发文分析
近年国家/地区发文量统计
| 国家/地区 | 数量 |
|---|---|
| England | 24 |
| USA | 22 |
| Turkey | 21 |
| India | 14 |
| Italy | 11 |
| Belgium | 5 |
| Canada | 5 |
| GERMANY (FED REP GER) | 5 |
| Netherlands | 5 |
| Poland | 5 |
近年机构发文量统计
| 机构 | 数量 |
|---|---|
| MANIPAL ACADEMY OF HIGHER EDUCATION (MAHE) | 5 |
| SHEFFIELD CHILDREN'S NHS FOUNDATION TRUST | 5 |
| UNIVERSITY OF LAUSANNE | 5 |
| UNIVERSITY OF LONDON | 5 |
| KK WOMEN'S & CHILDREN'S HOSPITAL | 4 |
| KU LEUVEN | 4 |
| MEDICAL UNIVERSITY OF WARSAW | 4 |
| UNIVERSITY OF AMSTERDAM | 4 |
| UNIVERSITY OF MANCHESTER | 4 |
| BIRMINGHAM WOMEN'S HOSPITAL | 3 |
近年文章引用他刊数据
| 文章名称 | 引用次数 |
|---|---|
| Mandibulofacial dysostosis Guion-Almeida type caused by ... | 5 |
| Expansion of phenotype of DDX3X syndrome: six new cases | 5 |
| Novel de novo mutation in ZBTB20 in primrose syndrome in... | 4 |
| Cantu syndrome, the changing phenotype: a report of the ... | 3 |
| Novel mutation in MASP1 gene in a new family with 3MC sy... | 3 |
| A novel Ser40Trp variant in IFITM5 in a family with oste... | 3 |
| SIX2 gene haploinsufficiency leads to a recognizable phe... | 3 |
| A novel homozygous variant in CANT1 in a patient with Ki... | 2 |
| Phenotypic delineation of a 12q21 deletion syndrome | 2 |
| A MECOM variant in an African American child with radiou... | 2 |
近年被他刊引用数据
| 期刊名称 | 引用次数 |
|---|---|
| AM J MED GENET A | 40 |
| CLIN DYSMORPHOL | 18 |
| EUR J MED GENET | 16 |
| CLIN GENET | 14 |
| MOL GENET GENOM MED | 10 |
| HUM MOL GENET | 9 |
| ORPHANET J RARE DIS | 9 |
| AM J HUM GENET | 7 |
| ANNU REV GENOM HUM G | 7 |
| GENES-BASEL | 7 |