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26篇 您的检索式：作者名="Coe BP"

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	题名	作者	年代	出处	被引量
1	Integrative genomic analyses identify BRF2 as a novel lineage-specific oncogene in lung squamous cell carcinoma显示文摘	Lockwood WW Chari R Coe BP	2010	PLoS Med2010，7，10：	1
2	Integrative genomic analyses identify BRF2 as a novel lineage-specific oncogene in lungsquamous cell carcinoma 显示文摘	Lockwood WW Chari R Coe BP	2010	PLoS Med2010，7，10：	1
3	A copy number variation morbidity map of developmental delay显示文摘	Cooper GM Coe BP Girirajan S	2011	Nat Genet2011，43，9：	1
4	Whole genome tilong path array CGH analysis of segmental copy number alterations in cervical cancer cell lines显示文摘	Lockwood WW Coe BP Willoams AC	2007	Int J Cancer2007，120，2：	1
5	Genomic and gene expression profiling of minute alterations of chromosome arm 1p in small cell lung carcinoma cells 显示文摘	Henderson LJ Coe BP Lee E	2005	B J Cancer2005，92，8：	1
6	Refining analyses of copy number variation identifies specific genes associated with developmental delay显示文摘	Coe BP Witherspoon K RosenfeldJA	2014	Nat Genet2014，46，10：	1
7	Integrative genomic analyses identify BRF2 as a novel lineage-specific oncogene in lung squamous cell carcinoma 显示文摘	Lockwood WW Chari R Coe BP	2010	PLoS Medicine2010，7，10：	1
8	A copy number variationmorbidity map of developmental delay显示文摘	Cooper GM Coe BP Girirajan S	2011	Nat Genet2011，43，：	1
9	Disruptive de no- vo mutations of DYRK1A lead to a syndromic form of autism and ID 显示文摘	VAN BON BW COE BP BERNIER R	2016	Mol Psychiatry2016，21，1：	1
10	Differential disruption of cell cycle pathways in small cell and non-small cell lung cancer显示文摘	Coe BP Lockwood WW Girard L	2006	Br J Cancer2006，94，2：	1
11	The genetic variability and commonality of neurodevelopmental disease显示文摘	Coe BP Girirajan S Eichler EE		0，，：	1
12	A copy number variation morbidity map of developmental delay显示文摘	Cooper GM Coe BP Girirajan S	2011	Nat Genet2011，43，9：	1
13	Genomic deregulation of the E2F/Rb pathway leads to activation of the oncogene EZH2 in small cell lung cancer显示文摘	Coe BP Thu KL Aviel-Ronen S	2013	PLos One2013，8，71：	1
14	Copy number variation detection and genotyping from exome sequence data显示文摘	Krumm N Sudmant PH Ko A O'Roak BJ Malig M Coe BP NHLBI Exome Sequencing Project Quinlan AR Nickerson DA Eichler EE		0，，：	1
15	Estimates ofpenetrance for recurrent pathogenic copy-number variations显示文摘	Rosenfeld JA Coe BP Eichler EE	2013	Genet Med2013，15，：	1
16	A copy number variation morbidity map of developmental delay显示文摘	Cooper GM Coe BP Girirajan S	2011	Nat Genet2011，43，：	1
17	Differential disruption of cell cycle pathways in small cell and non-small cell lung cancer显示文摘	Coe BP Lockwood WW Girard L	2006	Br J Cancer2006，94，12：	1
18	Genome structural variationdiscovery and genotyping显示文摘	Alkan C Coe BP Eichler EE	2011	Nat Rev Genet2011，，12：	1
19	Genome structural variation discovery and genotyping显示文摘	Alkan C Coe BP Eichler EE	2011	Nat Rev Genet2011，12，5：	1
20	Genome structural variation discovery and genotyping显示文摘	Alkan C Coe BP Eichler EE		0，，：	1

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