S
Stylianos E. Antonarakis
Researcher at University of Geneva
Publications - 758
Citations - 99393
Stylianos E. Antonarakis is an academic researcher from University of Geneva. The author has contributed to research in topics: Gene & Chromosome 21. The author has an hindex of 138, co-authored 746 publications receiving 93605 citations. Previous affiliations of Stylianos E. Antonarakis include Northwestern University & Gujarat University.
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Journal ArticleDOI
Genome-Wide Associations of Gene Expression Variation in Humans
Barbara E. Stranger,Matthew S. Forrest,Andrew G. Clark,Andrew G. Clark,Mark J Minichiello,Samuel Deutsch,Samuel Deutsch,Robert Lyle,Robert Lyle,Sarah E. Hunt,Brenda Kahl,Brenda Kahl,Stylianos E. Antonarakis,Stylianos E. Antonarakis,Simon Tavaré,Simon Tavaré,Simon Tavaré,Panagiotis Deloukas,Emmanouil T. Dermitzakis +18 more
TL;DR: The results suggest that regulatory polymorphism is widespread in the human genome and show that the 5-kb (phase I) HapMap has sufficient density to enable linkage disequilibrium mapping in humans.
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
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
Lu Chen,Lu Chen,Bing Ge,Francesco Paolo Casale,Louella Vasquez,Tony Kwan,Diego Garrido-Martín,Stephen Watt,Ying Yan,Kousik Kundu,Kousik Kundu,Simone Ecker,Avik Datta,David J. Richardson,Frances Burden,Frances Burden,Daniel Mead,Alice L. Mann,José M. Fernández,Sophia Rowlston,Sophia Rowlston,Steven P. Wilder,Samantha Farrow,Samantha Farrow,Xiaojian Shao,John J. Lambourne,Adriana Redensek,Cornelis A. Albers,Vyacheslav Amstislavskiy,Sofie Ashford,Sofie Ashford,Kim Berentsen,Lorenzo Bomba,Guillaume Bourque,David Bujold,Stephan Busche,Maxime Caron,Shu-Huang Chen,Warren A. Cheung,Oliver Delaneau,Emmanouil T. Dermitzakis,Heather Elding,Irina Colgiu,Frederik Otzen Bagger,Frederik Otzen Bagger,Frederik Otzen Bagger,Paul Flicek,Ehsan Habibi,Valentina Iotchkova,Valentina Iotchkova,Eva M. Janssen-Megens,Bowon Kim,Hans Lehrach,Ernesto Lowy,Amit Mandoli,Filomena Matarese,Matthew T. Maurano,John A. Morris,Vera Pancaldi,Farzin Pourfarzad,Karola Rehnström,Karola Rehnström,Augusto Rendon,Thomas Risch,Nilofar Sharifi,Marie-Michelle Simon,Marc Sultan,Alfonso Valencia,Klaudia Walter,Shuang-Yin Wang,Mattia Frontini,Mattia Frontini,Mattia Frontini,Stylianos E. Antonarakis,Laura Clarke,Marie-Laure Yaspo,Stephan Beck,Roderic Guigó,Daniel Rico,Joost H.A. Martens,Willem H. Ouwehand,Taco W. Kuijpers,Taco W. Kuijpers,Dirk S. Paul,Dirk S. Paul,Hendrik G. Stunnenberg,Oliver Stegle,Kate Downes,Kate Downes,Tomi Pastinen,Nicole Soranzo +90 more
TL;DR: High-resolution genetic, epigenetic, and transcriptomic profiling in three major human immune cell types from up to 197 individuals yields insights into cell-type-specific correlation between diverse genomic inputs, more generalizable correlations between these inputs, and defines molecular events that may underpin complex disease risk.
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Genetic structure of Europeans: a view from the North-East
Mari Nelis,Mari Nelis,Tõnu Esko,Tõnu Esko,Reedik Mägi,Fritz Zimprich,Alexander Zimprich,Draga Toncheva,Sena Karachanak,T. Piskackova,Ivan Balascak,Leena Peltonen,Eveliina Jakkula,Karola Rehnström,Mark Lathrop,Mark Lathrop,Simon Heath,Pilar Galan,Stefan Schreiber,Thomas Meitinger,Arne Pfeufer,H-Erich Wichmann,Béla Melegh,Noémi Polgár,Daniela Toniolo,Paolo Gasparini,Pio D'Adamo,Janis Klovins,Liene Nikitina-Zake,Vaidutis Kučinskas,Jūratė Kasnauskienė,Jan Lubinski,Tadeusz Dębniak,Svetlana A. Limborska,Andrey Khrunin,Xavier Estivill,Raquel Rabionet,Sara Marsal,Antonio Julià,Stylianos E. Antonarakis,Samuel Deutsch,Christelle Borel,Homa Attar,Maryline Gagnebin,Milan Macek,Michael Krawczak,Maido Remm,Andres Metspalu,Andres Metspalu +48 more
TL;DR: This analysis revealed that the genetic structure of the European population correlates closely with geography, and allows the creation of a comprehensive European genetic map that will greatly facilitate inter-population genetic studies including genome wide association studies (GWAS).
Journal ArticleDOI
Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.
TL;DR: An effort should be made to discover all common and rare copy number variants (CNVs) in the human population to enable systematic exploration of both SNPs and CNVs in association studies to identify the genomic contributors to the common disorders and complex traits.