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| 1 | Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies显示文摘 | Mefford HC Muhle H Ostertag P | 2010 | PLoS Genet2010，6，10： | 1 |
| 2 | Genotype to phenotype-discovery and characterization of novel genomic disorders in a 'genotype-first' era 显示文摘 | Mefford HC | 2009 | Genet Med2009，11，12： | 1 |
| 3 | Rare copy number variants are an important cause of epileptic encephalopathies显示文摘 | Mefford HC Yendle SC Hsu C | | 0，，06： | 1 |
| 4 | Genomics, intellectual disability, and autism显示文摘 | Mefford HC Batshaw ML Hoffman EP | 2012 | N Engl J Med2012，366，8： | 1 |
| 5 | Duplication hotspots, rare genomic disorders and common disease显示文摘 | Mefford HC Eichler EE | 2009 | Curr Opin Genet Dev2009，19，3： | 1 |
| 6 | Genetic contribution to common epilepsies 显示文摘 | Sisodiya SM Mefford HC | 2011 | Curt Opin Neurol2011，24，2： | 1 |
| 7 | Genome-wide copy number variation in epilepsy : novel susceptibility loci in idiopathic generalized and focal epilepsies 显示文摘 | Mefford HC Muhle H Ostertag P | 2010 | PLoS Genet2010，6，10： | 1 |
| 8 | Duplication hotspols, rare gen~ml- ic disorders, anti comm+m disease显示文摘 | MEFFORD HC EICHI ER EE | 2009 | Curr ()pin ( +met Dev2009，19，3： | 1 |
| 9 | Duplication hotspots, rare genomic disorders, and common disease 显示文摘 | Mefford HC Eichler EE | 2009 | Curt Opin Genet Dev2009，19，3： | 1 |
| 10 | The complex structure and dynamic evolution of human subtelomeres显示文摘 | Mefford HC Trask BJ | 2002 | Nat Rev Genet2002，3，2： | 1 |
| 11 | Thinking about cognition and epilepsy显示文摘 | Mefford HC | 2014 | Epilepsy Behav2014，41，12： | 1 |
| 12 | Duplication hotspots, rare genomic disorders, and common disease显示文摘 | Mefford HC Eichler EE | 2009 | Curr Opin Genet Dev2009，19，3： | 1 |
| 13 | Genome-wide copy number variation in epilepsy:Novel susceptibility loci in idiopathic generalized and focal epilepsies显示文摘 | Mefford HC Muhle H Ostertsg P | | 0，，05： | 1 |
| 14 | Rare copy number variants are an important cause of epileptic encephalopathies 显示文摘 | Mefford HC Yendle SC Hsu C | 2011 | Ann Neurol2011，70，6： | 1 |
| 15 | Duplication hotspots,rare genomic disorders,and common disease显示文摘 | Mefford HC Eichler EE | | 0，，03： | 1 |
| 16 | Rare copy number variants are an important cause of epileptic encephalopathies显示文摘 | Mefford HC Yendle SC Hsu C | | 0，，06： | 1 |
| 17 | Genotype to phenotype-discovery and characterization of novel genomic disorders in a 'genotype-first' era显示文摘 | Mefford HC | | 0，，12： | 1 |
| 18 | Duplication hotspots,rare genomic disorders,and common disease显示文摘 | Mefford HC Eichler EE | | 0，，03： | 1 |
| 19 | Further delineation of the 15q13 micradeletion and duplication syndromes:A clinical spectrum varying from non-pathogenic to a severe outcome显示文摘 | Van Bon BW Mefford HC Menten B | | 0，，08： | 1 |
| 20 | Duplication hotspots,rare genomic disorders, and common disease 显示文摘 | Mefford HC Eichler EE | 2009 | Curr Opin Genet Dev2009，19，3： | 1 |
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