Stephen T. Warren

35.7k citations

180 papers · 23.6k indexed · 8 hit papers · h-index 74

Impact in

Genetics top 0.01%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Cognitive Neuroscience top 0.1%
- Autism Spectrum Disorder Research

Papers in

Genetics 138
- Genetics and Neurodevelopmental Disorders 118
- Genomic variations and chromosomal abnormalities 33
Cognitive Neuroscience 47
- Autism Spectrum Disorder Research 44

Co-authors: Mark F. Bear Kimberly M. Huber Gary J. Bassell Peng Jin David L. Nelson William T. O'Donnell Victoria Brown Yue Feng
Journals: Human Molecular Genetics (12 papers)Proceedings of the National Academy of Sciences (11 papers)The American Journal of Human Genetics (9 papers)Genomics (7 papers)Nature Genetics (7 papers)
Partner nations: United States Netherlands United Kingdom

In The Last Decade

Stephen T. Warren

177 papers receiving 23.1k citations

Hit Papers

8 papers align trajectories log scale

Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function 2008 · 821 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2008 Neuron
2004 Trends in Neurosciences
2002 Proceedings of the National Academy of Sciences
2001 Cell
2001 Cell
1993 Science
1991 Science
1991 Cell

Peers

Countries citing papers authored by Stephen T. Warren

Since Specialization

Citations

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

Fields of papers citing papers by Stephen T. Warren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Stephen T. Warren, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Stephen T. Warren Line = papers co-authored together Stephen T. Warren links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Fragile X Syndrome Patient–Derived Neurons Developing in the Mouse Brain Show FMR1-Dependent Phenotypes Biological Psychiatry ·Marine Krzisch, Hao Wu, Bingbing Yuan, Troy W. Whitfield, X. Shawn Liu, Dongdong Fu, Carrie M. Garrett-Engele, Andrew Khalil, Tenzin Lungjangwa, Jennifer Shih, Aaron N. Chang, Stephen T. Warren, Angela Cacace, Kristin Andrykovich, Rosalie Rietjens, Owen B. Wallace, Mriganka Sur, Bhav Jain, Rudolf Jaenisch	2022	0
2	Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion Molecular Psychiatry ·Timothy P. Rutkowski, Ryan H. Purcell, Rebecca M. Pollak, Stephanie M. Grewenow, Georgette M. Gafford, Tamika Malone, Uswa A. Khan, Jason P. Schroeder, Michael P. Epstein, Gary J. Bassell, Stephen T. Warren, David Weinshenker, Tamara Caspary, Jennifer G. Mullé	2019	25
3	Where is the crowd Arrow@dit (Dublin Institute of Technology) ·Stephen T. Warren, Robert Gleasure, Philip O’Reilly, Joseph Feller, Shanping Li, Jerry Christoforo	2017	1
4	The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila Neurons Cell Reports ·Rick S. Bienkowski, Ayan Banerjee, J. Christopher Rounds, Jennifer Rha, Omotola F. Omotade, Christina Groß, Kevin J. Morris, Sara W. Leung, ChangHui Pak, Stephanie K. Jones, Michael R. Santoro, Stephen T. Warren, James Q. Zheng, Gary J. Bassell, Anita H. Corbett, Kenneth H. Moberg	2017	24
5	Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain Human Molecular Genetics ·Leila K. Myrick, Hideharu Hashimoto, Xiaodong Cheng, Stephen T. Warren	2014	82
6	A Chromatin-Dependent Role of the Fragile X Mental Retardation Protein FMRP in the DNA Damage Response DSpace@MIT (Massachusetts Institute of Technology) ·Roman Alpatov, Mika Nakamoto-Kinoshita, Andrés Blanco, Shuzhen Chen, Alexandra Stützer, Karim J. Armache, Matthew D. Simon, Chao Xu, Muzaffar Ali, Jernej Murn, Sladjana Prišić, Tatiana G. Kutateladze, Christopher R. Vakoc, Jinrong Min, Robert E. Kingston, Wolfgang Fischle, Stephen T. Warren, Yang Shi, Bluma J. Lesch, David C. Page	2014	2
7	Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum Human Molecular Genetics ·Tao Wang, Qian Pan, Lin Li, Keith E. Szulwach, Chun‐Xiao Song, Chuan He, Hao Wu, Stephen T. Warren, Peng Jin, Ranhui Duan, Xuekun Li	2012	131
8	Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective Annual Review of Pathology Mechanisms of Disease ·Michael R. Santoro, Steven M. Bray, Stephen T. Warren	2011	404
