Deborah A. McDermott

2.4k total citations · 1 hit paper
20 papers, 1.4k citations indexed

About

Deborah A. McDermott is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Deborah A. McDermott has authored 20 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Epidemiology and 7 papers in Genetics. Recurrent topics in Deborah A. McDermott's work include Congenital heart defects research (9 papers), Congenital Heart Disease Studies (7 papers) and BRCA gene mutations in cancer (3 papers). Deborah A. McDermott is often cited by papers focused on Congenital heart defects research (9 papers), Congenital Heart Disease Studies (7 papers) and BRCA gene mutations in cancer (3 papers). Deborah A. McDermott collaborates with scholars based in United States, Australia and United Kingdom. Deborah A. McDermott's co-authors include Craig T. Basson, Bruce B. Lerman, Calum A. MacRae, Patrick T. Ellinor, Günter Breithardt, Ludwig Thierfelder, Walter Birchmeier, Eric Schulze‐Bahr, Katja S. Grossmann and Matthias Paul and has published in prestigious journals such as New England Journal of Medicine, Circulation and Nature Genetics.

In The Last Decade

Deborah A. McDermott

18 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

2004 569 citations Brenda Gerull, Arnd Heuser et al. Nature Genetics profile →

Peers

Deborah A. McDermott

CCM

GENET

OSM

EPIDE

J M Chessells United Kingdom

Gábor Kovács Hungary

Chris Goumas Australia

Yoland Antill Australia

David E. Carter Canada

Louise Bath United Kingdom

Alessandra Carnevale Mexico

Christian Olsson Sweden

Victoria Murday United Kingdom

Elizabeth A. Putnam United States

J M Chessells United Kingdom

Deborah A. McDermott

136 ×0.2

CCM

398 ×0.9

205 ×0.8

GENET

29 ×0.1

OSM

98 ×0.6

EPIDE

Citations per year, relative to Deborah A. McDermott Deborah A. McDermott (= 1×) peers J M Chessells

Countries citing papers authored by Deborah A. McDermott

Since Specialization

Citations

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

Fields of papers citing papers by Deborah A. McDermott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah A. McDermott. 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 Deborah A. McDermott. The network helps show where Deborah A. McDermott may publish in the future.

Co-authorship network of co-authors of Deborah A. McDermott

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah A. McDermott. A scholar is included among the top collaborators of Deborah A. McDermott 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 Deborah A. McDermott. Deborah A. McDermott 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

McDermott, Deborah A., Jamie Fong, & Craig T. Basson. (2015). Holt-Oram Syndrome. Europe PMC (PubMed Central). 5 indexed citations

Baum, Fran, Angela Lawless, Toni Delany, et al.. (2014). Evaluation of Health in All Policies: concept, theory and application. Health Promotion International. 29(suppl 1). i130–i142. 93 indexed citations

Lin, Angela E., Craig T. Basson, Elizabeth Goldmuntz, et al.. (2008). Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management. Genetics in Medicine. 10(7). 469–494. 55 indexed citations

Arnett, Donna K., Alison E. Baird, Ruth Ann Barkley, et al.. (2007). Relevance of Genetics and Genomics for Prevention and Treatment of Cardiovascular Disease. Circulation. 115(22). 2878–2901. 142 indexed citations

McDermott, Deborah A., Santhi K. Ganesh, David M. Herrington, et al.. (2007). the Functional Genomics and Translational Biology Interdisciplinary Working Association Council on Epidemiology and Prevention, the Stroke Council, and Cardiovascular Disease: A Scientific Statement From the American Heart Relevance of Genetics and Genomics for Prevention and Treatment of. 1 indexed citations

Burton, Kimberly A., Deborah A. McDermott, David Wilkes, et al.. (2006). Haploinsufficiency at the Protein Kinase A RIα Gene Locus Leads to Fertility Defects in Male Mice and Men. Molecular Endocrinology. 20(10). 2504–2513. 50 indexed citations

Hatcher, Cathy J. & Deborah A. McDermott. (2006). Using the TBX5 transcription factor to grow and sculpt the heart. American Journal of Medical Genetics Part A. 140A(13). 1414–1418. 8 indexed citations

McDermott, Deborah A., Craig T. Basson, & Cathy J. Hatcher. (2006). Genetics of Cardiac Septation Defects and Their Pre-Implantation Diagnosis. Congenital Heart Disease. 126. 19–42. 3 indexed citations

McDermott, Deborah A., Michael Bressan, Jié He, et al.. (2005). TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome. Pediatric Research. 58(5). 981–986. 104 indexed citations

10.

Wilkes, David, Deborah A. McDermott, & Craig T. Basson. (2005). Clinical phenotypes and molecular genetic mechanisms of Carney complex. The Lancet Oncology. 6(7). 501–508. 66 indexed citations

11.

Gerull, Brenda, Arnd Heuser, Thomas Wichter, et al.. (2004). Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Nature Genetics. 36(11). 1162–1164. 569 indexed citations breakdown →

12.

Veugelers, Mark, Michael Bressan, & Deborah A. McDermott. (2004). Mutation of perinatal myosin heavy chain associated with a carney complex variant. ACC Current Journal Review. 13(10). 47–47.

13.

Veugelers, Mark, Michael Bressan, Deborah A. McDermott, et al.. (2004). Mutation of Perinatal Myosin Heavy Chain Associated with a Carney Complex Variant. New England Journal of Medicine. 351(5). 460–469. 94 indexed citations

14.

He, Jie, Deborah A. McDermott, Yan Song, et al.. (2003). Preimplantation genetic diagnosis of human congenital heart malformation and Holt–Oram syndrome. American Journal of Medical Genetics Part A. 126A(1). 93–98. 28 indexed citations

15.

Vaughan, Carl J., et al.. (2003). Molecular Genetic Analysis of PRKAG2 in Sporadic Wolff‐Parkinson‐White Syndrome. Journal of Cardiovascular Electrophysiology. 14(3). 263–268. 32 indexed citations

16.

Hatcher, Cathy J., et al.. (2003). Transcription factor cascades in congenital heart malformation. Trends in Molecular Medicine. 9(12). 512–515. 20 indexed citations

17.

Offit, Kenneth, Shlomit Gilad, Shoshana Paglin, et al.. (2002). Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancers.. PubMed. 8(12). 3813–9. 29 indexed citations

18.

Levine, Douglas A., Oscar Lin, R.R. Barakat, et al.. (2001). Risk of Endometrial Carcinoma Associated with BRCA Mutation. Gynecologic Oncology. 80(3). 395–398. 106 indexed citations

19.

Levine, Douglas A., Oscar Lin, Richard R. Barakat, et al.. (2001). Risk of Endometrial Carcinoma Associated With BRCA Mutation. Obstetrical & Gynecological Survey. 56(10). 619–620.

20.

McDermott, Deborah A., et al.. (1982). Attitudes towards Family Services in a Rural State. Family Relations. 31(1). 91–91. 4 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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