Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
277 | 3747 | 43.9 | 81% |
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 |
196 | 3 | GENETICS & HEREDITY//FRAGILE X SYNDROME//AMERICAN JOURNAL OF MEDICAL GENETICS | 53756 |
1566 | 2 | FRAGILE X SYNDROME//RETT SYNDROME//FRAGILE X | 7353 |
277 | 1 | FRAGILE X SYNDROME//FRAGILE X//FMR1 | 3747 |
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 | FRAGILE X SYNDROME | authKW | 6198800 | 27% | 76% | 998 |
2 | FRAGILE X | authKW | 2008829 | 9% | 76% | 326 |
3 | FMR1 | authKW | 1848534 | 7% | 81% | 281 |
4 | FMRP | authKW | 1413020 | 6% | 80% | 216 |
5 | FMR1 GENE | authKW | 1099156 | 4% | 92% | 146 |
6 | FXTAS | authKW | 833707 | 3% | 90% | 114 |
7 | PREMUTATION | authKW | 829603 | 3% | 92% | 111 |
8 | CGG REPEAT | authKW | 637803 | 2% | 94% | 83 |
9 | MIND | address | 407117 | 7% | 20% | 255 |
10 | FRAGILE X PREMUTATION | authKW | 344791 | 1% | 92% | 46 |
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 | 38198 | 42% | 0% | 1574 |
2 | Education, Special | 6187 | 4% | 1% | 157 |
3 | Neurosciences | 4464 | 22% | 0% | 818 |
4 | Rehabilitation | 1680 | 5% | 0% | 179 |
5 | Psychology, Developmental | 1588 | 4% | 0% | 146 |
6 | Clinical Neurology | 852 | 8% | 0% | 302 |
7 | Psychiatry | 831 | 6% | 0% | 241 |
8 | Behavioral Sciences | 648 | 3% | 0% | 128 |
9 | Pediatrics | 454 | 5% | 0% | 180 |
10 | Biochemistry & Molecular Biology | 321 | 12% | 0% | 464 |
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 | MIND | 407117 | 7% | 20% | 255 |
2 | CBG CLIN GENET | 195761 | 1% | 83% | 29 |
3 | BIOCHEM MOL MED | 183788 | 5% | 12% | 188 |
4 | CYTOMOL DIAGNOST | 114064 | 0% | 100% | 14 |
5 | MED INVEST NEURODEV DISORDERS MIND | 98112 | 1% | 38% | 32 |
6 | INTERDISCIPLINARY BRAIN SCI | 70814 | 1% | 23% | 38 |
7 | FRAGILE X TREATMENT | 57032 | 0% | 100% | 7 |
8 | PEDIAT NEUROL SCI BIOCHEM | 54990 | 0% | 75% | 9 |
9 | MED INVEST NEURODEV DISORDERS | 50741 | 0% | 35% | 18 |
10 | IST NEUROSCI SPERIMENTALI | 41899 | 0% | 86% | 6 |
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 | AMERICAN JOURNAL OF MEDICAL GENETICS | 194606 | 12% | 5% | 457 |
2 | JOURNAL OF NEURODEVELOPMENTAL DISORDERS | 38033 | 1% | 13% | 35 |
3 | AJIDD-AMERICAN JOURNAL ON INTELLECTUAL AND DEVELOPMENTAL DISABILITIES | 20276 | 1% | 10% | 26 |
4 | DEVELOPMENTAL BRAIN DYSFUNCTION | 19237 | 0% | 13% | 18 |
5 | HUMAN GENETICS | 18754 | 4% | 2% | 136 |
6 | JOURNAL OF MEDICAL GENETICS | 12310 | 3% | 2% | 94 |
7 | HUMAN MOLECULAR GENETICS | 12271 | 3% | 1% | 122 |
8 | CLINICAL GENETICS | 11993 | 2% | 2% | 87 |
9 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 10080 | 2% | 1% | 85 |
10 | AMERICAN JOURNAL OF HUMAN GENETICS | 9015 | 3% | 1% | 95 |
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 | FRAGILE X SYNDROME | 6198800 | 27% | 76% | 998 | Search FRAGILE+X+SYNDROME | Search FRAGILE+X+SYNDROME |
