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Sensitive and accurate detection of copy number variants using read depth of coverage

Genome Research, 2009-09, Vol.19 (9), p.1586-1592

2009

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The contribution of de novo coding mutations to autism spectrum disorder

Nature (London), 2014-11, Vol.515 (7526), p.216-221

2014

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Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

Neuron (Cambridge, Mass.), 2011-06, Vol.70 (5), p.886-897

2011

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High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

Neuron (Cambridge, Mass.), 2011-12, Vol.72 (6), p.951-963

2011

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IPCC7: Post-Quantum Encryption Scheme Based on a Perfect Dominating Set in 3-Regular Graph

IEEE access, 2024-01, Vol.12, p.1-1

2024

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Rates of contributory de novo mutation in high and low-risk autism families

Communications biology, 2021-09, Vol.4 (1), p.1026-10, Article 1026

2021

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Characterization of SLITRK1 variation in obsessive-compulsive disorder

PloS one, 2013-08, Vol.8 (8), p.e70376-e70376

2013

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Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm

Nucleic acids research, 2011-05, Vol.39 (10), p.e65-e65

2011

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De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

Molecular psychiatry, 2014-06, Vol.19 (6), p.652-658

2014

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature (London), 2012-05, Vol.485 (7397), p.242-245

2012

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Strong Association of De Novo Copy Number Mutations with Autism

Science (American Association for the Advancement of Science), 2007-04, Vol.316 (5823), p.445-449

2007

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Identification of genes and variants associated with quantitative traits using Bayesian factor screening

BMC proceedings, 2011-11, Vol.5 Suppl 9 (Suppl 9), p.S4-S4, Article S4

2011

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A tumour suppressor network relying on the polyamine–hypusine axis

Nature (London), 2012-07, Vol.487 (7406), p.244-248

2012

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AnnTools: a comprehensive and versatile annotation toolkit for genomic variants

Bioinformatics (Oxford, England), 2012-03, Vol.28 (5), p.724-725

2012

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Finding Disease Variants in Mendelian Disorders By Using Sequence Data: Methods and Applications

American journal of human genetics, 2011-12, Vol.89 (6), p.701-712

2011

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Sharing parental genomes by siblings concordant or discordant for autism

Cell genomics, 2023-06, Vol.3 (6), p.100319-100319, Article 100319

2023

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Novel patterns of genome rearrangement and their association with survival in breast cancer

Genome Research, 2006-12, Vol.16 (12), p.1465-1479

2006

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Mapping copy number variation by population-scale genome sequencing

Nature (London), 2011-02, Vol.470 (7332), p.59-65

2011

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Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA

Genomics (San Diego, Calif.), 2013-10, Vol.102 (4), p.270-277

2013

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Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

Human genetics, 2012-03, Vol.131 (3), p.435-442

2012

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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

Nature (London), 2011-06, Vol.474 (7349), p.114

2011

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Inferring haplotypes of copy number variations from high-throughput data with uncertainty

G3 : genes - genomes - genetics, 2011-06, Vol.1 (1), p.35-42

2011

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Sensitive and accurate detection of copy number variants using read depth of coverage

The contribution of de novo coding mutations to autism spectrum disorder

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

IPCC7: Post-Quantum Encryption Scheme Based on a Perfect Dominating Set in 3-Regular Graph

Rates of contributory de novo mutation in high and low-risk autism families

Characterization of SLITRK1 variation in obsessive-compulsive disorder

Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Strong Association of De Novo Copy Number Mutations with Autism

Identification of genes and variants associated with quantitative traits using Bayesian factor screening

A tumour suppressor network relying on the polyamine–hypusine axis

AnnTools: a comprehensive and versatile annotation toolkit for genomic variants

Finding Disease Variants in Mendelian Disorders By Using Sequence Data: Methods and Applications

Sharing parental genomes by siblings concordant or discordant for autism

Novel patterns of genome rearrangement and their association with survival in breast cancer

Mapping copy number variation by population-scale genome sequencing

Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA

Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

Inferring haplotypes of copy number variations from high-throughput data with uncertainty

Erratum: Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

Duplications of the Neuropeptide Receptor VIPR2 Confer Significant Risk for Schizophrenia

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