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GENETICS IN MEDICINE

2023年12月最新中科院分区表数据已经更新,欢迎查询! 如果您对期刊系统有任何需求或者问题,欢迎点击此处反馈给我们。

按期刊名首写字母查看 GENET MED最新评论:摘要主要说明论文的目的、所用的方法及取得的结果及意义。摘要里最多只需包括4个或5个最重要的观点、结果或含意。 (2021-12-30)


期刊名:   ISSN:   研究方向:   影响因子: -   SCI收录:
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GENETICS IN MEDICINE期刊基本信息Hello,您是该期刊的第41040位访客


基本信息 登录收藏
期刊名字GENETICS IN MEDICINEGENETICS IN MEDICINE

GENET MED
(此期刊被最新的JCR期刊SCIE收录)

LetPub评分
8.8
51人评分
我要评分

声誉
9.9

影响力
8.2

速度
7.1

期刊ISSN1098-3600
微信扫码收藏此期刊
E-ISSN1530-0366
2022-2023最新影响因子
(数据来源于搜索引擎)
8.8 点击查看影响因子趋势图
实时影响因子 截止2024年3月26日:6.17
2022-2023自引率6.80%点击查看自引率趋势图
五年影响因子8.9
h-index 111
CiteScore
CiteScoreSJRSNIPCiteScore排名
15.402.7452.761
学科分区排名百分位
大类:Medicine
小类:Genetics (clinical)
Q14 / 90

期刊简介
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.
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 231点击查看年文章数趋势图
Gold OA文章占比29.01%
研究类文章占比:
文章 ÷(文章 + 综述)
91.34%
WOS期刊SCI分区
2022-2023年最新版
WOS分区等级:1区

按学科分区JIF分区JIF排名JIF百分位
学科:GENETICS & HEREDITY
类别:SCIE
Q113/171
中科院《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
中科院SCI期刊分区
2023年12月最新升级版
点击查看中科院SCI期刊分区趋势图
大类学科小类学科Top期刊综述期刊
医学 3区1区1区
GENETICS & HEREDITY
遗传学
2区2区1区
中科院SCI期刊分区
2022年12月升级版
大类学科小类学科Top期刊综述期刊
医学 3区1区3区
GENETICS & HEREDITY
遗传学
2区1区1区
中科院SCI期刊分区
2021年12月旧的升级版
大类学科小类学科Top期刊综述期刊
医学 2区1区2区
GENETICS & HEREDITY
遗传学
1区2区1区
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
同领域相关期刊 GENETICS IN MEDICINE期刊近年CiteScore指标趋势图
该杂志的自引率趋势图 GENETICS IN MEDICINE中科院SCI期刊分区趋势图
该杂志的年文章数趋势图 同领域作者分享投稿经验
GENETICS IN MEDICINE上中国学者近期发表的论文  
  • 同领域相关期刊
  • 期刊CiteScore趋势图
  • 期刊自引率趋势图
  • 中科院SCI期刊分区趋势图
  • 年文章数趋势图
  • 该期刊中国学者近期发表论文
  • 中科院SCI期刊分区相关期刊
  • 同类著名期刊名称 h-index CiteScore
    NATURE REVIEWS GENETICS32073.20
    NATURE GENETICS52753.80
    TRENDS IN GENETICS20818.10
    Annual Review of Genetics17119.80
    AMERICAN JOURNAL OF HUMAN GENETICS28017.20
    Annual Review of Genomics and Human Genetics10415.10
    HUMAN GENETICS1269.70
    PLoS Genetics1949.00
    DNA RESEARCH897.10
    JOURNAL OF MEDICAL GENETICS1599.60
    中科院SCI期刊分区同大类学科的热搜期刊 浏览次数
    MEDICINE619265
    BIOMATERIALS526246
    BIOMEDICINE & PHARMACOTHERAPY484202
    Journal of Materials Chemistry B469614
    Frontiers in Pharmacology466085
    Frontiers in Immunology439181
    JOURNAL OF ETHNOPHARMACOLOGY419451
    COLLOIDS AND SURFACES B-BIOINTERFACES412320
    Frontiers in Oncology397003
    COMPUTERS IN BIOLOGY AND MEDICINE392181
  •  

    GENETICS IN MEDICINE GENETICS IN MEDICINE
    我来预测明年:
    稳步上升 表现平稳 逐渐下降  刷新
  •  

     
  •  

     
  •  

     
  • 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
  • 同大类学科的其他著名期刊名称 h-index CiteScore
    CA-A CANCER JOURNAL FOR CLINICIANS144642.90
    LANCET700133.20
    NEW ENGLAND JOURNAL OF MEDICINE933134.40
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION62245.40
    NATURE REVIEWS DRUG DISCOVERY289123.80
    BMJ-British Medical Journal015.30
    BMJ-British Medical Journal015.30
    NATURE REVIEWS IMMUNOLOGY35183.00
    NATURE MEDICINE497107.50
    Nature Reviews Disease Primers4860.90
    同分区等级的其他期刊名称 h-index CiteScore
    CA-A CANCER JOURNAL FOR CLINICIANS144642.90
    LANCET700133.20
    NEW ENGLAND JOURNAL OF MEDICINE933134.40
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION62245.40
    NATURE REVIEWS DRUG DISCOVERY289123.80
    NATURE REVIEWS MOLECULAR CELL BIOLOGY386164.40
    BMJ-British Medical Journal015.30
    BMJ-British Medical Journal015.30
    NATURE REVIEWS IMMUNOLOGY35183.00
    NATURE REVIEWS MICROBIOLOGY25060.20


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