相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions
Nandita Mukhopadhyay et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2021)
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios
Debashree Ray et al.
PLOS GENETICS (2021)
Association between MSX1 rs12532 polymorphism with nonsyndromic unilateral complete cleft lip and palate and tooth agenesis
Melissa Lancia et al.
ARCHIVES OF ORAL BIOLOGY (2020)
Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism
Nana Matoba et al.
TRANSLATIONAL PSYCHIATRY (2020)
A systematic scoping review of the genetic ancestry of the Brazilian population
Aracele Maria de Souza et al.
GENETICS AND MOLECULAR BIOLOGY (2019)
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts
John R. Shaffer et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2019)
Association between the FGFR1 rs13317 single nucleotide polymorphism and orbitale-nasion depth based on cephalometric images
Mohamed Adel et al.
JOURNAL OF HUMAN GENETICS (2018)
Potential genetic markers for nonsyndromic oral clefts in the Brazilian population: A systematic review and meta-analysis
Renato Assis Machado et al.
BIRTH DEFECTS RESEARCH (2018)
Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation
Karlijne Indencleef et al.
FRONTIERS IN GENETICS (2018)
Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 and non-syndromic oral clefts
Ana Camila Messetti et al.
JOURNAL OF ORAL PATHOLOGY & MEDICINE (2017)
Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting
Huan Liu et al.
NATURE COMMUNICATIONS (2017)
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Yanqin Yu et al.
NATURE COMMUNICATIONS (2017)
Contribution of FGFR1 Variants to Craniofacial Variations in East Asians
Mohamed Adel et al.
PLOS ONE (2017)
Preaxial Polydactyly Associated with a MSX1 Mutation and Report of Two Novel Mutations
Onnida Wattanarat et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2016)
Association between IRF6 and 8q24 Polymorphisms and Nonsyndromic Cleft Lip with or without Cleft Palate: Systematic Review and Meta-analysis
Kachin Wattanawong et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2016)
A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population
Tania Kawasaki de Araujo et al.
JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY (2016)
Association between IRF6 and 8q24 Polymorphisms and Nonsyndromic Cleft Lip with or without Cleft Palate: Systematic Review and Meta-analysis
Kachin Wattanawong et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2016)
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry
Andrea do Rego Borges et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2015)
Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum
A. Magariello et al.
EUROPEAN JOURNAL OF NEUROLOGY (2014)
Investigation of FGF1 and FGFR gene polymorphisms in a group of Iranian patients with nonsyndromic cleft lip with or without cleft palate
Zahra Rafiqdoost et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2014)
Polymorphisms at Regions 1p22.1 (rs560426) and 8q24 (rs1530300) Are Risk Markers for Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population
Elizabete Bagordakis et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2013)
Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)
Michael Gonzalez et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2013)
Polymorphisms in BMP4 and FGFR1 Genes Are Associated With Fracture Non-Union
Joao Matheus Guimaraes et al.
JOURNAL OF ORTHOPAEDIC RESEARCH (2013)
Three polymorphisms in IRF6 and 8q24 are associated with nonsyndromic cleft lip with or without cleft palate: Evidence from 20 studies
Meilin Wang et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2012)
Roles of SAM and DDHD domains in mammalian intracellular phospholipase A1 KIAA0725p
Hiroki Inoue et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2012)
Region 8q24 Is a Susceptibility Locus for Nonsyndromic Oral Clefting in Brazil
Luciano Abreu Brito et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2012)
Mutations in WNT10A are present in more than half of isolated hypodontia cases
Marie-Jose van den Boogaard et al.
JOURNAL OF MEDICAL GENETICS (2012)
Cleft lip and palate: understanding genetic and environmental influences
Michael J. Dixon et al.
NATURE REVIEWS GENETICS (2011)
Lack of association between IRF6 polymorphisms (rs2235371 and rs642961) and non-syndromic cleft lip and/or palate in a Brazilian population
L. M. R. Paranaiba et al.
ORAL DISEASES (2010)
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate
PA Jezewski et al.
JOURNAL OF MEDICAL GENETICS (2003)
分享论文