9	Local RNA Translation at the Synapse and in Disease: Figure 1. Journal of Neuroscience ·Liqun Liu‐Yesucevitz, Gary J. Bassell, Aaron D. Gitler, Anne C. Hart, Eric Klann, Joel D. Richter, Stephen T. Warren, Benjamin Wolozin	2011	239
10	Excess Phosphoinositide 3-Kinase Subunit Synthesis and Activity as a Novel Therapeutic Target in Fragile X Syndrome Journal of Neuroscience ·Christina Groß, M. Nakamoto, Xiaodi Yao, Chi-Bun Chan, So Y. Yim, Keqiang Ye, Stephen T. Warren, Gary J. Bassell	2010	197
11	FMRP Phosphorylation Reveals an Immediate-Early Signaling Pathway Triggered by Group I mGluR and Mediated by PP2A Journal of Neuroscience ·Usha Narayanan, Vijayalaxmi Nalavadi, M. Nakamoto, David C. Pallas, Stephanie Ceman, Gary J. Bassell, Stephen T. Warren	2007	187
12	The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development Proceedings of the National Academy of Sciences ·Robert Lu, Houping Wang, Zhe Liang, Li Ku, William T. O'Donnell, Wen Li, Stephen T. Warren, Yue Feng	2004	255
13	The fragile X mental retardation protein, FMRP, recognizes G‐quartets Mental Retardation and Developmental Disabilities Research Reviews ·Jennifer C. Darnell, Stephen T. Warren, Robert B. Darnell	2004	42
14	Altered synaptic plasticity in a mouse model of fragile X mental retardation Proceedings of the National Academy of Sciences ·Kimberly M. Huber, Sean Gallagher, Stephen T. Warren, Mark F. Bear Hit paper breakdown →	2002	1049
15	Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells Nature Genetics ·Bradford Coffee, Fuping Zhang, Stephen T. Warren, Daniel Reines	1999	247
16	Purified Recombinant Fmrp Exhibits Selective RNA Binding as an Intrinsic Property of the Fragile X Mental Retardation Protein Journal of Biological Chemistry ·Victoria Brown, Kersten M. Small, Lisa Lakkis, Yue Feng, Chris Gunter, Keith D. Wilkinson, Stephen T. Warren	1998	144
17	Genetic instabilities and hereditary neurological diseases Academic Press eBooks ·Robert D. Wells, Stephen T. Warren, M Sarmiento	1998	243
18	Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1 Human Molecular Genetics ·Chris Gunter, William Paradee, Dana C. Crawford, Katie Meadows, Jane Newman, Catherine B. Kunst, David L. Nelson, Charles E. Schwartz, Anna Murray, John MacPherson, S. L. Sherman, Stephen T. Warren	1998	59
19	Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes Human Molecular Genetics ·Ans M.W. van den Ouweland, Wout H. Deelen, Catherine B. Kunst, Maria-Luisa Giovannucci Uzielli, David L. Nelson, Stephen T. Warren, Ben A. Oostra, Dicky Halley	1994	34
20	Genetic Variation in Nigeria Human Heredity ·Ajovi B. Scott‐Emuakpor, Eserovwe Uviovo, Stephen T. Warren	1975	2

About Stephen T. Warren

Stephen T. Warren is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Cellular and Molecular Neuroscience and Aging, having authored 180 papers that have together received 23.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (118 papers), Autism Spectrum Disorder Research (44 papers), RNA modifications and cancer (41 papers), Genomic variations and chromosomal abnormalities (33 papers), Ubiquitin and proteasome pathways (23 papers), RNA Research and Splicing (19 papers), Epigenetics and DNA Methylation (19 papers) and Congenital heart defects research (18 papers). The work is most often cited by research in Genetics (15.9k citations), Cognitive Neuroscience (6.9k citations), Molecular Biology (17.3k citations), Cellular and Molecular Neuroscience (3.6k citations) and Developmental Neuroscience (782 citations). Stephen T. Warren has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Mark F. Bear, Kimberly M. Huber, Gary J. Bassell, Peng Jin, David L. Nelson, William T. O'Donnell, Victoria Brown, Yue Feng, Stephanie Ceman and Keith D. Wilkinson. Their work appears in journals such as Human Molecular Genetics, Proceedings of the National Academy of Sciences, The American Journal of Human Genetics, Genomics and Nature Genetics.

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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