B. Coe

Bradley P. Coe, B. Coe, S. Lam, 2013, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

EZH 2 is Required for Viability of SCLC Cells

Bradley P. Coe, B. Coe, S. Lam, 2013 .

A genetic model for neurodevelopmental disease

Bradley P. Coe, B. Coe, E. Eichler, 2012, Current Opinion in Neurobiology.

The genetic variability and commonality of neurodevelopmental disease

Bradley P. Coe, B. Coe, E. Eichler, 2012, American journal of medical genetics. Part C, Seminars in medical genetics.

Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes

Bradley P. Coe, B. Coe, C. Baker, 2018, Genetics in Medicine.

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity

Trygve E Bakken, Bradley P. Coe, B. Coe, 2018, Nature Genetics.

FACADE: a fast and sensitive algorithm for the segmentation and calling of high resolution array CGH data

Bradley P. Coe, B. Coe, C. MacAulay, 2010, Nucleic acids research.

Genomic markers for malignant progression in pulmonary adenocarcinoma with bronchioloalveolar features

Bradley P. Coe, B. Coe, W. Lam, 2008, Proceedings of the National Academy of Sciences.

Construction and optimization of chromosome arm-specific comparative genomic hybridization arrays for identifying genetic alterations in preinvasive lung cancers.

B. Coe, S. Lam, C. MacAulay, 2004, Chest.

Inverted duplication with terminal deletion of 5p and no cat‐like cry

Bradley P. Coe, B. Coe, J. Schein, 2008, American journal of medical genetics. Part A.

Integrative genomic and gene expression analysis of chromosome 7 identified novel oncogene loci in non-small cell lung cancer.

Bradley P. Coe, B. Coe, S. Lam, 2008, Genome.

Reﬁnement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder

Catarina D. Campbell, B. Coe, C. Baker, 2013 .

Copy-number variation and false positive prenatal aneuploidy screening results.

Matthew W. Snyder, J. Kitzman, J. Shendure, 2015, The New England journal of medicine.

Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia.

Bradley P. Coe, B. Coe, Niklas Krumm, 2013, American journal of human genetics.

Response to Benn

Bradley P. Coe, B. Coe, J. Rosenfeld, 2013, Genetics in Medicine.

SHORT REPORT Whole genome tiling path array CGH analysis of segmental copy number alterations in cervical cancer cell lines

Bradley P. Coe, B. Coe, C. MacAulay, 2006 .

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Richard A Marini, W. T. Harvey, B. Coe, 2020, Nature Communications.

Corrigendum: A copy number variation morbidity map of developmental delay

B. Coe, J. Rosenfeld, C. Baker, 2014, Nature Genetics.

B. Coe, E. Eichler, B. V. Bon, 2015 .

Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV.

Bradley P. Coe, B. Coe, C. Baker, 2016, American journal of human genetics.

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.

Sven Bergmann, Niklas Krumm, Bradley P. Coe, 2014, American journal of human genetics.

Genomic Patterns of De Novo Mutation in Simplex Autism

Len A. Pennacchio, Michael C. Zody, Archana Raja, 2017, Cell.

Copy number variations in the human genome and strategies for analysis.

Bradley P. Coe, B. Coe, W. Lam, 2010, Methods in molecular biology.

Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

Carlos S. Moreno, Carl Baker, Evan E. Eichler, 2011, PLoS genetics.

An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer

Raj Chari, Bradley P. Coe, Emily A. Vucic, 2010, BMC Systems Biology.

Genomic and gene expression profiling of minute alterations of chromosome arm 1p in small-cell lung carcinoma cells

Bradley P. Coe, B. Coe, W. Lam, 2005, British Journal of Cancer.

DNA amplification is a ubiquitous mechanism of oncogene activation in lung and other cancers

Bradley P. Coe, B. Coe, W. Lam, 2008, Oncogene.

Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications

B. Coe, E. Eichler, A. Sulovari, 2017, Genome Medicine.

Sequencing of sporadic Attention‐Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder

Karynne E. Patterson, Bradley P. Coe, B. Coe, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency

Kali T. Witherspoon, Bradley P. Coe, B. Coe, 2017, European Journal of Human Genetics.

