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Author Details
Full Name
Beth Wilmot
Affiliation
Knight Cancer Institute, Oregon Health & Science University
ORCID
Career Start Year
2004
Papers
64
H Index
25
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36264026
Secondary fusion proteins as a mechanism of BCR::ABL1 kinase-independent resistance in chronic myeloid leukaemia.
Br J Haematol
2023
36848718
The Oregon ADHD-1000: A new longitudinal data resource enriched for clinical cases and multiple levels of analysis.
Dev Cogn Neurosci
2023
34482403
Identification and prioritization of myeloid malignancy germline variants in a large cohort of adult patients with AML.
Blood
2022
35499387
Luxeptinib (CG-806) Targets FLT3 and Clusters of Kinases Operative in Acute Myeloid Leukemia.
Mol Cancer Ther
2022
35868306
Integrative analysis of drug response and clinical outcome in acute myeloid leukemia.
Cancer Cell
2022
36307214
Comprehensive molecular characterization of a rare case of Philadelphia chromosome-positive acute myeloid leukemia.
Cold Spring Harb Mol Case Stud
2022
35279027
Optimizing Translational Research for Exceptional Health and Life Span: A Systematic Narrative of Studies to Identify Translatable Therapeutic Target(s) for Exceptional Health Span in Humans.
J Gerontol A Biol Sci Med Sci
2022
31973781
Smaller total brain volume but not subcortical structure volume related to common genetic risk for ADHD.
Psychol Med
2021
33888254
NHLBI-CMREF Workshop Report on Pulmonary Vascular Disease Classification: JACC State-of-the-Art Review.
J Am Coll Cardiol
2021
34233449
Aurora A kinase as a target for therapy in <i>TCF3-HLF</i> rearranged acute lymphoblastic leukemia.
Haematologica
2021
31605387
Evaluating chronic emotional dysregulation and irritability in relation to ADHD and depression genetic risk in children with ADHD.
J Child Psychol Psychiatry
2020
32033925
Polygenic Risk Score-Derived Subcortical Connectivity Mediates Attention-Deficit/Hyperactivity Disorder Diagnosis.
Biol Psychiatry Cogn Neurosci Neuroimaging
2020
32066674
Large epigenome-wide association study of childhood ADHD identifies peripheral DNA methylation associated with disease and polygenic risk burden.
Transl Psychiatry
2020
33123685
Integrated analysis of patient samples identifies biomarkers for venetoclax efficacy and combination strategies in acute myeloid leukemia.
Nat Cancer
2020
30651561
Clinical resistance to crenolanib in acute myeloid leukemia due to diverse molecular mechanisms.
Nat Commun
2019
31667711
Polymorphisms in oxidative stress pathway genes and prostate cancer risk.
Cancer Causes Control
2019
31779979
What do functional genomics tell us about pathogenesis of AML?
Best Pract Res Clin Haematol
2019
31366621
Genomic landscape of neutrophilic leukemias of ambiguous diagnosis.
Blood
2019
29786871
Gender-Specific Effects of Selection for Drinking in the Dark on the Network Roles of Coding and Noncoding RNAs.
Alcohol Clin Exp Res
2018
30018082
Synthetic lethality of TNK2 inhibition in PTPN11-mutant leukemia.
Sci Signal
2018
29930110
Analysis of shared heritability in common disorders of the brain.
Science
2018
30333627
Functional genomic landscape of acute myeloid leukaemia.
Nature
2018
29496126
Working Memory and Vigilance as Multivariate Endophenotypes Related to Common Genetic Risk for Attention-Deficit/Hyperactivity Disorder.
J Am Acad Child Adolesc Psychiatry
2018
28630439
Recurrent cyclin D2 mutations in myeloid neoplasms.
Leukemia
2017
28439110
Characterization of the leukemogenic potential of distal cytoplasmic CSF3R truncation and missense mutations.
