORAL MAXILLO IAL RADIOL | 3 | 60% | 0.2% | 3 |
| 7 | EYE RADIAT ENVIRONM | 2 | 44% | 0.3% | 4 |
| 8 | ART SECT | 2 | 67% | 0.1% | 2 |
| 9 | INSERM CRI 9502 | 2 | 40% | 0.3% | 4 |
| 10 | DAVID INEZ MYERS GENET | 2 | 20% | 0.5% | 8 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000161784 | T CELL PROLYMPHOCYTIC LEUKEMIA//T PLL//TCL1 |
| 2 | 0.0000149916 | NIJMEGEN BREAKAGE SYNDROME//53BP1//NBS1 |
| 3 | 0.0000143413 | PREDICTIVE ASSAYS//INDIVIDUAL RADIOSENSITIVITY//NORMAL TISSUE RESPONSE |
| 4 | 0.0000109118 | G2 ASSAY//MUTAGEN SENSITIVITY//CHROMOSOMAL RADIOSENSITIVITY |
| 5 | 0.0000099070 | AOA2//ARSACS//APRATAXIN |
| 6 | 0.0000086814 | G2 REPAIR//CHROMATID TYPE ABERRATIONS//G2 M OVERRIDE |
| 7 | 0.0000084110 | DNA PK//DNA DEPENDENT PROTEIN KINASE//KU |
| 8 | 0.0000082688 | CHK1//RAD9//CLASPIN |
| 9 | 0.0000068440 | T OLIGOS//T OLIGO//MER PHENOTYPE |
| 10 | 0.0000054611 | FAK NAT BIOCHEM//GLIAL ENRICHED FRACTIONS//NEURONAL ENRICHED FRACTIONS |