E. Coonrod

发表

Developing genome and exome sequencing for candidate gene identification in inherited disorders: an integrated technical and bioinformatics approach.

Karl V Voelkerding, Emily M Coonrod, Jacob D Durtschi, 2013, Archives of pathology & laboratory medicine.

Clinical analysis of genome next-generation sequencing data using the Omicia platform

Martin G Reese, Archie Russell, Karl V Voelkerding, 2013, Expert review of molecular diagnostics.

Novel Hepatitis B Virus Capsid-Targeting Antiviral That Aggregates Core Particles and Inhibits Nuclear Entry of Viral Cores.

Andrew D. Huber, Emily M. Coonrod, S. Sarafianos, 2018, ACS infectious diseases.

Pan-cancer proteogenomic analysis reveals long and circular noncoding RNAs encoding peptides

Emily M. Coonrod, C. Maher, H. Dang, 2020, NAR cancer.

Arabidopsis has Two Functional Orthologs of the Yeast V‐ATPase Assembly Factor Vma21p

T. Stevens, K. Schumacher, Y. Stierhof, 2008, Traffic.

Homotypic vacuole fusion in yeast requires organelle acidification and not the V-ATPase membrane domain.

Lindsay N. Carpp, Emily M. Coonrod, T. Stevens, 2013, Developmental cell.

Condensation by DNA looping facilitates transfer of large DNA molecules into mammalian cells.

W. Montigny, S. Illenye, C. Houchens, 2001, Nucleic acids research.

The Heteroaryldihydropyrimidine Bay 38-7690 Induces Hepatitis B Virus Core Protein Aggregates Associated with Promyelocytic Leukemia Nuclear Bodies in Infected Cells

Andrew D. Huber, Emily M. Coonrod, S. Sarafianos, 2018, mSphere.

Pan-Cancer Analysis Reveals Recurrent BCAR4 Gene Fusions across Solid Tumors

Emily M. Coonrod, C. Maher, N. White, 2022, Molecular cancer research : MCR.

Next-Generation Sequencing: Principles for Clinical Application

Jacob D. Durtschi, Karl V. Voelkerding, Rebecca L. Margraf, 2016 .

Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency.

Emily M. Coonrod, L. Jorde, Karin Chen, 2013, American journal of human genetics.

VarBin, a novel method for classifying true and false positive variants in NGS data

Karl V. Voelkerding, Jacob Durtschi, Rebecca L. Margraf, 2013, BMC Bioinformatics.

Translating exome sequencing from research to clinical diagnostics

Karl V Voelkerding, Emily M Coonrod, Rebecca L Margraf, 2011, Clinical chemistry and laboratory medicine.

Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders

J. McElwee, L. Notarangelo, J. Walter, 2014, Journal of Clinical Immunology.

Estimated disease incidence of RAG1/2 mutations: A case report and querying the Exome Aggregation Consortium.

D. MacArthur, L. Notarangelo, J. Walter, 2017, The Journal of allergy and clinical immunology.

A novel germline PIGA mutation in Ferro‐Cerebro‐Cutaneous syndrome: A neurodegenerative X‐linked epileptic encephalopathy with systemic iron‐overload

Emily M. Coonrod, J. Opitz, J. Carey, 2014, American journal of medical genetics. Part A.

Report on the effects of fragment size, indexing, and read length on HLA sequencing on the Illumina MiSeq.

T. Profaizer, J. Delgado, A. Kumánovics, 2015, Human immunology.

The role of Fis1p–Mdv1p interactions in mitochondrial fission complex assembly

Emily M. Coonrod, J. Shaw, M. A. Karren, 2005, The Journal of cell biology.

CXXC5 variant in an immunodeficient patient with a progressive loss of hematopoietic cells.

K. Voelkerding, R. Margraf, J. Durtschi, 2020, The Journal of allergy and clinical immunology.

Characterization of cell-type specific circular RNAs associated with colorectal cancer metastasis

Emily M. Coonrod, H. Dang, Amy Ly, 2023, NAR cancer.

Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders

J. McElwee, L. Notarangelo, J. Walter, 2015, Journal of Clinical Immunology.

Ugo1p Is a Multipass Transmembrane Protein with a Single Carrier Domain Required for Mitochondrial Fusion

Emily M. Coonrod, J. Shaw, M. A. Karren, 2007, Traffic.

The Yeast vps Class E Mutants: The Beginning of the Molecular Genetic Analysis of Multivesicular Body Biogenesis

Emily M. Coonrod, T. Stevens, E. Coonrod, 2010, Molecular biology of the cell.

VarBin, a novel method for classifying true and false positive variants in NGS data

K. Voelkerding, R. Margraf, J. Durtschi, 2013, BMC Bioinformatics.

TACI mutation p.Lys154Ter identified in Good Syndrome.

K. Voelkerding, R. Margraf, J. Durtschi, 2013, Clinical Immunology.