(Q33905163)

29 July 2017

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. (English)

1 reference

single-nucleotide polymorphism

29 July 2017

1 reference

Margaret A. Pericak-Vance

inferred from title

author

17

Margaret A Pericak-Vance

0 references

Kyriacos Markianos

Kyriacos Markianos

15

0 references

Ellen M. Wijsman

Ellen Wijsman

5

0 references

Steven Buyske

Steven Buyske

7

0 references

Lincoln Stein

19

Lincoln Stein

1 reference

29 July 2017

1

Tara C Matise

1 reference

29 July 2017

Andrew G Clark

3

1 reference

ORCID Public Data File 2021

Jeremy Heil

14

Jeremy Heil

1 reference

29 July 2017

12

Stephen Glanowski

1 reference

29 July 2017

23

Emily S Winn-Deen

1 reference

29 July 2017

16

Ivy McMullen

1 reference

29 July 2017

Ravi Sachidanandam

2

1 reference

29 July 2017

Leonid Kruglyak

4

1 reference

29 July 2017

Jerzy Kakol

6

1 reference

29 July 2017

Buena Chui

8

1 reference

29 July 2017

Patrick Cohen

9

1 reference

29 July 2017

Claudia de Toma

10

1 reference

29 July 2017

Margaret Ehm

11

1 reference

29 July 2017

Chunsheng He

13

1 reference

29 July 2017

Arkadiy Silbergleit

18

1 reference

29 July 2017

Michael Wagner

20

1 reference

29 July 2017

Alexander F Wilson

21

1 reference

29 July 2017

Jeffrey D Winick

22

1 reference

29 July 2017

Carl T Yamashiro

24

1 reference

29 July 2017

Howard M Cann

25

1 reference

29 July 2017

Eric Lai

26

1 reference

29 July 2017

Arthur L Holden

27

1 reference

29 July 2017

language of work or name

English

0 references

publication date

3 July 2003

1 reference

American Journal of Human Genetics

29 July 2017

1 reference

29 July 2017

73

1 reference

29 July 2017

271-284

1 reference

29 July 2017

2

1 reference

High throughput genotyping technologies

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

A high-resolution recombination map of the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Progress in high throughput SNP genotyping methods

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

An automated computer system to support ultra high throughput SNP genotyping.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Detection and integration of genotyping errors in statistical genetics

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Efficient multipoint linkage analysis through reduction of inheritance space

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Initial sequencing and analysis of the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

The Sequence of the Human Genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Genotyping for human whole-genome scans: past, present, and future

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Allegro, a new computer program for multipoint linkage analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Equivalence of single- and multilocus markers: power to detect linkage with composite markers derived from biallelic loci

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

A fast and scalable radiation hybrid map construction and integration strategy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia. A clinical and molecular genetic study of 28 United Kingdom families.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Comprehensive human genetic maps: individual and sex-specific variation in recombination

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

The future of genetic studies of complex human diseases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Faster sequential genetic linkage computations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Strategies for multilocus linkage analysis in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Construction of multilocus genetic linkage maps in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

A second-generation linkage map of the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Avoiding recomputation in linkage analysis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180367

Bias in multipoint linkage analysis arising from map misspecification

29 October 2018

1 reference

12 December 2020

Chromosome-based method for rapid computer simulation in human genetic linkage analysis

1 reference

12 December 2020

Multipoint linkage analysis. A cautionary note

1 reference

12 December 2020

The new genomics: global views of biology

1 reference

12 December 2020

The use of a genetic map of biallelic markers in linkage studies

1 reference

12 December 2020

Variations on a theme: cataloging human DNA sequence variation

1 reference

12 December 2020

Identifiers

DOI

10.1086/377137

1 reference

release_ghd6cp5xfffaxdpppf4nmngkka

29 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ghd6cp5xfffaxdpppf4nmngkka

24 November 2022

mapped directly with Wikidata item

PMCID

1180367

1 reference

29 July 2017

1 reference