Class information for:
Level 1: AOA2//ARSACS//APRATAXIN

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
19037 458 38.5 83%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1789 5796 HEREDITARY SPASTIC PARAPLEGIA//FRIEDREICHS ATAXIA//FRIEDREICH ATAXIA

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 AOA2 Author keyword 65 95% 5% 21
2 ARSACS Author keyword 41 85% 5% 22
3 APRATAXIN Author keyword 33 77% 5% 23
4 AOA1 Author keyword 31 92% 3% 12
5 TDP1 Author keyword 23 69% 4% 20
6 TYROSYL DNA PHOSPHODIESTERASE Author keyword 23 100% 2% 10
7 SENATAXIN Author keyword 21 75% 3% 15
8 TYROSYL DNA PHOSPHODIESTERASE 1 Author keyword 15 82% 2% 9
9 ALS4 Author keyword 12 86% 1% 6
10 SCAN1 Author keyword 11 100% 1% 6

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 AOA2 65 95% 5% 21 Search AOA2 Search AOA2
2 ARSACS 41 85% 5% 22 Search ARSACS Search ARSACS
3 APRATAXIN 33 77% 5% 23 Search APRATAXIN Search APRATAXIN
4 AOA1 31 92% 3% 12 Search AOA1 Search AOA1
5 TDP1 23 69% 4% 20 Search TDP1 Search TDP1
6 TYROSYL DNA PHOSPHODIESTERASE 23 100% 2% 10 Search TYROSYL+DNA+PHOSPHODIESTERASE Search TYROSYL+DNA+PHOSPHODIESTERASE
7 SENATAXIN 21 75% 3% 15 Search SENATAXIN Search SENATAXIN
8 TYROSYL DNA PHOSPHODIESTERASE 1 15 82% 2% 9 Search TYROSYL+DNA+PHOSPHODIESTERASE+1 Search TYROSYL+DNA+PHOSPHODIESTERASE+1
9 ALS4 12 86% 1% 6 Search ALS4 Search ALS4
10 SCAN1 11 100% 1% 6 Search SCAN1 Search SCAN1

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 EARLY ONSET ATAXIA 83 94% 7% 30
2 TDP1 70 86% 8% 36
3 ARSACS 66 79% 9% 42
4 OCULAR MOTOR APRAXIA 39 54% 11% 51
5 CHARLEVOIX SAGUENAY 35 64% 8% 35
6 APRATAXIN GENE MUTATIONS 30 100% 3% 12
7 CEREBELLAR ATROPHY HMSNCA 26 100% 2% 11
8 PROTEIN APRATAXIN 25 73% 4% 19
9 SENATAXIN 23 72% 4% 18
10 RECESSIVE SPASTIC ATAXIA 22 58% 6% 26

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Molecular underpinnings of Aprataxin RNA/DNA deadenylase function and dysfunction in neurological disease 2015 3 65 52%
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: An overview 2011 18 29 93%
Single-strand break repair and genetic disease 2008 239 162 25%
Defective DNA repair and Neurodegenerative disease 2007 127 80 41%
The Autosomal Recessive Cerebellar Ataxias 2012 63 52 25%
A single strand that links multiple neuropathologies in human disease 2013 11 142 42%
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: Study of a family and review of the literature 2008 7 18 100%
Recognition and Repair of Chemically Heterogeneous Structures at DNA Ends 2015 2 212 17%
Clinical features and molecular genetics of autosomal recessive cerebellar ataxias 2007 102 124 23%
Topoisomerase-mediated chromosomal break repair: an emerging player in many games 2015 1 158 24%

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 HELMY 6 80% 0.9% 4
2 NEUROBIOL MOL NEUROPATHOL 2 44% 0.9% 4
3 DYNAM GENOME UNIT 2 67% 0.4% 2
4 RADIAT BIOL ONCOL 2 30% 1.3% 6
5 MAMMALIAN GENOME STABIL GRP 1 100% 0.4% 2
6 NUCLE ACID CHEM GRP 1 100% 0.4% 2
7 WELLCOME TRUST DNA REPAIR GRP 1 100% 0.4% 2
8 CANC UK DRUG DISCOVERY UNIT 1 30% 0.7% 3
9 DEV THER EUT BRANCH 1 12% 1.5% 7
10 MOL NEUROBIOL NEUROPATHOL 1 25% 0.7% 3

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000141399 FRIEDREICH ATAXIA//FRIEDREICHS ATAXIA//FRATAXIN
2 0.0000128860 CONGENITAL OCULAR MOTOR APRAXIA//JAMES PARKINSON//OCULAR MOTOR APRAXIA
3 0.0000112293 MARINESCO SJOGREN SYNDROME//MICRO SYNDROME//WARBURG MICRO SYNDROME
4 0.0000110309 TRNA SPLICING//POLYNUCLEOTIDE KINASE//SPLICING ENDONUCLEASE
5 0.0000099070 ATAXIA TELANGIECTASIA//ATM GENE//ATAXIA TELEANGIECTASIA
6 0.0000098323 APE1//AP ENDONUCLEASE//APE1 REF 1
7 0.0000096010 TOPOISOMERASE II//ICRF 193//DNA TOPOISOMERASE II
8 0.0000077273 MACHADO JOSEPH DISEASE//SPINOCEREBELLAR ATAXIA//SCA2
9 0.0000066988 NIJMEGEN BREAKAGE SYNDROME//53BP1//NBS1
10 0.0000061126 HEREDITARY SPASTIC PARAPLEGIA//SPG4//SPASTIN