《Human Mutation》雜志的最新年發文量為34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 約3.0個月 。
Human Mutation 雜志發文統計
文章名稱引用次數
- Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion53
- Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss36
- Mutational spectrum in a worldwide study of 700 families with BRCA1 or BRCA2 mutations34
- ClinVar at five years: Delivering on the promise33
- A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/325
- ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation25
- Iranome: A catalog of genomic variations in the Iranian population22
- Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification21
- MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains20
- ClinVar database of global familial hypercholesterolemia-associated DNA variants20
國家/地區發文量
- USA300
- GERMANY (FED REP GER)115
- France112
- Italy104
- England103
- Australia76
- Netherlands76
- Spain66
- Canada65
- CHINA MAINLAND64
