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| Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation RC Allen, HY Zoghbi, AB Moseley, HM Rosenblatt, JW Belmont American journal of human genetics 51 (6), 1229, 1992 | 1978 | 1992 |
| Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, DW Stockton, C Amos, ... Nature genetics 15 (1), 62-69, 1997 | 1936 | 1997 |
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| Diseases of unstable repeat expansion: mechanisms and common principles JR Gatchel, HY Zoghbi Nature Reviews Genetics 6 (10), 743-755, 2005 | 1024 | 2005 |
| A protein–protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration J Lim, T Hao, C Shaw, AJ Patel, G Szabó, JF Rual, CJ Fisk, N Li, ... Cell 125 (4), 801-814, 2006 | 985 | 2006 |
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| Postnatal neurodevelopmental disorders: meeting at the synapse? HY Zoghbi Science 302 (5646), 826-830, 2003 | 833 | 2003 |
