Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
15871 | 687 | 36.9 | 79% |
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 |
180 | 3 | DUCHENNE MUSCULAR DYSTROPHY//DYSTROPHIN//MUSCULAR DYSTROPHY | 56784 |
991 | 2 | DUCHENNE MUSCULAR DYSTROPHY//DYSTROPHIN//MUSCULAR DYSTROPHY | 10483 |
15871 | 1 | FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY//FSHD//DUX4 | 687 |
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 | FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY | authKW | 4570908 | 19% | 77% | 133 |
2 | FSHD | authKW | 2765734 | 11% | 84% | 74 |
3 | DUX4 | authKW | 1521161 | 5% | 93% | 37 |
4 | D4Z4 | authKW | 1294320 | 5% | 94% | 31 |
5 | FACIOSCAPULOHUMERAL DYSTROPHY | authKW | 916978 | 4% | 74% | 28 |
6 | SMCHD1 | authKW | 457156 | 2% | 86% | 12 |
7 | FACIOSCAPULOHUMERAL | authKW | 448163 | 2% | 92% | 11 |
8 | FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY FSHD | authKW | 426677 | 2% | 80% | 12 |
9 | 4Q35 | authKW | 311123 | 1% | 100% | 7 |
10 | FSHD1 | authKW | 311123 | 1% | 100% | 7 |
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 | Genetics & Heredity | 5323 | 37% | 0% | 253 |
2 | Clinical Neurology | 4593 | 36% | 0% | 247 |
3 | Neurosciences | 883 | 23% | 0% | 155 |
4 | Biochemistry & Molecular Biology | 303 | 21% | 0% | 145 |
5 | Cell Biology | 131 | 9% | 0% | 62 |
6 | Biotechnology & Applied Microbiology | 124 | 7% | 0% | 49 |
7 | Rehabilitation | 42 | 2% | 0% | 14 |
8 | Cell & Tissue Engineering | 33 | 1% | 0% | 5 |
9 | Pediatrics | 30 | 3% | 0% | 23 |
10 | Medicine, Research & Experimental | 22 | 3% | 0% | 23 |
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 | WELLSTONE PROGRAM | 272230 | 1% | 88% | 7 |
2 | LAZIO SECT | 133338 | 0% | 100% | 3 |
3 | INSERM UMR S MED GENET FUNCT GENOM 910 | 88892 | 0% | 100% | 2 |
4 | INT PHD PROGRAM CELLULAR MOL BIOL | 88892 | 0% | 100% | 2 |
5 | NEUROL PATHOL HUMAN GENET | 88892 | 0% | 100% | 2 |
6 | UMR 5239UCBL1IFR128 | 88892 | 0% | 100% | 2 |
7 | REFERENCE MALAD NEUROMUSCULAI | 84010 | 2% | 13% | 15 |
8 | MEDEX | 80001 | 0% | 60% | 3 |
9 | NEUROMUSCULAR BIOL DIS GRP | 79362 | 1% | 36% | 5 |
10 | HUMAN CLIN GENET | 64673 | 5% | 4% | 35 |
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 | 49135 | 7% | 2% | 51 |
2 | MUSCLE & NERVE | 10019 | 6% | 1% | 40 |
3 | SKELETAL MUSCLE | 8279 | 1% | 3% | 6 |
4 | HUMAN MOLECULAR GENETICS | 5233 | 5% | 0% | 34 |
5 | JOURNAL OF MEDICAL GENETICS | 4035 | 3% | 0% | 23 |
6 | AMERICAN JOURNAL OF HUMAN GENETICS | 3427 | 4% | 0% | 25 |
7 | NEUROLOGY | 2678 | 5% | 0% | 36 |
8 | EUROPEAN JOURNAL OF HUMAN GENETICS | 1734 | 2% | 0% | 12 |
9 | ANNALS OF NEUROLOGY | 1098 | 2% | 0% | 14 |
10 | CURRENT OPINION IN NEUROLOGY | 1087 | 1% | 0% | 7 |
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 | FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY | 4570908 | 19% | 77% | 133 | Search FACIOSCAPULOHUMERAL+MUSCULAR+DYSTROPHY | Search FACIOSCAPULOHUMERAL+MUSCULAR+DYSTROPHY |
2 | FSHD | 2765734 | 11% | 84% | 74 | Search FSHD | Search FSHD |
