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D-Index & Metrics

Genetics

D-Index
61
Citations
21827
World Ranking
3026
National Ranking
1319

Overview

Bradley P. Coe is affiliated with the University of Washington in the United States and focuses their research primarily in the domain of Biochemistry, Genetics, and Molecular Biology. Their scholarly work spans 34 publications within this broad field, with particular emphasis on Genetics, exhibiting 27 contributions. Other notable subfields include Cancer Research, Molecular Biology, Pulmonary and Respiratory Medicine, and Plant Science.

The scientist's research centers on key topics such as:

  • Genomics and Rare Diseases
  • Genomic variations and chromosomal abnormalities
  • Genetics and Neurodevelopmental Disorders
  • Cancer Genomics and Diagnostics
  • Genetic Associations and Epidemiology
  • Glioma Diagnosis and Treatment
  • Brain Metastases and Treatment

Bradley P. Coe has authored multiple papers, some of which have garnered significant citations in various high-impact journals. Selected recent publications include:

  • Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders, 2020, Nature Communications
  • Recent ultra-rare inherited variants implicate new autism candidate risk genes, 2021, Nature Genetics
  • Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations, 2020, Nature Communications
  • Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group, 2023, Genetics in Medicine
  • Recent ultra-rare inherited mutations identify novel autism candidate risk genes, 2020, bioRxiv (Cold Spring Harbor Laboratory)

The frequent publication venues for Coe's work include Nature Communications, Cancer Genetics, Genetics in Medicine Open, Nature Genetics, and Genetics in Medicine.

Coe collaborates regularly with several co-authors, including Laura K. Conlin, Evan E. Eichler, Vaidehi Jobanputra, Kendra Hoekzema, and Arvis Sulovari. These partnerships have contributed to multiple joint publications and research efforts.

Best Publications

  • Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

    Brian J. O’Roak;Laura Vives;Santhosh Girirajan;Emre Karakoc

  • Genome structural variation discovery and genotyping

    Can Alkan;Bradley P. Coe;Evan E. Eichler;Evan E. Eichler

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

    Brian J. O’Roak;Laura Vives;Wenqing Fu;Jarrett D. Egertson

  • A copy number variation morbidity map of developmental delay

    Gregory M Cooper;Bradley P Coe;Santhosh Girirajan;Jill A Rosenfeld

  • Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development

    Raphael Bernier;Christelle Golzio;Bo Xiong;Holly A. Stessman

  • A tiling resolution DNA microarray with complete coverage of the human genome.

    Adrian S. Ishkanian;Chad A. Malloff;Spencer K. Watson;Ronald J. DeLeeuw

  • Copy number variation detection and genotyping from exome sequence data

    Niklas Krumm;Peter H. Sudmant;Arthur Ko;Brian J. O'Roak

  • Refining analyses of copy number variation identifies specific genes associated with developmental delay

    Bradley P. Coe;Kali Witherspoon;Jill A. Rosenfeld;Bregje W M Van Bon;Bregje W M Van Bon

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

    Sébastien Jacquemont;Bradley P. Coe;Micha Hersch;Michael H. Duyzend

  • Excess of rare, inherited truncating mutations in autism.

    Niklas Krumm;Tychele N. Turner;Carl Baker;Laura Vives

  • Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants

    Santhosh Girirajan;Jill A. Rosenfeld;Bradley P. Coe;Sumit Parikh

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

    Holly A.F. Stessman;Bo Xiong;Bo Xiong;Bradley P. Coe;Tianyun Wang

  • Global diversity, population stratification, and selection of human copy-number variation

    Peter H. Sudmant;Swapan Mallick;Swapan Mallick;Bradley J. Nelson;Fereydoun Hormozdiari

  • Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

    Santhosh Girirajan;Zoran Brkanac;Bradley P. Coe;Carl Baker

  • A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP

    Céline Helsmoortel;Anneke T Vulto-van Silfhout;Bradley P Coe;Geert Vandeweyer

  • De novo genic mutations among a Chinese autism spectrum disorder cohort

    Tianyun Wang;Hui Guo;Bo Xiong;Holly A.F. Stessman

  • Estimates of penetrance for recurrent pathogenic copy-number variations.

    Jill A. Rosenfeld;Bradley P. Coe;Evan E. Eichler;Howard Cuckle

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

    Santhosh Girirajan;Megan Y. Dennis;Carl Baker;Maika Malig

  • Genomic Patterns of De Novo Mutation in Simplex Autism

    Tychele N. Turner;Bradley P. Coe;Diane E. Dickel;Kendra Hoekzema

  • Corrigendum: A copy number variation morbidity map of developmental delay

    Gregory M Cooper;Bradley P Coe;Santhosh Girirajan;Jill A Rosenfeld

Frequent Co-Authors

Evan E. Eichler
Evan E. Eichler University of Washington
Wan L. Lam
Wan L. Lam BC Cancer Research Centre
Raphael Bernier
Raphael Bernier University of Washington
Stephen Lam
Stephen Lam University of British Columbia
Corrado Romano
Corrado Romano I.R.C.C.S. Oasi Maria SS
Jozef Gecz
Jozef Gecz University of Adelaide
Jill A. Rosenfeld
Jill A. Rosenfeld Baylor College of Medicine
Carl Baker
Carl Baker National Institute of Arthritis and Musculoskeletal and Skin Diseases
John D. Minna
John D. Minna The University of Texas Southwestern Medical Center
Ann Nordgren
Ann Nordgren Karolinska University Hospital

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