Clan Genomics and the Complex Architecture of Human Disease

A map of human genome variation from population-scale sequencing

Nature · 2010 · 8K citations · Full text

Human Variation, Medicine, Genetics +6

A haplotype map of the human genome

Nature · 2005 · 5.9K citations · Full text

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan et al. · Nature Genetics · 1999 · 5K citations

Chromatin, Genome Instability, Transcriptional Regulation +11

A second generation human haplotype map of over 3.1 million SNPs

Liuda Ziaugra, Chibuzor Nkwodimmah, Missy Dixon et al. · Nature · 2007 · 4.5K citations · Full text

Haplotype Determination, Genotype-phenotype Association, Medicine +7

α-Synuclein Locus Triplication Causes Parkinson's Disease

Andrew Singleton · Science · 2003 · 4.3K citations

Mitophagy, Farnesyltransferase Inhibition, Social Sciences +16