Darrel Waggoner

8.0k total citations · 2 hit papers
65 papers, 3.2k citations indexed

About

Darrel Waggoner is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Darrel Waggoner has authored 65 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 33 papers in Molecular Biology and 9 papers in Physiology. Recurrent topics in Darrel Waggoner's work include Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (12 papers) and Congenital heart defects research (7 papers). Darrel Waggoner is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (12 papers) and Congenital heart defects research (7 papers). Darrel Waggoner collaborates with scholars based in United States, Australia and United Kingdom. Darrel Waggoner's co-authors include Jonathan D. Gitlin, Thomas B. Bartnikas, Ruby Leah B. Casareno, Philip C. Wong, Jeffrey D. Rothstein, Lino Tessarollo, Jamuna R. Subramaniam, Donald L. Price, S. Bruce Dowton and Valeria Culotta and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Darrel Waggoner

63 papers receiving 3.2k 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.

The Role of Copper in Neurodegenerative Disease

1999 759 citations Darrel Waggoner, Thomas B. Bartnikas et al. profile →
Synopsis of Guidelines for the Clinical Management of Cerebral Cavernous Malformations: Consensus Recommendations Based on Systematic Literature Review by the Angioma Alliance Scientific Advisory Board Clinical Experts Panel

2017 269 citations Darrel Waggoner et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Darrel Waggoner United States	24	1.5k	812	670	516	400	65	3.2k
Elizabeth A. Leibold United States	36	2.3k 1.6×	148 0.2×	1.5k 2.2×	117 0.2×	228 0.6×	45	4.7k
Seymour Packman United States	44	2.6k 1.8×	551 0.7×	1.4k 2.1×	227 0.4×	252 0.6×	135	6.5k
Makoto Yanagisawa Japan	31	3.2k 2.2×	367 0.5×	181 0.3×	249 0.5×	69 0.2×	57	4.8k
Lisbeth Birk Møller Denmark	33	1.5k 1.1×	407 0.5×	1.2k 1.8×	96 0.2×	48 0.1×	109	3.3k
Enrica Migliaccio Italy	32	4.7k 3.2×	391 0.5×	274 0.4×	108 0.2×	167 0.4×	45	7.4k
Paul J. Lockhart Australia	34	2.3k 1.6×	820 1.0×	1.5k 2.2×	1.2k 2.3×	37 0.1×	126	5.2k
Zeynep Tümer Denmark	39	3.4k 2.3×	1.9k 2.3×	1.5k 2.2×	139 0.3×	48 0.1×	180	5.7k
Tara M. DeSilva United States	30	956 0.7×	84 0.1×	158 0.2×	352 0.7×	201 0.5×	49	2.7k
Paolo Santambrogio Italy	43	2.4k 1.6×	166 0.2×	2.0k 2.9×	426 0.8×	29 0.1×	95	5.6k
Rosalba Carrozzo Italy	38	4.0k 2.7×	845 1.0×	185 0.3×	209 0.4×	46 0.1×	143	5.3k

Countries citing papers authored by Darrel Waggoner

Since Specialization

Citations

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

Fields of papers citing papers by Darrel Waggoner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Darrel Waggoner

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

Waggoner, Darrel, et al.. (2021). The relationship between performance on the medical genetics and genomics in-training and certifying examinations. Genetics in Medicine. 24(1). 225–231.

Waggoner, Darrel, Karen E. Wain, Adrian M. Dubuc, et al.. (2018). Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 20(10). 1105–1113. 46 indexed citations

Conboy, Erin, Filippo Pinto e Vairo, Darrel Waggoner, et al.. (2017). Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation. SHILAP Revista de lepidopterología. 2017. 1–4. 13 indexed citations

Beck, David B., Megan T. Cho, Francisca Millan, et al.. (2016). A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. Neurogenetics. 17(3). 173–178. 25 indexed citations

Metelitsina, T.I., Darrel Waggoner, & Michael A. Grassi. (2015). BATTEN DISEASE CAUSED BY A NOVEL MUTATION IN THE PPT1 GENE. Retinal Cases & Brief Reports. 10(3). 211–213. 3 indexed citations

Bhoj, Elizabeth, Sara Halbach, Donna M. McDonald‐McGinn, et al.. (2013). Expanding the spectrum of microdeletion 4q21 syndrome: A partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and pierre robin sequence. American Journal of Medical Genetics Part A. 161(9). 2327–2333. 19 indexed citations

Chong, Jessica X., Rebecca Ouwenga, Rebecca L. Anderson, Darrel Waggoner, & Carole Ober. (2012). A Population-Based Study of Autosomal-Recessive Disease-Causing Mutations in a Founder Population. The American Journal of Human Genetics. 91(4). 608–620. 44 indexed citations

Ross, Lainie Friedman & Darrel Waggoner. (2012). Parents: Critical Stakeholders in Expanding Newborn Screening. The Journal of Pediatrics. 161(3). 385–389. 12 indexed citations

Çalışkan, Minal, Jessica X. Chong, Lawrence H. Uricchio, et al.. (2011). Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13. Human Molecular Genetics. 20(7). 1285–1289. 78 indexed citations

10.

Waggoner, Darrel & Christopher Tan. (2011). Expanding newborn screening for lysosomal disorders: Opportunities and challenges. PubMed. 17(1). 9–14. 9 indexed citations

11.

Thienpont, Bernard, Litu Zhang, Alex V. Postma, et al.. (2010). Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans. The American Journal of Human Genetics. 86(6). 839–849. 72 indexed citations

12.

Nowaczyk, Małgorzata J.M., Melissa T. Carter, Jie Xu, et al.. (2008). Paternal deletion 6q24.3: A new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance. American Journal of Medical Genetics Part A. 146A(3). 354–360. 20 indexed citations

13.

MacLeod, Heather, Peter Pytel, Robert L. Wollmann, et al.. (2007). A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex. Neuromuscular Disorders. 17(4). 285–289. 16 indexed citations

14.

Waggoner, Darrel & Christa Lese Martin. (2006). Integration of internet-based genetic databases into the medical school pre-clinical and clinical curriculum. Genetics in Medicine. 8(6). 379–382. 16 indexed citations

15.

Waggoner, Darrel, et al.. (2005). Calibration of 6q subtelomere deletions to define genotype/phenotype correlations. Clinical Genetics. 67(5). 396–403. 60 indexed citations

16.

Tatton‐Brown, Katrina, Jenny Douglas, Kim Coleman, et al.. (2005). Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations. The American Journal of Human Genetics. 77(2). 193–204. 221 indexed citations

17.

Waggoner, Darrel, Gordana Raca, Katherine O. Welch, et al.. (2005). NSD1 analysis for Sotos syndrome: Insights and perspectives from the clinical laboratory. Genetics in Medicine. 7(8). 524–533. 41 indexed citations

18.

Bartnikas, Thomas B., Darrel Waggoner, Ruby Leah B. Casareno, et al.. (2000). Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase. Mammalian Genome. 11(5). 409–411. 12 indexed citations

19.

Waggoner, Darrel, Bettina Drisaldi, Thomas B. Bartnikas, et al.. (2000). Brain Copper Content and Cuproenzyme Activity Do Not Vary with Prion Protein Expression Level. Journal of Biological Chemistry. 275(11). 7455–7458. 151 indexed citations

20.

Waggoner, Darrel, et al.. (1999). Deletion of 1q in a patient with acrofacial dysostosis. American Journal of Medical Genetics. 82(4). 301–304. 22 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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