A genome-wide association study identifies multiple loci for variation in human ear morphology

The genetics of auricular development and malformation: New findings in model systems driving future directions for microtia research

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Transcriptional Profiling of Wnt3a Mutants Identifies Sp Transcription Factors as Essential Effectors of the Wnt/β-catenin Pathway in Neuromesodermal Stem Cells

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Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals

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A survey on ear biometrics

(2013) Ayman Abaza et al.   ACM COMPUTING SURVEYS

Modeling Recent Human Evolution in Mice by Expression of a Selected EDAR Variant

(2013) Yana G. Kamberov et al.   CELL

Mouse Hoxa2 mutations provide a model for microtia and auricle duplication

(2013) M. Minoux et al.   DEVELOPMENT

The adaptive variant EDARV370A is associated with straight hair in East Asians

(2013) Jingze Tan et al.   HUMAN GENETICS

Improved Heritability Estimation from Genome-wide SNPs

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The development of an automatic recognition system for earmark and earprint comparisons

(2012) Stéphane Junod et al.   FORENSIC SCIENCE INTERNATIONAL

Effects of an Asian-specific nonsynonymous EDAR variant on multiple dental traits

(2012) Jeong-Heuy Park et al.   JOURNAL OF HUMAN GENETICS

MultiPhen: Joint Model of Multiple Phenotypes Can Increase Discovery in GWAS

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FaST linear mixed models for genome-wide association studies

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GCTA: A Tool for Genome-wide Complex Trait Analysis

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LocusZoom: regional visualization of genome-wide association scan results

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METAL: fast and efficient meta-analysis of genomewide association scans

(2010) C. J. Willer et al.   BIOINFORMATICS

Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy

(2010) Paulien Smits et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A morphometric study of the human ear

(2010) K. Skaria Alexander et al.   Journal of Plastic Reconstructive and Aesthetic Surgery

MorphoJ: an integrated software package for geometric morphometrics

(2010) CHRISTIAN PETER KLINGENBERG   Molecular Ecology Resources

A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population

(2010) Mitsuko Nakashima et al.   NATURE GENETICS

A Common Variation in EDAR Is a Genetic Determinant of Shovel-Shaped Incisors

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Molecular aspects of hypohidrotic ectodermal dysplasia

(2009) Marja L. Mikkola   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Age- and sex-related changes in the normal human ear

(2009) Chiarella Sforza et al.   FORENSIC SCIENCE INTERNATIONAL

Fast model-based estimation of ancestry in unrelated individuals

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Heritability of human cranial dimensions: comparing the evolvability of different cranial regions

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Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening

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Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size

(2009) Nicole Soranzo et al.   PLoS Genetics

TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome

(2008) Ekkehart Lausch et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia

(2008) Akihiro Fujimoto et al.   HUMAN GENETICS

Enhanced ectodysplasin-A receptor (EDAR) signaling alters multiple fiber characteristics to produce the East Asian hair form

(2008) Chunyan Mou et al.   HUMAN MUTATION

Many sequence variants affecting diversity of adult human height

(2008) Daniel F Gudbjartsson et al.   NATURE GENETICS

Identification of ten loci associated with height highlights new biological pathways in human growth

(2008) Guillaume Lettre et al.   NATURE GENETICS

Positive Selection in East Asians for an EDAR Allele that Enhances NF-κB Activation

(2008) Jarosław Bryk et al.   PLoS One