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Newsletter articlesFull Text
INTERNATIONAL PATENT: CITY OF HOPE, THE TRANSLATIONAL GENOMICS RESEARCH INSTITUTE, RANGASAMY, SAMPATHKUMAR, NARAYANAN, VINODH FILES APPLICATION FOR "COMPOSITIONS FOR RESTORING MECP2 GENE FUNCTION AND...
Publisher:Washington, D.C: HT Digital Streams Limited
Journal title:US Fed News Service, Including US State News, 2023
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ArticlesPeer ReviewedFull Text
Epigenetics, Autism Spectrum, and Neurodevelopmental Disorders
Author / Creator:Rangasamy, Sampathkumar ; D’Mello, Santosh R. ; Narayanan, Vinodh
Publisher:Boston: Springer US
Journal title:Neurotherapeutics, 2013-10, Vol.10 (4), p.742-756
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ArticlesPeer ReviewedFull Text
Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex
Author / Creator:Wie, Jinhong ; Bharthur, Apoorva ; Wolfgang, Morgan ; Narayanan, Vinodh ; Ramsey, Keri ; Aranda, Kimberly ; Zhang, Qi ; Zhou, Yandong ; Ren, Dejian
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2020-07, Vol.11 (1), p.3351-3351, Article 3351
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ArticlesPeer ReviewedFull Text
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases
Author / Creator:De La Vega, Francisco M. ; Chowdhury, Shimul ; Moore, Barry ; Frise, Erwin ; McCarthy, Jeanette ; Hernandez, Edgar Javier ; Wong, Terence ; James, Kiely ; Guidugli, Lucia ; Agrawal, Pankaj B. ; Genetti, Casie A. ; Brownstein, Catherine A. ; Beggs, Alan H. ; Löscher, Britt-Sabina ; Franke, Andre ; Boone, Braden ; Levy, Shawn E. ; Õunap, Katrin ; Pajusalu, Sander ; Huentelman, Matt ; Ramsey, Keri ; Naymik, Marcus ; Narayanan, Vinodh ; Veeraraghavan, Narayanan ; Billings, Paul ; Reese, Martin G. ; Yandell, Mark ; Kingsmore, Stephen F.
Publisher:England: BioMed Central Ltd
Journal title:Genome medicine, 2021-10, Vol.13 (1), p.153-153, Article 153
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ArticlesPeer ReviewedFull Text
Improved methods for RNAseq-based alternative splicing analysis
Author / Creator:Halperin, Rebecca F. ; Hegde, Apurva ; Lang, Jessica D. ; Raupach, Elizabeth A. ; Legendre, Christophe ; Liang, Winnie S. ; LoRusso, Patricia M. ; Sekulic, Aleksandar ; Sosman, Jeffrey A. ; Trent, Jeffrey M. ; Rangasamy, Sampathkumar ; Pirrotte, Patrick ; Schork, Nicholas J.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2021-05, Vol.11 (1), p.10740-10740, Article 10740
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ArticlesPeer ReviewedFull Text
GABRG2 Variants Associated with Febrile Seizures
Author / Creator:Hernandez, Ciria C. ; Shen, Yanwen ; Hu, Ningning ; Shen, Wangzhen ; Narayanan, Vinodh ; Ramsey, Keri ; He, Wen ; Zou, Liping ; Macdonald, Robert L.
Publisher:Switzerland: MDPI AG
Journal title:Biomolecules (Basel, Switzerland), 2023-02, Vol.13 (3), p.414
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ArticlesPeer ReviewedFull Text
Reduced neuronal size and mTOR pathway activity in the Mecp2 A140V Rett syndrome mouse model
Author / Creator:Rangasamy, Sampathkumar ; Olfers, Shannon ; Gerald, Brittany ; Hilbert, Alex ; Svejda, Sean ; Narayanan, Vinodh
Publisher:England: Faculty of 1000 Ltd
Journal title:F1000 research, 2016, Vol.5, p.2269-2269
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ArticlesPeer ReviewedFull Text
A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome
Author / Creator:Schrauwen, Isabelle ; Szelinger, Szabolcs ; Siniard, Ashley L. ; Kurdoglu, Ahmet ; Corneveaux, Jason J. ; Malenica, Ivana ; Richholt, Ryan ; Van Camp, Guy ; De Both, Matt ; Swaminathan, Shanker ; Turk, Mari ; Ramsey, Keri ; Craig, David W. ; Narayanan, Vinodh ; Huentelman, Matthew J.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-07, Vol.10 (7), p.e0131797-e0131797
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ArticlesPeer ReviewedFull Text
Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation
Author / Creator:Jentarra, Garilyn M ; Olfers, Shannon L ; Rice, Stephen G ; Srivastava, Nishit ; Homanics, Gregg E ; Blue, Mary ; Naidu, SakkuBai ; Narayanan, Vinodh
Publisher:England: BioMed Central Ltd
Journal title:BMC neuroscience, 2010-02, Vol.11 (1), p.19-19, Article 19
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ArticlesPeer ReviewedFull Text
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood
