(Q46660448)

English

IBDfinder and SNPsetter: tools for pedigree-independent identification of autozygous regions in individuals with recessive inherited disease

scientific article published in June 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

IBDfinder and SNPsetter: tools for pedigree-independent identification of autozygous regions in individuals with recessive inherited disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

David T. Bonthron

5

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

author name string

Ian M Carr

1

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

Eamonn Sheridan

2

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

Bruce E Hayward

3

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

Alexander F Markham

4

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

publication date

1 June 2009

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

30

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

6

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

960-967

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

The size distribution of homozygous segments in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

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Lack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germline

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of information due to ambiguous haplotyping of SNPs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

A global disorder of imprinting in the human female germ line.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

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Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

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Estimation of the inbreeding coefficient through use of genomic data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

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On the relative abundance of bird species

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

Autozygosity mapping, complex consanguinity, and autosomal recessive disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

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Convergent adaptation of human lactase persistence in Africa and Europe

1 reference

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7 January 2021

based on heuristic

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Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

Quantification of homozygosity in consanguineous individuals with autosomal recessive disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

A new method for autozygosity mapping using single nucleotide polymorphisms (SNPs) and EXCLUDEAR.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20974

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.20974

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/19405095

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