《Genetics In Medicine》雜志的最新年發文量為164篇。
這表明該刊在每年都會精選并發表一定數量的高質量文章，以保持其在遺傳學領域的學術影響力。
該刊聚焦于醫學-遺傳學領域的前沿研究，致力于推動該領域新技術和新知識的傳播與應用。同時它積極鼓勵研究人員詳細發表其高質量的實驗研究和理論成果。
該刊的平均審稿周期約為 偏慢,4-8周 約1.3 weeks。
Genetics In Medicine 雜志發文統計
文章名稱引用次數
- Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature80
- Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test56
- BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors56
- Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders49
- False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care46
- Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification framework45
- Meeting the challenges of implementing rapid genomic testing in acute pediatric care33
- Long-read genome sequencing identifies causal structural variation in a Mendelian disease33
- Somatic TP53 variants frequently confound germ-line testing results31
- Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 133 families with developmental disorders31
國家/地區發文量
- USA702
- England175
- Canada133
- Netherlands131
- GERMANY (FED REP GER)123
- Australia118
- France116
- Italy80
- Belgium67
- CHINA MAINLAND62
