Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
2452 | 3593 | 44.1 | 87% |
Classes in level above (level 3) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
96 | 73697 | DNA METHYLATION//FRAGILE X SYNDROME//RETT SYNDROME |
Classes in level below (level 1) |
ID, lev. below | Publications | Label for level below |
---|---|---|
615 | 3160 | GENOMIC IMPRINTING//H19//BECKWITH WIEDEMANN SYNDROME |
22355 | 328 | DLK1//PREF 1//FETAL ANTIGEN 2 |
32628 | 105 | ARHI//NEURONATIN//APLASIA RAS HOMOLOG MEMBER I |
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 | GENOMIC IMPRINTING | Author keyword | 388 | 52% | 15% | 523 |
2 | H19 | Author keyword | 231 | 73% | 5% | 175 |
3 | BECKWITH WIEDEMANN SYNDROME | Author keyword | 135 | 56% | 5% | 165 |
4 | SILVER RUSSELL SYNDROME | Author keyword | 127 | 74% | 3% | 93 |
5 | IGF2 | Author keyword | 92 | 47% | 4% | 144 |
6 | IMPRINTING | Author keyword | 91 | 24% | 9% | 338 |
7 | DLK1 | Author keyword | 86 | 76% | 2% | 60 |
8 | LOSS OF IMPRINTING | Author keyword | 79 | 87% | 1% | 39 |
9 | IMPRINTED GENES | Author keyword | 52 | 59% | 2% | 58 |
10 | H19 GENE | Author keyword | 38 | 78% | 1% | 25 |
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 | GENOMIC IMPRINTING | 388 | 52% | 15% | 523 | Search GENOMIC+IMPRINTING | Search GENOMIC+IMPRINTING |
2 | H19 | 231 | 73% | 5% | 175 | Search H19 | Search H19 |
3 | BECKWITH WIEDEMANN SYNDROME | 135 | 56% | 5% | 165 | Search BECKWITH+WIEDEMANN+SYNDROME | Search BECKWITH+WIEDEMANN+SYNDROME |
4 | SILVER RUSSELL SYNDROME | 127 | 74% | 3% | 93 | Search SILVER+RUSSELL+SYNDROME | Search SILVER+RUSSELL+SYNDROME |
5 | IGF2 | 92 | 47% | 4% | 144 | Search IGF2 | Search IGF2 |
6 | IMPRINTING | 91 | 24% | 9% | 338 | Search IMPRINTING | Search IMPRINTING |
7 | DLK1 | 86 | 76% | 2% | 60 | Search DLK1 | Search DLK1 |
8 | LOSS OF IMPRINTING | 79 | 87% | 1% | 39 | Search LOSS+OF+IMPRINTING | Search LOSS+OF+IMPRINTING |
9 | IMPRINTED GENES | 52 | 59% | 2% | 58 | Search IMPRINTED+GENES | Search IMPRINTED+GENES |
10 | H19 GENE | 38 | 78% | 1% | 25 | Search H19+GENE | Search H19+GENE |
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 | BECKWITH WIEDEMANN SYNDROME | 311 | 39% | 17% | 622 |
2 | H19 | 295 | 69% | 7% | 249 |
3 | IGF2 | 232 | 66% | 6% | 215 |
4 | H19 GENE | 205 | 61% | 6% | 218 |
5 | MOUSE H19 GENE | 174 | 77% | 3% | 117 |
6 | FACTOR II GENE | 114 | 44% | 5% | 194 |
7 | SILVER RUSSELL SYNDROME | 111 | 52% | 4% | 152 |
8 | H19 IGF2 LOCUS | 110 | 78% | 2% | 72 |
9 | REPRESSIVE HISTONE METHYLATION | 101 | 67% | 3% | 91 |
10 | GROWTH FACTOR II | 99 | 24% | 10% | 365 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
The role and interaction of imprinted genes in human fetal growth | 2015 | 4 | 67 | 70% |
Genomic imprinting: Parental influence on the genome | 2001 | 1204 | 108 | 72% |
Genomic imprinting: the emergence of an epigenetic paradigm | 2011 | 153 | 96 | 74% |
Epigenetic reprogramming in mammalian development | 2001 | 1386 | 61 | 36% |
The role of genomic imprinting in biology and disease: an expanding view | 2014 | 21 | 144 | 42% |
Molecular Findings in BeckwithWiedemann Syndrome | 2013 | 23 | 96 | 85% |
Non-conflict theories for the evolution of genomic imprinting | 2014 | 9 | 44 | 80% |
The origin and evolution of genomic imprinting and viviparity in mammals | 2013 | 31 | 109 | 63% |
The H19 locus: Role of an imprinted non-coding RNA in growth and development | 2010 | 98 | 93 | 70% |
A census of mammalian imprinting | 2005 | 334 | 56 | 57% |
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 | DEV GENET IMPRINTING | 32 | 42% | 1.6% | 59 |
2 | MOL GENET EPIGENET | 21 | 73% | 0.4% | 16 |
3 | IMPRINTING CANC GRP | 17 | 72% | 0.4% | 13 |
4 | WESSEX GENET SERV | 15 | 88% | 0.2% | 7 |
5 | INORGAN ORGAN CHEM BIOCHEM | 12 | 63% | 0.3% | 12 |
6 | WELLCOME CRC CANC DEV BIOL | 9 | 45% | 0.4% | 15 |
7 | DEV GENET PROGRAMME | 8 | 29% | 0.6% | 22 |
8 | PROGRAMME DEV GENET | 7 | 67% | 0.2% | 6 |
9 | EXPLORAT FONCT ENDOCRINIENNES | 6 | 33% | 0.4% | 14 |
10 | BIOCHEM MOL BIOL BRANCH | 6 | 100% | 0.1% | 4 |
Related classes at same level (level 2) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000058082 | PRADER WILLI SYNDROME//ANGELMAN SYNDROME//PAR 4 |
2 | 0.0000057872 | XIST//X CHROMOSOME INACTIVATION//TSIX |
3 | 0.0000026116 | SOTOS SYNDROME//WEAVER SYNDROME//CEREBRAL GIGANTISM |
4 | 0.0000025846 | DNA METHYLATION//EPIGENETICS//HISTONE DEACETYLASE INHIBITOR |
5 | 0.0000019826 | DLX4//DLX3//CANC DEV BIOL MATERNAL FETAL BIOL |
6 | 0.0000017993 | HYDATIDIFORM MOLE//GESTATIONAL TROPHOBLASTIC NEOPLASIA//GESTATIONAL TROPHOBLASTIC DISEASES |
7 | 0.0000017785 | WILMS TUMOR//WT1//RHABDOID TUMOR |
8 | 0.0000014059 | VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//PSEUDOHYPOPARATHYROIDISM |
9 | 0.0000011279 | REPRODUCTIVE BIOLOGY//NUCLEAR TRANSFER//OOCYTE |
10 | 0.0000008372 | WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE |