Molecular Genetics & Genomic Medicine
SCIE國際簡稱：MOL GENET GENOM MED 參考譯名：分子遺傳學和基因組醫學
主要研究方向：Biochemistry, Genetics and Molecular Biology-Genetics 非預警期刊 審稿周期： 14 Weeks
《分子遺傳學和基因組醫學》(Molecular Genetics & Genomic Medicine)是一本由John Wiley and Sons Inc.出版的以Biochemistry, Genetics and Molecular Biology-Genetics為研究特色的國際期刊，發表該領域相關的原創研究文章、評論文章和綜述文章，及時報道該領域相關理論、實踐和應用學科的最新發現，旨在促進該學科領域科學信息的快速交流。該期刊是一本開放期刊，近三年沒有被列入預警名單。
Molecular Genetics & Genomic Medicine is a peer-reviewed journal for rapid dissemination of quality research related to the dynamically developing areas of human, molecular and medical genetics. The journal publishes original research articles covering findings in phenotypic, molecular, biological, and genomic aspects of genomic variation, inherited disorders and birth defects. The broad publishing spectrum of Molecular Genetics & Genomic Medicine includes rare and common disorders from diagnosis to treatment. Examples of appropriate articles include reports of novel disease genes, functional studies of genetic variants, in-depth genotype-phenotype studies, genomic analysis of inherited disorders, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and approaches to clinical diagnosis. Molecular Genetics & Genomic Medicine provides a scientific home for next generation sequencing studies of rare and common disorders, which will make research in this fascinating area easily and rapidly accessible to the scientific community. This will serve as the basis for translating next generation sequencing studies into individualized diagnostics and therapeutics, for day-to-day medical care.
Molecular Genetics & Genomic Medicine publishes original research articles, reviews, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented.
Molecular Genetics & Genomic Medicine期刊信息
- ISSN：2324-9269
- 出版語言：English
- 是否OA：開放
- E-ISSN：2324-9269
- 出版地區：United States
- 是否預警：否
- 出版商：John Wiley and Sons Inc.
- 出版周期：6 issues/year
- 創刊時間：2013
- 開源占比：0.7303
- Gold OA文章占比：68.56%
- OA被引用占比：1
- 出版國人文章占比：0.32
- 出版撤稿占比：0
- 研究類文章占比：87.24%
Molecular Genetics & Genomic Medicine CiteScore評價數據（2024年最新版）
| CiteScore | SJR | SNIP | CiteScore 指數 | ||||||||||||||||
| 4.2 | 0.633 | 0.696 |
|
名詞解釋：CiteScore 是衡量期刊所發表文獻的平均受引用次數，是在 Scopus 中衡量期刊影響力的另一個指標。當年CiteScore 的計算依據是期刊最近4年（含計算年度）的被引次數除以該期刊近四年發表的文獻數。例如，2022年的 CiteScore 計算方法為：2022年的 CiteScore =2019-2022年收到的對2019-2022年發表的文件的引用數量÷2019-2022年發布的文獻數量 注：文獻類型包括：文章、評論、會議論文、書籍章節和數據論文。
Molecular Genetics & Genomic Medicine中科院評價數據
中科院 2023年12月升級版
| Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
| 否 | 否 | 醫學 | 4區 | GENETICS & HEREDITY 遺傳學 | 4區 |
中科院 2022年12月升級版
| Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
| 否 | 否 | 醫學 | 4區 | GENETICS & HEREDITY 遺傳學 | 4區 |
中科院 2021年12月舊的升級版
| Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
| 否 | 否 | 醫學 | 4區 | GENETICS & HEREDITY 遺傳學 | 4區 |
中科院 2021年12月基礎版
| Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
| 否 | 否 | 醫學 | 4區 | GENETICS & HEREDITY 遺傳學 | 4區 |
中科院 2021年12月升級版
| Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
| 否 | 否 | 醫學 | 4區 | GENETICS & HEREDITY 遺傳學 | 4區 |
中科院 2020年12月舊的升級版
| Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
| 否 | 否 | 醫學 | 4區 | GENETICS & HEREDITY 遺傳學 | 4區 |
Molecular Genetics & Genomic Medicine JCR評價數據（2023-2024年最新版）
| 按JIF指標學科分區 | 收錄子集 | 分區 | 排名 | 百分位 |
| 學科：GENETICS & HEREDITY | SCIE | Q4 | 147 / 191 |
23.3% |
| 按JCI指標學科分區 | 收錄子集 | 分區 | 排名 | 百分位 |
| 學科：GENETICS & HEREDITY | SCIE | Q3 | 142 / 191 |
25.92% |
Molecular Genetics & Genomic Medicine歷年數據統計
影響因子
中科院分區
Molecular Genetics & Genomic Medicine中國學者發文選摘
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1、The effect of growth hormone treatment in children with novel BPTF gene variants: A report of two cases and literature review
Author: Wu, Wenyong; Chen, Ruimin
Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2066
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2、A novel splicing variant of VCAN identified in a Chinese family initially diagnosed with familial exudative vitreoretinopathy
Author: Zhong, Junwei; Shi, Jie; Zhang, Xiaotian; Xu, Ke; Zhang, Xiaohui; Xie, Yue; Li, Yang
Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 2, pp. -. DOI: 10.1002/mgg3.2083
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3、Association of demographic and clinical factors with risk of acute pancreatitis: An exposure-wide Mendelian randomization study
Author: Tang, Qiu-Yi; Yang, Qi; Yu, Xian-Qiang; Liu, Yu-Xiu; Tong, Zhi-Hui; Li, Bai-Qiang; Chen, Ya-Ting; Yu, Evan Yi-Wen; Li, Wei-Qin
Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2091
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4、Compound heterozygous loss-of-function variants in BRAT1 cause lethal neonatal rigidity and multifocal seizure syndrome
Author: Li, Shan; Yu, Shunan; Zhang, Yanzhuo; Wang, Ying; Jiang, Xu; Wu, Chengai
Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2092
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5、Nance-Horan syndrome pedigree due to a novel microdeletion and skewed X chromosome inactivation
Author: Huang, Yazhou; Ma, Linya; Zhang, Zhaoxia; Nie, Shujuan; Zhou, Yuan; Zhang, Jibo; Wang, Chao; Fang, Xingxin; Quan, Yingting; He, Ting; Liu, Anhui; Peng, Dan
Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 2, pp. -. DOI: 10.1002/mgg3.2100
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6、The compound heterozygous mutations of c.607G > a and c.657delC in the FAH gene are associated with renal damage with hereditary tyrosinemia type 1 (HT1)
Author: Chi, Huan; Gan, Chun; Jiang, Yaru; Chen, Dan; Qiu, Jiawen; Yang, Qing; Chen, Yaxi; Wang, Mo; Yang, Haiping; Jiang, Wei; Li, Qiu
Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2090
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7、A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4
Author: Yang, Kun; Wang, Xi; Wang, Wei-Qian; Han, Ming-Yu; Hu, Li-Min; Kang, Dong-Yang; Yang, Jin-Yuan; Liu, Min; Gao, Xue; Yuan, Yong-Yi; Xu, Jin-Cao
Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 3, pp. -. DOI: 10.1002/mgg3.2103
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8、BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity
Author: Yang, Shangying; Li, Zhen; Cheng, Wanyu; Ma, Meijiao; Qi, Rui; Rui, Xue; Ren, Yinghua; Sheng, Xunlun; Rong, Weining
Journal: MOLECULAR GENETICS & GENOMIC MEDICINE. 2023; Vol. 11, Issue 1, pp. -. DOI: 10.1002/mgg3.2095
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