Harro Seelaar

Harro Seelaar

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Harro Seelaar

Publications by authors named "Harro Seelaar"

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33Publications

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Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia.

Authors:
Lieke H H Meeter Rebecca M E Steketee Dina Salkovic Maartje E Vos Murray Grossman Corey T McMillan David J Irwin Adam L Boxer Julio C Rojas Nicholas T Olney Anna Karydas Bruce L Miller Yolande A L Pijnenburg Frederik Barkhof Raquel Sánchez-Valle Albert Lladó Sergi Borrego-Ecija Janine Diehl-Schmid Timo Grimmer Oliver Goldhardt Alexander F Santillo Oskar Hansson Susanne Vestberg Barbara Borroni Alessandro Padovani Daniela Galimberti Elio Scarpini Jonathan D Rohrer Ione O C Woollacott Matthis Synofzik Carlo Wilke Alexandre de Mendonca Rik Vandenberghe Luisa Benussi Roberta Ghidoni Giuliano Binetti Wiro J Niessen Janne M Papma Harro Seelaar Lize C Jiskoot Frank Jan de Jong Laura Donker Kaat Marta Del Campo Charlotte E Teunissen Esther E Bron Esther Van den Berg John C Van Swieten

J Neurol Neurosurg Psychiatry 2019 Sep 23;90(9):997-1004. Epub 2019 May 23.

Alzheimer Center and Department of Neurology, Erasmus MC, Rotterdam, The Netherlands

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http://jnnp.bmj.com/lookup/doi/10.1136/jnnp-2018-319784
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http://dx.doi.org/10.1136/jnnp-2018-319784DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820157PMC
September 2019

Three VCP Mutations in Patients with Frontotemporal Dementia.

Authors:
Tsz Hang Wong Cyril Pottier David C Hondius Lieke H H Meeter Jeroen G J van Rooij Shami Melhem Rick van Minkelen Cornelia M van Duijn Annemieke J M Rozemuller Harro Seelaar Rosa Rademakers John C van Swieten

J Alzheimers Dis 2018 ;65(4):1139-1146

Alzheimer center and Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.

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http://dx.doi.org/10.3233/JAD-180301DOI Listing
August 2019

Refining the Spectrum of Neuronal Intranuclear Inclusion Disease: A Case Report.

Authors:
Chiara Cupidi Anke A Dijkstra Shami Melhem Meike W Vernooij Lies-Anne Severijnen Renate K Hukema Annemieke J M Rozemuller Manuela Neumann John C van Swieten Harro Seelaar

J Neuropathol Exp Neurol 2019 Jul;78(7):665-670

Department of Neurology.

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http://dx.doi.org/10.1093/jnen/nlz043DOI Listing
July 2019

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

Novel CSF biomarkers in genetic frontotemporal dementia identified by proteomics.

Authors:
Emma L van der Ende Lieke H Meeter Christoph Stingl Jeroen G J van Rooij Marcel P Stoop Diana A T Nijholt Raquel Sanchez-Valle Caroline Graff Linn Öijerstedt Murray Grossman Corey McMillan Yolande A L Pijnenburg Robert Laforce Giuliano Binetti Luisa Benussi Roberta Ghidoni Theo M Luider Harro Seelaar John C van Swieten

Ann Clin Transl Neurol 2019 Apr 7;6(4):698-707. Epub 2019 Mar 7.

Department of Neurology Erasmus Medical Center PO Box 2040 3015 GD Rotterdam The Netherlands.

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https://onlinelibrary.wiley.com/doi/abs/10.1002/acn3.745
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http://dx.doi.org/10.1002/acn3.745DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469343PMC
April 2019

HR23B pathology preferentially co-localizes with p62, pTDP-43 and poly-GA in C9ORF72-linked frontotemporal dementia and amyotrophic lateral sclerosis.

