Publications Authored by Huei-Hsin Chiang

Confirmation of high frequency of C9orf72 mutations in patients with frontotemporal dementia from Sweden.

Authors:

Linn Öijerstedt Huei-Hsin Chiang Jenny Björkström Charlotte Forsell Lena Lilius Anna-Karin Lindström Håkan Thonberg Caroline Graff

Neurobiol Aging 2019 Mar 27. Epub 2019 Mar 27.

Division for Neurogeriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Karolinska University Hospital, Theme Aging, Unit for Hereditary Dementias QA12, Stockholm, Sweden. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2019.03.009	DOI Listing

March 2019

Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.

Authors:

Håkan Thonberg Huei-Hsin Chiang Lena Lilius Charlotte Forsell Anna-Karin Lindström Charlotte Johansson Jenny Björkström Steinunn Thordardottir Kristel Sleegers Christine Van Broeckhoven Annica Rönnbäck Caroline Graff

Acta Neuropathol Commun 2017 06 9;5(1):43. Epub 2017 Jun 9.

Department NVS, Center for Alzheimer Research, Division for Neurogeriatrics, Karolinska Institutet, Huddinge, Sweden.

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http://dx.doi.org/10.1186/s40478-017-0441-9	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465543	PMC

June 2017

No common founder for C9orf72 expansion mutation in Sweden.

Authors:

Huei-Hsin Chiang Charlotte Forsell Anna-Karin Lindström Lena Lilius Håkan Thonberg Inger Nennesmo Caroline Graff

J Hum Genet 2017 Feb 25;62(2):321-324. Epub 2016 Aug 25.

Department of NVS, Division for Neurogeriatrics, Karolinska Institutet, Center for Alzheimer Research, Huddinge, Sweden.

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http://dx.doi.org/10.1038/jhg.2016.108	DOI Listing

February 2017

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort.

Hum Mutat 2015 Dec 14;36(12):1226-35. Epub 2015 Oct 14.

Neurodegenerative Brain Diseases Group, Department of Molecular Genetics, VIB, Antwerp, Belgium.

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http://dx.doi.org/10.1002/humu.22908	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057316	PMC

December 2015

Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study.

Neurobiol Aging 2015 May 19;36(5):2005.e15-22. Epub 2015 Feb 19.

Department of Molecular Genetics, VIB, Antwerp, Belgium; Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium; Laboratory of Neurochemistry and Behavior, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S01974580150011	Publisher Site
http://dx.doi.org/10.1016/j.neurobiolaging.2015.02.014	DOI Listing

May 2015

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.

Authors:

Julie van der Zee Tim Van Langenhove Gabor G Kovacs Lubina Dillen William Deschamps Sebastiaan Engelborghs Radoslav Matěj Mathieu Vandenbulcke Anne Sieben Bart Dermaut Katrien Smets Philip Van Damme Céline Merlin Annelies Laureys Marleen Van Den Broeck Maria Mattheijssens Karin Peeters Luisa Benussi Giuliano Binetti Roberta Ghidoni Barbara Borroni Alessandro Padovani Silvana Archetti Pau Pastor Cristina Razquin Sara Ortega-Cubero Isabel Hernández Mercè Boada Agustín Ruiz Alexandre de Mendonça Gabriel Miltenberger-Miltényi Frederico Simões do Couto Sandro Sorbi Benedetta Nacmias Silvia Bagnoli Caroline Graff Huei-Hsin Chiang Håkan Thonberg Robert Perneczky Janine Diehl-Schmid Panagiotis Alexopoulos Giovanni B Frisoni Christian Bonvicini Matthis Synofzik Walter Maetzler Jennifer Müller vom Hagen Ludger Schöls Tobias B Haack Tim M Strom Holger Prokisch Oriol Dols-Icardo Jordi Clarimón Alberto Lleó Isabel Santana Maria Rosário Almeida Beatriz Santiago Michael T Heneka Frank Jessen Alfredo Ramirez Raquel Sanchez-Valle Albert Llado Ellen Gelpi Stayko Sarafov Ivailo Tournev Albena Jordanova Eva Parobkova Gian Maria Fabrizi Silvia Testi Eric Salmon Thomas Ströbel Patrick Santens Wim Robberecht Peter De Jonghe Jean-Jacques Martin Patrick Cras Rik Vandenberghe Peter Paul De Deyn Marc Cruts Kristel Sleegers Christine Van Broeckhoven

Acta Neuropathol 2014 Sep 5;128(3):397-410. Epub 2014 Jun 5.

Department of Molecular Genetics, VIB, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00401-014-1298-7	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131163	PMC

September 2014

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)70065-1	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112126	PMC

July 2014

Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.

Authors:

Huei-Hsin Chiang Charlotte Forsell Lena Lilius Linn Öijerstedt Steinunn Thordardottir Krishnan Shanmugarajan Marie Westerlund Inger Nennesmo Håkan Thonberg Caroline Graff

Eur J Hum Genet 2013 Nov 6;21(11):1260-5. Epub 2013 Mar 6.

Department of NVS, Karolinska Institutet, KI-Alzheimer Disease Research Center, Stockholm, Sweden.

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http://www.nature.com/articles/ejhg201337	Publisher Site
http://dx.doi.org/10.1038/ejhg.2013.37	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798842	PMC