Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
9970 | 1039 | 34.1 | 85% |
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 | HEREDITARY SPASTIC PARAPLEGIA | Author keyword | 321 | 77% | 21% | 216 |
2 | SPG4 | Author keyword | 151 | 95% | 5% | 52 |
3 | SPASTIN | Author keyword | 121 | 82% | 7% | 70 |
4 | SPG11 | Author keyword | 72 | 91% | 3% | 30 |
5 | HEREDITARY SPASTIC PARAPARESIS | Author keyword | 48 | 72% | 4% | 38 |
6 | ATLASTIN | Author keyword | 45 | 94% | 2% | 16 |
7 | SPAST | Author keyword | 44 | 100% | 2% | 16 |
8 | THIN CORPUS CALLOSUM | Author keyword | 35 | 81% | 2% | 21 |
9 | SPASTIC PARAPLEGIA | Author keyword | 33 | 48% | 5% | 50 |
10 | SPG7 | Author keyword | 30 | 100% | 1% | 12 |
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 | HEREDITARY SPASTIC PARAPLEGIA | 321 | 77% | 21% | 216 | Search HEREDITARY+SPASTIC+PARAPLEGIA | Search HEREDITARY+SPASTIC+PARAPLEGIA |
2 | SPG4 | 151 | 95% | 5% | 52 | Search SPG4 | Search SPG4 |
3 | SPASTIN | 121 | 82% | 7% | 70 | Search SPASTIN | Search SPASTIN |
4 | SPG11 | 72 | 91% | 3% | 30 | Search SPG11 | Search SPG11 |
5 | HEREDITARY SPASTIC PARAPARESIS | 48 | 72% | 4% | 38 | Search HEREDITARY+SPASTIC+PARAPARESIS | Search HEREDITARY+SPASTIC+PARAPARESIS |
6 | ATLASTIN | 45 | 94% | 2% | 16 | Search ATLASTIN | Search ATLASTIN |
7 | SPAST | 44 | 100% | 2% | 16 | Search SPAST | Search SPAST |
8 | THIN CORPUS CALLOSUM | 35 | 81% | 2% | 21 | Search THIN+CORPUS+CALLOSUM | Search THIN+CORPUS+CALLOSUM |
9 | SPASTIC PARAPLEGIA | 33 | 48% | 5% | 50 | Search SPASTIC+PARAPLEGIA | Search SPASTIC+PARAPLEGIA |
10 | SPG7 | 30 | 100% | 1% | 12 | Search SPG7 | Search SPG7 |
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 | PARAPARESIS | 186 | 69% | 15% | 160 |
2 | THIN CORPUS CALLOSUM | 136 | 84% | 7% | 74 |
3 | SPG4 | 109 | 92% | 4% | 44 |
4 | SPATACSIN | 70 | 89% | 3% | 32 |
5 | SPG4 MUTATIONS | 65 | 95% | 2% | 21 |
6 | ATLASTIN | 52 | 87% | 3% | 26 |
7 | CHROMOSOME 2P | 50 | 63% | 5% | 50 |
8 | HEREDITARY SPASTIC PARAPLEGIA | 49 | 29% | 13% | 140 |
9 | 15Q13 15 | 44 | 100% | 2% | 16 |
10 | SPG3A | 44 | 100% | 2% | 16 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance | 2012 | 60 | 145 | 83% |
Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms | 2013 | 40 | 210 | 70% |
Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms | 2008 | 187 | 123 | 77% |
Cellular Pathways of Hereditary Spastic Paraplegia | 2012 | 56 | 139 | 46% |
Hereditary spastic paraplegias: membrane traffic and the motor pathway | 2011 | 86 | 115 | 52% |
Hereditary spastic paraplegia | 2006 | 135 | 106 | 81% |
Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology | 2015 | 1 | 198 | 64% |
Hereditary spastic paraplegia: Advances in genetic research | 1996 | 125 | 20 | 90% |
Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms | 2014 | 6 | 226 | 70% |
Weaving the Web of ER Tubules | 2011 | 38 | 30 | 80% |
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 | CELLULAR NEUROL UNIT | 9 | 45% | 1.4% | 15 |
2 | GENET CYTOGENET | 4 | 13% | 3.1% | 32 |
3 | MED GENETSECT NEUROGENET | 4 | 75% | 0.3% | 3 |
4 | UMR S679 | 4 | 23% | 1.4% | 15 |
5 | FEDERAT NEUROSCI IFR70 | 3 | 57% | 0.4% | 4 |
6 | IZKF JR GRP | 3 | 60% | 0.3% | 3 |
7 | PHYS BIOPHYS E22 | 3 | 60% | 0.3% | 3 |
8 | NEUROGENET BRANCH | 3 | 11% | 2.3% | 24 |
9 | NEUROSCI MED BIOTECHNOL | 2 | 44% | 0.4% | 4 |
10 | NEUROMUSCULAR NEUROREHABIL UNIT | 2 | 67% | 0.2% | 2 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000080705 | OXYSTEROL BINDING PROTEIN//OXYSTEROL BINDING PROTEINS//OSBP |
2 | 0.0000075804 | STYLET TRACK//COLORECTAL NEOPLASMS PATHOLOGY//DRUG IN ADHESIVE PATCHES |
3 | 0.0000061126 | AOA2//ARSACS//APRATAXIN |
4 | 0.0000055166 | CONGENITAL GENERALIZED LIPODYSTROPHY//SEIPIN//BSCL2 |
5 | 0.0000052964 | MACHADO JOSEPH DISEASE//SPINOCEREBELLAR ATAXIA//SCA2 |
6 | 0.0000046296 | MARINESCO SJOGREN SYNDROME//MICRO SYNDROME//WARBURG MICRO SYNDROME |
7 | 0.0000044951 | ATP DEPENDENT PROTEASES//CLPB//FTSH |
8 | 0.0000043663 | DAP3//ICT1//MITOCHONDRIAL RIBOSOMAL PROTEINS |
9 | 0.0000043315 | FRIEDREICH ATAXIA//FRIEDREICHS ATAXIA//FRATAXIN |
10 | 0.0000040747 | PKAN//HALLERVORDEN SPATZ SYNDROME//NBIA |