Sergio E. Baranzini

ORCID: 0000-0003-0067-194X
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About
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Research Areas
  • Multiple Sclerosis Research Studies
  • Bioinformatics and Genomic Networks
  • Cytokine Signaling Pathways and Interactions
  • Gut microbiota and health
  • Gene expression and cancer classification
  • Systemic Lupus Erythematosus Research
  • Biomedical Text Mining and Ontologies
  • Genetic Associations and Epidemiology
  • T-cell and B-cell Immunology
  • RNA Research and Splicing
  • Olfactory and Sensory Function Studies
  • RNA regulation and disease
  • Advanced Chemical Sensor Technologies
  • Viral Infections and Immunology Research
  • Immunotherapy and Immune Responses
  • Gene Regulatory Network Analysis
  • Immune Cell Function and Interaction
  • Computational Drug Discovery Methods
  • Clostridium difficile and Clostridium perfringens research
  • MicroRNA in disease regulation
  • interferon and immune responses
  • T-cell and Retrovirus Studies
  • Neurogenesis and neuroplasticity mechanisms
  • Rheumatoid Arthritis Research and Therapies
  • Neuroinflammation and Neurodegeneration Mechanisms

University of California, San Francisco
2016-2025

Universidad Católica de Santa Fe
2024

University of Cambridge
2022

Aberdeen Royal Infirmary
2021

NHS Grampian
2021

QB3
2021

Brigham and Women's Hospital
2020

Universidad San Pablo
2020

Broad Institute
2020

McGill University
2014-2020

Stephen Sawcer Garrett Hellenthal Matti Pirinen Chris C. A. Spencer Nikolaos A. Patsopoulos and 95 more Loukas Moutsianas Alexander Dilthey Zhan Su Colin Freeman Sarah Hunt Sarah Edkins Emma Gray David R. Booth Simon Potter An Goris Gavin Band Annette Oturai Amy Strange Janna Saarela Céline Bellenguez Bertrand Fontaine Matthew Gillman Bernhard Hemmer Rhian Gwilliam Frauke Zipp Alagurevathi Jayakumar Roland Martinꝉ Stephen Leslie Stanley Hawkins Eleni Giannoulatou Sandra D’Alfonso Hannah Blackburn Filippo Martinelli Boneschi Jennifer Liddle Hanne F. Harbo M. L. Perez Anne Spurkland Matthew Waller Marcin P. Mycko Michelle Ricketts Manuel Comabella Naomi Hammond Ingrid Kockum Owen T McCann Maria Ban Pamela Whittaker Anu Kemppinen Paul A. Weston Clive Hawkins Sara Widaa John Zajicek Serge Dronov Neil P. Robertson Suzannah J. Bumpstead Lisa F. Barcellos Rathi Ravindrarajah Roby Abraham Lars Alfredsson Kristin Ardlie Cristin Aubin Amie Baker K. Baker Sergio E. Baranzini Laura Bergamaschi Roberto Bergamaschi Allan Bernstein Achim Berthele Mike Boggild Jonathan P. Bradfield David Brassat Simon Broadley Dorothea Buck Helmut Butzkueven Ruggero Capra William M. Carroll Paola Cavalla Elisabeth Gulowsen Celius Sabine Cepok Rosetta Chiavacci Françoise Clerget‐Darpoux Katleen Clysters Gıancarlo Comı M. Cossburn Isabelle Cournu‐Rebeix Mathew Cox Wendy Cozen Bruce Cree Anne H. Cross Daniele Cusi Mark J. Daly Emma Davis Paul I. W. de Bakker Marc Debouverie Marie D’hooghe Katherine Dixon Rita Dobosi Bénédicte Dubois David Ellinghaus Irina Elovaara Federica Esposito

10.1038/nature10251 article EN Nature 2011-08-01
Ashley Beecham Nikolaos A. Patsopoulos Dionysia K. Xifara Mary F. Davis Anu Kemppinen and 95 more Chris Cotsapas Tejas Shah Chris C. A. Spencer David J. Booth An Goris Annette Oturai Janna Saarela Bertrand Fontaine Bernhard Hemmer Claes Martin Frauke Zipp Sandra D’Alfonso Filippo Martinelli Boneschi Bruce Taylor Hanne F. Harbo Ingrid Kockum Jan Hillert Tomas Olsson Maria Ban Jorge R. Oksenberg Rogier Hintzen Lisa F. Barcellos Cristina Agliardi Lars Alfredsson Mehdi Alizadeh Carl A. Anderson Robert Andrews Helle Bach Søndergaard Amie Baker Gavin Band Sergio E. Baranzini Nadia Barizzone Jeffrey C. Barrett Céline Bellenguez Laura Bergamaschi Luisa Bernardinelli Achim Berthele Viola Biberacher Thomas M.C. Binder Hannah Blackburn Izaura Lima Bomfim Paola Brambilla Simon Broadley Bruno Brochet Lou Brundin Dorothea Buck Helmut Butzkueven Stacy J. Caillier William Camu Wassila Carpentier Paola Cavalla Elisabeth Gulowsen Celius Irène Coman Gıancarlo Comı Lucia Corrado Leentje Cosemans Isabelle Cournu‐Rebeix Bruce Cree Daniele Cusi Vincent Damotte Gilles Defer Silvia Delgado Panos Deloukas Alessia Di Sapio Alexander Dilthey Peter Donnelly Bénédicte Dubois Martin Duddy Sarah Edkins Irina Elovaara Federica Esposito Nikos Evangelou Barnaby Fiddes Judith Field André Franke Colin Freeman Irene Y. Frohlich Daniela Galimberti Christian Gieger Pierre‐Antoine Gourraud Christiane Graetz Andrew Graham Verena Grummel Clara Guaschino Athena Hadjixenofontos Hákon Hákonarson Christopher Halfpenny Gillian Hall Per Hall Anders Hamsten James Harley Timothy Harrower Clive Hawkins Garrett Hellenthal Charles Hillier

