Skip to Main Content

Author Details

Erin L Crowgey
Nemours Children's Hospital Delaware
2009
35
12
PMIDPaper TitleJournal TitlePublished Year
36479909KMT2A-D pathogenicity, prevalence, and variation according to a population database.Cancer Med2023
36479909KMT2A-D pathogenicity, prevalence, and variation according to a population database.Cancer Med2023
37250111Machine learning classifier approaches for predicting response to RTK-type-III inhibitors demonstrate high accuracy using transcriptomic signatures and <i>ex vivo</i> data.Bioinform Adv2023
37250111Machine learning classifier approaches for predicting response to RTK-type-III inhibitors demonstrate high accuracy using transcriptomic signatures and <i>ex vivo</i> data.Bioinform Adv2023
35310842Impact of Early Feeding: Metagenomics Analysis of the Infant Gut Microbiome.Front Cell Infect Microbiol2022
36016357CD24 Expression Dampens the Basal Antiviral State in Human Neuroblastoma Cells and Enhances Permissivity to Zika Virus Infection.Viruses2022
35485600A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.J Am Med Inform Assoc2022
36123353Integrated stem cell signature and cytomolecular risk determination in pediatric acute myeloid leukemia.Nat Commun2022
36556199DNA Methylation Analysis Reveals Distinct Patterns in Satellite Cell-Derived Myogenic Progenitor Cells of Subjects with Spastic Cerebral Palsy.J Pers Med2022
35045124Genomic surveillance of SARS-CoV-2 in the state of Delaware reveals tremendous genomic diversity.PLoS One2022
35310842Impact of Early Feeding: Metagenomics Analysis of the Infant Gut Microbiome.Front Cell Infect Microbiol2022
35485600A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.J Am Med Inform Assoc2022
36556199DNA Methylation Analysis Reveals Distinct Patterns in Satellite Cell-Derived Myogenic Progenitor Cells of Subjects with Spastic Cerebral Palsy.J Pers Med2022
36123353Integrated stem cell signature and cytomolecular risk determination in pediatric acute myeloid leukemia.Nat Commun2022
36016357CD24 Expression Dampens the Basal Antiviral State in Human Neuroblastoma Cells and Enhances Permissivity to Zika Virus Infection.Viruses2022
35045124Genomic surveillance of SARS-CoV-2 in the state of Delaware reveals tremendous genomic diversity.PLoS One2022
33987836Transcriptional analysis of muscle tissue and isolated satellite cells in spastic cerebral palsy.Dev Med Child Neurol2021
33987836Transcriptional analysis of muscle tissue and isolated satellite cells in spastic cerebral palsy.Dev Med Child Neurol2021
34557398The PNPLA3 rs738409 Variant but not MBOAT7 rs641738 is a Risk Factor for Nonalcoholic Fatty Liver Disease in Obese U.S. Children of Hispanic Ethnicity.Pediatr Gastroenterol Hepatol Nutr2021
34547772CBFB-MYH11 fusion transcripts distinguish acute myeloid leukemias with distinct molecular landscapes and outcomes.Blood Adv2021
34557398The PNPLA3 rs738409 Variant but not MBOAT7 rs641738 is a Risk Factor for Nonalcoholic Fatty Liver Disease in Obese U.S. Children of Hispanic Ethnicity.Pediatr Gastroenterol Hepatol Nutr2021
34547772CBFB-MYH11 fusion transcripts distinguish acute myeloid leukemias with distinct molecular landscapes and outcomes.Blood Adv2021
32224839Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples.Genomics Inform2020
32131829Error-corrected sequencing strategies enable comprehensive detection of leukemic mutations relevant for diagnosis and minimal residual disease monitoring.BMC Med Genomics2020
