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Publications in Genetics

Oxime-Based Linker Libraries as a General Approach for the Rapid Generation and Screening of Multidentate Inhibitors

Nature Protocols

Molecular Biology

English

Human Mutations in NDE1 Cause Extreme Microcephaly With Lissencephaly

American Journal of Human Genetics

English

Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway

American Journal of Human Genetics

English

Comprehensive Measurement of Respiratory Activity in Permeabilized Cells Using Extracellular Flux Analysis

Nature Protocols

Molecular Biology

English

Computational Protein–ligand Docking and Virtual Drug Screening With the AutoDock Suite

Nature Protocols

Molecular Biology

English

Genome-Wide Association Analysis for Multiple Continuous Secondary Phenotypes

American Journal of Human Genetics

English

A Genome-Wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases

American Journal of Human Genetics

English

The Orphan Disease Networks

American Journal of Human Genetics

English

Somatic Mutations in NEK9 Cause Nevus Comedonicus

American Journal of Human Genetics

English

A Permutation Procedure to Correct for Confounders in Case-Control Studies, Including Tests of Rare Variation

American Journal of Human Genetics

English