(Q46530826)

22 December 2017

title

Genome-wide association analyses identify variants in developmental genes associated with hypospadias (English)

1 reference

22 December 2017

genome-wide association study

main subject

0 references

author

Mads Vilhelm Hollegaard

10

1 reference

22 December 2017

Lude Franke

15

1 reference

22 December 2017

Agneta Nordenskjöld

17

1 reference

22 December 2017

Izabella Baranowska Körberg

6

Izabella Baranowska Körberg

0 references

Mads Melbye

19

Mads Melbye

0 references

Bjarke Feenstra

Bjarke Feenstra

2

0 references

Tune H Pers

Tune H Pers

4

0 references

Frank Geller

Frank Geller

1

0 references

Joel Hirschhorn

14

Joel N Hirschhorn

1 reference

22 December 2017

author name string

Lisbeth Carstensen

3

1 reference

22 December 2017

Iris A L M van Rooij

5

1 reference

22 December 2017

Izabella Baranowska Körberg

6

1 reference

22 December 2017

Shweta Choudhry

7

1 reference

22 December 2017

Juha M Karjalainen

8

1 reference

22 December 2017

Tine H Schnack

9

1 reference

22 December 2017

Wout F J Feitz

11

1 reference

22 December 2017

Nel Roeleveld

12

1 reference

22 December 2017

David M Hougaard

13

1 reference

22 December 2017

Laurence S Baskin

16

1 reference

22 December 2017

Loes F M van der Zanden

18

1 reference

22 December 2017

language of work or name

English

0 references

publication date

10 August 2014

1 reference

22 December 2017

published in

Nature Genetics

1 reference

22 December 2017

volume

46

1 reference

22 December 2017

issue

9

1 reference

22 December 2017

page(s)

957-963

1 reference

22 December 2017

Urethral seam formation and hypospadias.

cites work

1 reference

Aetiology of hypospadias: a systematic review of genes and environment

21 January 2018

1 reference

Hypospadias: anatomy, etiology, and technique

21 January 2018

1 reference

Is hypospadias a genetic, endocrine or environmental disease, or still an unexplained malformation?

21 January 2018

1 reference

Common variants in DGKK are strongly associated with risk of hypospadias

21 January 2018

1 reference

A map of human genome variation from population-scale sequencing

21 January 2018

1 reference

LocusZoom: regional visualization of genome-wide association scan results

21 January 2018

1 reference

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

21 January 2018

1 reference

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

21 January 2018

1 reference

A method and server for predicting damaging missense mutations

21 January 2018

1 reference

Identification of deleterious mutations within three human genomes

21 January 2018

1 reference

MutationTaster evaluates disease-causing potential of sequence alterations

21 January 2018

1 reference

Genome-wide association study identifies four loci associated with eruption of permanent teeth

21 January 2018

1 reference

Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances

21 January 2018

1 reference

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

21 January 2018

1 reference

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

21 January 2018

1 reference

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

21 January 2018

1 reference

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility

21 January 2018

1 reference

Genome-wide association study identifies five loci associated with lung function

21 January 2018

1 reference

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

21 January 2018

1 reference

Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

21 January 2018

1 reference

Systematic identification of trans eQTLs as putative drivers of known disease associations

21 January 2018

1 reference

GCTA: a tool for genome-wide complex trait analysis

21 January 2018

1 reference

Estimating missing heritability for disease from genome-wide association studies

21 January 2018

1 reference

Diacylglycerol kinase K variants impact hypospadias in a California study population

21 January 2018

1 reference

HOX homeobox genes exhibit spatial and temporal changes in expression during human skin development

21 January 2018

1 reference

21 January 2018

Human HOX gene mutations

1 reference

The eyes absent gene: genetic control of cell survival and differentiation in the developing Drosophila eye.

21 January 2018

1 reference

Six1 and Eya1 are critical regulators of peri-cloacal mesenchymal progenitors during genitourinary tract development.

21 January 2018

1 reference

Comparative gene expression analysis of genital tubercle development reveals a putative appendicular Wnt7 network for the epidermal differentiation

21 January 2018

1 reference

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

21 January 2018

1 reference

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

21 January 2018

1 reference

Genome-wide meta-analysis identifies new susceptibility loci for migraine

21 January 2018

1 reference

Genomic control for association studies

21 January 2018

1 reference

Genotype imputation for genome-wide association studies

21 January 2018

1 reference

A linear complexity phasing method for thousands of genomes

21 January 2018

1 reference

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

21 January 2018

1 reference

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

METAL: fast and efficient meta-analysis of genomewide association scans

21 January 2018

1 reference

Quantifying heterogeneity in a meta-analysis

21 January 2018

1 reference

Identifying a high fraction of the human genome to be under selective constraint using GERP++.

21 January 2018

1 reference

SMIM1 underlies the Vel blood group and influences red blood cell traits

21 January 2018

1 reference

A human phenome-interactome network of protein complexes implicated in genetic disorders

21 January 2018

1 reference

The mouse genome database: genotypes, phenotypes, and models of human disease

21 January 2018

1 reference

Reactome: a database of reactions, pathways and biological processes

21 January 2018

1 reference

KEGG for integration and interpretation of large-scale molecular data sets

21 January 2018

1 reference

Gene ontology: tool for the unification of biology

21 January 2018

1 reference

Clustering by passing messages between data points

21 January 2018

1 reference

APCluster: an R package for affinity propagation clustering

21 January 2018

1 reference

A travel guide to Cytoscape plugins

21 January 2018

1 reference

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

21 January 2018

1 reference

Familial Aggregation of Hypospadias: A Cohort Study

21 January 2018

1 reference

Mutation screening of BMP4, BMP7, HOXA4 and HOXB6 genes in Chinese patients with hypospadias

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25108383

12 December 2020

inferred from PubMed ID database lookup

Loss of Bmp7 and Fgf8 signaling in Hoxa13-mutant mice causes hypospadia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25108383

12 December 2020

inferred from PubMed ID database lookup

A Wilcoxon-type test for trend

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25108383

12 December 2020

inferred from PubMed ID database lookup

New Methods for Detecting Lineage-Specific Selection

1 reference

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.3063

1 reference

22 December 2017

1 reference

22 December 2017