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

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
22273 388 33.1 74%


Bar chart of Publication_year

Last years might be incomplete

Hierarchy of classes
The table includes all classes above and classes immediately below the current class.


Cluster id Level Cluster label #P
0 4 BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY 4064930
603 3       HUNTINGTONS DISEASE//SPINOCEREBELLAR ATAXIA//POLYGLUTAMINE 14359
1711 2             SPINOCEREBELLAR ATAXIA//HEREDITARY SPASTIC PARAPLEGIA//FRIEDREICHS ATAXIA 6674
22273 1                   ARSACS//AOA2//SENATAXIN 388

Terms with highest relevance score


rank Term termType Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 ARSACS authKW 1743473 6% 92% 24
2 AOA2 authKW 1731369 6% 100% 22
3 SENATAXIN authKW 1291367 5% 86% 19
4 APRATAXIN authKW 1156857 5% 70% 21
5 AOA1 authKW 655818 3% 83% 10
6 ALS4 authKW 550890 2% 100% 7
7 ATAXIA WITH OCULOMOTOR APRAXIA TYPE 2 authKW 550890 2% 100% 7
8 OCULAR MOTOR APRAXIA authKW 524651 3% 67% 10
9 SETX authKW 457878 2% 73% 8
10 OCULOMOTOR APRAXIA authKW 437205 3% 56% 10

Web of Science journal categories


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 Clinical Neurology 4020 44% 0% 172
2 Genetics & Heredity 1269 24% 0% 95
3 Neurosciences 466 22% 0% 85
4 Ophthalmology 316 8% 0% 32
5 Anthropology 285 4% 0% 17
6 Demography 234 2% 0% 8
7 Pediatrics 108 7% 0% 26
8 Biochemistry & Molecular Biology 73 16% 0% 61
9 Neuroimaging 70 2% 0% 7
10 Biology 22 3% 0% 11

Address terms


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 NUCLE ACID CHEM GRP 157397 1% 100% 2
2 RADIAT BIOL ONCOL 141649 2% 30% 6
3 NEUROBIOL MOL NEUROPATHOL 139904 1% 44% 4
4 AS 6 78699 0% 100% 1
5 AUSTRALIA ARMY MALARIA 78699 0% 100% 1
6 BORN BUNGE FDNMOL GENET 78699 0% 100% 1
7 BRAIN OURCE BRANCH BRAIN DIS 78699 0% 100% 1
8 BRAIN SPINAL CORD INSERM U1127 78699 0% 100% 1
9 CERVEAU MOELLE EPINIERECNRSUMR 7225 78699 0% 100% 1
10 CHAU QUEBEC 78699 0% 100% 1

Journals


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 NEUROGENETICS 10536 2% 1% 9
2 HUMAN BIOLOGY 3376 2% 0% 9
3 CEREBELLUM 3122 2% 1% 6
4 NEURO-OPHTHALMOLOGY 2992 2% 1% 7
5 REVUE NEUROLOGIQUE 2786 3% 0% 13
6 BMC MEDICAL GENETICS 1949 2% 0% 6
7 COMMUNITY GENETICS 1904 1% 1% 2
8 DNA REPAIR 1885 2% 0% 7
9 JOURNAL OF THE NEUROLOGICAL SCIENCES 1737 4% 0% 15
10 SAGGI-NEUROPSICOLOGIA INFANTILE PSICOPEDAGOGIA RIABILITAZIONE 1572 0% 2% 1

Author Key Words


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class		 LCSH search Wikipedia search
1 ARSACS 1743473 6% 92% 24 Search ARSACS Search ARSACS
2 AOA2 1731369 6% 100% 22 Search AOA2 Search AOA2
3 SENATAXIN 1291367 5% 86% 19 Search SENATAXIN Search SENATAXIN
4 APRATAXIN 1156857 5% 70% 21 Search APRATAXIN Search APRATAXIN
5 AOA1 655818 3% 83% 10 Search AOA1 Search AOA1
6 ALS4 550890 2% 100% 7 Search ALS4 Search ALS4
7 ATAXIA WITH OCULOMOTOR APRAXIA TYPE 2 550890 2% 100% 7 Search ATAXIA+WITH+OCULOMOTOR+APRAXIA+TYPE+2 Search ATAXIA+WITH+OCULOMOTOR+APRAXIA+TYPE+2
8 OCULAR MOTOR APRAXIA 524651 3% 67% 10 Search OCULAR+MOTOR+APRAXIA Search OCULAR+MOTOR+APRAXIA
9 SETX 457878 2% 73% 8 Search SETX Search SETX
10 OCULOMOTOR APRAXIA 437205 3% 56% 10 Search OCULOMOTOR+APRAXIA Search OCULOMOTOR+APRAXIA

Core articles
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c:
(1) Number of references referring to publications in the class.
(2) Share of total number of active references referring to publications in the class.
(3) Age of the article. New articles get higher score than old articles.
(4) Citation rate, normalized to year.


