L
Lilia I. Abramova
Researcher at Russian Academy
Publications - 88
Citations - 3633
Lilia I. Abramova is an academic researcher from Russian Academy. The author has contributed to research in topics: Schizophrenia & Genotype. The author has an hindex of 17, co-authored 87 publications receiving 3430 citations.
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Journal ArticleDOI
Common variants conferring risk of schizophrenia
Hreinn Stefansson,Hreinn Stefansson,Roel A. Ophoff,Roel A. Ophoff,Roel A. Ophoff,Stacy Steinberg,Stacy Steinberg,Ole A. Andreassen,Sven Cichon,Dan Rujescu,Thomas Werge,Olli Pietilainen,Ole Mors,Preben Bo Mortensen,Engilbert Sigurdsson,Omar Gustafsson,Mette Nyegaard,Annamari Tuulio-Henriksson,Andres Ingason,Thomas Hansen,Jaana Suvisaari,Jouko Lönnqvist,Tiina Paunio,Anders D. Børglum,Anders D. Børglum,Annette M. Hartmann,Anders Fink-Jensen,Merete Nordentoft,David M. Hougaard,Bent Nørgaard-Pedersen,Yvonne Böttcher,Jes Olesen,René Breuer,Hans-Jürgen Möller,Ina Giegling,Henrik B. Rasmussen,Sally Timm,Manuel Mattheisen,István Bitter,János Réthelyi,Brynja B. Magnusdottir,Thordur Sigmundsson,Pall I. Olason,Gisli Masson,Jeffrey R. Gulcher,Magnús Haraldsson,Ragnheidur Fossdal,Thorgeir E. Thorgeirsson,Unnur Thorsteinsdottir,Unnur Thorsteinsdottir,Mirella Ruggeri,Sarah Tosato,Barbara Franke,Eric Strengman,Lambertus A. Kiemeney,Ingrid Melle,Srdjan Djurovic,Lilia I. Abramova,Kaleda Vg,Julio Sanjuán,Rosa de Frutos,Elvira Bramon,Evangelos Vassos,Gillian Fraser,Ulrich Ettinger,Marco Picchioni,Nicholas Walker,T. Toulopoulou,Anna C. Need,Dongliang Ge,Joeng Lim Yoon,Kevin V. Shianna,Nelson B. Freimer,Rita M. Cantor,Robin M. Murray,Augustine Kong,Vera Golimbet,Angel Carracedo,Celso Arango,Javier Costas,Erik G. Jönsson,Lars Terenius,Ingrid Agartz,Hannes Petursson,Markus M. Nöthen,Marcella Rietschel,Paul M. Matthews,Pierandrea Muglia,Leena Peltonen,David St Clair,David Goldstein,Kari Stefansson,Kari Stefansson,David A. Collier,David A. Collier +94 more
TL;DR: Findings implicating the MHC region are consistent with an immune component to schizophrenia risk, whereas the association with NRGN and TCF4 points to perturbation of pathways involved in brain development, memory and cognition.
Journal ArticleDOI
Genome-wide association study reveals two new risk loci for bipolar disorder
Thomas W. Mühleisen,Thomas W. Mühleisen,Markus Leber,Markus Leber,Thomas G. Schulze,Jana Strohmaier,Franziska Degenhardt,Jens Treutlein,Manuel Mattheisen,Manuel Mattheisen,Andreas J. Forstner,Johannes Schumacher,René Breuer,Sandra Meier,Stefan Herms,Stefan Herms,Per Hoffmann,André Lacour,Stephanie H. Witt,Andreas Reif,Bertram Müller-Myhsok,Bertram Müller-Myhsok,Susanne Lucae,Wolfgang Maier,M.P. Schwarz,Helmut Vedder,Jutta Kammerer-Ciernioch,Andrea Pfennig,Michael Bauer,Martin Hautzinger,Susanne Moebus,Lutz Priebe,Piotr M. Czerski,Joanna Hauser,Jolanta Lissowska,Neonila Szeszenia-Dabrowska,Paul Brennan,James McKay,Adam Wright,Adam Wright,Philip B. Mitchell,Philip B. Mitchell,Janice M. Fullerton,Janice M. Fullerton,Peter R. Schofield,Peter R. Schofield,Grant W. Montgomery,Sarah E. Medland,Scott D. Gordon,Nicholas G. Martin,Valery Krasnow,Alexander Chuchalin,Gulja Babadjanova,Galina Pantelejeva,Lilia I. Abramova,Alexander S. Tiganov,Alexey Polonikov,Elza Khusnutdinova,Martin Alda,Paul Grof,Guy A. Rouleau,Gustavo Turecki,Catherine Laprise,Fabio Rivas,Fermín Mayoral,Manolis Kogevinas,Maria Grigoroiu-Serbanescu,Peter Propping,Tim Becker,Tim Becker,Marcella Rietschel,Markus M. Nöthen,Sven Cichon +72 more
TL;DR: Results from the largest BD GWAS to date are presented by investigating 2.3 million single-nucleotide polymorphisms (SNPs) in a sample of 24,025 patients and controls and detecting 56 genome-wide significant SNPs in five chromosomal regions including previously reported risk loci ANK3, ODZ4 and TRANK1.
