Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
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Title
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
Authors
Keywords
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Journal
Scientific Reports
Volume 7, Issue 1, Pages -
Publisher
Springer Nature
Online
2017-10-30
DOI
10.1038/s41598-017-15062-9
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Note: Only part of the references are listed.- Reference-based phasing using the Haplotype Reference Consortium panel
- (2016) Po-Ru Loh et al. NATURE GENETICS
- A reference panel of 64,976 haplotypes for genotype imputation
- (2016) NATURE GENETICS
- Next-generation genotype imputation service and methods
- (2016) Sayantan Das et al. NATURE GENETICS
- Testing Rare-Variant Association without Calling Genotypes Allows for Systematic Differences in Sequencing between Cases and Controls
- (2016) Yi-Juan Hu et al. PLoS Genetics
- Batteries
- (2015) Brian Owens NATURE
- Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic
- (2014) Andriy Derkach et al. BIOINFORMATICS
- MutationTaster2: mutation prediction for the deep-sequencing age
- (2014) Jana Marie Schwarz et al. NATURE METHODS
- Comparison of Methods to Account for Relatedness in Genome-Wide Association Studies with Family-Based Data
- (2014) Jakris Eu-ahsunthornwattana et al. PLoS Genetics
- Molecular Defects in the Motor Adaptor BICD2 Cause Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance
- (2013) Kristien Peeters et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy
- (2013) Kornelia Neveling et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in POFUT1, Encoding Protein O-fucosyltransferase 1, Cause Generalized Dowling-Degos Disease
- (2013) Ming Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- TNXB Mutations Can Cause Vesicoureteral Reflux
- (2013) R. A. Gbadegesin et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT
- (2013) Vivienne C.M. Neeve et al. MITOCHONDRION
- Common variants in the HLA-DRB1–HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
- (2013) Michaela Fakiola et al. NATURE GENETICS
- Deletion of Fibroblast Growth Factor Receptor 2 from the Peri-Wolffian Duct Stroma Leads to Ureteric Induction Abnormalities and Vesicoureteral Reflux
- (2013) Kenneth A. Walker et al. PLoS One
- A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development
- (2013) J. M. Darlow et al. Molecular Genetics & Genomic Medicine
- Titin mutation segregates with hereditary myopathy with early respiratory failure
- (2012) Gerald Pfeffer et al. BRAIN
- Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration
- (2012) H. Thorvaldsdottir et al. BRIEFINGS IN BIOINFORMATICS
- Cohort Profile: The ‘Children of the 90s’—the index offspring of the Avon Longitudinal Study of Parents and Children
- (2012) Andy Boyd et al. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
- Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
- (2011) R. E. Dickinson et al. BLOOD
- Primary, Nonsyndromic Vesicoureteric Reflux and Nephropathy in Sibling Pairs: A United Kingdom Cohort for a DNA Bank
- (2011) H. J. Lambert et al. Clinical Journal of the American Society of Nephrology
- The GUDMAP database - an online resource for genitourinary research
- (2011) S. D. Harding et al. DEVELOPMENT
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
- (2011) Stephen Sawcer et al. NATURE
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- FaST linear mixed models for genome-wide association studies
- (2011) Christoph Lippert et al. NATURE METHODS
- LocusZoom: regional visualization of genome-wide association scan results
- (2010) R. J. Pruim et al. BIOINFORMATICS
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- High Incidence of Vesicoureteral Reflux in Mice With Fgfr2 Deletion in Kidney Mesenchyma
- (2010) David S. Hains et al. JOURNAL OF UROLOGY
- Variance component model to account for sample structure in genome-wide association studies
- (2010) Hyun Min Kang et al. NATURE GENETICS
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5
- (2009) Christine E Briggs et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux
- (2009) H. J. Cordell et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- A Recessive Gene for Primary Vesicoureteral Reflux Maps to Chromosome 12p11-q13
- (2009) P. L. Weng et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- (2009) Prateek Kumar et al. Nature Protocols
- Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24
- (2009) S. Ashraf et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Vesicoureteral Reflux
- (2008) G. Williams et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- GUDMAP: The Genitourinary Developmental Molecular Anatomy Project
- (2008) A. P. McMahon et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity
- (2008) Maria Luisa Conte et al. PEDIATRIC NEPHROLOGY
- Role of Fibroblast Growth Factor Receptor 2 in Kidney Mesenchyme
- (2008) David Hains et al. PEDIATRIC RESEARCH
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