Steven Keiles

1.2k total citations
13 papers, 558 citations indexed

About

Steven Keiles is a scholar working on Pulmonary and Respiratory Medicine, Surgery and Genetics. According to data from OpenAlex, Steven Keiles has authored 13 papers receiving a total of 558 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pulmonary and Respiratory Medicine, 3 papers in Surgery and 3 papers in Genetics. Recurrent topics in Steven Keiles's work include Cystic Fibrosis Research Advances (6 papers), Neonatal Respiratory Health Research (4 papers) and BRCA gene mutations in cancer (3 papers). Steven Keiles is often cited by papers focused on Cystic Fibrosis Research Advances (6 papers), Neonatal Respiratory Health Research (4 papers) and BRCA gene mutations in cancer (3 papers). Steven Keiles collaborates with scholars based in United States, India and Germany. Steven Keiles's co-authors include Anja Kammesheidt, Aaron J. Stuenkel, Elizabeth Chao, Tina Pesaran, Virginia Speare, Elaine Chen, Stephanie Gandomi, Jill S. Dolinsky, Erika Palmaer and Holly LaDuca and has published in prestigious journals such as PLoS ONE, Gut and Genetics in Medicine.

In The Last Decade

Steven Keiles

13 papers receiving 541 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven Keiles United States 8 281 141 131 120 118 13 558
H Ozçelik Canada 9 414 1.5× 64 0.5× 160 1.2× 112 0.9× 67 0.6× 15 644
Yvonne Engwall Sweden 7 161 0.6× 115 0.8× 95 0.7× 271 2.3× 107 0.9× 9 508
Rachel T. Klein United States 10 354 1.3× 55 0.4× 205 1.6× 299 2.5× 45 0.4× 15 600
Inbal Kedar Israel 15 155 0.6× 42 0.3× 67 0.5× 108 0.9× 61 0.5× 42 383
Heidi Rothenmund Canada 12 220 0.8× 141 1.0× 288 2.2× 279 2.3× 47 0.4× 21 732
Anne Naumer United States 7 127 0.5× 77 0.5× 109 0.8× 44 0.4× 54 0.5× 16 447
Jacqueline Mersch United States 3 333 1.2× 25 0.2× 148 1.1× 123 1.0× 78 0.7× 9 544
Maran J.W. Olderode-Berends Netherlands 10 101 0.4× 59 0.4× 155 1.2× 239 2.0× 24 0.2× 14 457
Brita Thode Germany 10 95 0.3× 108 0.8× 49 0.4× 101 0.8× 39 0.3× 18 381

Countries citing papers authored by Steven Keiles

Since Specialization
Citations

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

Fields of papers citing papers by Steven Keiles

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven Keiles

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

All Works

13 of 13 papers shown
1.
LaDuca, Holly, Aaron J. Stuenkel, Jill S. Dolinsky, et al.. (2014). Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. Genetics in Medicine. 16(11). 830–837. 237 indexed citations
2.
Chong, Hansook Kim, Tao Wang, Hsiao-Mei Lu, et al.. (2014). The Validation and Clinical Implementation of BRCAplus: A Comprehensive High-Risk Breast Cancer Diagnostic Assay. PLoS ONE. 9(5). e97408–e97408. 57 indexed citations
3.
Hoffman, Jodi D., Nicole Schreiber‐Agus, Ruth Kornreich, et al.. (2014). The Ashkenazi Jewish carrier screening panel: evolution, status quo, and disparities. Prenatal Diagnosis. 34(12). 1161–1167. 15 indexed citations
4.
Langfelder-Schwind, E., Barbara Karczeski, Michelle N. Strecker, et al.. (2013). Molecular Testing for Cystic Fibrosis Carrier Status Practice Guidelines: Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 23(1). 5–15. 22 indexed citations
5.
Beer, Sebastian, András Szabó, Steven Keiles, et al.. (2012). Comprehensive functional analysis of chymotrypsin C ( CTRC ) variants reveals distinct loss-of-function mechanisms associated with pancreatitis risk. Gut. 62(11). 1616–1624. 72 indexed citations
6.
Nakagawa, Sachiko, Wei Sun, José Carlos Ferreira, et al.. (2012). Platelet Hexosaminidase A Enzyme Assay Effectively Detects Carriers Missed by Targeted DNA Mutation Analysis. JIMD Reports. 6. 1–6. 4 indexed citations
7.
Keiles, Steven, Ruth Koepke, Richard B. Parad, & Martin Kharrazi. (2011). Impact of IVS8-(TG)m(T)n on IRT and sweat chloride levels in newborns identified by California CF newborn screening. Journal of Cystic Fibrosis. 11(3). 257–260. 6 indexed citations
8.
Carroll, John L., et al.. (2010). Report of two patients with associated conditions in addition to cystic fibrosis. Journal of Cystic Fibrosis. 9(4). 269–271. 3 indexed citations
9.
Keiles, Steven. (2009). 2008 National Society of Genetic Counselors Presidential Address: The NSGC Should Do Something About That… and We Are. Journal of Genetic Counseling. 18(2). 105–108. 1 indexed citations
10.
Havasi, Viktória, Steven Keiles, Tina Hambuch, Eric J. Sorscher, & Anja Kammesheidt. (2008). The role of the F508C mutation in congenital bilateral absence of the vas deferens. Genetics in Medicine. 10(12). 910–914. 3 indexed citations
11.
Kammesheidt, Anja, Martin Kharrazi, Stephen M. Graham, et al.. (2006). Comprehensive genetic analysis of the cystic fibrosis transmembrane conductance regulator from dried blood specimens – Implications for newborn screening. Genetics in Medicine. 8(9). 557–562. 32 indexed citations
12.
Keiles, Steven & Anja Kammesheidt. (2006). Identification of CFTR, PRSS1, and SPINK1 Mutations in 381 Patients With Pancreatitis. Pancreas. 33(3). 221–227. 72 indexed citations
13.
Schrijver, Iris, Sudha Ramalingam, S. Ramalingam, et al.. (2005). Diagnostic Testing by CFTR Gene Mutation Analysis in a Large Group of Hispanics. Journal of Molecular Diagnostics. 7(2). 289–299. 34 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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