| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. | Am J Hum Genet | 2010 | 4.95 |
| 2 | Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. | Proc Natl Acad Sci U S A | 2011 | 3.99 |
| 3 | Reduced transcript expression of genes affected by inherited and de novo CNVs in autism. | Eur J Hum Genet | 2011 | 1.48 |
| 4 | Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51. | Am J Hum Genet | 2010 | 1.31 |