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Author Details
Full Name
Raju Kucherlapati
Affiliation
Harvard Medical School
ORCID
Career Start Year
1973
Papers
341
H Index
96
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36693150
Impact of Precision Medicine in Oncology.
Cancer J
2023
36693150
Impact of Precision Medicine in Oncology.
Cancer J
2023
35138907
A functional genomic approach to actionable gene fusions for precision oncology.
Sci Adv
2022
35138907
A functional genomic approach to actionable gene fusions for precision oncology.
Sci Adv
2022
31610796
Global impact of somatic structural variation on the DNA methylome of human cancers.
Genome Biol
2019
31772821
Optical imaging with a novel cathepsin-activatable probe for enhanced detection of colorectal cancer.
Am J Nucl Med Mol Imaging
2019
31610796
Global impact of somatic structural variation on the DNA methylome of human cancers.
Genome Biol
2019
31416464
An enhanced genetic model of colorectal cancer progression history.
Genome Biol
2019
31772821
Optical imaging with a novel cathepsin-activatable probe for enhanced detection of colorectal cancer.
Am J Nucl Med Mol Imaging
2019
31416464
An enhanced genetic model of colorectal cancer progression history.
Genome Biol
2019
29996110
A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases.
Cell Rep
2018
29996110
A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases.
Cell Rep
2018
27741356
MIIP haploinsufficiency induces chromosomal instability and promotes tumour progression in colorectal cancer.
J Pathol
2017
28512244
Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer.
Cancer Res
2017
28528867
A Pan-Cancer Proteogenomic Atlas of PI3K/AKT/mTOR Pathway Alterations.
Cancer Cell
2017
29069730
Inhibition of colorectal cancer genomic copy number alterations and chromosomal fragile site tumor suppressor FHIT and WWOX deletions by DNA mismatch repair.
Oncotarget
2017
27741356
MIIP haploinsufficiency induces chromosomal instability and promotes tumour progression in colorectal cancer.
J Pathol
2017
28179651
Oliver Smithies (1925-2017).
Nature
2017
28292439
Integrated Molecular Characterization of Uterine Carcinosarcoma.
Cancer Cell
2017
28292439
Integrated Molecular Characterization of Uterine Carcinosarcoma.
Cancer Cell
2017
28179651
Oliver Smithies (1925-2017).
Nature
2017
29069730
Inhibition of colorectal cancer genomic copy number alterations and chromosomal fragile site tumor suppressor FHIT and WWOX deletions by DNA mismatch repair.
Oncotarget
2017
28512244
Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer.
Cancer Res
2017
28528867
A Pan-Cancer Proteogenomic Atlas of PI3K/AKT/mTOR Pathway Alterations.
Cancer Cell
2017
26947078
Multilevel Genomics-Based Taxonomy of Renal Cell Carcinoma.
Cell Rep
2016
27153396
Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome Sequencing.
Am J Hum Genet
2016
26947078
Multilevel Genomics-Based Taxonomy of Renal Cell Carcinoma.
Cell Rep
2016
27153396
Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome Sequencing.
Am J Hum Genet
2016
26086041
Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry.
JAMA Oncol
2015
26086041
Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry.
JAMA Oncol
2015
26342024
MAPRE1 as a plasma biomarker for early-stage colorectal cancer and adenomas.
Cancer Prev Res (Phila)
2015
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
26342024
MAPRE1 as a plasma biomarker for early-stage colorectal cancer and adenomas.
Cancer Prev Res (Phila)
2015
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
24534818
Cardiovascular disease in Noonan syndrome.
Arch Dis Child
2014
25313082
Characterization of HPV and host genome interactions in primary head and neck cancers.
Proc Natl Acad Sci U S A
2014
25049390
Next-generation sequencing identifies rare variants associated with Noonan syndrome.
Proc Natl Acad Sci U S A
2014
24534818
Cardiovascular disease in Noonan syndrome.
Arch Dis Child
2014
25214561
Clinical significance of CTNNB1 mutation and Wnt pathway activation in endometrioid endometrial carcinoma.
J Natl Cancer Inst
2014
25155756
The somatic genomic landscape of chromophobe renal cell carcinoma.
Cancer Cell
2014
25057314
An EGFR targeted PET imaging probe for the detection of colonic adenocarcinomas in the setting of colitis.
Theranostics
2014
25214561
Clinical significance of CTNNB1 mutation and Wnt pathway activation in endometrioid endometrial carcinoma.
J Natl Cancer Inst
2014
25313082
Characterization of HPV and host genome interactions in primary head and neck cancers.
Proc Natl Acad Sci U S A
2014
25057314
An EGFR targeted PET imaging probe for the detection of colonic adenocarcinomas in the setting of colitis.
Theranostics
2014
25049390
Next-generation sequencing identifies rare variants associated with Noonan syndrome.
Proc Natl Acad Sci U S A
2014
25155756
The somatic genomic landscape of chromophobe renal cell carcinoma.
Cancer Cell
2014
23562608
Apc deficiency alters pulmonary epithelial cell fate and inhibits Nkx2.1 via triggering TGF-beta signaling.
Dev Biol
2013
24120142
The somatic genomic landscape of glioblastoma.
Cell
2013
24204966
The CHC22 clathrin-GLUT4 transport pathway contributes to skeletal muscle regeneration.
PLoS One
2013
23935891
Genotype directed therapy in murine mismatch repair deficient tumors.
PLoS One
2013
1 - 50 of 682
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Co-authored papers
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Broad Institute
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