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 em 2010

Germline genetic landscape of pediatric central nervous system tumors

Por Muskens, Ivo S, Zhang, Chenan, de Smith, Adam J, Biegel, Jaclyn A, Walsh, Kyle M, Wiemels, Joseph L
Publicado no Neuro Oncol (2019)

Non-additive and epistatic effects of HLA polymorphisms contributing to risk of adult glioma

Por Zhang, Chenan, de Smith, Adam J., Smirnov, Ivan V., Wiencke, John K., Wiemels, Joseph L., Witte, John S., Walsh, Kyle M.
Publicado no J Neurooncol (2017)

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 no PLoS One (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 no Neurooncol Adv (2020)

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 em 2008

GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL

Por Walsh, Kyle M., de Smith, Adam J., Chokkalingam, Anand P., Metayer, Catherine, Roberts, William, Barcellos, Lisa F., Wiemels, Joseph L., Buffler, Patricia A.
Publicado em 2013

Germline variants in predisposition genes in children with Down syndrome and acute lymphoblastic leukemia

Por Winer, Peleg, Muskens, Ivo S., Walsh, Kyle M., Vora, Ajay, Moorman, Anthony V., Wiemels, Joseph L., Roberts, Irene, Roy, Anindita, de Smith, Adam J.
Publicado no Blood Adv (2020)

Germline cancer predisposition variants and pediatric glioma: a population-based study in California

Por Muskens, Ivo S, de Smith, Adam J, Zhang, Chenan, Hansen, Helen M, Morimoto, Libby, Metayer, Catherine, Ma, Xiaomei, Walsh, Kyle M, Wiemels, Joseph L
Publicado no Neuro Oncol (2020)

Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion

Por Martins-Taylor, Kristen, Hsiao, Jack S., Chen, Pin-Fang, Glatt-Deeley, Heather, De Smith, Adam J., Blakemore, Alexandra I.F., Lalande, Marc, Chamberlain, Stormy J.
Publicado em 2014

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 no Front Genet (2018)

Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype

Por Walsh, Kyle M., de Smith, Adam J., Chokkalingam, Anand P., Metayer, Catherine, Dahl, Gary V., Hsu, Ling-i, Barcellos, Lisa F., Wiemels, Joseph L., Buffler, Patricia A.
Publicado em 2013

Genetic contribution to variation in DNA methylation at maternal smoking-sensitive loci in exposed neonates

Por Gonseth, Semira, de Smith, Adam J., Roy, Ritu, Zhou, Mi, Lee, Seung-Tae, Shao, Xiaorong, Ohja, Juhi, Wrensch, Margaret R., Walsh, Kyle M., Metayer, Catherine, Wiemels, Joseph L.
Publicado no Epigenetics (2016)

Periconceptional folate consumption is associated with neonatal DNA methylation modifications in neural crest regulatory and cancer development genes

Por Gonseth, Semira, Roy, Ritu, Houseman, E Andres, de Smith, Adam J, Zhou, Mi, Lee, Seung-Tae, Nusslé, Sébastien, Singer, Amanda W, Wrensch, Margaret R, Metayer, Catherine, Wiemels, Joseph L
Publicado no Epigenetics (2015)

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 no Oncotarget (2016)

A germ-line deletion of APOBEC3B does not contribute to subtype-specific childhood acute lymphoblastic leukemia etiology

Por Wallace, Amelia D., Francis, Stephen S., Shao, Xiaorong, de Smith, Adam J., Walsh, Kyle M., Mckean-Cowdin, Roberta, Ma, Xiaomei, Dahl, Gary, Barcellos, Lisa F., Wiemels, Joseph L., Metayer, Catherine
Publicado no Haematologica (2018)

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 no Leukemia (2015)

Common genetic variants associated with telomere length confer risk for neuroblastoma and other childhood cancers

Por Walsh, Kyle M., Whitehead, Todd P., de Smith, Adam J., Smirnov, Ivan V., Park, Minsun, Endicott, Alyson A., Francis, Stephen S., Codd, Veryan, Samani, Nilesh J., Metayer, Catherine, Wiemels, Joseph L.
Publicado no Carcinogenesis (2016)

Tobacco Smoke and Ras Mutations Among Latino and Non-Latino Children with Acute Lymphoblastic Leukemia

Por Kaur, Maneet, de Smith, Adam J., Selvin, Steve, Zhang, Luoping, Cunningham, Marc, Kang, Michelle W., Hansen, Helen M., Cooper, Robert M., McKean-Cowdin, Roberta, Wiemels, Joseph L., Metayer, Catherine
Publicado no Arch Med Res (2016)

Two HLA class II gene variants are independently associated with pediatric osteosarcoma risk

Por Zhang, Chenan, Wiemels, Joseph L., Hansen, Helen M., Gonzalez-Maya, Julio, Endicott, Alyson A., de Smith, Adam J., Smirnov, Ivan V., Witte, John S., Morimoto, Libby M., Metayer, Catherine, Walsh, Kyle M.
Publicado no Cancer Epidemiol Biomarkers Prev (2018)