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American Journal Of Medical Genetics Part A

American Journal Of Medical Genetics Part A杂志,由Wiley-Liss Inc.出版,于2003年创刊,Semimonthly,出版语言English,ISSN:1552-4825,E-ISSN:1552-4833。

投稿咨询
American Journal Of Medical Genetics Part A
American Journal Of Medical Genetics Part A
American Journal Of Medical Genetics Part A
SCI SCIE

杂志介绍

JCR分区
Q4
中科院分区
3区
影响因子
1.7
CiteScore
3.4
期刊收录
SCI、SCIE

American Journal Of Medical Genetics Part A(中文译名:《美国医学遗传学杂志 A 部分》),ISSN:1552-4825,EISSN:1552-4833,是Wiley-Liss Inc.出版的国际性学术期刊,创刊于2003年,以Semimonthly形式稳定发行,2026年总发文量约330篇。该刊采用非OA开放访问,学科归属为生物 - 遗传学。该刊是生物、遗传学领域的国际权威刊物,已被SCI(科学引文索引)、SCIE(科学引文索引扩展版)等国际主流学术数据库收录。2026年期刊影响因子达1.7,2025年期刊CiteScore为3.4,2025年期刊自引率约11.8%,在中科院期刊分区体系中位列生物学大类3区,在所属学科领域具备高学术影响力与国际认可度。American Journal Of Medical Genetics Part A长期聚焦生物、遗传学及相关产业的技术应用前沿,平均审稿周期较快,2-4周,审稿流程高效稳定。在稿件录用评判中,该刊将创新性与前沿性作为核心遴选标准,重点收录能够对生物、遗传学领域的落地与发展产生实质性推动价值的研究成果。

从全球发文格局来看,USACanada、Italy、England、Netherlands、GERMANY (FED REP GER)、France等为核心发文国家与地区;UNIVERSITY OF CALIFORNIA SYSTEMUNIVERSITY OF PENNSYLVANIA、CHILDRENS HOSPITAL OF PHILADELPHIA、HARVARD UNIVERSITY、UNIVERSITY OF WASHINGTON、BAYLOR COLLEGE OF MEDICINE、BOSTON CHILDREN'S HOSPITAL等高校与科研机构是期刊的主要发文单位。

期刊评价

名词解释:

影响因子(Impact Factor, IF):指该期刊前两年发表的文章,在第三年的平均被引用次数。它反映了期刊的近期平均影响力和热度。

中科院分区:中科院分区表是国内主流的学术期刊分级评价工具,核心意义是建立跨学科可比的统一评价标尺,为职称评审、学位授予、科研立项等科研管理工作提供标准化量化依据,同时帮助科研人员筛选优质期刊、规避学术风险,适配国内本土化的科研评价需求。

期刊分区表

《新锐期刊分区表》(2026年3月发布)

大类学科 小类学科 Top期刊 综述期刊
生物学
3区
GENETICS & HEREDITY 遗传学
3区

期刊分区表(2025年3月升级版)

大类学科 小类学科 Top期刊 综述期刊
生物学
3区
GENETICS & HEREDITY 遗传学
4区

期刊分区表(2023年12月升级版)

大类学科 小类学科 Top期刊 综述期刊
生物学
4区
GENETICS & HEREDITY 遗传学
4区

JCR分区

2025-2026年最新版

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 149 / 192

22.7

学科:GENETICS & HEREDITY SCIE Q3 143 / 192

25.78

2024-2025年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:GENETICS & HEREDITY SCIE Q3 135 / 192

29.9

学科:GENETICS & HEREDITY SCIE Q3 134 / 192

30.47


中国学者近期发文

1
Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficienc

Author:Williams, Aaron; Divin, Kristian; Burrage, Lindsay C.; Craigen, William J.; Scaglia, Fernando; Soler-alfonso, Claudia; Sutton, V. Reid; Glinton, Kevin E.; Marom, Ronit

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmg.a.70154

2
Identification of a Novel AMER1 Variant and Craniofacial Phenotypic Spectrum in Osteopathia Striata with Cranial Sclerosi

Author:Chen, Qing; Wang, Xin; Liu, Nianke; Yuan, Wenjun; Song, Yaling

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmg.a.70164

3
Differentiated In Vitro Efficacy of BYL719, ARQ092, and Rapamycin on Fibroblasts Isolated From a Chinese PIK3CA-Related Overgrowth Spectrum Individual With a Novel Varian

Author:Xiong, Fei; Wang, Qian; Wang, Shi-Qi; Zheng, Miao; Zhong, Hai-Yan; Zou, Ming-Li; Yuan, Si-Ming

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmg.a.70099

4
KRT6A Variant Underlies Pachyonychia Congenita: Insights Into Protein Aggregation and PPAR Signalin

Author:Ren, Yaqiong; Niu, Wensi; Cao, Yue; Zhang, Yuan; Hua, Jun; Wang, Hongying

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmg.a.70091

5
Evaluating the Diagnostic Yield of Prenatal Trio Exome Sequencing in Families With a History of Developmental Delay and Intellectual Disabilit

Author:Feng, Zhanke; Liu, Wenxin; Li, Huanyun; Wu, Shitong; Zhou, Runying; Chen, Xiaohang; Yao, Yingxin; Kong, Xiangdong

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmg.a.70111

6
A Novel Gain-of-Function ITPR1 Variant Associated With a Movement Disorder Characterized by Tremor and Dystoni

Author:Theberge, Emilie T.; Sun, Bo; Wang, Ruiwu; Mohajeri, Arezoo; Van Karnebeek, Clara D. M.; Boerkoel, Cornelius F.; Huynh, Stephanie; Horvath, Gabriella; Chen, S. R. Wayne; Lehman, Anna

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmga.70069

7
Clinical Insights From a Case of Sifrim-Hitz-Weiss Syndrome With a CHD4 Variant: Expanding the Phenotypic Spectrum and Its Response to Growth Hormone Therap

Author:Zhang, Jianmei; Chen, Shuangzhong; Dong, Guanping; Yang, Suhong; Wang, Ping; Zhou, Qiong; Wang, Pingping

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmg.a.70084

8
A Novel KCNQ2 Gain-of-Function Variant I134N Causes Severe Developmental and Epileptic Encephalopath

Author:Zeng, Fengmei; Ye, Xiaoying; Gao, Zhaobing; Tian, Fuyun; Shen, Yanwen

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmga.70044

9
Genetic and Clinical Features of FOXL2-Associated Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Based on 11 Chinese Families and Literature Revie

Author:Dong, Yijun; Xiao, Xueshan; Li, Shiqiang; Jia, Xiaoyun; Sun, Wenmin; Zhang, Qingjiong; Yi, Zhen

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2026; Vol. , Issue , pp. -. DOI: 10.1002/ajmga.70058

10
Identification of a Novel FGFR2 Gene Mutation (c.514_515delinsCT, p.Ala172Leu) in a Chinese Neonate With Apert Syndrome: A Case Repor

Author:Pan, Dongxue; Yang, Xiufang

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2025; Vol. , Issue , pp. -. DOI: 10.1002/ajmg.a.64158


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American Journal Of Medical Genetics Part A

国际简称:AM J MED GENET A参考译名:美国医学遗传学杂志 A 部分

年发文量:330 CiteScore:3.4 是否预警:否 Gold OA文章占比:37.01% 研究类文章占比:97.27%

杂志社联系方式:WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030

American Journal Of Medical Genetics Part A