《Familial Cancer》重点专注发布遗传学-医学领域的新研究，旨在促进和传播该领域相关的新技术和新知识。鼓励该领域研究者详细地发表他们的高质量实验研究和理论结果。该杂志创刊至今，在遗传学-医学领域，有较高影响力，对来稿文章质量要求较高，稿件投稿过审难度较大。欢迎广大同领域研究者投稿该杂志。
| CiteScore | SJR | SNIP | CiteScore排名 | |||
|---|---|---|---|---|---|---|
| 4.1 | 1.016 | 0.759 | 学科类别 | 分区 | 排名 | 百分位 |
|
大类：大类：Medicine
小类：小类：Oncology
|
Q3 | 205/404 | 49% | |||
|
大类：大类：Medicine
小类：小类：Genetics(clinical)
|
Q3 | 57/99 | 42% | |||
|
大类：大类：Medicine
小类：小类：Genetics
|
Q3 | 205/347 | 41% | |||
|
大类：大类：Medicine
小类：小类：CancerResearch
|
Q3 | 151/230 | 34% | |||
| 按JIF指标学科分区 | 收录子集 | 分区 | 排名 | 百分位 |
|---|---|---|---|---|
| 学科：GENETICS & HEREDITY | SCIE | Q3 | 130 / 191 | 32.2% |
| 学科：ONCOLOGY | SCIE | Q3 | 241 / 322 | 25.3% |
| 按JCI指标学科分区 | 收录子集 | 分区 | 排名 | 百分位 |
|---|---|---|---|---|
| 学科：GENETICS & HEREDITY | SCIE | Q4 | 146 / 191 | 23.82% |
| 学科：ONCOLOGY | SCIE | Q3 | 237 / 322 | 26.55% |
文章名称
引用次数
The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice
15
Physician interpretation of variants of uncertain significance
14
Hereditary gastric cancer: whats new? Update 2013-2018
11
Recent advances in Lynch syndrome
10
Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in TP53 germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinic
10
Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Mori
9
Moving into the mainstream: healthcare professionals views of implementing treatment focussed genetic testing in breast cancer care
8
Inequities in multi-gene hereditary cancer testing: lower diagnostic yield and higher VUS rate in individuals who identify as Hispanic, African or Asian and Pacific Islander as compared to European
8
Association between miR-146a rs2910164 polymorphism and specific cancer susceptibility: an updated meta-analysis
8
An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review
7
国家/地区
发文量
TUSA
68
TNetherlands
39
TEngland
29
TAustralia
23
TFrance
18
TCanada
15
TGERMANY (FED REP GER)
15
TItaly
9
TSweden
9
TBrazil
8
