國際簡稱:GENET MED 參考譯名:醫學遺傳學
主要研究方向:醫學-遺傳學 非預警期刊 審稿周期: 偏慢,4-8周 約1.3 weeks
《醫學遺傳學》(Genetics In Medicine)是一本由ELSEVIER出版的以醫學-遺傳學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。該期刊是一本未開放期刊,近三年沒有被列入預警名單。該期刊享有很高的科學聲譽,影響因子不斷增加,發行量也同樣高。
Genetics in Medicine (GIM) is the official journal of the American College of Medical Genetics and Genomics. The journal's mission is to enhance the knowledge, understanding, and practice of medical genetics and genomics through publications in clinical and laboratory genetics and genomics, including ethical, legal, and social issues as well as public health. As genetics and genomics continue to increase in importance and relevance in medical practice, the journal will be an accessible and authoritative resource for the dissemination of medical genetic knowledge to all medical providers through appropriate original research, reviews, commentaries, standards, and guidelines. GIM encourages research that combats racism, includes diverse populations and is written by authors from diverse and underrepresented backgrounds.
CiteScore | SJR | SNIP | CiteScore 指數 | ||||||||
15.2 | 2.697 | 2.538 |
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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。
Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
是 | 否 | 醫學 | 1區 | GENETICS & HEREDITY 遺傳學 | 1區 |
Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
是 | 否 | 醫學 | 1區 | GENETICS & HEREDITY 遺傳學 | 1區 |
Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
是 | 否 | 醫學 | 1區 | GENETICS & HEREDITY 遺傳學 | 1區 |
Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
是 | 否 | 醫學 | 1區 | GENETICS & HEREDITY 遺傳學 | 1區 |
Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
是 | 否 | 醫學 | 1區 | GENETICS & HEREDITY 遺傳學 | 1區 |
Top期刊 | 綜述期刊 | 大類學科 | 小類學科 | ||
是 | 否 | 醫學 | 1區 | GENETICS & HEREDITY 遺傳學 | 1區 |
按JIF指標學科分區 | 收錄子集 | 分區 | 排名 | 百分位 |
學科:GENETICS & HEREDITY | SCIE | Q1 | 18 / 191 |
90.8% |
按JCI指標學科分區 | 收錄子集 | 分區 | 排名 | 百分位 |
學科:GENETICS & HEREDITY | SCIE | Q1 | 11 / 191 |
94.5% |
Author: Miyake, Christina Y.; Lay, Erica J.; Soler-Alfonso, Claudia; Glinton, Kevin E.; Houck, Kimberly M.; Tosur, Mustafa; Moran, Nancy E.; Stephens, Sara B.; Scaglia, Fernando; Howard, Taylor S.; Kim, Jeffrey J.; Pham, Tam Dam; Valdes, Santiago O.; Li, Na; Murali, Chaya N.; Zhang, Lilei; Kava, Maina; Yim, Deane; Beach, Cheyenne; Webster, Gregory; Liberman, Leonardo; Janson, Christopher M.; Kannankeril, Prince J.; Baxter, Samantha; Singer-Berk, Moriel; Wood, Jordan; Mackenzie, Samuel J.; Sacher, Michael; Ghaloul-Gonzalez, Lina; Pedroza, Claudia; Morris, Shaine A.; Ehsan, Saad A.; Azamian, Mahshid S.; Lalani, Seema R.
Journal: GENETICS IN MEDICINE. 2023; Vol. 25, Issue 4, pp. -. DOI: 10.1016/j.gim.2022.11.020
Author: Yang L1,2, Kong Y3, Dong X2, Hu L3, Lin Y2, Chen X3, Ni Q2, Lu Y2, Wu B2, Wang H2, Lu QR4, Zhou W5,6,7.
Journal: Genet Med. 2019 Mar;21(3):564-571. doi: 10.1038/s41436-018-0091-8. Epub 2018 Jun 21.
Author: Garbade SF1, Shen N1,2, Himmelreich N1, Haas D1, Trefz FK1, Hoffmann GF1, Burgard P3, Blau N4,5.
