Andrew Bjonnes

3.3k total citations
15 papers, 272 citations indexed

About

Andrew Bjonnes is a scholar working on Pathology and Forensic Medicine, Public Health, Environmental and Occupational Health and Molecular Biology. According to data from OpenAlex, Andrew Bjonnes has authored 15 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pathology and Forensic Medicine, 4 papers in Public Health, Environmental and Occupational Health and 3 papers in Molecular Biology. Recurrent topics in Andrew Bjonnes's work include Pregnancy and preeclampsia studies (3 papers), Ovarian function and disorders (3 papers) and Reproductive Biology and Fertility (3 papers). Andrew Bjonnes is often cited by papers focused on Pregnancy and preeclampsia studies (3 papers), Ovarian function and disorders (3 papers) and Reproductive Biology and Fertility (3 papers). Andrew Bjonnes collaborates with scholars based in United States, Greece and Jordan. Andrew Bjonnes's co-authors include Richa Saxena, Corrine K. Welt, R. Georgiadis, Vasiliki Koika, Brendan J. Keating, Neoklis A. Georgopoulos, Dimitrios Panidis, Archana Tare, Jiankang Li and Ruth Hopkins and has published in prestigious journals such as Journal of Clinical Oncology, Brain and The Journal of Physical Chemistry C.

In The Last Decade

Andrew Bjonnes

15 papers receiving 266 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew Bjonnes United States 9 63 52 51 49 47 15 272
Li Cui China 9 62 1.0× 28 0.5× 33 0.6× 19 0.4× 23 0.5× 31 357
Ming‐Chao Huang Taiwan 11 67 1.1× 100 1.9× 14 0.3× 44 0.9× 64 1.4× 33 367
Y. H. Meng United States 11 50 0.8× 15 0.3× 15 0.3× 46 0.9× 8 0.2× 30 336
J. Gulcher Iceland 5 49 0.8× 15 0.3× 26 0.5× 167 3.4× 48 1.0× 7 418
Tianci Chu China 13 117 1.9× 15 0.3× 87 1.7× 5 0.1× 18 0.4× 20 396
R Mutani Italy 9 32 0.5× 44 0.8× 32 0.6× 28 0.6× 6 0.1× 13 302
Kim Bui United States 6 152 2.4× 51 1.0× 40 0.8× 57 1.2× 13 0.3× 7 413
Reeti Mehra India 10 32 0.5× 76 1.5× 25 0.5× 22 0.4× 4 0.1× 37 288
Mélanie Steffens Germany 11 84 1.3× 104 2.0× 33 0.6× 30 0.6× 17 0.4× 20 355
Callum Smith United Kingdom 9 107 1.7× 10 0.2× 31 0.6× 6 0.1× 35 0.7× 19 406

Countries citing papers authored by Andrew Bjonnes

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Bjonnes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Bjonnes

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

All Works

15 of 15 papers shown
1.
Zhang, Jianguo, Archana Tare, James F. Gusella, et al.. (2020). CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids. UNC Libraries. 5 indexed citations
2.
Tse, Julie Y., Alexei Protopopov, Meaghan Russell, et al.. (2018). Characterization of tumor mutation burden (TMB) and microsatellite instability (MSI) interplay for gastroesophageal adenocarcinoma (GA) and colorectal carcinoma (CRC).. Journal of Clinical Oncology. 36(5_suppl). 22–22. 3 indexed citations
3.
Vuzman, Dana, Ruobai Sun, Cheryl Eifert, et al.. (2017). Tumor mutation burden derived from large NGS panel as biomarker for immunotherapy response.. Journal of Clinical Oncology. 35(15_suppl). e23077–e23077. 4 indexed citations
4.
Sun, Ruobai, Pablo Cingolani, Angeliki Pantazi, et al.. (2017). Germline and somatic SNVS calling in NGS panel tumor samples: Approaches to optimize tumor only genomic analysis for cancer precision medicine.. Journal of Clinical Oncology. 35(15_suppl). e13011–e13011. 1 indexed citations
5.
Saxena, Richa, Robert M. Plenge, Andrew Bjonnes, et al.. (2017). A Multinational Arab Genome‐Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis. Arthritis & Rheumatology. 69(5). 976–985. 23 indexed citations
6.
Eichler, Florian, Jiankang Li, Yiran Guo, et al.. (2016). CSF1Rmosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids. Brain. 139(6). 1666–1672. 53 indexed citations
7.
Bjonnes, Andrew, Richa Saxena, & Corrine K. Welt. (2016). Relationship between polycystic ovary syndrome and ancestry in European Americans. Fertility and Sterility. 106(7). 1772–1777. 8 indexed citations
8.
Spracklen, Cassandra N., Caitlin J. Smith, Audrey F. Saftlas, et al.. (2016). Genetic predisposition to elevated levels of C-reactive protein is associated with a decreased risk for preeclampsia. Hypertension in Pregnancy. 36(1). 30–35. 3 indexed citations
9.
Chang, Anne‐Marie, Andrew Bjonnes, Daniel Aeschbach, et al.. (2016). Circadian gene variants influence sleep and the sleep electroencephalogram in humans. Chronobiology International. 33(5). 561–573. 27 indexed citations
10.
Saxena, Richa, Neoklis A. Georgopoulos, Tawnie Braaten, et al.. (2015). Han Chinese polycystic ovary syndrome risk variants in women of European ancestry: relationship to FSH levels and glucose tolerance. Human Reproduction. 30(6). 1454–1459. 29 indexed citations
11.
Saxena, Richa, Andrew Bjonnes, Neoklis A. Georgopoulos, et al.. (2015). Gene variants associated with age at menopause are also associated with polycystic ovary syndrome, gonadotrophins and ovarian volume. Human Reproduction. 30(7). 1697–1703. 16 indexed citations
12.
Smith, Caitlin J., Audrey F. Saftlas, Cassandra N. Spracklen, et al.. (2015). Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia. American Journal of Hypertension. 29(1). 17–24. 16 indexed citations
13.
Sapkota, Bishwa R., Ruth Hopkins, Andrew Bjonnes, et al.. (2015). Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study. The Journal of Steroid Biochemistry and Molecular Biology. 158. 149–156. 39 indexed citations
14.
Spracklen, Cassandra N., Audrey F. Saftlas, Elizabeth W. Triche, et al.. (2014). Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia. American Journal of Hypertension. 28(7). 915–923. 17 indexed citations
15.
Bjonnes, Andrew, et al.. (2010). Distance- and Wavelength-Dependent Dielectric Function of Au Nanoparticles by Angle-Resolved Surface Plasmon Resonance Imaging. The Journal of Physical Chemistry C. 114(19). 8837–8843. 28 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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