Richard E. Straub

40.0k total citations · 3 hit papers
129 papers, 12.9k citations indexed

About

Richard E. Straub is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Richard E. Straub has authored 129 papers receiving a total of 12.9k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Genetics, 47 papers in Molecular Biology and 31 papers in Cellular and Molecular Neuroscience. Recurrent topics in Richard E. Straub's work include Genetic Associations and Epidemiology (35 papers), Genomic variations and chromosomal abnormalities (17 papers) and Schizophrenia research and treatment (17 papers). Richard E. Straub is often cited by papers focused on Genetic Associations and Epidemiology (35 papers), Genomic variations and chromosomal abnormalities (17 papers) and Schizophrenia research and treatment (17 papers). Richard E. Straub collaborates with scholars based in United States, Ireland and United Kingdom. Richard E. Straub's co-authors include Daniel R. Weinberger, Michael Egan, Joseph H. Callicott, Bhaskar Kolachana, Terry E. Goldberg, Joel E. Kleinman, Chiara Maria Mazzanti, David Goldman, F. Anthony O’Neill and Kenneth S. Kendler and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Richard E. Straub

126 papers receiving 12.6k 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.

Effect of COMT Val ^108/158 Met genotype on frontal lobe function and risk for schizophrenia

2001 1.9k citations Michael Egan, Terry E. Goldberg et al. Proceedings of the National Academy of Sciences profile →
The Brain-Derived Neurotrophic Factor val66met Polymorphism and Variation in Human Cortical Morphology

2004 724 citations Lukas Pezawas, Beth A. Verchinski et al. Journal of Neuroscience profile →
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, Yunlong Ma et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Richard E. Straub United States	60	5.0k	4.5k	3.7k	3.0k	2.7k	129	12.9k
Thomas M. Hyde United States	65	6.3k 1.3×	3.0k 0.7×	3.9k 1.0×	3.1k 1.0×	2.5k 0.9×	258	15.0k
Markus M. Nöthen Germany	67	6.0k 1.2×	5.3k 1.2×	4.0k 1.1×	2.5k 0.8×	3.8k 1.4×	521	18.1k
Barbara K. Lipska United States	57	4.8k 1.0×	2.1k 0.5×	5.9k 1.6×	3.5k 1.2×	2.4k 0.9×	122	12.6k
George Kirov United Kingdom	62	4.1k 0.8×	5.4k 1.2×	2.0k 0.5×	1.6k 0.5×	3.3k 1.2×	198	11.3k
Ryota Hashimoto Japan	52	3.2k 0.6×	1.9k 0.4×	2.6k 0.7×	2.1k 0.7×	2.5k 0.9×	314	10.0k
Pat Levitt United States	79	7.7k 1.5×	4.0k 0.9×	8.0k 2.2×	5.4k 1.8×	1.8k 0.7×	304	22.3k
Joel E. Kleinman United States	79	8.4k 1.7×	3.8k 0.8×	6.5k 1.8×	3.8k 1.3×	3.9k 1.4×	323	19.7k
Schahram Akbarian United States	65	8.0k 1.6×	4.3k 1.0×	3.9k 1.1×	3.3k 1.1×	1.1k 0.4×	178	14.1k
Peter Propping Germany	68	6.0k 1.2×	3.7k 0.8×	4.3k 1.2×	1.5k 0.5×	3.1k 1.1×	329	16.1k
Joseph A. Gogos United States	60	6.8k 1.4×	3.9k 0.9×	4.8k 1.3×	3.1k 1.0×	1.1k 0.4×	136	13.2k

Countries citing papers authored by Richard E. Straub

Since Specialization

Citations

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

Fields of papers citing papers by Richard E. Straub

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard E. Straub. 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 Richard E. Straub. The network helps show where Richard E. Straub may publish in the future.