De novo genic mutations among a Chinese autism spectrum disorder cohort

Zev N. Kronenberg, Bradley P. Coe, B. Coe, 2016, Nature Communications.

Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.

Bradley P. Coe, B. Coe, J. Schuurs-Hoeijmakers, 2016, American journal of human genetics.

Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development

Jay Shendure, Serafino Buono, Hilde Peeters, 2014, Cell.

Kali T. Witherspoon, Bradley P. Coe, B. Coe, 2014, Nature Genetics.

Hotspots of missense mutation identify novel neurodevelopmental disorder genes and functional domains

Bradley P. Coe, B. Coe, K. Friend, 2017, Nature Neuroscience.

Characteristics of de novo structural changes in the human genome

Alexander Schönhuth, Edwin Cuppen, Victor Guryev, 2015, Genome research.

Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID

Kali T. Witherspoon, Bradley P. Coe, R Bernier, 2016, Molecular Psychiatry.

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

B. Coe, K. Friend, P. Lockhart, 2017, Nature Genetics.

Resource Genomic Patterns of De Novo Mutation in Simplex Autism Graphical Abstract Highlights

B. Coe, E. Eichler, F. Hormozdiari, 2022 .

Recent ultra-rare inherited variants implicate new autism candidate risk genes

Trygve E Bakken, Bradley P. Coe, B. Coe, 2021, Nature Genetics.

Gain of a region on 7p22.3, containing MAD1L1, is the most frequent event in small‐cell lung cancer cell lines

Calum MacAulay, Luc Girard, Bradley P. Coe, 2006, Genes, chromosomes & cancer.

The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant

Bradley P. Coe, Jessie H. Conta, B. Coe, 2015, European Journal of Human Genetics.

Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus

Mitchell R. Vollger, Bradley P. Coe, A. Pang, 2019, PLoS genetics.

A high-quality human reference panel reveals the complexity and distribution of genomic structural variants

Alexandros Kanterakis, Mark Santcroos, David van Enckevort, 2016, Nature Communications.

Differential disruption of cell cycle pathways in small cell and non-small cell lung cancer

Bradley P. Coe, B. Coe, S. Lam, 2006, British Journal of Cancer.

Divergent Genomic and Epigenomic Landscapes of Lung Cancer Subtypes Underscore the Selection of Different Oncogenic Pathways during Tumor Development

John D. Minna, John Yee, Raj Chari, 2011, PloS one.

Integrative Genomic Analyses Identify BRF2 as a Novel Lineage-Specific Oncogene in Lung Squamous Cell Carcinoma

Calum MacAulay, John D. Minna, John Yee, 2010, PLoS medicine.

Genomic Deregulation of the E2F/Rb Pathway Leads to Activation of the Oncogene EZH2 in Small Cell Lung Cancer

Bradley P. Coe, B. Coe, S. Lam, 2013, PloS one.

Integrative Genomic Analyses Identifies GGA2 as a Cooperative Driver of EGFR‐Mediated Lung Tumorigenesis

Bradley P. Coe, B. Coe, S. Lam, 2019, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Estimates of penetrance for recurrent pathogenic copy-number variations

Bradley P. Coe, B. Coe, J. Rosenfeld, 2012, Genetics in Medicine.

A family study implicates GBE1 in the etiology of autism spectrum disorder

Bradley P. Coe, B. Coe, N. Brown, 2021, Human mutation.

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model

Bradley P. Coe, B. Coe, C. Baker, 2018, Molecular Autism.

Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.

Bradley P. Coe, Mahshid S. Azamian, Lisa T. Emrick, 2016, American journal of human genetics.

Overexpression of LRP12, a gene contained within an 8q22 amplicon identified by high-resolution array CGH analysis of oral squamous cell carcinomas

Bradley P. Coe, B. Coe, W. Lam, 2004, Oncogene.

