Steven E. Boyden

1.2k total citations
15 papers, 356 citations indexed

About

Steven E. Boyden is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Physiology. According to data from OpenAlex, Steven E. Boyden has authored 15 papers receiving a total of 356 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Cardiology and Cardiovascular Medicine and 3 papers in Physiology. Recurrent topics in Steven E. Boyden's work include Muscle Physiology and Disorders (4 papers), Mast cells and histamine (3 papers) and Urticaria and Related Conditions (2 papers). Steven E. Boyden is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Mast cells and histamine (3 papers) and Urticaria and Related Conditions (2 papers). Steven E. Boyden collaborates with scholars based in United States, Japan and Portugal. Steven E. Boyden's co-authors include Louis M. Kunkel, Hirsh D. Komarow, Daniel L. Kastner, Ana Olivera, Elicia Estrella, Peter B. Kang, Dean D. Metcalfe, Colleen Satorius, Linda M. Scott and A.J. Pakstis and has published in prestigious journals such as New England Journal of Medicine, PLoS ONE and Journal of Allergy and Clinical Immunology.

In The Last Decade

Steven E. Boyden

13 papers receiving 352 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Steven E. Boyden United States	9	218	86	58	57	54	15	356
Véronique Bolduc United States	10	355 1.6×	48 0.6×	119 2.1×	36 0.6×	59 1.1×	19	492
Sinan Çomu Türkiye	8	165 0.8×	63 0.7×	87 1.5×	32 0.6×	21 0.4×	15	404
Mark D. Ware Canada	11	385 1.8×	138 1.6×	74 1.3×	22 0.4×	30 0.6×	15	583
Imen Dorboz France	14	492 2.3×	57 0.7×	94 1.6×	24 0.4×	23 0.4×	30	650
Isabelle Cournu‐Rebeix France	8	219 1.0×	79 0.9×	24 0.4×	31 0.5×	43 0.8×	12	443
Avery R. Soderman United States	8	327 1.5×	119 1.4×	85 1.5×	15 0.3×	12 0.2×	9	599
Hailing Yang United States	6	181 0.8×	87 1.0×	28 0.5×	15 0.3×	27 0.5×	10	376
Alice Abdel Aleem Egypt	13	216 1.0×	28 0.3×	119 2.1×	15 0.3×	52 1.0×	24	376
Carlo Arduino Italy	11	230 1.1×	47 0.5×	158 2.7×	8 0.1×	17 0.3×	25	490
Akiko Hamaguchi Japan	6	345 1.6×	121 1.4×	48 0.8×	13 0.2×	8 0.1×	6	518

Countries citing papers authored by Steven E. Boyden

Since Specialization

Citations

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

Fields of papers citing papers by Steven E. Boyden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven E. Boyden

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

All Works

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15 of 15 papers shown

Wen, Ting, Steven E. Boyden, Robert G. Lewis, et al.. (2025). Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing. Blood Advances. 9(10). 2443–2452.

Longo, Nicola, Robert G. Lewis, Thomas J. Nicholas, et al.. (2024). Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon‐level Array, and RNA sequencing. American Journal of Medical Genetics Part A. 194(5). e63516–e63516. 1 indexed citations

Wen, Ting, Andrew Farrell, Rong Mao, et al.. (2022). Rapid genome sequencing identifies a novel de novoSNAP25variant for neonatal congenital myasthenic syndrome. Molecular Case Studies. 8(7). a006242–a006242. 5 indexed citations

Naranjo, Andrea, Geethani Bandara, Yun Bai, et al.. (2020). Critical Signaling Events in the Mechanoactivation of Human Mast Cells through p.C492Y-ADGRE2. Journal of Investigative Dermatology. 140(11). 2210–2220.e5. 21 indexed citations

Salas‐Huetos, Albert, Frank Tüttelmann, Margot J. Wyrwoll, et al.. (2020). Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia. Human Genetics. 140(1). 217–227. 32 indexed citations

Salas‐Huetos, Albert, Frank Tüttelmann, Margot J. Wyrwoll, et al.. (2020). Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia. Human Genetics. 140(1). 229–229.

Komarow, Hirsh D., Andrea Naranjo, Margery Smelkinson, et al.. (2020). Mechanical Activation of ADGRE2 Causes Calcium-dependent Activation of PI3K and MAPK Pathways Driving Mast Cell Degranulation and PGD2 Production. Journal of Allergy and Clinical Immunology. 145(2). AB186–AB186. 1 indexed citations

Faridi, Rabia, Risa Tona, Alessandra Brofferio, et al.. (2018). Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome. Human Mutation. 40(2). 162–176. 27 indexed citations

Boyden, Steven E., Avanti Desai, Glenn Cruse, et al.. (2016). Vibratory Urticaria Associated with a Missense Variant in ADGRE2. New England Journal of Medicine. 374(7). 656–663. 130 indexed citations

10.

Mitsuhashi, Satomi, Steven E. Boyden, Elicia Estrella, et al.. (2013). Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2. Neuromuscular Disorders. 23(12). 975–980. 31 indexed citations

11.

Boyden, Steven E., Genri Kawahara, Jennifer A. Myers, et al.. (2012). Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores. Neurogenetics. 13(2). 115–124. 57 indexed citations

12.

Boyden, Steven E., Anna R. Duncan, Elicia Estrella, et al.. (2011). Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE. BMC Medical Genetics. 12(1). 87–87. 17 indexed citations

13.

Boyden, Steven E. & Louis M. Kunkel. (2010). High-Density Genomewide Linkage Analysis of Exceptional Human Longevity Identifies Multiple Novel Loci. PLoS ONE. 5(8). e12432–e12432. 17 indexed citations

14.

Boyden, Steven E., Mustafa A. Salih, Anna R. Duncan, et al.. (2010). Efficient identification of novel mutations in patients with limb girdle muscular dystrophy. Neurogenetics. 11(4). 449–455. 14 indexed citations

15.

Dimitrakov, Jordan D., et al.. (2005). 303: Single Nucleotide Polymorphism (SNP) Analysis of Autosomal Dominant Interstitial Cystitis: A Family-Based Study. The Journal of Urology. 173(4S). 84–84. 3 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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