Brandon Wormley

11.3k total citations · 1 hit paper
22 papers, 2.0k citations indexed

About

Brandon Wormley is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Brandon Wormley has authored 22 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Physiology. Recurrent topics in Brandon Wormley's work include Genetic Associations and Epidemiology (10 papers), Nicotinic Acetylcholine Receptors Study (4 papers) and Autism Spectrum Disorder Research (4 papers). Brandon Wormley is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Nicotinic Acetylcholine Receptors Study (4 papers) and Autism Spectrum Disorder Research (4 papers). Brandon Wormley collaborates with scholars based in United States, Ireland and United Kingdom. Brandon Wormley's co-authors include Kenneth S. Kendler, Brien P. Riley, F. Anthony O’Neill, Dermot Walsh, Yunlong Ma, Richard E. Straub, Maxim V. Myakishev, Bradley T. Webb, Judy L. Silberg and Debra L. Foley and has published in prestigious journals such as PLoS ONE, Stroke and Biological Psychiatry.

In The Last Decade

Brandon Wormley

22 papers receiving 1.9k 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.

Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Ortholog of the Mouse Dysbindin Gene, Is Associated with Schizophrenia

2002 619 citations Richard E. Straub, Yuxin Jiang et al. The American Journal of Human Genetics profile →

Peers

Brandon Wormley

GENET

CMN

Virginia L. Willour United States

Janice M. Fullerton Australia

Sibylle G. Schwab Germany

Bradley T. Webb United States

Mónica Bayés Spain

Alan R. Sanders United States

Ronnen H. Segman Israel

Guiqing Cai United States

M. Trixler Hungary

Yana V. Syagailo Germany

Virginia L. Willour United States

Brandon Wormley

665 ×0.9

788 ×1.1

GENET

408 ×0.8

CMN

346 ×1.1

209 ×0.7

Citations per year, relative to Brandon Wormley Brandon Wormley (= 1×) peers Virginia L. Willour

Countries citing papers authored by Brandon Wormley

Since Specialization

Citations

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

Fields of papers citing papers by Brandon Wormley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brandon Wormley

This figure shows the co-authorship network connecting the top 25 collaborators of Brandon Wormley. A scholar is included among the top collaborators of Brandon Wormley 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 Brandon Wormley. Brandon Wormley 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

Docherty, Anna R., Tim B. Bigdeli, Alexis C. Edwards, et al.. (2015). Genome-wide gene pathway analysis of psychotic illness symptom dimensions based on a new schizophrenia-specific model of the OPCRIT. Schizophrenia Research. 164(1-3). 181–186. 14 indexed citations

Edwards, Alexis C., Tim B. Bigdeli, Anna R. Docherty, et al.. (2015). Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes: Table 1.. Schizophrenia Bulletin. 42(2). 279–287. 27 indexed citations

Bigdeli, Tim B., Brion S. Maher, Zhongming Zhao, et al.. (2011). Comprehensive Gene-Based Association Study of a Chromosome 20 Linked Region Implicates Novel Risk Loci for Depressive Symptoms in Psychotic Illness. PLoS ONE. 6(12). e21440–e21440. 6 indexed citations

Riley, Brien P., Po‐Hsiu Kuo, Brion S. Maher, et al.. (2009). The dystrobrevin binding protein 1 (DTNBP1) gene is associated with schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample. Schizophrenia Research. 115(2-3). 245–253. 29 indexed citations

Fanous, Ayman H., Zhongming Zhao, Edwin J.C.G. van den Oord, et al.. (2009). Association study of SNAP25 and schizophrenia in Irish family and case–control samples. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(2). 663–674. 18 indexed citations

Bergen, Sarah E., Ayman H. Fanous, Po‐Hsiu Kuo, et al.. (2009). No association of dysbindin with symptom factors of schizophrenia in an Irish case–control sample. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(2). 700–705. 3 indexed citations

Riley, Brien P., Dawn L. Thiselton, Brion S. Maher, et al.. (2009). Replication of association between schizophrenia and ZNF804A in the Irish Case–Control Study of Schizophrenia sample. Molecular Psychiatry. 15(1). 29–37. 166 indexed citations

Prom‐Wormley, Elizabeth, L. J. Eaves, Debra L. Foley, et al.. (2008). Monoamine oxidase A and childhood adversity as risk factors for conduct disorder in females. Psychological Medicine. 39(4). 579–590. 60 indexed citations

Vladimirov, Vladimir I., Brion S. Maher, Brandon Wormley, et al.. (2008). The trace amine associated receptor (TAAR6) gene is not associated with schizophrenia in the Irish Case-Control Study of Schizophrenia (ICCSS) sample. Schizophrenia Research. 107(2-3). 249–254. 9 indexed citations

10.

Thiselton, Dawn L., Vladimir I. Vladimirov, Po‐Hsiu Kuo, et al.. (2007). AKT1 Is Associated with Schizophrenia Across Multiple Symptom Dimensions in the Irish Study of High Density Schizophrenia Families. Biological Psychiatry. 63(5). 449–457. 126 indexed citations

11.

Vladimirov, Vladimir I., Dawn L. Thiselton, Po‐Hsiu Kuo, et al.. (2007). A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families. Molecular Psychiatry. 12(9). 842–853. 26 indexed citations

12.

Riley, Brien P., Gursharan Kalsi, Po‐Hsiu Kuo, et al.. (2006). Alcohol dependence is associated with the ZNF699 gene, a human locus related to Drosophila hangover, in the Irish affected sib pair study of alcohol dependence (IASPSAD) sample. Molecular Psychiatry. 11(11). 1025–1031. 23 indexed citations

13.

Foley, Debra L., Lindon J. Eaves, Brandon Wormley, et al.. (2004). Childhood Adversity, Monoamine Oxidase A Genotype, and Risk for ConductDisorder. Archives of General Psychiatry. 61(7). 738–738. 373 indexed citations

14.

Straub, Richard E., Yuxin Jiang, Charles J. MacLean, et al.. (2002). Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Ortholog of the Mouse Dysbindin Gene, Is Associated with Schizophrenia. The American Journal of Human Genetics. 71(2). 337–348. 619 indexed citations breakdown →

15.

Straub, Richard E., C J MacLean, Yunlong Ma, et al.. (2002). Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes. Molecular Psychiatry. 7(6). 542–559. 110 indexed citations

16.

Sullivan, Patrick F., Michael C. Neale, Michael Silverman, et al.. (2001). An association study of DRD5 with smoking initiation and progression to nicotine dependence. American Journal of Medical Genetics. 105(3). 259–265. 42 indexed citations

17.

Silverman, Michael A., Michael C. Neale, Patrick F. Sullivan, et al.. (2000). Haplotypes of four novel single nucleotide polymorphisms in the nicotinic acetylcholine receptor β2‐subunit (CHRNB2) gene show no association with smoking initiation or nicotine dependence. American Journal of Medical Genetics. 96(5). 646–653. 1 indexed citations

18.

Straub, Richard E., Patrick F. Sullivan, Yunlong Ma, et al.. (1999). Susceptibility genes for nicotine dependence: a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit further study. Molecular Psychiatry. 4(2). 129–144. 136 indexed citations

19.

Rosenblum, William I. & Brandon Wormley. (1995). Selective Depression of Endothelium-Dependent Dilations During Cerebral Ischemia. Stroke. 26(10). 1877–1882. 15 indexed citations

20.

Rosenblum, William I., M. Danielle McDonald, & Brandon Wormley. (1989). Calcium ionophore and acetylcholine dilate arterioles on the mouse brain by different mechanisms.. Stroke. 20(10). 1391–1395. 29 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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