Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
1825 | 2470 | 34.7 | 74% |
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 |
222 | 3 | MYOTONIC DYSTROPHY//ALDOSTERONE//PHYSIOLOGY | 49798 |
2003 | 2 | MYOTONIC DYSTROPHY//MYOTONIA//MYOTONIC DYSTROPHY TYPE 1 | 5494 |
1825 | 1 | MYOTONIC DYSTROPHY//MYOTONIC DYSTROPHY TYPE 1//MYOTONIC DYSTROPHY TYPE 2 | 2470 |
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 | MYOTONIC DYSTROPHY | authKW | 6162561 | 26% | 77% | 646 |
2 | MYOTONIC DYSTROPHY TYPE 1 | authKW | 1384452 | 5% | 88% | 127 |
3 | MYOTONIC DYSTROPHY TYPE 2 | authKW | 649698 | 2% | 91% | 58 |
4 | CTG REPEAT | authKW | 573691 | 2% | 81% | 57 |
5 | PROXIMAL MYOTONIC MYOPATHY | authKW | 409235 | 1% | 95% | 35 |
6 | STEINERTS DISEASE | authKW | 373905 | 1% | 92% | 33 |
7 | CONGENITAL MYOTONIC DYSTROPHY | authKW | 372534 | 1% | 84% | 36 |
8 | DM1 | authKW | 258837 | 1% | 63% | 33 |
9 | MUSCLEBLIND | authKW | 249270 | 1% | 92% | 22 |
10 | DMPK | authKW | 226777 | 1% | 54% | 34 |
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 | 10785 | 29% | 0% | 726 |
2 | Genetics & Heredity | 4426 | 19% | 0% | 458 |
3 | Neurosciences | 2198 | 19% | 0% | 476 |
4 | Biochemistry & Molecular Biology | 961 | 20% | 0% | 498 |
5 | Cell Biology | 368 | 8% | 0% | 204 |
6 | Anesthesiology | 290 | 2% | 0% | 59 |
7 | Cardiac & Cardiovascular System | 282 | 6% | 0% | 136 |
8 | Pediatrics | 140 | 4% | 0% | 90 |
9 | Pathology | 99 | 3% | 0% | 62 |
10 | Medicine, General & Internal | 95 | 5% | 0% | 115 |
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 | MUSCLE HISTOPATHOL MOL BIOL | 71912 | 0% | 73% | 8 |
2 | DIPARTIMENTO BIOL MOL BIOTECNOL | 61803 | 0% | 100% | 5 |
3 | IRCCS POLICLIN SAN DONATO | 59712 | 1% | 13% | 36 |
4 | GRIMN | 49443 | 0% | 100% | 4 |
5 | CARDIOMYOL GENET SECT | 44494 | 0% | 60% | 6 |
6 | CLIN MALAD NEUROMUSCULAI | 41627 | 0% | 42% | 8 |
7 | NEUROMUSCULAR CLIN | 39040 | 1% | 20% | 16 |
8 | NEUROMUSCULAR NEUROL RARE DIS | 32959 | 0% | 67% | 4 |
9 | SCI EDUC PSYCHOL | 28593 | 0% | 26% | 9 |
10 | ECOBES RECH TRANSFERT | 28087 | 0% | 45% | 5 |
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 | 36106 | 3% | 4% | 83 |
2 | HUMAN MOLECULAR GENETICS | 11082 | 4% | 1% | 94 |
3 | MUSCLE & NERVE | 9466 | 3% | 1% | 74 |
4 | BASIC AND APPLIED MYOLOGY | 5347 | 0% | 6% | 7 |
5 | JOURNAL OF MEDICAL GENETICS | 4066 | 2% | 1% | 44 |
6 | JOURNAL OF NEUROLOGY | 3873 | 2% | 1% | 44 |
7 | NEUROLOGY | 2594 | 3% | 0% | 68 |
8 | JOURNAL OF THE NEUROLOGICAL SCIENCES | 1992 | 2% | 0% | 41 |
9 | ACTA NEUROLOGICA SCANDINAVICA | 1666 | 1% | 0% | 29 |
10 | AMERICAN JOURNAL OF HUMAN GENETICS | 1521 | 1% | 0% | 32 |
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 | MYOTONIC DYSTROPHY | 6162561 | 26% | 77% | 646 | Search MYOTONIC+DYSTROPHY | Search MYOTONIC+DYSTROPHY |
