M. Bevova

发表

Direct chromosome-length haplotyping by single-cell sequencing

Victor Guryev, Mark Hills, Ashley D Sanders, 2016, Genome research.

Bloom syndrome cells display sister chromatid exchanges at actively transcribed G4 motifs

M. Hills, V. Guryev, D. Spierings, 2016 .

The Genetics of MDD – A Review of Challenges and Opportunities

P. Heutink, W. Hoogendijk, M. Bevova, 2014 .

A Fine-Mapping Study of 7 Top Scoring Genes from a GWAS for Major Depressive Disorder

B. Penninx, G. Willemsen, D. Boomsma, 2012, PloS one.

Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1

J. López-Sendón, P. Heutink, S. Jain, 2015, Cerebellum.

Cytotoxic Activity of Mellitin Expressed by Recombinant Vectors in Cells of Acholeplasma laidlawii and Mycoplasma hominis

V. Govorun, N. M. Aleksandrova, M. Bevova, 2004, Russian Journal of Genetics.

Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

Cisca Wijmenga, Begoña Diosdado, Eric Strengman, 2005, Nature Genetics.

The New Coronavirus COVID-19 Infection

Y. Aulchenko, S. Netesov, M. Bevova, 2020, Molecular Genetics, Microbiology and Virology.

New coronavirus infection COVID-19

Y. Aulchenko, S. Netesov, M. Bevova, 2020, Molecular Genetics Microbiology and Virology (Russian version).

Using mouse models to dissect the genetics of obesity.

G. Brockmann, M. Bevova, 2002, Trends in genetics : TIG.

Chromosome-Wise Dissection of the Genome of the Extremely Big Mouse Line DU6i

Y. Aulchenko, G. Brockmann, M. Bevova, 2006, Genetics.

Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases.

B. Franke, A. Zhernakova, C. Wijmenga, 2007, American journal of human genetics.

Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia

J. López-Sendón, P. Heutink, P. Rizzu, 2014, Clinical genetics.

Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity.

P. Lockhart, A. Vanderver, S. Grimmond, 2013, American journal of human genetics.

Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP.

A. Zhernakova, C. Wijmenga, H. Boezen, 2008, American journal of human genetics.

Multiple independent variants in 6 q 21-22 associated with susceptibility to celiac disease in the Dutch , Finnish and Hungarian populations

A. Zhernakova, C. Wijmenga, J. Kere, 2011 .

Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria.

E. Sistermans, M. McDonald, T. Ben-Omran, 2013, American journal of human genetics.

Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitisAn unusual case of ascites

C. Wijmenga, D. Heel, M. Wapenaar, 2007, Gut.

A common polymorphism in the ABCB1 gene is associated with side effects of PGP-dependent antidepressants in a large naturalistic Dutch cohort

P. Heutink, Y. Milaneschi, B. Penninx, 2015, The Pharmacogenomics Journal.

The TRAF1-C5 region on chromosome 9q33 is associated with multiple autoimmune diseases

C. Wijmenga, J. Houwing-Duistermaat, L. H. van den Berg, 2009, Annals of the rheumatic diseases.

Resequencing Three Candidate Genes for Major Depressive Disorder in a Dutch Cohort

B. Penninx, D. Boomsma, E. D. de Geus, 2013, PloS one.

Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1

J. López-Sendón, P. Heutink, S. Jain, 2015, The Cerebellum.

Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1

J. López-Sendón, P. Heutink, Shu-Bing Qian, 2015, Cerebellum.