Bradley P. Coe

20.0k total citations · 3 hit papers
66 papers, 5.8k citations indexed

About

Bradley P. Coe is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Bradley P. Coe has authored 66 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 44 papers in Genetics and 13 papers in Cancer Research. Recurrent topics in Bradley P. Coe's work include Genomic variations and chromosomal abnormalities (41 papers), Genomics and Chromatin Dynamics (12 papers) and Genomics and Rare Diseases (11 papers). Bradley P. Coe is often cited by papers focused on Genomic variations and chromosomal abnormalities (41 papers), Genomics and Chromatin Dynamics (12 papers) and Genomics and Rare Diseases (11 papers). Bradley P. Coe collaborates with scholars based in United States, Canada and Italy. Bradley P. Coe's co-authors include Evan E. Eichler, Can Alkan, Wan L. Lam, Calum MacAulay, Niklas Krumm, Jill A. Rosenfeld, Raphael Bernier, Tychele N. Turner, Santhosh Girirajan and Carl Baker and has published in prestigious journals such as New England Journal of Medicine, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Bradley P. Coe

65 papers receiving 5.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Genome structural variation discovery and genotyping

2011 1.0k citations Can Alkan, Bradley P. Coe et al. profile →
A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders

2014 375 citations Sébastien Jacquemont, Bradley P. Coe et al. The American Journal of Human Genetics profile →
Excess of rare, inherited truncating mutations in autism

2015 345 citations Niklas Krumm, Tychele N. Turner et al. Nature Genetics profile →

Peers

Countries citing papers authored by Bradley P. Coe

Since Specialization

Citations

This map shows the geographic impact of Bradley P. Coe's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bradley P. Coe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bradley P. Coe more than expected).

Fields of papers citing papers by Bradley P. Coe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bradley P. Coe. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bradley P. Coe. The network helps show where Bradley P. Coe may publish in the future.

