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Author Details
Full Name
Michael F Walsh
Affiliation
Memorial Sloan Kettering Cancer Center
ORCID
Career Start Year
2004
Papers
83
H Index
31
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35944238
Regulation of Laboratory-Developed Tests in Preventive Oncology: Emerging Needs and Opportunities.
J Clin Oncol
2023
37845474
Neoplasia risk in patients with Lynch syndrome treated with immune checkpoint blockade.
Nat Med
2023
37738546
Germline Pathogenic Variants and Genetic Counseling by Ancestry in Patients With Epithelial Ovarian Cancer.
JCO Precis Oncol
2023
37262391
Prevalence and Clinical Implications of Mismatch Repair-Proficient Colorectal Cancer in Patients With Lynch Syndrome.
JCO Precis Oncol
2023
36744932
Comprehensive analysis of germline drivers in endometrial cancer.
J Natl Cancer Inst
2023
36735656
Mutant-RB1 circulating tumor DNA in the blood of unilateral retinoblastoma patients: What happens during enucleation surgery: A pilot study.
PLoS One
2023
36593350
Expanded genetic testing of GIST patients identifies high proportion of non-syndromic patients with germline alterations.
NPJ Precis Oncol
2023
36346689
NBN Pathogenic Germline Variants are Associated with Pan-Cancer Susceptibility and In Vitro DNA Damage Response Defects.
Clin Cancer Res
2023
36115772
Gene-based Confirmatory Germline Testing Following Tumor-only Sequencing of Prostate Cancer.
Eur Urol
2023
34810208
Multiple Primary Cancers in Patients Undergoing Tumor-Normal Sequencing Define Novel Associations.
Cancer Epidemiol Biomarkers Prev
2022
35585047
Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers.
Nat Commun
2022
35477182
Germline Pathogenic Variants Impact Clinicopathology of Advanced Lung Cancer.
Cancer Epidemiol Biomarkers Prev
2022
35442743
Toward more streamlined testing in pediatric oncology.
Sci Adv
2022
35675575
Concurrent Germline <i>BRCA1</i>/<i>2</i> and Mismatch Repair Mutations in Young-Onset Pancreatic and Colorectal Cancer: The Importance of Comprehensive Germline and Somatic Characterization to Inform Therapeutic Options.
JCO Precis Oncol
2022
35346574
Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndrome.
Genet Med
2022
35833951
Inherited Germline Cancer Susceptibility Gene Variants in Individuals with Non-Muscle-Invasive Bladder Cancer.
Clin Cancer Res
2022
35971132
Diagnostic yield and clinical relevance of expanded genetic testing for cancer patients.
Genome Med
2022
36041233
Disparities in cancer genetics care by race/ethnicity among pan-cancer patients with pathogenic germline variants.
Cancer
2022
35904492
Impaired Proteolysis of Noncanonical RAS Proteins Drives Clonal Hematopoietic Transformation.
Cancer Discov
2022
36265117
Germline <i>SMARCA4</i> Deletion as a Driver of Uterine Cancer: An Atypical Presentation.
JCO Precis Oncol
2022
35074424
Comprehensive assessment of germline pathogenic variant detection in tumor-only sequencing.
Ann Oncol
2022
34949653
Cancer-Causative Mutations Occurring in Early Embryogenesis.
Cancer Discov
2022
34863587
Inherited TP53 Variants and Risk of Prostate Cancer.
Eur Urol
2022
34675114
Clinical and Functional Significance of TP53 Exon 4-Intron 4 Splice Junction Variants.
Mol Cancer Res
2022
33466343
Molecular Changes in Retinoblastoma beyond <i>RB1</i>: Findings from Next-Generation Sequencing.
Cancers (Basel)
2021
36247821
<i>RB1</i> Circulating Tumor DNA in the Blood of Patients with Unilateral Retinoblastoma: Before and after Intra-arterial Chemotherapy.
Ophthalmol Sci
2021
33579957
The acquisition of molecular drivers in pediatric therapy-related myeloid neoplasms.
Nat Commun
2021
34654685
Germline Variants Identified in Patients with Early-onset Renal Cell Carcinoma Referred for Germline Genetic Testing.
Eur Urol Oncol
2021
34741162
The context-specific role of germline pathogenicity in tumorigenesis.
