Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate. (Q52681596)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29489415%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

title

Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate (English)

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18 March 2020

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11

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Fadekemi Olufunmilayo Oginni

18 March 2020

14

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18 March 2020

Chika K Onwuamah

17

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18 March 2020

21

Mary L Marazita

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18 March 2020

16

Rosemary Audu

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18 March 2020

author name string

Lord Jephthah Joojo Gowans

1

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18 March 2020

Ganiyu Oseni

2

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18 March 2020

Peter A Mossey

3

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18 March 2020

Wasiu Lanre Adeyemo

4

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18 March 2020

Mekonen A Eshete

5

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18 March 2020

Tamara D Busch

6

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18 March 2020

Peter Donkor

7

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18 March 2020

Solomon Obiri-Yeboah

8

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18 March 2020

Gyikua Plange-Rhule

9

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18 March 2020

Alexander A Oti

10

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18 March 2020

Peter B Olaitan

12

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18 March 2020

Babatunde S Aregbesola

13

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18 March 2020

Seidu A Bello

15

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18 March 2020

Pius Agbenorku

18

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18 March 2020

Mobolanle O Ogunlewe

19

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18 March 2020

Lukman O Abdur-Rahman

20

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18 March 2020

A A Adeyemo

22

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18 March 2020

Jeffrey C Murray

23

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18 March 2020

Azeez Butali

24

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18 March 2020

language of work or name

English

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publication date

28 February 2018

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Cleft Palate: Craniofacial Journal

18 March 2020

published in

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18 March 2020

volume

55

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18 March 2020

page(s)

736-742

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18 March 2020

issue

5

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Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity

18 March 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunities

25 August 2018

1 reference

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Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population.

25 August 2018

1 reference

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Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa

25 August 2018

1 reference

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Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway

25 August 2018

1 reference

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Epidemiology of oral clefts 2012: an international perspective.

25 August 2018

1 reference

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Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders.

25 August 2018

1 reference

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Genetic determination of human facial morphology: links between cleft-lips and normal variation

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Cleft lip and palate: understanding genetic and environmental influences

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome "tiling path" BAC array in a girl with heart defect, cleft palate, and developmental delay.

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

DRM/GREMLIN (CKTSF1B1) maps to human chromosome 15 and is highly expressed in adult and fetal brain

25 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6081638

25 August 2018

Identifiers

DOI

10.1177/1055665618754948

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29489415%20AND%20SRC:MED&resulttype=core&format=json

18 March 2020

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18 March 2020

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