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| 基本信息 | 登录收藏 | |||||||||||||||||||||
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期刊名字 | GENETICS IN MEDICINE GENET MED （此期刊被最新的JCR期刊SCIE收录） LetPub评分 8.8
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声誉 9.9 影响力 8.2 速度 7.1 | |||||||||||||||||||||
| 期刊ISSN | 1098-3600 | 微信扫码收藏此期刊 | ||||||||||||||||||||
| E-ISSN | 1530-0366 | |||||||||||||||||||||
| 2023-2024最新影响因子 （数据来源于搜索引擎） | 6.6 点击查看影响因子趋势图 | |||||||||||||||||||||
| 实时影响因子 | 截止2024年10月29日：4.237 | |||||||||||||||||||||
| 2023-2024自引率 | 6.10%点击查看自引率趋势图 | |||||||||||||||||||||
| 五年影响因子 | 7.4 | |||||||||||||||||||||
| JCI期刊引文指标 | 2 | |||||||||||||||||||||
| h-index | 111 | |||||||||||||||||||||
| CiteScore （ 2024年最新版） |
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| 期刊简介 |
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| 期刊官方网站 | https://www.journals.elsevier.com/genetics-in-medicine | |||||||||||||||||||||
| 期刊投稿网址 | https://www.editorialmanager.com/genetmed/default.aspx | |||||||||||||||||||||
| 作者指南网址 | https://www.elsevier.com/journals/genetics-in-medicine/1098-3600/guide-for-authors | |||||||||||||||||||||
| 期刊语言要求 | Language Please write your text in good English (American or British usage is accepted, but not a mixture of these). Authors who feel their English language manuscript may require editing to eliminate possible grammatical or spelling errors and to conform to correct scientific English may wish to use the English Language Editing service. 经LetPub语言功底雄厚的美籍native English speaker精心编辑的稿件，不仅能满足GENETICS IN MEDICINE的语言要求，还能让GENETICS IN MEDICINE编辑和审稿人得到更好的审稿体验，让稿件最大限度地被GENETICS IN MEDICINE编辑和审稿人充分理解和公正评估。LetPub的专业SCI论文编辑服务（包括SCI论文英语润色，同行资深专家修改润色，SCI论文专业翻译，SCI论文格式排版，专业学术制图等）帮助作者准备稿件，已助力全球15万+作者顺利发表论文。部分发表范例可查看：服务好评 论文致谢 。 提交文稿 | |||||||||||||||||||||
| 是否OA开放访问 | No 备注：Archive content is freely available after 12 months. | |||||||||||||||||||||
| 通讯方式 | ELSEVIER SCIENCE INC, STE 800, 230 PARK AVE, NEW YORK, USA, NY, 10169 | |||||||||||||||||||||
| 出版商 | ELSEVIER | |||||||||||||||||||||
| 涉及的研究方向 | 医学-遗传学 | |||||||||||||||||||||
| 出版国家或地区 | USA | |||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||
| 出版周期 | Monthly | |||||||||||||||||||||
| 出版年份 | 1998 | |||||||||||||||||||||
| 年文章数 | 164点击查看年文章数趋势图 | |||||||||||||||||||||
| Gold OA文章占比 | 65.65% | |||||||||||||||||||||
| 研究类文章占比： 文章 ÷（文章 + 综述） | 91.46% | |||||||||||||||||||||
| WOS期刊SCI分区 （ 2023-2024年最新版） | WOS分区等级：1区
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| 中国科学院《国际期刊预警 名单（试行）》名单 | 2024年02月发布的2024版：不在预警名单中 2023年01月发布的2023版：不在预警名单中 2021年12月发布的2021版：不在预警名单中 2020年12月发布的2020版：不在预警名单中 | |||||||||||||||||||||
| 中国科学院SCI期刊分区 （ 2023年12月最新升级版） | 点击查看中国科学院SCI期刊分区趋势图
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| 中国科学院SCI期刊分区 （ 2022年12月升级版） |
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| 中国科学院SCI期刊分区 （ 2021年12月旧的升级版） |
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| SCI期刊收录coverage | Science Citation Index Expanded (SCIE) (2020年1月，原SCI撤销合并入SCIE，统称SCIE) Scopus (CiteScore) | |||||||||||||||||||||
| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1098-3600%5BISSN%5D | |||||||||||||||||||||
| 平均审稿速度 | 网友分享经验： 偏慢,4-8周 来源Elsevier官网： 平均1.3 weeks | |||||||||||||||||||||
| 平均录用比例 | 网友分享经验： 较易 来源Elsevier官网： 26% | |||||||||||||||||||||
| LetPub助力发表 | 经LetPub编辑的稿件平均录用比例是未经润色的稿件的1.5倍，平均审稿时间缩短40%。众多作者在使用LetPub的专业SCI论文编辑服务（包括SCI论文英语润色，同行资深专家修改润色，SCI论文专业翻译，SCI论文格式排版，专业学术制图等）后论文在GENETICS IN MEDICINE顺利发表。
快看看作者怎么说吧：服务好评 论文致谢 | |||||||||||||||||||||
| 编辑信息 |
