首页 国际期刊 医学期刊 期刊详情(非官网)
400-808-1701

Prenatal Diagnosis

Prenatal Diagnosis杂志,由John Wiley and Sons Ltd出版,于1981年创刊,Monthly,出版语言English,ISSN:0197-3851,E-ISSN:1097-0223。

投稿咨询
Prenatal Diagnosis
Prenatal Diagnosis
Prenatal Diagnosis
SCI SCIE

杂志介绍

JCR分区
Q1
中科院分区
3区
影响因子
3.1
CiteScore
4.7
期刊收录
SCI、SCIE

Prenatal Diagnosis(中文译名:《产前诊断》),ISSN:0197-3851,EISSN:1097-0223,是John Wiley and Sons Ltd出版的国际性学术期刊,创刊于1981年,以Monthly形式稳定发行,2026年总发文量约177篇。该刊采用非OA开放访问,学科归属为医学 - 妇产科学。该刊是医学、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3.1,2025年期刊CiteScore为4.7,2025年期刊自引率约19.4%,在中科院期刊分区体系中位列医学大类3区,在所属学科领域具备高学术影响力与国际认可度。Prenatal Diagnosis长期聚焦医学、遗传学及相关产业的技术应用前沿,平均审稿周期约2月,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,重点收录能够对医学、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,USACHINA MAINLAND、England、France、Australia、Belgium、Canada等为核心发文国家与地区;UNIVERSITY OF LONDONKU LEUVEN、ASSISTANCE PUBLIQUE HOPITAUX PARIS (APHP)、BAYLOR COLLEGE OF MEDICINE、UNIVERSITY OF TORONTO、UNIVERSITY OF MELBOURNE、UNIVERSITY OF CALIFORNIA SYSTEM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
医学
3区
GENETICS & HEREDITY 遗传学 OBSTETRICS & GYNECOLOGY 妇产科学
3区 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
医学
2区
GENETICS & HEREDITY 遗传学 OBSTETRICS & GYNECOLOGY 妇产科学
2区 3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
医学
2区
GENETICS & HEREDITY 遗传学 OBSTETRICS & GYNECOLOGY 妇产科学
2区 2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 Q2 74 / 192

61.7

学科:OBSTETRICS & GYNECOLOGY SCIE Q1 33 / 143

77.3

学科:GENETICS & HEREDITY SCIE Q2 69 / 192

64.32

学科:OBSTETRICS & GYNECOLOGY SCIE Q2 56 / 143

61.19

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 Q2 86 / 192

55.5

学科:OBSTETRICS & GYNECOLOGY SCIE Q1 31 / 141

78.4

学科:GENETICS & HEREDITY SCIE Q2 75 / 192

61.2

学科:OBSTETRICS & GYNECOLOGY SCIE Q2 58 / 141

59.22


中国学者近期发文

1
Prenatal Diagnosis of Arthrogryposis Multiplex Congenita (AMC): Ultrasound and Genetic Findings in 69 Fetuses From 67 Unrelated Familie

Author:Yao, Tingting; Yuan, Limin; Dong, Xiaozhen; Wang, Yishan; Zhang, Chunshuang; Liu, Ling; Cheng, Guomei

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70122

2
Accurate Detection of Multiple Chromosome Rearrangements and Copy Number Variations by PacBio Sequencing in Complex Chromosomal Abnormalit

Author:Liu, Lili; Kang, Kai; Wang, Hao; Sun, Longhao; Wang, Dan; Wang, Na; Sheng, Qing; Zang, Zhan; Gu, Mengnan; Xu, Yiting; Feng, Wenting; Kong, Lingyin; Liang, Bo; Cao, Donghua

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70120

3
Genetic Investigation of Fetal Left-Right Laterality Defects Identified in the Second Trimester of Pregnanc

Author:Yu, Qiu-Xia; Guo, Jia-Chun; Zhang, Yong-Ling; Jing, Xiang-Yi; Li, Si-Yun; Li, Dong-Zhi

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70152

4
Fetal Sylvian Fissure Maturation in Congenital Heart Disease and Its Relation to Expected Brain Arterial Oxygen Saturation: A Longitudinal Stud

Author:Xiong, Xiaowei; Cui, Yuanjie; Hou, Chenxiao; Yi, Lina; Zhong, Shangjin; Zhang, Na; Wu, Qingqing

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70100

5
Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidne

Author:Yu, Qiu-Xia; Ni, Yu-Tong; Zhang, Yong-Ling; Xiao, Zhi-Qing; Li, Si-Yun; Jiang, Fan; Li, Dong-Zhi

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70086

6
Low-Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 Fetuse

Author:Pan, Lijuan; Wu, Jiayu; Zhang, Yi; Liang, Desheng; Yuan, Jing; Wang, Jue; Shen, Yinchen; Lu, Junjie; Xia, Aihua; Zhang, Zhenhui; Li, Jinchen; Li, Zhuo; Wu, Lingqian

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70114

7
Recurrent Male Hydrops Fetalis Reveals Hidden Incontinentia Pigmenti: Lessons From Pseudogene-Interfered Genomic Diagnosi

Author:Cao, Chunge; Zhang, Yao; Yang, Yingjun; Wei, Xing; Sun, Luming

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70105

8
Prenatal Variable Expressivity of a Maternal FGFR1 Truncating Variant in Consecutive Pregnancies: A Dual-Generation Case Repor

Author:Jing, Huining; Wang, Hao; Xu, Bocheng; Liu, Shanling; Wang, He; Zhang, Zhu

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70121

9
Twin Reversed Arterial Perfusion (TRAP) Sequence: Proposal for Morphologic Classification System Predicting Natural Histor

Author:Lu, Li; Li, Li; Gan, Quan; Cheng, Chen; Zhao, Sheng; Yang, Xiao-Hong

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70125

10
Prenatal Tympanic Ring Anomaly Without Microtia: A Subtle Clue Toward Severe Early-Onset Monogenic Disorder

Author:Lam, Yung Hang; Shi, Mengmeng; Dong, Zirui; Choy, Kwong Wai; Leung, Tak Yeung; Cao, Ye

Journal: PRENATAL DIAGNOSIS. 2026; Vol. , Issue , pp. -. DOI: 10.1002/pd.70131


在线咨询

Prenatal Diagnosis

国际简称:PRENATAL DIAG参考译名:产前诊断

年发文量:177 CiteScore:4.7 是否预警:否 Gold OA文章占比:48.68% 研究类文章占比:86.44%

杂志社联系方式:JOHN WILEY & SONS LTD, THE ATRIUM, SOUTHERN GATE, CHICHESTER, ENGLAND, W SUSSEX, PO19 8SQ

Prenatal Diagnosis