Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
9519 | 1148 | 30.9 | 73% |
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 |
2439 | 2 | GENOMIC IMPRINTING//BECKWITH WIEDEMANN SYNDROME//SILVER RUSSELL SYNDROME | 4075 |
9519 | 1 | SILVER RUSSELL SYNDROME//BECKWITH WIEDEMANN SYNDROME//UNIPARENTAL DISOMY | 1148 |
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 | SILVER RUSSELL SYNDROME | authKW | 2297951 | 9% | 80% | 108 |
2 | BECKWITH WIEDEMANN SYNDROME | authKW | 2257543 | 14% | 52% | 163 |
3 | UNIPARENTAL DISOMY | authKW | 950374 | 10% | 32% | 112 |
4 | RUSSELL SILVER SYNDROME | authKW | 827522 | 3% | 84% | 37 |
5 | MACROGLOSSIA | authKW | 468312 | 4% | 41% | 43 |
6 | WIEDEMANN BECKWITH SYNDROME | authKW | 434411 | 2% | 78% | 21 |
7 | ISODISOMY | authKW | 351728 | 2% | 58% | 23 |
8 | BECKWITH WIEDEMANN | authKW | 284961 | 1% | 71% | 15 |
9 | HETERODISOMY | authKW | 280928 | 1% | 81% | 13 |
10 | TONGUE REDUCTION | authKW | 215435 | 1% | 90% | 9 |
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 | 18909 | 53% | 0% | 608 |
2 | Pediatrics | 2870 | 18% | 0% | 205 |
3 | Dentistry, Oral Surgery & Medicine | 392 | 5% | 0% | 59 |
4 | Obstetrics & Gynecology | 382 | 6% | 0% | 72 |
5 | Endocrinology & Metabolism | 73 | 4% | 0% | 50 |
6 | Otorhinolaryngology | 39 | 2% | 0% | 19 |
7 | Medical Ethics | 30 | 0% | 0% | 4 |
8 | Radiology, Nuclear Medicine & Medical Imaging | 27 | 3% | 0% | 37 |
9 | Pathology | 26 | 2% | 0% | 24 |
10 | Surgery | 22 | 5% | 0% | 55 |
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 | WESSEX GENET SERV | 162906 | 1% | 88% | 7 |
2 | EXPLORAT FONCT ENDOCRINIENNES | 151288 | 1% | 36% | 16 |
3 | CLIN PEDIAT GENET UNIT | 106389 | 0% | 100% | 4 |
4 | MOL GENET EPIGENET | 106377 | 1% | 40% | 10 |
5 | RSS SGA EDUC FUND | 79791 | 0% | 100% | 3 |
6 | IMPRINTING CANC GRP | 65271 | 1% | 27% | 9 |
7 | CLIN PEDIAT GENET | 59842 | 0% | 75% | 3 |
8 | 3 HP | 53194 | 0% | 100% | 2 |
9 | ACT MOL BIOL FETAL DEV | 53194 | 0% | 100% | 2 |
10 | ENDOCRINOL DIABETOL CHILDREN REFERENCE RA | 53194 | 0% | 100% | 2 |
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 PART A | 30215 | 7% | 1% | 81 |
2 | JOURNAL OF MEDICAL GENETICS | 23787 | 6% | 1% | 72 |
3 | AMERICAN JOURNAL OF MEDICAL GENETICS | 18912 | 7% | 1% | 79 |
4 | EUROPEAN JOURNAL OF HUMAN GENETICS | 13426 | 4% | 1% | 43 |
5 | MEDIZINISCHE GENETIK | 9229 | 1% | 4% | 9 |
6 | ANNALES DE GENETIQUE | 6686 | 1% | 1% | 17 |
7 | CLINICAL GENETICS | 5647 | 3% | 1% | 33 |
8 | CLINICAL EPIGENETICS | 5289 | 1% | 2% | 9 |
9 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 5238 | 1% | 1% | 15 |
10 | PRENATAL DIAGNOSIS | 3691 | 2% | 1% | 28 |
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 | SILVER RUSSELL SYNDROME | 2297951 | 9% | 80% | 108 | Search SILVER+RUSSELL+SYNDROME | Search SILVER+RUSSELL+SYNDROME |
2 | BECKWITH WIEDEMANN SYNDROME | 2257543 | 14% | 52% | 163 | Search BECKWITH+WIEDEMANN+SYNDROME | Search BECKWITH+WIEDEMANN+SYNDROME |
3 | UNIPARENTAL DISOMY | 950374 | 10% | 32% | 112 | Search UNIPARENTAL+DISOMY | Search UNIPARENTAL+DISOMY |
4 | RUSSELL SILVER SYNDROME | 827522 | 3% | 84% | 37 | Search RUSSELL+SILVER+SYNDROME | Search RUSSELL+SILVER+SYNDROME |
5 | MACROGLOSSIA | 468312 | 4% | 41% | 43 | Search MACROGLOSSIA | Search MACROGLOSSIA |
