Family-based study shows heterogeneity of a susceptibility locus on chromosome 8q24 for nonsyndromic cleft lip and palate

Por Blanton, Susan H., Burt, Amber, Stal, Samuel, Mulliken, John B., Garcia, Elizabeth, Hecht, Jacqueline T.
Publicado em 2010

Ethnic heterogeneity of IRF6 AP-2α binding site promoter SNP association with nonsyndromic cleft lip and palate

Por Blanton, Susan H., Burt, Amber, Garcia, Elizabeth, Mulliken, John B., Stal, Samuel, Hecht, Jacqueline T.
Publicado em 2010

Combined neurodevelopmental exposure to deltamethrin and corticosterone is associated with Nr3c1 hypermethylation in the midbrain of male mice

Por Vester, Aimée I., Hermetz, Karen, Burt, Amber, Everson, Todd, Marsit, Carmen J., Caudle, William M.
Publicado no Neurotoxicol Teratol (2020)

Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate

Por Chiquet, Brett T., Blanton, Susan H., Burt, Amber, Ma, Deqiong, Stal, Samuel, Mulliken, John B., Hecht, Jacqueline T.
Publicado em 2008

Nonsyndromic cleft lip and palate: CRISPLD Genes and the Folate Gene Pathway Connection

Por Chiquet, Brett T., Henry, Robin, Burt, Amber, Mulliken, John B., Stal, Samuel, Blanton, Susan H., Hecht, Jacqueline T.
Publicado em 2010

Associations between single nucleotide polymorphisms in the FAS pathway and acute kidney injury

Por Bhatraju, Pavan, Hsu, Christine, Mukherjee, Paramita, Glavan, Bradford J., Burt, Amber, Mikacenic, Carmen, Himmelfarb, Jonathan, Wurfel, Mark
Publicado no Crit Care (2015)

Fitness among individuals with early childhood deafness: studies in alumni families from Gallaudet University

Por BLANTON, SUSAN H., NANCE, WALTER E., NORRIS, VIRGINIA W., WELCH, KATHERINE O., BURT, AMBER, PANDYA, ARTI, ARNOS, KATHLEEN S.
Publicado em 2009

Dietary fatty acid intake is associated with paraoxonase 1 activity in a cohort-based analysis of 1,548 subjects

Por Kim, Daniel Seung, Maden, Sean K, Burt, Amber A, Ranchalis, Jane E, Furlong, Clement E, Jarvik, Gail P
Publicado em 2013

Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate

Por Chiquet, Brett T, Hashmi, Syed S, Henry, Robin, Burt, Amber, Mulliken, John B, Stal, Samuel, Bray, Molly, Blanton, Susan H, Hecht, Jacqueline T
Publicado em 2009

Vitamin D Receptor Gene as a Candidate Gene for Parkinson Disease

Por BUTLER, MEGAN W., BURT, AMBER, EDWARDS, TODD L., ZUCHNER, STEPHAN, SCOTT, WILLIAM K., MARTIN, EDEN R., VANCE, JEFFERY M., WANG, LIYONG
Publicado em 2011

Effects of dietary components on high-density lipoprotein measures in a cohort of 1,566 participants

Por Kim, Daniel Seung, Burt, Amber A, Ranchalis, Jane E, Jarvik, Leah E, Eintracht, Jason F, Furlong, Clement E, Jarvik, Gail P
Publicado em 2014

Altered Transmission of HOX and Apoptotic SNPs Identify a Potential Common Pathway for Clubfoot

Por Ester, Audrey R., Weymouth, Katelyn S., Burt, Amber, Wise, Carol, Scott, Allison, Gurnett, Christina A, Dobbs, Matthew B., Blanton, Susan H., Hecht, Jacqueline T.
Publicado em 2009

Novel gene-by-environment interactions: APOB and NPC1L1 variants affect the relationship between dietary and total plasma cholesterol

Por Kim, Daniel S., Burt, Amber A., Ranchalis, Jane E., Jarvik, Ella R., Rosenthal, Elisabeth A., Hatsukami, Thomas S., Furlong, Clement E., Jarvik, Gail P.
Publicado em 2013

Maternal circadian disruption is associated with variation in placental DNA methylation

Por Clarkson-Townsend, Danielle A., Everson, Todd M., Deyssenroth, Maya A., Burt, Amber A., Hermetz, Karen E., Hao, Ke, Chen, Jia, Marsit, Carmen J.
Publicado no PLoS One (2019)

Placental lncRNA expression associated with placental cadmium concentrations and birth weight

Por Hussey, Michael R, Burt, Amber, Deyssenroth, Maya A, Jackson, Brian P, Hao, Ke, Peng, Shouneng, Chen, Jia, Marsit, Carmen J, Everson, Todd M
Publicado no Environ Epigenet (2020)

Joint Linkage and Association Analysis with Exome Sequence Data Implicates SLC25A40 in Hypertriglyceridemia

Por Rosenthal, Elisabeth A., Ranchalis, Jane, Crosslin, David R., Burt, Amber, Brunzell, John D., Motulsky, Arno G., Nickerson, Deborah A., Wijsman, Ellen M., Jarvik, Gail P.
Publicado em 2013

Additional Common Polymorphisms in the PON Gene Cluster Predict PON1 Activity but Not Vascular Disease

Por Kim, Daniel S., Burt, Amber A., Ranchalis, Jane E., Richter, Rebecca J., Marshall, Julieann K., Eintracht, Jason F., Rosenthal, Elisabeth A., Furlong, Clement E., Jarvik, Gail P.
Publicado em 2012

Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL

Por Kim, Daniel S., Burt, Amber A., Crosslin, David R., Robertson, Peggy D., Ranchalis, Jane E., Boyko, Edward J., Nickerson, Deborah A., Furlong, Clement E., Jarvik, Gail P.
Publicado em 2013

HDL‐3 is a Superior Predictor of Carotid Artery Disease in a Case‐Control Cohort of 1725 Participants

Por Kim, Daniel Seung, Burt, Amber A., Rosenthal, Elisabeth A., Ranchalis, Jane E., Eintracht, Jason F., Hatsukami, Thomas S., Furlong, Clement E., Marcovina, Santica, Albers, John J., Jarvik, Gail P.
Publicado no J Am Heart Assoc (2014)

A Genome-Wide Map of AAV-Mediated Human Gene Targeting

Por Deyle, David R., Hansen, R. Scott, Cornea, Anda M., Li, Li B., Burt, Amber A., Alexander, Ian E., Sandstrom, Richard S., Stamatoyannopoulos, John A., Wei, Chia-Lin, Russell, David W.
Publicado no Nat Struct Mol Biol (2014)