Alexey Vedernikov

ORCID: 0009-0002-1297-5035
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About
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Research Areas
  • Genetic Associations and Epidemiology
  • Parkinson's Disease Mechanisms and Treatments
  • Bioinformatics and Genomic Networks
  • Nuclear Receptors and Signaling
  • Genetics and Neurodevelopmental Disorders
  • T-cell and B-cell Immunology
  • Neurological diseases and metabolism
  • MicroRNA in disease regulation
  • Alzheimer's disease research and treatments
  • Bipolar Disorder and Treatment
  • Tryptophan and brain disorders
  • Immune responses and vaccinations
  • Immunotherapy and Immune Responses
  • Pharmaceutical studies and practices
  • Nutrition, Genetics, and Disease
  • Health, Environment, Cognitive Aging
  • Fungal and yeast genetics research
  • Silk-based biomaterials and applications
  • Occupational exposure and asthma
  • RNA modifications and cancer
  • Food Allergy and Anaphylaxis Research
  • Digestive system and related health
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Science, Research, and Medicine
  • Parathyroid Disorders and Treatments

Clinical Hospital No. 8
2024

Cardiff University
2012-2016

Medical Research Council
2013-2015

Monash University
2015

Chemical Pharmaceutical Research Institute
1980

Vavilov Institute of General Genetics
1977

Russian Academy of Sciences
1974

Valentina Escott‐Price Céline Bellenguez Li‐San Wang Seung‐Hoan Choi Denise Harold and 95 more Lesley Jones Peter Holmans Amy Gerrish Alexey Vedernikov Alexander Richards Anita L. DeStefano Jean‐Charles Lambert Carla A. Ibrahim‐Verbaas Adam C. Naj Rebecca Sims Gyungah Jun Joshua C. Bis Gary W. Beecham Benjamin Grenier‐Boley Giancarlo Russo Tricia A. Thornton‐Wells Nicola Denning Albert V. Smith Vincent Chouraki Charlene Thomas M. Arfan Ikram Diana Zélénika Badri N. Vardarajan Yoichiro Kamatani Chiao‐Feng Lin Helena Schmidt Brian W. Kunkle Melanie Dunstan Maria Vronskaya Andrew D. Johnson Agustı́n Ruiz Marie‐Thérèse Bihoreau Christiane Reitz Florence Pasquier Paul Hollingworth Olivier Hanon Annette L. Fitzpatrick Joseph D. Buxbaum Dominique Campion Paul K. Crane Clinton T. Baldwin Tim Becker Vilmundur Guðnason Carlos Cruchaga David Craig Najaf Amin Claudine Berr Lorna M. Lopez Philip L. De Jager Vincent Deramecourt Janet Johnston Denis A. Evans Simon Lovestone Luc Letenneur Isabel Hernández David C. Rubinsztein Gudny Eiriksdottir Kristel Sleegers Alison Goate Nathalie Fiévet Matthew J. Huentelman Michael Gill Kristelle Brown M. Ilyas Kamboh Lina Keller Pascale Barberger‐Gateau Bernadette McGuinness Eric B. Larson Amanda Myers Carole Dufouil Stephen Todd David Wallon Seth Love Ekaterina Rogaeva John Gallacher Peter St George‐Hyslop Jordi Clarimón Alberto Lleó Antony Bayer Debby W. Tsuang Lei Yu Magda Tsolaki Paola Bossù Gianfranco Spalletta Petroula Proitsi John Collinge Sandro Sorbi Florentino Sanchez‐García Nick C. Fox John Hardy María Cándida Déniz Naranjo Paolo Bosco Robert Clarke Carol Brayne Daniela Galimberti

Background Alzheimer's disease is a common debilitating dementia with known heritability, for which 20 late onset susceptibility loci have been identified, but more remain to be discovered. This study sought identify new genes, using an alternative gene-wide analytical approach tests patterns of association within in the powerful genome-wide dataset International Genomics Project Consortium, comprising over 7 m genotypes from 25,580 cases and 48,466 controls. Principal Findings In addition...

