| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1104995190 |
| P356 | DOI | 10.1186/S12864-018-4865-9 |
| P932 | PMC publication ID | 6008943 |
| P698 | PubMed publication ID | 29921221 |
| P2093 | author name string | Seung-Hwan Lee | |
| Bermseok Oh | |||
| Chol Shin | |||
| Jong Yeol Kim | |||
| Seongwon Cha | |||
| Jong-Sik Kim | |||
| Ah Yeon Park | |||
| Nam Han Cho | |||
| Ji Eun Lim | |||
| Si Woo Lee | |||
| Ji-One Kang | |||
| Jeong Min Nam | |||
| Jun-Hyeong Do | |||
| Kwang-Man Woo | |||
| P2860 | cites work | A genome-wide association study identifies five loci influencing facial morphology in Europeans | Q21563366 |
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| The phenotype of survivors of campomelic dysplasia | Q24678969 | ||
| Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology | Q26714036 | ||
| Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence | Q28235961 | ||
| Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1 | Q28261277 | ||
| Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2 | Q28305170 | ||
| Mapping the genetic architecture of gene expression in human liver | Q28472693 | ||
| Systematic identification of trans eQTLs as putative drivers of known disease associations | Q28659854 | ||
| METAL: fast and efficient meta-analysis of genomewide association scans | Q29547217 | ||
| Annotation of functional variation in personal genomes using RegulomeDB | Q29614867 | ||
| LocusZoom: regional visualization of genome-wide association scan results | Q29614868 | ||
| Development of an integrated Sasang constitution diagnosis method using face, body shape, voice, and questionnaire information. | Q30528517 | ||
| Heritability maps of human face morphology through large-scale automated three-dimensional phenotyping | Q33576636 | ||
| The ontology of craniofacial development and malformation for translational craniofacial research | Q33699401 | ||
| Innate immune activity conditions the effect of regulatory variants upon monocyte gene expression | Q33783132 | ||
| The assessment of facial variation in 4747 British school children. | Q34024858 | ||
| Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position | Q34161075 | ||
| The HIrisPlex system for simultaneous prediction of hair and eye colour from DNA. | Q34295623 | ||
| Self-perception, social skills, adjustment, and inhibition in young adolescents with craniofacial anomalies. | Q51149981 | ||
| Analysis of Sasang constitutional types using facial features with compensation for photographic distance. | Q53707778 | ||
| Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patients. | Q54765390 | ||
| Comparison of some cephalometric distances and corresponding facial proportions with regard to heritability | Q67919744 | ||
| Facial disfigurement: problems and management of social interaction and implications for mental health | Q68601733 | ||
| Heritability of craniofacial characteristics between parents and offspring estimated from lateral cephalograms | Q81483816 | ||
| Genetic variability in the regulation of gene expression in ten regions of the human brain | Q34398489 | ||
| Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans | Q34475541 | ||
| Bone mineral density-associated polymorphisms are associated with obesity-related traits in Korean adults in a sex-dependent manner | Q34541541 | ||
| Modeling 3D facial shape from DNA | Q35126094 | ||
| Identification of novel craniofacial regulatory domains located far upstream of SOX9 and disrupted in Pierre Robin sequence | Q35318805 | ||
| New insights into craniofacial morphogenesis | Q36037960 | ||
| Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape. | Q36112972 | ||
| A classification method of normal and overweight females based on facial features for automated medical applications | Q36167807 | ||
| LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants | Q36226921 | ||
| HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease | Q36435043 | ||
| Recent advances in craniofacial morphogenesis | Q36471176 | ||
| A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation | Q36919863 | ||
| Diversity of WD-repeat proteins | Q37299807 | ||
| Long-range regulation at the SOX9 locus in development and disease | Q37497734 | ||
| Detection and interpretation of shared genetic influences on 42 human traits | Q37552665 | ||
| SNP genotyping through the melting analysis of unlabelled oligonucleotide applied on dilute PCR amplicon | Q38334237 | ||
| Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. | Q38820711 | ||
| Developmental validation of the HIrisPlex system: DNA-based eye and hair colour prediction for forensic and anthropological usage | Q39250529 | ||
| Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment | Q47180877 | ||
| Modification of the Integrated Sasang Constitutional Diagnostic Model. | Q47556004 | ||
| Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia | Q47819908 | ||
| A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits | Q47936547 | ||
| Genome-wide mapping of global-to-local genetic effects on human facial shape. | Q49830752 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genome-wide association study | Q1098876 |
| P304 | page(s) | 481 | |
| P577 | publication date | 2018-06-19 | |
| P1433 | published in | BMC Genomics | Q15765854 |
| P1476 | title | Identification of five novel genetic loci related to facial morphology by genome-wide association studies. | |
| P478 | volume | 19 |
| Q97525573 | A review of genetics of nasal development and morphological variation |
| Q58553642 | Facial Genetics: A Brief Overview |
| Q91908341 | Hunting for genes that shape human faces: Initial successes and challenges for the future |
| Q60958909 | Identification of gene biomarkers in patients with postmenopausal osteoporosis |
| Q104111399 | Insights into the genetic architecture of the human face |
| Q83225870 | Novel genetic loci affecting facial shape variation in humans |
| Q90640851 | The age distribution of facial metrics in two large Korean populations |
| Q92990704 | Whole-exome sequencing identified four loci influencing craniofacial morphology in northern Han Chinese |
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