Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2

High-throughput discovery of novel developmental phenotypes

(2016) Mary E. Dickinson et al.   NATURE

A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation

(2016) Kaustubh Adhikari et al.   Nature Communications

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

(2016) John R. Shaffer et al.   PLoS Genetics

Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape

(2016) Joanne B. Cole et al.   PLoS Genetics

Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels

(2015) W. Lu et al.   HUMAN MOLECULAR GENETICS

Kabuki syndrome genesKMT2DandKDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development

(2015) Peter M. Van Laarhoven et al.   HUMAN MOLECULAR GENETICS

Modeling 3D Facial Shape from DNA

(2014) Peter Claes et al.   PLoS Genetics

Detecting Genetic Association of Common Human Facial Morphological Variation Using High Density 3D Image Registration

(2013) Shouneng Peng et al.   PLoS Computational Biology

Genome-wide Association Study of Three-Dimensional Facial Morphology Identifies a Variant in PAX3 Associated with Nasion Position

(2012) Lavinia Paternoster et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects

(2012) Frances M K Williams et al.   ANNALS OF THE RHEUMATIC DISEASES

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

Improved whole-chromosome phasing for disease and population genetic studies

(2012) Olivier Delaneau et al.   NATURE METHODS

A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans

(2012) Fan Liu et al.   PLoS Genetics

Epigenetic integration of the developing brain and face

(2011) Trish E. Parsons et al.   DEVELOPMENTAL DYNAMICS

Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1

(2011) A. M. Slavotinek et al.   JOURNAL OF MEDICAL GENETICS

Cleft lip and palate: understanding genetic and environmental influences

(2011) Michael J. Dixon et al.   NATURE REVIEWS GENETICS

Genotype Imputation with Thousands of Genomes

(2011) Bryan Howie et al.   G3-Genes Genomes Genetics

Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice

(2011) Lisenka E. L. M. Vissers et al.   PLoS Genetics

Quality control and quality assurance in genotypic data for genome-wide association studies

(2010) Cathy C. Laurie et al.   GENETIC EPIDEMIOLOGY

3D digital stereophotogrammetry: a practical guide to facial image acquisition

(2010) Carrie L Heike et al.   Head & Face Medicine

FREM1 Mutations Cause Bifid Nose, Renal Agenesis, and Anorectal Malformations Syndrome

(2009) Anas M. Alazami et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics