Jane M. DeLuca

696 total citations
31 papers, 484 citations indexed

About

Jane M. DeLuca is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and General Health Professions. According to data from OpenAlex, Jane M. DeLuca has authored 31 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 8 papers in General Health Professions. Recurrent topics in Jane M. DeLuca's work include Prenatal Screening and Diagnostics (6 papers), Genomics and Rare Diseases (5 papers) and Metabolism and Genetic Disorders (5 papers). Jane M. DeLuca is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomics and Rare Diseases (5 papers) and Metabolism and Genetic Disorders (5 papers). Jane M. DeLuca collaborates with scholars based in United States, Italy and Austria. Jane M. DeLuca's co-authors include Sally A. Norton, Georgianne L. Arnold, Margaret H. Kearney, Ronald M. Epstein, Benjamin L. Mazer, Supriya G. Mohile, Maureen Metzger, Stewart C. Alexander, Robert Gramling and Timothy E. Quill and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Patient Education and Counseling.

In The Last Decade

Jane M. DeLuca

31 papers receiving 471 citations

Peers

Jane M. DeLuca
Margaret Sahhar Australia
Ruth Horn United Kingdom
Nancy Steinberg Warren United States
Katherine Ackerman Porter United States
Mary Gallagher United States
Ellen Giarelli United States
Claudia Wiesemann Germany
Anthony L. Back United States
Jerome H. Chin United States
Rose Geransar Canada
Margaret Sahhar Australia
Jane M. DeLuca
Citations per year, relative to Jane M. DeLuca Jane M. DeLuca (= 1×) peers Margaret Sahhar

Countries citing papers authored by Jane M. DeLuca

Since Specialization
Citations

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

Fields of papers citing papers by Jane M. DeLuca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jane M. DeLuca. 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 Jane M. DeLuca. The network helps show where Jane M. DeLuca may publish in the future.

Co-authorship network of co-authors of Jane M. DeLuca

This figure shows the co-authorship network connecting the top 25 collaborators of Jane M. DeLuca. A scholar is included among the top collaborators of Jane M. DeLuca 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 Jane M. DeLuca. Jane M. DeLuca 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.
Sarasua, Sara M., Jane M. DeLuca, Curtis Rogers, et al.. (2023). Head Size in Phelan–McDermid Syndrome: A Literature Review and Pooled Analysis of 198 Patients Identifies Candidate Genes on 22q13. Genes. 14(3). 540–540. 4 indexed citations
2.
Schleif, William, Sara M. Sarasua, & Jane M. DeLuca. (2023). Preanalytic and Analytic Quality System Considerations in Noncoding RNA Biomarker Development for Clinical Diagnostics. Genetic Testing and Molecular Biomarkers. 27(5). 172–182. 2 indexed citations
3.
DeLuca, Jane M., et al.. (2023). Pancreatic Cancer and the Family Connection: The Role of Advanced Practitioners in Screening and Educating Genetically At-Risk Individuals. Journal of the Advanced Practitioner in Oncology. 14(6). 533–539. 2 indexed citations
4.
Boyd, Jessica M., et al.. (2023). Providers’ Perspectives Related to Parents’ Choice of Pediatric Provider of Record and Newborn Screening: A Qualitative Study. Journal of Primary Care & Community Health. 14. 4277810434–4277810434. 1 indexed citations
5.
Chen, Sunny, et al.. (2023). Weight Loss Is a Strong Predictor of Memory Disorder Independent of Genetic Influences. Genes. 14(8). 1563–1563. 1 indexed citations
6.
DeLuca, Jane M., et al.. (2023). Familial pancreatic cancer: a case study and review of the psychosocial effects of diagnoses on families. Hereditary Cancer in Clinical Practice. 21(1). 17–17. 1 indexed citations
7.
Sarasua, Sara M., et al.. (2022). Genetics providers’ experiences using telehealth: A grounded theory approach. Journal of Genetic Counseling. 31(5). 1155–1163. 4 indexed citations
8.
Chen, Sunny, Sara M. Sarasua, Jane M. DeLuca, et al.. (2022). TOMM40 genetic variants associated with healthy aging and longevity: a systematic review. BMC Geriatrics. 22(1). 667–667. 14 indexed citations
9.
Sarasua, Sara M., et al.. (2021). Comprehensive investigation of the phenotype of MEF2C‐related disorders in human patients: A systematic review. American Journal of Medical Genetics Part A. 185(12). 3884–3894. 14 indexed citations
10.
DeLuca, Jane M., et al.. (2020). Similarities and differences in key diagnosis, treatment, and management approaches for PAH deficiency in the United States and Europe. Orphanet Journal of Rare Diseases. 15(1). 266–266. 9 indexed citations
11.
Bernabéu, A, J A Ortíz, Belén Lledó, et al.. (2017). Abstracts for 2017 Foundation for Reproductive Medicine Translational Reproductive Biology and Clinical Reproductive Endocrinology Conference. Journal of Assisted Reproduction and Genetics. 34(10). 1385–1402. 1 indexed citations
12.
DeLuca, Jane M.. (2017). Public Attitudes Toward Expanded Newborn Screening. Journal of Pediatric Nursing. 38. e19–e23. 19 indexed citations
13.
Alexander, Stewart C., Susan Ladwig, Sally A. Norton, et al.. (2014). Emotional Distress and Compassionate Responses in Palliative Care Decision-Making Consultations. Journal of Palliative Medicine. 17(5). 579–584. 24 indexed citations
14.
Mazer, Benjamin L., et al.. (2014). “Speaking-for” and “speaking-as”: Pseudo-surrogacy in physician–patient–companion medical encounters about advanced cancer. Patient Education and Counseling. 96(1). 36–42. 34 indexed citations
15.
Staffler, Alex, et al.. (2014). Premature newborns with fatal intrauterine herpes simplex virus‐1 infection: first report of twins and review of the literature. Journal of the European Academy of Dermatology and Venereology. 29(6). 1216–1220. 30 indexed citations
16.
Mazer, Benjamin L., et al.. (2013). In search of compassion: a new taxonomy of compassionate physician behaviours. Health Expectations. 18(5). 1672–1685. 46 indexed citations
17.
DeLuca, Jane M., et al.. (2013). Implications of Newborn Screening for Nurses. Journal of Nursing Scholarship. 45(1). 25–33. 18 indexed citations
18.
Gramling, Robert, Sally A. Norton, Susan Ladwig, et al.. (2012). Direct Observation of Prognosis Communication in Palliative Care: A Descriptive Study. Journal of Pain and Symptom Management. 45(2). 202–212. 27 indexed citations
19.
Norton, Sally A., Bethel Ann Powers, Madeline H. Schmitt, et al.. (2011). Navigating Tensions: Integrating Palliative Care Consultation Services Into an Academic Medical Center Setting. Journal of Pain and Symptom Management. 42(5). 680–690. 16 indexed citations
20.
Arnold, Georgianne L., et al.. (2002). Protein insufficiency and linear growth restriction in phenylketonuria. The Journal of Pediatrics. 141(2). 243–246. 43 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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