Leukemia
2017
28360221
<i>NFAT5</i> and <i>SLC4A10</i> Loci Associate with Plasma Osmolality.
J Am Soc Nephrol
2017
28332277
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet
2017
28652245
Unpaired Extracellular Cysteine Mutations of CSF3R Mediate Gain or Loss of Function.
Cancer Res
2017
27004716
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.
Am J Med Genet B Neuropsychiatr Genet
2016
26304033
Methylomic analysis of salivary DNA in childhood ADHD identifies altered DNA methylation in VIPR2.
J Child Psychol Psychiatry
2016
26677978
Identification and Characterization of Tyrosine Kinase Nonreceptor 2 Mutations in Leukemia through Integration of Kinase Inhibitor Screening and Genomic Analysis.
Cancer Res
2016
26708334
HitWalker2: visual analytics for precision medicine and beyond.
Bioinformatics
2016
25043339
Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects.
J Bone Miner Res
2015
26625308
Src and STAT3 inhibitors synergize to promote tumor inhibition in renal cell carcinoma.
Oncotarget
2015
26367794
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Nature
2015
26177520
Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus.
PLoS One
2015
26032424
Therapeutically Targetable ALK Mutations in Leukemia.
Cancer Res
2015
26059482
Gene set analysis: A step-by-step guide.
Am J Med Genet B Neuropsychiatr Genet
2015
25924931
plethy: management of whole body plethysmography data in R.
BMC Bioinformatics
2015
25652416
Splicing landscape of the eight collaborative cross founder strains.
BMC Genomics
2015
23929584
Genetic susceptibility to chronic otitis media with effusion: candidate gene single nucleotide polymorphisms.
Laryngoscope
2014
25459302
â¿¿Pitfalls in the application of gene set analysis to genetics studiesâ¿¿: a response.
Trends Genet
2014
25154796
Functional and genomic context in pathway analysis of GWAS data.
Trends Genet
2014
25172470
Analysis considerations for utilizing RNA-Seq to characterize the brain transcriptome.
Int Rev Neurobiol
2014
24374554
The genetics of gene expression in complex mouse crosses as a tool to study the molecular underpinnings of behavior traits.
Mamm Genome
2014
23096700
Copy number variation analysis in 98 individuals with PHACE syndrome.
J Invest Dermatol
2013
28824928
PHENOTYPIC VARIABILITY IN INDIVIDUALS WITH TYPE V OSTEOGENESIS IMPERFECTA WITH IDENTICAL IFITM5 MUTATIONS.
J Rare Disord
2013
24286512
Comparison of methods to identify aberrant expression patterns in individual patients: augmenting our toolkit for precision medicine.
Genome Med
2013
23656643
Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML.
N Engl J Med
2013
23704919
Androgen receptor promotes ligand-independent prostate cancer progression through c-Myc upregulation.
PLoS One
2013
1 - 50 of 64
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Oregon Health & Science University, University of California Berkeley
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Jeffrey W Tyner
Oregon Health & Science University School of Medicine
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Brian J Druker
Oregon Health & Science University
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Michael A Mooney
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Christopher A Eide
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Joel T Nigg
Oregon Health & Science University
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Marc M Loriaux
Knight Cancer Institute, Oregon Health & Science University
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Cristina E Tognon
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Robert Hitzemann
Portland Alcohol Research Center, Oregon Health and Science University
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Peter Ryabinin
Knight Cancer Institute Oregon Health & Science University Portland Oregon USA.
Co-authored papers
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Julia E Maxson
Knight Cancer Institute, Oregon Health & Science University
Co-authored papers
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Bill H Chang
Oregon Health and Science University
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Robert P Searles
Oregon Health & Science University
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7
Haijiao Zhang
Oregon Health & Science University, Knight Cancer Institute
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Michael W Deininger
University of Utah Huntsman Cancer Institute
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Samuel B Luty
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Stephen V Faraone
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