3 | DUX4 | 1521161 | 5% | 93% | 37 | Search DUX4 | Search DUX4 |
4 | D4Z4 | 1294320 | 5% | 94% | 31 | Search D4Z4 | Search D4Z4 |
5 | FACIOSCAPULOHUMERAL DYSTROPHY | 916978 | 4% | 74% | 28 | Search FACIOSCAPULOHUMERAL+DYSTROPHY | Search FACIOSCAPULOHUMERAL+DYSTROPHY |
6 | SMCHD1 | 457156 | 2% | 86% | 12 | Search SMCHD1 | Search SMCHD1 |
7 | FACIOSCAPULOHUMERAL | 448163 | 2% | 92% | 11 | Search FACIOSCAPULOHUMERAL | Search FACIOSCAPULOHUMERAL |
8 | FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY FSHD | 426677 | 2% | 80% | 12 | Search FACIOSCAPULOHUMERAL+MUSCULAR+DYSTROPHY+FSHD | Search FACIOSCAPULOHUMERAL+MUSCULAR+DYSTROPHY+FSHD |
9 | 4Q35 | 311123 | 1% | 100% | 7 | Search 4Q35 | Search 4Q35 |
10 | FSHD1 | 311123 | 1% | 100% | 7 | Search FSHD1 | Search FSHD1 |
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 | TAWIL, R , VAN DER MAAREL, SM , TAPSCOTT, SJ , (2014) FACIOSCAPULOHUMERAL DYSTROPHY: THE PATH TO CONSENSUS ON PATHOPHYSIOLOGY.SKELETAL MUSCLE. VOL. 4. ISSUE . P. - | 100 | 86% | 31 |
2 | RICCI, G , ZATZ, M , TUPLER, R , (2014) FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY: MORE COMPLEX THAN IT APPEARS.CURRENT MOLECULAR MEDICINE. VOL. 14. ISSUE 8. P. 1052 -1068 | 98 | 89% | 2 |
3 | GATICA, LV , ROSA, AL , (2016) A COMPLEX INTERPLAY OF GENETIC AND EPIGENETIC EVENTS LEADS TO ABNORMAL EXPRESSION OF THE DUX4 GENE IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY.NEUROMUSCULAR DISORDERS. VOL. 26. ISSUE 12. P. 844 -852 | 92 | 84% | 0 |
4 | LEK, A , RAHIMOV, F , JONES, PL , KUNKEL, LM , (2015) EMERGING PRECLINICAL ANIMAL MODELS FOR FSHD.TRENDS IN MOLECULAR MEDICINE. VOL. 21. ISSUE 5. P. 295 -306 | 63 | 95% | 7 |
5 | RICHARDS, M , COPPEE, F , THOMAS, N , BELAYEW, A , UPADHYAYA, M , (2012) FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY (FSHD): AN ENIGMA UNRAVELLED?.HUMAN GENETICS. VOL. 131. ISSUE 3. P. 325 -340 | 73 | 87% | 22 |
6 | CABIANCA, DS , GABELLINI, D , (2010) FSHD: COPY NUMBER VARIATIONS ON THE THEME OF MUSCULAR DYSTROPHY.JOURNAL OF CELL BIOLOGY. VOL. 191. ISSUE 6. P. 1049-1060 | 96 | 71% | 24 |
7 | HEWITT, JE , (2015) LOSS OF EPIGENETIC SILENCING OF THE DUX4 TRANSCRIPTION FACTOR GENE IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY.HUMAN MOLECULAR GENETICS. VOL. 24. ISSUE . P. R17 -R23 | 68 | 87% | 4 |
8 | SACCONI, S , SALVIATI, L , DESNUELLE, C , (2015) FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1852. ISSUE 4. P. 607 -614 | 64 | 93% | 3 |
9 | SALORT-CAMPANA, E , NGUYEN, K , LEVY, N , POUGET, J , ATTARIAN, S , (2013) CLINICAL AND MOLECULAR DIAGNOSIS OF FACIOSCAPULOHUMERAL DYSTROPHY TYPE 1 (FSHD1) IN 2012.REVUE NEUROLOGIQUE. VOL. 169. ISSUE 8-9. P. 573-582 | 75 | 85% | 0 |
10 | HIMEDA, CL , JONES, TI , JONES, PL , (2015) FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY AS A MODEL FOR EPIGENETIC REGULATION AND DISEASE.ANTIOXIDANTS & REDOX SIGNALING. VOL. 22. ISSUE 16. P. 1463 -1482 | 98 | 58% | 3 |
Classes with closest relation at Level 1 |