2 | FRAGILE X | 2008829 | 9% | 76% | 326 | Search FRAGILE+X | Search FRAGILE+X |
3 | FMR1 | 1848534 | 7% | 81% | 281 | Search FMR1 | Search FMR1 |
4 | FMRP | 1413020 | 6% | 80% | 216 | Search FMRP | Search FMRP |
5 | FMR1 GENE | 1099156 | 4% | 92% | 146 | Search FMR1+GENE | Search FMR1+GENE |
6 | FXTAS | 833707 | 3% | 90% | 114 | Search FXTAS | Search FXTAS |
7 | PREMUTATION | 829603 | 3% | 92% | 111 | Search PREMUTATION | Search PREMUTATION |
8 | CGG REPEAT | 637803 | 2% | 94% | 83 | Search CGG+REPEAT | Search CGG+REPEAT |
9 | FRAGILE X PREMUTATION | 344791 | 1% | 92% | 46 | Search FRAGILE+X+PREMUTATION | Search FRAGILE+X+PREMUTATION |
10 | FRAXA | 335598 | 1% | 94% | 44 | Search FRAXA | Search FRAXA |
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 | LOESCH, D , HAGERMAN, R , (2012) UNSTABLE MUTATIONS IN THE FMR1 GENE AND THE PHENOTYPES.TANDEM REPEAT POLYMORPHISMS: GENETIC PLASTICITY, NEURAL DIVERSITY AND DISEASE. VOL. 769. ISSUE . P. 78-114 | 227 | 95% | 15 |
2 | GROSS, C , HOFFMANN, A , BASSELL, GJ , BERRY-KRAVIS, EM , (2015) THERAPEUTIC STRATEGIES IN FRAGILE X SYNDROME: FROM BENCH TO BEDSIDE AND BACK.NEUROTHERAPEUTICS. VOL. 12. ISSUE 3. P. 584 -608 | 198 | 90% | 7 |
3 | SANTORO, MR , BRAY, SM , WARREN, ST , (2012) MOLECULAR MECHANISMS OF FRAGILE X SYNDROME: A TWENTY-YEAR PERSPECTIVE.ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 7. VOL. 7. ISSUE . P. 219-245 | 126 | 86% | 138 |
4 | DE RUBEIS, S , FERNANDEZ, E , BUZZI, A , DI MARINO, D , BAGNI, C , (2012) MOLECULAR AND CELLULAR ASPECTS OF MENTAL RETARDATION IN THE FRAGILE X SYNDROME: FROM GENE MUTATION/S TO SPINE DYSMORPHOGENESIS.SYNAPTIC PLASTICITY: DYNAMICS, DEVELOPMENT AND DISEASE. VOL. 970. ISSUE . P. 517-551 | 179 | 84% | 15 |
5 | COOK, D , NURO, E , MURAI, KK , (2014) INCREASING OUR UNDERSTANDING OF HUMAN COGNITION THROUGH THE STUDY OF FRAGILE X SYNDROME.DEVELOPMENTAL NEUROBIOLOGY. VOL. 74. ISSUE 2. P. 147-177 | 227 | 63% | 7 |
6 | SETHNA, F , MOON, C , WANG, HB , (2014) FROM FMRP FUNCTION TO POTENTIAL THERAPIES FOR FRAGILE X SYNDROME.NEUROCHEMICAL RESEARCH. VOL. 39. ISSUE 6. P. 1016-1031 | 151 | 86% | 5 |
7 | RAJAN-BABU, IS , CHONG, SS , (2016) MOLECULAR CORRELATES AND RECENT ADVANCEMENTS IN THE DIAGNOSIS AND SCREENING OF FMR1-RELATED DISORDERS.GENES. VOL. 7. ISSUE 10. P. - | 138 | 95% | 0 |
8 | GALLAGHER, A , HALLAHAN, B , (2012) FRAGILE X-ASSOCIATED DISORDERS: A CLINICAL OVERVIEW.JOURNAL OF NEUROLOGY. VOL. 259. ISSUE 3. P. 401-413 | 124 | 91% | 38 |
9 | BAGNI, C , OOSTRA, BA , (2013) FRAGILE X SYNDROME: FROM PROTEIN FUNCTION TO THERAPY.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 161. ISSUE 11. P. 2809-2821 | 132 | 84% | 27 |
10 | HAGERMAN, PJ , HAGERMAN, RJ , (2015) FRAGILE X-ASSOCIATED TREMOR/ATAXIA SYNDROME.YEAR IN NEUROLOGY AND PSYCHIATRY. VOL. 1338. ISSUE . P. 58 -70 | 109 | 82% | 23 |
Classes with closest relation at Level 1 |