A Genetic Model for Neurodevelopmental Disease

بواسطة Coe, Bradley P., Girirajan, Santhosh, Eichler, Evan E.
منشور في 2012

The Genetic Variability and Commonality of Neurodevelopmental Disease

بواسطة COE, BRADLEY P., GIRIRAJAN, SANTHOSH, EICHLER, EVAN E.
منشور في 2012

Genome structural variation discovery and genotyping

بواسطة Alkan, Can, Coe, Bradley P., Eichler, Evan E.
منشور في 2011

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

بواسطة Coe, Bradley P., Chari, Raj, MacAulay, Calum, Lam, Wan L.
منشور في 2010

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

بواسطة Chari, Raj, Coe, Bradley P, Vucic, Emily A, Lockwood, William W, Lam, Wan L
منشور في 2010

Estimates of penetrance for recurrent pathogenic copy-number variations

بواسطة Rosenfeld, Jill A., Coe, Bradley P., Eichler, Evan E., Cuckle, Howard, Shaffer, Lisa G.
منشور في 2013

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

بواسطة Wilfert, Amy B., Sulovari, Arvis, Turner, Tychele N., Coe, Bradley P., Eichler, Evan E.
الحاوية / القاعدة Genome Med (2017)

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

بواسطة Chi, Bryan, deLeeuw, Ronald J, Coe, Bradley P, MacAulay, Calum, Lam, Wan L
منشور في 2004

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

بواسطة Mamiya, Ping C., Richards, Todd L., Coe, Bradley P., Eichler, Evan E., Kuhl, Patricia K.
الحاوية / القاعدة Proc Natl Acad Sci U S A (2016)

EZH2 promotes E2F driven SCLC tumorigenesis through modulation of apoptosis and cell cycle regulation

بواسطة Hubaux, Roland, Thu, Kelsie L., Coe, Bradley P., MacAulay, Calum, Lam, Stephen, Lam, Wan L.
منشور في 2013

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

بواسطة Chi, Bryan, deLeeuw, Ronald J, Coe, Bradley P, Ng, Raymond T, MacAulay, Calum, Lam, Wan L
منشور في 2008

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

بواسطة Duyzend, Michael H., Nuttle, Xander, Coe, Bradley P., Baker, Carl, Nickerson, Deborah A., Bernier, Raphael, Eichler, Evan E.
الحاوية / القاعدة Am J Hum Genet (2016)

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

بواسطة Sapkota, Yadav, Ghosh, Sunita, Lai, Raymond, Coe, Bradley P., Cass, Carol E., Yasui, Yutaka, Mackey, John R., Damaraju, Sambasivarao
منشور في 2013

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

بواسطة Aviel-Ronen, Sarit, Qi Zhu, Chang, Coe, Bradley P, Liu, Ni, Watson, Spencer K, Lam, Wan L, Tsao, Ming Sound
منشور في 2006

A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders

بواسطة Jacquemont, Sébastien, Coe, Bradley P., Hersch, Micha, Duyzend, Michael H., Krumm, Niklas, Bergmann, Sven, Beckmann, Jacques S., Rosenfeld, Jill A., Eichler, Evan E.
منشور في 2014

SIGMA: A System for Integrative Genomic Microarray Analysis of Cancer Genomes

بواسطة Chari, Raj, Lockwood, William W, Coe, Bradley P, Chu, Anna, Macey, Devon, Thomson, Andrew, Davies, Jonathan J, MacAulay, Calum, Lam, Wan L
منشور في 2006

SIGMA(2): A system for the integrative genomic multi-dimensional analysis of cancer genomes, epigenomes, and transcriptomes

بواسطة Chari, Raj, Coe, Bradley P, Wedseltoft, Craig, Benetti, Marie, Wilson, Ian M, Vucic, Emily A, MacAulay, Calum, Ng, Raymond T, Lam, Wan L
منشور في 2008

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

بواسطة Coe, Bradley P., Thu, Kelsie L., Aviel-Ronen, Sarit, Vucic, Emily A., Gazdar, Adi F., Lam, Stephen, Tsao, Ming-Sound, Lam, Wan L.
منشور في 2013

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

بواسطة Lonergan, Kim M., Chari, Raj, Coe, Bradley P., Wilson, Ian M., Tsao, Ming-Sound, Ng, Raymond T., MacAulay, Calum, Lam, Stephen, Lam, Wan L.
منشور في 2010

Copy number variation detection and genotyping from exome sequence data

بواسطة Krumm, Niklas, Sudmant, Peter H., Ko, Arthur, O'Roak, Brian J., Malig, Maika, Coe, Bradley P., Quinlan, Aaron R., Nickerson, Deborah A., Eichler, Evan E.
منشور في 2012