Intermediate phenotypes underlying osteosarcoma risk

por Semmes, Eleanor C., Zhang, Chenan, Walsh, Kyle M.
Publicado 2018

Telomere length connects melanoma and glioma predispositions

por Endicott, Alyson A., Taylor, Jennie W., Walsh, Kyle M.
Publicado 2016

Beyond Anxiety and Grief: Mapping the Emotional Landscape of Parents Facing a Childhood Cancer Diagnosis

por Sheikh, Shanzeh, Wimberly, Courtney E., Towry, Lisa, Walsh, Kyle M.
Publicado 2023

Disease risk prediction with rare and common variants

por Wu, Chengqing, Walsh, Kyle M, DeWan, Andrew T, Hoh, Josephine, Wang, Zuoheng
Publicado 2011

Shared genomic architecture between COVID-19 severity and numerous clinical and physiologic parameters revealed by LD score regression analysis

por Byun, Jinyoung, Han, Younghun, Walsh, Kyle M., Park, Amy S., Bondy, Melissa L., Amos, Christopher I.
Publicado 2022

Associations between genetic variants of KIF5B, FMN1, and MGAT3 in the cadherin pathway and pancreatic cancer risk

por Zhao, Lingling, Liu, Hongliang, Luo, Sheng, Moorman, Patricia G., Walsh, Kyle M., Li, Wei, Wei, Qingyi
Publicado 2020

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

por Zhao, Linlu, Triche, Elizabeth W, Walsh, Kyle M, Bracken, Michael B, Saftlas, Audrey F, Hoh, Josephine, Dewan, Andrew T
Publicado 2012

Whole-exome sequencing of a pedigree segregating asthma

por DeWan, Andrew T, Egan, Kathryn Brigham, Hellenbrand, Karen, Sorrentino, Keli, Pizzoferrato, Nicole, Walsh, Kyle M, Bracken, Michael B
Publicado 2012

Genetic variation associated with childhood and adult stature and risk of MYCN‐amplified neuroblastoma

por Semmes, Eleanor C., Shen, Erica, Cohen, Jennifer L., Zhang, Chenan, Wei, Qingyi, Hurst, Jillian H., Walsh, Kyle M.
Publicado 2020

Physician, patient, and caregiver support for a formal certification in pediatric neuro-oncology: A survey-based report from the SNO pediatrics working group

por Lindsay, Holly B, Cheng, Sylvia, Fisher, Paul Graham, Peters, Katherine B, Walsh, Kyle M, Ashley, David M, Huang, Annie
Publicado 2023

The joint impacts of sex and race/ethnicity on incidence of grade 1 versus grades 2–3 meningioma across the lifespan

por Walsh, Kyle M, Price, Mackenzie, Neff, Corey, Komisarow, Jordan M, Wimberly, Courtney E, Kruchko, Carol, Barnholtz-Sloan, Jill S, Ostrom, Quinn T
Publicado 2023

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

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

ADCC-activating antibodies correlate with decreased risk of congenital human cytomegalovirus transmission

por Semmes, Eleanor C., Miller, Itzayana G., Rodgers, Nicole, Phan, Caroline T., Hurst, Jillian H., Walsh, Kyle M., Stanton, Richard J., Pollara, Justin, Permar, Sallie R.
Publicado 2023

Three novel genetic variants in NRF2 signaling pathway genes are associated with pancreatic cancer risk

por Yang, Wenjun, Liu, Hongliang, Duan, Bensong, Xu, Xinyuan, Carmody, Dennis, Luo, Sheng, Walsh, Kyle M., Abbruzzese, James L., Zhang, Xuefeng, Chen, Xiaoxin, Wei, Qingyi
Publicado 2019

Capicua (CIC) mutations in gliomas in association with MAPK activation for exposing a potential therapeutic target

por Darabi, Sourat, Xiu, Joanne, Samec, Timothy, Kesari, Santosh, Carrillo, Jose, Aulakh, Sonikpreet, Walsh, Kyle M., Sengupta, Soma, Sumrall, Ashley, Spetzler, David, Glantz, Michael, Demeure, Michael J.
Publicado 2023

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

Pleiotropic MLLT10 variation confers risk of meningioma and estrogen-mediated cancers

por Walsh, Kyle M, Zhang, Chenan, Calvocoressi, Lisa, Hansen, Helen M, Berchuck, Andrew, Schildkraut, Joellen M, Bondy, Melissa L, Wrensch, Margaret, Wiemels, Joseph L, Claus, Elizabeth B
Publicado 2022

The shared genetic architecture between epidemiological and behavioral traits with lung cancer

por Pettit, Rowland W., Byun, Jinyoung, Han, Younghun, Ostrom, Quinn T., Edelson, Jacob, Walsh, Kyle M., Bondy, Melissa L., Hung, Rayjean J., McKay, James D., Amos, Christopher I.
Publicado 2021