Transcriptome Profiles of Carcinoma-in-Situ and Invasive Non-Small Cell Lung Cancer as Revealed by SAGE

Raj Chari, Bradley P. Coe, Wan L. Lam, 2010, PloS one.

SeeGH – A software tool for visualization of whole genome array comparative genomic hybridization data

Calum MacAulay, Bradley P. Coe, Wan L. Lam, 2004, BMC Bioinformatics.

High-resolution array CGH increases heterogeneity tolerance in the analysis of clinical samples.

Calum MacAulay, Cathie Garnis, B. Coe, 2005, Genomics.

SIGMA2: A system for the integrative genomic multi-dimensional analysis of cancer genomes, epigenomes, and transcriptomes

Calum MacAulay, Raymond T. Ng, Raj Chari, 2008, BMC Bioinformatics.

Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissues

Bradley P. Coe, B. Coe, W. Lam, 2006, BMC Genomics.

MD-SeeGH: a platform for integrative analysis of multi-dimensional genomic data

Calum MacAulay, Raymond T. Ng, Bradley P. Coe, 2008, BMC Bioinformatics.

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

Bradley P. Coe, M. Pirinen, C. Spencer, 2014, Human molecular genetics.

Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation

Bradley P. Coe, Allen D. Delaney, B. Coe, 2011, BMC Medical Genomics.

Comparative genomic hybridization on BAC arrays.

B. Coe, W. Lam, R. Chari, 2009, Methods in molecular biology.

The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism

B. Coe, A. V. Vulto-van Silfhout, B. D. de Vries, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

Germline DNA Copy Number Aberrations Identified as Potential Prognostic Factors for Breast Cancer Recurrence

Bradley P. Coe, B. Coe, J. Mackey, 2013, PloS one.

High‐resolution chromosome arm 5p array CGH analysis of small cell lung carcinoma cell lines

Bradley P. Coe, Calum Macaulay, Cathie Garnis, 2005, Genes, chromosomes & cancer.

A sequence-based approach to identify reference genes for gene expression analysis

Bradley P. Coe, B. Coe, S. Lam, 2010, BMC Medical Genomics.

Whole genome tiling path array CGH analysis of segmental copy number alterations in cervical cancer cell lines

Calum MacAulay, Bradley P. Coe, B. Coe, 2007, International journal of cancer.

Rare and de novo duplications containing SHOX in clubfoot

B. Coe, M. Dobbs, B. Sadler, 2020, Journal of Medical Genetics.

Brain white matter structure and COMT gene are linked to second-language learning in adults

Patricia K Kuhl, Bradley P. Coe, Evan E Eichler, 2016, Proceedings of the National Academy of Sciences.

risk factor for psychosis

Bradley P. Coe, M. Pirinen, C. Freeman, 2014 .

Novel regions of amplification on 8q distinct from the MYC locus and frequently altered in oral dysplasia and cancer

Bradley P. Coe, B. Coe, W. Lam, 2004, Genes, chromosomes & cancer.

Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes

B. Coe, C. Baker, E. Eichler, 2018, Genetics in Medicine.

Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations.

Bradley P. Coe, B. Coe, E. Eichler, 2022, European journal of medical genetics.

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Joseph T. Glessner, Bradley P. Coe, B. Coe, 2020, Nature Communications.

Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease

Bradley P. Coe, Albee Y. Ling, S. Gabriel, 2019, The New England journal of medicine.

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

B. Coe, E. Eichler, J. Glessner, 2020, Nature Communications.

You want Ketchup with your DNA Chips? An Overview of Expression Microarrays

Bradley Coe, B. Coe, 2003 .

Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry

Bradley P. Coe, B. Coe, D. Nickerson, 2016, Transfusion.

Comment re: a comparison of DNA copy number profiling platforms.

B. Coe, C. MacAulay, W. Lam, 2008, Cancer Research.

SeeGH – A software tool for visualization of whole genome array comparative genomic hybridization data

Bradley P. Coe, B. Coe, R. deLeeuw, 2004, BMC Bioinformatics.