Authors:
Frederike W Riemslagh Hannes Lans Harro Seelaar Lies-Anne W F M Severijnen Shamiram Melhem Wim Vermeulen Eleonora Aronica R Jeroen Pasterkamp John C van Swieten Rob Willemsen

Acta Neuropathol Commun 2019 03 13;7(1):39. Epub 2019 Mar 13.

Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1186/s40478-019-0694-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416930PMC
March 2019

EIF2AK3 variants in Dutch patients with Alzheimer's disease.

Authors:
Tsz Hang Wong Sven J van der Lee Jeroen G J van Rooij Lieke H H Meeter Petra Frick Shamiram Melhem Harro Seelaar M Arfan Ikram Annemieke J Rozemuller Henne Holstege Marc Hulsman Andre Uitterlinden Manuela Neumann Jeroen J M Hoozemans Cornelia M van Duijn Rosa Rademakers John C van Swieten

Neurobiol Aging 2019 01 24;73:229.e11-229.e18. Epub 2018 Aug 24.

Alzheimer Center and Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands; Alzheimer Center, Department of Neurology, VU University Medical Center, Amsterdam, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2018.08.016DOI Listing
January 2019

Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations.

Authors:
Tsz Hang Wong Harro Seelaar Shamiram Melhem Annemieke J M Rozemuller John C van Swieten

Neurobiol Aging 2019 Jan 29. Epub 2019 Jan 29.

Alzheimer Center and Department of Neurology, Erasmus Medical Center, Rotterdam, the Netherlands; Alzheimer Center and Department of Neurology, VU University Medical Center, Amsterdam, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2019.01.015DOI Listing
January 2019

Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia.

Authors:
David Bergeron Maria L Gorno-Tempini Gil D Rabinovici Miguel A Santos-Santos William Seeley Bruce L Miller Yolande Pijnenburg M Antoinette Keulen Colin Groot Bart N M van Berckel Wiesje M van der Flier Philip Scheltens Jonathan D Rohrer Jason D Warren Jonathan M Schott Nick C Fox Raquel Sanchez-Valle Oriol Grau-Rivera Ellen Gelpi Harro Seelaar Janne M Papma John C van Swieten John R Hodges Cristian E Leyton Olivier Piguet Emily J Rogalski Marsel M Mesulam Lejla Koric Kristensen Nora Jeéreémie Pariente Bradford Dickerson Ian R Mackenzie Ging-Yuek R Hsiung Serge Belliard David J Irwin David A Wolk Murray Grossman Matthew Jones Jennifer Harris David Mann Julie S Snowden Patricio Chrem-Mendez Ismael L Calandri Alejandra A Amengual Carole Miguet-Alfonsi Eloi Magnin Giuseppe Magnani Roberto Santangelo Vincent Deramecourt Florence Pasquier Niklas Mattsson Christer Nilsson Oskar Hansson Julia Keith Mario Masellis Sandra E Black Jordi A Matías-Guiu María-Nieves Cabrera-Martin Claire Paquet Julien Dumurgier Marc Teichmann Marie Sarazin Michel Bottlaender Bruno Dubois Christopher C Rowe Victor L Villemagne Rik Vandenberghe Elias Granadillo Edmond Teng Mario Mendez Philipp T Meyer Lars Frings Alberto Lleó Rafael Blesa Juan Fortea Sang Won Seo Janine Diehl-Schmid Timo Grimmer Kristian Steen Frederiksen Pascual Sánchez-Juan Gaël Chételat Willemijn Jansen Rémi W Bouchard Robert Jr Laforce Pieter Jelle Visser Rik Ossenkoppele

Ann Neurol 2018 11;84(5):729-740

Alzheimer center Amsterdam, Amsterdam UMC, Amsterdam Neuroscience, VU University, Amsterdam, the Netherlands.

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http://dx.doi.org/10.1002/ana.25333DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354051PMC
November 2018

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

Neuropsychiatric Symptoms Complicating the Diagnosis of Alzheimer's Disease: A Case Report.

