Víctor Andrade

ORCID: 0000-0003-0682-269X
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Alzheimer's disease research and treatments
  • Genetic Associations and Epidemiology
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Tryptophan and brain disorders
  • Epigenetics and DNA Methylation
  • Bioinformatics and Genomic Networks
  • Nutrition, Genetics, and Disease
  • Dementia and Cognitive Impairment Research
  • Genetics and Neurodevelopmental Disorders
  • Genomic variations and chromosomal abnormalities
  • Fatty Acid Research and Health
  • SARS-CoV-2 and COVID-19 Research
  • Cancer-related gene regulation
  • Folate and B Vitamins Research
  • Liver Disease Diagnosis and Treatment
  • Health, Environment, Cognitive Aging
  • Atherosclerosis and Cardiovascular Diseases
  • Neurogenesis and neuroplasticity mechanisms
  • Parkinson's Disease Mechanisms and Treatments
  • Wnt/β-catenin signaling in development and cancer
  • Humic Substances and Bio-Organic Studies
  • Protease and Inhibitor Mechanisms
  • Cardiovascular Disease and Adiposity
  • Congenital heart defects research
  • COVID-19 Clinical Research Studies

University of Cologne
2019-2023

University Hospital Bonn
2020-2023

University Hospital Cologne
2022-2023

Molecular Biology Consortium
2023

University of Chile
2017-2023

University of Stavanger
2021

University of Bonn
2019

Universidad Andrés Bello
2016-2018

Millennium Institute for Integrative Biology
2018

Céline Bellenguez Fahri Küçükali Iris E. Jansen Luca Kleineidam Sonia Moreno‐Grau and 95 more Najaf Amin Adam C. Naj Rafael Campos‐Martin Benjamin Grenier‐Boley Víctor Andrade Peter Holmans Anne Boland Vincent Damotte Sven J. van der Lee Marcos R. Costa Teemu Kuulasmaa Qiong Yang Itziar de Rojas Joshua C. Bis Amber Yaqub Ivana Nedeljković Julien Chapuis Shahzad Ahmad Vilmantas Giedraitis Dag Aarsland Pablo García‐González Carla Abdelnour Emilio Alarcón‐Martín Daniel Alcolea Montserrat Alegret Ignacio Álvarez Victoria Álvarez Nicola J. Armstrong Anthoula Tsolaki Carmen Antúnez Ildebrando Appollonio Marina Arcaro Silvana Archetti Alfonso Arias Pastor Beatrice Arosio Lavinia Athanasiu Henri Bailly Nerisa Banaj Miquel Baquero Sandra Barral Alexa S. Beiser Ana Belén Pastor Jennifer E. Below Penelope Benchek Luisa Benussi Claudine Berr Céline Besse Valentina Bessi Giuliano Binetti Alessandra Bizarro Rafael Blesa Merçé Boada Eric Boerwinkle Barbara Borroni Silvia Boschi Paola Bossù Geir Bråthen Jan Bressler Catherine Bresner Henry Brodaty Keeley J. Brookes Luis I. Brusco Dolores Buiza‐Rueda Katharina Bürger Vanessa Burholt William S. Bush Miguel Calero Laura B. Cantwell Geneviève Chêne Jaeyoon Chung Michael L. Cuccaro Ángel Carracedo Roberta Cecchetti Laura Cervera‐Carles Camille Charbonnier Hung‐Hsin Chen Caterina Chillotti Simona Ciccone Jurgen A.H.R. Claassen Christopher Clark Elisa Conti Anaïs Corma‐Gómez Emanuele Maria Costantini Carlo Custodero Delphine Daian Carolina Dalmasso Antonio Daniele Efthimios Dardiotis Jean‐François Dartigues Peter Paul De Deyn Kátia de Paiva Lopes Lot D. de Witte Stéphanie Debette Jürgen Deckert Teodoro del Ser

Abstract Characterization of the genetic landscape Alzheimer’s disease (AD) and related dementias (ADD) provides a unique opportunity for better understanding associated pathophysiological processes. We performed two-stage genome-wide association study totaling 111,326 clinically diagnosed/‘proxy’ AD cases 677,663 controls. found 75 risk loci, which 42 were new at time analysis. Pathway enrichment analyses confirmed involvement amyloid/tau pathways highlighted microglia implication. Gene...

