Jamie McDonald

5.4k total citations · 1 hit paper
52 papers, 2.6k citations indexed

About

Jamie McDonald is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Surgery. According to data from OpenAlex, Jamie McDonald has authored 52 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 33 papers in Pulmonary and Respiratory Medicine and 20 papers in Surgery. Recurrent topics in Jamie McDonald's work include Vascular Anomalies and Treatments (41 papers), Tracheal and airway disorders (31 papers) and Vascular Malformations and Hemangiomas (17 papers). Jamie McDonald is often cited by papers focused on Vascular Anomalies and Treatments (41 papers), Tracheal and airway disorders (31 papers) and Vascular Malformations and Hemangiomas (17 papers). Jamie McDonald collaborates with scholars based in United States, Canada and Spain. Jamie McDonald's co-authors include Pınar Bayrak‐Toydemir, Whitney Wooderchak‐Donahue, Kevin J. Whitehead, David A. Stevenson, Reed E. Pyeritz, Rong Mao, Franklin J. Miller, Pinar Bayrak‐Toydemir, Susan O. Lewin and Wei Tang and has published in prestigious journals such as Nature Genetics, Neurology and PEDIATRICS.

In The Last Decade

Jamie McDonald

52 papers receiving 2.6k citations

Hit Papers

align trajectories sort by overperformance

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.

Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era

2015 523 citations Jamie McDonald, Whitney Wooderchak‐Donahue et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jamie McDonald United States	23	1.4k	1.1k	672	440	435	52	2.6k
Pınar Bayrak‐Toydemir United States	27	1.0k 0.7×	968 0.8×	585 0.9×	1.1k 2.5×	1.1k 2.4×	77	3.5k
Whitney Wooderchak‐Donahue United States	16	472 0.3×	387 0.3×	319 0.5×	335 0.8×	211 0.5×	27	1.3k
Gabriela M. Repetto Chile	21	420 0.3×	534 0.5×	321 0.5×	936 2.1×	651 1.5×	67	2.1k
Antonio López Spain	28	598 0.4×	116 0.1×	78 0.1×	393 0.9×	101 0.2×	71	2.2k
Mark J. Pettenati United States	36	620 0.4×	299 0.3×	265 0.4×	2.1k 4.9×	998 2.3×	148	5.1k
Owen Williams United Kingdom	31	288 0.2×	133 0.1×	139 0.2×	1.4k 3.2×	150 0.3×	82	3.2k
Teresa Casals Spain	27	501 0.4×	1.9k 1.7×	313 0.5×	515 1.2×	460 1.1×	81	2.7k
Paola Corti Italy	21	213 0.1×	104 0.1×	102 0.2×	512 1.2×	149 0.3×	65	1.4k
Stephen J. Lauer United States	25	295 0.2×	404 0.4×	868 1.3×	514 1.2×	112 0.3×	54	2.4k
Sudha Srinivasan United States	16	104 0.1×	72 0.1×	133 0.2×	824 1.9×	589 1.4×	25	1.5k

Countries citing papers authored by Jamie McDonald

Since Specialization

Citations

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

Fields of papers citing papers by Jamie McDonald

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jamie McDonald

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

White, Andrew J., Félix Ratjen, Jamie McDonald, et al.. (2023). Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. Journal of Clinical Medicine. 12(7). 2704–2704. 10 indexed citations

McDonald, Jamie, David A. Stevenson, Andrea Hanson‐Kahn, et al.. (2023). Frequency of epistaxis and telangiectasia in patients with hereditary hemorrhagic telangiectasia (HHT) in comparison with the general population: Curaçao diagnostic criteria revisited. Genetics in Medicine. 25(8). 100865–100865. 10 indexed citations

McDonald, Jamie, et al.. (2023). The Shunt of It. CHEST Journal. 163(5). e201–e205. 1 indexed citations

White, Andrew J., Félix Ratjen, Jamie McDonald, et al.. (2023). Reply to Eker et al. Comment on “Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. J. Clin. Med. 2023, 12, 2704”. Journal of Clinical Medicine. 12(23). 7462–7462. 3 indexed citations

