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Author Details
Full Name
J Lynn Fink
Affiliation
The University of Queensland Diamantina Institute, The University of Queensland
ORCID
Career Start Year
1997
Papers
57
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36727564
Genome-wide exploration reveals distinctive northern and southern variants of Clonorchis sinensis in the Far East.
Mol Ecol Resour
2023
36773702
Minimizing Sample Failure Rates for Challenging Clinical Tumor Samples.
J Mol Diagn
2023
36331241
Exquisitely Platinum-Sensitive Triple-Negative Breast Cancer, Time for <i>BRCA</i> Methylation Testing?
JCO Precis Oncol
2022
33202420
EBV-associated primary CNS lymphoma occurring after immunosuppression is a distinct immunobiological entity.
Blood
2021
33865912
Subtype-Specific Analyses Reveal Infiltrative Basal Cell Carcinomas Are Highly Interactive with their Environment.
J Invest Dermatol
2021
32813714
Marked mitochondrial genetic variation in individuals and populations of the carcinogenic liver fluke Clonorchis sinensis.
PLoS Negl Trop Dis
2020
33575589
Comparative performance of the BGI and Illumina sequencing technology for single-cell RNA-sequencing.
NAR Genom Bioinform
2020
32076493
Erratum: <i>PTEN</i> deletion drives acute myeloid leukemia resistance to MEK inhibitors.
Oncotarget
2020
31974379
Chromosome arm aneuploidies shape tumour evolution and drug response.
Nat Commun
2020
31461379
Progression of Disease Within 24 Months in Follicular Lymphoma Is Associated With Reduced Intratumoral Immune Infiltration.
J Clin Oncol
2019
30046162
Subclonal evolution in disease progression from MGUS/SMM to multiple myeloma is characterised by clonal stability.
Leukemia
2019
29316705
Translocation Breakpoints Preferentially Occur in Euchromatin and Acrocentric Chromosomes.
Cancers (Basel)
2018
30239706
Single-cell RNA-seq reveals dynamic transcriptome profiling in human early neural differentiation.
Gigascience
2018
30564295
Using genomics to better define high-risk MGUS/SMM patients.
Oncotarget
2018
29783973
Erythrocyte microRNA sequencing reveals differential expression in relapsing-remitting multiple sclerosis.
BMC Med Genomics
2018
29133595
Targeted Next-Generation Sequencing for Detecting <i>MLL</i> Gene Fusions in Leukemia.
Mol Cancer Res
2018
27856273
Hypermutation In Pancreatic Cancer.
Gastroenterology
2017
28199314
Whole-genome landscape of pancreatic neuroendocrine tumours.
Nature
2017
28466550
Cutting edge genomics reveal new insights into tumour development, disease progression and therapeutic impacts in multiple myeloma.
Br J Haematol
2017
28953865
Corrigendum: Whole-genome landscape of pancreatic neuroendocrine tumours.
Nature
2017
26909576
Genomic analyses identify molecular subtypes of pancreatic cancer.
Nature
2016
25719666
Whole genomes redefine the mutational landscape of pancreatic cancer.
Nature
2015
26503049
Corrigendum: Whole-genome characterization of chemoresistant ovarian cancer.
Nature
2015
26172396
Integrated genomic and transcriptomic analysis of human brain metastases identifies alterations of potential clinical significance.
J Pathol
2015
26017449
Whole-genome characterization of chemoresistant ovarian cancer.
Nature
2015
24500968
Genome-wide DNA methylation patterns in pancreatic ductal adenocarcinoma reveal epigenetic deregulation of SLIT-ROBO, ITGA2 and MET signaling.
Int J Cancer
2014
25351503
Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis.
Nat Commun
2014
25005691
A workflow to increase verification rate of chromosomal structural rearrangements using high-throughput next-generation sequencing.
Biotechniques
2014
23900255
Computational approaches to identify functional genetic variants in cancer genomes.
Nat Methods
2013
24250782
Somatic point mutation calling in low cellularity tumors.
PLoS One
2013
23103869
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes.
Nature
2012
23049875
qpure: A tool to estimate tumor cellularity from genome-wide single-nucleotide polymorphism profiles.
PLoS One
2012
20429930
Integration of open access literature into the RCSB Protein Data Bank using BioLit.
BMC Bioinformatics
2010
20181245
Word add-in for ontology recognition: semantic enrichment of scientific literature.
BMC Bioinformatics
2010
19377474
The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line.
Nat Genet
2009
17986452
LOCATE: a mammalian protein subcellular localization database.
Nucleic Acids Res
2008
19112480
I am not a scientist, I am a number.
PLoS Comput Biol
2008
18515836
BioLit: integrating biological literature with databases.
Nucleic Acids Res
2008
18636105
Computational biology resources lack persistence and usability.
PLoS Comput Biol
2008
18211718
Towards defining the nuclear proteome.
Genome Biol
2008
18229722
Intrinsic evaluation of text mining tools may not predict performance on realistic tasks.
Pac Symp Biocomput
2008
18369428
Open access: taking full advantage of the content.
PLoS Comput Biol
2008
17688439
DomainDraw: a macromolecular feature drawing program.
In Silico Biol
2007
16381849
LOCATE: a mouse protein subcellular localization database.
Nucleic Acids Res
2006
17254308
Evaluation and comparison of mammalian subcellular localization prediction methods.
BMC Bioinformatics
2006
16504016
PhosphoregDB: the tissue and sub-cellular distribution of mammalian protein kinases and phosphatases.
BMC Bioinformatics
2006
16683029
Differential use of signal peptides and membrane domains is a common occurrence in the protein output of transcriptional units.
PLoS Genet
2006
16643283
Subcellular localization of mammalian type II membrane proteins.
Traffic
2006
15735688
IL-2- and STAT5-regulated cytokine gene expression in cells expressing the Tax protein of HTLV-1.
Oncogene
2005
12520018
The PlantsP and PlantsT Functional Genomics Databases.
Nucleic Acids Res
2003
1 - 50 of 57
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