Co-authorship network of co-authors of Richard E. Straub

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Jaffe, Andrew E., Richard E. Straub, Joo Heon Shin, et al.. (2018). Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis. Nature Neuroscience. 21(8). 1117–1125. 211 indexed citations

Jaffe, Andrew E., Ran Tao, Alexis L. Norris, et al.. (2017). qSVA framework for RNA quality correction in differential expression analysis. Proceedings of the National Academy of Sciences. 114(27). 7130–7135. 59 indexed citations

Li, Ming, Andrew E. Jaffe, Richard E. Straub, et al.. (2016). A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus. Nature Medicine. 22(6). 649–656. 108 indexed citations

Morita, Yukitaka, Joseph H. Callicott, Dwight Dickinson, et al.. (2014). Characteristics of the Cation Cotransporter NKCC1 in Human Brain: Alternate Transcripts, Expression in Development, and Potential Relationships to Brain Function and Schizophrenia. Journal of Neuroscience. 34(14). 4929–4940. 46 indexed citations

Hyde, T M, Barbara K. Lipska, Tanweer Ali, et al.. (2011). Expression of GABA Signaling Molecules KCC2, NKCC1, and GAD1 in Cortical Development and Schizophrenia. Journal of Neuroscience. 31(30). 11088–11095. 244 indexed citations

Tan, Hao Yang, Kristin K. Nicodemus, Richard E. Straub, et al.. (2009). PREFRONTAL BRAIN SYSTEMS IN SCHIZOPHRENIA AND PUTATIVE INTERACTING DOPAMINERGIC GENE MECHANISMS. Schizophrenia Bulletin. 35. 183–184. 1 indexed citations

Fanous, Ayman H., Michael C. Neale, Bradley T. Webb, et al.. (2008). Novel Linkage to Chromosome 20p Using Latent Classes of Psychotic Illness in 270 Irish High-Density Families. Biological Psychiatry. 64(2). 121–127. 47 indexed citations

Buckholtz, Joshua W., Andreas Meyer‐Lindenberg, Robyn A. Honea, et al.. (2007). Allelic Variation in RGS4 Impacts Functional and Structural Connectivity in the Human Brain. Journal of Neuroscience. 27(7). 1584–1593. 75 indexed citations

Buckholtz, Joshua W., Steven Sust, Hao Yang Tan, et al.. (2007). Imaging epistasis in vivo: COMT and RGS4. Molecular Psychiatry. 12(10). 885–885. 7 indexed citations

10.

Goldberg, Terry E., Jennifer E. Iudicello, Brita Elvevåg, et al.. (2007). BDNF Val66Met polymorphism significantly affects d′ in verbal recognition memory at short and long delays. Biological Psychology. 77(1). 20–24. 65 indexed citations

11.

Lipska, Barbara K., Shruti N. Mitkus, Thomas M. Hyde, et al.. (2006). RGS4 mRNA expression in postmortem human cortex is associated with COMT Val158Met genotype and COMT enzyme activity. Human Molecular Genetics. 15(18). 2804–2812. 39 indexed citations

12.

Gornick, Michele C., Anjené Addington, Alexandra Sporn, et al.. (2005). Dysbindin (DTNBP1, 6p22.3) is Associated with Childhood-Onset Psychosis and Endophenotypes Measured by the Premorbid Adjustment Scale (PAS). Journal of Autism and Developmental Disorders. 35(6). 831–838. 68 indexed citations

13.

Bobb, Aaron J., Anjené Addington, Ellen Sidransky, et al.. (2005). Support for association between ADHD and two candidate genes: NET1 and DRD1. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 134B(1). 67–72. 166 indexed citations

14.

Pezawas, Lukas, Beth A. Verchinski, Venkata S. Mattay, et al.. (2004). The Brain-Derived Neurotrophic Factor val66met Polymorphism and Variation in Human Cortical Morphology. Journal of Neuroscience. 24(45). 10099–10102. 724 indexed citations breakdown →

15.

Numakawa, Tadahiro, Yuki Yagasaki, Tetsuya Ishimoto, et al.. (2004). Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia. Human Molecular Genetics. 13(21). 2699–2708. 285 indexed citations

16.

Straub, Richard E., Barbara K. Lipska, Michael Egan, et al.. (2002). Allelic variation in GAD1 (GAD67) is associated with schizophrenia and influences cortical function and gene expression. Molecular Psychiatry. 12(9). 854–869. 214 indexed citations

17.

Straub, Richard E.. (2002). Reading and Responding to Student Writing: A Heuristic for Reflective Practice. Freshman English news. 30(1). 15–60. 6 indexed citations

18.

Egan, Michael, Terry E. Goldberg, Bhaskar Kolachana, et al.. (2001). Effect of COMT Val ^108/158 Met genotype on frontal lobe function and risk for schizophrenia. Proceedings of the National Academy of Sciences. 98(12). 6917–6922. 1877 indexed citations breakdown →

19.

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

20.

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

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.

Explore authors with similar magnitude of impact