High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases (Q31139643)

29 June 2017

High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases (English)

1 reference

29 June 2017

8

1 reference

29 June 2017

7

0 references

Thomas Illig

6

object named as

Thomas Illig

0 references

Stefan Schreiber

10

object named as

Stefan Schreiber

1 reference

ORCID Public Data File 2021

29 June 2017

1 reference

author name string

Nicole Herbon

1

1 reference

29 June 2017

Monika Werner

2

1 reference

29 June 2017

Christine Braig

3

1 reference

29 June 2017

Henning Gohlke

4

1 reference

29 June 2017

Gaby Dütsch

5

1 reference

29 June 2017

Annette Lantermann

9

1 reference

29 June 2017

Ezio Bonifacio

11

1 reference

29 June 2017

Annette Ziegler

12

1 reference

29 June 2017

Sibylle Schwab

13

1 reference

29 June 2017

Dieter Wildenauer

14

1 reference

29 June 2017

Dirk van den Boom

15

1 reference

29 June 2017

Andreas Braun

16

1 reference

29 June 2017

Michael Knapp

17

1 reference

29 June 2017

Peter Reitmeir

18

1 reference

29 June 2017

Matthias Wjst

19

1 reference

29 June 2017

1 May 2003

1 reference

29 June 2017

1 reference

29 June 2017

81

1 reference

29 June 2017

510-518

1 reference

29 June 2017

5

1 reference

Genetic dissection of complex traits: an overview

29 June 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Genomewide scans of complex human diseases: true linkage is hard to find

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Haplotype tagging for the identification of common disease genes

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortium

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Recombination within the human MHC.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography, chromosome recombination frequency and selection

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

A Genome-wide Search for Linkage to Asthma22See the Appendix

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

HLA associations in type 1 diabetes: merging genetics and immunology

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Large-scale determination of SNP allele frequencies in DNA pools using MALDI-TOF mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Population genetics--making sense out of sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

On the allelic spectrum of human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

NOD2 (CARD15), the first susceptibility gene for Crohn's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

The map problem: a comparison of genetic and sequence-based physical maps

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

An evaluation of the draft human genome sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Stratification analysis of MICA triplet repeat polymorphisms and HLA antigens associated with ulcerative colitis in Japanese

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Independent contribution of HLA-DRB1 and TNF alpha promoter polymorphisms to the susceptibility to Crohn's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Association between quantitative traits underlying asthma and the HLA-DRB1 locus in a family-based population sample

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Autoantibody appearance and risk for development of childhood diabetes in offspring of parents with type 1 diabetes: the 2-year analysis of the German BABYDIAB Study

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Detection of RET proto-oncogene codon 634 mutations using mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

Genomic control for association studies

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2802%2900035-6

7 January 2021

10.1016/S0888-7543(02)00035-6

Identifiers

DOI

1 reference

29 June 2017

1 reference