J. Murray

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

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.

Variants of developmental genes (TGFA, TGFB3, and MSX1) and their associations with orofacial clefts: A case‐parent triad analysis

R. T. Lie, Jack A. Taylor, A. Wilcox, 2003, Genetic epidemiology.

The Pitx2 protein in mouse development

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

Sequence evaluation of FGF and FGFR gene conserved non‐coding elements in non‐syndromic cleft lip and palate cases

J. Murray, B. Riley, J. C. Murray, 2007, American journal of medical genetics. Part A.

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.

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.

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

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

DNA methylation differences in monozygotic twins with Van der Woude syndrome

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

Identity by descent and candidate gene mapping of Richieri‐Costa and Pereira syndrome

J. Murray, A. Richieri‐Costa, D. Moretti-Ferreira, 2003, 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.

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

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

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

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

Renal Venous Thrombosis Complicating Acute Myeloid Leukemia with Hyperleukocytosis

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

Heritability of glutathione and related metabolites in stored red blood cells.

B. Darbro, J. Hess, G. Buettner, 2014, Free radical biology & medicine.

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.

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.

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.

Genetic linkage relationships of Charcot‐Marie‐Tooth disease (HMSN‐Ib) to chromosome 1 markers

T. Bird, J. Murray, Phillip F. Chance, 1987, Neurology.

A randomised study of “wet wraps” versus conventional treatment for atopic eczema

G. Galloway, L. Gardener, D. Hindley, 2005, Archives of Disease in Childhood.

Two novel point mutations in the long‐range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly

A. Bowcock, J. Morcuende, M. Dobbs, 2007, American journal of medical genetics. Part A.

MSX1 and TGFB3 Contribute to Clefting in South America

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

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4

J. Weber, K. Buetow, A. Kwitek, 1992, Nature genetics.

Identification of a Dominant Negative Homeodomain Mutation in Rieger Syndrome*

K. P. Murphy, D. Harris, I. Saadi, 2001, The Journal of Biological Chemistry.

In a Vietnamese population, MSX1 variants contribute to cleft lip and palate

M. Marazita, J. Murray, K. Shimozato, 2004, Genetics in Medicine.

Anthropometric charts for infants with trisomies 21, 18, or 13 born between 22 weeks gestation and term: The VON charts

J. Horbar, N. Boghossian, J. Carpenter, 2012, American journal of medical genetics. Part A.

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.

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

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

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.

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

Reinhold Schmidt, Stefan Ropele, Sudha Seshadri, 2013, Nature Genetics.

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

M. Jarvelin, L. Coin, M. Fornage, 2013, Nature Genetics.

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.

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.

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.

Clinical Pathology Case: Hyperimmunoglobulin E Syndrome (Job's Syndrome)

J. Murray, D. Murphey, Gary B. Strong, 2001, Pediatric pathology & molecular medicine.

FAT4 identified as a potential modifier of orofacial cleft laterality

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

Lymphoblastic Lymphoma Following Prenatal Exposure to Phenytoin

R. Hurwitz, R. Hill, S. Hegemier, 1996, Journal of pediatric hematology/oncology.

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 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.

Preliminary molecular studies on blepharocheilodontic syndrome

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

PVRL1 variants contribute to non‐syndromic cleft lip and palate in multiple populations

K. Christensen, S. Daack-Hirsch, E. Castilla, 2006, American journal of medical genetics. Part A.

Metabolic heritability at birth: implications for chronic disease research

J. Murray, K. Ryckman, L. Jelliffe‐Pawlowski, 2014, Human Genetics.

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

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

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.

Double paternal nondisjunction in an infant with transient neonatal diabetes mellitus and Klinefelter syndrome

S. Patil, M. Tansey, T. Félix, 2007, American journal of medical genetics. Part A.

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.

Outcomes of Infants and Young Children With Relapsed Medulloblastoma After Initial Craniospinal Irradiation–Sparing Approaches: An International Cohort Study

P. Northcott, J. Finlay, H. Toledano, 2022, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Lipoprotein Lipase Gene Mutations and the Genetic Susceptibility of Preeclampsia

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

Replication of a genome-wide association study of birth weight in preterm neonates.

D. Weeks, K. Doheny, E. Pugh, 2012, The Journal of pediatrics.

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

T. Beaty, D. Cutler, Xuefang Zhao, 2022, medRxiv.

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).

K H Buetow, J C Murray, J. Weber, 1994, Science.

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

T. Beaty, G. Shaw, D. Cutler, 2023, medRxiv.

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.

Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate

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

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

S. Weinberg, M. Marazita, J. Hecht, 2023, American journal of medical genetics. Part A.

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.

P. M. Falk, P. Green, M. Spence, 1990, American journal of human genetics.