Editor-in-Chief Robert D. Steiner University of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin, United States of America Deputy Editor-in-Chief David T. Miller, MD, PhD Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, United States of America | |||||||||||||||||||||
| 期刊常用信息链接 |
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| 中国学者近期发表的论文 | |
| 1. | Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients 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 PubMed DOI |
| 2. | Clinical and genetic spectrum of a large cohort of children with epilepsy in China. 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. PubMed DOI |
| 3. | Allelic phenotype values: a model for genotype-based phenotype prediction in phenylketonuria. 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. PubMed DOI |
| 4. | Correction: A homozygous FANCM frameshift pathogenic variant causes male infertility. 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. PubMed DOI |
| 5. | CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies. 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. PubMed DOI |
| 6. | A new clinical screening strategy and prevalence estimation for glucokinase variant-induced diabetes in an adult Chinese population. 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. PubMed DOI |
| 7. | TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. 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] PubMed DOI |
| 8. | Insights into genetics, human biology and disease gleaned from family based genomic studies. 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. PubMed DOI |
| 9. | Xrare: a machine learning method jointly modeling phenotypes and genetic evidence for rare disease diagnosis. Author: Li Q1, Zhao K1, Bustamante CD2,3, Ma X4,5, Wong WH6,7. Journal: Genet Med. 2019 Jan 24. doi: 10.1038/s41436-019-0439-8. [Epub ahead of print] PubMed DOI |
| 10. | Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome. Author: van der Sluijs PJ1, Jansen S2, Vergano SA3, Adachi-Fukuda M4, Alanay Y5, AlKindy A6, Baban A7, Bayat A8, Beck-Wödl S9, Berry K10, Bijlsma EK1, Bok LA11, Brouwer AFJ12, van der Burgt I13, Campeau PM14, Canham N15,16, Chrzanowska K17, Chu YWY18, Chung BHY18, Dahan K19, De Rademaeker M20, Destree A19, Dudding-Byth T21, Earl R22, Elcioglu N23, Elias ER24, Fagerberg C25, Gardham A15, Gener B26, Gerkes EH27, Grasshoff U9, van Haeringen A1, Heitink KR28, Herkert JC27, den Hollander NS1, Horn D29, Hunt D30, Kant SG1, Kato M31, Kayserili H32, Kersseboom R33, Kilic E34, Krajewska-Walasek M17, Lammers K35, Laulund LW36, Lederer D19, Lees M37, López-González V38, Maas S39, Mancini GMS33, Marcelis C2, Martinez F40, Maystadt I19, McGuire M41, McKee S42, Mehta S43, Metcalfe K44, Milunsky J45, Mizuno S46, Moeschler JB47, Netzer C48, Ockeloen CW2, Oehl-Jaschkowitz B49, Okamoto N50, Olminkhof SNM51, Orellana C40, Pasquier L52, Pottinger C53, Riehmer V48, Robertson SP54, Roifman M55,56, Rooryck C57, Ropers FG58, Rosello M40, Ruivenkamp CAL1, Sagiroglu MS59, Sallevelt SCEH60, Calvo AS61, Simsek-Kiper PO62, Soares G63, Solaeche L64, Sonmez FM65, Splitt M66, Steenbeek D28, Stegmann APA60, Stumpel CTRM60, Tanabe S67, Uctepe E68, Utine GE62, Veenstra-Knol HE27, Venkateswaran S69, Vilain C70,71, Vincent-Delorme C72, Vulto-van Silfhout AT2, Wheeler P73, Wilson GN74, Wilson LC37, Wollnik B75, Kosho T76, Wieczorek D77, Eichler E78, Pfundt R2, de Vries BBA2, Clayton-Smith J44, Santen GWE79. Journal: Genet Med. 2019 Jan 29. doi: 10.1038/s41436-018-0368-y. [Epub ahead of print] PubMed DOI |
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