Authors:
Willem S Eikelboom Jeroen G J van Rooij Esther van den Berg Michiel Coesmans Lize C Jiskoot Ellen Singleton Rik Ossenkoppele John C van Swieten Harro Seelaar Janne M Papma

J Alzheimers Dis 2018 ;66(4):1363-1369

Department of Neurology, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.

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http://dx.doi.org/10.3233/JAD-180700DOI Listing
January 2018

Cerebral blood flow in presymptomatic MAPT and GRN mutation carriers: A longitudinal arterial spin labeling study.

Authors:
Elise G P Dopper Vicky Chalos Eidrees Ghariq Tom den Heijer Anne Hafkemeijer Lize C Jiskoot Inge de Koning Harro Seelaar Rick van Minkelen Matthias J P van Osch Serge A R B Rombouts John C van Swieten

Neuroimage Clin 2016 3;12:460-5. Epub 2016 Aug 3.

Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands; Department of Clinical Genetics, VU Medical Center, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.nicl.2016.08.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011170PMC
November 2017

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

Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia.

Authors:
Elise G P Dopper Serge A R B Rombouts Lize C Jiskoot Tom den Heijer J Roos A de Graaf Inge de Koning Anke R Hammerschlag Harro Seelaar William W Seeley Ilya M Veer Mark A van Buchem Patrizia Rizzu John C van Swieten

Neurology 2014 Jul;83(2):e19-26

From the Departments of Neurology (E.G.P.D., L.C.J., T.d.H., H.S., J.C.v.S.), Epidemiology (T.d.H.), and Neuropsychology (J.R.A.d.G., I.d.K.), Erasmus Medical Center, Rotterdam; Department of Radiology (E.G.P.D., S.A.R.B.R., I.M.V., M.A.v.B.), Leiden University Medical Center; Departments of Neurology (E.G.P.D.) and Clinical Genetics (A.R.H., P.R., J.C.v.S.), VU Medical Center, Amsterdam; Leiden Institute for Brain and Cognition (S.A.R.B.R., I.M.V., M.A.v.B.) and Institute of Psychology (S.A.R.B.R., I.M.V.), Leiden University; Department of Neurology (T.d.H.), Sint Franciscus Gasthuis, Rotterdam, the Netherlands; and Department of Neurology (W.W.S.) and Memory and Aging Center (W.W.S.), University of California, San Francisco.

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http://www.neurology.org/content/early/2013/02/06/WNL.0b013e
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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000058
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http://dx.doi.org/10.1212/WNL.0000000000000583DOI Listing
July 2014

PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology.

Authors:
Tsz Hang Wong Wang Zheng Chiu Guido J Breedveld Ka Wan Li Annemieke J M H Verkerk David Hondius Renate K Hukema Harro Seelaar Petra Frick Lies-Anne Severijnen Gert-Jan Lammers Joyce H G Lebbink Sjoerd G van Duinen Wouter Kamphorst Annemieke J Rozemuller E Bert Bakker Manuela Neumann Rob Willemsen Vincenzo Bonifati August B Smit John van Swieten

Brain 2014 May 9;137(Pt 5):1361-73. Epub 2014 Apr 9.

1 Department of Neurology, Erasmus Medical Centre, 3015 CE Rotterdam, The Netherlands.

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http://dx.doi.org/10.1093/brain/awu067DOI Listing
May 2014

Episodic memory impairment in frontotemporal dementia; a ⁹⁹mTc- HMPAO SPECT study.

Authors:
Janne M Papma Harro Seelaar Inge de Koning Djo Hasan Ambroos Reijs Roelf Valkema Niels D Prins John C van Swieten

Curr Alzheimer Res 2013 Mar;10(3):332-9

Department of Neurology, Erasmus MC - University Medical Center, Rotterdam, The Netherlands.

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http://dx.doi.org/10.2174/1567205011310030013DOI Listing
March 2013

Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia.

