Steven B. Bleyl

2.9k total citations
42 papers, 1.4k citations indexed

About

Steven B. Bleyl is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Steven B. Bleyl has authored 42 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 14 papers in Genetics and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Steven B. Bleyl's work include Congenital heart defects research (17 papers), Congenital Heart Disease Studies (10 papers) and Cardiomyopathy and Myosin Studies (8 papers). Steven B. Bleyl is often cited by papers focused on Congenital heart defects research (17 papers), Congenital Heart Disease Studies (10 papers) and Cardiomyopathy and Myosin Studies (8 papers). Steven B. Bleyl collaborates with scholars based in United States, Netherlands and Sweden. Steven B. Bleyl's co-authors include John C. Carey, Gary C. Schoenwolf, Theodore J. Pysher, Kenneth Ward, Thomas K. Chin, Philippa H. Francis‐West, Philip R. Brauer, Luciana T. Pagotto, Victor Thompson and Sarah T. South and has published in prestigious journals such as Journal of the American College of Cardiology, PLoS ONE and PEDIATRICS.

In The Last Decade

Steven B. Bleyl

41 papers receiving 1.4k 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 B. Bleyl United States 20 869 483 302 276 229 42 1.4k
Bianca Hogers Netherlands 18 917 1.1× 319 0.7× 419 1.4× 137 0.5× 293 1.3× 19 1.3k
Siobhan Loughna United Kingdom 18 1.0k 1.2× 314 0.7× 177 0.6× 176 0.6× 182 0.8× 32 1.4k
Clement Lo United States 19 1.7k 1.9× 205 0.4× 284 0.9× 259 0.9× 118 0.5× 25 2.3k
Susan Fernbach United States 15 1.2k 1.4× 851 1.8× 370 1.2× 289 1.0× 424 1.9× 20 2.1k
Kérsti K. Linask United States 32 1.8k 2.1× 550 1.1× 367 1.2× 320 1.2× 302 1.3× 64 2.5k
Jasper J. van der Smagt Netherlands 22 623 0.7× 610 1.3× 113 0.4× 483 1.8× 50 0.2× 48 1.5k
Paul Grossfeld United States 22 1.7k 1.9× 756 1.6× 343 1.1× 716 2.6× 893 3.9× 53 2.9k
Ingrid M.B.H. van de Laar Netherlands 18 321 0.4× 213 0.4× 164 0.5× 329 1.2× 189 0.8× 40 963
Ravi Karra United States 17 1.4k 1.6× 341 0.7× 460 1.5× 138 0.5× 296 1.3× 42 1.8k
Marco Ritelli Italy 25 474 0.5× 163 0.3× 245 0.8× 1.1k 3.8× 86 0.4× 79 1.6k

Countries citing papers authored by Steven B. Bleyl

Since Specialization
Citations

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

Fields of papers citing papers by Steven B. Bleyl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven B. Bleyl

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

All Works

20 of 20 papers shown
1.
Bentley, Dawn, Christine Miller, Rong Mao, et al.. (2022). Evaluating use of changing technologies for rapid next-generation sequencing in pediatrics. Pediatric Research. 92(5). 1364–1369. 10 indexed citations
2.
Mason, Clinton C., Jennifer H. Garvin, Marc S. Williams, et al.. (2021). A qualitative study of prevalent laboratory information systems and data communication patterns for genetic test reporting. Genetics in Medicine. 23(11). 2171–2177. 2 indexed citations
3.
4.
Segal, Michael M., Alanna Kulchak Rahm, Grant M. Wood, et al.. (2017). Experience with Integrating Diagnostic Decision Support Software with Electronic Health Records: Benefits versus Risks of Information Sharing. eGEMs (Generating Evidence & Methods to improve patient outcomes). 5(1). 23–23. 11 indexed citations
5.
Hinton, Robert B., Kim L. McBride, Steven B. Bleyl, et al.. (2015). Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach. PMC. 2 indexed citations
6.
Bowles, Neil E., Chuanchau J. Jou, Cammon B. Arrington, et al.. (2015). Exome analysis of a family with Wolff–Parkinson–White syndrome identifies a novel disease locus. American Journal of Medical Genetics Part A. 167(12). 2975–2984. 10 indexed citations
7.
Bleyl, Steven B., et al.. (2014). Phenotype of a patient with contiguous deletion of TBX5 and TBX3: Expanding the disease spectrum. American Journal of Medical Genetics Part A. 164(5). 1304–1309. 13 indexed citations
8.
Bleyl, Steven B., et al.. (2014). Clinical Exome Sequencing Identifies a Novel TUBB4A Mutation in a Child With Static Hypomyelinating Leukodystrophy. Pediatric Neurology. 50(6). 608–611. 25 indexed citations
9.
Puchalski, Michael D., et al.. (2014). DOES GENOTYPE PREDICT AGE OF ONSET OF CARDIOMYOPATHY IN PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY?. Journal of the American College of Cardiology. 63(12). A600–A600. 1 indexed citations
10.
Arrington, Cammon B., Steven B. Bleyl, Norisada Matsunami, et al.. (2012). Exome Analysis of a Family With Pleiotropic Congenital Heart Disease. Circulation Cardiovascular Genetics. 5(2). 175–182. 48 indexed citations
11.
Arrington, Cammon B., et al.. (2012). Non-synonymous variants in pre-B cell leukemia homeobox (PBX) genes are associated with congenital heart defects. European Journal of Medical Genetics. 55(4). 235–237. 23 indexed citations
12.
Arrington, Cammon B., Steven B. Bleyl, Nori Matsunami, et al.. (2012). A family‐based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia. American Journal of Medical Genetics Part A. 158A(12). 3137–3147. 22 indexed citations
13.
Bhoj, Elizabeth, Purita Ramos, Linda A. Baker, et al.. (2011). Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development. European Journal of Human Genetics. 19(5). 540–546. 19 indexed citations
14.
Ohta, Sho, et al.. (2011). Detection of isoform‐specific fibroblast growth factor receptors by whole‐mount in situ hybridization in early chick embryos. Developmental Dynamics. 240(6). 1537–1547. 11 indexed citations
15.
Bleyl, Steven B., Yukio Saijoh, Noortje A.M. Bax, et al.. (2010). Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms. Human Molecular Genetics. 19(7). 1286–1301. 51 indexed citations
16.
Paxton, Christian N., Steven B. Bleyl, Susan C. Chapman, & Gary C. Schoenwolf. (2009). Identification of differentially expressed genes in early inner ear development. Gene Expression Patterns. 10(1). 31–43. 28 indexed citations
17.
Bax, Noortje A.M., Heleen Lie‐Venema, Rebecca Vicente‐Steijn, et al.. (2009). Platelet‐derived growth factor is involved in the differentiation of second heart field‐derived cardiac structures in chicken embryos. Developmental Dynamics. 238(10). 2658–2669. 25 indexed citations
18.
Bleyl, Steven B., Janice L. B. Byrne, Sarah T. South, et al.. (2007). Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes. American Journal of Medical Genetics Part A. 143A(23). 2785–2795. 13 indexed citations
19.
Bleyl, Steven B., Lorenzo D. Botto, John C. Carey, et al.. (2006). Analysis of a Scottish founder effect narrows the TAPVR‐1 gene interval to chromosome 4q12. American Journal of Medical Genetics Part A. 140A(21). 2368–2373. 18 indexed citations
20.
Chapman, Susan C., et al.. (2006). Restricted expression of Fgf16 within the developing chick inner ear. Developmental Dynamics. 235(8). 2276–2281. 20 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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