| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Highly effective SNP-based association mapping and management of recessive defects in livestock. | Nat Genet | 2008 | 2.68 |
| 2 | The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering. | J Neurosci | 2004 | 1.75 |
| 3 | Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. | Nat Genet | 2006 | 1.49 |
| 4 | The glycinergic system in human startle disease: a genetic screening approach. | Front Mol Neurosci | 2010 | 1.02 |
| 5 | Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease. | J Biol Chem | 2012 | 0.93 |
| 6 | A critical role for glycine transporters in hyperexcitability disorders. | Front Mol Neurosci | 2008 | 0.84 |