Derek Van Booven

1.8k total citations
29 papers, 1.1k citations indexed

About

Derek Van Booven is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Derek Van Booven has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Cognitive Neuroscience. Recurrent topics in Derek Van Booven's work include CRISPR and Genetic Engineering (4 papers), RNA and protein synthesis mechanisms (4 papers) and Autism Spectrum Disorder Research (4 papers). Derek Van Booven is often cited by papers focused on CRISPR and Genetic Engineering (4 papers), RNA and protein synthesis mechanisms (4 papers) and Autism Spectrum Disorder Research (4 papers). Derek Van Booven collaborates with scholars based in United States, Spain and United Kingdom. Derek Van Booven's co-authors include Sharon Marsh, Howard L. McLeod, Teri E. Klein, Michelle Whirl‐Carrillo, Russ B. Altman, Katrin Sangkuhl, Michael L. Cuccaro, Margaret A. Pericak‐Vance, Eden R. Martin and Patrice L. Whitehead and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Development.

In The Last Decade

Derek Van Booven

28 papers receiving 1.0k citations

Peers

Derek Van Booven

GENET

PHARM

ONCOL

Nancy Contel United States

Martine Dumont Canada

Denise L. Walker United States

Mohammad Reza Hojjati United States

Ryszard Wiaderkiewicz Poland

Yasue Horiuchi Japan

Santa Mammana Italy

Kiyoshi Egawa Japan

Li Zou China

Shiro Minami Japan

Nancy Contel United States

Derek Van Booven

463 ×1.0

289 ×1.2

GENET

89 ×0.4

88 ×0.6

PHARM

92 ×0.9

ONCOL

Citations per year, relative to Derek Van Booven Derek Van Booven (= 1×) peers Nancy Contel

Countries citing papers authored by Derek Van Booven

Since Specialization

Citations

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

Fields of papers citing papers by Derek Van Booven

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Derek Van Booven. 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 Derek Van Booven. The network helps show where Derek Van Booven may publish in the future.

Co-authorship network of co-authors of Derek Van Booven

This figure shows the co-authorship network connecting the top 25 collaborators of Derek Van Booven. A scholar is included among the top collaborators of Derek Van Booven 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 Derek Van Booven. Derek Van Booven 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

Gamer, Jackson, Derek Van Booven, Rajendra P. Pangeni, et al.. (2025). Stress-Induced Changes in Immune Signatures in ME/CFS Patients Determined by Transcriptome Analysis. Methods in molecular biology. 2920. 103–112.

Nissanka, Nadee, et al.. (2024). Absence of both MGME1 and POLG EXO abolishes mtDNA whereas absence of either creates unique mtDNA duplications. Journal of Biological Chemistry. 300(4). 107128–107128. 3 indexed citations

Bacman, Sandra R., Milena Pinto, Derek Van Booven, et al.. (2024). mitoTALEN reduces the mutant mtDNA load in neurons. Molecular Therapy — Nucleic Acids. 35(1). 102132–102132. 10 indexed citations

Harikumar, Kuzhuvelil B., Matthew Dunworth, Andrew J. Ewald, et al.. (2022). DOT1L Is a Novel Cancer Stem Cell Target for Triple-Negative Breast Cancer. Clinical Cancer Research. 28(9). 1948–1965. 48 indexed citations

Qureshi, Rehana, et al.. (2022). Estrone, the major postmenopausal estrogen, binds ERa to induce SNAI2, epithelial-to-mesenchymal transition, and ER+ breast cancer metastasis. Cell Reports. 41(7). 111672–111672. 20 indexed citations

Booven, Derek Van, Mengying Li, J. Sunil Rao, et al.. (2021). Alcohol use disorder causes global changes in splicing in the human brain. Translational Psychiatry. 11(1). 2–2. 25 indexed citations

Booven, Derek Van, et al.. (2021). The effect of stress on the transcriptomes of circulating immune cells in patients with Gulf War Illness. Life Sciences. 281. 119719–119719. 4 indexed citations

Camarena, Vladimir, David Sant, Derek Van Booven, et al.. (2019). Oscillatory cAMP signaling rapidly alters H3K4 methylation. Life Science Alliance. 3(1). e201900529–e201900529. 5 indexed citations

Silva, José & Derek Van Booven. (2018). Analysis of diet-induced differential methylation, expression, and interactions of lncRNA and protein-coding genes in mouse liver. Scientific Reports. 8(1). 11537–11537. 11 indexed citations

10.

Hokayem, Jimmy El, Elena Artimovich, André W. Phillips, et al.. (2018). Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons. Scientific Reports. 8(1). 8423–8423. 55 indexed citations

11.

Griswold, Anthony J., Derek Van Booven, Michael L. Cuccaro, et al.. (2017). Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder. Neurogenetics. 19(1). 17–26. 5 indexed citations

12.

Silva, José, Guerline Lambert, Derek Van Booven, & Claes Wahlestedt. (2016). Epigenomic and metabolic responses of hypothalamic POMC neurons to gestational nicotine exposure in adult offspring. Genome Medicine. 8(1). 93–93. 11 indexed citations

13.

Griswold, Anthony J., Nicole Dueker, Derek Van Booven, et al.. (2015). Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Molecular Autism. 6(1). 43–43. 46 indexed citations

14.

Yang, Cuixia, Hongwei Shao, Derek Van Booven, et al.. (2015). Epigenetic reprogramming of melanoma cells by vitamin C treatment. Clinical Epigenetics. 7(1). 51–51. 73 indexed citations

15.

Bademci, Güney, Oscar Diaz‐Horta, Shengru Guo, et al.. (2014). Identification of Copy Number Variants Through Whole-Exome Sequencing in Autosomal Recessive Nonsyndromic Hearing Loss. Genetic Testing and Molecular Biomarkers. 18(9). 658–661. 26 indexed citations

16.

Cukier, Holly N., Nicole Dueker, Susan H. Slifer, et al.. (2014). Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders. Molecular Autism. 5(1). 1–1. 252 indexed citations

17.

Gonzalez, Michael, Derek Van Booven, Eric Powell, et al.. (2013). GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis. Human Mutation. 34(6). 842–846. 48 indexed citations

18.

Cappola, Thomas P., Scot J. Matkovich, Wei Wang, et al.. (2011). Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation. Proceedings of the National Academy of Sciences. 108(6). 2456–2461. 76 indexed citations

19.

Booven, Derek Van, Sharon Marsh, Howard L. McLeod, et al.. (2010). Cytochrome P450 2C9-CYP2C9. Pharmacogenetics and Genomics. 20(4). 277–281. 190 indexed citations

20.

Marsh, Sharon, et al.. (2006). Ethnic Differences in Pharmacogenetically Relevant Genes. Current Drug Targets. 7(12). 1641–1648. 48 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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