Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
4780 | 1654 | 35.6 | 79% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
2321 | 4046 | VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//PSEUDOHYPOPARATHYROIDISM |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | VELOCARDIOFACIAL SYNDROME | Author keyword | 278 | 74% | 13% | 208 |
2 | DIGEORGE SYNDROME | Author keyword | 245 | 64% | 15% | 242 |
3 | VELO CARDIO FACIAL SYNDROME | Author keyword | 121 | 75% | 5% | 86 |
4 | 22Q112 DELETION SYNDROME | Author keyword | 112 | 70% | 6% | 93 |
5 | 22Q11 DELETION SYNDROME | Author keyword | 109 | 78% | 4% | 73 |
6 | 22Q11 DELETION | Author keyword | 91 | 73% | 4% | 69 |
7 | 22Q112 DELETION | Author keyword | 87 | 78% | 3% | 57 |
8 | VCFS | Author keyword | 58 | 73% | 3% | 45 |
9 | 22Q11 | Author keyword | 58 | 66% | 3% | 54 |
10 | 22Q112 | Author keyword | 32 | 68% | 2% | 28 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | VELOCARDIOFACIAL SYNDROME | 278 | 74% | 13% | 208 | Search VELOCARDIOFACIAL+SYNDROME | Search VELOCARDIOFACIAL+SYNDROME |
2 | DIGEORGE SYNDROME | 245 | 64% | 15% | 242 | Search DIGEORGE+SYNDROME | Search DIGEORGE+SYNDROME |
3 | VELO CARDIO FACIAL SYNDROME | 121 | 75% | 5% | 86 | Search VELO+CARDIO+FACIAL+SYNDROME | Search VELO+CARDIO+FACIAL+SYNDROME |
4 | 22Q112 DELETION SYNDROME | 112 | 70% | 6% | 93 | Search 22Q112+DELETION+SYNDROME | Search 22Q112+DELETION+SYNDROME |
5 | 22Q11 DELETION SYNDROME | 109 | 78% | 4% | 73 | Search 22Q11+DELETION+SYNDROME | Search 22Q11+DELETION+SYNDROME |
6 | 22Q11 DELETION | 91 | 73% | 4% | 69 | Search 22Q11+DELETION | Search 22Q11+DELETION |
7 | 22Q112 DELETION | 87 | 78% | 3% | 57 | Search 22Q112+DELETION | Search 22Q112+DELETION |
8 | VCFS | 58 | 73% | 3% | 45 | Search VCFS | Search VCFS |
9 | 22Q11 | 58 | 66% | 3% | 54 | Search 22Q11 | Search 22Q11 |
10 | 22Q112 | 32 | 68% | 2% | 28 | Search 22Q112 | Search 22Q112 |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | CARDIO FACIAL SYNDROME | 636 | 60% | 42% | 694 |
2 | VELOCARDIOFACIAL SYNDROME | 516 | 76% | 22% | 359 |
3 | CHROMOSOME 22Q11 | 246 | 79% | 9% | 155 |
4 | DIGEORGE SYNDROME | 236 | 47% | 22% | 370 |
5 | DIGEORGE VELOCARDIOFACIAL SYNDROME | 104 | 90% | 3% | 45 |
6 | ANOMALY FACE SYNDROME | 79 | 79% | 3% | 50 |
7 | CHROMOSOME 22Q112 | 75 | 80% | 3% | 47 |
8 | FUNCTIONAL COMT POLYMORPHISM | 68 | 100% | 1% | 22 |
9 | SYNDROME VCFS | 68 | 100% | 1% | 22 |
10 | MICRODELETIONS | 64 | 30% | 11% | 176 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes | 2007 | 183 | 117 | 82% |
Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome | 2014 | 17 | 51 | 63% |
Velo-cardio-facial syndrome: 30 Years of study | 2008 | 144 | 52 | 85% |
Practical guidelines for managing adults with 22q11.2 deletion syndrome | 2015 | 2 | 61 | 85% |
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia | 2010 | 125 | 169 | 50% |
Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion Syndrome | 2010 | 65 | 77 | 73% |
The 22q11.2 Deletion Syndrome as a Window into Complex Neuropsychiatric Disorders Over the Lifespan | 2014 | 10 | 97 | 64% |
Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome? | 2012 | 18 | 58 | 84% |
Immunological aspects of 22q11.2 deletion syndrome | 2012 | 23 | 88 | 64% |
Schizophrenia and velo-cardio-facial syndrome | 2002 | 156 | 36 | 58% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | CLIN GENET PROGRAM | 21 | 41% | 2.4% | 39 |
2 | DIAG TREATMENT STUDY VELOCARDIO IAL SYNDR | 11 | 100% | 0.4% | 6 |
3 | HUMAN GENET MOL BIOL | 7 | 15% | 2.5% | 41 |
4 | BEHAV NEUROGENET | 5 | 26% | 1.1% | 18 |
5 | COMMUN DISORDER UNIT | 4 | 67% | 0.2% | 4 |
6 | SERV MEDICOPEDAGOG | 4 | 75% | 0.2% | 3 |
7 | ADOLESCENCE CLIN PSYCHOL UNIT | 4 | 40% | 0.5% | 8 |
8 | DALGLISH FAMILY HEARTS MINDS CLIN DELET SYNDROM | 3 | 100% | 0.2% | 3 |
9 | HUMAN GENET LEUVEN | 3 | 100% | 0.2% | 3 |
10 | SERV MED MOL | 3 | 100% | 0.2% | 3 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000107978 | HDR SYNDROME//KENNY CAFFEY SYNDROME//HYPOPARATHYROIDISM |
2 | 0.0000094030 | HYPERPROLINEMIA//HYPERPROLINEMIA TYPE II//SUPERIOR MESENTERIC FLOW |
3 | 0.0000073120 | CAT EYE SYNDROME//SUPERNUMERARY MARKER CHROMOSOMES//SMALL SUPERNUMERARY MARKER CHROMOSOME |
4 | 0.0000070946 | SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5 |
5 | 0.0000066375 | ABSENT PULMONARY VALVE//ABSENT PULMONARY VALVE SYNDROME//ABSENT AORTIC VALVE |
6 | 0.0000066013 | DIRECTORATE CHILD WOMENS HLTH//THYMIC INDEX//FETAL THYMUS |
7 | 0.0000061662 | INTERRUPTED AORTIC ARCH//AORTOPULMONARY WINDOW//HEMITRUNCUS |
8 | 0.0000059683 | HEART DEVELOPMENT//SECOND HEART FIELD//NKX2 5 |
9 | 0.0000056219 | HOLT ORAM SYNDROME//TBX3//TBX2 |
10 | 0.0000055357 | EOSINOPHILIC ULCER//RIGA FEDE DISEASE//NEONATAL TEETH |