Matt Baker

Matt Baker

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Matt Baker

Matt Baker

Publications by authors named "Matt Baker"

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Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.

Authors:
Cyril Pottier Yingxue Ren Ralph B Perkerson Matt Baker Gregory D Jenkins Marka van Blitterswijk Mariely DeJesus-Hernandez Jeroen G J van Rooij Melissa E Murray Elizabeth Christopher Shannon K McDonnell Zachary Fogarty Anthony Batzler Shulan Tian Cristina T Vicente Billie Matchett Anna M Karydas Ging-Yuek Robin Hsiung Harro Seelaar Merel O Mol Elizabeth C Finger Caroline Graff Linn Öijerstedt Manuela Neumann Peter Heutink Matthis Synofzik Carlo Wilke Johannes Prudlo Patrizia Rizzu Javier Simon-Sanchez Dieter Edbauer Sigrun Roeber Janine Diehl-Schmid Bret M Evers Andrew King M Marsel Mesulam Sandra Weintraub Changiz Geula Kevin F Bieniek Leonard Petrucelli Geoffrey L Ahern Eric M Reiman Bryan K Woodruff Richard J Caselli Edward D Huey Martin R Farlow Jordan Grafman Simon Mead Lea T Grinberg Salvatore Spina Murray Grossman David J Irwin Edward B Lee EunRan Suh Julie Snowden David Mann Nilufer Ertekin-Taner Ryan J Uitti Zbigniew K Wszolek Keith A Josephs Joseph E Parisi David S Knopman Ronald C Petersen John R Hodges Olivier Piguet Ethan G Geier Jennifer S Yokoyama Robert A Rissman Ekaterina Rogaeva Julia Keith Lorne Zinman Maria Carmela Tartaglia Nigel J Cairns Carlos Cruchaga Bernardino Ghetti Julia Kofler Oscar L Lopez Thomas G Beach Thomas Arzberger Jochen Herms Lawrence S Honig Jean Paul Vonsattel Glenda M Halliday John B Kwok Charles L White Marla Gearing Jonathan Glass Sara Rollinson Stuart Pickering-Brown Jonathan D Rohrer John Q Trojanowski Vivianna Van Deerlin Eileen H Bigio Claire Troakes Safa Al-Sarraj Yan Asmann Bruce L Miller Neill R Graff-Radford Bradley F Boeve William W Seeley Ian R A Mackenzie John C van Swieten Dennis W Dickson Joanna M Biernacka Rosa Rademakers

Acta Neuropathol 2019 Jun 9;137(6):879-899. Epub 2019 Feb 9.

Department of Neuroscience, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.

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http://link.springer.com/10.1007/s00401-019-01962-9
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http://dx.doi.org/10.1007/s00401-019-01962-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533145PMC
June 2019

Clinicopathologic correlations in a family with a mutation presenting as primary progressive aphasia and primary lateral sclerosis.

Amyotroph Lateral Scler Frontotemporal Degener 2019 Jun 27:1-8. Epub 2019 Jun 27.

a Division of Neuropathology , University of British Columbia , Vancouver , Canada.

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http://dx.doi.org/10.1080/21678421.2019.1632347DOI Listing
June 2019