10.1371/journal.pone.0094661 article EN cc-by PLoS ONE 2014-06-12
Lesley Jones Jean‐Charles Lambert Weixin Wang Seung‐Hoan Choi Denise Harold and 95 more Alexey Vedernikov Valentina Escott‐Price Timothy Stone Alexander Richards Céline Bellenguez Carla A. Ibrahim‐Verbaas Adam C. Naj Rebecca Sims Amy Gerrish Gyungah Jun Anita L. DeStefano Joshua C. Bis Gary W. Beecham Benjamin Grenier‐Boley Giancarlo Russo Tricia A. Thornton‐Wells Nicola Jones Albert V. Smith Vincent Chouraki Charlene Thomas M. Arfan Ikram Diana Zélénika Badri N. Vardarajan Yoichiro Kamatani Chiao‐Feng Lin Helena Schmidt Brian W. Kunkle Melanie Dunstan Agustı́n Ruiz Marie‐Thérèse Bihoreau Christiane Reitz Florence Pasquier Paul Hollingworth Olivier Hanon Annette L. Fitzpatrick Joseph D. Buxbaum Dominique Campion Paul K. Crane Tim Becker Vilmundur Guðnason Carlos Cruchaga David W. Craig Najaf Amin Claudine Berr Oscar L. López Philip L. De Jager Vincent Deramecourt Janet Johnston Denis A. Evans Simon Lovestone Luc Letteneur Johanes Kornhuber Lluís Tárraga David C. Rubinsztein Gudny Eiriksdottir Kristel Sleegers Alison Goate Nathalie Fiévet Matthew J. Huentelman Michael Gill Valur Emilsson Kristelle Brown M. Ilyas Kamboh Lina Keller Pascale Barberger‐Gateau Bernadette McGuinness Eric B. Larson Amanda Myers Carole Dufouil Stephen Todd David Wallon Seth Love Patrick G. Kehoe Ekaterina Rogaeva John Gallacher Peter St George‐Hyslop Jordi Clarimón Alberti Lleὀ Antony Bayer Debby W. Tsuang Lei Yu Magda Tsolaki Paola Bossù Gianfranco Spalletta Petroula Proitsi John Collinge Sandro Sorbi Florentino Sanchez‐García Nick C. Fox John Hardy María Cándida Déniz Naranjo Cristina Razquín Paola Bosco Robert Clarke Carol Brayne

Abstract Background Late‐onset Alzheimer's disease (AD) is heritable with 20 genes showing genome‐wide association in the International Genomics of Project (IGAP). To identify biology underlying disease, we extended these genetic data a pathway analysis. Methods The ALIGATOR and GSEA algorithms were used IGAP to associated functional pathways correlated gene expression networks human brain. Results identified an excess curated biological enrichment association. Enriched areas included immune...

10.1016/j.jalz.2014.05.1757 article EN Alzheimer s & Dementia 2014-12-19

Neuroticism is a personality trait of fundamental importance for psychological wellbeing and public health. It strongly associated with major depressive disorder (MDD) several other psychiatric conditions. Although neuroticism heritable, attempts to identify the alleles involved in previous studies have been limited by relatively small sample sizes heterogeneity measurement neuroticism. Here we report genome-wide association study 91,370 participants UK Biobank cohort combined meta-analysis...

10.1101/032417 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2015-11-20

Progress in instrumental diagnostics, as well increased awareness among doctors about rare diseases, is steadily leading to an number of patients diagnosed with cardiac amyloidosis. Regardless amyloid formation route, damage the main cause mortality systemic The article presents a unique clinical observation hereditary transthyretin (ATTR) amyloidosis mixed phenotype detection during skeletal scintigraphy. In patient severe shortness breath, based on results radiological research,...

10.20996/1819-6446-2024-3031 article EN cc-by Rational Pharmacotherapy in Cardiology 2024-07-02

In the last two years, nine new susceptibility genes for Alzheimer's disease (AD) have been identified. These findings increased our understanding of and highlighted biological pathways. However these novel AD genes, plus APOE only account approximately a third predicted genetic risk. Therefore large part component is still to be determined.miRNAs are class non-coding which thought an important element post-translational machinery. Abnormalities in miRNA expression mediated gene regulation...

10.1016/j.jalz.2012.05.1788 article EN Alzheimer s & Dementia 2012-07-01
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