Related references
Note: Only part of the references are listed.A Genome-wide Comparison of the Functional Properties of Rare and Common Genetic Variants in Humans
Qianqian Zhu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Initial impact of the sequencing of the human genome
Eric S. Lander
NATURE (2011)
Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes
Erin L. Heinzen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Genetic Heterogeneity in Human Disease
Jon McClellan et al.
CELL (2010)
Sensitivity of Noninvasive Prenatal Detection of Fetal Aneuploidy from Maternal Plasma Using Shotgun Sequencing Is Limited Only by Counting Statistics
H. Christina Fan et al.
PLOS ONE (2010)
Copy-number variants in neurodevelopmental disorders: promises and challenges
Alison K. Merikangas et al.
TRENDS IN GENETICS (2009)