Pitx2 Regulates Procollagen Lysyl Hydroxylase (Plod) Gene Expression: Implications for the Pathology of Rieger Syndrome

por Hjalt, Tord A., Amendt, Brad A., Murray, Jeffrey C.
Publicado 2001

Hyperglycemia as a risk factor for the development of retinopathy of prematurity

por Mohamed, Shakir, Murray, Jeffrey C, Dagle, John M, Colaizy, Tarah
Publicado 2013

The effects of oral clefts on hospital use throughout the lifespan

por Wehby, George L, Pedersen, Dorthe Almind, Murray, Jeffrey C, Christensen, Kaare
Publicado 2012

Psychiatric Diagnoses in Individuals with Non-Syndromic Oral Clefts: A Danish Population-Based Cohort Study

por Pedersen, Dorthe Almind, Wehby, George L., Murray, Jeffrey C., Christensen, Kaare
Publicado 2016

Polymorphisms of CYP51A1 from Cholesterol Synthesis: Associations with Birth Weight and Maternal Lipid Levels and Impact on CYP51 Protein Structure

por Lewińska, Monika, Zelenko, Urska, Merzel, Franci, Golic Grdadolnik, Simona, Murray, Jeffrey C., Rozman, Damjana
Publicado 2013

Interactions between PDA-associated polymorphisms and genetic ancestry alter ductus arteriosus gene expression

por Clyman, Ronald I., Hills, Nancy K., Dagle, John M., Murray, Jeffrey C., Kelsey, Keegan
Publicado 2021

Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger syndrome

por Maciolek, Nicole L, Alward, Wallace LM, Murray, Jeffrey C, Semina, Elena V, McNally, Mark T
Publicado 2006

Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases

por Leslie, Elizabeth J., Standley, Jennifer, Compton, John, Bale, Sherri, Schutte, Brian C., Murray, Jeffrey C.
Publicado 2013

Genetic associations with neonatal thyroid stimulating hormone levels

por Alul, Farah Y., Shchelochkov, Oleg A., Berberich, Stanton L., Murray, Jeffrey C., Ryckman, Kelli K.
Publicado 2013

Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia

por Brémond-Gignac, Dominique, Bitoun, Pierre, Reis, Linda M., Copin, Henri, Murray, Jeffrey C., Semina, Elena V.
Publicado 2010

Transcriptome landscape of the human placenta

por Kim, Jinsil, Zhao, Keyan, Jiang, Peng, Lu, Zhi-xiang, Wang, Jinkai, Murray, Jeffrey C, Xing, Yi
Publicado 2012

Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations

por Yang, Tian, Jia, Zhonglin, Bryant-Pike, Whitney, Chandrasekhar, Anand, Murray, Jeffrey C, Fritzsch, Bernd, Bassuk, Alexander G
Publicado 2014

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development

por Mueller, Kathryn L., Murray, Jeffrey C., Michaelson, Jacob J., Christiansen, Morten H., Reilly, Sheena, Tomblin, J. Bruce
Publicado 2016

A novel nonsense mutation in keratin 10 causes a familial case of recessive epidermolytic ichthyosis

por Gutierrez, Jeydith A, Hannoush, Zeina C, Vargas, Luis G, Momany, Allison, Garcia, Carmen C, Murray, Jeffrey C, Dunnwald, Martine
Publicado 2013

Candidate gene and locus analysis of myopia

por Mutti, Donald O., Cooper, Margaret E., O'Brien, Sarah, Jones, Lisa A., Marazita, Mary L., Murray, Jeffrey C., Zadnik, Karla
Publicado 2007

Cost-effectiveness of a gestational age metabolic algorithm for preterm and small-for-gestational-age classification

por Coyle, Kathryn, Quan, Amanda My Linh, Wilson, Lindsay A., Hawken, Steven, Bota, A. Brianne, Coyle, Doug, Murray, Jeffrey C., Wilson, Kumanan
Publicado 2021

Validation of gestational age determination from ultrasound or a metabolic gestational age algorithm using exact date of conception in a cohort of newborns conceived using assisted...

por Hawken, Steven, Olibris, Brieanne, Ducharme, Robin, Bota, A. Brianne, Murray, Jeffrey C., Potter, Beth K., Walker, Mark, Chakraborty, Pranesh, Wilson, Kumanan
Publicado 2022

X-Linked Genes and Risk of Orofacial Clefts: Evidence from Two Population-Based Studies in Scandinavia

por Jugessur, Astanand, Skare, Øivind, Lie, Rolv T., Wilcox, Allen J., Christensen, Kaare, Christiansen, Lene, Nguyen, Truc Trung, Murray, Jeffrey C., Gjessing, Håkon K.
Publicado 2012

Genome-Wide Analysis of DNA Methylation in Human Amnion

por Kim, Jinsil, Pitlick, Mitchell M., Christine, Paul J., Schaefer, Amanda R., Saleme, Cesar, Comas, Belén, Cosentino, Viviana, Gadow, Enrique, Murray, Jeffrey C.
Publicado 2013

Association of Amino Acids with Common Complications of Prematurity

por Ryckman, Kelli K, Dagle, John M, Shchelochkov, Oleg A, Ehinger, Noah, Poole, Stanley D., Berberich, Stanton L., Reese, Jeff, Murray, Jeffrey C
Publicado 2013