Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 32628 | 105 | 31.5 | 91% |
Classes in level above (level 2) |
| ID, lev. above |
Publications | Label for level above |
|---|---|---|
| 2452 | 3593 | GENOMIC IMPRINTING//H19//BECKWITH WIEDEMANN 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 | ARHI | Author keyword | 23 | 74% | 16% | 17 |
| 2 | NEURONATIN | Author keyword | 17 | 68% | 14% | 15 |
| 3 | APLASIA RAS HOMOLOG MEMBER I | Author keyword | 3 | 100% | 3% | 3 |
| 4 | DIRAS3 | Author keyword | 2 | 50% | 3% | 3 |
| 5 | NNAT | Author keyword | 2 | 36% | 4% | 4 |
| 6 | APLASIA RAS HOMOLOGUE MEMBER I ARHI | Author keyword | 1 | 100% | 2% | 2 |
| 7 | NOEY2 | Author keyword | 1 | 100% | 2% | 2 |
| 8 | OB GYN HOSP | Address | 1 | 50% | 2% | 2 |
| 9 | PATERNALLY EXPRESSED | Author keyword | 1 | 100% | 2% | 2 |
| 10 | ANALYSIS OF POLYMORPHISM | Author keyword | 1 | 50% | 1% | 1 |
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 | ARHI | 23 | 74% | 16% | 17 | Search ARHI | Search ARHI |
| 2 | NEURONATIN | 17 | 68% | 14% | 15 | Search NEURONATIN | Search NEURONATIN |
| 3 | APLASIA RAS HOMOLOG MEMBER I | 3 | 100% | 3% | 3 | Search APLASIA+RAS+HOMOLOG+MEMBER+I | Search APLASIA+RAS+HOMOLOG+MEMBER+I |
| 4 | DIRAS3 | 2 | 50% | 3% | 3 | Search DIRAS3 | Search DIRAS3 |
| 5 | NNAT | 2 | 36% | 4% | 4 | Search NNAT | Search NNAT |
| 6 | APLASIA RAS HOMOLOGUE MEMBER I ARHI | 1 | 100% | 2% | 2 | Search APLASIA+RAS+HOMOLOGUE+MEMBER+I+ARHI | Search APLASIA+RAS+HOMOLOGUE+MEMBER+I+ARHI |
| 7 | NOEY2 | 1 | 100% | 2% | 2 | Search NOEY2 | Search NOEY2 |
| 8 | PATERNALLY EXPRESSED | 1 | 100% | 2% | 2 | Search PATERNALLY+EXPRESSED | Search PATERNALLY+EXPRESSED |
| 9 | ANALYSIS OF POLYMORPHISM | 1 | 50% | 1% | 1 | Search ANALYSIS+OF+POLYMORPHISM | Search ANALYSIS+OF+POLYMORPHISM |
| 10 | MIGRATION SUPPRESSION | 1 | 50% | 1% | 1 | Search MIGRATION+SUPPRESSION | Search MIGRATION+SUPPRESSION |
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 | ARHI | 19 | 80% | 11% | 12 |
| 2 | DIRAS3 | 6 | 100% | 4% | 4 |
| 3 | GENE ARHI | 6 | 100% | 4% | 4 |
| 4 | ARHI DIRAS3 | 3 | 100% | 3% | 3 |
| 5 | SUPPRESSOR GENE ARHI | 3 | 50% | 4% | 4 |
| 6 | DISTAL CHROMOSOME 2 | 3 | 60% | 3% | 3 |
| 7 | HUMAN NEURONATIN GENE | 1 | 50% | 2% | 2 |
| 8 | RENDERS RESISTANCE | 1 | 50% | 1% | 1 |
| 9 | 1P31 | 0 | 33% | 1% | 1 |
| 10 | REGULATES GLYCOGEN SYNTHESIS | 0 | 33% | 1% | 1 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
|---|---|---|---|---|
| Neuronatin gene: Imprinted and misfolded Studies in Lafora disease, diabetes and cancer may implicate NNAT-aggregates as a common downstream participant in neuronal loss | 2014 | 3 | 62 | 48% |
| Biochemistry and biology of ARHI (DIRAS3), an imprinted tumor suppressor gene whose expression is lost in ovarian and breast cancers | 2006 | 19 | 31 | 42% |
| Tools to study the function of the Ras-related, estrogen-regulated growth inhibitor in breast cancer | 2008 | 1 | 17 | 6% |
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 | OB GYN HOSP | 1 | 50% | 1.9% | 2 |
| 2 | SAHLGRENSKA CARDIOVASC METABOL | 1 | 50% | 1.0% | 1 |
| 3 | FUJIAN NEUROSURG | 0 | 17% | 1.0% | 1 |
| 4 | ONCOL WUXI | 0 | 14% | 1.0% | 1 |
| 5 | MOL CELLULAR BIOL MOL CELL GENET | 0 | 13% | 1.0% | 1 |
| 6 | SKIN SUR E SENSING | 0 | 13% | 1.0% | 1 |
| 7 | CHINESE HUMAN GENOME SHANGHAI | 0 | 11% | 1.0% | 1 |
| 8 | OFF TRANSLAT | 0 | 11% | 1.0% | 1 |
| 9 | ANIM GENET BREEDING REPROD PLATEAU MT R | 0 | 10% | 1.0% | 1 |
| 10 | HLTH SCI B151 | 0 | 100% | 1.0% | 1 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000151681 | GENOMIC IMPRINTING//H19//BECKWITH WIEDEMANN SYNDROME |
| 2 | 0.0000146644 | TID1//HRFI//DNAJB1 |
| 3 | 0.0000074362 | MIR 1260B//NOUVEL HOP ESTAING//DIETARY COMPOUNDS |
| 4 | 0.0000065302 | TAISHO FUNCT GENOM//MULTIPHOTON DETECTION//ADAPTER TAGGED COMPETITIVE PCR |
| 5 | 0.0000060831 | LAFORA DISEASE//POLYGLUCOSAN BODIES//UNVERRICHT LUNDBORG DISEASE |
| 6 | 0.0000055097 | REM2//RRAD//RGK |
| 7 | 0.0000052660 | DIFFERENTIAL DISPLAY//MRNA DIFFERENTIAL DISPLAY//ANIM NUTR FEED YUNNAN PROV |
| 8 | 0.0000052207 | MUSASHI1//MUSASHI//MUSASHI 2 |
| 9 | 0.0000049477 | PSEUDOHYPOPARATHYROIDISM//ALBRIGHT HEREDITARY OSTEODYSTROPHY//ALBRIGHTS HEREDITARY OSTEODYSTROPHY |
| 10 | 0.0000046512 | GFI1B//GFI1//ZELLBIOL TUMORFOR |