Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
96 | 73697 | 36.9 | 76% |
Classes in level above (level 4) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
0 | 3633673 | BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//MED |
Classes in level below (level 2) |
ID, lev. below |
Publications | Label for level below |
---|---|---|
348 | 16958 | DNA METHYLATION//EPIGENETICS//HISTONE DEACETYLASE INHIBITOR |
409 | 16055 | WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE |
955 | 10314 | TURNER SYNDROME//SRY//TURNERS SYNDROME |
1959 | 5166 | RBM5//MEIOTIC DRIVE//HUMAN CHROMOSOME 3 |
2040 | 4888 | FRAGILE X SYNDROME//FRAGILE X//FMR1 |
2321 | 4046 | VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//PSEUDOHYPOPARATHYROIDISM |
2452 | 3593 | GENOMIC IMPRINTING//H19//BECKWITH WIEDEMANN SYNDROME |
2539 | 3300 | RETT SYNDROME//MECP2//MECP2 GENE |
2836 | 2461 | PRADER WILLI SYNDROME//ANGELMAN SYNDROME//PAR 4 |
3008 | 2083 | SMITH LEMLI OPITZ SYNDROME//INCONTINENTIA PIGMENTI//CHONDRODYSPLASIA PUNCTATA |
3134 | 1736 | XIST//X CHROMOSOME INACTIVATION//TSIX |
3229 | 1493 | WILLIAMS SYNDROME//WILLIAMS BEUREN SYNDROME//SUPRAVALVULAR AORTIC STENOSIS |
3508 | 1004 | KABUKI SYNDROME//KABUKI MAKE UP SYNDROME//TRICHORHINOPHALANGEAL SYNDROME |
3834 | 600 | SOTOS SYNDROME//WEAVER SYNDROME//CEREBRAL GIGANTISM |
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 | DNA METHYLATION | Author keyword | 1489 | 38% | 4% | 3091 |
2 | FRAGILE X SYNDROME | Author keyword | 1436 | 77% | 1% | 967 |
3 | RETT SYNDROME | Author keyword | 1401 | 84% | 1% | 775 |
4 | PRADER WILLI SYNDROME | Author keyword | 1276 | 84% | 1% | 700 |
5 | AMERICAN JOURNAL OF MEDICAL GENETICS | Journal | 1083 | 32% | 4% | 2796 |
6 | WILLIAMS SYNDROME | Author keyword | 964 | 83% | 1% | 551 |
7 | TURNER SYNDROME | Author keyword | 837 | 74% | 1% | 625 |
8 | GENOMIC IMPRINTING | Author keyword | 830 | 70% | 1% | 696 |
9 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | Journal | 725 | 34% | 2% | 1752 |
10 | ANGELMAN SYNDROME | Author keyword | 639 | 84% | 0% | 348 |
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 | DNA METHYLATION | 1489 | 38% | 4% | 3091 | Search DNA+METHYLATION | Search DNA+METHYLATION |
2 | FRAGILE X SYNDROME | 1436 | 77% | 1% | 967 | Search FRAGILE+X+SYNDROME | Search FRAGILE+X+SYNDROME |
3 | RETT SYNDROME | 1401 | 84% | 1% | 775 | Search RETT+SYNDROME | Search RETT+SYNDROME |
4 | PRADER WILLI SYNDROME | 1276 | 84% | 1% | 700 | Search PRADER+WILLI+SYNDROME | Search PRADER+WILLI+SYNDROME |
5 | WILLIAMS SYNDROME | 964 | 83% | 1% | 551 | Search WILLIAMS+SYNDROME | Search WILLIAMS+SYNDROME |
6 | TURNER SYNDROME | 837 | 74% | 1% | 625 | Search TURNER+SYNDROME | Search TURNER+SYNDROME |
7 | GENOMIC IMPRINTING | 830 | 70% | 1% | 696 | Search GENOMIC+IMPRINTING | Search GENOMIC+IMPRINTING |
8 | ANGELMAN SYNDROME | 639 | 84% | 0% | 348 | Search ANGELMAN+SYNDROME | Search ANGELMAN+SYNDROME |
9 | EPIGENETICS | 590 | 26% | 3% | 1939 | Search EPIGENETICS | Search EPIGENETICS |
10 | MECP2 | 563 | 80% | 0% | 352 | Search MECP2 | Search MECP2 |
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 | DNA METHYLATION | 1343 | 27% | 6% | 4353 |
