(Q33778721)

29 July 2017

title

Microarray-based maps of copy-number variant regions in European and sub-Saharan populations (English)

1 reference

Andreas Papassotiropoulos

29 July 2017

1 reference

Christian Vogler

1

0 references

object named as

Andreas Papassotiropoulos

14

1 reference

ORCID Public Data File 2021

Iris-Tatjana Kolassa

11

object named as

Iris-Tatjana Kolassa

1 reference

29 July 2017

Dominique de Quervain

13

object named as

Dominique J-F de Quervain

1 reference

29 July 2017

12

Thomas Elbert

1 reference

29 July 2017

8

Attila Stetak

1 reference

29 July 2017

7

Bianca Auschra

1 reference

29 July 2017

10

Vanja Vukojevic

1 reference

29 July 2017

Leo Gschwind

2

1 reference

29 July 2017

Benno Röthlisberger

3

1 reference

29 July 2017

Andreas Huber

4

1 reference

29 July 2017

Isabel Filges

5

1 reference

29 July 2017

Peter Miny

6

1 reference

29 July 2017

Philippe Demougin

9

1 reference

29 July 2017

language of work or name

English

0 references

publication date

16 December 2010

1 reference

29 July 2017

1 reference

29 July 2017

volume

5

1 reference

29 July 2017

issue

12

1 reference

29 July 2017

page(s)

e15246

1 reference

Creative Commons Attribution 4.0 International

29 July 2017

copyright license

start time

16 December 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

The 1000 Genomes Project: new opportunities for research and social challenges

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Methodological challenges of genome-wide association analysis in Africa

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Comparing CNV detection methods for SNP arrays

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Mechanisms of change in gene copy number

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Trauma, poverty and mental health among Somali and Rwandese refugees living in an African refugee settlement - an epidemiological study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

CNV-seq, a new method to detect copy number variation using high-throughput sequencing

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Integrated detection and population-genetic analysis of SNPs and copy number variation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Genotype, haplotype and copy-number variation in worldwide human populations

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Going the distance: human population genetics in a clinal world.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Relative impact of nucleotide and copy number variation on gene expression phenotypes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

A faster circular binary segmentation algorithm for the analysis of array CGH data

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Global variation in copy number in the human genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Primate segmental duplications: crucibles of evolution, diversity and disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Structural variation in the human genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Segmental duplications and copy-number variation in the human genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Large-scale copy number polymorphism in the human genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Role of evolutionary history on haplotype block structure in the human genome: implications for disease mapping

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Genetic structure of human populations

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

The structure of haplotype blocks in the human genome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002949

Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genome.

4 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0015246

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21179565

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33: clinical and array-CGH study of a benign phenotype in a three-generation family

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21179565

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0015246

1 reference

29 July 2017

0 references

1 reference

29 July 2017

1 reference