Author / Creator:Levy, Michael A ; Beck, David B ; Metcalfe, Kay ; Douzgou Sofia ; Sivagamy, Sithambaram ; Cottrell Trudie ; Ansar Muhammad ; Kerkhof, Jennifer ; Mignot Cyril ; Marie-Christine, Nougues ; Keren, Boris ; Moore, Hannah W ; Oegema Renske ; Giltay, Jacques C ; Simon, Marleen ; van Jaarsveld Richard H ; Bos, Jessica ; Mieke, van Haelst ; Mahdi, Motazacker M ; Boon Elles M J ; Santen Gijs W E ; Ruivenkamp Claudia A L ; Alders Marielle ; Romeo, Luperchio Teresa ; Boukas Leandros ; Ramsey, Keri ; Narayanan Vinodh ; Bradley, Schaefer G ; Bonasio Roberto ; Doheny, Kimberly F ; Stevenson, Roger E ; Banka Siddharth ; Sadikovic Bekim ; Fahrner, Jill A
Publisher:London: Nature Publishing Group
Journal title:Npj genomic medicine, 2021-11, Vol.6 (1)
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ArticlesPeer ReviewedFull Text
Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders
Author / Creator:Frankel, Eric ; Podder, Avijit ; Sharifi, Megan ; Pillai, Roshan ; Belnap, Newell ; Ramsey, Keri ; Dodson, Julius ; Venugopal, Pooja ; Brzezinski, Molly ; Llaci, Lorida ; Gerald, Brittany ; Mills, Gabrielle ; Sanchez-Castillo, Meredith ; Balak, Chris D. ; Szelinger, Szabolcs ; Jepsen, Wayne M. ; Siniard, Ashley L. ; Richholt, Ryan ; Naymik, Marcus ; Schrauwen, Isabelle ; Craig, David W. ; Piras, Ignazio S. ; Huentelman, Matthew J. ; Schork, Nicholas J. ; Narayanan, Vinodh ; Rangasamy, Sampathkumar
Publisher:Switzerland: MDPI AG
Journal title:Cells (Basel, Switzerland), 2023-05, Vol.12 (10), p.1437
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ArticlesPeer ReviewedFull Text
Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing
Author / Creator:Szelinger, Szabolcs ; Malenica, Ivana ; Corneveaux, Jason J. ; Siniard, Ashley L. ; Kurdoglu, Ahmet A. ; Ramsey, Keri M. ; Schrauwen, Isabelle ; Trent, Jeffrey M. ; Narayanan, Vinodh ; Huentelman, Matthew J. ; Craig, David W.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-12, Vol.9 (12), p.e113036-e113036
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ArticlesPeer ReviewedFull Text
Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disability
Author / Creator:Banuelos, Erika ; Ramsey, Keri ; Belnap, Newell ; Krishnan, Malavika ; Balak, Chris D. ; Szelinger, Szabolcs ; Siniard, Ashley L. ; Russell, Megan ; Richholt, Ryan ; De Both, Matt ; Piras, Ignazio ; Naymik, Marcus ; Claasen, Ana M. ; Rangasamy, Sampathkumar ; Huentelman, Matthew J. ; Craig, David W. ; Campeau, Philippe M. ; Narayanan, Vinodh ; Schrauwen, Isabelle
Publisher:England: Faculty of 1000 Ltd
Journal title:F1000 research, 2017, Vol.6, p.553-553
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ArticlesPeer ReviewedFull Text
Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations
Author / Creator:Ramsey, Keri ; Belnap, Newell ; Bonfitto, Anna ; Jepsen, Wayne ; Naymik, Marcus ; Sanchez‐Castillo, Meredith ; Craig, David W. ; Szelinger, Szabolcs ; Huentelman, Matthew J. ; Narayanan, Vinodh ; Rangasamy, Sampath
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2022-02, Vol.10 (2), p.e1857-n/a
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ArticlesPeer ReviewedFull Text
Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities [version 1; peer review: 2 app...
Author / Creator:Narayanan, Mohan ; Ramsey, Keri ; Grebe, Theresa ; Schrauwen, Isabelle ; Szelinger, Szabolcs ; Huentelman, Matthew ; Craig, David ; Narayanan, Vinodh
Publisher:England: F1000Research
Journal title:F1000 research, 2015, Vol.4, p.912-912
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ArticlesPeer ReviewedFull Text
Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood
Author / Creator:Levy, Michael A ; Beck, David B ; Metcalfe, Kay ; Douzgou Sofia ; Sivagamy, Sithambaram ; Cottrell Trudie ; Ansar Muhammad ; Kerkhof, Jennifer ; Mignot Cyril ; Marie-Christine, Nougues ; Keren, Boris ; Moore, Hannah W ; Oegema Renske ; Giltay, Jacques C ; Simon, Marleen ; van Jaarsveld Richard H ; Bos, Jessica ; Mieke, van Haelst ; Mahdi, Motazacker M ; Boon Elles M J ; Santen Gijs W E ; Ruivenkamp Claudia A L ; Alders Marielle ; Romeo, Luperchio Teresa ; Boukas Leandros ; Ramsey, Keri ; Narayanan Vinodh ; Bradley, Schaefer G ; Bonasio Roberto ; Doheny, Kimberly F ; Stevenson, Roger E ; Banka Siddharth ; Sadikovic Bekim ; Fahrner, Jill A
Publisher:London: Nature Publishing Group
Journal title:Npj genomic medicine, 2021-11, Vol.6 (1)
