Kellen D. Winden

3.2k total citations · 1 hit paper
28 papers, 2.1k citations indexed

About

Kellen D. Winden is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Kellen D. Winden has authored 28 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Physiology. Recurrent topics in Kellen D. Winden's work include Genetics and Neurodevelopmental Disorders (7 papers), Tuberous Sclerosis Complex Research (4 papers) and Pluripotent Stem Cells Research (4 papers). Kellen D. Winden is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Tuberous Sclerosis Complex Research (4 papers) and Pluripotent Stem Cells Research (4 papers). Kellen D. Winden collaborates with scholars based in United States, Germany and Poland. Kellen D. Winden's co-authors include Daniel H. Geschwind, Mustafa Şahin, Anatol Bragin, Elior Peles, Brett S. Abrahams, Olga Peñagarikano, Hongmei Dong, Lisa I. Sonnenblick, Peyman Golshani and Joel Almajano and has published in prestigious journals such as Nature, Cell and Journal of Biological Chemistry.

In The Last Decade

Kellen D. Winden

26 papers receiving 2.1k 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.

Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits

2011 794 citations Olga Peñagarikano, Brett S. Abrahams et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kellen D. Winden United States	16	1.1k	778	663	398	212	28	2.1k
Chiara Verpelli Italy	30	1.5k 1.4×	856 1.1×	565 0.9×	939 2.4×	208 1.0×	56	2.6k
Paul A. Tooney Australia	29	1.8k 1.6×	631 0.8×	356 0.5×	357 0.9×	136 0.6×	60	3.0k
Harrison W. Gabel United States	23	2.2k 1.9×	1.1k 1.4×	416 0.6×	397 1.0×	139 0.7×	36	2.9k
Steven W. Flavell United States	20	1.4k 1.3×	463 0.6×	411 0.6×	962 2.4×	212 1.0×	28	2.9k
Chang‐Hyuk Kwon United States	17	1.6k 1.4×	625 0.8×	466 0.7×	625 1.6×	225 1.1×	19	3.0k
Thomas Portmann United States	10	1.8k 1.6×	524 0.7×	666 1.0×	1.1k 2.7×	123 0.6×	11	2.7k
Irina Voineagu Australia	18	2.3k 2.1×	1.3k 1.7×	994 1.5×	440 1.1×	105 0.5×	34	3.3k
T. Grant Belgard United States	16	1.5k 1.3×	608 0.8×	627 0.9×	407 1.0×	146 0.7×	22	2.6k
Kimberly A. Aldinger United States	25	1.3k 1.1×	613 0.8×	365 0.6×	344 0.9×	72 0.3×	48	2.3k
Sonia Cohen United States	15	1.4k 1.2×	1.1k 1.4×	615 0.9×	639 1.6×	111 0.5×	31	2.3k

Countries citing papers authored by Kellen D. Winden

Since Specialization

Citations

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

Fields of papers citing papers by Kellen D. Winden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kellen D. Winden. 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 Kellen D. Winden. The network helps show where Kellen D. Winden may publish in the future.

Co-authorship network of co-authors of Kellen D. Winden

This figure shows the co-authorship network connecting the top 25 collaborators of Kellen D. Winden. A scholar is included among the top collaborators of Kellen D. Winden 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 Kellen D. Winden. Kellen D. Winden 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

D’Amore, Angelica, Maria Sundberg, Rui Lin, et al.. (2025). Phenotypic rescue via mTOR inhibition in neuron-specific Pten knockout mice reveals AKT and mTORC1-site specific changes. Molecular Psychiatry. 30(7). 3077–3089.

Saber, Wardiya Afshar, et al.. (2025). Neuronal hyperactivity becomes mTORC1 independent due to transcriptional changes in tuberous sclerosis complex disease models. Cell Reports. 44(12). 116664–116664.

