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

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

#	Work	Indexed citations
1	Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population 2024 ·Human Genomics ·Ewa Goljan, (unknown), Asma I. Tahir, Mohamed El-Kalioby, Brian F. Meyer, Dorota Monies	2
2	Evaluation of predictive performance of fetal urinary inflammatory markers of postnatal kidney function in fetuses with posterior urethral valves 2024 ·Pediatric Nephrology ·(unknown), Audrey Casemayou, (unknown), Benjamin Breuil, Marcin Tkaczyk, Małgorzata Stańczyk, Krzysztof Szaflik, (unknown), Stéphane Decramer, Julie Klein, Joost P. Schanstra, Brian F. Meyer	1
3	Wild-type S100A3 and S100A13 restore calcium homeostasis and mitigate mitochondrial dysregulation in pulmonary fibrosis patient-derived cells 2023 ·Frontiers in Cell and Developmental Biology ·(unknown), (unknown), Mohammed Khalid, (unknown), Maher Al‐Saif, Faiqa Imtiaz, Khushnooda Ramzan, (unknown), Ayodele Alaiya, Brian F. Meyer, Sergei P. Atamas, Kate S. Collison, Khalid S.A. Khabar, Jeffrey D. Hasday, Futwan Al‐Mohanna	2
4	β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model 2021 ·Molecular Cancer Therapeutics ·Minjing Zou, (unknown), (unknown), (unknown), Monther Al‐Alwan, Ibrahim Al‐Jammaz, Khalid S.A. Khabar, Falah Almohanna, Abdullah M. Assiri, Brian F. Meyer, Ali S. Alzahrani, Futwan Al‐Mohanna, Yufei Shi	8
5	Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets 2019 ·Bone ·(unknown), Minjing Zou, (unknown), (unknown), (unknown), Roua A. Al‐Rijjal, Brian F. Meyer, Yufei Shi	26
6	Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders 2019 ·Parkinsonism & Related Disorders ·Saeed Bohlega, Hussam Abou‐Al‐Shaar, (unknown), (unknown), (unknown), Brian F. Meyer, Dorota Monies, Edward Cupler, Amr Al‐Saif	20
7	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 2018 ·Frontiers in Immunology ·Hamoud Al‐Mousa, (unknown), (unknown), (unknown), Mohamed Abouelhoda, (unknown), Dorota Monies, Brian F. Meyer, Abbas Hawwari, Majed Dasouki	54
8	De novo truncating variants in WHSC1 recapitulate the Wolf–Hirschhorn (4p16.3 microdeletion) syndrome phenotype 2018 ·Genetics in Medicine ·Nada Derar, Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, Dorota Monies, Mohamed Abouelhoda, Brian F. Meyer, Nabil Moghrabi, Fowzan S. Alkuraya	21
9	Cyp24a1 Attenuation Limits Progression of BrafV600E -Induced Papillary Thyroid Cancer Cells and Sensitizes Them to BRAFV600E Inhibitor PLX4720 2017 ·Cancer Research ·Minjing Zou, Essa Y. Baitei, (unknown), Futwan Al‐Mohanna, Ranjit S. Parhar, René St‐Arnaud, Shioko Kimura, Catrin Pritchard, Ali S. Alzahrani, Abdullah M. Assiri, Brian F. Meyer, Yufei Shi	17
10	Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype 2017 ·American Journal of Medical Genetics Part A ·Ruqaiah Altassan, (unknown), Tariq Masoodi, (unknown), Ola Khalifa, Hamad Alzaidan, Nadia Sakati, (unknown), Zuhair N. Al‐Hassnan, Yousef Binamer, (unknown), William J. Wade, Zayed Al‐Zayed, (unknown), (unknown), Brian F. Meyer, (unknown), Salma M. Wakil	15
11	Clinical and genetic features of anoctaminopathy in Saudi Arabia 2015 ·Neurosciences ·Saeed Bohlega, (unknown), Ahmad Abulaban, (unknown), Hindi Al‐Hindi, Brian F. Meyer	16
12	IL-12 immunotherapy of Braf-induced papillary thyroid cancer in a mouse model 2015 ·Laboratory Investigation ·Ranjit S. Parhar, Minjing Zou, Futwan Al‐Mohanna, Essa Y. Baitei, Abdullah M. Assiri, Brian F. Meyer, Yufei Shi	26
13	Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency 2014 ·PMC ·Ravikumar Balasubramanian, Jin‐Ho Choi, Ludmila Francescatto, Jason R. Willer, Edward R. Horton, (unknown), Konstantina M. Stanković, Lacey Plummer, Cassandra Buck, Richard Quinton, Todd D. Nebesio, Verónica Mericq, Paulina M. Merino, Brian F. Meyer, Dorota Monies, James F. Gusella, (unknown), Nicholas Katsanis, William F. Crowley	2
14	Perceptions of Colorectal Cancer Screening in Urban African American Clinic Patients: Differences by Gender and Screening Status 2010 ·Journal of Cancer Education ·Sarah Bauerle Bass, Thomas F. Gordon, Sheryl Burt Ruzek, (unknown), Stephanie Ward, Anuradha Paranjape, Karen Lin, Brian F. Meyer, Dominique G. Ruggieri	62
15	Novel homozygous mutation in DSP causing skin fragility-woolly hair syndrome: report of a large family and review of the desmoplakin-related phenotypes 2010 ·Clinical Genetics ·Mohammed Al‐Owain, Salma M. Wakil, (unknown), (unknown), (unknown), Mansoor A. Haider, Hindi Al‐Hindi, Ali Awaji, (unknown), Batoul Baz, (unknown), Brian F. Meyer	18
16	Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease 2008 ·Genetics in Medicine ·Namik Kaya, Faiqa Imtiaz, Dilek Çolak, Moeenaldeen AlSayed, Ali Al‐Odaib, (unknown), Bashayer Al‐Mubarak, Mohammad Al-Owain, Hesham Aldhalaan, Aziza Chedrawi, Zuhair N. Al‐Hassnan, Serdar Coşkun, Nadia Sakati, Pinar T. Ozand, Brian F. Meyer	17
17	Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome 2008 ·The American Journal of Human Genetics ·Anas M. Alazami, Amr Al‐Saif, Abdulaziz Alsemari, Saeed Bohlega, Soumaya Zlitni, Fatema Alzahrani, Prashant Bavi, Namik Kaya, Dilek Çolak, Hanif Khalak, (unknown), Borut Peterlin, Sumita Danda, Kailash P. Bhatia, Susanne A. Schneider, Nadia Sakati, Christopher A. Walsh, Futwan Al‐Mohanna, Brian F. Meyer, Fowzan S. Alkuraya	94
18	Familial Blepharophimosis-Like Syndrome with Esotropia, Uveal Coloboma, and Short Stature 2006 ·Ophthalmic Genetics ·Arif O. Khan, (unknown), Mohammed A. Aldahmesh, (unknown), Brian F. Meyer	1
19	The detection of rhodamine 123 efflux at low levels of drug resistance 1996 ·British Journal of Haematology ·(unknown), (unknown), (unknown), Wendy N. Erber, Brian F. Meyer	41
20	Brine Shrimp: A Convenient General Bioassay for Active Plant Constituents breakdown → 1982 ·Planta Medica ·Brian F. Meyer, N. R. Ferrigni, (unknown), Linda Jacobsen, D. E. NICHOLS, J. McLaughlin	3856

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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