Jeffrey C Murray


Ontology type: schema:Person     


Person Info

NAME

Jeffrey C

SURNAME

Murray

Publications in SciGraph latest 50 shown

  • 2017-03 Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate in HUMAN GENETICS
  • 2015-03 Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy in PEDIATRIC RESEARCH
  • 2013-05 Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases in GENETICS IN MEDICINE
  • 2013-03 The heritability of metabolic profiles in newborn twins in HEREDITY
  • 2012-12 Oral cleft prevention program (OCPP) in BMC PEDIATRICS
  • 2012-12 Outcome of Extremely Preterm Infants (<1,000 g) With Congenital Heart Defects From the National Institute of Child Health and Human Development Neonatal Research Network in PEDIATRIC CARDIOLOGY
  • 2012-11 No observed association for mitochondrial SNPs with preterm delivery and related outcomes in PEDIATRIC RESEARCH
  • 2012-06 Detectable clonal mosaicism from birth to old age and its relationship to cancer in NATURE GENETICS
  • 2012-05 Common variants at 6q22 and 17q21 are associated with intracranial volume in NATURE GENETICS
  • 2012-05 Common variants at 12q15 and 12q24 are associated with infant head circumference in NATURE GENETICS
  • 2012-03 Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis in NATURE GENETICS
  • 2012-02 Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn in PEDIATRIC RESEARCH
  • 2012-02 Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis in NATURE GENETICS
  • 2011-12 The effect of systematic pediatric care on neonatal mortality and hospitalizations of infants born with oral clefts in BMC PEDIATRICS
  • 2011-09 Active choice but not too active: Public perspectives on biobank consent models in GENETICS IN MEDICINE
  • 2011-07 Replication of Genetic Associations in the Inflammation, Complement, and Coagulation Pathways With Intraventricular Hemorrhage in LBW Preterm Neonates in PEDIATRIC RESEARCH
  • 2011-03 Cleft lip and palate: understanding genetic and environmental influences in NATURE REVIEWS GENETICS
  • 2010-11 292 A Genome-Wide Association Study of Spontaneous Preterm Delivery in PEDIATRIC RESEARCH
  • 2009-06 The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-02 Genetic Contributions to the Development of Retinopathy of Prematurity in PEDIATRIC RESEARCH
  • 2008-09 Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts in GENETICS IN MEDICINE
  • 2008-03 The Effects of Prenatal Use of Folic Acid and Other Dietary Supplements on Early Child Development in MATERNAL AND CHILD HEALTH JOURNAL
  • 2006-12 Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger syndrome in BMC MEDICAL GENETICS
  • 2005-10 15 Single Nucleotide Polymorphisms in Smooth Muscle Regulation Genes as Risk Factors for Spontaneous Preterm Delivery. in PEDIATRIC RESEARCH
  • 2004-06 In a Vietnamese population, MSX1 variants contribute to cleft lip and palate in GENETICS IN MEDICINE
  • 2000-09 Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease in NATURE GENETICS
  • 1999-04 High Throughput Sequence Analysis of the 1 Megabase Region Containing the Van der Woude Locus in PEDIATRIC RESEARCH
  • 1998-02 The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 1993-09 The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus in HUMAN GENETICS
  • 1992-09 Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4 in NATURE GENETICS
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