6 | WIEDEMANN BECKWITH SYNDROME | 434411 | 2% | 78% | 21 | Search WIEDEMANN+BECKWITH+SYNDROME | Search WIEDEMANN+BECKWITH+SYNDROME |
7 | ISODISOMY | 351728 | 2% | 58% | 23 | Search ISODISOMY | Search ISODISOMY |
8 | BECKWITH WIEDEMANN | 284961 | 1% | 71% | 15 | Search BECKWITH+WIEDEMANN | Search BECKWITH+WIEDEMANN |
9 | HETERODISOMY | 280928 | 1% | 81% | 13 | Search HETERODISOMY | Search HETERODISOMY |
10 | TONGUE REDUCTION | 215435 | 1% | 90% | 9 | Search TONGUE+REDUCTION | Search TONGUE+REDUCTION |
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 | MUSSA, A , RUSSO, S , LARIZZA, L , RICCIO, A , FERRERO, GB , (2016) (EPI)GENOTYPE-PHENOTYPE CORRELATIONS IN BECKWITH-WIEDEMANN SYNDROME: A PARADIGM FOR GENOMIC MEDICINE.CLINICAL GENETICS. VOL. 89. ISSUE 4. P. 403 -415 | 69 | 82% | 5 |
2 | MUSSA, A , DI CANDIA, S , RUSSO, S , CATANIA, S , DE PELLEGRIN, M , DI LUZIO, L , FERRARI, M , TORTORA, C , MEAZZINI, MC , BRUSATI, R , ET AL (2016) RECOMMENDATIONS OF THE SCIENTIFIC COMMITTEE OF THE ITALIAN BECKWITH-WIEDEMANN SYNDROME ASSOCIATION ON THE DIAGNOSIS, MANAGEMENT AND FOLLOW-UP OF THE SYNDROME.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 59. ISSUE 1. P. 52 -64 | 53 | 71% | 4 |
3 | MUSSA, A , RUSSO, S , DE CRESCENZO, A , FRESCHI, A , CALZARI, L , MAITZ, S , MACCHIAIOLO, M , MOLINATTO, C , BALDASSARRE, G , MARIANI, M , ET AL (2016) (EPI)GENOTYPE-PHENOTYPE CORRELATIONS IN BECKWITH-WIEDEMANN SYNDROME.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 24. ISSUE 2. P. 183 -190 | 35 | 83% | 10 |
4 | WEKSBERG, R , SHUMAN, C , BECKWITH, JB , (2010) BECKWITH-WIEDEMANN SYNDROME.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 18. ISSUE 1. P. 8 -14 | 43 | 90% | 154 |
5 | WAKELING, EL , BRIOUDE, F , LOKULO-SODIPE, O , O'CONNELL, SM , SALEM, J , BLIEK, J , CANTON, APM , CHRZANOWSKA, KH , DAVIES, JH , DIAS, RP , ET AL (2017) DIAGNOSIS AND MANAGEMENT OF SILVER-RUSSELL SYNDROME: FIRST INTERNATIONAL CONSENSUS STATEMENT.NATURE REVIEWS ENDOCRINOLOGY. VOL. 13. ISSUE 2. P. 105 -124 | 77 | 58% | 0 |
6 | ISHIDA, M , (2016) NEW DEVELOPMENTS IN SILVER-RUSSELL SYNDROME AND IMPLICATIONS FOR CLINICAL PRACTICE.EPIGENOMICS. VOL. 8. ISSUE 4. P. 563 -580 | 63 | 71% | 0 |
7 | EGGERMANN, T , SPENGLER, S , GOGIEL, M , BEGEMANN, M , ELBRACHT, M , (2012) EPIGENETIC AND GENETIC DIAGNOSIS OF SILVER-RUSSELL SYNDROME.EXPERT REVIEW OF MOLECULAR DIAGNOSTICS. VOL. 12. ISSUE 5. P. 459 -471 | 46 | 92% | 13 |
8 | EGGERMANN, T , (2010) RUSSELL-SILVER SYNDROME.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 154C. ISSUE 3. P. 355-364 | 41 | 98% | 47 |
9 | AZZI, S , HABIB, WA , NETCHINE, I , (2014) BECKWITH-WIEDEMANN AND RUSSELL-SILVER SYNDROMES: FROM NEW MOLECULAR INSIGHTS TO THE COMPREHENSION OF IMPRINTING REGULATION.CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY. VOL. 21. ISSUE 1. P. 30 -38 | 48 | 70% | 18 |
10 | RUSSO, S , CALZARI, L , MUSSA, A , MAININI, E , CASSINA, M , DI CANDIA, S , CLEMENTI, M , GUZZETTI, S , TABANO, S , MIOZZO, M , ET AL (2016) A MULTI-METHOD APPROACH TO THE MOLECULAR DIAGNOSIS OF OVERT AND BORDERLINE 11P15.5 DEFECTS UNDERLYING SILVER-RUSSELL AND BECKWITH-WIEDEMANN SYNDROMES.CLINICAL EPIGENETICS. VOL. 8. ISSUE . P. - | 35 | 90% | 1 |
Classes with closest relation at Level 1 |