Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 19199 | 451 | 22.3 | 43% |
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 | PARTIAL DUPLICATION 9Q | Author keyword | 6 | 100% | 1% | 4 |
| 2 | CHROMOSOME VARIANT | Author keyword | 4 | 75% | 1% | 3 |
| 3 | CHROMOSOME 9 | Author keyword | 4 | 14% | 6% | 27 |
| 4 | PERICENTRIC INVERSION | Author keyword | 4 | 16% | 5% | 21 |
| 5 | PARTIAL TRISOMY 9Q | Author keyword | 3 | 100% | 1% | 3 |
| 6 | EUCHROMATIC VARIANT | Author keyword | 3 | 60% | 1% | 3 |
| 7 | TRISOMY 9Q | Author keyword | 3 | 60% | 1% | 3 |
| 8 | EUCHROMATIC VARIANTS | Author keyword | 2 | 67% | 0% | 2 |
| 9 | HETEROMORPHISM | Author keyword | 2 | 16% | 2% | 9 |
| 10 | CHROMOSOME 9 VARIANT | Author keyword | 1 | 100% | 0% | 2 |
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 | PARTIAL DUPLICATION 9Q | 6 | 100% | 1% | 4 | Search PARTIAL+DUPLICATION+9Q | Search PARTIAL+DUPLICATION+9Q |
| 2 | CHROMOSOME VARIANT | 4 | 75% | 1% | 3 | Search CHROMOSOME+VARIANT | Search CHROMOSOME+VARIANT |
| 3 | CHROMOSOME 9 | 4 | 14% | 6% | 27 | Search CHROMOSOME+9 | Search CHROMOSOME+9 |
| 4 | PERICENTRIC INVERSION | 4 | 16% | 5% | 21 | Search PERICENTRIC+INVERSION | Search PERICENTRIC+INVERSION |
| 5 | PARTIAL TRISOMY 9Q | 3 | 100% | 1% | 3 | Search PARTIAL+TRISOMY+9Q | Search PARTIAL+TRISOMY+9Q |
| 6 | EUCHROMATIC VARIANT | 3 | 60% | 1% | 3 | Search EUCHROMATIC+VARIANT | Search EUCHROMATIC+VARIANT |
| 7 | TRISOMY 9Q | 3 | 60% | 1% | 3 | Search TRISOMY+9Q | Search TRISOMY+9Q |
| 8 | EUCHROMATIC VARIANTS | 2 | 67% | 0% | 2 | Search EUCHROMATIC+VARIANTS | Search EUCHROMATIC+VARIANTS |
| 9 | HETEROMORPHISM | 2 | 16% | 2% | 9 | Search HETEROMORPHISM | Search HETEROMORPHISM |
| 10 | CHROMOSOME 9 VARIANT | 1 | 100% | 0% | 2 | Search CHROMOSOME+9+VARIANT | Search CHROMOSOME+9+VARIANT |
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 | SECONDARY CONSTRICTION REGION | 23 | 86% | 3% | 12 |
| 2 | PARTIAL TRISOMY 9Q | 13 | 80% | 2% | 8 |
| 3 | EUCHROMATIC BAND | 11 | 100% | 1% | 6 |
| 4 | 9QH | 9 | 83% | 1% | 5 |
| 5 | QH | 9 | 83% | 1% | 5 |
| 6 | EXTRA BAND | 6 | 80% | 1% | 4 |
| 7 | G POSITIVE BAND | 6 | 80% | 1% | 4 |
| 8 | C BAND PATTERN | 4 | 75% | 1% | 3 |
| 9 | INV9 | 4 | 75% | 1% | 3 |
| 10 | CHROMOSOME 9 VARIANT | 3 | 100% | 1% | 3 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references | % act. ref. to same field |
|---|---|---|---|---|
| Homozygosity for pericentric inversions of chromosome 9 in a patient's parents with stillbirth - Report of a new case and review of literature | 2006 | 2 | 23 | 52% |
| Directly transmitted unbalanced chromosome abnormalities and euchromatic variants | 2005 | 96 | 142 | 10% |
| Chromosome abnormalities without phenotypic consequences | 2007 | 12 | 53 | 17% |
| PARTIAL TRISOMY 9Q RESULTING FROM A FAMILIAL TRANSLOCATION T(9-16)(Q32-Q24) | 1984 | 15 | 3 | 67% |
| ASPECTS OF EVALUATION, SIGNIFICANCE, AND EVOLUTION OF HUMAN C-BAND HETEROMORPHISM | 1982 | 54 | 28 | 54% |
| Homozygosity for constitutional chromosomal rearrangements: a systematic review with reference to origin, ascertainment and phenotype | 2010 | 1 | 39 | 13% |
| NONDISJUNCTION OF CHROMOSOMES IN MAN - HYPOTHESES AND FACTS | 1988 | 1 | 12 | 33% |
| STRUCTURAL ORGANIZATION OF HETEROCHROMATIN IN THE HUMAN GENOME | 1987 | 0 | 20 | 40% |
| CYTOGENETIC STUDIES OF PROSTATIC-CANCER | 1991 | 1 | 80 | 19% |
| CHROMOSOMES - AGING - LONGEVITY | 1986 | 0 | 34 | 29% |
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 | BONE MARROW TRANSPLANTAT UNIV | 1 | 50% | 0.2% | 1 |
| 2 | EA 1533 GENET REPROD HUMAINE | 1 | 50% | 0.2% | 1 |
| 3 | IMMUNOCHEM IMMUNOPATHOL INSERM U108 | 1 | 50% | 0.2% | 1 |
| 4 | KANAZAWA RED CROSS HOSP | 1 | 50% | 0.2% | 1 |
| 5 | REPROD STEM CELLS ENGN | 1 | 50% | 0.2% | 1 |
| 6 | SERV FISIOPATOL FETAL | 1 | 50% | 0.2% | 1 |
| 7 | FOOD PHARMACEUT DEV S | 0 | 33% | 0.2% | 1 |
| 8 | MEIR HOSPSACKLER MED | 0 | 33% | 0.2% | 1 |
| 9 | BREEDING BIOL GRP | 0 | 25% | 0.2% | 1 |
| 10 | GENET REF WESSEX | 0 | 25% | 0.2% | 1 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000166126 | PRODUCTS OF CONCEPTION//RECURRENT MISCARRIAGE//RECURRENT PREGNANCY LOSS PROGRAM |
| 2 | 0.0000163644 | SATELLITE DNA//HIGHER ORDER REPEATS//SATELLITE DNA EVOLUTION |
| 3 | 0.0000158896 | HETEROCHROMATINIZATION//SATELLITE ASSOCIATION//ECTOPIC NUCLEOLUS ORGANIZER REGION |
| 4 | 0.0000116475 | TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P |
| 5 | 0.0000106396 | CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME |
| 6 | 0.0000099485 | CAT EYE SYNDROME//SUPERNUMERARY MARKER CHROMOSOMES//SMALL SUPERNUMERARY MARKER CHROMOSOME |
| 7 | 0.0000099189 | MEIOTIC SEGREGATION//SPERM ANEUPLOIDY//SPERM FISH |
| 8 | 0.0000099018 | DOUBLE ANEUPLOIDY//NONDISJUNCTION//48 XXY 21 |
| 9 | 0.0000075106 | RUBINSTEIN TAYBI SYNDROME//CORNEAL KELOID//TRISOMY 16Q |
| 10 | 0.0000061606 | CONFINED PLACENTAL MOSAICISM//UNIPARENTAL DISOMY//TRISOMY 9 |