Winden, Kellen D., Juan Pablo Ruíz, & Mustafa Şahin. (2024). Construction destruction: Contribution of dyregulated proteostasis to neurodevelopmental disorders. Current Opinion in Neurobiology. 90. 102934–102934. 1 indexed citations

Saffari, Afshin, Wardiya Afshar Saber, Lara Wahlster, et al.. (2024). High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature Communications. 15(1). 584–584. 9 indexed citations

Winden, Kellen D., et al.. (2023). Increased degradation of FMRP contributes to neuronal hyperexcitability in tuberous sclerosis complex. Cell Reports. 42(8). 112838–112838. 7 indexed citations

Saber, Wardiya Afshar, Kellen D. Winden, Xutong Shi, et al.. (2023). ALDH5A1-deficient iPSC-derived excitatory and inhibitory neurons display cell type specific alterations. Neurobiology of Disease. 190. 106386–106386. 8 indexed citations

Chang, Margaret H., Anaïs Levescot, Nathan Nelson-Maney, et al.. (2021). Arthritis flares mediated by tissue-resident memory T cells in the joint. Cell Reports. 37(4). 109902–109902. 68 indexed citations

Sundberg, Maria, Richard S. Smith, Kellen D. Winden, et al.. (2021). 16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro. Nature Communications. 12(1). 2897–2897. 35 indexed citations

Dalal, Jasbir, Kellen D. Winden, Catherine L. Salussolia, et al.. (2021). Loss of Tsc1 in cerebellar Purkinje cells induces transcriptional and translation changes in FMRP target transcripts. eLife. 10. 11 indexed citations

10.

Winden, Kellen D., et al.. (2019). Biallelic Mutations inTSC2Lead to Abnormalities Associated with Cortical Tubers in Human iPSC-Derived Neurons. Journal of Neuroscience. 39(47). 9294–9305. 61 indexed citations

11.

Winden, Kellen D., Darius Ebrahimi‐Fakhari, & Mustafa Şahin. (2018). Abnormal mTOR Activation in Autism. Annual Review of Neuroscience. 41(1). 1–23. 150 indexed citations

12.

Sundberg, Maria, Ivan Tochitsky, David E. Buchholz, et al.. (2018). Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin. Molecular Psychiatry. 23(11). 2167–2183. 75 indexed citations

13.

Ercan, Ebru, Juliette M. Han, Alessia Di Nardo, et al.. (2017). Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex. The Journal of Experimental Medicine. 214(3). 681–697. 78 indexed citations

14.

Winden, Kellen D., Anatol Bragin, Jerome Engel, & Dan Geschwind. (2015). Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy. Neurobiology of Disease. 78. 35–44. 15 indexed citations

15.

Konopka, Geneviève, Tara Friedrich, Jeremy Davis‐Turak, et al.. (2012). Human-Specific Transcriptional Networks in the Brain. Neuron. 75(4). 601–617. 182 indexed citations

16.

Peñagarikano, Olga, Brett S. Abrahams, Edward I. Herman, et al.. (2011). Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits. Cell. 147(1). 235–246. 794 indexed citations breakdown →

17.

Sagi, Sarah A., Christian Lessard, Kellen D. Winden, et al.. (2011). Substrate Sequence Influences γ-Secretase Modulator Activity, Role of the Transmembrane Domain of the Amyloid Precursor Protein. Journal of Biological Chemistry. 286(46). 39794–39803. 30 indexed citations

18.

Winden, Kellen D., Stanislav L. Karsten, Anatol Bragin, et al.. (2011). A Systems Level, Functional Genomics Analysis of Chronic Epilepsy. PLoS ONE. 6(6). e20763–e20763. 61 indexed citations

19.

Rosen, Ezra Y., Eric Wexler, Giovanni Coppola, et al.. (2011). Functional Genomic Analyses Identify Pathways Dysregulated by Progranulin Deficiency, Implicating Wnt Signaling. Neuron. 71(6). 1030–1042. 100 indexed citations

20.

Coppola, Giovanni, Kellen D. Winden, Geneviève Konopka, Fuying Gao, & Daniel H. Geschwind. (2009). Expression and network analysis of Illumina microarray data. Protocol Exchange. 1 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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