Emanuela V Volpi

Emanuela V Volpi

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Emanuela V Volpi

Emanuela V Volpi

Publications by authors named "Emanuela V Volpi"

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DNA damage in obesity: Initiator, promoter and predictor of cancer.

Mutat Res 2018 Oct - Dec;778:23-37. Epub 2018 Aug 17.

Department of Biomedical Sciences, Faculty of Science and Technology, University of Westminster, 115 New Cavendish Street, London W1W 6UW, UK. Electronic address:

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http://dx.doi.org/10.1016/j.mrrev.2018.08.002DOI Listing
April 2019

Corrigendum: Whole genome analysis of a schistosomiasis-transmitting freshwater snail.

Authors:
Coen M Adema LaDeana W Hillier Catherine S Jones Eric S Loker Matty Knight Patrick Minx Guilherme Oliveira Nithya Raghavan Andrew Shedlock Laurence Rodrigues do Amaral Halime D Arican-Goktas Juliana G Assis Elio Hideo Baba Olga L Baron Christopher J Bayne Utibe Bickham-Wright Kyle K Biggar Michael Blouin Bryony C Bonning Chris Botka Joanna M Bridger Katherine M Buckley Sarah K Buddenborg Roberta Lima Caldeira Julia Carleton Omar S Carvalho Maria G Castillo Iain W Chalmers Mikkel Christensens Sandra Clifton Celine Cosseau Christine Coustau Richard M Cripps Yesid Cuesta-Astroz Scott F Cummins Leon Di Stefano Nathalie Dinguirard David Duval Scott Emrich Cédric Feschotte Rene Feyereisen Peter FitzGerald Catrina Fronick Lucinda Fulton Richard Galinier Sandra G Gava Michael Geusz Kathrin K Geyer Gloria I Giraldo-Calderón Matheus de Souza Gomes Michelle A Gordy Benjamin Gourbal Christoph Grunau Patrick C Hanington Karl F Hoffmann Daniel Hughes Judith Humphries Daniel J Jackson Liana K Jannotti-Passos Wander de Jesus Jeremias Susan Jobling Bishoy Kamel Aurélie Kapusta Satwant Kaur Joris M Koene Andrea B Kohn Dan Lawson Scott P Lawton Di Liang Yanin Limpanont Sijun Liu Anne E Lockyer Ty Anna L Lovato Fernanda Ludolf Vince Magrini Donald P McManus Monica Medina Milind Misra Guillaume Mitta Gerald M Mkoji Michael J Montague Cesar Montelongo Leonid L Moroz Monica C Munoz-Torres Umar Niazi Leslie R Noble Francislon S Oliveira Fabiano S Pais Anthony T Papenfuss Rob Peace Janeth J Pena Emmanuel A Pila Titouan Quelais Brian J Raney Jonathan P Rast David Rollinson Izinara C Rosse Bronwyn Rotgans Edwin J Routledge Kathryn M Ryan Larissa L S Scholte Kenneth B Storey Martin Swain Jacob A Tennessen Chad Tomlinson Damian L Trujillo Emanuela V Volpi Anthony J Walker Tianfang Wang Ittiprasert Wannaporn Wesley C Warren Xiao-Jun Wu Timothy P Yoshino Mohammed Yusuf Si-Ming Zhang Min Zhao Richard K Wilson

Nat Commun 2017 08 23;8:16153. Epub 2017 Aug 23.

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http://dx.doi.org/10.1038/ncomms16153DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569240PMC
August 2017

Whole genome analysis of a schistosomiasis-transmitting freshwater snail.

Authors:
Coen M Adema LaDeana W Hillier Catherine S Jones Eric S Loker Matty Knight Patrick Minx Guilherme Oliveira Nithya Raghavan Andrew Shedlock Laurence Rodrigues do Amaral Halime D Arican-Goktas Juliana G Assis Elio Hideo Baba Olga L Baron Christopher J Bayne Utibe Bickham-Wright Kyle K Biggar Michael Blouin Bryony C Bonning Chris Botka Joanna M Bridger Katherine M Buckley Sarah K Buddenborg Roberta Lima Caldeira Julia Carleton Omar S Carvalho Maria G Castillo Iain W Chalmers Mikkel Christensens Sandra Clifton Celine Cosseau Christine Coustau Richard M Cripps Yesid Cuesta-Astroz Scott F Cummins Leon di Stephano Nathalie Dinguirard David Duval Scott Emrich Cédric Feschotte Rene Feyereisen Peter FitzGerald Catrina Fronick Lucinda Fulton Richard Galinier Sandra G Gava Michael Geusz Kathrin K Geyer Gloria I Giraldo-Calderón Matheus de Souza Gomes Michelle A Gordy Benjamin Gourbal Christoph Grunau Patrick C Hanington Karl F Hoffmann Daniel Hughes Judith Humphries Daniel J Jackson Liana K Jannotti-Passos Wander de Jesus Jeremias Susan Jobling Bishoy Kamel Aurélie Kapusta Satwant Kaur Joris M Koene Andrea B Kohn Dan Lawson Scott P Lawton Di Liang Yanin Limpanont Sijun Liu Anne E Lockyer TyAnna L Lovato Fernanda Ludolf Vince Magrini Donald P McManus Monica Medina Milind Misra Guillaume Mitta Gerald M Mkoji Michael J Montague Cesar Montelongo Leonid L Moroz Monica C Munoz-Torres Umar Niazi Leslie R Noble Francislon S Oliveira Fabiano S Pais Anthony T Papenfuss Rob Peace Janeth J Pena Emmanuel A Pila Titouan Quelais Brian J Raney Jonathan P Rast David Rollinson Izinara C Rosse Bronwyn Rotgans Edwin J Routledge Kathryn M Ryan Larissa L S Scholte Kenneth B Storey Martin Swain Jacob A Tennessen Chad Tomlinson Damian L Trujillo Emanuela V Volpi Anthony J Walker Tianfang Wang Ittiprasert Wannaporn Wesley C Warren Xiao-Jun Wu Timothy P Yoshino Mohammed Yusuf Si-Ming Zhang Min Zhao Richard K Wilson

