Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
17533 | 531 | 22.3 | 63% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
409 | 16055 | WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE |
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 | WOLF HIRSCHHORN SYNDROME | Author keyword | 217 | 85% | 21% | 114 |
2 | 4P DELETION | Author keyword | 65 | 95% | 4% | 21 |
3 | PITT ROGERS DANKS SYNDROME | Author keyword | 23 | 100% | 2% | 10 |
4 | 4Q DELETION | Author keyword | 18 | 89% | 2% | 8 |
5 | WOLF HIRSCHHORN | Author keyword | 18 | 89% | 2% | 8 |
6 | 4Q DELETION SYNDROME | Author keyword | 17 | 100% | 2% | 8 |
7 | LETM1 | Author keyword | 17 | 75% | 2% | 12 |
8 | 4Q SYNDROME | Author keyword | 15 | 82% | 2% | 9 |
9 | WHS | Author keyword | 15 | 88% | 1% | 7 |
10 | 4P SYNDROME | Author keyword | 14 | 100% | 1% | 7 |
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 | WOLF HIRSCHHORN SYNDROME | 217 | 85% | 21% | 114 | Search WOLF+HIRSCHHORN+SYNDROME | Search WOLF+HIRSCHHORN+SYNDROME |
2 | 4P DELETION | 65 | 95% | 4% | 21 | Search 4P+DELETION | Search 4P+DELETION |
3 | PITT ROGERS DANKS SYNDROME | 23 | 100% | 2% | 10 | Search PITT+ROGERS+DANKS+SYNDROME | Search PITT+ROGERS+DANKS+SYNDROME |
4 | 4Q DELETION | 18 | 89% | 2% | 8 | Search 4Q+DELETION | Search 4Q+DELETION |
5 | WOLF HIRSCHHORN | 18 | 89% | 2% | 8 | Search WOLF+HIRSCHHORN | Search WOLF+HIRSCHHORN |
6 | 4Q DELETION SYNDROME | 17 | 100% | 2% | 8 | Search 4Q+DELETION+SYNDROME | Search 4Q+DELETION+SYNDROME |
7 | LETM1 | 17 | 75% | 2% | 12 | Search LETM1 | Search LETM1 |
8 | 4Q SYNDROME | 15 | 82% | 2% | 9 | Search 4Q+SYNDROME | Search 4Q+SYNDROME |
9 | WHS | 15 | 88% | 1% | 7 | Search WHS | Search WHS |
10 | 4P SYNDROME | 14 | 100% | 1% | 7 | Search 4P+SYNDROME | Search 4P+SYNDROME |
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 | 4P SYNDROME | 76 | 100% | 5% | 24 |
2 | WHS CRITICAL REGION | 40 | 82% | 4% | 23 |
3 | ROGERS DANKS SYNDROME | 35 | 86% | 3% | 18 |
4 | 4Q SYNDROME | 35 | 81% | 4% | 21 |
5 | PARTIAL TRISOMY 4Q | 24 | 82% | 3% | 14 |
6 | WHS | 18 | 89% | 2% | 8 |
7 | WOLF HIRSCHHORN SYNDROME | 16 | 23% | 11% | 59 |
8 | CHROMOSOME 4 | 15 | 19% | 13% | 71 |
9 | DEL4Q12Q211 | 12 | 86% | 1% | 6 |
10 | SYNDROME WHS | 12 | 86% | 1% | 6 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature | 2014 | 4 | 41 | 44% |
The etiology of Wolf-Hirschhorn syndrome | 2005 | 79 | 58 | 33% |
Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature | 2012 | 4 | 43 | 81% |
Seizure and EEG patterns in Wolf-Hirschhorn (4p-) syndrome | 2005 | 16 | 23 | 87% |
Clinical and Genomic Characterization of Distal Duplications and Deletions of Chromosome 4q: Study of Two Cases and Review of the Literature | 2009 | 19 | 21 | 62% |
CLINICAL MANIFESTATIONS OF TRISOMY 4P SYNDROME | 1995 | 38 | 22 | 77% |
Del(4)(pter->q33:) case report and review of the literature | 1997 | 11 | 6 | 100% |
Mild phenotype in interstitial 4p deletion: Another patient and review of the literature | 1997 | 8 | 12 | 92% |
Wolf-Hirschhorn syndrome and infantile epileptic encephalopathy. Case report and literature review | 2007 | 0 | 21 | 86% |
Wolf-Hirschhorn syndrome - Review of the literature and three case studies | 1998 | 4 | 15 | 100% |
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 DYSMORPHOL UNIT | 4 | 75% | 0.6% | 3 |
2 | CYTOGENET MICROARRAY S | 2 | 67% | 0.4% | 2 |
3 | CLIN PEDIAT GD DE MARCHI | 2 | 50% | 0.6% | 3 |
4 | UNITA OSPED PATOL NEONATALE | 1 | 100% | 0.4% | 2 |
5 | CANC MED SCI MED | 1 | 50% | 0.2% | 1 |
6 | DAEJEON REG CANC MED SCI | 1 | 50% | 0.2% | 1 |
7 | HPSERV PEDIAT | 1 | 50% | 0.2% | 1 |
8 | IST SCI STELLA MARIS | 1 | 50% | 0.2% | 1 |
9 | MALATTIE METAB GENET | 1 | 50% | 0.2% | 1 |
10 | MED EDUC PLANNING | 1 | 50% | 0.2% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000210440 | TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P |
2 | 0.0000164776 | RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15 |
3 | 0.0000138990 | TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY |
4 | 0.0000131216 | SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5 |
5 | 0.0000105698 | PALLISTER KILLIAN SYNDROME//TETRASOMY 12P//TRISOMY 12P |
6 | 0.0000096150 | COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT CCR//COMPLEX CHROMOSOMAL REARRANGEMENTS |
7 | 0.0000094072 | CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME |
8 | 0.0000089982 | SATB1//2Q DELETION//SATB2 |
9 | 0.0000087911 | FETAL GENDER//HUMAN FETAL NEURONS//NEWBORN INTENS CARE |
10 | 0.0000081542 | JACOBSEN SYNDROME//11Q SYNDROME//11Q TERMINAL DELETION DISORDER |