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Marianna Bevova

Research Profile

Physiology

Genes & Molecular Sequences

Procedures

Chromosome Mapping

Concepts & Ideas

Disorders

Chemicals & Drugs

Geographic Areas

Netherlands

Living Beings

Mouse

Anatomy

Co-author Network

Publications

TOP 3
Ryan J Taft; Marjo S van der Knaap; Adeline Vanderver; Ishwar C Verma; Truus E M Abbink; Marianna R Bevova; Susan Blaser; Joanna Crawford; Stephen A Damiani; Irenaeus F M de Coo; Sean M Grimmond; Monica Juneja; Richard J Leventer; Paul J Lockhart; David Miller; Kate Pope; Petra J W Pouwels; Prab Prabhakar; Julian Raiman; Tena Rosser; Kelin Ru; Johanna Schmidt; Cas Simons; Nicole I Wolf
Mutations in DARS Cause Hypomyelination with Brain Stem and Spinal Cord Involvement and Leg Spasticity.
Benjamin Nota; Jean-Marc Nuoffer; Rossella Parini; Ana Pop; Marie-Hélène Read; Axel Renneberg; René Santer; Erik A Sistermans; Thomas Strahleck; Eduard A Struys; Marjo S van der Knaap; Silvy J M van Dooren; Emile Van Schaftingen; Magalie Barth; Tawfeg Ben-Omran; Marianna R Bevova; Pascale de Lonlay; Matilde R Fernandez Ojeda; Georg F Hoffmann; Cornelis Jakobs; Erwin E W Jansen; Warsha A Kanhai; Martijn Kranendijk; Marie T McDonald; Alf Meberg; Ania C Muntau; Aggie W M Nieuwint; Gajja S Salomons
Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria.
Eva C Verbeek; Gonneke Willemsen; Ingrid M C Bakker; Marianna R Bevova; Zoltán Bochdanovits; Dorret I Boomsma; Eco J de Geus; Witte J G Hoogendijk; Brenda W Penninx; Patrizia Rizzu; Johannes H Smit; David Sondervan; Peter Heutink
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder.

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All Publications

2013: Ryan J Taft; Marjo S van der Knaap; Adeline Vanderver; Ishwar C Verma; Truus E M Abbink; Marianna R Bevova; Susan Blaser; Joanna Crawford; Stephen A Damiani; Irenaeus F M de Coo; Sean M Grimmond; Monica Juneja; Richard J Leventer; Paul J Lockhart; David Miller; Kate Pope; Petra J W Pouwels; Prab Prabhakar; Julian Raiman; Tena Rosser; Kelin Ru; Johanna Schmidt; Cas Simons; Nicole I Wolf
Mutations in DARS Cause Hypomyelination with Brain Stem and Spinal Cord Involvement and Leg Spasticity.
American journal of human genetics 2013;92(5):774-80.
2013: Benjamin Nota; Jean-Marc Nuoffer; Rossella Parini; Ana Pop; Marie-Hélène Read; Axel Renneberg; René Santer; Erik A Sistermans; Thomas Strahleck; Eduard A Struys; Marjo S van der Knaap; Silvy J M van Dooren; Emile Van Schaftingen; Magalie Barth; Tawfeg Ben-Omran; Marianna R Bevova; Pascale de Lonlay; Matilde R Fernandez Ojeda; Georg F Hoffmann; Cornelis Jakobs; Erwin E W Jansen; Warsha A Kanhai; Martijn Kranendijk; Marie T McDonald; Alf Meberg; Ania C Muntau; Aggie W M Nieuwint; Gajja S Salomons
Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria.
American journal of human genetics 2013;92(4):627-31.
2012: Eva C Verbeek; Gonneke Willemsen; Ingrid M C Bakker; Marianna R Bevova; Zoltán Bochdanovits; Dorret I Boomsma; Eco J de Geus; Witte J G Hoogendijk; Brenda W Penninx; Patrizia Rizzu; Johannes H Smit; David Sondervan; Peter Heutink
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder.
PloS one 2012;7(5):e37384.
2011: Elisabet Einarsdottir; Katri Kaukinen; Juha Kere; Ilma Korponay-Szabo; Lotta L E Koskinen; Kalle Kurppa; Markku Mäki; M Luisa Mearin; Alienke Monsuur; Chris Mulder; Ruben van't Slot; Cisca Wijmenga; Alexandra Zhernakova; Marianna R Bevova; Päivi Saavalainen
Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations.
European journal of human genetics : EJHG 2011;19(6):682-6.
2008: Alexandra Zhernakova; Eleanora M Festen; Lude Franke; Gosia Trynka; Cleo C van Diemen; Alienke J Monsuur; Marianna R Bevova; Rian M Nijmeijer; Ruben van 't Slot; Roel Heijmans; H Marike Boezen; David A van Heel; Ad van Bodegraven; Pieter C F Stokkers; Cisca Wijmenga; J Bart A Crusius; Rinse Weersma
Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP.
American journal of human genetics 2008;82(5):1202-10.
2007: Alexandra Zhernakova; Behrooz Alizadeh; Marianna R Bevova; Miek A van Leeuwen; Marieke Coenen; Barbara Franke; Lude Franke; Marcel D Posthumus; David A van Heel; Gerrit van der Steege; Timothy Radstake; Pilar Barrera; Bart O Roep; Bobby P C Koeleman; Cisca Wijmenga
Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases.
American journal of human genetics 2007;81(6):1284-8.
2006: Marianna R Bevova; Yurii Aulchenko; Soner Aksu; Ulla Renne; Gudrun A Brockmann
Chromosome-wise dissection of the genome of the extremely big mouse line DU6i.
Genetics 2006;172(1):401-10.
2005: Alienke J Monsuur; Paul I W de Bakker; Behrooz Alizadeh; Alexandra Zhernakova; Marianna R Bevova; Eric Strengman; Lude Franke; Ruben van't Slot; Martine J Van Belzen; Ineke C M Lavrijsen; Begoña Diosdado; Mark J Daly; Chris J J Mulder; M Luisa Mearin; Jos W R Meijer; Gerrit A Meijer; Erica van Oort; Martin C Wapenaar; Bobby P C Koeleman; Cisca Wijmenga
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect.
Nature genetics 2005;37(12):1341-4.
2002: Gudrun A Brockmann; Marianna R Bevova
Using mouse models to dissect the genetics of obesity.
Trends in genetics : TIG 2002;18(7):367-76.