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Author Details
Full Name
Andrew D Skol
Affiliation
The University of Chicago
ORCID
Career Start Year
2001
Papers
57
H Index
26
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36349721
Inherited cancer predisposing mutations in patients with therapy-related myeloid neoplasms.
Br J Haematol
2023
36349721
Inherited cancer predisposing mutations in patients with therapy-related myeloid neoplasms.
Br J Haematol
2023
34775477
PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors.
Pharmacogenomics J
2022
35617957
Genetic changes associated with relapse in favorable histology Wilms tumor: A Children's Oncology Group AREN03B2 study.
Cell Rep Med
2022
34983928
Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.
Nat Commun
2022
34775477
PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors.
Pharmacogenomics J
2022
34934177
Correction to: PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors.
Pharmacogenomics J
2022
35617957
Genetic changes associated with relapse in favorable histology Wilms tumor: A Children's Oncology Group AREN03B2 study.
Cell Rep Med
2022
34983928
Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.
Nat Commun
2022
34934177
Correction to: PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors.
Pharmacogenomics J
2022
33419763
Functional Common and Rare <i>ERBB2</i> Germline Variants Cooperate in Familial and Sporadic Cancer Susceptibility.
Cancer Prev Res (Phila)
2021
33419763
Functional Common and Rare <i>ERBB2</i> Germline Variants Cooperate in Familial and Sporadic Cancer Susceptibility.
Cancer Prev Res (Phila)
2021
32913072
The impact of sex on gene expression across human tissues.
Science
2020
31901248
Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2.
Am J Hum Genet
2020
32913072
The impact of sex on gene expression across human tissues.
Science
2020
33164750
Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes.
Elife
2020
31901248
Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2.
Am J Hum Genet
2020
33164750
Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes.
Elife
2020
30385613
Genetic Variants of <i>VEGFA</i> and <i>FLT4</i> Are Determinants of Survival in Renal Cell Carcinoma Patients Treated with Sorafenib.
Cancer Res
2019
30385613
Genetic Variants of <i>VEGFA</i> and <i>FLT4</i> Are Determinants of Survival in Renal Cell Carcinoma Patients Treated with Sorafenib.
Cancer Res
2019
28973033
Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.
PLoS One
2017
28979163
A p53-regulated apoptotic gene signature predicts treatment response and outcome in pediatric acute lymphoblastic leukemia.
Cancer Manag Res
2017
28973033
Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.
PLoS One
2017
29296818
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.
Blood Adv
2017
29117357
Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma.
J Natl Cancer Inst
2017
28163169
Does MAOA increase susceptibility to prenatal stress in young children?
Neurotoxicol Teratol
2017
28163169
Does MAOA increase susceptibility to prenatal stress in young children?
Neurotoxicol Teratol
2017
29296818
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.
Blood Adv
2017
28979163
A p53-regulated apoptotic gene signature predicts treatment response and outcome in pediatric acute lymphoblastic leukemia.
Cancer Manag Res
2017
29117357
Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma.
J Natl Cancer Inst
2017
26868379
A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.
Nat Commun
2016
26868379
A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.
Nat Commun
2016
26480299
Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.
Inflamm Bowel Dis
2016
27716388
The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance.
Breast Cancer Res
2016
26480299
Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.
Inflamm Bowel Dis
2016
27716388
The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance.
Breast Cancer Res
2016
25338677
Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.
Genes Immun
2015
29771652
Establishing a translational genomics infrastructure in pediatric cancer: the GREAT KIDS experience.
Per Med
2015
25338677
Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.
Genes Immun
2015
25766683
Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci.
BMC Genomics
2015
26014803
Integrated genomic analysis suggests MLL3 is a novel candidate susceptibility gene for familial nasopharyngeal carcinoma.
Cancer Epidemiol Biomarkers Prev
2015
29771652
Establishing a translational genomics infrastructure in pediatric cancer: the GREAT KIDS experience.
Per Med
2015
26014803
Integrated genomic analysis suggests MLL3 is a novel candidate susceptibility gene for familial nasopharyngeal carcinoma.
Cancer Epidemiol Biomarkers Prev
2015
25766683
Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci.
BMC Genomics
2015
24186849
Discovery and functional assessment of gene variants in the vascular endothelial growth factor pathway.
Hum Mutat
2014
24186849
Discovery and functional assessment of gene variants in the vascular endothelial growth factor pathway.
Hum Mutat
2014
24753543
Shared and independent colorectal cancer risk alleles in TGFβ-related genes in African and European Americans.
Carcinogenesis
2014
24882388
Radiation-induced apoptosis varies among individuals and is modified by sex and age.
Int J Radiat Biol
2014
24920014
A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus.
Nat Commun
2014
24753543
Shared and independent colorectal cancer risk alleles in TGFβ-related genes in African and European Americans.
Carcinogenesis
2014
1 - 50 of 114
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