Generalized Admixture Mapping for Complex Traits

por Zhu, Bin, Ashley-Koch, Allison E., Dunson, David B.
Publicado 2013

Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data

por Mei, Hao, Ma, Deqiong, Ashley-Koch, Allison, Martin, Eden R
Publicado 2005

Exome Analysis of Two Limb-Girdle Muscular Dystrophy Families: Mutations Identified and Challenges Encountered

por McDonald, Kristin K., Stajich, Jeffrey, Blach, Colette, Ashley-Koch, Allison E., Hauser, Michael A.
Publicado 2012

Association of Variant rs4790904 in Protein Kinase C Alpha with Posttraumatic Stress Disorder in a U.S. Caucasian and African-American Veteran Sample

por Liu, Yutao, Rimmler, Jacqueline, Dennis, Michelle F., Ashley-Koch, Allison E., Hauser, Michael A., Beckham, Jean C.
Publicado 2013

Bipolar Disorder, Brain-Derived Neurotrophic Factor (BDNF) Val66Met Polymorphism and Brain Morphology

por Teh, Cheryl Ann, Lee, Tih-Shih, Kuchibhatla, Margaratha, Ashley-Koch, Allison, MacFall, James, Krishnan, Ranga, Beyer, John
Publicado 2012

Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease

por Doss, Jennifer F., Jonassaint, Jude C., Garrett, Melanie E., Ashley-Koch, Allison E., Telen, Marilyn J., Chi, Jen-Tsan
Publicado 2016

Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one‐carbon metabolism networks

por Hillman, Paul, Baker, Craig, Hebert, Luke, Brown, Michael, Hixson, James, Ashley‐Koch, Allison, Morrison, Alanna C., Northrup, Hope, Au, Kit Sing
Publicado 2020

Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients

por Hebert, Luke, Hillman, Paul, Baker, Craig, Brown, Michael, Ashley-Koch, Allison, Hixson, James E., Morrison, Alanna C., Northrup, Hope, Au, Kit Sing
Publicado 2020

Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy

por Garrett, Melanie E., Soldano, Karen L., Erwin, Kyle N., Zhang, Yingze, Gordeuk, Victor R., Gladwin, Mark T., Telen, Marilyn J., Ashley-Koch, Allison E.
Publicado 2022

ANGIOTENSIN RECEPTOR GENE POLYMORPHISMS AND TWO-YEAR CHANGE IN HYPERINTENSE LESION VOLUME IN MEN

por Taylor, Warren D., Steffens, David C., Ashley-Koch, Allison, Payne, Martha E., MacFall, James R., Potocky, Christopher F., Krishnan, K. Ranga R.
Publicado 2009

An Examination of the Association between 5-HTTLPR, Combat Exposure, and PTSD Diagnosis among U.S. Veterans

por Liu, Yutao, Garrett, Melanie E., Dennis, Michelle F., Green, Kimberly T., Ashley-Koch, Allison E., Hauser, Michael A., Beckham, Jean C., Kimbrel, Nathan A.
Publicado 2015

In vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress

por Anderson, Blair R., Howell, David N., Soldano, Karen, Garrett, Melanie E., Katsanis, Nicholas, Telen, Marilyn J., Davis, Erica E., Ashley-Koch, Allison E.
Publicado 2015

Correction: In vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress

por Anderson, Blair R., Howell, David N., Soldano, Karen, Garrett, Melanie E., Katsanis, Nicholas, Telen, Marilyn J., Davis, Erica E., Ashley-Koch, Allison E.
Publicado 2015

Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular Degeneration

por Tan, Perciliz L., Garrett, Melanie E., Willer, Jason R., Campochiaro, Peter A., Campochiaro, Betsy, Zack, Donald J., Ashley-Koch, Allison E., Katsanis, Nicholas
Publicado 2017

Integrative single-nucleus multi-omics analysis prioritizes candidate cis and trans regulatory networks and their target genes in Alzheimer’s disease brains

por Gamache, Julia, Gingerich, Daniel, Shwab, E. Keats, Barrera, Julio, Garrett, Melanie E., Hume, Cordelia, Crawford, Gregory E., Ashley-Koch, Allison E., Chiba-Falek, Ornit
Publicado 2023

Adjusting for covariates on a slippery slope: linkage analysis of change over time

por Rampersaud, Evadnie, Allen, Andrew, Li, Yi-Ju, Shao, Yujun, Bass, Meredyth, Haynes, Carol, Ashley-Koch, Allison, Martin, Eden R, Schmidt, Silke, Hauser, Elizabeth R
Publicado 2003

RNA sequencing of isolated cell populations expressing human APOL1 G2 risk variant reveals molecular correlates of sickle cell nephropathy in zebrafish podocytes

por Bundy, Joseph L., Anderson, Blair R., Francescatto, Ludmila, Garrett, Melanie E., Soldano, Karen L., Telen, Marilyn J., Davis, Erica E., Ashley-Koch, Allison E.
Publicado 2019

Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

por Markunas, Christina A., Soldano, Karen, Dunlap, Kaitlyn, Cope, Heidi, Asiimwe, Edgar, Stajich, Jeffrey, Enterline, David, Grant, Gerald, Fuchs, Herbert, Gregory, Simon G., Ashley-Koch, Allison E.
Publicado 2013

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics

por Markunas, Christina A, Lock, Eric, Soldano, Karen, Cope, Heidi, Ding, Chien-Kuang C, Enterline, David S, Grant, Gerald, Fuchs, Herbert, Ashley-Koch, Allison E, Gregory, Simon G
Publicado 2014

Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts

por Nouraie, Mehdi, Ashley-Koch, Allison E., Garrett, Melanie E., Sritharan, Nithya, Zhang, Yingze, Little, Jane, Gordeuk, Victor R., Gladwin, Mark T., Telen, Marilyn J., Kato, Gregory J.
Publicado 2020