Nicole C. Meyer

7.3k total citations
44 papers, 2.4k citations indexed

About

Nicole C. Meyer is a scholar working on Immunology, Nephrology and Molecular Biology. According to data from OpenAlex, Nicole C. Meyer has authored 44 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Immunology, 15 papers in Nephrology and 12 papers in Molecular Biology. Recurrent topics in Nicole C. Meyer's work include Complement system in diseases (16 papers), Renal Diseases and Glomerulopathies (15 papers) and Hearing, Cochlea, Tinnitus, Genetics (11 papers). Nicole C. Meyer is often cited by papers focused on Complement system in diseases (16 papers), Renal Diseases and Glomerulopathies (15 papers) and Hearing, Cochlea, Tinnitus, Genetics (11 papers). Nicole C. Meyer collaborates with scholars based in United States, Iran and Belgium. Nicole C. Meyer's co-authors include Richard J. Smith, Yuzhou Zhang, Carla Nester, Hossein Najmabadi, Kimia Kahrizi, Susan Strome, Kai Wang, Sanjeev Sethi, Nicolò Ghiringhelli Borsa and Fengxiao Bu and has published in prestigious journals such as PLANT PHYSIOLOGY, Current Biology and Genetics.

In The Last Decade

Nicole C. Meyer

43 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicole C. Meyer United States 28 920 785 740 385 311 44 2.4k
Ramiro Ramírez‐Solis United Kingdom 23 213 0.2× 2.4k 3.0× 268 0.4× 80 0.2× 29 0.1× 39 3.2k
Patrick Nitschké France 33 1.1k 1.2× 1.9k 2.5× 67 0.1× 348 0.9× 56 0.2× 78 3.7k
Hans‐Georg Frank Germany 28 1.0k 1.1× 1.1k 1.5× 11 0.0× 204 0.5× 268 0.9× 87 3.4k
Lingqian Wu China 24 187 0.2× 1.2k 1.5× 31 0.0× 102 0.3× 71 0.2× 186 2.4k
Makoto Hiroi Japan 27 205 0.2× 685 0.9× 61 0.1× 23 0.1× 158 0.5× 145 2.9k
Valérie Delague France 28 344 0.4× 1.7k 2.2× 81 0.1× 53 0.1× 42 0.1× 91 2.6k
Landian Hu China 30 183 0.2× 1.9k 2.4× 57 0.1× 45 0.1× 75 0.2× 79 2.6k
Hiroyoshi Ishizaki Japan 22 344 0.4× 982 1.3× 75 0.1× 24 0.1× 51 0.2× 27 1.7k
Daniel Dufort Canada 27 475 0.5× 2.5k 3.2× 25 0.0× 16 0.0× 129 0.4× 49 3.6k
Martin Stehling Germany 32 1.0k 1.1× 2.3k 2.9× 26 0.0× 297 0.8× 7 0.0× 68 4.1k

Countries citing papers authored by Nicole C. Meyer

Since Specialization
Citations

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

Fields of papers citing papers by Nicole C. Meyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicole C. Meyer