Authors:
Elise G P Dopper Serge A R B Rombouts Lize C Jiskoot Tom den Heijer J Roos A de Graaf Inge de Koning Anke R Hammerschlag Harro Seelaar William W Seeley Ilya M Veer Mark A van Buchem Patrizia Rizzu John C van Swieten

Neurology 2013 Feb 6;80(9):814-23. Epub 2013 Feb 6.

Department of Neurology, Erasmus Medical Center, Rotterdam, the Netherlands.

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http://www.neurology.org/content/early/2013/02/06/WNL.0b013e
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http://www.neurology.org/cgi/doi/10.1212/WNL.0b013e31828407b
Publisher Site
http://dx.doi.org/10.1212/WNL.0b013e31828407bcDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598452PMC
February 2013

Midcingulate involvement in progressive supranuclear palsy and tau positive frontotemporal dementia.

Authors:
Wang Zheng Chiu Janne M Papma Inge de Koning Laura Donker Kaat Harro Seelaar Ambroos E M Reijs Roelf Valkema Djo Hasan Agnita J W Boon John Cornelis van Swieten

J Neurol Neurosurg Psychiatry 2012 Sep 25;83(9):910-5. Epub 2012 Jun 25.

Department of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1136/jnnp-2011-302035DOI Listing
September 2012

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

Authors:
Javier Simón-Sánchez Elise G P Dopper Petra E Cohn-Hokke Renate K Hukema Nayia Nicolaou Harro Seelaar J Roos A de Graaf Inge de Koning Natasja M van Schoor Dorly J H Deeg Marion Smits Joost Raaphorst Leonard H van den Berg Helenius J Schelhaas Christine E M De Die-Smulders Danielle Majoor-Krakauer Annemieke J M Rozemuller Rob Willemsen Yolande A L Pijnenburg Peter Heutink John C van Swieten

Brain 2012 Mar 1;135(Pt 3):723-35. Epub 2012 Feb 1.

Department of Clinical Genetics, VU University Medical Centre, 1007 MB Amsterdam, The Netherlands.

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http://dx.doi.org/10.1093/brain/awr353DOI Listing
March 2012

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.

Authors:
Elise G P Dopper Harro Seelaar Wang Zheng Chiu Inge de Koning Rick van Minkelen Matthew C Baker Annemieke J M Rozemuller Rosa Rademakers John C van Swieten

J Mol Neurosci 2011 Nov 24;45(3):354-8. Epub 2011 Aug 24.

Department of Neurology, Erasmus Medical Center, 's-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands.

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http://link.springer.com/10.1007/s12031-011-9626-z
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http://dx.doi.org/10.1007/s12031-011-9626-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207131PMC
November 2011

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.

Authors:
Alan E Renton Elisa Majounie Adrian Waite Javier Simón-Sánchez Sara Rollinson J Raphael Gibbs Jennifer C Schymick Hannu Laaksovirta John C van Swieten Liisa Myllykangas Hannu Kalimo Anders Paetau Yevgeniya Abramzon Anne M Remes Alice Kaganovich Sonja W Scholz Jamie Duckworth Jinhui Ding Daniel W Harmer Dena G Hernandez Janel O Johnson Kin Mok Mina Ryten Danyah Trabzuni Rita J Guerreiro Richard W Orrell James Neal Alex Murray Justin Pearson Iris E Jansen David Sondervan Harro Seelaar Derek Blake Kate Young Nicola Halliwell Janis Bennion Callister Greg Toulson Anna Richardson Alex Gerhard Julie Snowden David Mann David Neary Michael A Nalls Terhi Peuralinna Lilja Jansson Veli-Matti Isoviita Anna-Lotta Kaivorinne Maarit Hölttä-Vuori Elina Ikonen Raimo Sulkava Michael Benatar Joanne Wuu Adriano Chiò Gabriella Restagno Giuseppe Borghero Mario Sabatelli David Heckerman Ekaterina Rogaeva Lorne Zinman Jeffrey D Rothstein Michael Sendtner Carsten Drepper Evan E Eichler Can Alkan Ziedulla Abdullaev Svetlana D Pack Amalia Dutra Evgenia Pak John Hardy Andrew Singleton Nigel M Williams Peter Heutink Stuart Pickering-Brown Huw R Morris Pentti J Tienari Bryan J Traynor

Neuron 2011 Oct 21;72(2):257-68. Epub 2011 Sep 21.