10.1038/s41588-022-01024-z article EN cc-by Nature Genetics 2022-04-01
Itziar de Rojas Sonia Moreno‐Grau Niccoló Tesi Benjamin Grenier‐Boley Víctor Andrade and 95 more Iris E. Jansen Nancy L. Pedersen Najada Stringa Anna Zettergren Isabel Hernández Laura Montrreal Carmen Antúnez Anna Antonell Rick M. Tankard Joshua C. Bis Rebecca Sims Céline Bellenguez Inés Quintela Antonio González-Pérez Miguel Calero Emilio Franco‐Macías Juan Macı́as Rafael Blesa Laura Cervera‐Carles Manuel Menéndez‐González Ana Frank José Luís Royo Fermín Moreno Raquel Huerto Vilas Miquel Baquero Mónica Díez-Fairén Carmen Lage Sebastián García‐Madrona Pablo García‐González Emilio Alarcón‐Martín Sergi Valero Óscar Sotolongo‐Grau Abbe Ullgren Adam C. Naj Afina W. Lemstra Alba Benaque Alba Pérez‐Cordón Alberto Benussi Alberto Rábano Alessandro Padovani Alessio Squassina Alexandre de Mendonça Alfonso Arias Pastor Almar A. L. Kok Alun Meggy Ana Belén Pastor Ana Espinosa Anaïs Corma‐Gómez Angel Martín Montes Ángela Sanabria Anita L. DeStefano Anja Schneider Annakaisa Haapasalo Anne Kinhult Ståhlbom Anne Tybjærg‐Hansen Annette M. Hartmann Annika Spottke Arturo Corbatón Anchuelo Arvid Rongve Barbara Borroni Beatrice Arosio Benedetta Nacmias Børge G. Nordestgaard Brian W. Kunkle Camille Charbonnier Carla Abdelnour Carlo Masullo Carmen Martínez Rodríguez Carmen Muñoz-Fernández Carole Dufouil Caroline Graff Catarina B. Ferreira Caterina Chillotti Chandra A. Reynolds Chiara Fenoglio Christine Van Broeckhoven Christopher Clark Claudia Pisanu Claudia L. Satizábal Clive Holmes Dolores Buiza‐Rueda Dag Aarsland Dan Rujescu Daniel Alcolea Daniela Galimberti David Wallon Davide Seripa Edna Grünblatt Efthimios Dardiotis Emrah Düzel Elio Scarpini Elisa Conti Elisa Rubino Ellen Gelpí Eloy Rodríguez‐Rodríguez

Genetic discoveries of Alzheimer's disease are the drivers our understanding, and together with polygenetic risk stratification can contribute towards planning feasible efficient preventive curative clinical trials. We first perform a large genetic association study by merging all available case-control datasets by-proxy results (discovery n = 409,435 validation size 58,190). Here, we add six variants associated (near APP, CHRNE, PRKD3/NDUFAF7, PLCG2 two exonic in SHARPIN gene). Assessment...

