Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. (Q33998487)

30 July 2017

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

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30 July 2017

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13

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30 July 2017

Sandra Daack-Hirsch

8

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Mauricio Arcos-Burgos

Mauricio Arcos-Burgos

4

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Joan Bailey-Wilson

Joan E Bailey-Wilson

21

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Matthew Edwards

Matthew Edwards

27

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Mary L. Marazita

1

Mary L Marazita

1 reference

30 July 2017

Jeffrey C Murray

2

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30 July 2017

Andrew C Lidral

3

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30 July 2017

Margaret E Cooper

5

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30 July 2017

Toby Goldstein

6

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30 July 2017

Brion S Maher

7

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30 July 2017

Rebecca Schultz

9

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30 July 2017

M Adela Mansilla

10

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30 July 2017

L Leigh Field

11

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30 July 2017

You-e Liu

12

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30 July 2017

Sue Malcolm

14

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30 July 2017

Robin Winter

15

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30 July 2017

Ajit Ray

16

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30 July 2017

Lina Moreno

17

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30 July 2017

Consuelo Valencia

18

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30 July 2017

Katherine Neiswanger

19

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30 July 2017

Diego F Wyszynski

20

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30 July 2017

Hasan Albacha-Hejazi

22

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30 July 2017

Terri H Beaty

23

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30 July 2017

Iain McIntosh

24

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30 July 2017

Jacqueline B Hetmanski

25

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30 July 2017

Gökhan Tunçbilek

26

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30 July 2017

Louise Harkin

28

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30 July 2017

Rodney Scott

29

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30 July 2017

Laurence G Roddick

30

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30 July 2017

language of work or name

English

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publication date

4 June 2004

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American Journal of Human Genetics

30 July 2017

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30 July 2017

75

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30 July 2017

2

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30 July 2017

161-173

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Identification of SATB2 as the cleft palate gene on 2q32-q33.

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Fox's in development and disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Distribution of the titf2/foxe1 gene product is consistent with an important role in the development of foregut endoderm, palate, and hair.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Gene/environment causes of cleft lip and/or palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

The significance of not finding a gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Power to detect linkage based on multiple sets of data in the presence of locus heterogeneity: comparative evaluation of model-based linkage methods for affected sib pair data.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Implementing a unified approach to family-based tests of association.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

A chromosomal deletion map of human malformations.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Improved set of short-tandem-repeat polymorphisms for screening the human genome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Faster sequential genetic linkage computations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

A General Model for the Genetic Analysis of Pedigree Data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: a reanalysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Familial recurrence-pattern analysis of cleft lip with or without cleft palate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

TP63 mutation and clefting modifier genes in an EEC syndrome family

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Determining trait locus position from multipoint analysis: accuracy and power of three different statistics.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Meta-analysis of genome searches

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

Lods, wrods, and mods: the interpretation of lod scores calculated under different models.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1216052

A genome‐wide scan for loci predisposing to non‐syndromic cleft lip with or without cleft palate in two large Syrian families

29 October 2018

1 reference

12 December 2020

Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2

1 reference

12 December 2020

Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India

1 reference

12 December 2020

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

1 reference

12 December 2020

Transforming growth factor alpha locus and nonsyndromic cleft lip with or without cleft palate: a reappraisal

1 reference

12 December 2020

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1086/422475

1 reference

30 July 2017

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30 July 2017

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