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ArticlesPeer ReviewedFull Text
Evidence for population variation in TSC1 and TSC2 gene expression
Author / Creator:Jentarra, Garilyn M ; Rice, Stephen G ; Olfers, Shannon ; Saffen, David ; Narayanan, Vinodh
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2011-02, Vol.12 (1), p.29-29, Article 29
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ArticlesPeer ReviewedFull Text
Simultaneous recordings of ocular microtremor and microsaccades with a piezoelectric sensor and a video-oculography system
Author / Creator:McCamy, Michael B. ; Collins, Niamh ; Otero-Millan, Jorge ; Al-Kalbani, Mohammed ; Macknik, Stephen L. ; Coakley, Davis ; Troncoso, Xoana G. ; Boyle, Gerard ; Narayanan, Vinodh ; Wolf, Thomas R. ; Martinez-Conde, Susana
Publisher:United States: PeerJ. Ltd
Journal title:PeerJ (San Francisco, CA), 2013-02, Vol.1, p.e14-e14
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ArticlesFull Text
Arizona Biotech: In the Trenches - Dr. Vinodh Narayanan
Author / Creator:Keating, Gina
Publisher:Phoenix: American City Business Journals
Journal title:The Business Journal, 2004-12, Vol.25 (12), p.35
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ArticlesPeer ReviewedFull Text
Duchenne Muscular Dystrophy in Two Half-Brothers Due to Inherited 306 Kb Inverted Insertion of 10p15.1 into Intron 44 of the Dp427m Transcript of the DMD Gene
Author / Creator:Jepsen, Wayne M. ; Fazenbaker, Andrew ; Ramsey, Keri ; Bonfitto, Anna ; Naymik, Marcus ; Turner, Bryce ; Sloan, Jennifer ; Tiwari, Nishant ; Bernes, Saunder M. ; Neilson, Derek E. ; Sanchez-Castillo, Meredith ; Huentelman, Matt J. ; Narayanan, Vinodh
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-11, Vol.25 (22), p.11922
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INTERNATIONAL PATENT: CITY OF HOPE, THE TRANSLATIONAL GENOMICS RESEARCH INSTITUTE, RANGASAMY, SAMPATHKUMAR, NARAYANAN, VINODH FILES APPLICATION FOR "COMPOSITIONS FOR RESTORING MECP2 GENE FUNCTION AND...

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Epigenetics, Autism Spectrum, and Neurodevelopmental Disorders

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Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex

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Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases

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Improved methods for RNAseq-based alternative splicing analysis

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GABRG2 Variants Associated with Febrile Seizures

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Reduced neuronal size and mTOR pathway activity in the Mecp2 A140V Rett syndrome mouse model

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A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome

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Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

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Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

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Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders

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Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing

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Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disability

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Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations

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Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities [version 1; peer review: 2 app...

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Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

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Evidence for population variation in TSC1 and TSC2 gene expression

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Simultaneous recordings of ocular microtremor and microsaccades with a piezoelectric sensor and a video-oculography system

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Arizona Biotech: In the Trenches - Dr. Vinodh Narayanan

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Duchenne Muscular Dystrophy in Two Half-Brothers Due to Inherited 306 Kb Inverted Insertion of 10p15.1 into Intron 44 of the Dp427m Transcript of the DMD Gene

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