Neuromuscular Diseases Research Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.neuron.2011.09.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200438PMC
October 2011

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia.

Authors:
Katya Rascovsky John R Hodges David Knopman Mario F Mendez Joel H Kramer John Neuhaus John C van Swieten Harro Seelaar Elise G P Dopper Chiadi U Onyike Argye E Hillis Keith A Josephs Bradley F Boeve Andrew Kertesz William W Seeley Katherine P Rankin Julene K Johnson Maria-Luisa Gorno-Tempini Howard Rosen Caroline E Prioleau-Latham Albert Lee Christopher M Kipps Patricia Lillo Olivier Piguet Jonathan D Rohrer Martin N Rossor Jason D Warren Nick C Fox Douglas Galasko David P Salmon Sandra E Black Marsel Mesulam Sandra Weintraub Brad C Dickerson Janine Diehl-Schmid Florence Pasquier Vincent Deramecourt Florence Lebert Yolande Pijnenburg Tiffany W Chow Facundo Manes Jordan Grafman Stefano F Cappa Morris Freedman Murray Grossman Bruce L Miller

Brain 2011 Sep 2;134(Pt 9):2456-77. Epub 2011 Aug 2.

Department of Neurology, Perelman School of Medicine, University of Pennsylvania, 3400 Spruce Street, 3 West Gates, Philadelphia, PA 19104, USA.

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http://brain.oxfordjournals.org/content/brain/134/9/2456.ful
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http://www.brain.oxfordjournals.org/cgi/doi/10.1093/brain/aw
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http://dx.doi.org/10.1093/brain/awr179DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170532PMC
September 2011

Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review.

Authors:
Harro Seelaar Jonathan D Rohrer Yolande A L Pijnenburg Nick C Fox John C van Swieten

J Neurol Neurosurg Psychiatry 2011 May 22;82(5):476-86. Epub 2010 Oct 22.

Department of Neurology, Erasmus MC - University Medical Centre Rotterdam, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1136/jnnp.2010.212225DOI Listing
May 2011

Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders.

Authors:
Tibor Hortobágyi Claire Troakes Agnes L Nishimura Caroline Vance John C van Swieten Harro Seelaar Andrew King Safa Al-Sarraj Boris Rogelj Christopher E Shaw

Acta Neuropathol 2011 Apr 1;121(4):519-27. Epub 2011 Mar 1.

Department of Clinical Neuroscience, King's College London, MRC Centre for Neurodegeneration Research, Institute of Psychiatry, De Crespigny Park, London SE58AF, UK.

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http://dx.doi.org/10.1007/s00401-011-0813-3DOI Listing
April 2011

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.

Authors:
Alice S Chen-Plotkin Maria Martinez-Lage Patrick M A Sleiman William Hu Robert Greene Elisabeth McCarty Wood Shaoxu Bing Murray Grossman Gerard D Schellenberg Kimmo J Hatanpaa Myron F Weiner Charles L White William S Brooks Glenda M Halliday Jillian J Kril Marla Gearing Thomas G Beach Neill R Graff-Radford Dennis W Dickson Rosa Rademakers Bradley F Boeve Stuart M Pickering-Brown Julie Snowden John C van Swieten Peter Heutink Harro Seelaar Jill R Murrell Bernardino Ghetti Salvatore Spina Jordan Grafman Jeffrey A Kaye Randall L Woltjer Marsel Mesulam Eileen Bigio Albert Lladó Bruce L Miller Ainhoa Alzualde Fermin Moreno Jonathan D Rohrer Ian R A Mackenzie Howard H Feldman Ronald L Hamilton Marc Cruts Sebastiaan Engelborghs Peter P De Deyn Christine Van Broeckhoven Thomas D Bird Nigel J Cairns Allison Goate Matthew P Frosch Peter F Riederer Nenad Bogdanovic Virginia M Y Lee John Q Trojanowski Vivianna M Van Deerlin

