Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
16874 | 630 | 30.4 | 70% |
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 |
207 | 3 | MULTIPLE SCLEROSIS//MYASTHENIA GRAVIS//MULTIPLE SCLEROSIS JOURNAL | 52279 |
1365 | 2 | MYASTHENIA GRAVIS//THYMOMA//THYMIC CARCINOMA | 8240 |
16874 | 1 | CONGENITAL MYASTHENIC SYNDROME//TUBULAR AGGREGATES//CONGENITAL MYASTHENIA | 630 |
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 | CONGENITAL MYASTHENIC SYNDROME | authKW | 4372005 | 19% | 74% | 122 |
2 | TUBULAR AGGREGATES | authKW | 1211669 | 6% | 71% | 35 |
3 | CONGENITAL MYASTHENIA | authKW | 712461 | 3% | 70% | 21 |
4 | SLOW CHANNEL CONGENITAL MYASTHENIC SYNDROME | authKW | 440612 | 2% | 91% | 10 |
5 | DOK7 | authKW | 390966 | 2% | 73% | 11 |
6 | SLOW CHANNEL SYNDROME | authKW | 366529 | 2% | 69% | 11 |
7 | RAPSYN | authKW | 362247 | 3% | 36% | 21 |
8 | DOK 7 | authKW | 301985 | 1% | 69% | 9 |
9 | TRANSIENT NEONATAL MYASTHENIA GRAVIS | authKW | 290805 | 1% | 100% | 6 |
10 | LIMB GIRDLE MYASTHENIA | authKW | 249260 | 1% | 86% | 6 |
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 | 11494 | 58% | 0% | 367 |
2 | Neurosciences | 3253 | 42% | 0% | 266 |
3 | Pediatrics | 673 | 12% | 0% | 76 |
4 | Genetics & Heredity | 200 | 9% | 0% | 55 |
5 | Obstetrics & Gynecology | 137 | 5% | 0% | 33 |
6 | Pathology | 112 | 4% | 0% | 28 |
7 | Psychiatry | 34 | 4% | 0% | 24 |
8 | Anesthesiology | 21 | 1% | 0% | 9 |
9 | Physiology | 9 | 2% | 0% | 15 |
10 | Medicine, Research & Experimental | 7 | 3% | 0% | 16 |
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 | UNITE FONCT CARDIOGENET MYOGENET | 215896 | 1% | 64% | 7 |
2 | MUSCLE | 127309 | 3% | 15% | 17 |
3 | NEUROSCI GRP | 101077 | 9% | 4% | 55 |
4 | MOL MED NEUROSCI GRP | 96935 | 0% | 100% | 2 |
5 | UNITE CLIN PATHOL MUSCULAIRE | 96935 | 0% | 100% | 2 |
6 | FRIEDRICH BAUR | 83563 | 5% | 6% | 31 |
7 | RECEPTOR BIOL | 81882 | 3% | 10% | 17 |
8 | SERV ELE OPHYSIOL | 77543 | 1% | 40% | 4 |
9 | NEUROL GERIATR MED PALLIAT CARE | 64622 | 0% | 67% | 2 |
10 | UNITAT PATOL NEUROMUSCULAR | 55386 | 1% | 29% | 4 |
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 | NEUROMUSCULAR DISORDERS | 41712 | 7% | 2% | 45 |
2 | MUSCLE & NERVE | 13237 | 7% | 1% | 44 |
3 | NEUROLOGY | 3807 | 7% | 0% | 41 |
4 | BRAIN | 2464 | 3% | 0% | 18 |
5 | JOURNAL OF CHILD NEUROLOGY | 1939 | 2% | 0% | 14 |
6 | ANNALS OF NEUROLOGY | 1776 | 3% | 0% | 17 |
7 | PEDIATRIC NEUROLOGY | 1631 | 2% | 0% | 12 |
8 | CURRENT OPINION IN NEUROLOGY | 1552 | 1% | 0% | 8 |
9 | ANNALS OF THE NEW YORK ACADEMY OF SCIENCES | 1452 | 6% | 0% | 35 |
10 | REVUE NEUROLOGIQUE | 1452 | 2% | 0% | 12 |
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 | CONGENITAL MYASTHENIC SYNDROME | 4372005 | 19% | 74% | 122 | Search CONGENITAL+MYASTHENIC+SYNDROME | Search CONGENITAL+MYASTHENIC+SYNDROME |
2 | TUBULAR AGGREGATES | 1211669 | 6% | 71% | 35 | Search TUBULAR+AGGREGATES | Search TUBULAR+AGGREGATES |
3 | CONGENITAL MYASTHENIA | 712461 | 3% | 70% | 21 | Search CONGENITAL+MYASTHENIA | Search CONGENITAL+MYASTHENIA |
