Class information for:
Level 3: GENETICS & HEREDITY//FRAGILE X SYNDROME//AMERICAN JOURNAL OF MEDICAL GENETICS

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
196 53756 34.0 72%


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
395 2             GENETICS & HEREDITY//ANNALES DE GENETIQUE//HOLOPROSENCEPHALY 16816
898 2             TURNER SYNDROME//KLINEFELTER SYNDROME//PREMATURE OVARIAN FAILURE 11325
1566 2             FRAGILE X SYNDROME//RETT SYNDROME//FRAGILE X 7353
2439 2             GENOMIC IMPRINTING//BECKWITH WIEDEMANN SYNDROME//SILVER RUSSELL SYNDROME 4075
2731 2             DOWN SYNDROME//DYRK1A//TS65DN 3262
2900 2             PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A 2794
3091 2             WILLIAMS SYNDROME//WILLIAMS BEUREN SYNDROME//SUPRAVALVULAR AORTIC STENOSIS 2359
3109 2             VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//22Q112 DELETION SYNDROME 2322
3243 2             PSEUDOHYPOPARATHYROIDISM//FAHRS DISEASE//MENINGIOANGIOMATOSIS 1993
3882 2             SOTOS SYNDROME//NSD1//WEAVER SYNDROME 857
4078 2             KABUKI SYNDROME//SCHIMKE IMMUNO OSSEOUS DYSPLASIA//KABUKI MAKE UP SYNDROME 600

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 GENETICS & HEREDITY WoSSC 485206 40% 4% 21299
2 FRAGILE X SYNDROME authKW 478156 2% 80% 1052
3 AMERICAN JOURNAL OF MEDICAL GENETICS journal 461953 5% 31% 2676
4 RETT SYNDROME authKW 414390 2% 85% 861
5 TURNER SYNDROME authKW 410288 2% 79% 915
6 PRADER WILLI SYNDROME authKW 374696 1% 87% 763
7 AMERICAN JOURNAL OF MEDICAL GENETICS PART A journal 332173 3% 32% 1843
8 WILLIAMS SYNDROME authKW 308577 1% 89% 613
9 DOWN SYNDROME authKW 276484 3% 30% 1652
10 GENOMIC IMPRINTING authKW 226912 1% 62% 647

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 485206 40% 4% 21299
2 Obstetrics & Gynecology 36617 9% 2% 4620
3 Pediatrics 26621 9% 1% 4607
4 Education, Special 25480 2% 4% 1232
5 Reproductive Biology 18616 4% 2% 2138
6 Developmental Biology 13473 4% 2% 1905
7 Medical Ethics 9091 1% 4% 448
8 Rehabilitation 8396 3% 1% 1609
9 Andrology 6146 1% 3% 386
10 Cell Biology 5672 7% 1% 3937

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 MED GENET 150276 6% 9% 3231
2 CYTOGENET 106053 1% 25% 750
3 HUMAN GENET 101936 5% 7% 2849
4 CLIN GENET 79784 2% 12% 1202
5 PEDIAT 55350 10% 2% 5405
6 WESSEX REG GENET 44972 0% 44% 180
7 MIND 43278 1% 24% 317
8 GENET 40108 5% 3% 2444
9 MOL HUMAN GENET 37460 1% 11% 593
10 CLIN COMMUNITY HLTH NURSING 24716 0% 37% 118

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 461953 5% 31% 2676
2 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 332173 3% 32% 1843
3 ANNALES DE GENETIQUE 184150 1% 53% 611
4 JOURNAL OF MEDICAL GENETICS 151060 2% 22% 1248
5 CLINICAL GENETICS 139560 2% 22% 1125
6 PRENATAL DIAGNOSIS 123309 2% 20% 1109
7 HUMAN GENETICS 111318 2% 16% 1260
8 GENETIC COUNSELING 94828 1% 42% 398
9 EUROPEAN JOURNAL OF MEDICAL GENETICS 93319 1% 38% 434
10 MOLECULAR CYTOGENETICS 60430 0% 47% 228

