Bryan C. Bjork

4.0k total citations · 1 hit paper
20 papers, 2.3k citations indexed

About

Bryan C. Bjork is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Bryan C. Bjork has authored 20 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Bryan C. Bjork's work include Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (8 papers) and Innovations in Medical Education (4 papers). Bryan C. Bjork is often cited by papers focused on Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (8 papers) and Innovations in Medical Education (4 papers). Bryan C. Bjork collaborates with scholars based in United States, United Kingdom and Sweden. Bryan C. Bjork's co-authors include David R. Beier, Michael A. Rudnicki, Hediye Erdjument‐Bromage, Patrick Seale, Shihuan Kuang, Bruce M. Spiegelman, Srikripa Devarakonda, Anthony Scimè, Sherry Chin and Wenli Yang and has published in prestigious journals such as Nature, PLoS ONE and Development.

In The Last Decade

Bryan C. Bjork

20 papers receiving 2.3k citations

Hit Papers

PRDM16 controls a brown fat/skeletal muscle switch 2008 2026 2014 2020 2008 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bryan C. Bjork United States 13 1.5k 839 789 353 315 20 2.3k
Jonathan M. Peterson United States 26 1.2k 0.8× 1.2k 1.4× 667 0.8× 504 1.4× 66 0.2× 52 2.4k
Masaji Sakaguchi Japan 17 678 0.4× 386 0.5× 1.5k 1.9× 293 0.8× 158 0.5× 37 2.3k
Emidio E. Pistilli United States 29 944 0.6× 238 0.3× 1.5k 1.8× 209 0.6× 154 0.5× 58 2.2k
Lisa Agatea Italy 10 556 0.4× 556 0.7× 1.0k 1.3× 80 0.2× 59 0.2× 12 1.6k
Tea Shavlakadze Australia 23 944 0.6× 200 0.2× 1.3k 1.7× 82 0.2× 120 0.4× 40 2.4k
Matthew P. Krause Canada 20 548 0.4× 211 0.3× 683 0.9× 111 0.3× 160 0.5× 29 1.4k
John Babraj United Kingdom 25 1.7k 1.1× 166 0.2× 1.4k 1.7× 260 0.7× 183 0.6× 53 4.1k
Cory M. Dungan United States 25 763 0.5× 87 0.1× 1.0k 1.3× 84 0.2× 141 0.4× 49 1.5k
Merly C. Vogt United States 13 529 0.3× 323 0.4× 537 0.7× 74 0.2× 92 0.3× 18 1.7k
Takafumi Tsuchiya Japan 19 528 0.3× 407 0.5× 450 0.6× 82 0.2× 158 0.5× 56 1.8k

Countries citing papers authored by Bryan C. Bjork

Since Specialization
Citations

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

Fields of papers citing papers by Bryan C. Bjork

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bryan C. Bjork. 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 Bryan C. Bjork. The network helps show where Bryan C. Bjork may publish in the future.

Co-authorship network of co-authors of Bryan C. Bjork

This figure shows the co-authorship network connecting the top 25 collaborators of Bryan C. Bjork. A scholar is included among the top collaborators of Bryan C. Bjork 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 Bryan C. Bjork. Bryan C. Bjork 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.
Zhang, Hongji, et al.. (2022). PRDM16 expression and function in mammalian cochlear development. Developmental Dynamics. 251(10). 1666–1683. 6 indexed citations
2.
Jones, Jennifer, et al.. (2021). PRDM16 regulates a temporal transcriptional program to promote progression of cortical neural progenitors. Development. 148(6). 12 indexed citations
3.
Wu, Meng, et al.. (2020). Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex. Journal of Developmental Biology. 8(4). 30–30. 9 indexed citations
4.
Bjork, Bryan C., Angela C. Gomez, Jennifer Jones, et al.. (2018). Prdm16 and Mecom mutants exhibit cleft secondary palate as a result of perturbations that affect different stages of palatogenesis. The FASEB Journal. 32(S1). 2 indexed citations
5.
Schnütgen, Frank, Qi Dai, Jennifer Jones, et al.. (2017). Generation of a multipurpose Prdm16 mouse allele by targeted gene trapping. Disease Models & Mechanisms. 10(7). 909–922. 10 indexed citations
6.
Wilson, Nathan R., Kanagaraj Palaniyandi, Eric C. Liao, et al.. (2016). SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delamination. Scientific Reports. 6(1). 17735–17735. 28 indexed citations
7.
Winkle, Lon J. Van, Bryan C. Bjork, Nalini Chandar, et al.. (2014). Critical Thinking and Reflection on Community Service for a Medical Biochemistry Course Raise Students’ Empathy, Patient-Centered Orientation, and Examination Scores. Medical Science Educator. 24(3). 279–290. 12 indexed citations
8.
Winkle, Lon J. Van, Susan Cornell, Nancy Fjortoft, et al.. (2013). Critical Thinking and Reflection Exercises in a Biochemistry Course to Improve Prospective Health Professions Students’ Attitudes Toward Physician-Pharmacist Collaboration. American Journal of Pharmaceutical Education. 77(8). 169–169. 32 indexed citations
9.
Winkle, Lon J. Van, Sophie La Salle, Bryan C. Bjork, et al.. (2013). Challenging Medical Students to Confront their Biases: A Case Study Simulation Approach. Medical Science Educator. 23(2). 217–224. 10 indexed citations
10.
Winkle, Lon J. Van, Bryan C. Bjork, Nalini Chandar, et al.. (2012). Interprofessional Workshop to Improve Mutual Understanding Between Pharmacy and Medical Students. American Journal of Pharmaceutical Education. 76(8). 150–150. 39 indexed citations
11.
Kamp, Anna, Michael Peterson, Karen L. Svenson, et al.. (2010). Genome-wide identification of mouse congenital heart disease loci. Human Molecular Genetics. 19(16). 3105–3113. 15 indexed citations
12.
Bjork, Bryan C., Yuko Fujiwara, Shannon W. Davis, et al.. (2010). A Transient Transgenic RNAi Strategy for Rapid Characterization of Gene Function during Embryonic Development. PLoS ONE. 5(12). e14375–e14375. 13 indexed citations
13.
Letra, Ariadne, Manika Govil, Toby McHenry, et al.. (2010). Novel Cleft Susceptibility Genes in Chromosome 6q. Journal of Dental Research. 89(9). 927–932. 23 indexed citations
14.
Bjork, Bryan C., et al.. (2009). Prdm16 is required for normal palatogenesis in mice. Human Molecular Genetics. 19(5). 774–789. 110 indexed citations
15.
Seale, Patrick, Bryan C. Bjork, Wenli Yang, et al.. (2008). PRDM16 controls a brown fat/skeletal muscle switch. Nature. 454(7207). 961–967. 1835 indexed citations breakdown →
16.
Bjork, Bryan C., et al.. (2008). SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs. Mammalian Genome. 19(10-12). 687–690. 5 indexed citations
17.
Moran, Jennifer L., Andrew D. Bolton, Pamela V. Tran, et al.. (2006). Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse. Genome Research. 16(3). 436–440. 75 indexed citations
18.
Watanabe, Yoriko, Jeffrey C. Murray, Bryan C. Bjork, et al.. (2001). Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41. Human Mutation. 18(5). 422–434. 1 indexed citations
19.
Schutte, Brian C., Bryan C. Bjork, Simon G. Gregory, et al.. (2000). A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.. PubMed. 10(1). 81–94. 46 indexed citations
20.
Schutte, Brian C., Ann M. Basart, Yoriko Watanabe, et al.. (1999). Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome. American Journal of Medical Genetics. 84(2). 145–150. 54 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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