Class information for:
Level 1: GENOMIC IMPRINTING//H19//BECKWITH WIEDEMANN SYNDROME

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
615 3160 45.3 87%


Bar chart of Publication_year

Last years might be incomplete

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 GENOMIC IMPRINTING Author keyword 375 52% 16% 516
2 H19 Author keyword 231 73% 6% 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% 5% 144
6 IMPRINTING Author keyword 84 23% 10% 325
7 LOSS OF IMPRINTING Author keyword 79 87% 1% 39
8 IMPRINTED GENES Author keyword 47 57% 2% 56
9 H19 GENE Author keyword 38 78% 1% 25
10 RUSSELL SILVER SYNDROME Author keyword 35 72% 1% 28

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 375 52% 16% 516 Search GENOMIC+IMPRINTING Search GENOMIC+IMPRINTING
2 H19 231 73% 6% 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% 5% 144 Search IGF2 Search IGF2
6 IMPRINTING 84 23% 10% 325 Search IMPRINTING Search IMPRINTING
7 LOSS OF IMPRINTING 79 87% 1% 39 Search LOSS+OF+IMPRINTING Search LOSS+OF+IMPRINTING
8 IMPRINTED GENES 47 57% 2% 56 Search IMPRINTED+GENES Search IMPRINTED+GENES
9 H19 GENE 38 78% 1% 25 Search H19+GENE Search H19+GENE
10 RUSSELL SILVER SYNDROME 35 72% 1% 28 Search RUSSELL+SILVER+SYNDROME Search RUSSELL+SILVER+SYNDROME

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 310 39% 20% 621
2 H19 284 69% 8% 246
3 IGF2 226 65% 7% 213
4 H19 GENE 202 61% 7% 217
5 MOUSE H19 GENE 174 77% 4% 117
6 FACTOR II GENE 113 44% 6% 193
7 SILVER RUSSELL SYNDROME 111 52% 5% 152
8 H19 IGF2 LOCUS 110 78% 2% 72
9 REPRESSIVE HISTONE METHYLATION 101 67% 3% 91
10 GROWTH FACTOR II 98 24% 11% 363

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 63%
Genomic imprinting: Parental influence on the genome 2001 1204 108 71%
Genomic imprinting: the emergence of an epigenetic paradigm 2011 153 96 74%
Epigenetic reprogramming in mammalian development 2001 1386 61 36%
Molecular Findings in BeckwithWiedemann Syndrome 2013 23 96 85%
The role of genomic imprinting in biology and disease: an expanding view 2014 21 144 40%
The H19 locus: Role of an imprinted non-coding RNA in growth and development 2010 98 93 70%
Non-conflict theories for the evolution of genomic imprinting 2014 9 44 77%
A census of mammalian imprinting 2005 334 56 57%
The origin and evolution of genomic imprinting and viviparity in mammals 2013 31 109 61%

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 30 41% 1.8% 58
2 MOL GENET EPIGENET 21 73% 0.5% 16
3 IMPRINTING CANC GRP 17 72% 0.4% 13
4 WESSEX GENET SERV 15 88% 0.2% 7
5 WELLCOME CRC CANC DEV BIOL 9 45% 0.5% 15
6 DEV GENET PROGRAMME 8 29% 0.7% 22
7 PROGRAMME DEV GENET 7 67% 0.2% 6
8 EXPLORAT FONCT ENDOCRINIENNES 6 33% 0.4% 14
9 FR GENET 8 2 6 100% 0.1% 4
10 MOL GENET IGMM 5 63% 0.2% 5

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000151681 ARHI//NEURONATIN//APLASIA RAS HOMOLOG MEMBER I
2 0.0000143600 DLK1//PREF 1//FETAL ANTIGEN 2
3 0.0000092688 TRANSGENERATIONAL//METASTABLE EPIALLELE//TRANSGENERATIONAL EPIGENETIC INHERITANCE
4 0.0000084143 PARTHENOGENETIC EMBRYONIC STEM CELL//HEART DIS CARDIOTHORAC SURG//PARTHENOGENETIC STEM CELLS
5 0.0000082902 XIST//X CHROMOSOME INACTIVATION//TSIX
6 0.0000078485 CONFINED PLACENTAL MOSAICISM//UNIPARENTAL DISOMY//TRISOMY 9
7 0.0000075461 DNMT3B//DNA METHYLTRANSFERASE//DNMT1
8 0.0000074008 PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A
9 0.0000064987 PSEUDOHYPOPARATHYROIDISM//ALBRIGHT HEREDITARY OSTEODYSTROPHY//ALBRIGHTS HEREDITARY OSTEODYSTROPHY
10 0.0000064916 CTCF//CONTROL GENET PROC//ENHANCER BLOCKING