10.1038/s41467-021-22491-8 article EN cc-by Nature Communications 2021-06-07
Céline Bellenguez Fahri Küçükali Iris E. Jansen Víctor Andrade Sonia Moreno‐Grau and 95 more Najaf Amin Adam C. Naj Benjamin Grenier‐Boley Rafael Campos‐Martin Peter Holmans Anne Boland Luca Kleineidam Vincent Damotte Sven J. van der Lee Teemu Kuulasmaa Qiong Yang Itziar de Rojas Joshua C. Bis Amber Yaqub Ivana Nedeljković Marcos R. Costa Julien Chapuis Shahzad Ahmad Vilmantas Giedraitis Merçé Boada Dag Aarsland Pablo García‐González Carla Abdelnour Emilio Alarcón‐Martín Montserrat Alegret Ignacio Álvarez Victoria Álvarez Nicola J. Armstrong Anthoula Tsolaki Carmen Antúnez Ildebrando Appollonio Marina Arcaro Silvana Archetti Alfonso Arias Pastor Beatrice Arosio Lavinia Athanasiu Henri Bailly Nerisa Banaj Miquel Baquero Ana Belén Pastor Luisa Benussi Claudine Berr Céline Besse Valentina Bessi Giuliano Binetti Alessandra Bizzarro Daniel Alcolea Rafael Blesa Barbara Borroni Silvia Boschi Paola Bossù Geir Bråthen Catherine Bresner Keeley J. Brookes Luis I. Brusco Katharina Bürger María J. Bullido Vanessa Burholt William S. Bush Miguel Calero Carole Dufouil Ángel Carracedo Roberta Cecchetti Laura Cervera‐Carles Camille Charbonnier Caterina Chillotti Henry Brodaty Simona Ciccone Jurgen A.H.R. Claassen Christopher Clark Elisa Conti Anaïs Corma‐Gómez Emanuele Maria Costantini Carlo Custodero Delphine Daian Carolina Dalmasso Antonio Daniele Efthimios Dardiotis Jean‐François Dartigues Peter Paul De Deyn Kátia de Paiva Lopes Lot D. de Witte Stéphanie Debette Jürgen Deckert Teodoro del Ser Nicola Denning Anita L. DeStefano Martin Dichgans Janine Diehl‐Schmid Mónica Díez-Fairén Paolo Rossi Srdjan Djurovic Emmanuelle Duron Emrah Düzel Sebastiaan Engelborghs

ABSTRACT Alzheimer’s disease (AD) is a severe and incurable neurodegenerative disease, the failure to find effective treatments suggests that underlying pathology remains poorly understood. Due its strong heritability, deciphering genetic landscape of AD related dementia (ADD) unique opportunity advance our knowledge. We completed meta-analysis genome-wide association studies (39,106 clinically AD-diagnosed cases, 46,828 proxy-ADD cases 401,577 controls) with most promising signals...

10.1101/2020.10.01.20200659 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2020-10-04

Abstract Alzheimer’s disease has a long asymptomatic phase that offers substantial time window for intervention. Using this of opportunity will require early diagnostic and prognostic biomarkers to detect pathology at predementia stages, thus allowing identification patients who most probably progress dementia the type benefit from specific disease-modifying therapies. Consequently, we searched CSF proteins associated with progression along clinical staging. We measured levels 184 in samples...

10.1093/brain/awac024 article EN Brain 2022-01-25

Mosaic loss of chromosome Y (mLOY) is a common ageing-related somatic event and has been previously associated with Alzheimer’s disease (AD). However, mLOY estimation from genotype microarray data only reflects the degree subjects at moment DNA sampling. Therefore, phenotype associations AD can be severely age-confounded in context genome-wide association studies. Here, we applied Mendelian randomisation to construct an age-independent polygenic risk score (mloy-PRS) using 114 autosomal...

10.3390/ijms24020898 article EN International Journal of Molecular Sciences 2023-01-04

Alzheimer's disease (AD) is a neurodegenerative characterized by progressive cognitive impairment of patients, affecting around 12% people older than 65 years old. WHO estimated that over 48.6 million all the world suffer this disease. On basis cumulative results on our research, we have postulated neuroimmunomodulation hypothesis appears to provide reasonable explanation both preclinical and clinical observations. In context, long-term activation innate immune system triggers an anomalous...

