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Author Details

Andrew D Skol
The University of Chicago
2001
57
26
PMIDPaper TitleJournal TitlePublished Year
36349721Inherited cancer predisposing mutations in patients with therapy-related myeloid neoplasms.Br J Haematol2023
36349721Inherited cancer predisposing mutations in patients with therapy-related myeloid neoplasms.Br J Haematol2023
34775477PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors.Pharmacogenomics J2022
35617957Genetic changes associated with relapse in favorable histology Wilms tumor: A Children's Oncology Group AREN03B2 study.Cell Rep Med2022
34983928Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.Nat Commun2022
34775477PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors.Pharmacogenomics J2022
34934177Correction to: PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors.Pharmacogenomics J2022
35617957Genetic changes associated with relapse in favorable histology Wilms tumor: A Children's Oncology Group AREN03B2 study.Cell Rep Med2022
34983928Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.Nat Commun2022
34934177Correction to: PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors.Pharmacogenomics J2022
33419763Functional Common and Rare <i>ERBB2</i> Germline Variants Cooperate in Familial and Sporadic Cancer Susceptibility.Cancer Prev Res (Phila)2021
33419763Functional Common and Rare <i>ERBB2</i> Germline Variants Cooperate in Familial and Sporadic Cancer Susceptibility.Cancer Prev Res (Phila)2021
32913072The impact of sex on gene expression across human tissues.Science2020
31901248Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2.Am J Hum Genet2020
32913072The impact of sex on gene expression across human tissues.Science2020
33164750Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes.Elife2020
31901248Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2.Am J Hum Genet2020
33164750Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes.Elife2020
30385613Genetic Variants of <i>VEGFA</i> and <i>FLT4</i> Are Determinants of Survival in Renal Cell Carcinoma Patients Treated with Sorafenib.Cancer Res2019
30385613Genetic Variants of <i>VEGFA</i> and <i>FLT4</i> Are Determinants of Survival in Renal Cell Carcinoma Patients Treated with Sorafenib.Cancer Res2019
28973033Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.PLoS One2017
28979163A p53-regulated apoptotic gene signature predicts treatment response and outcome in pediatric acute lymphoblastic leukemia.Cancer Manag Res2017
28973033Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.PLoS One2017
29296818Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.Blood Adv2017
29117357Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma.J Natl Cancer Inst2017
28163169Does MAOA increase susceptibility to prenatal stress in young children?Neurotoxicol Teratol2017
28163169Does MAOA increase susceptibility to prenatal stress in young children?Neurotoxicol Teratol2017
29296818Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.Blood Adv2017
28979163A p53-regulated apoptotic gene signature predicts treatment response and outcome in pediatric acute lymphoblastic leukemia.Cancer Manag Res2017
29117357Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma.J Natl Cancer Inst2017
26868379A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.Nat Commun2016
26868379A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.Nat Commun2016
26480299Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.Inflamm Bowel Dis2016
27716388The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance.Breast Cancer Res2016
26480299Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.Inflamm Bowel Dis2016
27716388The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance.Breast Cancer Res2016
25338677Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.Genes Immun2015
29771652Establishing a translational genomics infrastructure in pediatric cancer: the GREAT KIDS experience.Per Med2015
25338677Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.Genes Immun2015
25766683Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci.BMC Genomics2015
26014803Integrated genomic analysis suggests MLL3 is a novel candidate susceptibility gene for familial nasopharyngeal carcinoma.Cancer Epidemiol Biomarkers Prev2015
29771652Establishing a translational genomics infrastructure in pediatric cancer: the GREAT KIDS experience.Per Med2015
26014803Integrated genomic analysis suggests MLL3 is a novel candidate susceptibility gene for familial nasopharyngeal carcinoma.Cancer Epidemiol Biomarkers Prev2015
25766683Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci.BMC Genomics2015
24186849Discovery and functional assessment of gene variants in the vascular endothelial growth factor pathway.Hum Mutat2014
24186849Discovery and functional assessment of gene variants in the vascular endothelial growth factor pathway.Hum Mutat2014
24753543Shared and independent colorectal cancer risk alleles in TGFβ-related genes in African and European Americans.Carcinogenesis2014
24882388Radiation-induced apoptosis varies among individuals and is modified by sex and age.Int J Radiat Biol2014
24920014A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus.Nat Commun2014
24753543Shared and independent colorectal cancer risk alleles in TGFβ-related genes in African and European Americans.Carcinogenesis2014
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European Bioinformatics Institute
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UPMC Hillman Cancer Center
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University of Texas MD Anderson Cancer Center
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University of Geneva
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