(Q21091121)

English

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia

scientific article

Maternal Genes and Facial Clefts in Offspring: A Comprehensive Search for Genetic Associations in Two Population-Based Cleft Studies from Scandinavia

In more languages

Statements

scholarly article

0 references

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia (English)

0 references

Abee Lowman Boyles

8

object named as

Abee Lowman Boyles

author given names

Abee Lowman

author last names

Boyles

1 reference

10 August 2022

Sandra Daack-Hirsch

9

object named as

Sandra Daack-Hirsch

author given names

Sandra

author last names

Daack-Hirsch

1 reference

10 August 2022

5

object named as

Allen James Wilcox

author given names

Allen James

author last names

Wilcox

1 reference

10 August 2022

Kaare Christensen

7

object named as

Kaare Christensen

author given names

Kaare

author last names

Christensen

1 reference

10 August 2022

author name string

Astanand Jugessur

1

author given names

Astanand

author last names

Jugessur

1 reference

10 August 2022

Min Shi

2

author given names

Min

author last names

Shi

1 reference

10 August 2022

Håkon Kristian Gjessing

3

author given names

Håkon Kristian

author last names

Gjessing

1 reference

10 August 2022

Rolv Terje Lie

4

author given names

Rolv Terje

author last names

Lie

1 reference

10 August 2022

Clarice Ring Weinberg

6

author given names

Clarice Ring

author last names

Weinberg

1 reference

10 August 2022

Truc Trung Nguyen

10

author given names

Truc Trung

author last names

Nguyen

1 reference

10 August 2022

Lene Christiansen

11

author given names

Lene

author last names

Christiansen

1 reference

10 August 2022

Andrew Carl Lidral

12

author given names

Andrew Carl

author last names

Lidral

1 reference

10 August 2022

Jeffrey Clark Murray

13

author given names

Jeffrey Clark

author last names

Murray

1 reference

10 August 2022

language of work or name

0 references

publication date

2010

0 references

0 references

5

0 references

e11493

0 references

7

0 references

copyright license

Creative Commons Attribution 4.0 International

9 July 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Folic acid supplements and risk of facial clefts: national population based case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Contributions of PTCH gene variants to isolated cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

https://pubmed.ncbi.nlm.nih.gov/20634891

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

p53 activates expression of HIC-1, a new candidate tumour suppressor gene on 17p13.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Robinow syndrome: phenotypic variability in a family with a novel intragenic ROR2 mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Filamin B mutations cause chondrocyte defects in skeletal development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Filamins as integrators of cell mechanics and signalling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

Maternal rescue of transforming growth factor-beta 1 null mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

19 March 2017

A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

The genetics of isolated orofacial clefts: from genotypes to subphenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Familial risk of oral clefts by morphological type and severity: population based cohort study of first degree relatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Identification of risk-related haplotypes with the use of multiple SNPs from nuclear families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Orofacial clefting: recent insights into a complex trait

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Changing lifestyles and oral clefts occurrence in Denmark

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

The many faces of filamin: a versatile molecular scaffold for cell motility and signalling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Long term follow up study of survival associated with cleft lip and palate at birth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Do parents of children with congenital malformations have a higher cancer risk? A nationwide study in Denmark

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Genotype relative risks: methods for design and analysis of candidate-gene association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Maternal effects in human cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

12 September 2017

Wnt5a regulates directional cell migration and cell proliferation via Ror2-mediated noncanonical pathway in mammalian palate development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

27 September 2017

Isolation and embryonic expression of the novel mouse gene Hic1, the homologue of HIC1, a candidate gene for the Miller-Dieker syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

30 May 2018

Onset of endogenous synthesis of epidermal growth factor in neonatal mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

30 May 2018

Plots of P-values to evaluate many tests simultaneously

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011493

21 January 2018

Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011493

21 January 2018

Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller-Dieker syndrome.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011493

21 January 2018

Distinguishing the Effects of Maternal and Offspring Genes through Studies of "Case-Parent Triads"

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011493

21 January 2018

Autosomal dominant spondylocarpotarsal synostosis syndrome: phenotypic homogeneity and genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

29 November 2018

Case-parent triads: estimating single- and double-dose effects of fetal and maternal disease gene haplotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901336

29 November 2018

Genome-scan for loci involved in cleft lip with or without cleft palate in consanguineous families from Turkey

1 reference

https://pubmed.ncbi.nlm.nih.gov/20634891

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0011493

0 references

2010PLoSO...511493J

0 references

0 references

0 references

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q21091121&oldid=1870220781"