Arch Neurol 2011 Apr;68(4):488-97

Center for Neurodegenerative Disease Research, Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, 19104, USA.

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http://dx.doi.org/10.1001/archneurol.2011.53DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160280PMC
April 2011

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.

Authors:
Hazel Urwin Keith A Josephs Jonathan D Rohrer Ian R Mackenzie Manuela Neumann Astrid Authier Harro Seelaar John C Van Swieten Jeremy M Brown Peter Johannsen Jorgen E Nielsen Ida E Holm Dennis W Dickson Rosa Rademakers Neill R Graff-Radford Joseph E Parisi Ronald C Petersen Kimmo J Hatanpaa Charles L White Myron F Weiner Felix Geser Vivianna M Van Deerlin John Q Trojanowski Bruce L Miller William W Seeley Julie van der Zee Samir Kumar-Singh Sebastiaan Engelborghs Peter P De Deyn Christine Van Broeckhoven Eileen H Bigio Han-Xiang Deng Glenda M Halliday Jillian J Kril David G Munoz David M Mann Stuart M Pickering-Brown Valerie Doodeman Gary Adamson Shabnam Ghazi-Noori Elizabeth M C Fisher Janice L Holton Tamas Revesz Martin N Rossor John Collinge Simon Mead Adrian M Isaacs

Acta Neuropathol 2010 Jul 20;120(1):33-41. Epub 2010 May 20.

UCL Institute of Neurology, London, UK.

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http://dx.doi.org/10.1007/s00401-010-0698-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887939PMC
July 2010

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration.

Authors:
Harro Seelaar Kirsten Y Klijnsma Inge de Koning Aad van der Lugt Wang Zheng Chiu Asma Azmani Annemieke J M Rozemuller John C van Swieten

J Neurol 2010 May 28;257(5):747-53. Epub 2009 Nov 28.

Department of Neurology, Erasmus MC, University Medical Center Rotterdam, Room Hs 611, s-Gravendijkwal 230, 3015 CE Rotterdam, The Netherlands.

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http://dx.doi.org/10.1007/s00415-009-5404-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864899PMC
May 2010

Survival in progressive supranuclear palsy and frontotemporal dementia.

Authors:
Wang Zheng Chiu L D Kaat Harro Seelaar Sonia M Rosso Agnita Jw Boon Wouter Kamphorst John C van Swieten

J Neurol Neurosurg Psychiatry 2010 Apr;81(4):441-5

Department of Neurology, Erasmus University Medical Centre Rotterdam, Room Hs 611, 's-Gravendijkwal 230, 3015 CE Rotterdam, The Netherlands.

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http://dx.doi.org/10.1136/jnnp.2009.195719DOI Listing
April 2010

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.

