(Q24568378)

16

0 references

Olivier Goureau

15

Olivier Goureau

0 references

Said El Shamieh

Said El Shamieh

1

0 references

Christina Zeitz

Christina Zeitz

17

0 references

Isabelle Audo

Isabelle Audo

18

0 references

Vanessa Démontant

6

Vanessa Démontant

0 references

Marion Neuillé

2

Marion Neuillé

0 references

Marie-Elise Lancelot

10

Marie-Elise Lancelot

0 references

Thierry Léveillard

13

Thierry Léveillard

0 references

Angélique Terray

3

Angélique Terray

0 references

Saddek Mohand-Saïd

14

Saddek Mohand-Saïd

0 references

Elise Orhan

4

Elise Orhan

0 references

Mélanie Letexier

11

Mélanie Letexier

0 references

Fiona Boyard

9

Fiona Boyard

0 references

Aline Antonio

8

Aline Antonio

0 references

Christelle Michiels

7

Christelle Michiels

0 references

author name string

Christel Condroyer

5

0 references

Jean-Paul Saraiva

American Journal of Human Genetics

12

0 references

language of work or name

English

0 references

publication date

3 April 2014

0 references

published in

0 references

volume

94

0 references

issue

4

0 references

page(s)

625-33

0 references

cites work

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness

1 reference

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Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa

24 March 2017

1 reference

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TOPORS, implicated in retinal degeneration, is a cilia-centrosomal protein

24 March 2017

1 reference

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A map of human genome variation from population-scale sequencing

24 March 2017

1 reference

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Discovery and functional analysis of a retinitis pigmentosa gene, C2ORF71

24 March 2017

1 reference

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The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary cilium

24 March 2017

1 reference

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A quantitative atlas of mitotic phosphorylation

24 March 2017

1 reference

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Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy

24 March 2017

1 reference

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Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy

24 March 2017

1 reference

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The Plk1 target Kizuna stabilizes mitotic centrosomes to ensure spindle bipolarity

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

24 March 2017

1 reference

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Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Positional cloning of the gene for X-linked retinitis pigmentosa 2

24 March 2017

1 reference

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A method and server for predicting damaging missense mutations

24 March 2017

1 reference

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Mutations in RAB28, encoding a farnesylated small GTPase, are associated with autosomal-recessive cone-rod dystrophy

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Integrating common and rare genetic variation in diverse human populations

7 April 2017

1 reference

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

When cilia go bad: cilia defects and ciliopathies

7 April 2017

1 reference

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Evolution and functional impact of rare coding variation from deep sequencing of human exomes

7 April 2017

1 reference

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7 April 2017

1 reference

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Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosa

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosa

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

C-NAP1 and rootletin restrain DNA damage-induced centriole splitting and facilitate ciliogenesis.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Non-syndromic retinal ciliopathies: translating gene discovery into therapy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Transcriptional code and disease map for adult retinal cell types.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Novel C2orf71 mutations account for ∼1% of cases in a large French arRP cohort.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Transcriptome analysis and molecular signature of human retinal pigment epithelium

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

EYS is a major gene for rod-cone dystrophies in France.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Spectrum of rhodopsin mutations in French autosomal dominant rod-cone dystrophy patients

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Centrosome biogenesis and function: centrosomics brings new understanding

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Centriole/basal body morphogenesis and migration during ciliogenesis in animal cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

An evaluation of genetic distances for use with microsatellite loci.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Microtubules in the spermatids of stick insects

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980423

Molecular Mechanisms Controlling Midline Crossing by Precerebellar Neurons

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24680887

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2014.03.005

1 reference

1 reference

1 reference

PubMed publication ID

24680887

1 reference