Class information for:
Level 2: FRAGILE X SYNDROME//RETT SYNDROME//FRAGILE X

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
1566 7353 40.5 82%


Bar chart of Publication_year

Last years might be incomplete

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
2548 1                   RETT SYNDROME//MECP2//CDKL5 2211
8667 1                   X LINKED MENTAL RETARDATION//XLMR//PQBP1 1230
30657 1                   KBG SYNDROME//AARSKOG SCOTT SYNDROME//FGD1 165

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 3208701 14% 77% 1006
2 RETT SYNDROME authKW 2900714 11% 83% 841
3 FRAGILE X authKW 1074214 5% 77% 334
4 MECP2 authKW 1039120 5% 70% 357
5 FMR1 authKW 961936 4% 82% 284
6 FMRP authKW 726529 3% 81% 217
7 X LINKED MENTAL RETARDATION authKW 564977 2% 74% 183
8 FMR1 GENE authKW 559973 2% 92% 146
9 FXTAS authKW 424735 2% 90% 114
10 PREMUTATION authKW 422647 2% 92% 111

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 72220 41% 1% 3034
2 Clinical Neurology 7347 15% 0% 1101
3 Neurosciences 6144 19% 0% 1380
4 Education, Special 5843 3% 1% 216
5 Pediatrics 4105 9% 0% 664
6 Rehabilitation 2122 4% 0% 288
7 Psychology, Developmental 1834 3% 0% 225
8 Psychiatry 928 5% 0% 379
9 Biochemistry & Molecular Biology 884 14% 0% 1004
10 Behavioral Sciences 530 2% 0% 175

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 212122 4% 20% 258
2 WESTERN SYDNEY GENET PROGRAM 105524 1% 40% 64
3 CBG CLIN GENET 99729 0% 83% 29
4 BIOCHEM MOL MED 93472 3% 12% 188
5 RETT SYNDROME 66642 0% 94% 17
6 RETT 58369 0% 94% 15
7 CYTOMOL DIAGNOST 58112 0% 100% 14
8 GENET DISORDERS COGNIT BEHAV 51494 0% 56% 22
9 MED INVEST NEURODEV DISORDERS MIND 49966 0% 38% 32
10 GENET EPIGENET CONTROL GENE EXP S 41852 0% 92% 11

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 239746 10% 8% 711
2 BRAIN & DEVELOPMENT 71813 3% 7% 251
3 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 46495 3% 4% 255
4 JOURNAL OF NEURODEVELOPMENTAL DISORDERS 37959 1% 19% 49
5 JOURNAL OF MEDICAL GENETICS 29587 3% 4% 204
6 HUMAN MOLECULAR GENETICS 23593 3% 2% 237
7 CLINICAL GENETICS 22511 2% 3% 167
8 EUROPEAN JOURNAL OF HUMAN GENETICS 16463 2% 3% 121
9 HUMAN GENETICS 16438 2% 2% 179
10 AMERICAN JOURNAL OF HUMAN GENETICS 14856 2% 2% 171

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 3208701 14% 77% 1006 Search FRAGILE+X+SYNDROME Search FRAGILE+X+SYNDROME
2 RETT SYNDROME 2900714 11% 83% 841 Search RETT+SYNDROME Search RETT+SYNDROME
3 FRAGILE X 1074214 5% 77% 334 Search FRAGILE+X Search FRAGILE+X
4 MECP2 1039120 5% 70% 357 Search MECP2 Search MECP2
5 FMR1 961936 4% 82% 284 Search FMR1 Search FMR1
6 FMRP 726529 3% 81% 217 Search FMRP Search FMRP
7 X LINKED MENTAL RETARDATION 564977 2% 74% 183 Search X+LINKED+MENTAL+RETARDATION Search X+LINKED+MENTAL+RETARDATION
8 FMR1 GENE 559973 2% 92% 146 Search FMR1+GENE Search FMR1+GENE
9 FXTAS 424735 2% 90% 114 Search FXTAS Search FXTAS
10 PREMUTATION 422647 2% 92% 111 Search PREMUTATION Search PREMUTATION

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 LIYANAGE, VRB , RASTEGAR, M , (2014) RETT SYNDROME AND MECP2.NEUROMOLECULAR MEDICINE. VOL. 16. ISSUE 2. P. 231-264 217 80% 14
4 LEONARD, H , COBB, S , DOWNS, J , (2017) CLINICAL AND BIOLOGICAL PROGRESS OVER 50 YEARS IN RETT SYNDROME.NATURE REVIEWS NEUROLOGY. VOL. 13. ISSUE 1. P. 37 -51 193 95% 0
5 CHAHROUR, M , ZOGHBI, HY , (2007) THE STORY OF RETT SYNDROME: FROM CLINIC TO NEUROBIOLOGY.NEURON. VOL. 56. ISSUE 3. P. 422-437 113 94% 531
6 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. 219-245 127 86% 138
7 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
8 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
9 LOMBARDI, LM , BAKER, SA , ZOGHBI, HY , (2015) MECP2 DISORDERS: FROM THE CLINIC TO MICE AND BACK.JOURNAL OF CLINICAL INVESTIGATION. VOL. 125. ISSUE 8. P. 2914 -2923 117 87% 24
10 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

Classes with closest relation at Level 2


Rank Class id link
1 3091 WILLIAMS SYNDROME//WILLIAMS BEUREN SYNDROME//SUPRAVALVULAR AORTIC STENOSIS
2 2900 PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A
3 2606 FHIT//WWOX//FRAGILE SITES
4 493 AUTISM//JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS//AUTISM SPECTRUM DISORDER
5 891 POSTSYNAPTIC DENSITY//LONG TERM POTENTIATION//SYNAPTIC PLASTICITY
6 898 TURNER SYNDROME//KLINEFELTER SYNDROME//PREMATURE OVARIAN FAILURE
7 3382 LISSENCEPHALY//SECKEL SYNDROME//LIS1
8 395 GENETICS & HEREDITY//ANNALES DE GENETIQUE//HOLOPROSENCEPHALY
9 2731 DOWN SYNDROME//DYRK1A//TS65DN
10 3882 SOTOS SYNDROME//NSD1//WEAVER SYNDROME

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