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

Authors:
Cyril Pottier Xiaolai Zhou Ralph B Perkerson Matt Baker Gregory D Jenkins Daniel J Serie Roberta Ghidoni Luisa Benussi Giuliano Binetti Adolfo López de Munain Miren Zulaica Fermin Moreno Isabelle Le Ber Florence Pasquier Didier Hannequin Raquel Sánchez-Valle Anna Antonell Albert Lladó Tammee M Parsons NiCole A Finch Elizabeth C Finger Carol F Lippa Edward D Huey Manuela Neumann Peter Heutink Matthis Synofzik Carlo Wilke Robert A Rissman Jaroslaw Slawek Emilia Sitek Peter Johannsen Jørgen E Nielsen Yingxue Ren Marka van Blitterswijk Mariely DeJesus-Hernandez Elizabeth Christopher Melissa E Murray Kevin F Bieniek Bret M Evers Camilla Ferrari Sara Rollinson Anna Richardson Elio Scarpini Giorgio G Fumagalli Alessandro Padovani John Hardy Parastoo Momeni Raffaele Ferrari Francesca Frangipane Raffaele Maletta Maria Anfossi Maura Gallo Leonard Petrucelli EunRan Suh Oscar L Lopez Tsz H Wong Jeroen G J van Rooij Harro Seelaar Simon Mead Richard J Caselli Eric M Reiman Marwan Noel Sabbagh Mads Kjolby Anders Nykjaer Anna M Karydas Adam L Boxer Lea T Grinberg Jordan Grafman Salvatore Spina Adrian Oblak M-Marsel Mesulam Sandra Weintraub Changiz Geula John R Hodges Olivier Piguet William S Brooks David J Irwin John Q Trojanowski Edward B Lee Keith A Josephs Joseph E Parisi Nilüfer Ertekin-Taner David S Knopman Benedetta Nacmias Irene Piaceri Silvia Bagnoli Sandro Sorbi Marla Gearing Jonathan Glass Thomas G Beach Sandra E Black Mario Masellis Ekaterina Rogaeva Jean-Paul Vonsattel Lawrence S Honig Julia Kofler Amalia C Bruni Julie Snowden David Mann Stuart Pickering-Brown Janine Diehl-Schmid Juliane Winkelmann Daniela Galimberti Caroline Graff Linn Öijerstedt Claire Troakes Safa Al-Sarraj Carlos Cruchaga Nigel J Cairns Jonathan D Rohrer Glenda M Halliday John B Kwok John C van Swieten Charles L White Bernardino Ghetti Jill R Murell Ian R A Mackenzie Ging-Yuek R Hsiung Barbara Borroni Giacomina Rossi Fabrizio Tagliavini Zbigniew K Wszolek Ronald C Petersen Eileen H Bigio Murray Grossman Vivianna M Van Deerlin William W Seeley Bruce L Miller Neill R Graff-Radford Bradley F Boeve Dennis W Dickson Joanna M Biernacka Rosa Rademakers

Lancet Neurol 2018 06 30;17(6):548-558. Epub 2018 Apr 30.

Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Electronic address:

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http://dx.doi.org/10.1016/S1474-4422(18)30126-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237181PMC
June 2018

Passive hip movement measurements related to dynamic motion during gait in hip osteoarthritis.

J Orthop Res 2016 10 3;34(10):1790-1797. Epub 2016 Mar 3.

Faculty of Health Professions, School of Physiotherapy, Dalhousie University, 4th Floor Forrest Building, 5869 University Ave, 15000, Halifax, Nova Scotia, Canada.

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http://dx.doi.org/10.1002/jor.23198DOI Listing
October 2016

Diffuse leukoencephalopathy with spheroids presenting as primary progressive aphasia.

Neurology 2015 Aug 22;85(7):652-3. Epub 2015 Jul 22.

From the Cognitive Neurology and Alzheimer's Disease Center (C.O., E.H.B., B.B., S.W., M.-M.M.), Northwestern University Feinberg School of Medicine, Chicago, IL; and the Mayo Clinic (M.C.B., R.R.), Jacksonville, FL.

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http://dx.doi.org/10.1212/WNL.0000000000001851DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4548282PMC
August 2015

PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease.

Brain 2015 Jun 20;138(Pt 6):e357. Epub 2014 Nov 20.

Department of Neuroscience, Mayo Clinic, Jacksonville, Florida, USA.

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http://dx.doi.org/10.1093/brain/awu332DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614132PMC
June 2015

Frontotemporal dementia and its subtypes: a genome-wide association study.

