Debra Lochner Doyle

1.3k total citations
18 papers, 835 citations indexed

About

Debra Lochner Doyle is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Debra Lochner Doyle has authored 18 papers receiving a total of 835 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Debra Lochner Doyle's work include BRCA gene mutations in cancer (9 papers), Prenatal Screening and Diagnostics (3 papers) and Genomics and Rare Diseases (2 papers). Debra Lochner Doyle is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Prenatal Screening and Diagnostics (3 papers) and Genomics and Rare Diseases (2 papers). Debra Lochner Doyle collaborates with scholars based in United States, Canada and Australia. Debra Lochner Doyle's co-authors include Donald L. Patrick, Susan Kinne, Robin L. Bennett, Robert G. Resta, Stefanie Uhrich, A.H. Bittles, Robert D. Steiner, C. Ronald Scott, Kwang‐Ting Cheng and Kerry Silvey and has published in prestigious journals such as American Journal of Public Health, Australasian Journal of Paramedicine and Genetics in Medicine.

In The Last Decade

Debra Lochner Doyle

16 papers receiving 787 citations

Peers

Debra Lochner Doyle

GENET

PPCH

PHEOH

GHP

Salma K. Marani United States

Judith Luce United States

Sue Gessler United Kingdom

Lindsay Fraser United Kingdom

Kate Butler Canada

Ilias Goranitis Australia

Juan Acuña United States

Jonathon Gray United Kingdom

Loane Skene Australia

Susan Fleming United States

Salma K. Marani United States

Debra Lochner Doyle

223 ×0.8

GENET

93 ×0.5

PPCH

156 ×1.2

PHEOH

130 ×1.3

GHP

100 ×1.3

Citations per year, relative to Debra Lochner Doyle Debra Lochner Doyle (= 1×) peers Salma K. Marani

Countries citing papers authored by Debra Lochner Doyle

Since Specialization

Citations

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

Fields of papers citing papers by Debra Lochner Doyle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Debra Lochner Doyle. 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 Debra Lochner Doyle. The network helps show where Debra Lochner Doyle may publish in the future.

Co-authorship network of co-authors of Debra Lochner Doyle

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

All Works

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18 of 18 papers shown

Murray, Michael F., Monica A. Giovanni, Debra Lochner Doyle, et al.. (2021). DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 23(6). 989–995. 39 indexed citations

Kaye, Celia I., Joann Bodurtha, Mathew J. Edick, et al.. (2019). Regional models of genetic services in the United States. Genetics in Medicine. 22(2). 381–388. 12 indexed citations

Hart, Ragan, Louis P. Garrison, Debra Lochner Doyle, et al.. (2019). Projected Cost-Effectiveness for 2 Gene-Drug Pairs Using a Multigene Panel for Patients Undergoing Percutaneous Coronary Intervention. Value in Health. 22(11). 1231–1239. 13 indexed citations

Doyle, Debra Lochner, Mindy Clyne, Juan L. Rodriguez, et al.. (2018). Proposed outcomes measures for state public health genomic programs. Genetics in Medicine. 20(9). 995–1003. 10 indexed citations

Purcell, Patricia L., et al.. (2017). Identification of Oral Clefts as a Risk Factor for Hearing LossDuring Newborn Hearing Screening. PubMed. 3(1). 21–28.

Doyle, Debra Lochner, Rawan I. Awwad, Jehannine Austin, et al.. (2016). 2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling. Journal of Genetic Counseling. 25(5). 868–879. 52 indexed citations

Guzauskas, Gregory F., et al.. (2012). Stakeholder perspectives on decision-analytic modeling frameworks to assess genetic services policy. Genetics in Medicine. 15(1). 84–87. 2 indexed citations

Harrison, Tabitha A., et al.. (2009). Billing for Medical Genetics and Genetic Counseling Services: A National Survey. Journal of Genetic Counseling. 19(1). 38–43. 26 indexed citations

Bennett, Robin L., et al.. (2008). Standardized Human Pedigree Nomenclature: Update and Assessment of the Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 17(5). 424–433. 166 indexed citations

10.

Laurino, Mercy, Robin L. Bennett, L. Baumeister, et al.. (2005). Genetic Evaluation and Counseling of Couples with Recurrent Miscarriage: Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 14(3). 165–181. 40 indexed citations

11.

Kinne, Susan, Donald L. Patrick, & Debra Lochner Doyle. (2004). Prevalence of Secondary Conditions Among People With Disabilities. American Journal of Public Health. 94(3). 443–445. 256 indexed citations

12.

Bennett, Robin L., Arno G. Motulsky, A.H. Bittles, et al.. (2002). Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors. Australasian Journal of Paramedicine. 11(2). 97–119. 138 indexed citations

13.

Austin, Melissa A., Donna K. Arnett, Terri H. Beaty, et al.. (2001). Opportunities for Public Health Genetics Trainees: Results of an Employer/Workplace Survey. Public Health Genomics. 4(3). 143–147. 3 indexed citations

14.

Doyle, Debra Lochner, et al.. (1995). Factors which influence the rate of receiving a routine second newborn screening test in Washington State. American Journal of Medical Genetics. 59(4). 417–420. 9 indexed citations

15.

Steinhaus, Kathryn A., Robin L. Bennett, Robert G. Resta, et al.. (1995). Inconsistencies in pedigree symbols in human genetics publications: A need for standardization. American Journal of Medical Genetics. 56(3). 291–295. 6 indexed citations

16.

Doyle, Debra Lochner & Phyllis Noerager Stern. (1992). Negotiating Self-Care in Rehabilitation Nursing. Rehabilitation Nursing. 17(6). 319–321. 10 indexed citations

17.

Abramowicz, Jacques S., Steven L. Warsof, Debra Lochner Doyle, Deborah F. Smith, & Donald L. Levy. (1989). Congenital cystic hygroma of the neck diagnosed prenatally: Outcome with normal and abnormal karyotype. Prenatal Diagnosis. 9(5). 321–327. 52 indexed citations

18.

HUSKISSON, E.C., J. A. Wojtulewski, Barbara M. Ansell, et al.. (1987). Problems in assessing the possible disease‐modifying effect of naproxen. International Journal of Clinical Practice. 41(1). 560–565. 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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