Bryce Schuler

549 total citations
10 papers, 223 citations indexed

About

Bryce Schuler is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Bryce Schuler has authored 10 papers receiving a total of 223 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in Bryce Schuler's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and BRCA gene mutations in cancer (2 papers). Bryce Schuler is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and BRCA gene mutations in cancer (2 papers). Bryce Schuler collaborates with scholars based in United States, Netherlands and France. Bryce Schuler's co-authors include Nicholas M. Negretti, Susan H. Guttentag, Timothy S. Blackwell, Jonathan A. Kropski, David S. Nichols, Nicholas E. Banovich, Arun C. Habermann, Jennifer M. S. Sucre, Erin J. Plosa and Christopher S. Jetter and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and Development.

In The Last Decade

Bryce Schuler

8 papers receiving 222 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bryce Schuler United States 5 69 67 63 42 32 10 223
Enrique Alfaro Spain 10 37 0.5× 47 0.7× 75 1.2× 31 0.7× 52 1.6× 35 254
Andrew Kwok United Kingdom 6 36 0.5× 52 0.8× 53 0.8× 18 0.4× 29 0.9× 10 189
Manuel A. Torres Acosta United States 4 58 0.8× 97 1.4× 70 1.1× 15 0.4× 32 1.0× 7 262
Leanne M. Bilawchuk Canada 6 54 0.8× 62 0.9× 72 1.1× 49 1.2× 119 3.7× 11 256
Katherine McAllister United Kingdom 9 47 0.7× 28 0.4× 88 1.4× 17 0.4× 17 0.5× 16 269
Junbin Wang China 7 23 0.3× 45 0.7× 41 0.7× 14 0.3× 21 0.7× 16 162
Giuseppe Paolicelli Italy 7 34 0.5× 37 0.6× 58 0.9× 18 0.4× 42 1.3× 9 205
Margarethe Konik Germany 8 42 0.6× 101 1.5× 68 1.1× 9 0.2× 10 0.3× 21 181
Fiona Henkel Germany 8 36 0.5× 38 0.6× 53 0.8× 15 0.4× 13 0.4× 12 237

Countries citing papers authored by Bryce Schuler

Since Specialization
Citations

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

Fields of papers citing papers by Bryce Schuler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bryce Schuler

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

All Works

10 of 10 papers shown
1.
Bastarache, Lisa, Rory J. Tinker, Bryce Schuler, et al.. (2025). Characterizing trends in clinical genetic testing: A single-center analysis of EHR data from 1.8 million patients over two decades. The American Journal of Human Genetics. 112(5). 1029–1038. 2 indexed citations
2.
Bick, Alexander, et al.. (2025). Benefits and barriers to broad implementation of genomic sequencing in the NICU. The American Journal of Human Genetics. 112(6). 1270–1285.
3.
4.
Schuler, Bryce, et al.. (2023). Collaborative efforts to improve genetic testing in the neonatal intensive care unit. Journal of Perinatology. 43(12). 1500–1505. 2 indexed citations
5.
Schuler, Bryce, et al.. (2022). Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases. Journal of Clinical Investigation. 132(7). 19 indexed citations
6.
Schuler, Bryce, et al.. (2022). eP234: SERPINA1 sequencing facilitates detection of undiagnosed Alpha-1 antitrypsin deficiency. Genetics in Medicine. 24(3). S148–S149. 2 indexed citations
7.
Negretti, Nicholas M., Erin J. Plosa, John T. Benjamin, et al.. (2021). A single-cell atlas of mouse lung development. Development. 148(24). 73 indexed citations
8.
Schuler, Bryce, Arun C. Habermann, Erin J. Plosa, et al.. (2020). Age-determined expression of priming protease TMPRSS2 and localization of SARS-CoV-2 in lung epithelium. Journal of Clinical Investigation. 131(1). 90 indexed citations
9.
Schuler, Bryce, Luyuan Li, Michal Mokrý, et al.. (2014). Major and Minor Group Rhinoviruses Elicit Differential Signaling and Cytokine Responses as a Function of Receptor-Mediated Signal Transduction. PLoS ONE. 9(4). e93897–e93897. 29 indexed citations
10.

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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2026