Familial Cancer
Familial Cancer is a journal indexed in SJR in Genetics and Oncology with an H index of 70. It has a price of 3190 €. It has an SJR impact factor of 1,018 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 1,018.
Familial Cancer focuses its scope in these topics and keywords: cancer, aspiration, risk, breast, women, increased, nipple, oxytocinassisted, middle, cancerlowlevel, ...
Metrics
Scimago and CountryOfPapers database fields
SJR Impact
1,018
H-index
70
Docs (year)
69
Docs 3y
148
Total refs
2783
Cites 3y
329
Citable 3y
138
Cites/Doc 2y
1.99
Ref/Doc
40.33
Immediate OA
3190 €
Embargoed OA
NPD
Non OA / Submission
0 €
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Researcher reviews
Best articles by citations
Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge
View moreIdentification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing
View moreReferral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinoma
View morePredictors of choosing life-long screening or prophylactic surgery in women at high and moderate risk for breast and ovarian cancer
View moreResponse to neo-adjuvant chemotherapy in BRCA1 and BRCA2 related stage III breast cancer
View moreThe impact of positive cancer family history on the clinical features and outcome of patients with non-small cell lung cancer
View moreTrends in colorectal cancer incidence and mortality in the Israeli Jewish ethnic populations
View moreTumor histology helps to identify Lynch syndrome among colorectal cancer patients
View moreTwo novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patients
View moreVestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review
View moreWhat motivates interest in attending a familial cancer genetics clinic?
View moreThe effect of oral 3,3'-diindolylmethane supplementation on the 2:16a-OHE ratio in BRCA1 mutation carriers
View morePredictive genetic testing in a young child: a case report
View morePeritoneal carcinoma in women with genetic susceptibility: implications for Jewish populations
View moreNon-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report
View moreNon-cancer endpoints in BRCA1/2 carriers after risk-reducing salpingo-oophorectomy
View moreNevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene
View moreMutation analysis of the PALB2 cancer predisposition gene in familial melanoma
View moreLow Prevalence of BRCA1 Exon Rearrangements in Familial and Young Sporadic Breast Cancer Patients
View moreLow prevalence of BRCA1 and BRCA2 mutations in the sporadic breast cancer of Spanish population
View moreLong-term outcomes of risk-reducing surgery in unaffected women at increased familial risk of breast and/or ovarian cancer
View moreLinkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
View moreImpact of computer-assisted data collection, evaluation and management on the cancer genetic counselor's time providing patient care
View moreIGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer
View more