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Author Details
Full Name
Kilannin Krysiak
Affiliation
Washington University School of Medicine
ORCID
Career Start Year
2007
Papers
44
H Index
19
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36373660
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.
Nucleic Acids Res
2023
37910143
Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.
Cancer Res Commun
2023
37493986
Mutations associated with progression in follicular lymphoma predict inferior outcomes at diagnosis: Alliance A151303.
Blood Adv
2023
36541006
Accessing clinical-grade genomic classification data through the ClinGen Data Platform.
Pac Symp Biocomput
2023
36571464
A comparative analysis of RAS variants in patients with disorders of somatic mosaicism.
Genet Med
2023
34780623
Phase 1/dose expansion trial of brentuximab vedotin and lenalidomide in relapsed or refractory diffuse large B-cell lymphoma.
Blood
2022
35475554
Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease.
Hum Mutat
2022
35568002
Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.
Cancer Genet
2022
35624339
A community approach to the cancer-variant-interpretation bottleneck.
Nat Cancer
2022
36063163
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
Genet Med
2022
35101336
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
Genet Med
2022
33288274
Corrigendum to "Haploinsufficiency of multiple del(5q) genes induce B cell abnormalities in mice" [Leuk. Res. 96C (2020) 106428].
Leuk Res
2021
34036230
Impact of a 40-Gene Targeted Panel Test on Physician Decision Making for Patients With Acute Myeloid Leukemia.
JCO Precis Oncol
2021
34164801
Heterozygous HMGB1 loss-of-function variants are associated with developmental delay and microcephaly.
Clin Genet
2021
32246132
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.
Nat Genet
2020
32739655
Haploinsufficiency of multiple del(5q) genes induce B cell abnormalities in mice.
Leuk Res
2020
30287923
Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples.
Genet Med
2019
31779674
Standard operating procedure for curation and clinical interpretation of variants in cancer.
Genome Med
2019
31796060
Text-mining clinically relevant cancer biomarkers for curation into the CIViC database.
Genome Med
2019
31390566
A Spontaneous Aggressive ERα+ Mammary Tumor Model Is Driven by Kras Activation.
Cell Rep
2019
31618044
Open-Sourced CIViC Annotation Pipeline to Identify and Annotate Clinically Relevant Variants Using Single-Molecule Molecular Inversion Probes.
JCO Clin Cancer Inform
2019
29074501
Single-agent ibrutinib in relapsed or refractory follicular lymphoma: a phase 2 consortium trial.
Blood
2018
30181556
The prognostic effects of somatic mutations in ER-positive breast cancer.
Nat Commun
2018
30224629
Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer.
Nat Commun
2018
30429476
Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer.
Nat Commun
2018
30311370
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.
Hum Mutat
2018
28064239
Recurrent somatic mutations affecting B-cell receptor signaling pathway genes in follicular lymphoma.
Blood
2017
28138153
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer.
Nat Genet
2017
28434888
Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS.
Bone
2017
28178280
Knockdown of HSPA9 induces TP53-dependent apoptosis in human hematopoietic progenitor cells.
PLoS One
2017
28874413
A Phase II Trial of Neoadjuvant MK-2206, an AKT Inhibitor, with Anastrozole in Clinical Stage II or III <i>PIK3CA</i>-Mutant ER-Positive and HER2-Negative Breast Cancer.
Clin Cancer Res
2017
27029710
A genomic case study of mixed fibrolamellar hepatocellular carcinoma.
Ann Oncol
2016
26531824
DGIdb 2.0: mining clinically relevant drug-gene interactions.
Nucleic Acids Res
2016
27681435
Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas.
Cell Rep
2016
27181063
Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia.
Exp Hematol
2016
27058228
A genomic analysis of Philadelphia chromosome-negative AML arising in patients with CML.
Blood Cancer J
2016
25550197
Reduced levels of Hspa9 attenuate Stat5 activation in mouse B cells.
Exp Hematol
2015
26645048
Optimizing cancer genome sequencing and analysis.
Cell Syst
2015
21123823
Knockdown of Hspa9, a del(5q31.2) gene, results in a decrease in hematopoietic progenitors in mice.
Blood
2011
22158538
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes.
Nat Genet
2011
20039246
Lipophilic pyridinium bisphosphonates: potent gammadelta T cell stimulators.
Angew Chem Int Ed Engl
2010
19309137
Lipophilic bisphosphonates as dual farnesyl/geranylgeranyl diphosphate synthase inhibitors: an X-ray and NMR investigation.
J Am Chem Soc
2009
18789701
Bisphosphonate inhibitors of ATP-mediated HIV-1 reverse transcriptase catalyzed excision of chain-terminating 3'-azido, 3'-deoxythymidine: a QSAR investigation.
Bioorg Med Chem
2008
17963374
Activity of sulfonium bisphosphonates on tumor cell lines.
J Med Chem
2007
1 - 44 of 44
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The Ohio State University
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