(Q34966316)

5 August 2017

title

A genome-wide linkage scan for quantitative trait loci influencing the craniofacial complex in humans (Homo sapiens sapiens). (English)

1 reference

5 August 2017

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quantitative trait locus

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4

John Blangero

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5 August 2017

6

Shelley A Cole

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5 August 2017

3

Michael C Mahaney

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5 August 2017

9

Roger M Siervogel

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5 August 2017

13

Bradford Towne

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5 August 2017

2

Dana L Duren

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5 August 2017

8

Wm Cameron Chumlea

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5 August 2017

10

Audrey C Choh

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5 August 2017

11

Ramzi W Nahhas

1 reference

5 August 2017

12

Miryoung Lee

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5 August 2017

Richard J Sherwood

1

1 reference

5 August 2017

Thomas D Dyer

series ordinal

5

1 reference

5 August 2017

Stefan A Czerwinski

series ordinal

7

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5 August 2017

publication date

15 February 2011

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5 August 2017

number of pages

12

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inferred from page(s)

published in

The Anatomical Record

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5 August 2017

volume

294

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5 August 2017

issue

4

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5 August 2017

page(s)

664-675

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Comparative gene expression analysis of avian embryonic facial structures reveals new candidates for human craniofacial disorders.

5 August 2017

cites work

1 reference

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8 July 2018

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Data and theory point to mainly additive genetic variance for complex traits

8 July 2018

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Status and potential commercial impact of stem cell-based treatments on dental and craniofacial regeneration

8 July 2018

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Craniofacial levels and the morphological maturation of the human skull

8 July 2018

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Tissue engineering of tooth crown, root, and periodontium.

8 July 2018

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Bioengineering and systems biology

8 July 2018

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The calmodulin pathway and evolution of elongated beak morphology in Darwin's finches

8 July 2018

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8 July 2018

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Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome.

8 July 2018

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8 July 2018

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A systems approach to discovering signaling and regulatory pathways--or, how to digest large interaction networks into relevant pieces.

8 July 2018

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Taking it to the max: the genetic and developmental mechanisms coordinating midfacial morphogenesis and dysmorphology

8 July 2018

1 reference

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Mathematical modelling of skeletal repair.

8 July 2018

1 reference

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Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

8 July 2018

1 reference

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Pleiotropy, homeostasis, and functional networks based on assays of cardiovascular traits in genetically randomized populations

8 July 2018

1 reference

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New strategies for craniofacial repair and replacement: a brief review

8 July 2018

1 reference

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Cranial skeletal biology.

8 July 2018

1 reference

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Tools and Techniques for Craniofacial Tissue Engineering

8 July 2018

1 reference

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Multiple hits during early embryonic development: digenic diseases and holoprosencephaly

8 July 2018

1 reference

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The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 gene

8 July 2018

1 reference

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Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly

8 July 2018

1 reference

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The craniofacial surgeon as amateur geneticist

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Morphogenesis of the medial region of the developing mandible is regulated by multiple signaling pathways

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

The human genome, implications for oral health and diseases, and dental education

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Hajdu--Cheney syndrome: evolution of phenotype and clinical problems

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Tissue-engineered composites of bone and cartilage for mandible condylar reconstruction

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Variance component methods for detecting complex trait loci

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination

8 July 2018

1 reference

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The role of sonic hedgehog in normal and abnormal craniofacial morphogenesis

8 July 2018

1 reference

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Linkage analysis narrows the critical region for oculodentodigital dysplasia to chromosome 6q22-q23

8 July 2018

1 reference

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Multipoint quantitative-trait linkage analysis in general pedigrees

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Pattern and process of growth of the abnormal human fetus.

8 July 2018

1 reference

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The functional matrix hypothesis revisited. 4. The epigenetic antithesis and the resolving synthesis

8 July 2018

1 reference

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Markov chain Monte Carlo segregation and linkage analysis for oligogenic models

8 July 2018

1 reference

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And the next 50 years? The future of recombinant DNA technology in oral medicine

8 July 2018

1 reference

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

8 July 2018

1 reference

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Gaussian models for genetic linkage analysis using complete high-resolution maps of identity by descent

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Experimental analysis of the control of expression of the homeobox-gene Msx-1 in the developing limb and face.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Recombinant DNA technology and oral medicine.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

The 1993-94 Généthon human genetic linkage map

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Research on craniofacial genetics and developmental biology: implications for the future of academic dentistry.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Pubertal spurts in cranial base and mandible. Comparisons within individuals.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

A second-generation linkage map of the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Late Elongation of the Cranial Base

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

The saddle angle: constancy or change?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Clinical manifestations and molecular investigation of 50 patients with Williams syndrome in the Greek population.

8 July 2018

1 reference

21 January 2018

1 reference

BMP gene delivery for alveolar bone engineering at dental implant defects.

21 January 2018

1 reference

Expression of WNT signalling pathway genes during chicken craniofacial development.

21 January 2018

1 reference

Ontogeny of robusticity of craniofacial traits in modern humans: a study of South American populations

21 January 2018

1 reference

Otodental syndrome, oculo-facio-cardio-dental (OFCD) syndrome, and lobodontia: dental disorders of interest to the pediatric radiologist.

21 January 2018

1 reference

Systems biology 101--what you need to know

21 January 2018

1 reference

A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.

21 January 2018

1 reference

Histological development and dynamic expression of Bmp2-6 mRNAs in the embryonic and postnatal mouse cranial base.

21 January 2018

1 reference

Osseous tissue engineering with gene therapy for facial bone reconstruction

21 January 2018

1 reference

Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly

21 January 2018

1 reference

Pure familial 6q21q22.1 duplication in two generations.

21 January 2018

1 reference

Growth of the mandible during pubescence.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091483

Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridization

26 October 2018

1 reference

The genetic map of craniofacial anomalies

21 January 2018

1 reference

12 December 2020

Elongation of the cranial base in girls during pubescence

1 reference

12 December 2020

Cranial base elongation in boys during pubescence

1 reference

12 December 2020

Temporal and spatial expression of genes for cartilage extracellular matrix proteins during avian mandibular arch development

1 reference

12 December 2020

Experimental analysis of Msx-1 and Msx-2 gene expression during chick mandibular morphogenesis

1 reference

12 December 2020

FGF signaling in mandibular skeletogenesis

1 reference

12 December 2020

Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia

1 reference

12 December 2020

Identifiers

DOI

10.1002/AR.21337

1 reference

release_whzxpjt3tzfs5njyxuk4t6gcue

5 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/whzxpjt3tzfs5njyxuk4t6gcue

24 November 2022

mapped directly with Wikidata item

PMC publication ID

3091483

1 reference

5 August 2017

1 reference