Clan Genomics and the Complex Architecture of Human Disease

References

Page 1

	Year	Citations
A map of human genome variation from population-scale sequencing Nature Human VariationMedicineGeneticsHuman Genome VariationGenetic Variation	2010	8K
A haplotype map of the human genome Nature	2005	5.9K
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, Nature Genetics ChromatinGenome InstabilityTranscriptional RegulationMendelian DisorderX-linked Mecp2	1999	5K
A second generation human haplotype map of over 3.1 million SNPs Liuda Ziaugra, Chibuzor Nkwodimmah, Missy Dixon, Nature Haplotype DeterminationGenotype-phenotype AssociationMedicineGeneticsHuman Polymorphism	2007	4.5K
α-Synuclein Locus Triplication Causes Parkinson's Disease Andrew Singleton Science MitophagyFarnesyltransferase InhibitionSocial SciencesCell AutophagyAutophagy	2003	4.3K
Accurate whole human genome sequencing using reversible terminator chemistry David Bentley, Shankar Balasubramanian, Harold Swerdlow, Nature	2008	3.7K
Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease Stefano Romeo, Julia Kozlitina, Chao Xing, Nature Genetics Metabolic SyndromeHepatologyGeneticsLiver PhysiologyGenetic Epidemiology	2008	3.3K
Integrating common and rare genetic variation in diverse human populations Nature Allelic VariantHaplotype DeterminationHuman VariationNatural SciencesGenetics	2010	3.1K
The Wellcome Trust Case Control Consortium, U.K. Kaspar Mossman Scientific American Data TrustArtsBusinessLawTrust	2008	2.7K
Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development Philip J. Stephens, Chris Greenman, Beiyuan Fu, Cell	2011	2.4K

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