Co-authorship network of co-authors of Bradley P. Coe

This figure shows the co-authorship network connecting the top 25 collaborators of Bradley P. Coe. A scholar is included among the top collaborators of Bradley P. Coe based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bradley P. Coe. Bradley P. Coe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Analytical Validation and Clinical Sensitivity of the Belay Summit Assay for the Detection of DNA Variants in Cerebrospinal Fluid of Primary and Metastatic Central Nervous System Cancer 2025 ·Journal of Molecular Diagnostics ·Qian Nie, Kala F. Schilter, Kyle M. Hernandez, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Kathryn J. Mitchell, David W. Ellis, (unknown), (unknown), Christopher Douville, Bradley P. Coe, Chetan Bettegowda, Honey V. Reddi	7
2	Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations 2022 ·European Journal of Medical Genetics ·Sultan Cingöz, (unknown), (unknown), Ezgi Karaca, Burcu Çelet Özden, Semra Hız Kurul, (unknown), Bradley P. Coe, Deborah A. Nickerson, Evan E. Eichler	1
3	Integrative Genomic Analyses Identifies GGA2 as a Cooperative Driver of EGFR-Mediated Lung Tumorigenesis 2018 ·Journal of Thoracic Oncology ·Hannah E. O’Farrell, Bryant Harbourne, Zimple Kurlawala, Yusuke Inoue, (unknown), Victor D. Martínez, Daniel Lu, Min Hee Oh, Bradley P. Coe, Kelsie L. Thu, Romel Somwar, Stephen Lam, Wan L. Lam, Arun M. Unni, Levi J. Beverly, William W. Lockwood	14
4	Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications 2017 ·Genome Medicine ·Amy B. Wilfert, Arvis Sulovari, Tychele N. Turner, Bradley P. Coe, Evan E. Eichler	91
5	Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region 2016 ·Genome Research ·Kiana Mohajeri, Stuart Cantsilieris, John Huddleston, Bradley J. Nelson, Bradley P. Coe, Catarina D. Campbell, Carl Baker, Lana Harshman, Katherine M. Munson, Zev Kronenberg, Milinn Kremitzki, Archana N. Raja, Claudia Rita Catacchio, Tina Graves, Richard K. Wilson, Mario Ventura, Evan E. Eichler	20
6	Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV 2015 ·The American Journal of Human Genetics ·Michael Duyzend, Xander Nuttle, Bradley P. Coe, Carl Baker, Deborah A. Nickerson, Raphael Bernier, Evan E. Eichler	44
7	A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders breakdown → 2014 ·The American Journal of Human Genetics ·Sébastien Jacquemont, Bradley P. Coe, Micha Hersch, Michael Duyzend, Niklas Krumm, Sven Bergmann, J. Beckmann, Jill A. Rosenfeld, Evan E. Eichler	375
8	Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in Schizophrenia 2013 ·The American Journal of Human Genetics ·(unknown), Tom Walsh, Süleyman Gülsüner, (unknown), Alex S. Nord, Molly Gasperini, Sarah B. Pierce, Cailyn H. Spurrell, Bradley P. Coe, Niklas Krumm, Ming K. Lee, Jonathan Sebat, Jon McClellan, Mary‐Claire King	28
9	Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder 2013 ·The American Journal of Human Genetics ·Santhosh Girirajan, Megan Y. Dennis, Carl Baker, Maika Malig, Bradley P. Coe, Colin Campbell, Kenneth M. K. Mark, Tiffany Vu, Can Alkan, Ze Cheng, Leslie G. Biesecker, Raphael Bernier, Evan E. Eichler	211
10	Copy Number Variations in the Human Genome and Strategies for Analysis 2010 ·Methods in molecular biology ·Emily A. Vucic, Kelsie L. Thu, (unknown), Wan L. Lam, Bradley P. Coe	3
11	A sequence-based approach to identify reference genes for gene expression analysis 2010 ·BMC Medical Genomics ·Raj Chari, Kim M. Lonergan, Larissa A. Pikor, Bradley P. Coe, Chang‐Qi Zhu, (unknown), Calum MacAulay, Ming‐Sound Tsao, Stephen Lam, Raymond T. Ng, Wan L. Lam	41
12	FACADE : a fast and sensitive algorithm for the segmentation and calling of high resolution array CGH data 2010 ·Nucleic Acids Research ·Bradley P. Coe, Raj Chari, Calum MacAulay, Wan L. Lam	11
13	DNA amplification is a ubiquitous mechanism of oncogene activation in lung and other cancers 2008 ·Oncogene ·William W. Lockwood, Raj Chari, Bradley P. Coe, Luc Girard, Calum MacAulay, Stephen Lam, Adi F. Gazdar, John D. Minna, Wan L. Lam	90
14	SIGMA2: A system for the integrative genomic multi-dimensional analysis of cancer genomes, epigenomes, and transcriptomes 2008 ·BMC Bioinformatics ·Raj Chari, Bradley P. Coe, (unknown), (unknown), Ian M. Wilson, Emily A. Vucic, Calum MacAulay, Raymond T. Ng, Wan L. Lam	30
15	Whole genome tiling path array CGH analysis of segmental copy number alterations in cervical cancer cell lines 2006 ·International Journal of Cancer ·William W. Lockwood, Bradley P. Coe, (unknown), Calum MacAulay, Wan L. Lam	34
16	SIGMA: A System for Integrative Genomic Microarray Analysis of Cancer Genomes 2006 ·BMC Genomics ·Raj Chari, William W. Lockwood, Bradley P. Coe, (unknown), (unknown), (unknown), Jonathan Davies, Calum MacAulay, Wan L. Lam	31
17	Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissues 2006 ·BMC Genomics ·Sarit Aviel‐Ronen, Chang‐Qi Zhu, Bradley P. Coe, Ni Liu, Spencer K. Watson, Wan L. Lam, Ming‐Sound Tsao	38
18	Gain of a region on 7p22.3, containing MAD1L1, is the most frequent event in small‐cell lung cancer cell lines 2005 ·Genes Chromosomes and Cancer ·Bradley P. Coe, (unknown), Bryan Chi, Luc Girard, John D. Minna, Adi F. Gazdar, Stephen Lam, Calum MacAulay, Wan L. Lam	47
19	A tiling resolution DNA microarray with complete coverage of the human genome 2004 ·Nature Genetics ·Adrian Ishkanian, Chad A. Malloff, Spencer K. Watson, Ronald J. deLeeuw, Bryan Chi, Bradley P. Coe, Antoine M. Snijders, Donna G. Albertson, Daniel Pinkel, Marco A. Marra, Victor Ling, Calum MacAulay, Wan L. Lam	475
20	Novel regions of amplification on 8q distinct from the MYC locus and frequently altered in oral dysplasia and cancer 2003 ·Genes Chromosomes and Cancer ·Cathie Garnis, Bradley P. Coe, Adrian Ishkanian, Lewei Zhang, Miriam P. Rosin, Wan L. Lam	53

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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