10.1038/ng.2770 article EN Nature Genetics 2013-09-29
Nikolaos A. Patsopoulos Sergio E. Baranzini Adam Santaniello Parisa Shoostari Chris Cotsapas and 95 more Garrett Wong Ashley Beecham Tojo James Joseph M. Replogle Ioannis S. Vlachos Cristin McCabe Tune H. Pers Aaron Brandes Charles C. White Brendan T Keenan Maria Cimpean Phoebe A. Winn Ioannis-Pavlos Panteliadis Allison Robbins Till F. M. Andlauer Onigiusz Zarzycki Bénédicte Dubois An Goris Helle Bach Søndergaard Finn Sellebjerg Per Soelberg Sorensen Henrik Ullum Lise Wegner Thørner Janna Saarela Isabelle Cournu‐Rebeix Vincent Damotte Bertrand Fontaine Léna Guillot‐Noël Mark Lathrop Sandra Vukusic Achim Berthele Viola Pongratz Dorothea Buck Christiane Gasperi Christiane Graetz Verena Grummel Bernhard Hemmer Muni Hoshi Benjamin Knier Thomas Korn Christina M. Lill Felix Luessi Mark Mühlau Frauke Zipp Efthimios Dardiotis Cristina Agliardi Antonio Amoroso Nadia Barizzone Maria Donata Benedetti Luisa Bernardinelli Paola Cavalla Ferdinando Clarelli Gıancarlo Comı Daniele Cusi Federica Esposito Laura Ferrè Daniela Galimberti Clara Guaschino Maurizio Leone Vittorio Martinelli Lucia Moiola Marco Salvetti Melissa Sorosina Domizia Vecchio Andrea Zauli Silvia Santoro Nicasio Mancini Miriam Zuccalà Julia Mescheriakova Cornelia M. van Duijn Steffan D. Bos Elisabeth Gulowsen Celius Anne Spurkland Manuel Comabella Xavier Montalbán Lars Alfredsson Izaura Lima Bomfim David Gómez-Cabrero Jan Hillert Maja Jagodic Magdalena Lindén Fredrik Piehl Ilijas Jelčić Roland Martinꝉ Mirela Sospedra Amie Baker Maria Ban Clive Hawkins Pirro G. Hysi Seema Kalra Fredrik Karpe Jyoti Khadake Geneviève Lachance Paul Molyneux Matthew Neville

We analyzed genetic data of 47,429 multiple sclerosis (MS) and 68,374 control subjects established a reference map the architecture MS that includes 200 autosomal susceptibility variants outside major histocompatibility complex (MHC), one chromosome X variant, 32 within extended MHC. used an ensemble methods to prioritize 551 putative genes implicate innate adaptive pathways distributed across cellular components immune system. Using expression profiles from purified human microglia, we...

10.1126/science.aav7188 article EN Science 2019-09-26

Significance We have experimentally investigated the immunoregulatory effects of human gut microbiota in multiple sclerosis (MS). identified specific bacteria that are associated with MS and demonstrated these regulate T lymphocyte-mediated adaptive immune responses contribute to proinflammatory environment vitro vivo. Thus, our results expand knowledge microbial regulation immunity may provide a basis for development microbiome-based therapeutics autoimmune diseases.

10.1073/pnas.1711235114 article EN Proceedings of the National Academy of Sciences 2017-09-11

There is emerging evidence that the commensal microbiota has a role in pathogenesis of multiple sclerosis (MS), putative autoimmune disease CNS. Here, we compared gut microbial composition 34 monozygotic twin pairs discordant for MS. While there were no major differences overall profiles, found significant increase some taxa such as Akkermansia untreated MS twins. Furthermore, most notably, when transplanted to transgenic mouse model spontaneous brain autoimmunity, twin-derived induced...

