Brian F. Meyer

13.0k total citations · 1 hit paper
160 papers, 7.6k citations indexed

About

Brian F. Meyer is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Brian F. Meyer has authored 160 papers receiving a total of 7.6k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 44 papers in Genetics and 23 papers in Oncology. Recurrent topics in Brian F. Meyer's work include RNA modifications and cancer (11 papers), Thyroid Cancer Diagnosis and Treatment (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Brian F. Meyer is often cited by papers focused on RNA modifications and cancer (11 papers), Thyroid Cancer Diagnosis and Treatment (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Brian F. Meyer collaborates with scholars based in Saudi Arabia, United States and Australia. Brian F. Meyer's co-authors include D. E. NICHOLS, Linda Jacobsen, J. McLaughlin, N. R. Ferrigni, Yufei Shi, Minjing Zou, Fowzan S. Alkuraya, Dorota Monies, Mohammed A. Aldahmesh and Salma M. Wakil and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Brian F. Meyer

156 papers receiving 7.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Brine Shrimp: A Convenient General Bioassay for Active Plant Constituents

1982 3.9k citations Brian F. Meyer, N. R. Ferrigni et al. Planta Medica profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brian F. Meyer Saudi Arabia	35	2.6k	1.8k	1.2k	1.0k	730	160	7.6k
Gian Luigi Russo Italy	50	3.5k 1.3×	1.0k 0.6×	410 0.4×	731 0.7×	582 0.8×	157	8.9k
Mei Sun China	49	4.0k 1.5×	2.4k 1.3×	1.5k 1.3×	2.0k 2.0×	432 0.6×	136	11.0k
Yoshinori Fujimoto Japan	41	3.5k 1.3×	1.3k 0.7×	427 0.4×	486 0.5×	285 0.4×	435	8.2k
Yoshimasa Nakamura Japan	59	5.9k 2.3×	4.9k 2.7×	438 0.4×	642 0.6×	316 0.4×	301	12.7k
Masashi Hosokawa Japan	52	2.9k 1.1×	557 0.3×	300 0.3×	786 0.8×	405 0.6×	237	9.4k
David R. Bickers United States	58	4.7k 1.8×	796 0.4×	726 0.6×	544 0.5×	255 0.3×	252	12.1k
Xin Zhao China	43	3.5k 1.3×	1.0k 0.6×	480 0.4×	1.6k 1.6×	392 0.5×	468	8.1k
Samuel M. Cohen United States	56	3.4k 1.3×	1.0k 0.6×	353 0.3×	873 0.9×	341 0.5×	328	10.8k
Eun‐Jung Park South Korea	49	4.5k 1.7×	966 0.5×	320 0.3×	403 0.4×	246 0.3×	253	8.6k
Patrick Borel France	58	2.9k 1.1×	872 0.5×	410 0.4×	1.7k 1.7×	731 1.0×	179	9.9k

Countries citing papers authored by Brian F. Meyer

Since Specialization

Citations

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

Fields of papers citing papers by Brian F. Meyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brian F. Meyer

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

All Works

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20 of 20 papers shown

Goljan, Ewa, et al.. (2024). Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population. Human Genomics. 18(1). 30–30. 2 indexed citations

Casemayou, Audrey, Benjamin Breuil, Marcin Tkaczyk, et al.. (2024). Evaluation of predictive performance of fetal urinary inflammatory markers of postnatal kidney function in fetuses with posterior urethral valves. Pediatric Nephrology. 40(4). 1023–1032. 1 indexed citations

Khalid, Mohammed, Maher Al‐Saif, Faiqa Imtiaz, et al.. (2023). Wild-type S100A3 and S100A13 restore calcium homeostasis and mitigate mitochondrial dysregulation in pulmonary fibrosis patient-derived cells. Frontiers in Cell and Developmental Biology. 11. 1282868–1282868. 2 indexed citations

Zou, Minjing, Monther Al‐Alwan, Ibrahim Al‐Jammaz, et al.. (2021). β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model. Molecular Cancer Therapeutics. 20(9). 1603–1613. 8 indexed citations

Zou, Minjing, et al.. (2019). Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets. Bone. 125. 186–193. 26 indexed citations

Bohlega, Saeed, Hussam Abou‐Al‐Shaar, Brian F. Meyer, et al.. (2019). Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders. Parkinsonism & Related Disorders. 64. 145–149. 20 indexed citations

Al‐Mousa, Hamoud, Mohamed Abouelhoda, Dorota Monies, et al.. (2018). High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots. Frontiers in Immunology. 9. 782–782. 54 indexed citations

Derar, Nada, Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, et al.. (2018). De novo truncating variants in WHSC1 recapitulate the Wolf–Hirschhorn (4p16.3 microdeletion) syndrome phenotype. Genetics in Medicine. 21(1). 185–188. 21 indexed citations

Zou, Minjing, Essa Y. Baitei, Futwan Al‐Mohanna, et al.. (2017). Cyp24a1 Attenuation Limits Progression of BrafV600E -Induced Papillary Thyroid Cancer Cells and Sensitizes Them to BRAFV600E Inhibitor PLX4720. Cancer Research. 77(8). 2161–2172. 17 indexed citations

10.

Altassan, Ruqaiah, Tariq Masoodi, Ola Khalifa, et al.. (2017). Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype. American Journal of Medical Genetics Part A. 173(4). 1009–1016. 15 indexed citations

11.

Bohlega, Saeed, et al.. (2015). Clinical and genetic features of anoctaminopathy in Saudi Arabia. Neurosciences. 20(2). 173–177. 16 indexed citations

12.

Parhar, Ranjit S., Minjing Zou, Futwan Al‐Mohanna, et al.. (2015). IL-12 immunotherapy of Braf-induced papillary thyroid cancer in a mouse model. Laboratory Investigation. 96(1). 89–97. 26 indexed citations

13.

Balasubramanian, Ravikumar, Jin‐Ho Choi, Ludmila Francescatto, et al.. (2014). Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency. PMC. 2 indexed citations

14.

Bass, Sarah Bauerle, Thomas F. Gordon, Sheryl Burt Ruzek, et al.. (2010). Perceptions of Colorectal Cancer Screening in Urban African American Clinic Patients: Differences by Gender and Screening Status. Journal of Cancer Education. 26(1). 121–128. 62 indexed citations

15.

Al‐Owain, Mohammed, Salma M. Wakil, Mansoor A. Haider, et al.. (2010). Novel homozygous mutation in DSP causing skin fragility-woolly hair syndrome: report of a large family and review of the desmoplakin-related phenotypes. Clinical Genetics. 80(1). 50–58. 18 indexed citations

16.

Kaya, Namik, Faiqa Imtiaz, Dilek Çolak, et al.. (2008). Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease. Genetics in Medicine. 10(9). 675–684. 17 indexed citations

17.

Alazami, Anas M., Amr Al‐Saif, Abdulaziz Alsemari, et al.. (2008). Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome. The American Journal of Human Genetics. 83(6). 684–691. 94 indexed citations

18.

Khan, Arif O., et al.. (2006). Familial Blepharophimosis-Like Syndrome with Esotropia, Uveal Coloboma, and Short Stature. Ophthalmic Genetics. 27(3). 79–82. 1 indexed citations

19.

Erber, Wendy N., et al.. (1996). The detection of rhodamine 123 efflux at low levels of drug resistance. British Journal of Haematology. 93(3). 650–655. 41 indexed citations

20.

Meyer, Brian F., et al.. (1982). Brine Shrimp: A Convenient General Bioassay for Active Plant Constituents. Planta Medica. 45(5). 31–34. 3856 indexed citations breakdown →

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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