A. Petrin

发表

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.

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 .

Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate

A. Adeyemo, T. Beaty, Erliang Zeng, 2021, Scientific Reports.

Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting.

Stephen S. Gisselbrecht, James M. Harris, W. Goessling, 2011, American journal of human genetics.

Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate

A. Adeyemo, T. Beaty, Erliang Zeng, 2022, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Genetic Studies in the Nigerian Population Implicate an MSX1 Mutation in Complex Oral Facial Clefting Disorders

J. Murray, P. Mossey, W. Adeyemo, 2011, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Replication of Genome Wide Association Identified Candidate Genes Confirm the Role of Common and Rare Variants in PAX7 and VAX1 in the Etiology of Nonsyndromic CL(P)

T. Beaty, M. Marazita, K. Cuenco, 2013, American journal of medical genetics. Part A.

DNA methylation differences in monozygotic twins with Van der Woude syndrome

M. Marazita, D. Moretti-Ferreira, J. Murray, 2023, Frontiers in Dental Medicine.

Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans

Lisa A. Lansdon, J. Murray, D. Houston, 2017, Genetics.

Further characterization of microdeletion syndrome involving 2p15‐p16.1

T. Félix, M. Sanseverino, J. Murray, 2010, American journal of medical genetics. Part A.

Identification of a microdeletion at the 7q33‐q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case

Jeffrey C Murray, Sthella Zanchetta, A. Richieri‐Costa, 2010, American journal of medical genetics. Part A.

Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P)

A. Adeyemo, Erliang Zeng, M. Marazita, 2021, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Variant Analyses of Candidate Genes in Orofacial Clefts in Multi-Ethnic Populations.

A. Adeyemo, M. Marazita, J. Murray, 2021, Oral diseases.

A Case of 3q29 Microdeletion Syndrome Involving Oral Cleft Inherited from a Nonaffected Mosaic Parent: Molecular Analysis and Ethical Implications

J. Murray, S. Daack-Hirsch, J. L'heureux, 2011, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus

M. Marazita, N. Sobreira, S. Lachke, 2021, Journal of dental research.

Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome

Siulan Vendramini-Pittoli, A. Richieri‐Costa, J. Murray, 2012, American journal of medical genetics. Part A.

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

T. Beaty, K. Christensen, S. Weinberg, 2017, Genetic epidemiology.

Non‐random distribution of deleterious mutations in the DNA and protein‐binding domains of IRF6 are associated with Van Der Woude syndrome

A. Adeyemo, M. Marazita, J. Murray, 2020, Molecular genetics & genomic medicine.

Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.

Tony Roscioli, Adebowale Adeyemo, Ying Zhu, 2016, Birth defects research.

Monozygotic twins with variable expression of Van der Woude Syndrome

J. Murray, R. Jobling, R. Ferrier, 2011, American Journal of Medical Genetics. Part A.

Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.

A. Adeyemo, S. Eliason, I. Saadi, 2016, Birth defects research.

Genetic Studies in the Nigerian Population Implicate an MSX1 Mutation in Complex Oral Facial Clefting Disorders

W. Adeyemo, M. Mansilla, C. Onwuamah, 2011, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

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.

DNA Methylation Effects on Van der Woude Syndrome Phenotypic Variability.

A. Butali, W. Awotoye, A. Petrin, 2024, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.