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Times Cited: 168
Times Cited: 168
Times Cited
Times Co-cited
Similarity
Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome.
Sergiu P Paşca, Thomas Portmann, Irina Voineagu, Masayuki Yazawa, Aleksandr Shcheglovitov, Anca M Paşca, Branden Cord, Theo D Palmer, Sachiko Chikahisa, Seiji Nishino,[...]. Nat Med 2011
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A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells.
Maria C N Marchetto, Cassiano Carromeu, Allan Acab, Diana Yu, Gene W Yeo, Yangling Mu, Gong Chen, Fred H Gage, Alysson R Muotri. Cell 2010
Maria C N Marchetto, Cassiano Carromeu, Allan Acab, Diana Yu, Gene W Yeo, Yangling Mu, Gong Chen, Fred H Gage, Alysson R Muotri. Cell 2010
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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar, Raffaella Bloise, Carlo Napolitano, Peter J Schwartz, Robert M Joseph, Karen Condouris,[...]. Cell 2004
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SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients.
Aleksandr Shcheglovitov, Olesya Shcheglovitova, Masayuki Yazawa, Thomas Portmann, Rui Shu, Vittorio Sebastiano, Anna Krawisz, Wendy Froehlich, Jonathan A Bernstein, Joachim F Hallmayer,[...]. Nature 2013
Aleksandr Shcheglovitov, Olesya Shcheglovitova, Masayuki Yazawa, Thomas Portmann, Rui Shu, Vittorio Sebastiano, Anna Krawisz, Wendy Froehlich, Jonathan A Bernstein, Joachim F Hallmayer,[...]. Nature 2013
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Cerebral organoids model human brain development and microcephaly.
Madeline A Lancaster, Magdalena Renner, Carol-Anne Martin, Daniel Wenzel, Louise S Bicknell, Matthew E Hurles, Tessa Homfray, Josef M Penninger, Andrew P Jackson, Juergen A Knoblich. Nature 2013
Madeline A Lancaster, Magdalena Renner, Carol-Anne Martin, Daniel Wenzel, Louise S Bicknell, Matthew E Hurles, Tessa Homfray, Josef M Penninger, Andrew P Jackson, Juergen A Knoblich. Nature 2013
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iPSC-derived forebrain neurons from FXS individuals show defects in initial neurite outgrowth.
Matthew E Doers, Michael T Musser, Robert Nichol, Erich R Berndt, Mei Baker, Timothy M Gomez, Su-Chun Zhang, Leonard Abbeduto, Anita Bhattacharyya. Stem Cells Dev 2014
Matthew E Doers, Michael T Musser, Robert Nichol, Erich R Berndt, Mei Baker, Timothy M Gomez, Su-Chun Zhang, Leonard Abbeduto, Anita Bhattacharyya. Stem Cells Dev 2014
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FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders.
Jessica Mariani, Gianfilippo Coppola, Ping Zhang, Alexej Abyzov, Lauren Provini, Livia Tomasini, Mariangela Amenduni, Anna Szekely, Dean Palejev, Michael Wilson,[...]. Cell 2015
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Assembly of functionally integrated human forebrain spheroids.
Fikri Birey, Jimena Andersen, Christopher D Makinson, Saiful Islam, Wu Wei, Nina Huber, H Christina Fan, Kimberly R Cordes Metzler, Georgia Panagiotakos, Nicholas Thom,[...]. Nature 2017
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Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
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Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome.
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Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.
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Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D culture.
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Modelling schizophrenia using human induced pluripotent stem cells.
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Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors.
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Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
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Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation.
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Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model.
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Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome.
Kun-Yong Kim, Eriona Hysolli, In-Hyun Park. Proc Natl Acad Sci U S A 2011
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Synaptic, transcriptional and chromatin genes disrupted in autism.
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Synaptic dysregulation in a human iPS cell model of mental disorders.
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Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy syndrome.
Georgia Panagiotakos, Christos Haveles, Arpana Arjun, Ralitsa Petrova, Anshul Rana, Thomas Portmann, Sergiu P Paşca, Theo D Palmer, Ricardo E Dolmetsch. Elife 2019
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The contribution of de novo coding mutations to autism spectrum disorder.
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Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure.
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Signaling defects in iPSC-derived fragile X premutation neurons.
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Rapid single-step induction of functional neurons from human pluripotent stem cells.
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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
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Mutant astrocytes differentiated from Rett syndrome patients-specific iPSCs have adverse effects on wild-type neurons.
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Directed differentiation and functional maturation of cortical interneurons from human embryonic stem cells.
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Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.
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Mouse model of Timothy syndrome recapitulates triad of autistic traits.
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Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells.
Achia Urbach, Ori Bar-Nur, George Q Daley, Nissim Benvenisty. Cell Stem Cell 2010
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CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons.
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Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling.
Stuart M Chambers, Christopher A Fasano, Eirini P Papapetrou, Mark Tomishima, Michel Sadelain, Lorenz Studer. Nat Biotechnol 2009
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CACNA1D de novo mutations in autism spectrum disorders activate Cav1.3 L-type calcium channels.
Alexandra Pinggera, Andreas Lieb, Bruno Benedetti, Michaela Lampert, Stefania Monteleone, Klaus R Liedl, Petronel Tuluc, Jörg Striessnig. Biol Psychiatry 2015
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Functional maturation of hPSC-derived forebrain interneurons requires an extended timeline and mimics human neural development.
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Modeling human cortical development in vitro using induced pluripotent stem cells.
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Altered neuronal network and rescue in a human MECP2 duplication model.
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Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons.
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Human cerebral cortex development from pluripotent stem cells to functional excitatory synapses.
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The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).
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Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome.
Masayuki Yazawa, Brian Hsueh, Xiaolin Jia, Anca M Pasca, Jonathan A Bernstein, Joachim Hallmayer, Ricardo E Dolmetsch. Nature 2011
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Ca(V)1 and Ca(V)2 channels engage distinct modes of Ca(2+) signaling to control CREB-dependent gene expression.
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A polygenic burden of rare disruptive mutations in schizophrenia.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.