Authors:
Raffaele Ferrari Dena G Hernandez Michael A Nalls Jonathan D Rohrer Adaikalavan Ramasamy John B J Kwok Carol Dobson-Stone William S Brooks Peter R Schofield Glenda M Halliday John R Hodges Olivier Piguet Lauren Bartley Elizabeth Thompson Eric Haan Isabel Hernández Agustín Ruiz Mercè Boada Barbara Borroni Alessandro Padovani Carlos Cruchaga Nigel J Cairns Luisa Benussi Giuliano Binetti Roberta Ghidoni Gianluigi Forloni Daniela Galimberti Chiara Fenoglio Maria Serpente Elio Scarpini Jordi Clarimón Alberto Lleó Rafael Blesa Maria Landqvist Waldö Karin Nilsson Christer Nilsson Ian R A Mackenzie Ging-Yuek R Hsiung David M A Mann Jordan Grafman Christopher M Morris Johannes Attems Timothy D Griffiths Ian G McKeith Alan J Thomas P Pietrini Edward D Huey Eric M Wassermann Atik Baborie Evelyn Jaros Michael C Tierney Pau Pastor Cristina Razquin Sara Ortega-Cubero Elena Alonso Robert Perneczky Janine Diehl-Schmid Panagiotis Alexopoulos Alexander Kurz Innocenzo Rainero Elisa Rubino Lorenzo Pinessi Ekaterina Rogaeva Peter St George-Hyslop Giacomina Rossi Fabrizio Tagliavini Giorgio Giaccone James B Rowe Johannes C M Schlachetzki James Uphill John Collinge Simon Mead Adrian Danek Vivianna M Van Deerlin Murray Grossman John Q Trojanowski Julie van der Zee William Deschamps Tim Van Langenhove Marc Cruts Christine Van Broeckhoven Stefano F Cappa Isabelle Le Ber Didier Hannequin Véronique Golfier Martine Vercelletto Alexis Brice Benedetta Nacmias Sandro Sorbi Silvia Bagnoli Irene Piaceri Jørgen E Nielsen Lena E Hjermind Matthias Riemenschneider Manuel Mayhaus Bernd Ibach Gilles Gasparoni Sabrina Pichler Wei Gu Martin N Rossor Nick C Fox Jason D Warren Maria Grazia Spillantini Huw R Morris Patrizia Rizzu Peter Heutink Julie S Snowden Sara Rollinson Anna Richardson Alexander Gerhard Amalia C Bruni Raffaele Maletta Francesca Frangipane Chiara Cupidi Livia Bernardi Maria Anfossi Maura Gallo Maria Elena Conidi Nicoletta Smirne Rosa Rademakers Matt Baker Dennis W Dickson Neill R Graff-Radford Ronald C Petersen David Knopman Keith A Josephs Bradley F Boeve Joseph E Parisi William W Seeley Bruce L Miller Anna M Karydas Howard Rosen John C van Swieten Elise G P Dopper Harro Seelaar Yolande A L Pijnenburg Philip Scheltens Giancarlo Logroscino Rosa Capozzo Valeria Novelli Annibale A Puca Massimo Franceschi Alfredo Postiglione Graziella Milan Paolo Sorrentino Mark Kristiansen Huei-Hsin Chiang Caroline Graff Florence Pasquier Adeline Rollin Vincent Deramecourt Florence Lebert Dimitrios Kapogiannis Luigi Ferrucci Stuart Pickering-Brown Andrew B Singleton John Hardy Parastoo Momeni

Lancet Neurol 2014 Jul;13(7):686-99

Laboratory of Neurogenetics, Department of Internal Medicine, Texas Tech University Health Science Center, Lubbock, Texas, USA.

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http://dx.doi.org/10.1016/S1474-4422(14)70065-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112126PMC
July 2014

A novel GRN mutation (GRN c.708+6_+9delTGAG) in frontotemporal lobar degeneration with TDP-43-positive inclusions: clinicopathologic report of 6 cases.

J Neuropathol Exp Neurol 2014 May;73(5):467-73

From the Departments of Pathology (ENB-I, EHB), Psychiatry and Behavioral Science (SW), and Neurology (MM), Northwestern University; Northwestern Cognitive Neurology and Alzheimer Disease Center (SW, MM, EHB); and Rush University Medical Center (JAS), Chicago, Illinois; Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania (ES, SEA, EM-W, VMVD, JQT); Department of Neurology, University of Iowa, Iowa City, Iowa (H-SS); Massachusetts General Hospital, Boston, Massachusetts (BTH, MPF); and Department of Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida (MCB, RR).