4 | SLOW CHANNEL CONGENITAL MYASTHENIC SYNDROME | 440612 | 2% | 91% | 10 | Search SLOW+CHANNEL+CONGENITAL+MYASTHENIC+SYNDROME | Search SLOW+CHANNEL+CONGENITAL+MYASTHENIC+SYNDROME |
5 | DOK7 | 390966 | 2% | 73% | 11 | Search DOK7 | Search DOK7 |
6 | SLOW CHANNEL SYNDROME | 366529 | 2% | 69% | 11 | Search SLOW+CHANNEL+SYNDROME | Search SLOW+CHANNEL+SYNDROME |
7 | RAPSYN | 362247 | 3% | 36% | 21 | Search RAPSYN | Search RAPSYN |
8 | DOK 7 | 301985 | 1% | 69% | 9 | Search DOK+7 | Search DOK+7 |
9 | TRANSIENT NEONATAL MYASTHENIA GRAVIS | 290805 | 1% | 100% | 6 | Search TRANSIENT+NEONATAL+MYASTHENIA+GRAVIS | Search TRANSIENT+NEONATAL+MYASTHENIA+GRAVIS |
10 | LIMB GIRDLE MYASTHENIA | 249260 | 1% | 86% | 6 | Search LIMB+GIRDLE+MYASTHENIA | Search LIMB+GIRDLE+MYASTHENIA |
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 | ENGEL, AG , (2012) CURRENT STATUS OF THE CONGENITAL MYASTHENIC SYNDROMES.NEUROMUSCULAR DISORDERS. VOL. 22. ISSUE 2. P. 99-111 | 64 | 66% | 59 |
2 | ENGEL, AG , SHEN, XM , SELCEN, D , SINE, SM , (2015) CONGENITAL MYASTHENIC SYNDROMES: PATHOGENESIS, DIAGNOSIS, AND TREATMENT.LANCET NEUROLOGY. VOL. 14. ISSUE 4. P. 420 -434 | 50 | 56% | 31 |
3 | HANTAI, D , RICHARD, P , KOENIG, J , EYMARD, B , (2004) CONGENITAL MYASTHENIC SYNDROMES.CURRENT OPINION IN NEUROLOGY. VOL. 17. ISSUE 5. P. 539-551 | 58 | 78% | 43 |
4 | ANDREUX, F , HANTAI, D , EYMARD, B , (2004) CONGENITAL MYASTHENIC SYNDROMES PHENOTYPIC EXPRESSION AND PATHOPHYSIOLOGICAL CHARACTERISATION.REVUE NEUROLOGIQUE. VOL. 160. ISSUE 2. P. 163-176 | 55 | 87% | 1 |
5 | ABICHT, A , DUSL, M , GALLENMULLER, C , GUERGUELTCHEVA, V , SCHARA, U , DELLA MARINA, A , WIBBELER, E , ALMARAS, S , MIHAYLOVA, V , VON DER HAGEN, M , ET AL (2012) CONGENITAL MYASTHENIC SYNDROMES: ACHIEVEMENTS AND LIMITATIONS OF PHENOTYPE-GUIDED GENE-AFTER-GENE SEQUENCING IN DIAGNOSTIC PRACTICE: A STUDY OF 680 PATIENTS.HUMAN MUTATION. VOL. 33. ISSUE 10. P. 1474-1484 | 33 | 92% | 26 |
6 | VRINTEN, C , VAN DER ZWAAG, AM , WEINREICH, SS , SCHOLTEN, RJPM , VERSCHUUREN, JJGM , (2014) EPHEDRINE FOR MYASTHENIA GRAVIS, NEONATAL MYASTHENIA AND THE CONGENITAL MYASTHENIC SYNDROMES.COCHRANE DATABASE OF SYSTEMATIC REVIEWS. VOL. . ISSUE 12. P. - | 48 | 64% | 0 |
7 | EYMARD, B , STOJKOVIC, T , STERNBERG, D , RICHARD, P , NICOLE, S , FOURNIER, E , BEHIN, A , LAFORET, P , SERVAIS, L , ROMERO, N , ET AL (2013) CONGENITAL MYASTHENIC SYNDROMES: DIFFICULTIES IN THE DIAGNOSIS, COURSE AND PROGNOSIS, AND THERAPY - THE FRENCH NATIONAL CONGENITAL MYASTHENIC SYNDROME NETWORK EXPERIENCE.REVUE NEUROLOGIQUE. VOL. 169. ISSUE . P. S45-S55 | 36 | 84% | 5 |
8 | EYMARD, B , HANTAI, D , FOURNIER, E , NICOLE, S , STERNBERG, D , RICHARD, P , FARDEAU, M , (2014) CONGENITAL MYASTHENIC SYNDROMES ; FRENCH EXPERIENCE.BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE. VOL. 198. ISSUE 2. P. 257 -270 | 37 | 79% | 0 |
9 | HARPER, CM , (2004) CONGENITAL MYASTHENIC SYNDROMES.SEMINARS IN NEUROLOGY. VOL. 24. ISSUE 1. P. 111-123 | 43 | 75% | 21 |
10 | ENGEL, AG , SHEN, XM , SELCEN, D , SINE, SM , (2010) WHAT HAVE WE LEARNED FROM THE CONGENITAL MYASTHENIC SYNDROMES.JOURNAL OF MOLECULAR NEUROSCIENCE. VOL. 40. ISSUE 1-2. P. 143 -153 | 33 | 75% | 43 |
Classes with closest relation at Level 1 |