X. Ye

发表

Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate.

T. Beaty, I. Ruczinski, E. Jabs, 2012, Birth defects research. Part A, Clinical and molecular teratology.

The Second Deletion Mutation in Exon 8 of EDA Gene in an XLHED Pedigree

W. Yin, Z. Bian, X. Ye, 2013, Dermatology.

Methylation State of the EDA Gene Promoter in Chinese X-Linked Hypohidrotic Ectodermal Dysplasia Carriers

W. Yin, Z. Bian, X. Ye, 2013, PloS one.

Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2011, Genetic epidemiology.

Keratinocytes modify fibroblast metabolism in hereditary gingival fibromatosis.

M. Fan, Z. Bian, J. W. Von den Hoff, 2008, Archives of oral biology.

Novel mutations in EVC cause aberrant splicing in Ellis–van Creveld syndrome

Chunyan Luo, Mairaj K. Ahmed, Lisong Shi, 2016, Molecular Genetics and Genomics.

A novel heterozygous deletion in the EVC2 gene causes Weyers acrofacial dysostosis

E. Jabs, M. Fan, Z. Bian, 2006, Human Genetics.

X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts.

R. T. Lie, T. Beaty, I. Ruczinski, 2013, European journal of oral sciences.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2010, Nature Genetics.

Genetic Factors Responsible for Cleft Lip and Palate

Mairaj K. Ahmed, X. Ye, 2022, Surgical Atlas of Cleft Palate and Palatal Fistulae.

Genome wide study of maternal and parent‐of‐origin effects on the etiology of orofacial clefts

R. T. Lie, T. Beaty, I. Ruczinski, 2012, American journal of medical genetics. Part A.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA 4

Hong Wang, Holger Schwender, Ingo Ruczinski, 2010 .

Evidence for gene-environment interaction in a genome wide study of isolated, non-syndromic cleft palate

Holger Schwender, Ingo Ruczinski, Alan F. Scott, 2011 .

Examining Markers in 8q24 to Explain Differences in Evidence for Association With Cleft Lip With/Without Cleft Palate Between Asians and Europeans

Holger Schwender, Ingo Ruczinski, Tao Wu, 2012, Genetic epidemiology.

Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate

Ingo Ruczinski, Alan F. Scott, Terri H. Beaty, 2010, Human Genetics.

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations

T. Beaty, E. Jabs, A. F. Scott, 2006, Human Genetics.

Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis

J. Richtsmeier, B. Reva, E. Jabs, 2016, Plastic and reconstructive surgery.

Review of the Genetic Basis of Jaw Malformations

P. Taub, Mairaj K. Ahmed, X. Ye, 2016, Journal of Pediatric Genetics.

A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3‐p23.3

L. Shi, Z. Bian, B. Peng, 2005, Clinical genetics.

Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.

W. Yin, Z. Bian, Q. Wang, 2009, Journal of clinical periodontology.

Novel mutations in EVC cause aberrant splicing in Ellis–van Creveld syndrome

Chunyan Luo, Mairaj K. Ahmed, Lisong Shi, 2016, Molecular Genetics and Genomics.

Genetic Basis of Nonsyndromic and Syndromic Tooth Agenesis

X. Ye, A. Attaie, 2016, Journal of Pediatric Genetics.

Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds.

W. Yin, Z. Bian, Lisong Shi, 2008, European journal of oral sciences.

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

Alexander F. Wilson, A. F. Wilson, J. Richtsmeier, 2012, Nature Genetics.

A genome wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP 2 and within BBS 9

Alexander F. Wilson, A. F. Wilson, J. Richtsmeier, 2012 .

Oral Clefting in China Over the Last Decade: 205,679 Patients

Peter J. Taub, Ethylin Wang Jabs, E. Jabs, 2014, Plastic and reconstructive surgery. Global open.

Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family

L. Edelmann, T. Haaf, R. Maroofian, 2017, Molecular Syndromology.

Identification of novel mutations of IRF6 gene in Chinese families with Van der Woude syndrome.

Z. Bian, M. Fan, Lisong Shi, 2005, International journal of molecular medicine.

Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations

T. Beaty, E. Jabs, A. F. Scott, 2010, European Journal of Human Genetics.

HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice.

E. Jabs, D. Hunter, C. Schubert, 2012, American journal of human genetics.

HOXB 1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb 1 [ superscript / ] Mice

E. Jabs, D. Hunter, C. Schubert, 2022 .

Joint Testing of Genotypic and Gene-Environment Interaction Identified Novel Association for BMP4 with Non-Syndromic CL/P in an Asian Population Using Data from an International Cleft Consortium

T. Beaty, E. Jabs, A. F. Scott, 2014, PloS one.

Evidence of Gene−Environment Interaction for Two Genes on Chromosome 4 and Environmental Tobacco Smoke in Controlling the Risk of Nonsyndromic Cleft Palate

T. Beaty, I. Ruczinski, M. Taub, 2014, PloS one.

Phenotypes and genotypes in 2 DGI families with different DSPP mutations.

M. Fan, Z. Bian, B. Peng, 2006, Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics.

Phenotypic findings in Chinese families with X-linked hypohydrotic ectodermal dysplasia.

W. Yin, Z. Bian, X. Ye, 2012, Archives of oral biology.

Increased expression of collagen prolyl 4-hydroxylases in Chinese patients with hereditary gingival fibromatosis.

M. Fan, Z. Bian, L. Meng, 2007, Archives of oral biology.

HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1[superscript −/−] Mice

E. Jabs, D. Hunter, C. Schubert, 2012 .

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Alan F Scott, Jeffrey C Murray, 2010, Nature Genetics.

Genome wide study of maternal and parent‐of‐origin effects on the etiology of orofacial clefts

R. T. Lie, T. Beaty, I. Ruczinski, 2012, American journal of medical genetics. Part A.