Kellen D. Winden

3.2k citations

28 papers · 2.1k indexed · 1 hit paper · h-index 16

Impact in

Developmental Neuroscience top 5%
- Neurogenesis and neuroplasticity mechanisms
Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research

Papers in ⓘ

Genetics 9
- Genetics and Neurodevelopmental Disorders 7
Molecular Biology 19
- RNA Research and Splicing 4
- Pluripotent Stem Cells Research 4
- Mitochondrial Function and Pathology 4
- RNA and protein synthesis mechanisms 3
- Congenital heart defects research 3
- Machine Learning in Bioinformatics 2

Co-authors: Daniel H. Geschwind (8 shared papers)Mustafa Şahin (16 shared papers)Anatol Bragin (3 shared papers)Peyman Golshani (1 shared paper)Joshua T. Trachtenberg (1 shared paper)Elior Peles (1 shared paper)Joel Almajano (1 shared paper)Hongmei Dong (1 shared paper)
Journals: Cell Reports (4 papers)Nature Communications (2 papers)Molecular Psychiatry (2 papers)Neuron (2 papers)Neurobiology of Disease (2 papers)
Partner nations: United States Germany Poland

In The Last Decade

Kellen D. Winden

26 papers receiving 2.1k citations

Hit Papers

align trajectories log scale

Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits 2011 · 794 citations

Peers

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-authors

The 25 scholars most cited alongside Kellen D. Winden, 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 Kellen D. Winden Line = papers co-authored together Kellen D. Winden links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits Cell ·Olga Peñagarikano, Brett S. Abrahams, Edward I. Herman, Kellen D. Winden, Amos Gdalyahu, Hongmei Dong, Lisa I. Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin, Peyman Golshani, Joshua T. Trachtenberg, Elior Peles, Daniel H. Geschwind Hit paper breakdown →	2011	794
2	Human-specific transcriptional regulation of CNS development genes by FOXP2 Nature ·Geneviève Konopka, Jamee M. Bomar, Kellen D. Winden, Giovanni Coppola, Zophonı́as O. Jónsson, Fuying Gao, Sophia Peng, Todd M. Preuss, James A. Wohlschlegel, Daniel H. Geschwind	2009	267
3	Human-Specific Transcriptional Networks in the Brain Neuron ·Geneviève Konopka, Tara Friedrich, Jeremy Davis‐Turak, Kellen D. Winden, Michael C. Oldham, Fuying Gao, Leslie Chen, Guang-Zhong Wang, Rui Luo, Todd M. Preuss, Daniel H. Geschwind	2012	182
4	Abnormal mTOR Activation in Autism Annual Review of Neuroscience ·Kellen D. Winden, Darius Ebrahimi‐Fakhari, Mustafa Şahin	2018	150
5	Functional Genomic Analyses Identify Pathways Dysregulated by Progranulin Deficiency, Implicating Wnt Signaling Neuron ·Ezra Y. Rosen, Eric Wexler, Revital Versano, Giovanni Coppola, Fuying Gao, Kellen D. Winden, Michael C. Oldham, Lauren Herl Martens, Ping Zhou, Robert V. Farese, Daniel H. Geschwind	2011	100
6	The organization of the transcriptional network in specific neuronal classes Molecular Systems Biology ·Kellen D. Winden, Michael C. Oldham, Károly Mirnics, Philip J. Ebert, Christo H. Swan, Pat Levitt, John L.R. Rubenstein, Steve Horvath, Daniel H. Geschwind	2009	89
7	Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex The Journal of Experimental Medicine ·Ebru Ercan, Juliette M. Han, Alessia Di Nardo, Kellen D. Winden, Min‐Joon Han, Leonie Hoyo, Afshin Saffari, Andrew Leask, Daniel H. Geschwind, Mustafa Şahin	2017	78
8	Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin Molecular Psychiatry ·Maria Sundberg, Ivan Tochitsky, David E. Buchholz, Kellen D. Winden, Ville Kujala, Kush Kapur, Deniz Cataltepe, Daria Turner, Min‐Joon Han, Clifford J. Woolf, Mary E. Hatten, Mustafa Şahin	2018	75
9	Arthritis flares mediated by tissue-resident memory T cells in the joint Cell Reports ·Margaret H. Chang, Anaïs Levescot, Nathan Nelson-Maney, Rachel B. Blaustein, Kellen D. Winden, Allyn Morris, Alexandra Wactor, Spoorthi Balu, Ricardo Grieshaber‐Bouyer, Kevin Wei, Lauren A. Henderson, Yoichiro Iwakura, Rachael A. Clark, Deepak A. Rao, Robert C. Fuhlbrigge, Peter A. Nigrović	2021	68
10	Biallelic Mutations inTSC2Lead to Abnormalities Associated with Cortical Tubers in Human iPSC-Derived Neurons Journal of Neuroscience ·Kellen D. Winden, Maria Sundberg, Cindy Yang, Syed M.A. Wafa, Sean Dwyer, Pin-Fang Chen, Elizabeth D. Buttermore, Mustafa Şahin	2019	61
