Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
17852 | 516 | 22.2 | 71% |
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 | CAT EYE SYNDROME | Author keyword | 46 | 76% | 6% | 32 |
2 | SUPERNUMERARY MARKER CHROMOSOMES | Author keyword | 27 | 83% | 3% | 15 |
3 | SMALL SUPERNUMERARY MARKER CHROMOSOME | Author keyword | 23 | 74% | 3% | 17 |
4 | SUPERNUMERARY MARKER CHROMOSOME | Author keyword | 17 | 47% | 5% | 27 |
5 | MARKER CHROMOSOME | Author keyword | 17 | 37% | 7% | 37 |
6 | SMALL SUPERNUMERARY MARKER CHROMOSOMES SSMC | Author keyword | 15 | 82% | 2% | 9 |
7 | SMALL SUPERNUMERARY MARKER CHROMOSOMES | Author keyword | 13 | 71% | 2% | 10 |
8 | RING CHROMOSOME 1 | Author keyword | 9 | 83% | 1% | 5 |
9 | SUPERNUMERARY MARKER | Author keyword | 6 | 71% | 1% | 5 |
10 | TRISOMY 19Q | Author keyword | 4 | 75% | 1% | 3 |
Web of Science journal categories |
Author Key Words |
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 | STRUCTURALLY ABNORMAL CHROMOSOMES | 68 | 84% | 7% | 37 |
2 | FISH APPROACH | 27 | 92% | 2% | 11 |
3 | PRENATAL DIAGNOSES | 26 | 87% | 3% | 13 |
4 | MICRO FISH | 20 | 100% | 2% | 9 |
5 | SSMC | 12 | 56% | 3% | 15 |
6 | MARKER CHROMOSOMES | 12 | 22% | 9% | 47 |
7 | CAT EYE SYNDROME | 11 | 30% | 6% | 32 |
8 | PROXIMAL 19Q TRISOMY | 8 | 100% | 1% | 5 |
9 | FISH CHARACTERIZATION | 7 | 67% | 1% | 6 |
10 | 16Q DELETION | 6 | 80% | 1% | 4 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Handling small supernumerary marker chromosomes in prenatal diagnostics | 2009 | 20 | 25 | 76% |
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity | 2013 | 3 | 39 | 79% |
Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics | 2007 | 71 | 116 | 24% |
Characterization of a supernumerary ring chromosome 1 mosaicism in two cell systems by molecular cytogenetic techniques and review of the literature | 2003 | 6 | 18 | 89% |
Prenatal diagnosis of supernumerary ring chromosome 1: Case report and review of the literature | 2007 | 2 | 30 | 83% |
Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature | 2003 | 5 | 19 | 68% |
First small supernumerary ring chromosome carrying 10q euchromatin in a patient with mild phenotype characterized by molecular cytogenetic techniques and review of the literature | 2005 | 4 | 19 | 53% |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review | 2013 | 0 | 45 | 56% |
DUPLICATION OF DISTAL-19Q - CLINICAL REPORT AND REVIEW | 1992 | 18 | 5 | 80% |
Cat eye syndrome and growth hormone deficiency with pituitary anomalies: A case report and review of the literature | 2013 | 0 | 18 | 39% |
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 | PLATEFORME GENOM IMRB 955 | 1 | 40% | 0.4% | 2 |
2 | CYTOGENET GENET | 1 | 33% | 0.4% | 2 |
3 | ABACID GENET | 1 | 50% | 0.2% | 1 |
4 | BALAGUE | 1 | 50% | 0.2% | 1 |
5 | BIOL MED GENET UNIT | 1 | 50% | 0.2% | 1 |
6 | CLIN CHILDREN JUVENILE MED | 1 | 50% | 0.2% | 1 |
7 | METAB INHERITED DISORDERS | 1 | 50% | 0.2% | 1 |
8 | NEONATOL PATHOL INTENS CARE | 1 | 50% | 0.2% | 1 |
9 | OTORYNOLARYNGOL | 1 | 50% | 0.2% | 1 |
10 | PEDIAT DIABETOL NEONATOL BIRTH DEFECTS | 1 | 50% | 0.2% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000238228 | SPECTRAL SIMILARITY MAPPING//FAST FISH//CHROMOSOME SPREADING |
2 | 0.0000230246 | PITT HOPKINS SYNDROME//18Q DELETION SYNDROME//18Q SYNDROME |
3 | 0.0000223094 | RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15 |
4 | 0.0000221945 | PALLISTER KILLIAN SYNDROME//TETRASOMY 12P//TRISOMY 12P |
5 | 0.0000183046 | COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT CCR//COMPLEX CHROMOSOMAL REARRANGEMENTS |
6 | 0.0000176667 | CONFINED PLACENTAL MOSAICISM//UNIPARENTAL DISOMY//TRISOMY 9 |
7 | 0.0000160737 | TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P |
8 | 0.0000144586 | TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY |
9 | 0.0000134159 | PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A |
10 | 0.0000120324 | SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME |