Bryce A. Seifert

2.0k total citations
15 papers, 229 citations indexed

About

Bryce A. Seifert is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Bryce A. Seifert has authored 15 papers receiving a total of 229 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Bryce A. Seifert's work include Genomics and Rare Diseases (4 papers), Genetic factors in colorectal cancer (4 papers) and BRCA gene mutations in cancer (3 papers). Bryce A. Seifert is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetic factors in colorectal cancer (4 papers) and BRCA gene mutations in cancer (3 papers). Bryce A. Seifert collaborates with scholars based in United States, Australia and United Kingdom. Bryce A. Seifert's co-authors include Jonathan S. Berg, James P. Evans, Daniel S. Marchuk, Kirk C. Wilhelmsen, H. Shelton Earp, Linda D. Cooley, Lina Shao, David T. Miller, Deborah Ritter and Michele C. Hayward and has published in prestigious journals such as SHILAP Revista de lepidopterología, Clinical Cancer Research and Journal of Investigative Dermatology.

In The Last Decade

Bryce A. Seifert

14 papers receiving 227 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bryce A. Seifert United States	7	140	90	82	67	40	15	229
Finn C. Nielsen Denmark	12	157 1.1×	166 1.8×	73 0.9×	46 0.7×	32 0.8×	14	271
Nur Diana Binte Ishak Singapore	8	86 0.6×	56 0.6×	38 0.5×	47 0.7×	80 2.0×	15	219
Makia J. Marafie Kuwait	11	154 1.1×	142 1.6×	79 1.0×	50 0.7×	37 0.9×	28	279
Wendy A. van Zelst-Stams Netherlands	5	53 0.4×	87 1.0×	58 0.7×	72 1.1×	45 1.1×	5	168
Olga Campos Spain	9	129 0.9×	138 1.5×	96 1.2×	100 1.5×	67 1.7×	18	270
Alfonso Hisado-Oliva Spain	7	160 1.1×	140 1.6×	21 0.3×	21 0.3×	16 0.4×	7	247
Mitchell W. Dillon United States	5	81 0.6×	127 1.4×	18 0.2×	15 0.2×	26 0.7×	7	202
Antoine Rousselin France	8	266 1.9×	296 3.3×	132 1.6×	88 1.3×	73 1.8×	11	471
Vera Riehmer Germany	7	54 0.4×	142 1.6×	46 0.6×	9 0.1×	33 0.8×	11	229
Tadeusz Dębniak Poland	9	160 1.1×	111 1.2×	69 0.8×	80 1.2×	67 1.7×	14	246

Countries citing papers authored by Bryce A. Seifert

Since Specialization

Citations

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

Fields of papers citing papers by Bryce A. Seifert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bryce A. Seifert. 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 Bryce A. Seifert. The network helps show where Bryce A. Seifert may publish in the future.

Co-authorship network of co-authors of Bryce A. Seifert

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Zainab, Rida, Justin Lack, Morgan Similuk, et al.. (2025). Genetic evaluation of pediatric pituitary adenomas and USP8-related genotype-phenotype correlations in Cushing’s disease. Pituitary. 28(5). 92–92.

Moses, Rachel Gore, Bryce A. Seifert, Siyuan Liu, et al.. (2024). Deep Screening for X Chromosome Parent-of-Origin Effects on Neurobehavioral and Neuroanatomical Phenotypes in 47,XXY Klinefelter Syndrome. SHILAP Revista de lepidopterología. 4(6). 100391–100391. 1 indexed citations

Seifert, Bryce A., et al.. (2024). Myotonic dystrophy type 1 testing, 2024 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 26(8). 101145–101145. 2 indexed citations

Mohsin, Noreen, Jia Yan, Paul Nghiem, et al.. (2024). Genetic Risk Factors for Early-Onset Merkel Cell Carcinoma. JAMA Dermatology. 160(2). 172–172. 6 indexed citations

Nghiem, Paul, Jenna Bergerson, Morgan Similuk, et al.. (2022). Early-Onset Merkel Cell Carcinoma is Associated with Germline Defects in DNA Repair Genes and a Rare Immunodeficiency. Journal of Investigative Dermatology. 142(10). 2839–2839. 1 indexed citations

Raca, Gordana, Caroline Astbury, Mauricio De Castro, et al.. (2022). Points to consider in the detection of germline structural variants using next-generation sequencing: A statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 25(2). 100316–100316. 24 indexed citations

Similuk, Morgan, Jia Yan, Bryce A. Seifert, et al.. (2022). eP083: Chromosomal microarray analysis as a supplement to exome sequencing in pediatric patients with suspected inborn errors of immunity. Genetics in Medicine. 24(3). S55–S55. 1 indexed citations

Shao, Lina, Yassmine Akkari, Linda D. Cooley, et al.. (2021). Chromosomal microarray analysis, including constitutional and neoplastic disease applications, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 23(10). 1818–1829. 28 indexed citations

Deignan, Joshua L., Caroline Astbury, Saurav Guha, et al.. (2020). Addendum: Technical standards and guidelines for spinal muscular atrophy testing. Genetics in Medicine. 23(12). 2462–2462. 3 indexed citations

10.

McDonald, Marie, et al.. (2020). An Unusual Association: Total Anomalous Pulmonary Venous Return and Aortic Arch Obstruction in Patients with Cat Eye Syndrome. Journal of Pediatric Genetics. 10(1). 35–38. 4 indexed citations

11.

Lee, Kristy, Bryce A. Seifert, Hermela Shimelis, et al.. (2018). Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels. Genetics in Medicine. 21(7). 1497–1506. 41 indexed citations

12.

Seifert, Bryce A., Jennifer McGlaughon, Sarah A. Jackson, et al.. (2018). Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework. Genetics in Medicine. 21(7). 1507–1516. 17 indexed citations

13.

Seifert, Bryce A., Marion Déjosez, & Thomas P. Zwaka. (2017). Ronin influences the DNA damage response in pluripotent stem cells. Stem Cell Research. 23. 98–104. 9 indexed citations

14.

Haskell, Gloria, Brian C. Jensen, Leigh Ann Samsa, et al.. (2017). Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease. Circulation Cardiovascular Genetics. 10(3). 29 indexed citations

15.

Seifert, Bryce A., Julianne O’Daniel, Daniel S. Marchuk, et al.. (2016). Germline Analysis from Tumor–Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings. Clinical Cancer Research. 22(16). 4087–4094. 63 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.

Explore authors with similar magnitude of impact