11	A Systems Level, Functional Genomics Analysis of Chronic Epilepsy PLoS ONE ·Kellen D. Winden, Stanislav L. Karsten, Anatol Bragin, Lili C. Kudo, Lauren Gehman, Josephine Ruidera, Daniel H. Geschwind, Jerome Engel	2011	61
12	Cell-type-specific miR-431 dysregulation in a motor neuron model of spinal muscular atrophy Human Molecular Genetics ·Mary H. Wertz, Kellen D. Winden, Pierre Neveu, Shi‐Yan Ng, Ebru Ercan, Mustafa Şahin	2016	37
13	16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro Nature Communications ·Maria Sundberg, Hannah Pinson, Richard S. Smith, Kellen D. Winden, Pooja Venugopal, Derek J.C. Tai, James F. Gusella, Michael E. Talkowski, Christopher A. Walsh, Max Tegmark, Mustafa Şahin	2021	35
14	Substrate Sequence Influences γ-Secretase Modulator Activity, Role of the Transmembrane Domain of the Amyloid Precursor Protein Journal of Biological Chemistry ·Sarah A. Sagi, Christian Lessard, Kellen D. Winden, Hiroko Maruyama, Jeremy C. Koo, Sascha Weggen, Thomas Kukar, Todd E. Golde, Edward H. Koo	2011	30
15	Megalencephaly and Macrocephaly Seminars in Neurology ·Kellen D. Winden, Christopher J. Yuskaitis, Annapurna Poduri	2015	23
16	Phenotypic Screen with TSC-Deficient Neurons Reveals Heat-Shock Machinery as a Druggable Pathway for mTORC1 and Reduced Cilia Cell Reports ·Alessia Di Nardo, Isadora Lenoël, Kellen D. Winden, Alina Rühmkorf, Meera E. Modi, Lee Barrett, Ebru Ercan-Herbst, Pooja Venugopal, Robert Behne, Carla A.M. Lopes, Robin J. Kleiman, Mónica Bettencourt‐Dias, Mustafa Şahin	2020	17
17	Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy Neurobiology of Disease ·Kellen D. Winden, Anatol Bragin, Jerome Engel, Dan Geschwind	2015	15
18	Loss of Tsc1 in cerebellar Purkinje cells induces transcriptional and translation changes in FMRP target transcripts eLife ·Jasbir Dalal, Kellen D. Winden, Catherine L. Salussolia, Maria Sundberg, Achint K. Singh, Truc Pham, Pingzhu Zhou, William T. Pu, Meghan T. Miller, Mustafa Şahin	2021	11
19	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 ·Afshin Saffari, Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian E. Alecu, M. L. ZIEGLER, Marlene Scheffold, Kellen D. Winden, Jed L. Hubbs, Elizabeth D. Buttermore, Lee Barrett, Georg H. H. Borner, Alexandra K. Davies, Darius Ebrahimi‐Fakhari, Mustafa Şahin	2024	9
20	ALDH5A1-deficient iPSC-derived excitatory and inhibitory neurons display cell type specific alterations Neurobiology of Disease ·Wardiya Afshar Saber, Nicole A. Teaney, Kellen D. Winden, Hellen Jumo, Xutong Shi, Gabrielle E. McGinty, Jed L. Hubbs, Cidi Chen, Itay Tokatly Latzer, Federico M. Gasparoli, Darius Ebrahimi‐Fakhari, Elizabeth D. Buttermore, Jean‐Baptiste Roullet, Phillip L. Pearl, Mustafa Şahin	2023	8

About Kellen D. Winden

Kellen D. Winden is a scholar working on Genetics, Molecular Biology, Cell Biology, Physiology and Genetics, having authored 28 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), RNA Research and Splicing (4 papers), Tuberous Sclerosis Complex Research (4 papers), Pluripotent Stem Cells Research (4 papers), Mitochondrial Function and Pathology (4 papers), RNA and protein synthesis mechanisms (3 papers), Congenital heart defects research (3 papers) and Machine Learning in Bioinformatics (2 papers). The work is most often cited by research in Developmental Neuroscience (156 citations), Cognitive Neuroscience (663 citations), Genetics (778 citations), Cellular and Molecular Neuroscience (398 citations) and Developmental Biology (43 citations). Kellen D. Winden has collaborated with scholars based in United States, Germany and Poland. Frequent co-authors include Daniel H. Geschwind, Mustafa Şahin, Anatol Bragin, Peyman Golshani, Joshua T. Trachtenberg, Elior Peles, Joel Almajano, Hongmei Dong, Olga Peñagarikano and Brett S. Abrahams. Their work appears in journals such as Cell Reports, Nature Communications, Molecular Psychiatry, Neuron and Neurobiology of Disease.

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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