Nat Commun 2017 05 16;8:15451. Epub 2017 May 16.

The McDonnell Genome Institute, Washington University, Saint Louis, Missouri 63108 USA.

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http://dx.doi.org/10.1038/ncomms15451DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440852PMC
May 2017

Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2.

Mol Cytogenet 2015 10;8:36. Epub 2015 Jun 10.

Faculty of Linguistics, Philology and Phonetics, University of Oxford, Walton Street, Oxford, OX1 2HG UK ; Faculty of Modern languages, University of Oxford, 47 Wellington Square, Oxford, OX1 2JF UK.

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http://dx.doi.org/10.1186/s13039-015-0148-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460787PMC
June 2015

Author reply: To PMID 24480711.

Ophthalmology 2015 Apr;122(4):e22

Moorfields Eye Hospital, London, UK; University College London, Institute of Ophthalmology, Bath Street, London, UK.

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http://dx.doi.org/10.1016/j.ophtha.2014.08.041DOI Listing
April 2015

De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.

J Med Genet 2014 Nov 16;51(11):737-47. Epub 2014 Sep 16.

Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, UK NIHR Biomedical Research Centre, Oxford, UK Craniofacial Unit, Department of Plastic and Reconstructive Surgery, Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, UK.

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http://dx.doi.org/10.1136/jmedgenet-2014-102582DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215269PMC
November 2014

Detailed phenotypic and genotypic characterization of bietti crystalline dystrophy.

Ophthalmology 2014 Jun 28;121(6):1174-84. Epub 2014 Jan 28.

Moorfields Eye Hospital, London, United Kingdom; Institute of Ophthalmology, University College London, London, United Kingdom.

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http://dx.doi.org/10.1016/j.ophtha.2013.11.042DOI Listing
June 2014

Comprehensive cytogenomic profile of the in vitro neuronal model SH-SY5Y.

Neurogenetics 2013 Feb 9;14(1):63-70. Epub 2012 Dec 9.

Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, OX3 7BN, Oxford, UK.

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http://dx.doi.org/10.1007/s10048-012-0350-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569589PMC
February 2013

Combining M-FISH and Quantum Dot technology for fast chromosomal assignment of transgenic insertions.

BMC Biotechnol 2011 Dec 13;11:121. Epub 2011 Dec 13.

Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, UK.

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http://dx.doi.org/10.1186/1472-6750-11-121DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266222PMC
December 2011

Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophy.

Invest Ophthalmol Vis Sci 2011 Aug 22;52(9):6617-23. Epub 2011 Aug 22.

Nuffield Laboratory of Ophthalmology and Oxford Eye Hospital Biomedical Research Centre, University of Oxford, John Radcliffe Hospital, United Kingdom.

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http://dx.doi.org/10.1167/iovs.11-7932DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175985PMC
August 2011

An improved technique for chromosomal analysis of human ES and iPS cells.

Stem Cell Rev Rep 2011 Jun;7(2):471-7

Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, OX3 7BN, Oxford, UK.

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http://dx.doi.org/10.1007/s12015-010-9224-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3073051PMC
June 2011

A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.

J Neurodev Disord 2011 Jun 12;3(2):124-31. Epub 2011 Feb 12.

Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, UK.

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http://dx.doi.org/10.1007/s11689-011-9076-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105230PMC
June 2011

Fluorescence in situ hybridization (FISH) for genomic investigations in rat.

Methods Mol Biol 2010 ;659:409-26

Department of Cardiovascular Medicine, John Radcliffe Hospital, Oxford, UK.

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http://dx.doi.org/10.1007/978-1-60761-789-1_32DOI Listing
December 2010

HAC stability in murine cells is influenced by nuclear localization and chromatin organization.

BMC Cell Biol 2009 Mar 6;10:18. Epub 2009 Mar 6.

Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, OX3 7BN, UK.

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http://dx.doi.org/10.1186/1471-2121-10-18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2674426PMC
March 2009

FISH glossary: an overview of the fluorescence in situ hybridization technique.

Biotechniques 2008 Oct;45(4):385-6, 388, 390 passim

Molecular Cytogenetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.2144/000112811DOI Listing
October 2008