Expression and association data strongly support JARID2 involvement in nonsyndromic cleft lip with or without cleft palate (Q33588767)

28 July 2017

Expression and association data strongly support JARID2 involvement in nonsyndromic cleft lip with or without cleft palate (English)

1 reference

cleft lip with or without cleft palate

28 July 2017

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1 reference

Anna Monica Rosaria Bianco

inferred from title

author

series ordinal

7

object named as

Anna Monica Bianco

1 reference

28 July 2017

Anna Savoia

6

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Luca Scapoli

object named as

Luca Scapoli

series ordinal

1

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Furio Pezzetti

series ordinal

3

object named as

Furio Pezzetti

1 reference

28 July 2017

8

Francesco Carinci

1 reference

28 July 2017

4

Annalisa Palmieri

1 reference

28 July 2017

2

Marcella Martinelli

1 reference

28 July 2017

5

Ambra Girardi

1 reference

28 July 2017

1 July 2010

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28 July 2017

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28 July 2017

31

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28 July 2017

7

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28 July 2017

794-800

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Haploview: analysis and visualization of LD and haplotype maps

28 July 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Common and rare variants in multifactorial susceptibility to common diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Human genetic factors in nonsyndromic cleft lip and palate: an update

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Mapping of three translocation breakpoints associated with orofacial clefting within 6p24 and identification of new transcripts within the region

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

On Confidence Intervals for Genotype Relative Risks and Attributable Risks from Case Parent Trio Designs for Candidate-Gene Studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

The family based association test method: strategies for studying general genotype--phenotype associations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Roles of JUMONJI in mouse embryonic development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

JUMONJI, a critical factor for cardiac development, functions as a transcriptional repressor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Cleft lip with or without cleft palate: implication of the heavy chain of non-muscle myosin IIA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

A decade of discoveries in cardiac biology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Splicing Factors Induce Cystic Fibrosis Transmembrane Regulator Exon 9 Skipping through a Nonevolutionary Conserved Intronic Element

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

JARID2 regulates binding of the Polycomb repressive complex 2 to target genes in ES cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Jarid2/Jumonji coordinates control of PRC2 enzymatic activity and target gene occupancy in pluripotent cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Combined segregation and linkage analysis of nonsyndromic orofacial cleft in two candidate regions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Evidence of linkage to 6p23 and genetic heterogeneity in nonsyndromic cleft lip with or without cleft palate

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Confidence intervals for genotype relative risks and allele frequencies from the case parent trio design for candidate-gene studies.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Multiplex relative risk and estimation of the number of loci underlying an inherited disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

The 6p deletion syndrome: a new orofacial clefting syndrome and its implications for antenatal screening.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21266

7 January 2021

Identifiers

DOI

10.1002/HUMU.21266

1 reference

28 July 2017

1 reference

PubMed ID

20506229