White, Andrew J., Dewi Clark, Murali M. Chakinala, et al.. (2020). Genotype–Phenotype Correlations in Children with HHT. Journal of Clinical Medicine. 9(9). 2714–2714. 16 indexed citations

McDonald, Jamie, et al.. (2020). Curaçao diagnostic criteria for hereditary hemorrhagic telangiectasia is highly predictive of a pathogenic variant in ENG or ACVRL1 (HHT1 and HHT2). Genetics in Medicine. 22(7). 1201–1205. 43 indexed citations

Stevenson, David A., et al.. (2019). Localization and age distribution of telangiectases in children and adolescents with hereditary hemorrhagic telangiectasia: A retrospective cohort study. Journal of the American Academy of Dermatology. 81(4). 950–955. 15 indexed citations

Ruiz, Lı́dia, Jamie McDonald, Whitney Wooderchak‐Donahue, et al.. (2019). Characterization of a family mutation in the 5’ untranslated region of the endoglin gene causative of hereditary hemorrhagic telangiectasia. Journal of Human Genetics. 64(4). 333–339. 7 indexed citations

Klostranec, Jesse, Long Chen, Shobhit Mathur, et al.. (2018). A theory for polymicrogyria and brain arteriovenous malformations in HHT. Neurology. 92(1). 34–42. 16 indexed citations

10.

Jiang, Xuan, Whitney Wooderchak‐Donahue, Jamie McDonald, et al.. (2018). Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia. Science Signaling. 11(513). 22 indexed citations

11.

Morris, Andrew M., Elissa Rennert‐May, Nick Daneman, et al.. (2018). Rationale and development of a business case for antimicrobial stewardship programs in acute care hospital settings. Antimicrobial Resistance and Infection Control. 7(1). 104–104. 12 indexed citations

12.

McDonald, Jamie, et al.. (2018). Vitamin D Levels are Associated with Epistaxis Severity and Bleeding Duration in Hereditary Hemorrhagic Telangiectasia. Biomarkers in Medicine. 12(4). 365–371. 2 indexed citations

13.

Soemedi, Rachel, Kamil J. Cygan, Christy L. Rhine, et al.. (2017). Pathogenic variants that alter protein code often disrupt splicing. Nature Genetics. 49(6). 848–855. 151 indexed citations

14.

Higa, Leigh Ann, et al.. (2015). Life experiences of individuals with hereditary hemorrhagic telangiectasia and disclosing outside the family: a qualitative analysis. Journal of Community Genetics. 7(1). 81–89. 8 indexed citations

15.

Wain, Karen E., Marissa S. Ellingson, Jamie McDonald, et al.. (2014). Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review. Genetics in Medicine. 16(8). 588–593. 54 indexed citations

16.

McDonald, Jamie, Pınar Bayrak‐Toydemir, & Reed E. Pyeritz. (2011). Hereditary hemorrhagic telangiectasia: An overview of diagnosis, management, and pathogenesis. Genetics in Medicine. 13(7). 607–616. 245 indexed citations

17.

McDonald, Jamie, et al.. (2009). Multiple Sequence Variants in Hereditary Hemorrhagic Telangiectasia Cases. Journal of Molecular Diagnostics. 11(6). 569–575. 14 indexed citations

18.

Bayrak‐Toydemir, Pınar, Jamie McDonald, Boaz A. Markewitz, et al.. (2006). Genotype–phenotype correlation in hereditary hemorrhagic telangiectasia: Mutations and manifestations*. American Journal of Medical Genetics Part A. 140A(5). 463–470. 157 indexed citations

19.

Mao, Rong, et al.. (2005). The Implication of De Novo 21-Hydroxylase Mutation in Clinical and Prenatal Molecular Diagnoses. Genetic Testing. 9(2). 121–125. 7 indexed citations

20.

Botkin, Jeffrey R., Ken R. Smith, Robert T. Croyle, et al.. (2003). Genetic testing for a BRCA1 mutation: Prophylactic surgery and screening behavior in women 2 years post testing. American Journal of Medical Genetics Part A. 118A(3). 201–209. 163 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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