2 | CGG REPEAT | 1025 | 83% | 1% | 581 |
3 | SUBEROYLANILIDE HYDROXAMIC ACID | 807 | 65% | 1% | 764 |
4 | CARDIO FACIAL SYNDROME | 725 | 63% | 1% | 729 |
5 | CPG BINDING PROTEIN 2 | 660 | 78% | 1% | 436 |
6 | FULL MUTATION | 626 | 92% | 0% | 243 |
7 | VELOCARDIOFACIAL SYNDROME | 570 | 79% | 1% | 370 |
8 | DE NOVO METHYLATION | 546 | 59% | 1% | 611 |
9 | MICRODELETIONS | 543 | 72% | 1% | 421 |
10 | MENTAL RETARDATION | 525 | 22% | 3% | 2079 |
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 | AMERICAN JOURNAL OF MEDICAL GENETICS | 1083 | 32% | 4% | 2796 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 725 | 34% | 2% | 1752 |
3 | ANNALES DE GENETIQUE | 546 | 57% | 1% | 651 |
4 | HUMAN GENETICS | 373 | 21% | 2% | 1610 |
5 | JOURNAL OF MEDICAL GENETICS | 368 | 24% | 2% | 1346 |
6 | CLINICAL GENETICS | 317 | 24% | 2% | 1159 |
7 | CYTOGENETICS AND CELL GENETICS | 251 | 25% | 1% | 856 |
8 | EPIGENETICS | 247 | 44% | 1% | 430 |
9 | GENETIC COUNSELING | 222 | 43% | 1% | 389 |
10 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 209 | 41% | 1% | 402 |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Function and information content of DNA methylation | 2015 | 26 | 115 | 72% |
Functions of DNA methylation: islands, start sites, gene bodies and beyond | 2012 | 627 | 96 | 72% |
Reversing DNA Methylation: Mechanisms, Genomics, and Biological Functions | 2014 | 104 | 209 | 80% |
DNA methylation patterns and epigenetic memory | 2002 | 2737 | 180 | 68% |
New and emerging HDAC inhibitors for cancer treatment | 2014 | 90 | 123 | 76% |
The fundamental role of epigenetic events in cancer | 2002 | 2978 | 107 | 59% |
Anticancer activities of histone deacetylase inhibitors | 2006 | 1390 | 198 | 73% |
DNA methylation: roles in mammalian development | 2013 | 277 | 196 | 62% |
Epigenetics and human obesity | 2015 | 11 | 111 | 74% |
Molecular origins of cancer: Epigenetics in cancer | 2008 | 1320 | 91 | 51% |
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 | CYTOGENET | 209 | 26% | 1.0% | 707 |
2 | CLIN GENET | 167 | 13% | 1.6% | 1171 |
3 | EPIGENET | 109 | 37% | 0.3% | 236 |
4 | WESSEX REG GENET | 107 | 46% | 0.2% | 175 |
5 | MOL HUMAN GENET | 96 | 14% | 0.9% | 644 |
6 | DEV GENET IMPRINTING | 83 | 61% | 0.1% | 87 |
7 | MIND | 82 | 25% | 0.4% | 287 |
8 | CLIN COMMUNITY HLTH NURSING | 52 | 37% | 0.1% | 110 |
9 | CBG CLIN GENET | 51 | 83% | 0.0% | 29 |
10 | CANC EPIGENET | 49 | 32% | 0.2% | 125 |
Related classes at same level (level 3) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000002834 | CHROMATIN//CHROMOSOMA//NUCLEAR ENVELOPE |
2 | 0.0000002557 | NUCHAL TRANSLUCENCY//TWIN TWIN TRANSFUSION SYNDROME//NON INVASIVE PRENATAL DIAGNOSIS |
3 | 0.0000001815 | CLEFT PALATE-CRANIOFACIAL JOURNAL//CRANIOSYNOSTOSIS//CLEFT PALATE |
4 | 0.0000001660 | GENOME EDITING//CAS9//CRISPR |
5 | 0.0000001653 | BIOINFORMATICS//BMC BIOINFORMATICS//MATHEMATICAL & COMPUTATIONAL BIOLOGY |
6 | 0.0000001637 | MICRORNA//MICRORNAS//MIRNA |
7 | 0.0000001444 | TRANSCRIPTION FACTOR//ETS 1//C JUN |
8 | 0.0000001385 | REPRODUCTIVE BIOLOGY//ANDROLOGY//SPERMATOZOA |
9 | 0.0000001271 | DEVELOPMENTAL BIOLOGY//DEVELOPMENT//DROSOPHILA |
10 | 0.0000001254 | MERKEL CELL CARCINOMA//P53//JC VIRUS |