Derek J.C. Tai

804 total citations
15 papers, 400 citations indexed

About

Derek J.C. Tai is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Derek J.C. Tai has authored 15 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Oncology. Recurrent topics in Derek J.C. Tai's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and CRISPR and Genetic Engineering (3 papers). Derek J.C. Tai is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and CRISPR and Genetic Engineering (3 papers). Derek J.C. Tai collaborates with scholars based in United States, Taiwan and United Kingdom. Derek J.C. Tai's co-authors include Yun‐Li Ma, Eminy H.Y. Lee, Wei‐Lun Hsu, Yen‐Chen Liu, Michael E. Talkowski, James F. Gusella, Yan‐Chu Chen, Mustafa Şahin, Serkan Erdin and Yiping Shen and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Journal of Neuroscience.

In The Last Decade

Derek J.C. Tai

15 papers receiving 397 citations

Peers

Countries citing papers authored by Derek J.C. Tai

Since Specialization

Citations

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

Fields of papers citing papers by Derek J.C. Tai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Derek J.C. Tai. 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 J.C. Tai. The network helps show where Derek J.C. Tai may publish in the future.

Co-authorship network of co-authors of Derek J.C. Tai

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing 2025 ·Cell Genomics ·(unknown), Joshua B. Black, (unknown), Alejandro Barrera, Susan A. Berry, (unknown), Xander Nuttle, (unknown), Derek J.C. Tai, Michael E. Talkowski, Nahid Iglesias, Charles A. Gersbach	4
2	Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries 2023 ·Cell Reports Methods ·Xander Nuttle, (unknown), Benjamin Currall, Mariana Moysés‐Oliveira, Kiana Mohajeri, (unknown), Diane Lucente, Rachita Yadav, Derek J.C. Tai, James F. Gusella, Michael E. Talkowski	1
3	Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell–Derived Neurons 2022 ·Biological Psychiatry ·Euan Parnell, (unknown), Marc P. Forrest, (unknown), (unknown), (unknown), (unknown), Marc Dos Santos, Nicolas H. Piguel, Derek J.C. Tai, Hanwen Zhang, Tracy S. Gertler, Dina Simkin, Alan R. Sanders, Michael E. Talkowski, Pablo V. Gejman, Evangelos Kiskinis, Jubao Duan, Peter Penzes	16
4	Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder 2022 ·Nature Communications ·Elaine T. Lim, Yingleong Chan, (unknown), Xiaoge Guo, Serkan Erdin, Derek J.C. Tai, Songlei Liu, (unknown), (unknown), Ying Chan, Jessica J. Chiang, Katharina Meyer, Xiaochang Zhang, Christopher A. Walsh, Bruce A. Yankner, Soumya Raychaudhuri, Joel N. Hirschhorn, James F. Gusella, Michael E. Talkowski, George M. Church	14
5	STATISTICAL AND FUNCTIONAL CONVERGENCE OF COMMON AND RARE VARIANT RISK FOR AUTISM SPECTRUM DISORDERS AT CHROMOSOME 16P 2022 ·European Neuropsychopharmacology ·Daniel J. Weiner, Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove, Jack B. Fu, Ajay Nadig, Jonathan Sebat, (unknown), David M. Hougaard, Anders D. Børglum, Michael E. Talkowski, Steve McCarroll, Elise Robinson	2
6	16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro 2021 ·Nature Communications ·Maria Sundberg, (unknown), Richard S. Smith, Kellen D. Winden, (unknown), Derek J.C. Tai, James F. Gusella, Michael E. Talkowski, Christopher A. Walsh, Max Tegmark, Mustafa Şahin	35
7	Restoring Wnt6 signaling ameliorates behavioral deficits in MeCP2 T158A mouse model of Rett syndrome 2020 ·Scientific Reports ·Wei‐Lun Hsu, Yun‐Li Ma, Yen‐Chen Liu, Derek J.C. Tai, Eminy H.Y. Lee	21
8	Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons 2020 ·Molecular Autism ·Catarina M. Seabra, Tatsiana Aneichyk, Serkan Erdin, Derek J.C. Tai, Celine de Esch, (unknown), Yu An, Poornima Manavalan, Ashok Ragavendran, Alexei Stortchevoi, Clemer Abad, Juan I. Young, Patrı́cia Maciel, Michael E. Talkowski, James F. Gusella	11
9	Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome 2019 ·American Journal of Medical Genetics Part A ·Philip M. Boone, Scott Paterson, Kiana Mohajeri, Wenmiao Zhu, Casie A. Genetti, Derek J.C. Tai, (unknown), Pankaj B. Agrawal, Carlos A. Bacino, Weimin Bi, Michael E. Talkowski, Benjamin M. Hogan, Lance H. Rodan	12
10	MeCP2 SUMOylation rescues Mecp2-mutant-induced behavioural deficits in a mouse model of Rett syndrome 2016 ·Nature Communications ·Derek J.C. Tai, Yen‐Chen Liu, Wei‐Lun Hsu, Yun‐Li Ma, (unknown), (unknown), Eminy H.Y. Lee	57
11	Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR 2016 ·Nature Neuroscience ·Derek J.C. Tai, Ashok Ragavendran, Poornima Manavalan, Alexei Stortchevoi, Catarina M. Seabra, Serkan Erdin, Ryan L. Collins, Ian Blumenthal, Xiaoli Chen, Yiping Shen, Mustafa Şahin, Chengsheng Zhang, Charles Lee, James F. Gusella, Michael E. Talkowski	53
12	CREB SUMOylation by the E3 Ligase PIAS1 Enhances Spatial Memory 2014 ·Journal of Neuroscience ·Yan‐Chu Chen, Wei‐Lun Hsu, Yun‐Li Ma, Derek J.C. Tai, Eminy H.Y. Lee	37
13	Novel role and mechanism of protein inhibitor of activated STAT1 in spatial learning 2010 ·The EMBO Journal ·Derek J.C. Tai, Wei‐Lun Hsu, Yen‐Chen Liu, Yun‐Li Ma, Eminy H.Y. Lee	37
14	A novel defense mechanism that is activated on amyloid-β insult to mediate cell survival: role of SGK1-STAT1/STAT2 signaling 2009 ·Cell Death and Differentiation ·Wei‐Lun Hsu, (unknown), Derek J.C. Tai, Yun‐Li Ma, Eminy H.Y. Lee	19
15	SGK1 Phosphorylation of IκB Kinase α and p300 Up-regulates NF-κB Activity and Increases N-Methyl-D-aspartate Receptor NR2A and NR2B Expression 2008 ·Journal of Biological Chemistry ·Derek J.C. Tai, (unknown), Yun‐Li Ma, Eminy H.Y. Lee	81

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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