Rank Reference # ref.
in cl.		 Shr. of ref. in
cl.		 Citations
1 TADA, M , YOKOSEKI, A , SATO, T , MAKIFUCHI, T , ONODERA, O , (2010) EARLY-ONSET ATAXIA WITH OCULAR MOTOR APRAXIA AND HYPOALBUMINEMIA/ATAXIA WITH OCULOMOTOR APRAXIA 1.DISEASES OF DNA REPAIR. VOL. 685. ISSUE . P. 21 -33 44 67% 1
2 BOUHLAL, Y , AMOURI, R , EL EUCH-FAYECHE, G , HENTATI, F , (2011) AUTOSOMAL RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY: AN OVERVIEW.PARKINSONISM & RELATED DISORDERS. VOL. 17. ISSUE 6. P. 418-422 27 93% 24
3 PRODI, E , GRISOLI, M , PANZERI, M , MINATI, L , FATTORI, F , ERBETTA, A , UZIEL, G , D'ARRIGO, S , TESSA, A , CIANO, C , ET AL (2013) SUPRATENTORIAL AND PONTINE MRI ABNORMALITIES CHARACTERIZE RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY. A COMPREHENSIVE STUDY OF AN ITALIAN SERIES.EUROPEAN JOURNAL OF NEUROLOGY. VOL. 20. ISSUE 1. P. 138-+ 24 89% 15
4 RUDENSKAYA, GE , KURKINA, MV , ZAKHAROVA, EY , (2012) ATAXIA WITH OCULOMOTOR APRAXIA: CLINICAL-GENETIC CHARACTERISTICS AND DNA-DIAGNOSTIC.ZHURNAL NEVROLOGII I PSIKHIATRII IMENI S S KORSAKOVA. VOL. 112. ISSUE 10. P. 58-63 25 93% 0
5 YOKOSEKI, A , ISHIHARA, T , KOYAMA, A , SHIGA, A , YAMADA, M , SUZUKI, C , SEKIJIMA, Y , MARUTA, K , TSUCHIYA, M , DATE, H , ET AL (2011) GENOTYPE-PHENOTYPE CORRELATIONS IN EARLY ONSET ATAXIA WITH OCULAR MOTOR APRAXIA AND HYPOALBUMINAEMIA.BRAIN. VOL. 134. ISSUE . P. 1387 -1399 24 96% 6
6 LIU, L , LI, XB , ZI, XH , SHEN, L , HU, ZM , HUANG, SX , YU, DL , LI, HB , XIA, K , TANG, BS , ET AL (2016) A NOVEL HEMIZYGOUS SACS MUTATION IDENTIFIED BY WHOLE EXOME SEQUENCING AND SNP ARRAY ANALYSIS IN A CHINESE ARSACS PATIENT.JOURNAL OF THE NEUROLOGICAL SCIENCES. VOL. 362. ISSUE . P. 111 -114 21 91% 1
7 ANHEIM, M , MONGA, B , FLEURY, M , CHARLES, P , BARBOT, C , SALIH, M , DELAUNOY, JP , FRITSCH, M , ARNING, L , SYNOFZIK, M , ET AL (2009) ATAXIA WITH OCULOMOTOR APRAXIA TYPE 2: CLINICAL, BIOLOGICAL AND GENOTYPE/PHENOTYPE CORRELATION STUDY OF A COHORT OF 90 PATIENTS.BRAIN. VOL. 132. ISSUE . P. 2688 -2698 27 71% 71
8 SCHELLENBERG, MJ , TUMBALE, PP , WILLIAMS, RS , (2015) MOLECULAR UNDERPINNINGS OF APRATAXIN RNA/DNA DEADENYLASE FUNCTION AND DYSFUNCTION IN NEUROLOGICAL DISEASE.PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY. VOL. 117. ISSUE 2-3. P. 157 -165 34 52% 5
9 ALI, Z , KLAR, J , JAMEEL, M , KHAN, K , FATIMA, A , RAININKO, R , BAIG, S , DAHL, N , (2016) NOVEL SACS MUTATIONS ASSOCIATED WITH INTELLECTUAL DISABILITY, EPILEPSY AND WIDESPREAD SUPRATENTORIAL ABNORMALITIES.JOURNAL OF THE NEUROLOGICAL SCIENCES. VOL. 371. ISSUE . P. 105 -111 25 76% 0
10 CASTELLOTTI, B , MARIOTTI, C , RIMOLDI, M , FANCELLU, R , PLUMARI, M , CAIMI, S , UZIEL, G , NARDOCCI, N , MORONI, I , ZORZI, G , ET AL (2011) ATAXIA WITH OCULOMOTOR APRAXIA TYPE1 (AOA1): NOVEL AND RECURRENT APRATAXIN MUTATIONS, COENZYME Q10 ANALYSES, AND CLINICAL FINDINGS IN ITALIAN PATIENTS.NEUROGENETICS. VOL. 12. ISSUE 3. P. 193-201 24 80% 10

Classes with closest relation at Level 1


Rank Class id link
1 32627 IGHMBP2//SMARD1//SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS
2 30096 MARINESCO SJOGREN SYNDROME//SIL1//WARBURG MICRO SYNDROME
3 19766 TRNA SPLICING//POLYNUCLEOTIDE KINASE//SPLICING ENDONUCLEASE
4 5917 ATAXIA TELANGIECTASIA//ATM//ATM GENE
5 3134 FRATAXIN//FRIEDREICHS ATAXIA//FRIEDREICH ATAXIA
6 2557 SPINOCEREBELLAR ATAXIA//MACHADO JOSEPH DISEASE//SCA2
7 19522 REPLICATION FORK BARRIER//FORK ARREST//REPLICATION TERMINATOR PROTEIN
8 16799 BROWN BOWEL SYNDROME//VITAMIN E DEFICIENCY//ALPHA TOCOPHEROL TRANSFER PROTEIN GENE
9 9176 HEREDITARY SPASTIC PARAPLEGIA//SPASTIN//SPG4
10 36093 CHRONIC NK CELL LEUKEMIA//FAMILY NODECODES//IDENTITY STATES

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