Heidi Cope

3.2k total citations
37 papers, 615 citations indexed

About

Heidi Cope is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Physiology. According to data from OpenAlex, Heidi Cope has authored 37 papers receiving a total of 615 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Public Health, Environmental and Occupational Health and 8 papers in Physiology. Recurrent topics in Heidi Cope's work include Lysosomal Storage Disorders Research (7 papers), Genomics and Rare Diseases (6 papers) and Spinal Dysraphism and Malformations (6 papers). Heidi Cope is often cited by papers focused on Lysosomal Storage Disorders Research (7 papers), Genomics and Rare Diseases (6 papers) and Spinal Dysraphism and Malformations (6 papers). Heidi Cope collaborates with scholars based in United States, Chile and Poland. Heidi Cope's co-authors include Allison E. Ashley‐Koch, Simon G. Gregory, Michael L. Cuccaro, Vandana Shashi, Karen Soldano, Yujun Shao, John R. Gilbert, Kelly Schoch, Melanie E. Garrett and Kimberly L. Raiford and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

Heidi Cope

33 papers receiving 607 citations

Peers

Heidi Cope

GENET

PHEOH

PPCH

Maria Arvio Finland

Satu Kivitie‐Kallio Finland

Clotilde Mircher France

Alison D. Archibald Australia

Erika F. Augustine United States

Alice Bonuccelli Italy

Sophie Dahoun Switzerland

Srinivasan Muthuswamy India

Felippe Borlot Canada

Marlene J. Huggins Canada

Maria Arvio Finland

Heidi Cope

260 ×0.9

GENET

153 ×1.0

129 ×0.9

111 ×0.8

PHEOH

96 ×1.1

PPCH

Citations per year, relative to Heidi Cope Heidi Cope (= 1×) peers Maria Arvio

Countries citing papers authored by Heidi Cope

Since Specialization

Citations

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

Fields of papers citing papers by Heidi Cope

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heidi Cope

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

All Works

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20 of 20 papers shown

Tzeng, Janice, et al.. (2024). Parent perspectives following newborn screening resulting in diagnoses of fragile X syndrome or fragile X premutation. Research in Developmental Disabilities. 148. 104719–104719.

Cope, Heidi, Emma Heslop, Alexandra Johnson, et al.. (2024). Clinician Perspectives of Gene Therapy as a Treatment Option for Duchenne Muscular Dystrophy. Journal of Neuromuscular Diseases. 11(5). 1085–1093.

Chong, Karen, David Chitayat, Kelly L. Gilmore, et al.. (2023). Diagnosis of TBC1D32‐associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy. American Journal of Medical Genetics Part A. 191(5). 1282–1292. 1 indexed citations

Chan, Kee, Zhanzhi Hu, Heidi Cope, et al.. (2023). NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders. International Journal of Neonatal Screening. 9(4). 63–63. 6 indexed citations

Kucera, Katerina S., Heidi Cope, Anne Wheeler, et al.. (2023). Two years of newborn screening for Duchenne muscular dystrophy as a part of the statewide Early Check research program in North Carolina. Genetics in Medicine. 26(1). 101009–101009. 9 indexed citations

Kucera, Katerina S., Verónica Robles, Heidi Cope, et al.. (2023). P497: Two years of newborn screening for Duchenne Muscular Dystrophy in North Carolina: Results from Early Check*. SHILAP Revista de lepidopterología. 1(1). 100544–100544.

Brock, Trisha, et al.. (2023). A humanized Caenorhabditis elegans model of hereditary spastic paraplegia-associated variants in KLC4. Disease Models & Mechanisms. 16(8). 3 indexed citations

Peay, Holly L., Rebecca Moultrie, Heidi Cope, et al.. (2022). Education and Consent for Population-Based DNA Screening: A Mixed-Methods Evaluation of the Early Check Newborn Screening Pilot Study. Frontiers in Genetics. 13. 891592–891592. 10 indexed citations

Huston, Sara, Mollie Minear, Azita Sadeghpour, et al.. (2018). Participant-Partners in Genetic Research: An Exome Study with Families of Children with Unexplained Medical Conditions. PubMed. 10(1). e2–e2. 2 indexed citations

10.

Nicole, Sophie, Loren Peña, Stephen R. Hooper, et al.. (2018). Characteristics of undiagnosed diseases network applicants: implications for referring providers. BMC Health Services Research. 18(1). 652–652. 23 indexed citations

11.

Deisseroth, Cole A., Johannes Birgmeier, Ethan E. Bodle, et al.. (2018). ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis. Genetics in Medicine. 21(7). 1585–1593. 62 indexed citations

12.

Cope, Heidi, et al.. (2018). Severe Cardiac Involvement Is Rare in Patients with Late-Onset Pompe Disease and the Common c.-32-13T>G Variant: Implications for Newborn Screening. The Journal of Pediatrics. 198. 308–312. 19 indexed citations

13.

Cope, Heidi, Rebecca C. Spillmann, Nicholas Stong, et al.. (2018). Further evidence for the involvement of EFL1 in a Shwachman–Diamond-like syndrome and expansion of the phenotypic features. Molecular Case Studies. 4(5). a003046–a003046. 22 indexed citations

14.

Case, Laura E., et al.. (2018). Early-onset of symptoms and clinical course of Pompe disease associated with the c.-32–13 T > G variant. Molecular Genetics and Metabolism. 126(2). 106–116. 15 indexed citations

15.

DeArmey, Stephanie, et al.. (2017). Treatment of profound thrombocytopenia in a patient with Gaucher disease type 1: Is there a role for substrate reduction therapy. Molecular Genetics and Metabolism Reports. 12. 82–84. 5 indexed citations

16.

Lock, Eric F., Karen Soldano, Melanie E. Garrett, et al.. (2015). Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation. BMC Genomics. 16(1). 11–11. 10 indexed citations

17.

Markunas, Christina A., Eric F. Lock, Karen Soldano, et al.. (2014). Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics. BMC Medical Genomics. 7(1). 39–39. 23 indexed citations

18.

Cope, Heidi, et al.. (2013). Outcome and life satisfaction of adults with myelomeningocele. Disability and health journal. 6(3). 236–243. 23 indexed citations

19.

Shao, Yujun, Kimberly L. Raiford, Chantelle M. Wolpert, et al.. (2002). Phenotypic Homogeneity Provides Increased Support for Linkage on Chromosome 2 in Autistic Disorder. The American Journal of Human Genetics. 70(4). 1058–1061. 136 indexed citations

20.

Grove, Bryon D., et al.. (1996). The role of gravin in endothelial wound healing. The FASEB Journal. 10(3). 1 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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