Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
5972 | 1481 | 37.0 | 85% |
Classes in level above (level 2) |
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 | DRAVET SYNDROME | Author keyword | 202 | 75% | 10% | 146 |
2 | SCN1A | Author keyword | 191 | 74% | 10% | 143 |
3 | GEFS | Author keyword | 87 | 74% | 4% | 64 |
4 | SEVERE MYOCLONIC EPILEPSY IN INFANCY | Author keyword | 82 | 85% | 3% | 44 |
5 | SEVERE MYOCLONIC EPILEPSY OF INFANCY | Author keyword | 70 | 87% | 2% | 34 |
6 | GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS | Author keyword | 55 | 92% | 1% | 22 |
7 | SMEI | Author keyword | 42 | 74% | 2% | 31 |
8 | LGI1 | Author keyword | 41 | 65% | 3% | 39 |
9 | STIRIPENTOL | Author keyword | 27 | 58% | 2% | 31 |
10 | SCN1A MUTATION | Author keyword | 27 | 83% | 1% | 15 |
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 | DRAVET SYNDROME | 202 | 75% | 10% | 146 | Search DRAVET+SYNDROME | Search DRAVET+SYNDROME |
2 | SCN1A | 191 | 74% | 10% | 143 | Search SCN1A | Search SCN1A |
3 | GEFS | 87 | 74% | 4% | 64 | Search GEFS | Search GEFS |
4 | SEVERE MYOCLONIC EPILEPSY IN INFANCY | 82 | 85% | 3% | 44 | Search SEVERE+MYOCLONIC+EPILEPSY+IN+INFANCY | Search SEVERE+MYOCLONIC+EPILEPSY+IN+INFANCY |
5 | SEVERE MYOCLONIC EPILEPSY OF INFANCY | 70 | 87% | 2% | 34 | Search SEVERE+MYOCLONIC+EPILEPSY+OF+INFANCY | Search SEVERE+MYOCLONIC+EPILEPSY+OF+INFANCY |
6 | GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS | 55 | 92% | 1% | 22 | Search GENERALIZED+EPILEPSY+WITH+FEBRILE+SEIZURES+PLUS | Search GENERALIZED+EPILEPSY+WITH+FEBRILE+SEIZURES+PLUS |
7 | SMEI | 42 | 74% | 2% | 31 | Search SMEI | Search SMEI |
8 | LGI1 | 41 | 65% | 3% | 39 | Search LGI1 | Search LGI1 |
9 | STIRIPENTOL | 27 | 58% | 2% | 31 | Search STIRIPENTOL | Search STIRIPENTOL |
10 | SCN1A MUTATION | 27 | 83% | 1% | 15 | Search SCN1A+MUTATION | Search SCN1A+MUTATION |
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 | SEVERE MYOCLONIC EPILEPSY | 431 | 67% | 26% | 390 |
2 | FEBRILE SEIZURES PLUS | 230 | 69% | 13% | 198 |
3 | NEURONAL SODIUM CHANNEL | 151 | 83% | 6% | 86 |
4 | DOMINANT PARTIAL EPILEPSY | 143 | 85% | 5% | 75 |
5 | SCN1A MUTATIONS | 143 | 88% | 5% | 67 |
6 | AUDITORY FEATURES | 128 | 82% | 5% | 74 |
7 | GENE SCN1A | 111 | 100% | 2% | 32 |
8 | SCN1A | 105 | 67% | 6% | 96 |
9 | GENERALIZED EPILEPSY | 105 | 34% | 17% | 250 |
10 | DRAVET SYNDROME | 73 | 58% | 6% | 83 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
Sodium channel mutations in epilepsy and other neurological disorders | 2005 | 228 | 76 | 58% |
Sodium channel SCN1A and epilepsy: Mutations and mechanisms | 2010 | 83 | 85 | 68% |
Na(V)1.1 channels and epilepsy | 2010 | 101 | 71 | 58% |
Mutations in GABA(A) receptor subunits associated with genetic epilepsies | 2010 | 69 | 45 | 71% |
A catalog of SCN1A variants | 2009 | 88 | 80 | 75% |
Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects | 2010 | 77 | 55 | 64% |
Clinical spectrum of SCN2A mutations | 2012 | 24 | 21 | 90% |
Epilepsy genetics - past, present, and future | 2011 | 44 | 68 | 57% |
Molecular genetics of Dravet syndrome | 2011 | 20 | 32 | 100% |
Epilepsy and mental retardation restricted to females: X-linked epileptic infantile encephalopathy of unusual inheritance | 2015 | 1 | 24 | 75% |
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 | CENT PATHOMECH EPILEPSY | 11 | 100% | 0.4% | 6 |
2 | REFERENCE EPILEPSIES RA | 9 | 44% | 1.0% | 15 |
3 | NEUROGENET GRP | 5 | 16% | 1.8% | 26 |
4 | CHILDRENS HOSP A MEYER | 5 | 23% | 1.1% | 17 |
5 | EPIDEMIOL BRAIN DISORDERS | 4 | 28% | 0.9% | 13 |
6 | EPILEPSY GENET GRP | 4 | 40% | 0.5% | 8 |
7 | PEDIAT HOSP A MEYER | 4 | 56% | 0.3% | 5 |
8 | SERV NEUROL METAB | 4 | 41% | 0.5% | 7 |
9 | MUSCULAR NEURODEGENERAT DIS UNIT | 4 | 16% | 1.4% | 20 |
10 | DIRECTORATE GENET MOL PATHOL | 3 | 57% | 0.3% | 4 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000164154 | FEBRILE SEIZURES//COMPLEX FEBRILE SEIZURE//FEBRILE CONVULSIONS |
2 | 0.0000161430 | JUVENILE MYOCLONIC EPILEPSY//PHOTOPAROXYSMAL RESPONSE//IDIOPATHIC GENERALIZED EPILEPSY |
3 | 0.0000149119 | HOT WATER EPILEPSY//BATHING EPILEPSY//REFLEX EPILEPSY |
4 | 0.0000133067 | RETIGABINE//FLUPIRTINE//KCNQ |
5 | 0.0000124779 | RUFINAMIDE//CLOBAZAM//LENNOX GASTAUT SYNDROME |
6 | 0.0000100624 | NOCTURNAL FRONTAL LOBE EPILEPSY//CYCLIC ALTERNATING PATTERN//ADNFLE |
7 | 0.0000087573 | WEST SYNDROME//INFANTILE SPASMS//HYPSARRHYTHMIA |
8 | 0.0000084087 | NEUROSCI REGENERAT//NAV17//NAV18 |
9 | 0.0000080866 | PAROXYSMAL KINESIGENIC DYSKINESIA//PRRT2//PAROXYSMAL KINESIGENIC CHOREOATHETOSIS |
10 | 0.0000077432 | TNFAIP1//KCTD7//KCTD10 |