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Justine Coppinger

Observed names: J Coppinger, J. Coppinger
ORCID: 0009-0000-4137-930X
Observed ORCID: 0009-0000-4137-930X
OpenAlex ID: A5041344323
Detection of low‐level mosaicism by array CGH in routine diagnostic specimens
2006 · Blake C. Ballif, Emily A. Rorem, et al. · American Journal of Medical Genetics Part A · 352
Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
2008 · Blake C Ballif, Aaron Theisen, et al. · Molecular Cytogenetics · 298
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Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound
2012 · Lisa G. Shaffer, Jill A. Rosenfeld, et al. · Prenatal Diagnosis · 267
Experience with microarray‐based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies
2012 · Lisa G. Shaffer, Mindy P. Dabell, et al. · Prenatal Diagnosis · 243
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The identification of microdeletion syndromes and other chromosome abnormalities: Cytogenetic methods of the past, new technologies for the future
2007 · Lisa G. Shaffer, Bassem A. Bejjani, et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 233
Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications
2009 · Jill A. Rosenfeld, Justine Coppinger, et al. · Journal of Neurodevelopmental Disorders · 207
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Comparison of microarray‐based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens
2008 · Lisa G. Shaffer, Justine Coppinger, et al. · Prenatal Diagnosis · 186
Whole‐genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray
2009 · Justine Coppinger, Sarah Alliman, et al. · Prenatal Diagnosis · 173
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region
2009 · J. Coppinger, D. McDonald-McGinn, et al. · Human Molecular Genetics · 104
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Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting
2010 · Idit Maya, Bella Davidov, et al. · Prenatal Diagnosis · 78
The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective
2014 · Gary J. Latham, Justine Coppinger, et al. · Frontiers in Genetics · 54
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The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes
2011 · Lisa G. Shaffer, Justine Coppinger, et al. · Prenatal Diagnosis · 44
Referral patterns for microarray testing in prenatal diagnosis
2012 · Lisa G. Shaffer, Mindy Preston Dabell, et al. · Prenatal Diagnosis · 42
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH
2009 · Sara Anne Adams, Justine Coppinger, et al. · Genetics in Medicine · 40
A blood biomarker test for brain amyloid impacts the clinical evaluation of cognitive impairment
2023 · Mark Monane, Kim G. Johnson, et al. · Annals of Clinical and Translational Neurology · 32
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Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2
2010 · S Alliman, J Coppinger, et al. · Clinical Genetics · 26
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes
2011 · Jill A Rosenfeld, Lindsey E Stephens, et al. · European Journal of Human Genetics · 21
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SCN8A mutation in a child presenting with seizures and developmental delays
2016 · Janet Malcolmson, Robert Kleyner, et al. · Molecular Case Studies · 19
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Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis
2012 · Allen N. Lamb, Jill A. Rosenfeld, et al. · Genetics in Medicine · 19
Referral patterns for microarray testing in prenatal diagnosis
2012 · Lisa G. Shaffer, Mindy Preston Dabell, et al. · Prenatal Diagnosis · 13
Experience With Microarray-Based Comparative Genomic Hybridization for Prenatal Diagnosis in Over 5000 Pregnancies
2013 · Lisa G. Shaffer, Mindy P. Dabell, et al. · Obstetrical & Gynecological Survey · 9
Early Alzheimer's diagnosis: U.S. primary care physicians and use of blood biomarkers
2026 · Jeffrey M. Burns, Susan Alford, et al. · Alzheimer s & Dementia · 7
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Comparison of Microarray-Based Detection Rates for Cytogenetic Abnormalities in Prenatal and Neonatal Specimens
2008 · Lisa G. Shaffer, Justine Coppinger, et al. · Obstetrical & Gynecological Survey · 6
Response to the letter by Collins and Schimke
2011 · Sara Anne (adams) Morton, Justine Coppinger, et al. · Genetics in Medicine · 3
Independent validation of the PrecivityAD2™ blood test to identify presence or absence of brain amyloid pathology in individuals with cognitive impairment
2025 · Justine Coppinger, Tim West, et al. · npj Dementia · 2
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Works count: 35
Citation count: 2,480
H-index: 19
I10-index: 20
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