Authors:
Vivianna M Van Deerlin Patrick M A Sleiman Maria Martinez-Lage Alice Chen-Plotkin Li-San Wang Neill R Graff-Radford Dennis W Dickson Rosa Rademakers Bradley F Boeve Murray Grossman Steven E Arnold David M A Mann Stuart M Pickering-Brown Harro Seelaar Peter Heutink John C van Swieten Jill R Murrell Bernardino Ghetti Salvatore Spina Jordan Grafman John Hodges Maria Grazia Spillantini Sid Gilman Andrew P Lieberman Jeffrey A Kaye Randall L Woltjer Eileen H Bigio Marsel Mesulam Safa Al-Sarraj Claire Troakes Roger N Rosenberg Charles L White Isidro Ferrer Albert Lladó Manuela Neumann Hans A Kretzschmar Christine Marie Hulette Kathleen A Welsh-Bohmer Bruce L Miller Ainhoa Alzualde Adolfo Lopez de Munain Ann C McKee Marla Gearing Allan I Levey James J Lah John Hardy Jonathan D Rohrer Tammaryn Lashley Ian R A Mackenzie Howard H Feldman Ronald L Hamilton Steven T Dekosky Julie van der Zee Samir Kumar-Singh Christine Van Broeckhoven Richard Mayeux Jean Paul G Vonsattel Juan C Troncoso Jillian J Kril John B J Kwok Glenda M Halliday Thomas D Bird Paul G Ince Pamela J Shaw Nigel J Cairns John C Morris Catriona Ann McLean Charles DeCarli William G Ellis Stefanie H Freeman Matthew P Frosch John H Growdon Daniel P Perl Mary Sano David A Bennett Julie A Schneider Thomas G Beach Eric M Reiman Bryan K Woodruff Jeffrey Cummings Harry V Vinters Carol A Miller Helena C Chui Irina Alafuzoff Päivi Hartikainen Danielle Seilhean Douglas Galasko Eliezer Masliah Carl W Cotman M Teresa Tuñón M Cristina Caballero Martínez David G Munoz Steven L Carroll Daniel Marson Peter F Riederer Nenad Bogdanovic Gerard D Schellenberg Hakon Hakonarson John Q Trojanowski Virginia M-Y Lee

Nat Genet 2010 Mar 14;42(3):234-9. Epub 2010 Feb 14.

[1] Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA. [2] These authors contributed equally to this work.

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http://dx.doi.org/10.1038/ng.536DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828525PMC
March 2010

Survival profiles of patients with frontotemporal dementia and motor neuron disease.

Authors:
William T Hu Harro Seelaar Keith A Josephs David S Knopman Bradley F Boeve Eric J Sorenson Leo McCluskey Lauren Elman Helenius J Schelhaas Joseph E Parisi Benno Kuesters Virginia M-Y Lee John Q Trojanowski Ronald C Petersen John C van Swieten Murray Grossman

Arch Neurol 2009 Nov;66(11):1359-64

Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.

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http://dx.doi.org/10.1001/archneurol.2009.253DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881327PMC
November 2009

Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population.

Authors:
Javier Simón-Sánchez Harro Seelaar Zoltán Bochdanovits Dorly J H Deeg John C van Swieten Peter Heutink

PLoS One 2009 Oct 22;4(10):e7494. Epub 2009 Oct 22.

Department of Clinical Genetics, Section of Medical Genomics, VU University Medical Centre, Amsterdam, The Netherlands.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0007494PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2761542PMC
October 2009

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.

Authors:
Harro Seelaar H Jurgen Schelhaas Asma Azmani Benno Küsters Sonia Rosso Danielle Majoor-Krakauer Maarten C de Rijk Patrizia Rizzu Ming ten Brummelhuis Pieter A van Doorn Wouter Kamphorst Rob Willemsen John C van Swieten

Brain 2007 May 14;130(Pt 5):1375-85. Epub 2007 Mar 14.

Department of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.

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https://academic.oup.com/brain/article-lookup/doi/10.1093/br
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http://dx.doi.org/10.1093/brain/awm024DOI Listing
May 2007

Progranulin mutations in Dutch familial frontotemporal lobar degeneration.

Authors:
Iraad F Bronner Patrizia Rizzu Harro Seelaar Saskia E van Mil Burcu Anar Asma Azmani Laura Donker Kaat Sonia Rosso Peter Heutink John C van Swieten

Eur J Hum Genet 2007 Mar 17;15(3):369-74. Epub 2007 Jan 17.

Department of Human Genetics, Section Medical Genomics, VU University Medical Center and VU University, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1038/sj.ejhg.5201772DOI Listing
March 2007