Journal ArticleDOI
Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder
Sven Cichon,Thomas W. Mühleisen,Franziska Degenhardt,Manuel Mattheisen,Xavier Miró,Jana Strohmaier,Michael Steffens,Christian Meesters,Stefan Herms,Moritz Weingarten,Lutz Priebe,Britta Haenisch,Michael Alexander,Jennifer Vollmer,René Breuer,Christine Schmäl,Peter Tessmann,Susanne Moebus,H.-Erich Wichmann,Stefan Schreiber,Bertram Müller-Myhsok,Susanne Lucae,Stéphane Jamain,Stéphane Jamain,Marion Leboyer,Marion Leboyer,Frank Bellivier,Frank Bellivier,Bruno Etain,Bruno Etain,Chantal Henry,Chantal Henry,Jean-Pierre Kahn,Simon Heath,Marian L. Hamshere,Michael Conlon O'Donovan,Michael John Owen,Nicholas John Craddock,Markus J. Schwarz,Helmut Vedder,Jutta Kammerer-Ciernioch,Andreas Reif,Johanna Sasse,Michael Bauer,Martin Hautzinger,Adam Wright,Adam Wright,Philip B. Mitchell,Philip B. Mitchell,Peter R. Schofield,Peter R. Schofield,Grant W. Montgomery,Sarah E. Medland,Scott D. Gordon,Nicholas G. Martin,Omar Gustafsson,Ole A. Andreassen,Ole A. Andreassen,Srdjan Djurovic,Srdjan Djurovic,Engilbert Sigurdsson,Stacy Steinberg,Hreinn Stefansson,Kari Stefansson,Kari Stefansson,Lejla Kapur-Pojskić,Liliana Oruc,Fabio Rivas,Fermín Mayoral,Alexander Chuchalin,Gulja Babadjanova,Alexander S. Tiganov,Galina Pantelejeva,Lilia I. Abramova,Maria Grigoroiu-Serbanescu,Carmen C. Diaconu,Piotr M. Czerski,Joanna Hauser,Andreas Zimmer,Mark Lathrop,Thomas G. Schulze,Thomas F. Wienker,Johannes Schumacher,Wolfgang Maier,Peter Propping,Marcella Rietschel,Markus M. Nöthen +86 more
TL;DR: Evidence is provided that NCAN encodes neurocan, an extracellular matrix glycoprotein, which is thought to be involved in cell adhesion and migration, and expression in mice is localized within cortical and hippocampal areas.
