Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
4352 | 1725 | 32.0 | 78% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
580 | 13536 | MICROSATELLITE INSTABILITY//LYNCH SYNDROME//HNPCC |
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 | FAMILIAL ADENOMATOUS POLYPOSIS | Author keyword | 99 | 31% | 15% | 264 |
2 | APC GENE | Author keyword | 93 | 61% | 6% | 98 |
3 | MUTYH | Author keyword | 51 | 63% | 3% | 51 |
4 | CRIBRIFORM MORULAR VARIANT | Author keyword | 45 | 94% | 1% | 16 |
5 | MUTYH ASSOCIATED POLYPOSIS | Author keyword | 41 | 81% | 1% | 25 |
6 | ADENOMATOUS POLYPOSIS COLI GENE | Author keyword | 33 | 71% | 2% | 27 |
7 | MYH | Author keyword | 29 | 63% | 2% | 29 |
8 | MYH GENE | Author keyword | 24 | 91% | 1% | 10 |
9 | FAP | Author keyword | 23 | 25% | 5% | 78 |
10 | TURCOTS SYNDROME | Author keyword | 20 | 63% | 1% | 20 |
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 | FAMILIAL ADENOMATOUS POLYPOSIS | 99 | 31% | 15% | 264 | Search FAMILIAL+ADENOMATOUS+POLYPOSIS | Search FAMILIAL+ADENOMATOUS+POLYPOSIS |
2 | APC GENE | 93 | 61% | 6% | 98 | Search APC+GENE | Search APC+GENE |
3 | MUTYH | 51 | 63% | 3% | 51 | Search MUTYH | Search MUTYH |
4 | CRIBRIFORM MORULAR VARIANT | 45 | 94% | 1% | 16 | Search CRIBRIFORM+MORULAR+VARIANT | Search CRIBRIFORM+MORULAR+VARIANT |
5 | MUTYH ASSOCIATED POLYPOSIS | 41 | 81% | 1% | 25 | Search MUTYH+ASSOCIATED+POLYPOSIS | Search MUTYH+ASSOCIATED+POLYPOSIS |
6 | ADENOMATOUS POLYPOSIS COLI GENE | 33 | 71% | 2% | 27 | Search ADENOMATOUS+POLYPOSIS+COLI+GENE | Search ADENOMATOUS+POLYPOSIS+COLI+GENE |
7 | MYH | 29 | 63% | 2% | 29 | Search MYH | Search MYH |
8 | MYH GENE | 24 | 91% | 1% | 10 | Search MYH+GENE | Search MYH+GENE |
9 | FAP | 23 | 25% | 5% | 78 | Search FAP | Search FAP |
10 | TURCOTS SYNDROME | 20 | 63% | 1% | 20 | Search TURCOTS+SYNDROME | Search TURCOTS+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 | FAP | 155 | 54% | 12% | 199 |
2 | CHROMOSOME 5Q21 | 117 | 51% | 10% | 164 |
3 | COLI GENE | 112 | 62% | 7% | 117 |
4 | APC GENE | 64 | 24% | 13% | 228 |
5 | OCULAR FUNDUS LESIONS | 60 | 79% | 2% | 38 |
6 | MYH ASSOCIATED POLYPOSIS | 56 | 76% | 2% | 39 |
7 | MULTIPLE COLORECTAL ADENOMAS | 51 | 79% | 2% | 33 |
8 | CONGENITAL HYPERTROPHY | 50 | 67% | 3% | 45 |
9 | MYH GENE | 47 | 88% | 1% | 22 |
10 | SOMATIC G C T A MUTATIONS | 43 | 54% | 3% | 56 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): A review of the literature | 2007 | 89 | 49 | 90% |
Guidelines for the clinical management of familial adenomatous polyposis (FAP) | 2008 | 160 | 80 | 43% |
The ABC of APC | 2001 | 442 | 198 | 39% |
Familial adenomatous polyposis | 2006 | 179 | 152 | 49% |
MUTYH-associated polyposis (MAP) | 2011 | 27 | 137 | 63% |
APC Germline Mutations in Individuals Being Evaluated for Familial Adenomatous Polyposis A Review of the Mayo Clinic Experience with 1591 Consecutive Tests | 2013 | 9 | 75 | 91% |
APC Polymorphisms and the Risk of Colorectal Neoplasia: A HuGE Review and Meta-Analysis | 2013 | 11 | 49 | 71% |
MUTYH-associated polyposis- From defect in base excision repair to clinical genetic testing | 2007 | 66 | 57 | 53% |
Familial adenomatous polyposis | 2009 | 95 | 92 | 32% |
Systematic review of the impact of registration and screening on colorectal cancer incidence and mortality in familial adenomatous polyposis and Lynch syndrome | 2013 | 10 | 47 | 55% |
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 | DANISH POLYPOSIS REGISTER | 8 | 62% | 0.5% | 8 |
2 | MOL POPULAT GENET | 6 | 14% | 2.2% | 38 |
3 | POLYPOSIS REGISTRY | 5 | 21% | 1.2% | 20 |
4 | BELGIAN POLYPOSIS PROJECT | 4 | 67% | 0.2% | 4 |
5 | ANGIOGENET ONCOGENET | 4 | 75% | 0.2% | 3 |
6 | ITALIAN REGISTRY HEREDITARY COLORECTAL TUMORS | 4 | 75% | 0.2% | 3 |
7 | F A | 3 | 57% | 0.2% | 4 |
8 | GRP HUMAN GENET | 3 | 22% | 0.7% | 12 |
9 | FAMILIAL BOWEL CANC CLIN | 3 | 60% | 0.2% | 3 |
10 | COLORECTAL TUMORS | 2 | 67% | 0.1% | 2 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000217482 | MIN MOUSE//MIN MICE//FAP MODEL |
2 | 0.0000117514 | MICROSATELLITE INSTABILITY//LYNCH SYNDROME//HNPCC |
3 | 0.0000115249 | INTER SIMPLE SEQUENCE REPEAT PCR//BIOPHYS CYTOMETRY//HOSP UNIV SALAMANCA IBSAL |
4 | 0.0000107687 | TUMORICIDAL POTENTIAL//V FES//CNRS URA 620 |
5 | 0.0000104555 | DESMOID TUMOR//AGGRESSIVE FIBROMATOSIS//FIBROMATOSIS |
6 | 0.0000095236 | PEUTZ JEGHERS SYNDROME//CRONKHITE CANADA SYNDROME//JUVENILE POLYPOSIS |
7 | 0.0000082718 | AMPULLA OF VATER//AMPULLARY ADENOMA//AMPULLECTOMY |
8 | 0.0000080085 | CEITOX UNIDEF//DOSE DEPENDENT TRANSITIONS//PSYCH HLTH |
9 | 0.0000070293 | BETA CATENIN//AXIN//WNT |
10 | 0.0000068499 | FLAT ADENOMA//DEPRESSED ADENOMA//POLYPOID GROWTH |