2 | MYOTONIC DYSTROPHY TYPE 1 | 1384452 | 5% | 88% | 127 | Search MYOTONIC+DYSTROPHY+TYPE+1 | Search MYOTONIC+DYSTROPHY+TYPE+1 |
3 | MYOTONIC DYSTROPHY TYPE 2 | 649698 | 2% | 91% | 58 | Search MYOTONIC+DYSTROPHY+TYPE+2 | Search MYOTONIC+DYSTROPHY+TYPE+2 |
4 | CTG REPEAT | 573691 | 2% | 81% | 57 | Search CTG+REPEAT | Search CTG+REPEAT |
5 | PROXIMAL MYOTONIC MYOPATHY | 409235 | 1% | 95% | 35 | Search PROXIMAL+MYOTONIC+MYOPATHY | Search PROXIMAL+MYOTONIC+MYOPATHY |
6 | STEINERTS DISEASE | 373905 | 1% | 92% | 33 | Search STEINERTS+DISEASE | Search STEINERTS+DISEASE |
7 | CONGENITAL MYOTONIC DYSTROPHY | 372534 | 1% | 84% | 36 | Search CONGENITAL+MYOTONIC+DYSTROPHY | Search CONGENITAL+MYOTONIC+DYSTROPHY |
8 | DM1 | 258837 | 1% | 63% | 33 | Search DM1 | Search DM1 |
9 | MUSCLEBLIND | 249270 | 1% | 92% | 22 | Search MUSCLEBLIND | Search MUSCLEBLIND |
10 | DMPK | 226777 | 1% | 54% | 34 | Search DMPK | Search DMPK |
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 | MEOLA, G , CARDANI, R , (2015) MYOTONIC DYSTROPHIES: AN UPDATE ON CLINICAL ASPECTS, GENETIC, PATHOLOGY, AND MOLECULAR PATHOMECHANISMS.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1852. ISSUE 4. P. 594 -606 | 165 | 94% | 17 |
2 | KRAHE, R , UDD, B , (2012) THE MYOTONIC DYSTROPHIES: MOLECULAR, CLINICAL, AND THERAPEUTIC CHALLENGES.LANCET NEUROLOGY. VOL. 11. ISSUE 10. P. 891-905 | 134 | 95% | 111 |
3 | KONIECZNY, P , STEPNIAK-KONIECZNA, E , SOBCZAK, K , (2014) MBNL PROTEINS AND THEIR TARGET RNAS, INTERACTION AND SPLICING REGULATION.NUCLEIC ACIDS RESEARCH. VOL. 42. ISSUE 17. P. 10873 -10887 | 114 | 91% | 13 |
4 | MEOLA, G , SANSONE, V , (2007) CEREBRAL INVOLVEMENT IN MYOTONIC DYSTROPHIES.MUSCLE & NERVE. VOL. 36. ISSUE 3. P. 294-306 | 110 | 95% | 100 |
5 | THORNTON, CA , (2014) MYOTONIC DYSTROPHY.NEUROLOGIC CLINICS. VOL. 32. ISSUE 3. P. 705 -+ | 94 | 95% | 20 |
6 | CHAU, A , KALSOTRA, A , (2015) DEVELOPMENTAL INSIGHTS INTO THE PATHOLOGY OF AND THERAPEUTIC STRATEGIES FOR DM1: BACK TO THE BASICS.DEVELOPMENTAL DYNAMICS. VOL. 244. ISSUE 3. P. 377 -390 | 110 | 80% | 8 |
7 | SICOT, G , GOMES-PEREIRA, M , (2013) RNA TOXICITY IN HUMAN DISEASE AND ANIMAL MODELS: FROM THE UNCOVERING OF A NEW MECHANISM TO THE DEVELOPMENT OF PROMISING THERAPIES.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1832. ISSUE 9. P. 1390-1409 | 135 | 67% | 14 |
8 | PETTERSSON, OJ , AAGAARD, L , JENSEN, TG , DAMGAARD, CK , (2015) MOLECULAR MECHANISMS IN DM1-A FOCUS ON FOCI.NUCLEIC ACIDS RESEARCH. VOL. 43. ISSUE 4. P. 2433 -2441 | 78 | 92% | 8 |
9 | KLEIN, AF , DASTIDAR, S , FURLING, D , CHUAH, MK , (2015) THERAPEUTIC APPROACHES FOR DOMINANT MUSCLE DISEASES: HIGHLIGHT ON MYOTONIC DYSTROPHY.CURRENT GENE THERAPY. VOL. 15. ISSUE 4. P. 329 -337 | 87 | 84% | 2 |
10 | JOHNSON, NE , HEATWOLE, CR , (2012) MYOTONIC DYSTROPHY: FROM BENCH TO BEDSIDE.SEMINARS IN NEUROLOGY. VOL. 32. ISSUE 3. P. 246-254 | 80 | 90% | 11 |
Classes with closest relation at Level 1 |