Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
22276 | 330 | 28.4 | 73% |
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 | COMPLEX CHROMOSOMAL REARRANGEMENT | Author keyword | 20 | 58% | 7% | 23 |
2 | COMPLEX CHROMOSOME REARRANGEMENT CCR | Author keyword | 13 | 80% | 2% | 8 |
3 | COMPLEX CHROMOSOMAL REARRANGEMENTS | Author keyword | 12 | 63% | 4% | 12 |
4 | COMPLEX CHROMOSOMAL REARRANGEMENT CCR | Author keyword | 12 | 86% | 2% | 6 |
5 | COMPLEX CHROMOSOME REARRANGEMENTS | Author keyword | 11 | 69% | 3% | 9 |
6 | COMPLEX CHROMOSOME REARRANGEMENT | Author keyword | 8 | 42% | 5% | 15 |
7 | CHROMOTHRIPSIS | Author keyword | 6 | 37% | 4% | 13 |
8 | CHROMOPLEXY | Author keyword | 2 | 67% | 1% | 2 |
9 | SERIAL REPLICATION SLIPPAGE | Author keyword | 2 | 67% | 1% | 2 |
10 | BALANCED COMPLEX CHROMOSOMAL REARRANGEMENT BCCR | Author keyword | 1 | 100% | 1% | 2 |
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 | 8 BREAKPOINTS | 15 | 88% | 2% | 7 |
2 | MATERNAL REARRANGEMENT | 6 | 100% | 1% | 4 |
3 | COMPLEX CHROMOSOMAL REARRANGEMENTS | 5 | 54% | 2% | 7 |
4 | CCR | 4 | 28% | 4% | 13 |
5 | COMPLEX CHROMOSOME REARRANGEMENTS | 4 | 75% | 1% | 3 |
6 | MALE CARRIER | 4 | 56% | 2% | 5 |
7 | CATASTROPHIC EVENT | 2 | 67% | 1% | 2 |
8 | COMPLEX CHROMOSOME REARRANGEMENT | 2 | 67% | 1% | 2 |
9 | NORMAL MOTHER | 2 | 67% | 1% | 2 |
10 | CHROMOTHRIPSIS | 2 | 24% | 2% | 8 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
Prevalence and clinical implications of chromothripsis in cancer genomes | 2014 | 9 | 30 | 43% |
De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: Report and review | 1998 | 53 | 69 | 74% |
Balanced Complex Chromosome Rearrangements: Reproductive Aspects. A Review | 2012 | 22 | 85 | 81% |
Chromothripsis and cancer: causes and consequences of chromosome shattering | 2012 | 72 | 40 | 35% |
Chromothripsis and Human Disease: Piecing Together the Shattering Process | 2012 | 43 | 17 | 47% |
Complex chromosomal rearrangement involving chromosomes 1, 4 and 22 in an infertile male: case report and literature review | 2009 | 8 | 19 | 95% |
De novo exceptional complex chromosomal rearrangement in a healthy fertile male: case report and review of the literature | 2011 | 4 | 25 | 92% |
Constitutional complex chromosomal rearrangements in a klinefelter patient: case report and review of literature | 2012 | 1 | 16 | 88% |
Balanced complex chromosome rearrangement in male infertility: case report and literature review | 2015 | 0 | 44 | 77% |
The role of microhomology in genomic structural variation | 2014 | 8 | 83 | 13% |
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 | CHROMOSOMAL GENET | 1 | 40% | 0.6% | 2 |
2 | SCDU GENET MED | 1 | 40% | 0.6% | 2 |
3 | CITOGENET MED GENET MOL | 1 | 23% | 0.9% | 3 |
4 | AO FATEBENEFRATELLI OFTALM | 1 | 50% | 0.3% | 1 |
5 | BUR CHILDRENS HLTH | 1 | 50% | 0.3% | 1 |
6 | CITOTEST | 1 | 50% | 0.3% | 1 |
7 | DIAG THER Y PREVENT NEUROHANDIC | 1 | 50% | 0.3% | 1 |
8 | DIP MED | 1 | 50% | 0.3% | 1 |
9 | GALTON S | 1 | 50% | 0.3% | 1 |
10 | GEN PERINATAL MATERNAL NEONATAL MED | 1 | 50% | 0.3% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000244213 | SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5 |
2 | 0.0000205080 | MEIOTIC SEGREGATION//SPERM ANEUPLOIDY//SPERM FISH |
3 | 0.0000191263 | TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P |
4 | 0.0000189803 | PRODUCTS OF CONCEPTION//RECURRENT MISCARRIAGE//RECURRENT PREGNANCY LOSS PROGRAM |
5 | 0.0000183046 | CAT EYE SYNDROME//SUPERNUMERARY MARKER CHROMOSOMES//SMALL SUPERNUMERARY MARKER CHROMOSOME |
6 | 0.0000180668 | CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME |
7 | 0.0000153523 | TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY |
8 | 0.0000140901 | CHROMOSOME 6Q DELETION//SIM1 GENE//6Q DELETION |
9 | 0.0000127244 | TRICHORHINOPHALANGEAL SYNDROME//TRPS1//TRICHO RHINO PHALANGEAL SYNDROME |
10 | 0.0000113462 | SPECTRAL SIMILARITY MAPPING//FAST FISH//CHROMOSOME SPREADING |