(Q33424084)

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Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta

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scholarly article

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Europe PubMed Central

PubMed publication ID

26 July 2017

Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

osteogenesis imperfecta

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Pierre Lindenbaum

11

object named as

Pierre Lindenbaum

0 references

Frédéric Tores

10

object named as

Frédéric Tores

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object named as

Anne Philippi

13

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author name string

Peter Brooks

1

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Europe PubMed Central

PubMed publication ID

26 July 2017

Charles Marcaillou

2

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Europe PubMed Central

PubMed publication ID

26 July 2017

Maud Vanpeene

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Jean-Paul Saraiva

4

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Daniel Stockholm

5

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Stephan Francke

6

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Reyna Favis

7

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Nadine Cohen

8

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Francis Rousseau

9

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Frédéric Tores

10

1 reference

Europe PubMed Central

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26 July 2017

Jörg Hager

12

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Europe PubMed Central

PubMed publication ID

26 July 2017

publication date

30 March 2009

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Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

16

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

copyright license

Creative Commons Attribution 2.0 Generic

30 March 2009

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April 2022 Public Data File from Crossref

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April 2022 Public Data File from Crossref

Detection of sharing by descent, long-range phasing and haplotype imputation

1 reference

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Next-generation DNA sequencing

1 reference

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A SNP streak model for the identification of genetic regions identical-by-descent

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1 reference

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A pragmatic suggestion for dealing with results for candidate genes obtained from genome wide association studies

1 reference

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Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.

1 reference

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Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

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Ranks of genuine associations in whole-genome scans.

1 reference

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Mismatch cleavage by single-strand specific nucleases

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Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

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MutS-DNA interactions and DNase protection analysis with surface plasmon resonance

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Searching for genetic determinants in the new millennium

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ATP hydrolysis-dependent formation of a dynamic ternary nucleoprotein complex with MutS and MutL.

1 reference

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21 June 2018

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

1 reference

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21 June 2018

Mutation detection using a novel plant endonuclease

1 reference

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21 June 2018

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

1 reference

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21 June 2018

Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances

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Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning

1 reference

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Fractionation of nucleic acids into single-stranded and double-stranded forms

1 reference

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A general statistical model for detecting complex-trait loci by using affected relative pairs in a genome search

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Mutation detection with MutH, MutL, and MutS mismatch repair proteins

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Genomic mismatch scanning in pedigrees.

1 reference

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1 reference

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The probability that related individuals share some section of genome identical by descent.

1 reference

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Abnormal alpha 2-chain in type I collagen from a patient with a form of osteogenesis imperfecta

1 reference

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1 reference

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1 reference

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1 reference

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Mismatch-stimulated killing

1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2679057

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Room temperature method for increasing the rate of DNA reassociation by many thousandfold: the phenol emulsion reassociation technique

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2679057

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1 reference

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31 October 2018

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1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

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based on heuristic

inferred from PubMed ID database lookup

Guilt by association

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Identity by Descent Process along the Chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct IBD mapping: identical-by-descent mapping without genotyping

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factors affecting the kinetics of DNA reassociation in phenol-water emulsion at high DNA concentrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteogenesis imperfecta is linked to both type I collagen structural genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Finding similarities and differences among genomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A biotinylated MutS fusion protein and its use in a rapid mutation screening technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic mismatch scanning identifies human genomic DNA shared identical by descent

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enrichment for loci identical-by-descent between pairs of mouse or human genomes by genomic mismatch scanning

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Who needs genetic markers?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage-disequilibrium mapping without genotyping

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proof of "disease causing" mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19331686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2156-10-16

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Dimensions Publication ID

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2156-10-16

9 September 2019

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

ResearchGate publication ID

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