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Author Details
Full Name
Bartlomiej Przychodzen
Affiliation
Vanda Pharmaceuticals Inc.
ORCID
Career Start Year
2010
Papers
86
H Index
36
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34756793
Corrigendum to "Assessing the potential correlation of polymorphisms in the IL6R with relative IL6 elevation in severely ill COVID-19 patients" [Cytokine 148 (2021) 155662].
Cytokine
2022
35598394
Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection.
Virology
2022
36327219
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
PLoS Genet
2022
35121493
Elevated plasma levels of CXCL16 in severe COVID-19 patients.
Cytokine
2022
33330999
Neurokinin-1 receptor antagonist tradipitant has mixed effects on itch in atopic dermatitis: results from EPIONE, a randomized clinical trial.
J Eur Acad Dermatol Venereol
2021
34551289
PBRM1 loss in kidney cancer unbalances the proximal tubule master transcription factor hub to repress proximal tubule differentiation.
Cell Rep
2021
34353696
Assessing the potential correlation of polymorphisms in the IL6R with relative IL6 elevation in severely ill COVID-19 patients'.
Cytokine
2021
33421484
Genomic and phenotypic characterization of Investigator Global Assessment (IGA) scale-based endotypes in atopic dermatitis.
J Am Acad Dermatol
2021
31413096
Genomics of therapy-related myeloid neoplasms.
Haematologica
2020
32004386
Distinctive and common features of moderate aplastic anaemia.
Br J Haematol
2020
31911633
Rare germline variant contributions to myeloid malignancy susceptibility.
Leukemia
2020
32361028
Amantadine disrupts lysosomal gene expression: A hypothesis for COVID19 treatment.
Int J Antimicrob Agents
2020
30618304
<i>BCOR</i> and <i>BCORL1</i> mutations in myelodysplastic syndromes (MDS): clonal architecture and impact on outcomes.
Leuk Lymphoma
2019
31869410
Therapy-related acute lymphoblastic leukemia is a distinct entity with adverse genetic features and clinical outcomes.
Blood Adv
2019
31772163
Invariant patterns of clonal succession determine specific clinical features of myelodysplastic syndromes.
Nat Commun
2019
31358855
The novel autophagy inhibitor ROC-325 augments the antileukemic activity of azacitidine.
Leukemia
2019
31320321
Distinct clinical and biological implications of <i>CUX1</i> in myeloid neoplasms.
Blood Adv
2019
31288594
Misidentification of <i>MLL3</i> and other mutations in cancer due to highly homologous genomic regions.
Leuk Lymphoma
2019
31018124
Development of a Cx46 Targeting Strategy for Cancer Stem Cells.
Cell Rep
2019
30898763
Subclonal STAT3 mutations solidify clonal dominance.
Blood Adv
2019
31070582
Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesis.
Elife
2019
30709865
Invariant phenotype and molecular association of biallelic <i>TET2</i> mutant myeloid neoplasia.
Blood Adv
2019
30655603
Mutation clonal burden and allogeneic hematopoietic cell transplantation outcomes in acute myeloid leukemia and myelodysplastic syndromes.
Bone Marrow Transplant
2019
29339439
<i>IDH1/2</i> Mutations Sensitize Acute Myeloid Leukemia to PARP Inhibition and This Is Reversed by IDH1/2-Mutant Inhibitors.
Clin Cancer Res
2018
30015632
Leukemogenic nucleophosmin mutation disrupts the transcription factor hub that regulates granulomonocytic fates.
J Clin Invest
2018
30322869
Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes.
Blood
2018
29749402
Clonal PIGA mosaicism and dynamics in paroxysmal nocturnal hemoglobinuria.
Leukemia
2018
29795413
Consequences of mutant TET2 on clonality and subclonal hierarchy.
Leukemia
2018
29797327
Transcriptomic rationale for synthetic lethality-targeting ERCC1 and CDKN1A in chronic myelomonocytic leukaemia.
Br J Haematol
2018
28935992
Distinct clinical and biological implications of various DNMT3A mutations in myeloid neoplasms.
Leukemia
2018
29099495
A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia.
Leukemia
2018
29321554
Mutations in DNMT3A, U2AF1, and EZH2 identify intermediate-risk acute myeloid leukemia patients with poor outcome after CR1.
Blood Cancer J
2018
29217782
Rational management approach to pure red cell aplasia.
Haematologica
2018
27992414
Dynamics of clonal evolution in myelodysplastic syndromes.
Nat Genet
2017
28111468
Deletion of Ptpn1 induces myeloproliferative neoplasm.
Leukemia
2017
28255022
Molecular features of early onset adult myelodysplastic syndrome.
Haematologica
2017
28223278
Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation.
Blood
2017
28318095
Clinicopathologic and molecular characterization of myeloid neoplasms with isolated t(6;9)(p23;q34).
Int J Lab Hematol
2017
29416752
Fanconi Anemia germline variants as susceptibility factors in aplastic anemia, MDS and AML.
Oncotarget
2017
28650479
AML1-ETO requires enhanced C/D box snoRNA/RNP formation to induce self-renewal and leukaemia.
Nat Cell Biol
2017
28555081
Genomic determinants of chronic myelomonocytic leukemia.
Leukemia
2017
28893734
Origins of myelodysplastic syndromes after aplastic anemia.
Blood
2017
28819282
Adding molecular data to prognostic models can improve predictive power in treated patients with myelodysplastic syndromes.
Leukemia
2017
28862700
Differences in genomic patterns and clinical outcomes between African-American and White patients with myelodysplastic syndromes.
Blood Cancer J
2017
28758902
GATA4 loss of function in liver cancer impedes precursor to hepatocyte transition.
J Clin Invest
2017
28031539
Recurrent genetic defects on chromosome 5q in myeloid neoplasms.
Oncotarget
2017
27773925
Complete mutational spectrum of the autophagy interactome: a novel class of tumor suppressor genes in myeloid neoplasms.
Leukemia
2017
26205084
Runx1 repression by histone deacetylation is critical for Setbp1-induced mouse myeloid leukemia development.
Leukemia
2016
26574844
Angioimmunoblastic T-cell Lymphomas With the RHOA p.Gly17Val Mutation Have Classic Clinical and Pathologic Features.
Am J Surg Pathol
2016
27983727
The complexity of interpreting genomic data in patients with acute myeloid leukemia.
Blood Cancer J
2016
1 - 50 of 86
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