10.3233/jad-170354 article EN Journal of Alzheimer s Disease 2017-08-22

Abstract Synaptic abnormalities have been described in individuals with autism spectrum disorders (ASD). The cell-adhesion molecule Neuroligin-3 (Nlgn3) has an essential role the function and maturation of synapses NLGN3 ASD-associated mutations disrupt hippocampal cortical function. Here we show that Wnt/β-catenin signaling increases Nlgn3 mRNA protein levels HT22 mouse cells primary cultures rat neurons. We characterized activity promoter constructs containing conserved putative T-cell...

10.1038/s41398-018-0093-y article EN cc-by Translational Psychiatry 2018-02-05

ABSTRACT BACKGROUND Disentangling the genetic constellation underlying Alzheimer’s disease (AD) is important. Doing so allows us to identify biological pathways AD, point towards novel drug targets and use variants for individualised risk predictions in modifying or prevention trials. In present work we report on largest genome-wide association study (GWAS) AD date show combined utility of proven loci precision medicine using polygenic scores (PRS). METHODS Three sets summary statistics were...

10.1101/19012021 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2019-11-15

Wnt/ β -catenin signaling modulates brain development and function its deregulation underlies pathological changes occurring in neurodegenerative neurodevelopmental disorders. Since one of the main effects is modulation target genes, present work we examined global transcriptional induced by short-term Wnt3a treatment (4 h) primary cultures rat hippocampal neurons. RNAseq experiments allowed identification 170 differentially expressed including known genes such as Notum, Axin2, Lef1, well...

10.1155/2016/4672841 article EN cc-by Neural Plasticity 2016-01-01

Background:Alzheimer's disease (AD) is a multifactorial disease, that involves neuroinflammatory processes in which microglial cells respond to "damage signals". The latter includes oligomeric tau, iron, oxidative free radicals, and other molecules promotes neuroinflammation the brain, prom oting neuronal death cognitive impairment. Since AD first cause of dementia elderly, its pharmacotherapy has limited efficacy, novel treatments are critical improve quality life patients. Multitarget...

10.3233/jad-200067 article EN Journal of Alzheimer s Disease 2020-05-08

Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder without cure, despite the enormous number of investigations and therapeutic approaches. AD consequence microglial responses to "damage signals", such as aggregated tau oligomers, which trigger neuro-inflammatory reaction, promoting misfolding cytoskeleton structure. Since most prevalent cause dementia in elderly (>60 years old), new treatments are essential improve well-being affected subjects. The pharmaceutical...

10.3390/ph16070960 article EN cc-by Pharmaceuticals 2023-07-04

According to the WHO, antimicrobial resistance is among top 10 threats global health. Due increased rates, an increase in mortality and morbidity of patients has been observed, with projections more than million deaths associated infections caused by antibacterial resistant microorganisms. Our research group developed a new family pyrimido-isoquinolin-quinones showing activities against multidrug-resistant Staphylococcus aureus. We have 3D-QSAR CoMFA CoMSIA studies (r2 = 0.938; 0.895), from...

10.3390/ph16111621 article EN cc-by Pharmaceuticals 2023-11-17

Evidence-based Nutraceutical Compounds (EBNC), containing bioactive principles of demonstrated efficacy and health security are opening solutions for a modern preventive medicine, as potential many chronic diseases the human beings. EBNC contain components diet that can be used prevention or treatment disease. They obtained through rigorous processes extraction from natural resources Good Manufacturing Practices (GMP) regulations, exhibit sound preclinical studies published in high impact...

