Justine Coppinger

2.5k total citations
24 papers, 1.5k citations indexed

About

Justine Coppinger is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Justine Coppinger has authored 24 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 5 papers in Plant Science. Recurrent topics in Justine Coppinger's work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (13 papers) and Genomics and Rare Diseases (5 papers). Justine Coppinger is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (13 papers) and Genomics and Rare Diseases (5 papers). Justine Coppinger collaborates with scholars based in United States, Canada and Israel. Justine Coppinger's co-authors include Lisa G. Shaffer, Blake C. Ballif, Bassem A. Bejjani, Beth S. Torchia, Jill A. Rosenfeld, Mindy Preston Dabell, J. Britt Ravnan, Jay W. Ellison, Allan J. Fisher and Anne M. Bandholz and has published in prestigious journals such as Alzheimer s & Dementia, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Justine Coppinger

22 papers receiving 1.4k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Justine Coppinger 1.2k 857 480 182 99 24 1.5k
Amber N. Pursley 1.1k 0.9× 690 0.8× 498 1.0× 250 1.4× 61 0.6× 28 1.4k
Beth S. Torchia 1.2k 1.0× 686 0.8× 693 1.4× 171 0.9× 109 1.1× 34 1.6k
Brigitte Benzacken 737 0.6× 426 0.5× 462 1.0× 156 0.9× 57 0.6× 61 1.3k
Carolina Sismani 735 0.6× 266 0.3× 515 1.1× 184 1.0× 38 0.4× 75 984
Peih-Shan Wu 803 0.7× 726 0.8× 391 0.8× 159 0.9× 212 2.1× 193 1.3k
J. O. Van Hemel 809 0.7× 356 0.4× 457 1.0× 193 1.1× 109 1.1× 38 1.1k
Sandra Chantot‐Bastaraud 939 0.8× 404 0.5× 759 1.6× 152 0.8× 40 0.4× 67 1.4k
F. J. Dill 579 0.5× 486 0.6× 242 0.5× 105 0.6× 112 1.1× 24 897
Vanna Pecile 499 0.4× 175 0.2× 443 0.9× 112 0.6× 70 0.7× 54 825
Sharon W. Horsley 1.3k 1.1× 367 0.4× 882 1.8× 436 2.4× 46 0.5× 30 1.8k

Countries citing papers authored by Justine Coppinger

Since Specialization
Citations

This map shows the geographic impact of Justine Coppinger'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 Justine Coppinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Justine Coppinger more than expected).

Fields of papers citing papers by Justine Coppinger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Justine Coppinger. 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 Justine Coppinger. The network helps show where Justine Coppinger may publish in the future.

Co-authorship network of co-authors of Justine Coppinger

This figure shows the co-authorship network connecting the top 25 collaborators of Justine Coppinger. A scholar is included among the top collaborators of Justine Coppinger 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 Justine Coppinger. Justine Coppinger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Alford, Susan, et al.. (2026). Early Alzheimer's diagnosis: U.S. primary care physicians and use of blood biomarkers. Alzheimer s & Dementia. 22(1). e70986–e70986.
2.
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Monane, Mark, Kim G. Johnson, B. Joy Snider, et al.. (2023). A blood biomarker test for brain amyloid impacts the clinical evaluation of cognitive impairment. Annals of Clinical and Translational Neurology. 10(10). 1738–1748. 19 indexed citations
4.
Tegay, David, Kenneth Ward, Justine Coppinger, et al.. (2016). SCN8A mutation in a child presenting with seizures and developmental delays. Molecular Case Studies. 2(6). a001073–a001073. 11 indexed citations
5.
Latham, Gary J., Justine Coppinger, Andrew G. Hadd, & Sarah L. Nolin. (2014). The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective. Frontiers in Genetics. 5. 244–244. 42 indexed citations
6.
Shaffer, Lisa G., Mindy Preston Dabell, Allan J. Fisher, et al.. (2013). Experience With Microarray-Based Comparative Genomic Hybridization for Prenatal Diagnosis in Over 5000 Pregnancies. Obstetrical & Gynecological Survey. 68(2). 93–95. 4 indexed citations
7.
Lamb, Allen N., Jill A. Rosenfeld, Justine Coppinger, et al.. (2012). Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis. Genetics in Medicine. 14(11). 914–921. 10 indexed citations
8.
Shaffer, Lisa G., Mindy Preston Dabell, Allan J. Fisher, et al.. (2012). Experience with microarray‐based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies. Prenatal Diagnosis. 32(10). 976–985. 163 indexed citations
9.
Coppinger, Justine, Blake C. Ballif, Lisa G. Shaffer, et al.. (2011). Response to the letter by Collins and Schimke. Genetics in Medicine. 13(11). 982–983. 2 indexed citations
10.
Shaffer, Lisa G., Justine Coppinger, Sarah Alliman, et al.. (2011). The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes. Prenatal Diagnosis. 31(8). 778–787. 33 indexed citations
11.
Maya, Idit, Bella Davidov, Liron Gershovitz, et al.. (2010). Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting. Prenatal Diagnosis. 30(12-13). 1131–1137. 61 indexed citations
12.
Alliman, Sarah, Justine Coppinger, Janet Marcadier, et al.. (2010). Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2. Clinical Genetics. 78(2). 162–168. 20 indexed citations
13.
Coppinger, Justine, Sulagna C. Saitta, Tracy Stroud, et al.. (2009). Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH. Genetics in Medicine. 11(5). 314–322. 30 indexed citations
14.
15.
Rosenfeld, Jill A., Justine Coppinger, Bassem A. Bejjani, et al.. (2009). Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications. Journal of Neurodevelopmental Disorders. 2(1). 26–38. 120 indexed citations
16.
Epstein, Leon G., Ali Jalali, Joshua V. Ross, et al.. (2008). Neuroimaging findings in children with rare or novel de novo chromosomal anomalies. Birth Defects Research Part A Clinical and Molecular Teratology. 82(4). 200–210. 1 indexed citations
17.
Ballif, Blake C., Aaron Theisen, Justine Coppinger, et al.. (2008). Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication. Molecular Cytogenetics. 1(1). 8–8. 176 indexed citations
18.
Shaffer, Lisa G., Justine Coppinger, Sarah Alliman, et al.. (2008). Comparison of microarray‐based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens. Prenatal Diagnosis. 28(9). 789–795. 102 indexed citations
19.
Shaffer, Lisa G., Bassem A. Bejjani, Beth S. Torchia, et al.. (2007). The identification of microdeletion syndromes and other chromosome abnormalities: Cytogenetic methods of the past, new technologies for the future. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(4). 335–345. 128 indexed citations
20.
Ballif, Blake C., Emily A. Rorem, Kyle Sundin, et al.. (2006). Detection of low‐level mosaicism by array CGH in routine diagnostic specimens. American Journal of Medical Genetics Part A. 140A(24). 2757–2767. 228 indexed citations

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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