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Cruchaga & Goate reply

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Cruchaga & Goate reply

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PLD3 variants in population studies

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PLD3 gene variants and Alzheimer's disease

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PLD3 and sporadic Alzheimer's disease risk

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Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

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PLD3 is accumulated on neuritic plaques in Alzheimer’s disease brains

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Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

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National Institute on Aging–Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease

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GENCODE: The reference human genome annotation for The ENCODE Project

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A Pan-European Study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

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National Institute on Aging–Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach

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The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer's disease

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Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing

(2011) Joke Reumers et al.   NATURE BIOTECHNOLOGY

A framework for variation discovery and genotyping using next-generation DNA sequencing data

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

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Fast and accurate short read alignment with Burrows-Wheeler transform

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Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays

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Differential regulation of apoptosis by caspase-mediated cleavage of phospholipase D isozymes

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