J. C. Murray

F. Oginni, P. Donkor, P. Mossey, 2018, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

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

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

Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?

S. Weinberg, M. Marazita, J. Hecht, 2023, medRxiv.

Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations

A. Adeyemo, M. Marazita, R. Braimah, 2016, Journal of dental research.

Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.

T. Beaty, M. Marazita, J. Murray, 2012, Birth defects research. Part A, Clinical and molecular teratology.

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.

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

T. Beaty, N. Prescott, R. Scott, 2004, American journal of human genetics.

Clinical and epidemiologic studies of cleft lip and palate in the Philippines.

K. Buetow, R. Munger, J. Murray, 1997, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Between-hospital variation in treatment and outcomes in extremely preterm infants.

Abhik Das, Seetha Shankaran, Jeffrey C Murray, 2015, The New England journal of medicine.

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.

Antagonistic signals between BMP4 and FGF8 define the expression of Pitx1 and Pitx2 in mouse tooth-forming anlage.

J. Murray, E. Semina, Yanding Zhang, 2000, Developmental biology.

Multiomic signals associated with maternal epidemiological factors contributing to preterm birth in low- and middle-income countries

J. Stringer, N. Aghaeepour, M. Snyder, 2023, Science advances.

X‐chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate

K. Christensen, M. Marazita, J. Murray, 2007, American journal of medical genetics. Part A.

Cleft palate, transforming growth factor alpha gene variants, and maternal exposures: Assessing gene‐environment interactions in case‐parent triads

Jeffrey C Murray, Astanand Jugessur, R. T. Lie, 2003, Genetic epidemiology.

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

J C Murray, R Pfundt, R. Pfundt, 2007, Journal of Medical Genetics.

Genomic strategy identifies a missense mutation in WD‐repeat domain 65 (WDR65) in an individual with Van der Woude syndrome

J. Kere, J. Murray, M. Peyrard-Janvid, 2011, American journal of medical genetics. Part A.

Neurodegenerative central nervous system Langerhans cell histiocytosis and coincident hydrocephalus treated with vincristine/cytosine arabinoside

Ricardo J. Flores, D. Hsu, C. Allen, 2010, Pediatric blood & cancer.

Mapping of the human complement factor I gene to 4q25.

K. Buetow, W. Sanger, C. Morton, 1989, Genomics.

Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes.

J. Carey, R. Ferrell, J. Eichner, 1987, Journal of medical genetics.

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35

C. Wijmenga, G. V. van Ommen, R. Frants, 1995, Muscle & nerve. Supplement.

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

S. Cichon, M. Nöthen, T. Beaty, 2012, Nature Genetics.

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.

Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants.

G. Shaw, C. Wasserman, C. D. O'Malley, 1996, American journal of human genetics.

Edinburgh Research Explorer Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

R. T. Lie, A. Visel, E. Green, 2018 .

Disrupted IRF6-NME1/2 Complexes as a Cause of Cleft Lip/Palate

J. Murray, T. Cox, E. Chu, 2017, Journal of dental research.

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

R. T. Lie, A. Wilcox, K. Doheny, 2016, Human molecular genetics.

Renal Venous Thrombosis Complicating Acute Myeloid Leukemia with Hyperleukocytosis

Z. Dreyer, M. Brandt, S. Dorfman, 1996, Journal of pediatric hematology/oncology.

Common variants at 6q22 and 17q21 are associated with intracranial volume

Wiro J Niessen, Clifford R Jack, Reinhold Schmidt, 2012, Nature Genetics.

Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts

J. Murray, H. van Bokhoven, R. Gorlin, 2002, Journal of medical genetics.

FAT4 identified as a potential modifier of orofacial cleft laterality

T. Beaty, S. Weinberg, M. Marazita, 2021, medRxiv.

The PAX1 locus at 20p11 is a modifier for bilateral cleft lip only

T. Beaty, D. Cutler, P. Claes, 2020, medRxiv.

DNA methylation differences in monozygotic twins with Van der Woude syndrome

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

Genome-wide analysis of copy number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes.

Lisa A. Lansdon, K. Mohlke, S. Girirajan, 2022, American journal of human genetics.

Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate

A. Adeyemo, F. Oginni, M. Marazita, 2018, Journal of dental research.

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

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

MSX1 and TGFB3 Contribute to Clefting in South America

M. Marazita, E. Castilla, M. Cooper, 2003, Journal of dental research.

INVITED EDITORIAL Face Facts: Genes, Environment, and Clefts

J. Murray, J. C. Murray, 2007 .

Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts.

