Regan Veith

1.3k total citations
10 papers, 243 citations indexed

About

Regan Veith is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Regan Veith has authored 10 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Regan Veith's work include Genomics and Rare Diseases (5 papers), BRCA gene mutations in cancer (3 papers) and Ethics in Clinical Research (2 papers). Regan Veith is often cited by papers focused on Genomics and Rare Diseases (5 papers), BRCA gene mutations in cancer (3 papers) and Ethics in Clinical Research (2 papers). Regan Veith collaborates with scholars based in United States, Australia and United Kingdom. Regan Veith's co-authors include David Bick, David Dimmock, Pippa Simpson, Kimberly A. Strong, Paul Coucke, Tammy M. Holm, Majed Dasouki, Pamela Trapane, Marjolijn Renard and Osman Başpınar and has published in prestigious journals such as Clinical Journal of the American Society of Nephrology, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Regan Veith

10 papers receiving 240 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Regan Veith United States	5	173	55	53	53	31	10	243
Helena Mörse Sweden	10	48 0.3×	83 1.5×	22 0.4×	169 3.2×	28 0.9×	19	312
Sabine Grill Germany	9	79 0.5×	48 0.9×	18 0.3×	27 0.5×	32 1.0×	22	259
Chantal Farra Lebanon	12	127 0.7×	71 1.3×	58 1.1×	42 0.8×	25 0.8×	38	341
Joel T. Gibson Australia	8	64 0.4×	94 1.7×	17 0.3×	8 0.2×	8 0.3×	9	238
Purificación García de Miguel Spain	7	51 0.3×	39 0.7×	30 0.6×	69 1.3×	4 0.1×	7	275
Georgios Adonakis Greece	11	32 0.2×	61 1.1×	47 0.9×	58 1.1×	13 0.4×	46	359
Janna A. Hol Netherlands	11	40 0.2×	192 3.5×	112 2.1×	19 0.4×	23 0.7×	22	310
Giuseppina Baldassarre Italy	11	186 1.1×	275 5.0×	25 0.5×	22 0.4×	13 0.4×	20	420
Anthony Audino United States	10	17 0.1×	50 0.9×	54 1.0×	74 1.4×	24 0.8×	33	257
J Lorenzo Bermejo Germany	9	108 0.6×	95 1.7×	27 0.5×	36 0.7×	60 1.9×	13	302

Countries citing papers authored by Regan Veith

Since Specialization

Citations

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

Fields of papers citing papers by Regan Veith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Regan Veith

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

All Works

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10 of 10 papers shown

Larson, Austin, Lisa Salz, Regan Veith, et al.. (2024). Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting. Frontiers in Pediatrics. 12. 1349519–1349519. 4 indexed citations

Mele, Caterina, Mathieu Lemaire, Paraskevas Iatropoulos, et al.. (2015). Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome. Clinical Journal of the American Society of Nephrology. 10(6). 1011–1019. 37 indexed citations

Lee, Daniel J., Regan Veith, David Dimmock, & Margaret M. Samyn. (2014). Hypertrophic Cardiomyopathy: A New Mutation Illustrates the Need for Family-Centered Care. Pediatric Cardiology. 35(8). 1474–1477. 2 indexed citations

Strong, Kimberly A., et al.. (2014). Views of nonmedical, health system professionals regarding the return of whole genome sequencing incidental findings.. PubMed. 113(5). 179–84. 11 indexed citations

Strong, Kimberly A., et al.. (2014). Views of primary care providers regarding the return of genome sequencing incidental findings. Clinical Genetics. 86(5). 461–468. 23 indexed citations

El‐Chammas, Khalil, Regan Veith, Neha Sekhri, et al.. (2012). Pancreatic insufficiency in Toriello–Carey syndrome: Report of a second patient. American Journal of Medical Genetics Part A. 158A(5). 1208–1211. 3 indexed citations

Worthey, Elizabeth A., David Bick, David Dimmock, et al.. (2012). Clinical diagnostic whole genome sequencing in a paediatric population: experience from our WGS genetics clinic. BMC Proceedings. 6(S6). 2 indexed citations

Bick, David, et al.. (2012). Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study. Clinical Genetics. 84(3). 230–236. 64 indexed citations

Quintero, Diana, et al.. (2011). A Rare Presentation of Neonatal Stridor. Clinical Pediatrics. 51(3). 294–296. 2 indexed citations

10.

Renard, Marjolijn, Tammy M. Holm, Regan Veith, et al.. (2010). Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency. European Journal of Human Genetics. 18(8). 895–901. 95 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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