Nat Genet
2021
34133209
Therapeutic Implications of Germline Testing in Patients With Advanced Cancers.
J Clin Oncol
2021
34250384
Prevalence and Characterization of Biallelic and Monoallelic <i>NTHL1</i> and <i>MSH3</i> Variant Carriers From a Pan-Cancer Patient Population.
JCO Precis Oncol
2021
34240179
Paired Tumor-Normal Sequencing Provides Insights Into the TP53-Related Cancer Spectrum in Patients With Li-Fraumeni Syndrome.
J Natl Cancer Inst
2021
34308366
Prospective pan-cancer germline testing using MSK-IMPACT informs clinical translation in 751 patients with pediatric solid tumors.
Nat Cancer
2021
31444830
Fumarate hydratase FH c.1431_1433dupAAA (p.Lys477dup) variant is not associated with cancer including renal cell carcinoma.
Hum Mutat
2020
31922925
Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based Screening.
J Clin Oncol
2020
31794323
Cancer Susceptibility Mutations in Patients With Urothelial Malignancies.
J Clin Oncol
2020
32676930
Utilization of clinical genetic counseling among childhood and young adult cancer survivors in a registry trial.
J Community Genet
2020
32422154
Recommendations for Long-Term Follow-up of Adults with Heritable Retinoblastoma.
Ophthalmology
2020
32386119
Whole-body magnetic resonance imaging as surveillance for subsequent malignancies in preadolescent, adolescent, and young adult survivors of germline retinoblastoma: An update.
Pediatr Blood Cancer
2020
32320050
11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood.
Cancer
2020
32532877
Reticular dysgenesis caused by an intronic pathogenic variant in <i>AK2</i>.
Cold Spring Harb Mol Case Stud
2020
30376427
Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-Cancer.
J Clin Oncol
2019
31645348
Histone H3K36I mutation in a metastatic histiocytic tumor of the skull and response to sarcoma chemotherapy.
Cold Spring Harb Mol Case Stud
2019
31768065
Activating mutations in CSF1R and additional receptor tyrosine kinases in histiocytic neoplasms.
Nat Med
2019
31648317
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.
Blood Adv
2019
32775946
Understanding inherited risk in unselected newly diagnosed patients with endometrial cancer.
JCO Precis Oncol
2019
32923861
Pathogenic Loss-of-Function Germline <i>TERT</i> Mutations in Patients With Solid Tumors.
JCO Precis Oncol
2019
30255452
A synonymous germline variant PALB2 c.18G>T (p.Gly6=) disrupts normal splicing in a family with pancreatic and breast cancers.
Breast Cancer Res Treat
2019
30894706
Correction: Toward automation of germline variant curation in clinical cancer genetics.
Genet Med
2019
30787465
Toward automation of germline variant curation in clinical cancer genetics.
Genet Med
2019
1 - 50 of 83
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row(s) 1 - 30 of 30
Collaborators
Michael F Berger
Co-authored papers
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The Fifth Affiliated Hospital, Sun Yat-sen University
Co-authored papers
23
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Co-authored papers
19
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Co-authored papers
12
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Kim E Nichols
St. Jude Children's Research Hospital
Co-authored papers
8
Katherine L Nathanson
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Co-authored papers
6
Barry S Taylor
Memorial Sloan Kettering Cancer Center
Co-authored papers
6
Wassim Abida
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Co-authored papers
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Jorge S Reis-Filho
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Co-authored papers
5
Nikolaus Schultz
Memorial Sloan Kettering Cancer Center
Co-authored papers
5
Britta Weigelt
Memorial Sloan Kettering Cancer Center
Co-authored papers
5
Jinghui Zhang
Changhai Hospital, Second Military Medical University
Co-authored papers
5
Michael J Morris
Memorial Sloan Kettering Cancer Center
Co-authored papers
4
Howard I Scher
Memorial Sloan Kettering Cancer Center
Co-authored papers
4
Fergus J Couch
Mayo Clinic
Co-authored papers
4
Pier Selenica
Memorial Sloan Kettering Cancer Center
Co-authored papers
4
Chimene Kesserwan
National Institutes of Health
Co-authored papers
3
John Easton
St Jude Children's Research Hospital
Co-authored papers
3
Abraham Ari Hakimi
Co-authored papers
3
Michael N Edmonson
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