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http://dx.doi.org/10.1097/NEN.0000000000000070DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109801PMC
May 2014

Psychosis and hallucinations in frontotemporal dementia with the C9ORF72 mutation: a detailed clinical cohort.

Cogn Behav Neurol 2013 Sep;26(3):146-54

Departments of *Clinical Neurological Sciences and †Pathology, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada ‡Department of Neuroscience, Mayo Clinic, Jacksonville, FL.

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http://dx.doi.org/10.1097/WNN.0000000000000008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090685PMC
September 2013

Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation.

Neuropathology 2013 Apr 18;33(2):122-33. Epub 2012 Jun 18.

Cognitive Neurology and Alzheimer Disease Center, Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA.

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http://dx.doi.org/10.1111/j.1440-1789.2012.01332.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449045PMC
April 2013

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.

Hum Mol Genet 2012 Aug 3;21(15):3500-12. Epub 2012 May 3.

Department of Neurology, University of California, Los Angeles, CA, USA.

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http://dx.doi.org/10.1093/hmg/dds161DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392107PMC
August 2012

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease.

Acta Neuropathol 2009 Nov 9;118(5):605-16. Epub 2009 Aug 9.

Institute of Neuropathology, University Hospital of Zürich, Zurich, Switzerland.

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http://dx.doi.org/10.1007/s00401-009-0581-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864784PMC
November 2009

A new subtype of frontotemporal lobar degeneration with FUS pathology.

Brain 2009 Nov 11;132(Pt 11):2922-31. Epub 2009 Aug 11.

Institute of Neuropathology, University Hospital of Zürich, Zürich, Switzerland.

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http://dx.doi.org/10.1093/brain/awp214DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768659PMC
November 2009

Gene expression study on peripheral blood identifies progranulin mutations.

Ann Neurol 2008 Jul;64(1):92-6

Department of Neurology, Program in Neurogenetics, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA.

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http://doi.wiley.com/10.1002/ana.21397
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http://dx.doi.org/10.1002/ana.21397DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2773201PMC
July 2008

Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions.

Acta Neuropathol 2007 May 7;113(5):601-6. Epub 2006 Dec 7.

Department of Neuroscience, Mayo Clinic College of Medicine, 4500 San Pablo Road, Jacksonville, FL 32224, USA.

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http://dx.doi.org/10.1007/s00401-006-0178-1DOI Listing
May 2007

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

Brain 2006 Nov;129(Pt 11):3081-90

Department of Pathology and Laboratory Medicine, University of British Columbia and Vancouver Coastal Health Vancouver, BC, Canada.

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http://dx.doi.org/10.1093/brain/awl271DOI Listing
November 2006

Characteristics of frontotemporal dementia patients with a Progranulin mutation.

Ann Neurol 2006 Sep;60(3):374-80

Cognitive Neuroscience Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1440, USA.

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http://doi.wiley.com/10.1002/ana.20969
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http://dx.doi.org/10.1002/ana.20969DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987739PMC
September 2006

Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation.

Am J Med Genet B Neuropsychiatr Genet 2004 Feb;125B(1):79-82

Institute of Psychiatry, Section of Old Age Psychiatry, Denmark Hill, London, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.b.20083DOI Listing
February 2004

Familial primary progressive aphasia.

Alzheimer Dis Assoc Disord 2003 Apr-Jun;17(2):106-12

Department of Neurology, Mayo Clinic Jacksonville, Jacksonville, Florida 32224, USA.

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August 2003

A family with a tau P301L mutation presenting with parkinsonism.

Parkinsonism Relat Disord 2002 Dec;9(2):121-3

Department of Neurology, Bronx VA Medical Center, NY 10468, USA.

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December 2002

Ducks in a row. Aligning incentives to improve profitability.

Authors:
Matt Baker

MGMA Connex 2002 Jul;2(6):44-7

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July 2002