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

W W Lockwood , R Chari , B P Coe , L Girard
Oncogene 27 ( 33) 4615 -4624

98
2008
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID

B W M van Bon , B P Coe , R Bernier , C Green
Molecular Psychiatry 21 ( 1) 126 -132

99
2016
Genomic and gene expression profiling of minute alterations of chromosome arm 1p in small-cell lung carcinoma cells.

L-J Henderson , B P Coe , E H L Lee , L Girard
British Journal of Cancer 92 ( 8) 1553 -1560

28
2005
Differential disruption of cell cycle pathways in small cell and non-small cell lung cancer

B P Coe , W W Lockwood , L Girard , R Chari
British Journal of Cancer 94 ( 12) 1927 -1935

91
2006
Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV

Michael H. Duyzend , Xander Nuttle , Bradley P. Coe , Carl Baker
American Journal of Human Genetics 98 ( 1) 45 -57

38
2016
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations

Seema R. Lalani , Pengfei Liu , Jill A. Rosenfeld , Levi B. Watkin
American Journal of Human Genetics 98 ( 2) 347 -357

38
2016
Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders

Fabienne Prieur , Julien Thevenon , Jozef Gecz , Marie Shaw
American Journal of Human Genetics 98 ( 3) 541 -552

80
2016
Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development

Raphael Bernier , Christelle Golzio , Bo Xiong , Holly A Stessman
Cell 158 ( 2) 263 -276

479
2014
Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder

Santhosh Girirajan , Megan Y. Dennis , Carl Baker , Maika Malig
American Journal of Human Genetics 92 ( 2) 221 -237

313
2013
Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in Schizophrenia

Jon M. McClellan , Mary-Claire King , Caitlin Rippey , Tom Walsh
American Journal of Human Genetics 93 ( 4) 697 -710

33
2013
A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders

Sébastien Jacquemont , Bradley P. Coe , Micha Hersch , Michael H. Duyzend
American Journal of Human Genetics 94 ( 3) 415 -425

305
2014
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

B. J. O'Roak , L. Vives , W. Fu , J. D. Egertson
Science 338 ( 6114) 1619 -1622

921
2012
Genomic markers for malignant progression in pulmonary adenocarcinoma with bronchioloalveolar features

S. Aviel-Ronen , B. P. Coe , S. K. Lau , G. da Cunha Santos
Proceedings of the National Academy of Sciences of the United States of America 105 ( 29) 10155 -10160

61
2008
Copy number variation detection and genotyping from exome sequence data

N. Krumm , P. H. Sudmant , A. Ko , B. J. O'Roak
Genome Research 22 ( 8) 1525 -1532

424
2012
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

M Kvarnung , T Wang , K Hoekzema , D Vecchio
European Journal of Human Genetics 28

2020
15 Techniques/Molecular

S Girirajan , JA Rosenfeld , BP Coe
Year Book of Pathology and Laboratory Medicine 2013 2013 285

2013
Integrative genomic and gene expression analysis of chromosome 7 identified novel oncogene loci in non-small cell lung cancer

Campbell JM , Lockwood WW , THP Buys , R Chari
GENETIC ALTERATIONS AND LINEAGE SPECIFICITY IN LUNG CANCER 49 -49

2009
EZH2 is over-expressed in SCLC as a result of genomic deregulation of the Rb/E2F pathway.

BP Coe , S Aviel-Ronen , Gazdar AF Andrea Pusic , JD Minna
THE ROLE OF SPECIFIC GENOMIC ALTERATIONS IN SMALL CELL LUNG CANCER AGGRESSIVENESS 144 -144

2008
2006