J
Jean-Louis Blouin
Researcher at University of Geneva
Publications - 114
Citations - 7948
Jean-Louis Blouin is an academic researcher from University of Geneva. The author has contributed to research in topics: Chromosome 21 & Primary ciliary dyskinesia. The author has an hindex of 43, co-authored 106 publications receiving 7651 citations. Previous affiliations of Jean-Louis Blouin include Geneva College & Johns Hopkins University School of Medicine.
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Journal ArticleDOI
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
Cathryn M. Lewis,Douglas F. Levinson,Lesley H. Wise,Lynn E. DeLisi,Richard E. Straub,Iiris Hovatta,Nigel Williams,Sibylle G. Schwab,Ann E. Pulver,Stephen V. Faraone,Linda M. Brzustowicz,Linda M. Brzustowicz,Charles A. Kaufmann,David L. Garver,Hugh Gurling,Eva Lindholm,Hilary Coon,Hans W. Moises,William Byerley,Sarah H. Shaw,Andrea Mesén,Robin Sherrington,F. Anthony O'Neill,Dermot Walsh,Kenneth S. Kendler,Jesper Ekelund,Tiina Paunio,Jouko Lönnqvist,Leena Peltonen,Leena Peltonen,Michael Conlon O'Donovan,Michael John Owen,Dieter B. Wildenauer,Wolfgang Maier,Gerald Nestadt,Jean-Louis Blouin,Stylianos E. Antonarakis,Bryan J. Mowry,Jeremy M. Silverman,Raymond R. Crowe,C. Robert Cloninger,Ming T. Tsuang,Dolores Malaspina,Jill M. Harkavy-Friedman,Dragan M. Svrakic,Anne S. Bassett,Jennifer A. Holcomb,Gursharan Kalsi,Andrew McQuillin,Jon Brynjolfson,Thordur Sigmundsson,Hannes Petursson,Elena Jazin,Tómas Zoega,Tómas Helgason +54 more
TL;DR: The GSMA produced significant genomewide evidence for linkage on chromosome 2q and suggests that some or all of these regions contain loci that increase susceptibility to schizophrenia in diverse populations.
Journal ArticleDOI
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
Ricardo Segurado,Sevilla D. Detera-Wadleigh,Douglas F. Levinson,Cathryn M. Lewis,Michael Gill,John I. Nurnberger,Nicholas John Craddock,J. Raymond DePaulo,Miron Baron,Elliot S. Gershon,Jenny Ekholm,Sven Cichon,Gustavo Turecki,Stephan Claes,John R. Kelsoe,Peter R. Schofield,Renee F. Badenhop,Renee F. Badenhop,Jean Morissette,Hilary Coon,Douglas Blackwood,L. Alison McInnes,Tatiana Foroud,Howard J. Edenberg,Theodore Reich,John P. Rice,Alison Goate,Melvin G. McInnis,Francis J. McMahon,Judith A. Badner,Lynn R. Goldin,Phil Bennett,Virginia L. Willour,Peter P. Zandi,Jianjun Liu,Conrad T. Gilliam,S H Juo,Wade H. Berrettini,Takeo Yoshikawa,Leena Peltonen,Leena Peltonen,Jouko Lönnqvist,Markus M. Nöthen,Johannes Schumacher,Christine Windemuth,Marcella Rietschel,Peter Propping,Wolfgang Maier,Martin Alda,Paul Grof,Guy A. Rouleau,Jurgen Del-Favero,Christine Van Broeckhoven,Julien Mendlewicz,Rolf Adolfsson,M. Anne Spence,Hermann Luebbert,L. J. Adams,Jennifer A. Donald,Philip B. Mitchell,Nicholas Barden,Eric Shink,William Byerley,Walter J. Muir,Peter M. Visscher,Stuart MacGregor,Hugh Gurling,Gursharan Kalsi,Andrew McQuillin,Michael Escamilla,Victor I. Reus,Pedro León,Nelson B. Freimer,Henrik Ewald,Torben A Kruse,Ole Mors,Uppala Radhakrishna,Jean-Louis Blouin,Stylianos E. Antonarakis,Nurten A. Akarsu +79 more
TL;DR: The present results for the very narrow model are promising but suggest that more and larger data sets are needed to support linkage, as well as suggest that linkage might be detected in certain populations or subsets of pedigrees.
Journal ArticleDOI
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
Jean-Louis Blouin,Beth A. Dombroski,Swapan K. Nath,Virginia K. Lasseter,Paula S. Wolyniec,Gerald Nestadt,Mary H. Thornquist,Gail Ullrich,John J. McGrath,Laura Kasch,Malgorzata Lamacz,Marion Thomas,Corinne Gehrig,Uppala Radhakrishna,Sarah E. Snyder,Katherine G. Balk,Karin J. Neufeld,Karen Swartz,Nicola DeMarchi,George N. Papadimitriou,Dimitris Dikeos,Costas N. Stefanis,Aravinda Chakravarti,Barton Childs,David E. Housman,Haig H. Kazazian,Stylianos E. Antonarakis,Ann E. Pulver +27 more
TL;DR: A genome-wide scan for schizophrenia susceptibility loci (SSL) using 452 microsatellite markers on 54 multiplex pedigrees is presented and it is more probable that chromosome 8 may be a false positive linkage.
Journal ArticleDOI
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia
Lucia Bartoloni,Jean-Louis Blouin,Yanzhen Pan,Corinne Gehrig,Amit K. Maiti,Nathalie Scamuffa,Colette Rossier,Mark Jorissen,Miguel Armengot,M Meeks,Hannah M. Mitchison,Eddie M. K. Chung,C. D. DeLozier-Blanchet,William J. Craigen,Stylianos E. Antonarakis +14 more
TL;DR: It is concluded that mutations in the coding region of DNAH11 account for situs inversus totalis and probably a minority of cases of PCD.
Journal ArticleDOI
DNAH5 Mutations Are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects
Nada Hornef,Heike Olbrich,Judit Horvath,Maimoona B Zariwala,Manfred Fliegauf,Niki T. Loges,Johannes H. Wildhaber,Peadar G. Noone,Marcus P. Kennedy,Stylianos E. Antonarakis,Jean-Louis Blouin,Lucia Bartoloni,Thomas Nüsslein,Peter Ahrens,Matthias Griese,Heiner Kuhl,Ralf Sudbrak,Michael R. Knowles,Richard Reinhardt,Heymut Omran +19 more
TL;DR: DNAH5 is frequently mutated in patients with PCD exhibiting outer dynein arm defects and mutations cluster in five exons.