| 缩写名/全名 |
J CLIN RES PEDIATR E
Journal of Clinical Research in Pediatric Endocrinology |
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| ISSN号 | 1308-5727 | ||||||||||||||||||||||||
| 研究方向 | ENDOCRINOLOGY & METABOLISM-PEDIATRICS | ||||||||||||||||||||||||
| 影响因子 | 2015:1.568, 2016:1.118, 2017:1.163, 2018:1.285, 2019:1.803, | ||||||||||||||||||||||||
| 出版国家 | TURKEY | ||||||||||||||||||||||||
| 出版周期 | |||||||||||||||||||||||||
| 年文章数 | 60 | ||||||||||||||||||||||||
| 出版年份 | 0 | ||||||||||||||||||||||||
| 是否OA | Yes | ||||||||||||||||||||||||
| 审稿周期(仅供参考) | |||||||||||||||||||||||||
| 录用比例 | |||||||||||||||||||||||||
| 投稿链接 | http://jcrpe.dergisi.org/login.php?page=0&nocache=b9697d0345753f300abd84d095c47bf8 | ||||||||||||||||||||||||
| 投稿官网 | http://jcrpe.org/home/ | ||||||||||||||||||||||||
| h-index | 30 | ||||||||||||||||||||||||
| CiteScore |
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| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1308-5727%5BISSN%5D | ||||||||||||||||||||||||
| 中科院SCI期刊分区 （ 2018年新版本） |
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| 中科院SCI期刊分区 （ 2020年新版本） |
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| 中国学者近期发表的论文 | |
| 1. | Novel Compound Heterozygous Variants in the LHCGR Gene in a Genetically Male Patient with Female External Genitalia Author: Yan M1, Dilihuma J1, Luo Y1, Reyilanmu B1, Shen Y2, Mireguli M1. Journal: J Clin Res Pediatr Endocrinol. 2019 May 28;11(2):211-217. doi: 10.4274/jcrpe.galenos.2018.2018.0197. Epub 2018 Nov 16. PubMed DOI |
| 2. | A Novel Nonsense Mutation of PHF6 in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann Syndrome. Author: Zhang X1, Fan Y1, Liu X1, Ang Zhu M2, Sun Y1, Yan H1, He Y1, Ye X1, Gu X1, Yu Y1. Journal: J Clin Res Pediatr Endocrinol. 2019 Jan 11. doi: 10.4274/jcrpe.0220. [Epub ahead of print] PubMed DOI |
| 3. | Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis. Author: Bao S, Cai JH, Yang SY, Ren Y, Feng T, Jin T, Li ZR. Journal: J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):135-43. doi: 10.4274/jcrpe.2259. Epub 2015 Dec 18. PubMed |
| 4. | Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis. Author: Liu S, Chai J, Zheng G, Li H, Lu D, Ge Y. Journal: J Clin Res Pediatr Endocrinol. 2016 Mar 5;8(1):21-5. doi: 10.4274/jcrpe.2456. Epub 2015 Dec 18. PubMed |
| 5. | A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism. Author: Zheng X, Ma SG, Qiu YL, Guo ML, Shao XJ. Journal: J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):224-7. doi: 10.4274/jcrpe.2380. Epub 2015 Dec 18. PubMed |
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