发文地区与机构
近年国家 / 地区发文量统计
| 国家 / 地区 | 发文量 |
|---|---|
| CHINA MAINLAND | 487 |
| USA | 239 |
| Italy | 62 |
| GERMANY (FED REP GER) | 45 |
| Canada | 44 |
| Japan | 40 |
| Iran | 39 |
| England | 32 |
| France | 31 |
| Netherlands | 31 |
近年机构发文量统计
| 机构 | 发文量 |
|---|---|
| SHANGHAI JIAO TONG UNIVERSITY | 35 |
| CHINESE ACADEMY OF MEDICAL SCIENCES - P... | 34 |
| CENTRAL SOUTH UNIVERSITY | 29 |
| BAYLOR COLLEGE OF MEDICINE | 26 |
| UNIVERSITY OF CALIFORNIA SYSTEM | 26 |
| HARVARD UNIVERSITY | 24 |
| CAPITAL MEDICAL UNIVERSITY | 22 |
| NORTHWEST UNIVERSITY XI'AN | 22 |
| FUDAN UNIVERSITY | 21 |
| CHINA MEDICAL UNIVERSITY | 19 |
文章引用情况
1
Association study between genetic polymorphisms in folate metabolism and gastric cancer susceptibility in Chinese Han population: A case-control study2
Retrotransposon insertion as a novel mutational event in Bardet-Biedl syndrome3
Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy4
Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism5
CBS mutations are good predictors for B6-responsiveness: A study based on the analysis of 35 Brazilian Classical Homocystinuria patients6
Whole-exome sequencing for variant discovery in blepharospasm7
Next-generation sequencing unravels extensive genetic alteration in recurrent ovarian cancer and unique genetic changes in drug-resistant recurrent ovarian cancer8
Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications9
Novel mutations of COL4A COL4A and COL4A5 genes in Chinese patients with Alport Syndrome using next generation sequence technique10
Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low-pass whole-genome sequencing