R. Munger, J. Murray, T. Burns, 1999, Teratology.

Search for genetic modifiers of IRF6 and genotype–phenotype correlations in Van der Woude and popliteal pterygium syndromes

M. Marazita, B. Schutte, E. Leslie, 2013, 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.

Whole exome association of rare deletions in multiplex oral cleft families

Ingo Ruczinski, Alexandre Bureau, Hasan Albacha-Hejazi, 2017, Genetic epidemiology.

Reevaluating surgery and re-irradiation for locally recurrent pediatric ependymoma—a multi-institutional study

S. McGovern, P. Dirks, Michael D. Taylor, 2021, Neuro-oncology advances.

Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1-p34.

K. Buetow, H. Harris, B. Emanuel, 1988, Genomics.

PITX2 and FOXC1 spectrum of mutations in ocular syndromes

U. Broeckel, J. Murray, L. Reis, 2012, European Journal of Human Genetics.

Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome.

E. Roeder, J. Murray, A. Lin, 2000, American journal of medical genetics.

Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers.

J. Weber, V. Sheffield, T. Hudson, 1995, Human molecular genetics.

The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus

C. Wijmenga, J. Wasmuth, R. Frants, 1993, Human Genetics.

Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines.

K. Buetow, R. Shiang, J. Murray, 1997, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes.

K. Buetow, S. Huson, J. Carey, 1987, Journal of Medical Genetics.

Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes

S. Weinberg, M. Marazita, E. Leslie, 2023, Human Genetics.

Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study

I. Ruczinski, M. Taub, A. F. Scott, 2013, Human Genetics.

Evidence for SNP‐SNP interaction identified through targeted sequencing of cleft case‐parent trios

T. Beaty, D. Koboldt, I. Ruczinski, 2017, Genetic epidemiology.

A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature

S. Scherer, R. Pfundt, H. Hakonarson, 2023, American journal of medical genetics. Part A.

Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36

C. Steyers, J. Morcuende, M. Dobbs, 2000, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Lipoprotein Lipase Gene Mutations and the Genetic Susceptibility of Preeclampsia

J. L. Smith, J. Murray, Y. J. Kim, 2001, Hypertension.

Association of single nucleotide polymorphisms in the thrombopoietin‐receptor gene, but not the thrombopoietin gene, with differences in platelet count

J. Widness, R. Strauss, J. Yankowitz, 2004, American journal of hematology.

Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice.

J. Murray, J. Graw, E. Semina, 2000, Human molecular genetics.

Using Family Data as a Verification Standard to Evaluate Copy Number Variation Calling Strategies for Genetic Association Studies

Caitlin P. McHugh, C. Laurie, M. Marazita, 2012, Genetic epidemiology.

Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19.

J. Murray, E. Semina, R. Reiter, 1997, Human molecular genetics.

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.

K. Christensen, B. Maher, M. Marazita, 2004, The New England journal of medicine.

Phenotypic and Pathologic Evaluation of the myd Mouse. A Candidate Model for Facioscapulohumeral Dystrophy

K. Mathews, R. Schelper, J. Murray, 1995, Journal of neuropathology and experimental neurology.

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

S. Cichon, T. Beaty, T. Wienker, 2012, Nature Genetics.

Search for genetic modifiers of IRF6 and genotype–phenotype correlations in Van der Woude and popliteal pterygium syndromes

M. Marazita, B. Schutte, E. Leslie, 2013, American journal of medical genetics. Part A.

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

Daniel E. Miller, M. Jarvelin, K. Hao, 2018, bioRxiv.

The Pitx2 protein in mouse development

B. Amendt, E. Semina, T. Hjalt, 2000, Developmental dynamics : an official publication of the American Association of Anatomists.

Targeted Newborn Metabolomics: Prediction of gestational age from cord blood

G. Dorsey, M. Kamya, E. Rogers, 2021, Journal of Perinatology.

Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate

H. Brand, S. Weinberg, M. Marazita, 2023, HGG advances.

Preliminary molecular studies on blepharocheilodontic syndrome

V. L. Gil-da-Silva-Lopes, E. Ramos, C. Martinhago, 2007, American journal of medical genetics. Part A.

Coeliac disease in twins

R. Gorlin, S. Daack-Hirsch, J. V. Bokhoven, 2002, Journal of medical genetics.

Possible roles of bilirubin and breast milk in protection against retinopathy of prematurity

J. Dawson, E. Bell, J. Dagle, 2011, Acta paediatrica.

Cytochrome P450 (CYP2D6) Genotype is Associated with Elevated Systolic Blood Pressure in Preterm Infants Following NICU Discharge

F. Morriss, Susan Haynes, J. Dagle, 2011 .