Marc P. Forrest

2.0k total citations
28 papers, 1.1k citations indexed

About

Marc P. Forrest is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Marc P. Forrest has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Marc P. Forrest's work include Genetics and Neurodevelopmental Disorders (13 papers), Neuroscience and Neuropharmacology Research (6 papers) and Congenital heart defects research (6 papers). Marc P. Forrest is often cited by papers focused on Genetics and Neurodevelopmental Disorders (13 papers), Neuroscience and Neuropharmacology Research (6 papers) and Congenital heart defects research (6 papers). Marc P. Forrest collaborates with scholars based in United States, United Kingdom and Germany. Marc P. Forrest's co-authors include Peter Penzes, Euan Parnell, Derek J. Blake, Enca Martin‐Rendon, Adrian J. Waite, Matthew Hill, Andrew J. Quantock, Jubao Duan, María Dolores Martin‐de‐Saavedra and Katherine E. Tansey and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Neuron.

In The Last Decade

Marc P. Forrest

26 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marc P. Forrest United States 17 676 465 288 186 108 28 1.1k
Constance Smith‐Hicks United States 15 555 0.8× 411 0.9× 413 1.4× 275 1.5× 95 0.9× 31 1.1k
Gaia Novarino Austria 18 784 1.2× 440 0.9× 196 0.7× 175 0.9× 164 1.5× 31 1.3k
Shane McCarthy United States 9 1.0k 1.5× 458 1.0× 324 1.1× 225 1.2× 67 0.6× 16 1.5k
James Gilbert United States 15 559 0.8× 305 0.7× 343 1.2× 249 1.3× 135 1.3× 18 1.1k
Trygve E. Bakken United States 16 849 1.3× 431 0.9× 217 0.8× 295 1.6× 45 0.4× 23 1.4k
Tzyy‐Nan Huang Taiwan 18 565 0.8× 380 0.8× 250 0.9× 291 1.6× 160 1.5× 34 1.0k
María Dolores Rubio Spain 13 593 0.9× 259 0.6× 367 1.3× 178 1.0× 139 1.3× 20 1.1k
Shuang Hao United States 10 455 0.7× 460 1.0× 265 0.9× 326 1.8× 101 0.9× 14 918
Silvia Bassani Italy 19 683 1.0× 267 0.6× 510 1.8× 117 0.6× 257 2.4× 27 1.2k
Erika Pedrosa United States 21 1.1k 1.6× 555 1.2× 204 0.7× 233 1.3× 60 0.6× 34 1.5k

Countries citing papers authored by Marc P. Forrest

Since Specialization
Citations

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

Fields of papers citing papers by Marc P. Forrest

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc P. Forrest. 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 Marc P. Forrest. The network helps show where Marc P. Forrest may publish in the future.

Co-authorship network of co-authors of Marc P. Forrest

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

All Works

20 of 20 papers shown
1.
Forrest, Marc P. & Peter Penzes. (2023). Mechanisms of copy number variants in neuropsychiatric disorders: From genes to therapeutics. Current Opinion in Neurobiology. 82. 102750–102750. 7 indexed citations
2.
Zhang, Siwei, Hanwen Zhang, Marc P. Forrest, et al.. (2023). Multiple genes in a single GWAS risk locus synergistically mediate aberrant synaptic development and function in human neurons. Cell Genomics. 3(9). 100399–100399. 9 indexed citations
3.
Forrest, Marc P., Marc Dos Santos, Nicolas H. Piguel, et al.. (2023). Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub. Nature Communications. 14(1). 825–825. 10 indexed citations
4.
Yoon, Sehyoun, Marc Dos Santos, Marc P. Forrest, et al.. (2023). Early developmental deletion of forebrain Ank2 causes seizure-related phenotypes by reshaping the synaptic proteome. Cell Reports. 42(7). 112784–112784. 5 indexed citations
5.
Kozlova, Alena, Siwei Zhang, Hanwen Zhang, et al.. (2022). Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons. The American Journal of Human Genetics. 109(8). 1500–1519. 9 indexed citations
6.
Parnell, Euan, Marc P. Forrest, Marc Dos Santos, et al.. (2022). Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell–Derived Neurons. Biological Psychiatry. 94(2). 153–163. 16 indexed citations
7.
Simkin, Dina, Carlos G. Vanoye, Reshma R. Desai, et al.. (2021). Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy. eLife. 10. 26 indexed citations
8.
Shapiro, Lauren P., María Dolores Martin‐de‐Saavedra, Christopher P. Pratt, et al.. (2020). Rapid 3D Enhanced Resolution Microscopy Reveals Diversity in Dendritic Spinule Dynamics, Regulation, and Function. Neuron. 107(3). 522–537.e6. 27 indexed citations
9.
Parnell, Euan, et al.. (2020). KALRN: A central regulator of synaptic function and synaptopathies. Gene. 768. 145306–145306. 31 indexed citations
10.
Gao, Ruoqi, Christopher P. Pratt, Sehyoun Yoon, et al.. (2019). CNTNAP2 is targeted to endosomes by the polarity protein PAR3. European Journal of Neuroscience. 51(4). 1074–1086. 7 indexed citations
11.
Torshizi, Abolfazl Doostparast, Chris Armoskus, Hanwen Zhang, et al.. (2019). Deconvolution of transcriptional networks identifies TCF4 as a master regulator in schizophrenia. Science Advances. 5(9). eaau4139–eaau4139. 40 indexed citations
12.
Schürmann, Britta, Katherine J. Kopeikina, Kristoffer Myczek, et al.. (2019). A novel role for the late-onset Alzheimer’s disease (LOAD)-associated protein Bin1 in regulating postsynaptic trafficking and glutamatergic signaling. Molecular Psychiatry. 25(9). 2000–2016. 37 indexed citations
13.
Gao, Ruoqi, Nicolas H. Piguel, María Dolores Martin‐de‐Saavedra, et al.. (2018). CNTNAP2 stabilizes interneuron dendritic arbors through CASK. Molecular Psychiatry. 23(9). 1832–1850. 37 indexed citations
14.
Forrest, Marc P., Euan Parnell, & Peter Penzes. (2018). Dendritic structural plasticity and neuropsychiatric disease. Nature reviews. Neuroscience. 19(4). 215–234. 315 indexed citations
15.
Forrest, Marc P., Hanwen Zhang, Winton Moy, et al.. (2017). Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci. Cell stem cell. 21(3). 305–318.e8. 80 indexed citations
16.
Smith, Katharine R., Kelly A. Jones, Katherine J. Kopeikina, et al.. (2017). Cadherin-10 Maintains Excitatory/Inhibitory Ratio through Interactions with Synaptic Proteins. Journal of Neuroscience. 37(46). 11127–11139. 18 indexed citations
17.
18.
Forrest, Marc P., Matthew Hill, David H. Kavanagh, et al.. (2017). The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability. Schizophrenia Bulletin. 44(5). 1100–1110. 69 indexed citations
19.
Forrest, Marc P., Matthew Hill, Andrew J. Quantock, Enca Martin‐Rendon, & Derek J. Blake. (2014). The emerging roles of TCF4 in disease and development. Trends in Molecular Medicine. 20(6). 322–331. 120 indexed citations
20.
Forrest, Marc P., et al.. (2012). Functional analysis ofTCF4missense mutations that cause Pitt-Hopkins syndrome. Human Mutation. 33(12). 1676–1686. 56 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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