Bradley T. Webb

32.8k total citations · 1 hit paper
86 papers, 3.3k citations indexed

About

Bradley T. Webb is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Bradley T. Webb has authored 86 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Genetics, 34 papers in Molecular Biology and 14 papers in Epidemiology. Recurrent topics in Bradley T. Webb's work include Genetic Associations and Epidemiology (51 papers), Genetic Mapping and Diversity in Plants and Animals (13 papers) and Alcohol Consumption and Health Effects (12 papers). Bradley T. Webb is often cited by papers focused on Genetic Associations and Epidemiology (51 papers), Genetic Mapping and Diversity in Plants and Animals (13 papers) and Alcohol Consumption and Health Effects (12 papers). Bradley T. Webb collaborates with scholars based in United States, United Kingdom and Ireland. Bradley T. Webb's co-authors include Kenneth S. Kendler, F. Anthony O’Neill, Dermot Walsh, Richard E. Straub, Charles J. MacLean, Yunlong Ma, Maxim V. Myakishev, Brien P. Riley, Brandon Wormley and Ayman H. Fanous and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Bioinformatics.

In The Last Decade

Bradley T. Webb

82 papers receiving 3.2k 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

Bradley T. Webb

GENET

CMN

PMH

Sibylle G. Schwab Germany

Andrew McQuillin United Kingdom

Alexander F. Wilson United States

Dai Zhang China

Silviu‐Alin Bacanu United States

Dieter B. Wildenauer Germany

Kathryn L. Evans United Kingdom

Brien P. Riley United States

Jonathan L. Haines United States

Dimitrios Avramopoulos United States

Sibylle G. Schwab Germany

Bradley T. Webb

1.2k ×0.8

GENET

1.0k ×0.8

641 ×1.2

CMN

473 ×1.1

PMH

400 ×1.0

Citations per year, relative to Bradley T. Webb Bradley T. Webb (= 1×) peers Sibylle G. Schwab

Countries citing papers authored by Bradley T. Webb

Since Specialization

Citations

This map shows the geographic impact of Bradley T. Webb'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 Bradley T. Webb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bradley T. Webb more than expected).

Fields of papers citing papers by Bradley T. Webb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bradley T. Webb. 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 Bradley T. Webb. The network helps show where Bradley T. Webb may publish in the future.

Co-authorship network of co-authors of Bradley T. Webb

This figure shows the co-authorship network connecting the top 25 collaborators of Bradley T. Webb. A scholar is included among the top collaborators of Bradley T. Webb 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 Bradley T. Webb. Bradley T. Webb 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

Stratford, Jeran K., Megan Ulmer Carnes, Ravi Mathur, et al.. (2025). Identifying compounds to treat opiate use disorder by leveraging multi-omic data integration and multiple drug repurposing databases. Translational Psychiatry. 15(1). 528–528.

White, Julie D., Bryan C. Quach, Shizhong Han, et al.. (2024). Alcohol Use Disorder–Associated DNA Methylation in the Nucleus Accumbens and Dorsolateral Prefrontal Cortex. Biological Psychiatry Global Open Science. 4(6). 100375–100375. 1 indexed citations

Alexander, Jeffry, Roseann E. Peterson, Michael F. Miles, et al.. (2023). Case-only exome variation analysis of severe alcohol dependence using a multivariate hierarchical gene clustering approach. PLoS ONE. 18(4). e0283985–e0283985. 2 indexed citations

Edwards, Alexis C., et al.. (2023). Multifaceted risk for non-suicidal self-injury only versus suicide attempt in a population-based cohort of adults. Journal of Affective Disorders. 333. 474–481. 5 indexed citations

Romero, Roberto, Jerome F. Strauss, Sonia S. Hassan, et al.. (2022). Study protocol to quantify the genetic architecture of sonographic cervical length and its relationship to spontaneous preterm birth. BMJ Open. 12(3). e053631–e053631. 3 indexed citations

Gillespie, Nathan A., Robert M. Kirkpatrick, Chandra A. Reynolds, et al.. (2022). Determining the stability of genome-wide factors in BMI between ages 40 to 69 years. PLoS Genetics. 18(8). e1010303–e1010303. 4 indexed citations

Bountress, Kaitlin E., Frank R. Wendt, Arpana Agrawal, et al.. (2021). Potential causal effect of posttraumatic stress disorder on alcohol use disorder and alcohol consumption in individuals of European descent: A Mendelian Randomization Study. Alcoholism Clinical and Experimental Research. 45(8). 1616–1623. 14 indexed citations

Savage, Jeanne E., Jessica E. Salvatore, Fazil Alıev, et al.. (2018). Polygenic Risk Score Prediction of Alcohol Dependence Symptoms Across Population‐Based and Clinically Ascertained Samples. Alcoholism Clinical and Experimental Research. 42(3). 520–530. 20 indexed citations

Edwards, Alexis C., Joseph D. Deak, Ian R. Gizer, et al.. (2018). Meta‐Analysis of Genetic Influences on Initial Alcohol Sensitivity. Alcoholism Clinical and Experimental Research. 42(12). 2349–2359. 19 indexed citations

10.

Lee, Donghyung, et al.. (2017). JEPEGMIX2: improved gene-level joint analysis of eQTLs in cosmopolitan cohorts. Bioinformatics. 34(2). 286–288. 6 indexed citations

11.

Peterson, Roseann E., Alexis C. Edwards, Silviu‐Alin Bacanu, et al.. (2017). The utility of empirically assigning ancestry groups in cross‐population genetic studies of addiction. American Journal on Addictions. 26(5). 494–501. 36 indexed citations

12.

Docherty, Anna R., Arden Moscati, Danielle M. Dick, et al.. (2017). Polygenic prediction of the phenome, across ancestry, in emerging adulthood. Psychological Medicine. 48(11). 1814–1823. 24 indexed citations

13.

Zhao, Zhongming, Bradley T. Webb, Peilin Jia, et al.. (2013). Association Study of 167 Candidate Genes for Schizophrenia Selected by a Multi-Domain Evidence-Based Prioritization Algorithm and Neurodevelopmental Hypothesis. PLoS ONE. 8(7). e67776–e67776. 94 indexed citations

14.

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

15.

Fanous, Ayman H., Michael C. Neale, Richard E. Straub, et al.. (2003). Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: A family based association study. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 125B(1). 69–78. 57 indexed citations

16.

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 →

17.

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

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.

Straub, Richard E., Charles J. MacLean, Rory Martin, et al.. (1998). A schizophrenia locus may be located in region 10p15-p11. American Journal of Medical Genetics. 81(4). 296–301. 111 indexed citations

20.

Webb, Bradley T., et al.. (1973). Hans Wolff (1920–1967): Memorial Lecture. Africa. 43(4). 350–350.

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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