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Author Details
Full Name
Jimmy C Lin
Affiliation
National Human Genome Research Institute, US National Institutes of Health
ORCID
Career Start Year
2008
Papers
33
H Index
22
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
30905807
Exome Sequencing of ABCB5 Identifies Recurrent Melanoma Mutations that Result in Increased Proliferative and Invasive Capacities.
J Invest Dermatol
2019
30905807
Exome Sequencing of ABCB5 Identifies Recurrent Melanoma Mutations that Result in Increased Proliferative and Invasive Capacities.
J Invest Dermatol
2019
30850615
Author Correction: RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells.
Sci Rep
2019
30850615
Author Correction: RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells.
Sci Rep
2019
29330521
RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells.
Sci Rep
2018
29330521
RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells.
Sci Rep
2018
26994145
MultiDimensional ClinOmics for Precision Therapy of Children and Adolescent Young Adults with Relapsed and Refractory Cancer: A Report from the Center for Cancer Research.
Clin Cancer Res
2016
26994145
MultiDimensional ClinOmics for Precision Therapy of Children and Adolescent Young Adults with Relapsed and Refractory Cancer: A Report from the Center for Cancer Research.
Clin Cancer Res
2016
26502337
Recurrent inactivating RASA2 mutations in melanoma.
Nat Genet
2015
26502337
Recurrent inactivating RASA2 mutations in melanoma.
Nat Genet
2015
24008424
Somatic mutations in MAP3K5 attenuate its proapoptotic function in melanoma through increased binding to thioredoxin.
J Invest Dermatol
2014
24008424
Somatic mutations in MAP3K5 attenuate its proapoptotic function in melanoma through increased binding to thioredoxin.
J Invest Dermatol
2014
25113440
Mutational and functional analysis of the tumor-suppressor PTPRD in human melanoma.
Hum Mutat
2014
25113440
Mutational and functional analysis of the tumor-suppressor PTPRD in human melanoma.
Hum Mutat
2014
23365548
Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing.
ScientificWorldJournal
2013
23901115
Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma.
Proc Natl Acad Sci U S A
2013
23644516
Mining exomic sequencing data to identify mutated antigens recognized by adoptively transferred tumor-reactive T cells.
Nat Med
2013
23590858
Overcoming the obstacles to returning genomic research results.
Genet Res (Camb)
2013
23631825
Translational utility of next-generation sequencing.
Genomics
2013
23365548
Computational and bioinformatics frameworks for next-generation whole exome and genome sequencing.
ScientificWorldJournal
2013
23901115
Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma.
Proc Natl Acad Sci U S A
2013
23631825
Translational utility of next-generation sequencing.
Genomics
2013
23644516
Mining exomic sequencing data to identify mutated antigens recognized by adoptively transferred tumor-reactive T cells.
Nat Med
2013
23590858
Overcoming the obstacles to returning genomic research results.
Genet Res (Camb)
2013
22260482
Delving into somatic variation in sporadic melanoma.
Pigment Cell Melanoma Res
2012
29776237
Personalizing rare disease research: how genomics is revolutionizing the diagnosis and treatment of rare disease.
Per Med
2012
23006843
Comparative exome sequencing of metastatic lesions provides insights into the mutational progression of melanoma.
BMC Genomics
2012
22260482
Delving into somatic variation in sporadic melanoma.
Pigment Cell Melanoma Res
2012
29776237
Personalizing rare disease research: how genomics is revolutionizing the diagnosis and treatment of rare disease.
Per Med
2012
23006843
Comparative exome sequencing of metastatic lesions provides insights into the mutational progression of melanoma.
BMC Genomics
2012
21163964
The genetic landscape of the childhood cancer medulloblastoma.
Science
2011
21163964
The genetic landscape of the childhood cancer medulloblastoma.
Science
2011
21499247
Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
Nat Genet
2011
21618342
Analysis of the disintegrin-metalloproteinases family reveals ADAM29 and ADAM7 are often mutated in melanoma.
Hum Mutat
2011
21946352
Exon capture analysis of G protein-coupled receptors identifies activating mutations in GRM3 in melanoma.
Nat Genet
2011
21946352
Exon capture analysis of G protein-coupled receptors identifies activating mutations in GRM3 in melanoma.
Nat Genet
2011
21618342
Analysis of the disintegrin-metalloproteinases family reveals ADAM29 and ADAM7 are often mutated in melanoma.
Hum Mutat
2011
21499247
Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
Nat Genet
2011
20424519
Novel somatic mutations in heterotrimeric G proteins in melanoma.
Cancer Biol Ther
2010
21047771
Mutational and functional analysis reveals ADAMTS18 metalloproteinase as a novel driver in melanoma.
Mol Cancer Res
2010
20516699
Protein microarrays for cancer diagnostics and therapy.
Med Princ Pract
2010
20424519
Novel somatic mutations in heterotrimeric G proteins in melanoma.
Cancer Biol Ther
2010
21047771
Mutational and functional analysis reveals ADAMTS18 metalloproteinase as a novel driver in melanoma.
Mol Cancer Res
2010
20516699
Protein microarrays for cancer diagnostics and therapy.
Med Princ Pract
2010
19264984
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene.
Science
2009
19264984
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene.
Science
2009
19584151
SMAD4 gene mutations are associated with poor prognosis in pancreatic cancer.
Clin Cancer Res
2009
19351817
Genetic mutations associated with cigarette smoking in pancreatic cancer.
Cancer Res
2009
19718025
Analysis of the tyrosine kinome in melanoma reveals recurrent mutations in ERBB4.
Nat Genet
2009
19426505
Identification of microbial DNA in human cancer.
BMC Med Genomics
2009
1 - 50 of 66
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