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Author Details
Full Name
Tamara L Lamprecht
Affiliation
St. Jude Children's Research Hospital
ORCID
Career Start Year
2010
Papers
24
H Index
19
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34778799
Integrative Genomic Analysis of Pediatric Myeloid-Related Acute Leukemias Identifies Novel Subtypes and Prognostic Indicators.
Blood Cancer Discov
2021
30046003
Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomes.
JCI Insight
2018
29891567
Clonal dynamics of donor-derived myelodysplastic syndrome after unrelated hematopoietic cell transplantation for high-risk pediatric B-lymphoblastic leukemia.
Cold Spring Harb Mol Case Stud
2018
28841212
Impact of Notch disruption on myeloid development.
Blood Cancer J
2017
28487541
Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome.
Leukemia
2017
28215704
CpG Island Hypermethylation Mediated by DNMT3A Is a Consequence of AML Progression.
Cell
2017
29146900
The genomic landscape of pediatric myelodysplastic syndromes.
Nat Commun
2017
27181063
Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia.
Exp Hematol
2016
26595813
PML-RARA requires DNA methyltransferase 3A to initiate acute promyelocytic leukemia.
J Clin Invest
2016
25600023
Epigenomic analysis of the HOX gene loci reveals mechanisms that may control canonical expression patterns in AML and normal hematopoietic cells.
Leukemia
2015
26305651
Association Between Mutation Clearance After Induction Therapy and Outcomes in Acute Myeloid Leukemia.
JAMA
2015
25487151
Role of TP53 mutations in the origin and evolution of therapy-related acute myeloid leukaemia.
Nature
2015
24656771
The R882H DNMT3A mutation associated with AML dominantly inhibits wild-type DNMT3A by blocking its ability to form active tetramers.
Cancer Cell
2014
24613412
Functional heterogeneity of genetically defined subclones in acute myeloid leukemia.
Cancer Cell
2014
23297133
Genomic impact of transient low-dose decitabine treatment on primary AML cells.
Blood
2013
23634996
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.
N Engl J Med
2013
23455394
Notch signaling in acute promyelocytic leukemia.
Leukemia
2013
22159024
Effect of circadian clock gene mutations on nonvisual photoreception in the mouse.
Invest Ophthalmol Vis Sci
2012
23056333
Expression and function of PML-RARA in the hematopoietic progenitor cells of Ctsg-PML-RARA mice.
PLoS One
2012
22817890
The origin and evolution of mutations in acute myeloid leukemia.
Cell
2012
22237025
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing.
Nature
2012
21436584
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression.
J Clin Invest
2011
21324882
Biome representational in silico karyotyping.
Genome Res
2011
21067377
DNMT3A mutations in acute myeloid leukemia.
N Engl J Med
2010
1 - 24 of 24
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10
Elaine R Mardis
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Washington University School of Medicine
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Washington University School of Medicine
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Sharon E Heath
Washington University School of Medicine.
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Timothy A Graubert
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John F DiPersio
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7
Peter Westervelt
Washington University School of Medicine
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David E Larson
McDonnell Genome Institute, Washington University School of Medicine
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Michelle O'Laughlin
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Lukas D Wartman
Washington University School of Medicine in St. Louis
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Li Ding
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