10.1073/pnas.1711233114 article EN Proceedings of the National Academy of Sciences 2017-09-11

Multiple sclerosis is a demyelinating disease, characterized by inflammation in the brain and spinal cord, possibly due to autoimmunity. Large-scale sequencing of cDNA libraries, derived from plaques dissected brains patients with multiple (MS), indicated an abundance transcripts for osteopontin (OPN). Microarray analysis cords rats paralyzed experimental autoimmune encephalomyelitis (EAE), model MS, also revealed increased OPN transcripts. Osteopontin-deficient mice were resistant...

10.1100/tsw.2002.326 article EN 2002-04-12

The progressive loss of CNS myelin in patients with multiple sclerosis (MS) has been proposed to result from the combined effects damage oligodendrocytes and failure remyelination. A common feature demyelinated lesions is presence oligodendrocyte precursors (OLPs) blocked at a premyelinating stage. However, mechanistic basis for inhibition repair incompletely understood. To identify novel regulators OLP differentiation, potentially dysregulated during repair, we performed genome-wide screen...

10.1101/gad.1806309 article EN Genes & Development 2009-06-10

The discovery and broad application of MRI in medicine has led to an increased awareness the number patients with incidental white matter pathology CNS. Routinely encountered clinical practice, natural history or evolution such individuals respect their risk developing multiple sclerosis (MS) is unclear.To investigate who exhibit imaging findings highly suggestive MS pathology.Detailed radiologic data were obtained from asymptomatic anomalies MS.The cohort consisted 41 female 3 male subjects...

10.1212/01.wnl.0000335764.14513.1a article EN Neurology 2008-12-11

Identical (or more correctly 'monozygotic') twins are widely used to study the contributions of genetics and environment human disease. A that focused on three pairs monozygotic twins, in which one twin had multiple sclerosis other did not, has brought latest techniques genome sequencing analysis this field, incidentally published first female sequences. Full sequences were determined for pair these two mRNA transcriptome epigenome CD4+ lymphocytes determined. The striking result is no...

10.1038/nature08990 article EN cc-by-nc-sa Nature 2010-04-01

Multiple sclerosis (MS), a chronic disorder of the central nervous system and common cause neurological disability in young adults, is characterized by moderate but complex risk heritability. Here we report results genome-wide association study performed 1000 prospective case series well-characterized individuals with MS group-matched controls using Sentrix® HumanHap550 BeadChip platform from Illumina. After stringent quality control data filtering, compared allele frequencies for 551 642...

10.1093/hmg/ddn388 article EN Human Molecular Genetics 2008-11-14

The ability to computationally predict whether a compound treats disease would improve the economy and success rate of drug approval. This study describes Project Rephetio systematically model efficacy based on 755 existing treatments. First, we constructed Hetionet (neo4j.het.io), an integrative network encoding knowledge from millions biomedical studies. v1.0 consists 47,031 nodes 11 types 2,250,197 relationships 24 types. Data were integrated 29 public resources connect compounds,...

10.7554/elife.26726 article EN cc-by eLife 2017-09-22

To characterize the accrual of long-term disability in a cohort actively treated multiple sclerosis (MS) patients and to assess whether clinical magnetic resonance imaging (MRI) data used trials have prognostic value.This is prospective study 517 managed MS enrolled at single center.More than 91% were retained, with ascertained up 10 years after baseline visit. At this last assessment, neurologic as measured by Expanded Disability Status Scale (EDSS) was stable or improved compared 41%...

10.1002/ana.24747 article EN cc-by-nc-nd Annals of Neurology 2016-07-27

Genome-wide association studies (GWAS) testing several hundred thousand SNPs have been performed in multiple sclerosis (MS) and other complex diseases. Typically, the number of markers which evidence for exceeds genome-wide significance threshold is very small, that do not exceed this are generally neglected. Classical statistical analysis these datasets MS revealed genes with known immunological functions. However, many showing modest may represent false negatives. We hypothesize certain...

10.1093/hmg/ddp120 article EN cc-by-nc Human Molecular Genetics 2009-03-13

Objective Rates of worsening and evolution to secondary progressive multiple sclerosis (MS) may be substantially lower in actively treated patients compared natural history studies from the pretreatment era. Nonetheless, our recently reported prospective cohort, more than half with relapsing MS accumulated significant new disability by 10th year follow‐up. Notably, “no evidence disease activity” at 2 years did not predict long‐term stability. Here, we determined what extent clinical relapses...

10.1002/ana.25463 article EN cc-by-nc Annals of Neurology 2019-03-09

Abstract In multiple sclerosis (MS), B cell–depleting therapy using monoclonal anti-CD20 Abs, including rituximab (RTX) and ocrelizumab, effectively reduces disease activity. Based on indirect evidence, it is generally believed that elimination of the Ag-presenting capabilities Ag nonspecific immune functions cells underlie therapeutic efficacy. However, a small subset T lymphocytes (T cells) was shown to also express CD20, but controversy prevails surrounding true existence this cell...

10.4049/jimmunol.1400118 article EN The Journal of Immunology 2014-06-16
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