Journal list Promote Sponsor
verified SJR 1,018 · Q2 • database Scopus / SJR & Web of Science indexed
Familial Cancer
Netherlands · Springer Science and Busines...
workspace_premium Q2 — Genetics lock Subscription

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, ...

ISSN: 1389-9600
Publisher: Springer Science and Business Media B.V.
Category: Genetics
Indexation: verifiedScopus / SJR verifiedWeb of Science
open_in_new Portal NPD menu_book Guidelines NPD
schedule CountryOfPapers database fields
SJR Impact Factor trending_up
1,018 Q2
H-index 70
Acceptance rate pie_chart
28% Selective
Source Acceptance_Rate
Time to publication hourglass_top
NPD
Field NPD
Publication cost (APC) payments
3.190 € Subscription
Non-OA path 0 €

Metrics

Scimago and CountryOfPapers database fields

Scopus / SJR Web of Science

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 €

shield Researcher voice

Name good journals. Call out predatory ones.

Share what peer review, fees, and timelines were really like. Praise fair editors. Flag APC traps, fake metrics, or spam solicitations — with facts from your submission.

Fair & fast peer review Clear APC / no surprise fees Suspected predatory Fake impact claims
rate_review Write an honest review

Researcher reviews

sentiment_dissatisfied No reviews yet — be the first to share an honest experience.
User
* Only to validate authenticity — identity is not shown publicly.

Best articles by citations

Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge

View more

Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing

View more

Referral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinoma

View more

Predictors of choosing life-long screening or prophylactic surgery in women at high and moderate risk for breast and ovarian cancer

View more

Response to neo-adjuvant chemotherapy in BRCA1 and BRCA2 related stage III breast cancer

View more

The impact of positive cancer family history on the clinical features and outcome of patients with non-small cell lung cancer

View more

Trends in colorectal cancer incidence and mortality in the Israeli Jewish ethnic populations

View more

Tumor histology helps to identify Lynch syndrome among colorectal cancer patients

View more

Two novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patients

View more

Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review

View more

What motivates interest in attending a familial cancer genetics clinic?

View more

The effect of oral 3,3'-diindolylmethane supplementation on the 2:16a-OHE ratio in BRCA1 mutation carriers

View more
SHOW MORE ARTICLES

Predictive genetic testing in a young child: a case report

View more

Peritoneal carcinoma in women with genetic susceptibility: implications for Jewish populations

View more

Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report

View more

Non-cancer endpoints in BRCA1/2 carriers after risk-reducing salpingo-oophorectomy

View more

Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene

View more

Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma

View more

Low Prevalence of BRCA1 Exon Rearrangements in Familial and Young Sporadic Breast Cancer Patients

View more

Low prevalence of BRCA1 and BRCA2 mutations in the sporadic breast cancer of Spanish population

View more

Long-term outcomes of risk-reducing surgery in unaffected women at increased familial risk of breast and/or ovarian cancer

View more

Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)

View more

Impact of computer-assisted data collection, evaluation and management on the cancer genetic counselor's time providing patient care

View more

IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer

View more

FAQs