32224843Accelerating next generation sequencing data analysis: an evaluation of optimized best practices for Genome Analysis Toolkit algorithms.Genomics Inform2020
32224839Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples.Genomics Inform2020
32636668Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors.Appl Clin Genet2020
33215070Implementation of a learning healthcare system for sickle cell disease.JAMIA Open2020
34467103Perspectives on Molecular Diagnostic Testing for the COVID-19 Pandemic in Delaware.Dela J Public Health2020
34467103Perspectives on Molecular Diagnostic Testing for the COVID-19 Pandemic in Delaware.Dela J Public Health2020
33215070Implementation of a learning healthcare system for sickle cell disease.JAMIA Open2020
32636668Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors.Appl Clin Genet2020
32131829Error-corrected sequencing strategies enable comprehensive detection of leukemic mutations relevant for diagnosis and minimal residual disease monitoring.BMC Med Genomics2020
32224843Accelerating next generation sequencing data analysis: an evaluation of optimized best practices for Genome Analysis Toolkit algorithms.Genomics Inform2020
30990720Mapping Citrullinated Sites in Multiple Organs of Mice Using Hypercitrullinated Library.J Proteome Res2019
34278055Whole genome metagenomic analysis of the gut microbiome of differently fed infants identifies differences in microbial composition and functional genes, including an absent CRISPR/Cas9 gene in the formula-fed cohort.Hum Microb J2019
31028937Development of a Novel Next-Generation Sequencing Assay for Carrier Screening in Old Order Amish and Mennonite Populations of Pennsylvania.J Mol Diagn2019
30990720Mapping Citrullinated Sites in Multiple Organs of Mice Using Hypercitrullinated Library.J Proteome Res2019
34278055Whole genome metagenomic analysis of the gut microbiome of differently fed infants identifies differences in microbial composition and functional genes, including an absent CRISPR/Cas9 gene in the formula-fed cohort.Hum Microb J2019
31028937Development of a Novel Next-Generation Sequencing Assay for Carrier Screening in Old Order Amish and Mennonite Populations of Pennsylvania.J Mol Diagn2019
29563102Protein <i>S</i>-Nitrosylation Controls Glycogen Synthase Kinase 3β Function Independent of Its Phosphorylation State.Circ Res2018
29925314Epigenetic machine learning: utilizing DNA methylation patterns to predict spastic cerebral palsy.BMC Bioinformatics2018
30010035A Systems Biology Approach for Studying Heterotopic Ossification: Proteomic Analysis of Clinical Serum and Tissue Samples.Genomics Proteomics Bioinformatics2018
29563102Protein <i>S</i>-Nitrosylation Controls Glycogen Synthase Kinase 3β Function Independent of Its Phosphorylation State.Circ Res2018
29618007Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibility.Hum Reprod2018
30010035A Systems Biology Approach for Studying Heterotopic Ossification: Proteomic Analysis of Clinical Serum and Tissue Samples.Genomics Proteomics Bioinformatics2018
29925314Epigenetic machine learning: utilizing DNA methylation patterns to predict spastic cerebral palsy.BMC Bioinformatics2018
29618007Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibility.Hum Reprod2018
28150249Mapping Biological Networks from Quantitative Data-Independent Acquisition Mass Spectrometry: Data to Knowledge Pipelines.Methods Mol Biol2017
28472996A survey of proteomic biomarkers for heterotopic ossification in blood serum.J Orthop Surg Res2017
  • 1 - 50 of 70