10.4172/2161-0460.1000456 article EN cc-by Journal of Alzheimer’s Disease & Parkinsonism 2018-01-01
Iris E. Jansen Sven J. van der Lee Duber Gomez‐Fonseca Itziar de Rojas Carolina Dalmasso and 95 more Benjamin Grenier‐Boley Anna Zettergren Aniket Mishra Muhammad Ali Víctor Andrade Céline Bellenguez Luca Kleineidam Fahri Küçükali Yun Ju Sung Niccoló Tesi Eleonora M. Vromen Douglas P. Wightman Daniel Alcolea Montserrat Alegret Ignacio Álvarez Philippe Amouyel Lavinia A Andresen Shahram Bahrami Henri Bailly Olivia Belbin Sverre Bergh Geert Jan Biessels Kaj Blennow Rafael Blesa Merçé Boada Anne Boland Katharina Büerger Ángel Carracedo Laura Cervera‐Carles Geneviève Chêne Jurgen A.H.R. Claassen Stéphanie Debette Jean‐François Deleuze Peter Paul De Deyn Janine Diehl‐Schmid Srdjan Djurovic Oriol Dols‐Icardo Carole Dufouil Emmanuelle Duron Emrah Düzel Tormod Fladby Juan Fortea Lutz Frölich Pablo García‐González María García‐Martínez Ina Giegling Oliver Goldhardt Timo Grimmer Annakaisa Haapasalo Harald Hampel Olivier Hanon Lucrezia Hausner Stefanie Heilmann‐Heimbach Seppo Helisalmi Michael T. Heneka Isabel Hernández Sanna‐Kaisa Herukka Henne Holstege Jonas Alexander Jarholm Silke Kern Anne‐Brita Knapskog Anne M. Koivisto Johannes Kornhuber Teemu Kuulasmaa Carmen Lage Christoph Laske Ville Leinonen Piotr Lewczuk Alberto Lleó Adolfo López de Munain Sara López‐García Wolfgang Maier Marta Marquié Merel O. Mol Laura Montrreal Fermín Moreno Sonia Moreno‐Grau Gaël Nicolas Markus M. Nöthen Adelina Orellana Lene Pålhaugen Janne M. Papma Florence Pasquier Robert Perneczky Oliver Peters Yolande A.L. Pijnenburg Julius Popp Daniëlle Posthuma Ana Pozueta Josef Priller Raquel Puerta Inés Quintela Inez Ramakers Eloy Rodríguez‐Rodríguez Dan Rujescu

Abstract Amyloid-beta 42 (Aβ42) and phosphorylated tau (pTau) levels in cerebrospinal fluid (CSF) reflect core features of the pathogenesis Alzheimer’s disease (AD) more directly than clinical diagnosis. Initiated by European Alzheimer & Dementia Biobank (EADB), largest collaborative effort on genetics underlying CSF biomarkers was established, including 31 cohorts with a total 13,116 individuals (discovery n = 8,074; replication 5,042 individuals). Besides APOE locus, novel associations...

10.1101/2022.03.08.22271043 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2022-03-09

ABSTRACT Mosaic loss of chromosome Y (mLOY) is a common ageing-related somatic event occurring exclusively in men and has been previously associated with Alzheimer’s disease (AD). However, mLOY estimation from genotype microarray data only reflects the degree subjects at moment DNA sampling. Therefore, phenotype associations AD can be severely age-confounded context genome-wide association studies. Here, we applied Mendelian randomization to construct an age-independent polygenic risk score...

10.1101/2022.07.20.22277657 preprint EN cc-by-nd medRxiv (Cold Spring Harbor Laboratory) 2022-07-22

Abstract Background The most relevant risk factor in Alzheimer’s disease (AD) is age. Aging a complex process involving several biological changes which lead to chronic cellular stress and sterile tissue inflammation. During aging cells become senescent seen as morphological secretion of immune signaling mediators associated with systemic low‐grade Interestingly, during neurodegenerative processes such AD, microglia, astrocytes, vascular unit senescent. To explore the potential connection...

10.1002/alz.062706 article EN Alzheimer s & Dementia 2023-06-01

Abstract Background Previous research reported the association between circulating Omega‐3 polyunsaturated fatty acids (PUFA) in blood and risk of dementia Alzheimer’s disease (AD). However, a large intervention study supplementing that this supplementation has only marginal effect on improvement cognitive performance after supplementation. Since PUFA metabolism shared processing enzymes, we explored whether relationship two main families PUFA, i.e., Omega‐6, might associate with...

10.1002/alz.065791 article EN Alzheimer s & Dementia 2023-06-01
Coming Soon ...