Journal ArticleDOI
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Stacy Steinberg,Simone de Jong,Ole A. Andreassen,Thomas Werge,Anders D. Børglum,Ole Mors,Preben Bo Mortensen,Omar Gustafsson,Omar Gustafsson,Javier Costas,Olli Pietilainen,Ditte Demontis,Sergi Papiol,Johanna Huttenlocher,Manuel Mattheisen,René Breuer,Evangelos Vassos,Ina Giegling,Gillian Fraser,Nicholas Walker,Annamari Tuulio-Henriksson,Jaana Suvisaari,Jouko Lönnqvist,Tiina Paunio,Ingrid Agartz,Ingrid Melle,Srdjan Djurovic,Eric Strengman,Gesche Jürgens,Birte Glenthøj,Lars Terenius,David M. Hougaard,Torben F. Ørntoft,Carsten Wiuf,Michael Didriksen,Mads V. Hollegaard,Merete Nordentoft,Ruud van Winkel,Gunter Kenis,Lilia I. Abramova,Kaleda Vg,Manuel Arrojo,Julio Sanjuán,Celso Arango,Swetlana Sperling,Moritz J. Rossner,Michele Ribolsi,Valentina Magni,Alberto Siracusano,Claus Christiansen,Lambertus A. Kiemeney,Jan H. Veldink,Leonard H. van den Berg,Andres Ingason,Pierandrea Muglia,Robin M. Murray,Markus M. Nöthen,Engilbert Sigurdsson,Hannes Petursson,Unnur Thorsteinsdottir,Augustine Kong,I. Alex Rubino,Marc De Hert,János Réthelyi,István Bitter,Erik G. Jönsson,Vera Golimbet,Angel Carracedo,Hannelore Ehrenreich,Nicholas John Craddock,Michael John Owen,Michael Conlon O'Donovan,Mirella Ruggeri,Sarah Tosato,Leena Peltonen,Roel A. Ophoff,David A. Collier,David St Clair,Marcella Rietschel,Sven Cichon,Hreinn Stefansson,Dan Rujescu,Kari Stefansson +82 more
TL;DR: An expanded set of variants in the major histocompatibility complex region, near neurogranin (NRGN) and in an intron of transcription factor 4 (TCF4), and two novel variants showing genome-wide significant association are found.
Journal ArticleDOI
Expanding the range of ZNF804A variants conferring risk of psychosis
Stacy Steinberg,Ole Mors,Anders D. Børglum,Anders D. Børglum,Omar Gustafsson,Omar Gustafsson,Thomas Werge,Preben Bo Mortensen,Ole A. Andreassen,Engilbert Sigurdsson,Thorgeir E. Thorgeirsson,Yvonne Böttcher,Pall I. Olason,Roel A. Ophoff,Roel A. Ophoff,Sven Cichon,Iris H Gudjonsdottir,Olli Pietiläinen,Olli Pietiläinen,Mette Nyegaard,Annamari Tuulio-Henriksson,Andres Ingason,Thomas Hansen,Lavinia Athanasiu,Jaana Suvisaari,Jan-Erik Lönnqvist,Tiina Paunio,Annette M. Hartmann,Gesche Jürgens,Merete Nordentoft,David M. Hougaard,Bent Nørgaard-Pedersen,René Breuer,H.-J. Möller,Ina Giegling,Birte Glenthøj,Henrik B. Rasmussen,M. Mattheisen,István Bitter,János Réthelyi,Thordur Sigmundsson,Ragnheidur Fossdal,Unnur Thorsteinsdottir,Unnur Thorsteinsdottir,Mirella Ruggeri,Sarah Tosato,Eric Strengman,Lambertus A. Kiemeney,Ingrid Melle,Srdjan Djurovic,Lilia I. Abramova,Kaleda Vg,Muriel Walshe,Elvira Bramon,Evangelos Vassos,Tao Li,Tao Li,Gillian Fraser,Neil Walker,Timothea Toulopoulou,J. Yoon,Nelson B. Freimer,Rita M. Cantor,Robin M. Murray,Augustine Kong,Vera Golimbet,Erik G. Jönsson,Lars Terenius,Ingrid Agartz,Hannes Petursson,Markus M. Nöthen,M. Rietschel,Leena Peltonen,Leena Peltonen,Dan Rujescu,David A. Collier,David A. Collier,Hreinn Stefansson,D St Clair,Kari Stefansson,Kari Stefansson +80 more
TL;DR: As it has been proposed that variants such as rs1344706[T]—common and with low relative risk—may also serve to identify regions harboring less common, higher-risk susceptibility alleles, ZNF804A is searched for large copy number variants (CNVs) in psychosis patients and patients with other psychiatric disorders and 39 481 controls.