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 478156 2% 80% 1052 Search FRAGILE+X+SYNDROME Search FRAGILE+X+SYNDROME
2 RETT SYNDROME 414390 2% 85% 861 Search RETT+SYNDROME Search RETT+SYNDROME
3 TURNER SYNDROME 410288 2% 79% 915 Search TURNER+SYNDROME Search TURNER+SYNDROME
4 PRADER WILLI SYNDROME 374696 1% 87% 763 Search PRADER+WILLI+SYNDROME Search PRADER+WILLI+SYNDROME
5 WILLIAMS SYNDROME 308577 1% 89% 613 Search WILLIAMS+SYNDROME Search WILLIAMS+SYNDROME
6 DOWN SYNDROME 276484 3% 30% 1652 Search DOWN+SYNDROME Search DOWN+SYNDROME
7 GENOMIC IMPRINTING 226912 1% 62% 647 Search GENOMIC+IMPRINTING Search GENOMIC+IMPRINTING
8 MENTAL RETARDATION 216356 2% 34% 1147 Search MENTAL+RETARDATION Search MENTAL+RETARDATION
9 ANGELMAN SYNDROME 175266 1% 85% 365 Search ANGELMAN+SYNDROME Search ANGELMAN+SYNDROME
10 KLINEFELTER SYNDROME 167036 1% 71% 414 Search KLINEFELTER+SYNDROME Search KLINEFELTER+SYNDROME

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. 78-114 228 96% 15
2 CASSIDY, SB , SCHWARTZ, S , MILLER, JL , DRISCOLL, DJ , (2012) PRADER-WILLI SYNDROME.GENETICS IN MEDICINE. VOL. 14. ISSUE 1. P. 10 -26 140 95% 202
3 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
4 MARTENS, MA , WILSON, SJ , REUTENS, DC , (2008) RESEARCH REVIEW: WILLIAMS SYNDROME: A CRITICAL REVIEW OF THE COGNITIVE, BEHAVIORAL, AND NEUROANATOMICAL PHENOTYPE.JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY. VOL. 49. ISSUE 6. P. 576 -608 183 96% 149
5 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 -51 195 96% 0
6 LIYANAGE, VRB , RASTEGAR, M , (2014) RETT SYNDROME AND MECP2.NEUROMOLECULAR MEDICINE. VOL. 16. ISSUE 2. P. 231-264 218 81% 14
7 NISTAL, M , PANIAGUA, R , GONZALEZ-PERAMATO, P , REYES-MUGICA, M , (2016) PERSPECTIVES IN PEDIATRIC PATHOLOGY, CHAPTER 16. KLINEFELTER SYNDROME AND OTHER ANOMALIES IN X AND Y CHROMOSOMES. CLINICAL AND PATHOLOGICAL ENTITIES.PEDIATRIC AND DEVELOPMENTAL PATHOLOGY. VOL. 19. ISSUE 4. P. 259 -277 196 83% 0
8 CHAHROUR, M , ZOGHBI, HY , (2007) THE STORY OF RETT SYNDROME: FROM CLINIC TO NEUROBIOLOGY.NEURON. VOL. 56. ISSUE 3. P. 422-437 114 95% 531
9 BONDY, CA , (2007) CLINICAL PRACTICE GUIDELINE - CARE OF GIRLS AND WOMEN WITH TURNER SYNDROME: A GUIDELINE OF THE TURNER SYNDROME STUDY GROUP.JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 92. ISSUE 1. P. 10 -25 136 91% 325
10 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. 219-245 128 87% 138

Classes with closest relation at Level 3


Rank Class id link
1 563 DNA METHYLATION//EPIGENETICS//METHYLATION
2 453 PRENATAL DIAGNOSIS//NUCHAL TRANSLUCENCY//OBSTETRICS & GYNECOLOGY
3 474 CLEFT PALATE-CRANIOFACIAL JOURNAL//CLEFT PALATE//CRANIOSYNOSTOSIS
4 167 REPRODUCTIVE BIOLOGY//THERIOGENOLOGY//ANDROLOGY
5 71 GENETICS & HEREDITY//CHROMATIN//CELL BIOLOGY
6 113 EDUCATION, SPECIAL//REHABILITATION//AUTISM
7 373 ENDOGENOUS RETROVIRUS//VIROLOGY//JOURNAL OF VIROLOGY
8 625 HYPOSPADIAS//ANORECTAL MALFORMATION//BLADDER EXSTROPHY
9 27 DEVELOPMENTAL BIOLOGY//DEVELOPMENT//AGR2
10 447 TCTP//TRANSLATIONALLY CONTROLLED TUMOR PROTEIN//GENETIC EPIDEMIOLOGY

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