Recommended Authors

James Fitch
The Institute for Genomic Medicine, Nationwide Children's Hospital
Career Start Year 2015
Number of shared co-authors 0
Xiaowei Zhan
Southwestern Medical Center, University of Texas
Career Start Year 2012
Number of shared co-authors 3
Benjamin J Kelly
Nationwide Children's Hospital
Career Start Year 2009
Number of shared co-authors 0
Kathleen M Fisch
Center for Computational Biology and Bioinformatics, University of California
Career Start Year 2009
Number of shared co-authors 0
Henrik Stranneheim
Karolinska Institutet
Career Start Year 2009
Number of shared co-authors 1
Jeffrey G Reid
Regeneron Pharmaceuticals, Inc.
Career Start Year 2007
Number of shared co-authors 2
Mark J Cowley
Children's Cancer Institute, Lowy Cancer Research Centre
Career Start Year 2006
Number of shared co-authors 0
Daniel C Koboldt
Institute for Genomic Medicine, Nationwide Children's Hospital
Career Start Year 2005
Number of shared co-authors 4
Ali Torkamani
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 3
Praveen F Cherukuri
Sanford School of Medicine, University of South Dakota
Career Start Year 2005
Number of shared co-authors 2
Robert Sebra
Icahn School of Medicine at Mount Sinai
Career Start Year 2004
Number of shared co-authors 2
Christopher E Mason
Feil Family Brain and Mind Research Institute.
Career Start Year 2004
Number of shared co-authors 1
David W Craig
University of Southern California
Career Start Year 2004
Number of shared co-authors 1
Sek Won Kong
Boston Children's Hospital, Seoul National University, Seoul National University Hospital
Career Start Year 2003
Number of shared co-authors 1
Yufeng Shen
Columbia University
Career Start Year 2002
Number of shared co-authors 7
Kai Wang
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 5
Eric W Klee
Mayo Clinic College of Medicine and Science
Career Start Year 2001
Number of shared co-authors 1
Stacey Gabriel
Broad Institute of MIT and Harvard
Career Start Year 2001
Number of shared co-authors 11
Yan W Asmann
Mayo Clinic
Career Start Year 2000
Number of shared co-authors 2
Nancy F Hansen
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2000
Number of shared co-authors 2
Michael N Edmonson
St. Jude Children's Research Hospital
Career Start Year 1999
Number of shared co-authors 7
Shawn Levy
HudsonAlpha Institute for Biotechnology
Career Start Year 1999
Number of shared co-authors 7
Sean McGrath
Harvard T.H. Chan School of Public Health
Career Start Year 1996
Number of shared co-authors 3
Steven J M Jones
University of British Columbia
Career Start Year 1995
Number of shared co-authors 6
Elizabeth A Worthey
Heersink School of Medicine, The University of Alabama at Birmingham
Career Start Year 1995
Number of shared co-authors 7
Robert S Fulton
McDonnell Genome Institute, Washington University School of Medicine
Career Start Year 1994
Number of shared co-authors 10
Jean-Pierre A Kocher
Mayo Clinic
Career Start Year 1991
Number of shared co-authors 1
Elaine R Mardis
The Ohio State University
Career Start Year 1988
Number of shared co-authors 14
Donna M Muzny
Baylor College of Medicine
Career Start Year 1988
Number of shared co-authors 17
James C Mullikin
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1985
Number of shared co-authors 3

Collaborators

Edward A Kolb
Co-authored papers 7
Jennifer E Van Eyk
Smidt Heart Institute, Cedars-Sinai Medical Center
Co-authored papers 6
Vidya Venkatraman
Co-authored papers 4
Yanling Liu
St. Jude Children's Research Hospital
Co-authored papers 2
Subha Madhavan
Innovation Center for Biomedical Informatics, Georgetown University Medical Center
Co-authored papers 2
Shawn W Polson
Co-authored papers 2
Rhonda E Ries
Clinical Research Division, Fred Hutchinson Cancer Research Center
Co-authored papers 2
Richard Aplenc
Children's Hospital of Philadelphia
Co-authored papers 2
Todd A Alonzo
Keck School of Medicine, University of Southern California
Co-authored papers 2
Xiaotu Ma
St. Jude Children's Research Hospital
Co-authored papers 2
Soheil Meshinchi
Fred Hutchinson Cancer Research Centre
Co-authored papers 2
Timothy J Triche
Center for Epigenetics, Van Andel Research Institute
Co-authored papers 2
Cathy H Wu
Georgetown University Medical Center
Co-authored papers 2
Mark A Hoffman
Children's Mercy Hospital
Co-authored papers 2
Jennifer T Wyffels
Co-authored papers 2
Samuel J Aronson
Georgetown University.
Co-authored papers 1
Katherine L Nathanson
Perelman School of Medicine, University of Pennsylvania, USA Abramson Cancer Center
Co-authored papers 1
Erin M Ramos
National Human Genome Research Institute
Co-authored papers 1
Timothy C Burn
Incyte Research Institute
Co-authored papers 1
Madison Goldrich
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 1
Janina M Jeff
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Co-authored papers 1
Samuel L Volchenboum
University of Chicago
Co-authored papers 1
Tejinder Rakhra-Burris
Center for Applied Genomics and Precision Medicine, Duke University
Co-authored papers 1
Mary V Relling
Departments of Pharmaceutical Sciences.
Co-authored papers 1
Lisa Bastarache
Vanderbilt University Medical Center
Co-authored papers 1
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 1
Hongzhan Huang
Co-authored papers 1
Jessica D Tenenbaum
Duke University
Co-authored papers 1
Dan M Roden
Vanderbilt University Medical Center
Co-authored papers 1
Stephen J Chanock
National Cancer Institute, National Institutes of Health
Co-authored papers 1
Release 1.2