This figure shows the co-authorship network connecting the top 25 collaborators of Nicole C. Meyer. A scholar is included among the top collaborators of Nicole C. Meyer 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 Nicole C. Meyer. Nicole C. Meyer 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.
Taylor, Amanda, Nicole C. Meyer, Sarah M. Roberts, et al.. (2023). Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 Glomerulopathy. Kidney International Reports. 9(2). 464–477. 8 indexed citations
2.
Zhang, Yuzhou, Nicolò Ghiringhelli Borsa, Nicole C. Meyer, et al.. (2020). Factor H Autoantibodies and Complement-Mediated Diseases. Frontiers in Immunology. 11. 607211–607211. 27 indexed citations
3.
Bu, Fengxiao, Yuzhou Zhang, Kai Wang, et al.. (2018). Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology. 29(12). 2809–2819. 48 indexed citations
4.
Bu, Fengxiao, Nicolò Ghiringhelli Borsa, M. B. Jones, et al.. (2015). High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies. Journal of the American Society of Nephrology. 27(4). 1245–1253. 74 indexed citations
5.
Ealy, Megan, Nicole C. Meyer, Isabelle Schrauwen, et al.. (2014). Rare Variants in BMP2 and BMP4 Found in Otosclerosis Patients Reduce Smad Signaling. Otology & Neurotology. 35(3). 395–400. 10 indexed citations
6.
Zhang, Yuzhou, Carla Nester, Mikkel‐Ole Skjoedt, et al.. (2014). Defining the Complement Biomarker Profile of C3 Glomerulopathy. Clinical Journal of the American Society of Nephrology. 9(11). 1876–1882. 66 indexed citations
7.
Bu, Fengxiao, Tara Maga, Nicole C. Meyer, et al.. (2013). Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology. 25(1). 55–64. 161 indexed citations
8.
Sethi, Sanjeev, Fernando C. Fervenza, Yuzhou Zhang, et al.. (2012). Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement. Kidney International. 83(2). 293–299. 139 indexed citations
9.
Zhang, Yuzhou, Nicole C. Meyer, Kai Wang, et al.. (2012). Causes of Alternative Pathway Dysregulation in Dense Deposit Disease. Clinical Journal of the American Society of Nephrology. 7(2). 265–274. 147 indexed citations
10.
Gázquez, Irene, José A. López‐Escámez, Antonia Ruíz Moreno, et al.. (2011). Functional Variants in NOS1 and NOS2A Are Not Associated with Progressive Hearing Loss in Ménière's Disease in a European Caucasian Population. DNA and Cell Biology. 30(9). 699–708. 9 indexed citations
11.
Bazazzadegan, Niloofar, Kimia Kahrizi, Nicole C. Meyer, et al.. (2011). Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss. American Journal of Medical Genetics Part A. 155(5). 1202–1211. 7 indexed citations
12.
Schrauwen, Isabelle, Megan Ealy, Erik Fransén, et al.. (2009). Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations. Human Genetics. 127(2). 155–162. 24 indexed citations
13.
Avenarius, Matthew R., Michael S. Hildebrand, Yuzhou Zhang, et al.. (2009). Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein. The American Journal of Human Genetics. 84(4). 505–510. 177 indexed citations
14.
Leykin, Igor, Ke Hao, Nicole C. Meyer, et al.. (2005). Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data. BMC Genetics. 6(1). 7–7. 20 indexed citations
15.
Kawasaki, Ichiro, Anahita Amiri, Yuan Fan, et al.. (2004). The PGL Family Proteins Associate With Germ Granules and Function Redundantly in Caenorhabditis elegans Germline Development. Genetics. 167(2). 645–661. 106 indexed citations
16.
Canman, Julie C., et al.. (2004). C. elegans PAR Proteins Function by Mobilizing and Stabilizing Asymmetrically Localized Protein Complexes. Current Biology. 14(10). 851–862. 153 indexed citations
17.
Chang, Eugene H., Maithilee Menezes, Nicole C. Meyer, et al.. (2004). Branchio-oto-renal syndrome: The mutation spectrum inEYA1and its phenotypic consequences. Human Mutation. 23(6). 582–589. 159 indexed citations
18.
Lauer, Peter, et al.. (1997). Clone–Contig and STS Maps of the Hereditary Hemochromatosis Region on Human Chromosome 6p21.3–p22. Genome Research. 7(5). 457–470. 20 indexed citations
19.
Ruddy, David A., Vince Lee, Gabriel A. Mintier, et al.. (1997). A 1.1-Mb Transcript Map of the Hereditary Hemochromatosis Locus. Genome Research. 7(5). 441–456. 71 indexed citations
20.
Close, Timothy J., Nicole C. Meyer, & J Radik. (1995). Nucleotide Sequence of a Gene Encoding a 58.5-Kilodalton Barley Dehydrin That Lacks a Serine Tract. PLANT PHYSIOLOGY. 107(1). 289–290. 22 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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