Novel insight into the etiology of ischemic stroke gained by integrative transcriptome-wide association study

por Jung, Junghyun, Lu, Zeyun, de Smith, Adam, Mancuso, Nicholas
Publicado 2023

Implications of copy number variation in people with chromosomal abnormalities: potential for greater variation in copy number state may contribute to variability of phenotype

por de Smith, Adam J., Trewick, Anne L., Blakemore, Alexandra I. F.
Publicado 2010

Incorporation of DNA methylation quantitative trait loci (mQTLs) in epigenome-wide association analysis: application to birthweight effects in neonatal whole blood

por Li, Shaobo, Mancuso, Nicholas, Metayer, Catherine, Ma, Xiaomei, de Smith, Adam J., Wiemels, Joseph L.
Publicado 2022

Associations between early‐life and in utero infections and cytomegalovirus‐positive acute lymphoblastic leukemia in children

por Gallant, Rachel E., Arroyo, Katti, Metayer, Catherine, Kang, Alice Y., de Smith, Adam J., Wiemels, Joseph L.
Publicado 2022

Exploring the genetic and epigenetic origins of juvenile myelomonocytic leukemia using newborn screening samples

por Behnert, Astrid, Meyer, Julia, Parsa, Jahan-Yar, Hechmer, Aaron, Loh, Mignon L., Olshen, Adam, de Smith, Adam J., Stieglitz, Elliot
Publicado 2021

Somatic Mutation Allelic Ratio Test Using ddPCR (SMART-ddPCR): An Accurate Method for Assessment of Preferential Allelic Imbalance in Tumor DNA

por de Smith, Adam J., Walsh, Kyle M., Hansen, Helen M., Endicott, Alyson A., Wiencke, John K., Metayer, Catherine, Wiemels, Joseph L.
Publicado 2015

Pediatric glioma and medulloblastoma risk and population demographics: a Poisson regression analysis

por Muskens, Ivo S, Feng, Qianxi, Francis, Stephen S, Walsh, Kyle M, Mckean-Cowdin, Roberta, Gauderman, William J, de Smith, Adam J, Wiemels, Joseph L
Publicado 2020

DNA methylation at birth in monozygotic twins discordant for pediatric acute lymphoblastic leukemia

por Nickels, Eric M., Li, Shaobo, Myint, Swe Swe, Arroyo, Katti, Feng, Qianxi, Siegmund, Kimberly D., de Smith, Adam J., Wiemels, Joseph L.
Publicado 2022

Evaluating Genomic Polygenic Risk Scores for Childhood Acute Lymphoblastic Leukemia in Latinos

por Jeon, Soyoung, Lo, Ying Chu, Morimoto, Libby M., Metayer, Catherine, Ma, Xiaomei, Wiemels, Joseph L., de Smith, Adam J., Chiang, Charleston W.K.
Publicado 2023

Evaluating genomic polygenic risk scores for childhood acute lymphoblastic leukemia in Latinos

por Jeon, Soyoung, Lo, Ying Chu, Morimoto, Libby M., Metayer, Catherine, Ma, Xiaomei, Wiemels, Joseph L., de Smith, Adam J., Chiang, Charleston W.K.
Publicado 2023

Small Deletion Variants Have Stable Breakpoints Commonly Associated with Alu Elements

por de Smith, Adam J., Walters, Robin G., Coin, Lachlan J. M., Steinfeld, Israel, Yakhini, Zohar, Sladek, Rob, Froguel, Philippe, Blakemore, Alexandra I. F.
Publicado 2008

Mitochondrial 1555 G>A variant as a potential risk factor for childhood glioblastoma

por Li, Shaobo, Gai, Xiaowu, Myint, Swe Swe, Arroyo, Katti, Morimoto, Libby, Metayer, Catherine, de Smith, Adam J, Walsh, Kyle M, Wiemels, Joseph L
Publicado 2022

To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes

por Wallace, Amelia D., Wendt, George A., Barcellos, Lisa F., de Smith, Adam J., Walsh, Kyle M., Metayer, Catherine, Costello, Joseph F., Wiemels, Joseph L., Francis, Stephen S.
Publicado 2018

Cytomegalovirus proteins, maternal pregnancy cytokines, and their impact on neonatal immune cytokine profiles and acute lymphoblastic leukemogenesis in children

por Wiemels, Joseph L., Wang, Rong, Zhou, Mi, Hansen, Helen, Gallant, Rachel, Jung, Junghyun, Mancuso, Nicholas, de Smith, Adam J., Metayer, Catherine, Kogan, Scott C., Ma, Xiaomei
Publicado 2022

Epigenomic signature of major congenital heart defects in newborns with Down syndrome

por Mouat, Julia S., Li, Shaobo, Myint, Swe Swe, Laufer, Benjamin I., Lupo, Philip J., Schraw, Jeremy M., Woodhouse, John P., de Smith, Adam J., LaSalle, Janine M.
Publicado 2023

Epigenomic signature of major congenital heart defects in newborns with Down syndrome

por Mouat, Julia S., Li, Shaobo, Myint, Swe Swe, Laufer, Benjamin I., Lupo, Philip J., Schraw, Jeremy M., Woodhouse, John P., de Smith, Adam J., LaSalle, Janine M.
Publicado 2023

Localized variation in ancestral admixture identifies pilocytic astrocytoma risk loci among Latino children

por Li, Shaobo, Chiang, Charleston W. K., Myint, Swe Swe, Arroyo, Katti, Chan, Tsz Fung, Morimoto, Libby, Metayer, Catherine, de Smith, Adam J., Walsh, Kyle M., Wiemels, Joseph L.
Publicado 2022

Clonal and microclonal mutational heterogeneity in high hyperdiploid acute lymphoblastic leukemia

por de Smith, Adam J., Ojha, Juhi, Francis, Stephen S., Sanders, Erica, Endicott, Alyson A., Hansen, Helen M., Smirnov, Ivan, Termuhlen, Amanda M., Walsh, Kyle M., Metayer, Catherine, Wiemels, Joseph L.
Publicado 2016

Increased burden of familial-associated early-onset cancer risk among minority Americans compared to non-Latino Whites

por Feng, Qianxi, Nickels, Eric, Muskens, Ivo S, de Smith, Adam J, Gauderman, W James, Yee, Amy C, Ricker, Charite, Mack, Thomas, Leavitt, Andrew D, Godley, Lucy A, Wiemels, Joseph L
Publicado 2021

A Functional Polymorphism in the CEBPE Gene Promoter Influences Acute Lymphoblastic Leukemia Risk through Interaction with the Hematopoietic Transcription Factor Ikaros

por Wiemels, Joseph L., de Smith, Adam J., Xiao, Jianqiao, Lee, Seung-Tae, Muench, Marcus O., Fomin, Marina E., Zhou, Mi, Hansen, Helen M., Termuhlen, Amanda, Metayer, Catherine, Walsh, Kyle M.
Publicado 2015