Large-scale placenta DNA methylation integrated analysis reveals fetal sex-specific differentially methylated CpG sites and regions

por Andrews, Shan V., Yang, Irene J., Froehlich, Karolin, Oskotsky, Tomiko, Sirota, Marina
Publicado 2022

“Gap hunting” to characterize clustered probe signals in Illumina methylation array data

por Andrews, Shan V., Ladd-Acosta, Christine, Feinberg, Andrew P., Hansen, Kasper D., Fallin, M. Daniele
Publicado 2016

Cross-tissue integration of genetic and epigenetic data offers insight into autism spectrum disorder

por Andrews, Shan V., Ellis, Shannon E., Bakulski, Kelly M., Sheppard, Brooke, Croen, Lisa A., Hertz-Picciotto, Irva, Newschaffer, Craig J., Feinberg, Andrew P., Arking, Dan E., Ladd-Acosta, Christine, Fallin, M. Daniele
Publicado 2017

Case-control meta-analysis of blood DNA methylation and autism spectrum disorder

por Andrews, Shan V., Sheppard, Brooke, Windham, Gayle C., Schieve, Laura A., Schendel, Diana E., Croen, Lisa A., Chopra, Pankaj, Alisch, Reid S., Newschaffer, Craig J., Warren, Stephen T., Feinberg, Andrew P., Fallin, M. Daniele, Ladd-Acosta, Christine
Publicado 2018

Understanding LRRK2 kinase activity in preclinical models and human subjects through quantitative analysis of LRRK2 and pT73 Rab10

por Wang, Xiang, Negrou, Elvira, Maloney, Michael T., Bondar, Vitaliy V., Andrews, Shan V., Montalban, Manuel, Llapashtica, Ceyda, Maciuca, Romeo, Nguyen, Hoang, Solanoy, Hilda, Arguello, Annie, Przybyla, Laralynne, Moerke, Nathan J., Huntwork-Rodriguez, Sarah, Henry, Anastasia G.
Publicado 2021

A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus

por Lanata, Cristina M., Paranjpe, Ishan, Nititham, Joanne, Taylor, Kimberly E., Gianfrancesco, Milena, Paranjpe, Manish, Andrews, Shan, Chung, Sharon A., Rhead, Brooke, Barcellos, Lisa F., Trupin, Laura, Katz, Patricia, Dall’Era, Maria, Yazdany, Jinoos, Sirota, Marina, Criswell, Lindsey A.
Publicado 2019

Author Correction: A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus

por Lanata, Cristina M., Paranjpe, Ishan, Nititham, Joanne, Taylor, Kimberly E., Gianfrancesco, Milena, Paranjpe, Manish, Andrews, Shan, Chung, Sharon A., Rhead, Brooke, Barcellos, Lisa F., Trupin, Laura, Katz, Patricia, Dall’Era, Maria, Yazdany, Jinoos, Sirota, Marina, Criswell, Lindsey A.
Publicado 2020

Elevated polygenic burden for autism is associated with differential DNA methylation at birth

por Hannon, Eilis, Schendel, Diana, Ladd-Acosta, Christine, Grove, Jakob, Hansen, Christine Søholm, Andrews, Shan V., Hougaard, David Michael, Bresnahan, Michaeline, Mors, Ole, Hollegaard, Mads Vilhelm, Bækvad-Hansen, Marie, Hornig, Mady, Mortensen, Preben Bo, Børglum, Anders D., Werge, Thomas, Pedersen, Marianne Giørtz, Nordentoft, Merete, Buxbaum, Joseph, Daniele Fallin, M., Bybjerg-Grauholm, Jonas, Reichenberg, Abraham, Mill, Jonathan
Publicado 2018

Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function

por Mortlock, Sally, Houshdaran, Sahar, Kosti, Idit, Rahmioglu, Nilufer, Nezhat, Camran, Vitonis, Allison F., Andrews, Shan V., Grosjean, Parker, Paranjpe, Manish, Horne, Andrew W., Jacoby, Alison, Lager, Jeannette, Opoku-Anane, Jessica, Vo, Kim Chi, Manvelyan, Evelina, Sen, Sushmita, Ghukasyan, Zhanna, Collins, Frances, Santamaria, Xavier, Saunders, Philippa, Kober, Kord, McRae, Allan F., Terry, Kathryn L., Vallvé-Juanico, Júlia, Becker, Christian, Rogers, Peter A. W., Irwin, Juan C., Zondervan, Krina, Montgomery, Grant W., Missmer, Stacey, Sirota, Marina, Giudice, Linda
Publicado 2023