J C Murray
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Explore the profile of J C Murray including associated specialties, affiliations and a list of published articles.
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324
Citations
6430
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Recent Articles
1.
Machado-Paula L, Romanowska J, Lie R, Hovey L, Doolittle B, Awotoye W, et al.
medRxiv
. 2025 Feb;
PMID: 39990564
Objectives: Nonsyndromic orofacial clefts (OFCs) etiology involves multiple genetic and environmental factors with over 60 identified risk loci; however, they account for only a minority of the estimated risk. Epigenetic...
2.
Liang K, Feliciano J, Marrone K, Murray J, Hann C, Anagnostou V, et al.
ESMO Open
. 2023 Dec;
9(1):102199.
PMID: 38071928
Background: Brain metastasis (BRM) is uncommon in gastroesophageal cancer. As such, clinicopathologic and molecular determinants of BRM and impact on clinical outcome remain incompletely understood. Methods: We retrospectively analyzed clinicopathologic...
3.
Petrin A, Zeng E, Thomas M, Moretti-Ferreira D, Marazita M, Xie X, et al.
Front Dent Med
. 2023 Mar;
4.
PMID: 36936396
Introduction: Van der Woude Syndrome (VWS) is an autosomal dominant disorder responsible for 2% of all syndromic orofacial clefts (OFCs) with being the primary causal gene (70%). Cases may present...
4.
Awotoye W, Comnick C, Pendleton C, Zeng E, Alade A, Mossey P, et al.
J Dent Res
. 2021 Oct;
101(4):465-472.
PMID: 34689653
Risk loci identified through genome-wide association studies have explained about 25% of the phenotypic variations in nonsyndromic orofacial clefts (nsOFCs) on the liability scale. Despite the notable sex differences in...
5.
Gray K, Kovacheva V, Mirzakhani H, Bjonnes A, Almoguera B, Wilson M, et al.
BJOG
. 2020 Aug;
128(1):55-65.
PMID: 32741103
Objective: To assess whether women with a genetic predisposition to medical conditions known to increase pre-eclampsia risk have an increased risk of pre-eclampsia in pregnancy. Design: Case-control study. Setting And...
6.
Dodds R, Murray J, Robinson S, Sayer A
Eur Geriatr Med
. 2020 Apr;
11(3):433-441.
PMID: 32297269
Purpose: The European Working Group on Sarcopenia in Older People 2 (EWGSOP2) consensus definition introduced the concept of probable sarcopenia as a basis on which to begin treatment. Our aims...
7.
Eshete M, Liu H, Li M, Adeyemo W, Gowans L, Mossey P, et al.
J Dent Res
. 2017 Sep;
97(1):41-48.
PMID: 28886269
In contrast to the progress that has been made toward understanding the genetic etiology of cleft lip with or without cleft palate, relatively little is known about the genetic etiology...
8.
Lansdon L, Bernabe H, Nidey N, Standley J, Schnieders M, Murray J
J Dent Res
. 2017 Aug;
96(11):1339-1345.
PMID: 28825856
Here we describe the genotype-phenotype correlations of diseases caused by variants in Fibroblast Growth Factor Receptor 1 ( FGFR1) and report a novel, de novo variant in FGFR1 in an...
9.
Parada-Sanchez M, Chu E, Cox L, Undurty S, Standley J, Murray J, et al.
J Dent Res
. 2017 Aug;
96(11):1330-1338.
PMID: 28767310
Mutations and common polymorphisms in interferon regulatory factor 6 ( IRF6) are associated with both syndromic and nonsyndromic forms of cleft lip/palate (CLP). To date, much of the focus on...
10.
Moreno Uribe L, Fomina T, Munger R, Romitti P, Jenkins M, Gjessing H, et al.
J Dent Res
. 2017 Jun;
96(11):1322-1329.
PMID: 28662356
Prior genome-wide association studies for oral clefts have focused on clinic-based samples with unclear generalizability. Prior samples were also small for investigating effects by cleft type and exclusively studied isolated...