(Q34200920)

English

Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure

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scholarly article

1 reference

Europe PubMed Central

31 July 2017

Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure (English)

1 reference

Europe PubMed Central

31 July 2017

Sandrine Caburet

object named as

Sandrine Caburet

1

0 references

object named as

Paul Laissue

8

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object named as

Giovanni Levi

12

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author name string

Petra Zavadakova

2

1 reference

Europe PubMed Central

31 July 2017

Ziva Ben-Neriah

3

1 reference

Europe PubMed Central

31 July 2017

Kamal Bouhali

4

1 reference

Europe PubMed Central

31 July 2017

Aurélie Dipietromaria

5

1 reference

Europe PubMed Central

31 July 2017

Céline Charon

6

1 reference

Europe PubMed Central

31 July 2017

Céline Besse

7

1 reference

Europe PubMed Central

31 July 2017

Vered Chalifa-Caspi

9

1 reference

Europe PubMed Central

31 July 2017

Sophie Christin-Maitre

10

1 reference

Europe PubMed Central

31 July 2017

Daniel Vaiman

11

1 reference

Europe PubMed Central

31 July 2017

Reiner A Veitia

13

1 reference

Europe PubMed Central

31 July 2017

Marc Fellous

14

1 reference

Europe PubMed Central

31 July 2017

language of work or name

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publication date

13 March 2012

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

7

1 reference

Europe PubMed Central

31 July 2017

e33412

1 reference

Europe PubMed Central

31 July 2017

3

1 reference

Europe PubMed Central

31 July 2017

copyright license

Creative Commons Attribution 4.0 International

13 March 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency

1 reference

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5 July 2018

Steroid regulation of drug-metabolizing cytochromes P450.

1 reference

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5 July 2018

KinSNP software for homozygosity mapping of disease genes using SNP microarrays

1 reference

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5 July 2018

Roles of E3 ubiquitin ligases in cell adhesion and migration

1 reference

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5 July 2018

Clinical practice. Primary ovarian insufficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Dlx genes pattern mammalian jaw primordium by regulating both lower jaw-specific and upper jaw-specific genetic programs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

C. elegans dss-1 is functionally conserved and required for oogenesis and larval growth

1 reference

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5 July 2018

Positive regulation of steroidogenic acute regulatory protein gene expression through the interaction between Dlx and GATA-4 for testicular steroidogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

NOBOX homeobox mutation causes premature ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Missense mutations in the BMP15 gene are associated with ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

An update: spontaneous premature ovarian failure is not an early menopause

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Molecular cloning of porcine growth differentiation factor 9 (GDF-9) cDNA and its role in early folliculogenesis: direct ovarian injection of GDF-9 gene fragments promotes early folliculogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Identification of novel mutations in FOXL2 associated with premature ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Premature ovarian failure: a systematic review on therapeutic interventions to restore ovarian function and achieve pregnancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Targeted deletion of the Vgf gene indicates that the encoded secretory peptide precursor plays a novel role in the regulation of energy balance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Genes and premature ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Atm-deficient mice: a paradigm of ataxia telangiectasia

1 reference

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5 July 2018

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

1 reference

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5 July 2018

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302824

5 July 2018

Turner's Syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0033412

21 January 2018

Ovarian histological findings in an adult patient with the steroidogenic acute regulatory protein (StAR) deficiency reveal the impairment of steroidogenesis by lipoid deposition

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0033412

21 January 2018

Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0033412

21 January 2018

Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0033412

21 January 2018

Premature ovarian failure

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0033412

21 January 2018

[Premature ovarian failure]

1 reference

https://pubmed.ncbi.nlm.nih.gov/22428046

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Premature ovarian failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/22428046

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Empty follicle syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22428046

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Premature ovarian failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/22428046

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel 30 bp deletion in the FOXL2 gene in a phenotypically normal woman with primary amenorrhoea: case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/22428046

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HaploPainter: a tool for drawing pedigrees with complex haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22428046

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0033412

1 reference

Europe PubMed Central

31 July 2017

2012PLoSO...733412C

0 references

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

ResearchGate publication ID

0 references

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