Class information for:
Level 1: FANCONI ANEMIA//FANCONI ANAEMIA//FANCD2

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
3521 1888 43.8 81%


Bar chart of Publication_year

Last years might be incomplete

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 FANCONI ANEMIA Author keyword 590 73% 24% 451
2 FANCONI ANAEMIA Author keyword 86 67% 4% 78
3 FANCD2 Author keyword 76 81% 2% 46
4 FANCONIS ANEMIA Author keyword 57 65% 3% 54
5 FANCA Author keyword 55 92% 1% 22
6 HUMAN GENET HEMATOL Address 48 76% 2% 34
7 FANCONIS ANAEMIA Author keyword 31 76% 1% 22
8 CLIN GENET HUMAN GENET Address 21 35% 3% 50
9 FANCG Author keyword 21 85% 1% 11
10 FANCM Author keyword 17 79% 1% 11

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 FANCONI ANEMIA 590 73% 24% 451 Search FANCONI+ANEMIA Search FANCONI+ANEMIA
2 FANCONI ANAEMIA 86 67% 4% 78 Search FANCONI+ANAEMIA Search FANCONI+ANAEMIA
3 FANCD2 76 81% 2% 46 Search FANCD2 Search FANCD2
4 FANCONIS ANEMIA 57 65% 3% 54 Search FANCONIS+ANEMIA Search FANCONIS+ANEMIA
5 FANCA 55 92% 1% 22 Search FANCA Search FANCA
6 FANCONIS ANAEMIA 31 76% 1% 22 Search FANCONIS+ANAEMIA Search FANCONIS+ANAEMIA
7 FANCG 21 85% 1% 11 Search FANCG Search FANCG
8 FANCM 17 79% 1% 11 Search FANCM Search FANCM
9 FANCC 15 77% 1% 10 Search FANCC Search FANCC
10 FANCONI 11 60% 1% 12 Search FANCONI Search FANCONI

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 FACC 151 95% 3% 52
2 MONOUBIQUITINATED FANCD2 131 87% 3% 65
3 NUCLEAR COMPLEX 108 68% 5% 95
4 FANCG XRCC9 94 97% 1% 28
5 FANCD2 81 73% 3% 61
6 CROSS LINK REPAIR 76 44% 7% 131
7 INDUCED APOPTOTIC RESPONSES 69 96% 1% 22
8 BRCA PATHWAY 63 83% 2% 35
9 ANEMIA CORE COMPLEX 55 82% 2% 32
10 GROUP A GENE 46 59% 3% 51

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Fanconi anaemia and the repair of Watson and Crick DNA crosslinks 2013 106 74 68%
Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins 2007 386 101 74%
How the Fanconi Anemia Pathway Guards the Genome 2009 238 155 76%
Why does the bone marrow fail in Fanconi anemia? 2014 19 87 71%
The Fanconi Anemia DNA Repair Pathway: Structural and Functional Insights into a Complex Disorder 2014 17 121 76%
Molecular pathogenesis of Fanconi anemia: recent progress 2006 204 135 79%
Regulation of DNA cross-link repair by the Fanconi anemia/BRCA pathway 2012 133 179 41%
DNA interstrand crosslink repair and cancer 2011 196 157 36%
The emerging genetic and molecular basis of Fanconi anaemia 2001 334 106 79%
Fanconi anaemia: genetics, molecular biology, and cancer-implications for clinical management in children and adults 2015 1 91 86%

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 HUMAN GENET HEMATOL 48 76% 1.8% 34
2 CLIN GENET HUMAN GENET 21 35% 2.6% 50
3 DNA DAMAGE SIGNALING 12 48% 1.0% 19
4 GENOME MAINTENANCE 10 57% 0.6% 12
5 LATE EFFECTS STUDIES 7 53% 0.5% 9
6 GRP MUTAGENESIS 5 40% 0.5% 10
7 CELLULAR MOL RADIAT ONCOL 4 47% 0.4% 7
8 LATE EFFECT STUDIES 4 38% 0.5% 9
9 DNA DAMAGE SIGNALINGSAKYO KU 4 75% 0.2% 3
10 GRP GENOME ABIL DNA REPAIR 4 75% 0.2% 3

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000096585 DYSKERATOSIS CONGENITA//HOYERAAL HREIDARSSON SYNDROME//DYSKERIN
2 0.0000072012 CHEK2//PALB2//SERV CIRUGIA GEN ESPECIALIDADES
3 0.0000072003 RAD51//HOMOLOGOUS RECOMBINATION//RAD52
4 0.0000068442 TRANSLESION SYNTHESIS//DNA POLYMERASE ETA//DNA DAMAGE TOLERANCE
5 0.0000066590 WERNER SYNDROME//ROTHMUND THOMSON SYNDROME//RECQ
6 0.0000056274 OLAPARIB//SYNTHETIC LETHALITY//PARP INHIBITOR
7 0.0000044312 XERODERMA PIGMENTOSUM//COCKAYNE SYNDROME//NUCLEOTIDE EXCISION REPAIR
8 0.0000040799 SHWACHMAN DIAMOND SYNDROME//SBDS//SHWACHMAN SYNDROME
9 0.0000039946 NIJMEGEN BREAKAGE SYNDROME//53BP1//NBS1
10 0.0000037547 APLASTIC ANEMIA//SEVERE APLASTIC ANEMIA//APLASTIC ANAEMIA