Journal: Genet Med. 2019 Mar;21(3):580-590. doi: 10.1038/s41436-018-0081-x. Epub 2018 Jul 12.
Author: Yin H1, Ma H1, Hussain S1, Zhang H1, Xie X1, Jiang L1, Jiang X1, Iqbal F1, Bukhari I1, Jiang H1, Ali A1, Zhong L1, Li T1, Fan S1, Zhang B1, Gao J1, Li Y1, Nazish J1, Khan T1, Khan M1, Zubair M1, Hao Q1, Fang H1, Huang J2, Huleihel M3, Sha J4, Pandita TK5, Zhang Y6, Shi Q7.
Journal: Genet Med. 2019 Jan;21(1):266. doi: 10.1038/s41436-018-0127-0.
Author: Cai H1, Qing X2, Niringiyumukiza JD1, Zhan X3, Mo D4, Zhou Y5, Shang X6,7.
Journal: Genet Med. 2019 Apr;21(4):826-836. doi: 10.1038/s41436-018-0262-7. Epub 2018 Sep 14.
Author: Ma Y1, Han X2, Zhou X1, Li Y3, Gong S1, Zhang S1, Cai X1, Zhou L1, Luo Y1, Li M1, Liu W1, Zhang X1, Ren Q1, Ji L4.
Journal: Genet Med. 2019 Apr;21(4):939-947. doi: 10.1038/s41436-018-0282-3. Epub 2018 Sep 24.
Author: Liu J1,2,3, Wu N4,5,6,7; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Yang N8,9,10, Takeda K11,12, Chen W1,13, Li W8,9, Du R14, Liu S1,2,15, Zhou Y2,16, Zhang L8,9, Liu Z2,17, Zuo Y1,2,15, Zhao S1,2, Blank R18, Pehlivan D14, Dong S8,9, Zhang J1,2,15, Shen J1,2,15, Si N19,20, Wang Y1, Liu G1,2,15, Li S1, Zhao Y1,2, Zhao H1, Chen Y1,2, Zhao Y1, Song X14, Hu J1, Lin M1,2,13, Tian Y1, Yuan B14, Yu K1, Niu Y2,21, Yu B1, Li X2,21, Chen J1,2, Yan Z1,2,13, Zhu Q1,2, Meng X19,20, Chen X22, Su J23, Zhao X19,20, Wang X20, Ming Y24, Li X25, Raggio CL26, Zhang B1, Weng X1,2,15, Zhang S2,27, Zhang X2,19,20, Watanabe K12, Matsumoto M12; Japan Early Onset Scoliosis Research Group, Jin L8, Shen Y28,29, Sobreira NL30, Posey JE14, Giampietro PF31, Valle D30; Baylor-Hopkins Center for Mendelian Genomics, Liu P14,32, Wu Z2,15,21, Ikegawa S11, Lupski JR14,33,34, Zhang F8,9,10, Qiu G35,36,37.
Journal: Genet Med. 2019 Jan 14. doi: 10.1038/s41436-018-0377-x. [Epub ahead of print]
Author: Posey JE1, O'Donnell-Luria AH2,3,4, Chong JX5, Harel T6, Jhangiani SN7, Coban Akdemir ZH8, Buyske S9,10, Pehlivan D8, Carvalho CMB8, Baxter S3, Sobreira N11, Liu P8,12, Wu N8,13, Rosenfeld JA8, Kumar S14, Avramopoulos D11, White JJ8,5, Doheny KF11,15, Witmer PD11,15, Boehm C11, Sutton VR8, Muzny DM7, Boerwinkle E7,16, Günel M17,18, Nickerson DA19, Mane S20, MacArthur DG2,3, Gibbs RA8,7, Hamosh A11, Lifton RP17,21,22, Matise TC9, Rehm HL2,3, Gerstein M14, Bamshad MJ5,19, Valle D11, Lupski JR23,24,25,26; Centers for Mendelian Genomics.
Journal: Genet Med. 2019 Apr;21(4):798-812. doi: 10.1038/s41436-018-0408-7. Epub 2019 Jan 18.
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