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Translational Oncology
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January 10, 2025
Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications
Romy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 16, 2024
Adenomas from individuals with pathogenic biallelic variants in the <i>MUTYH</i> and <i>NTHL1</i> genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications
Romy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Cancers
|
October 28, 2023
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
Romy Walker, Khalid Mahmood, Julia Como, et al.
Annual Review of Biomedical Data Science
|
April 25, 2024
Generating Clinical-Grade Gene-Disease Validity Classifications Through the ClinGen Data Platforms
Matt W Wright, Courtney L Thaxton, Tristan Nelson, et al.
Genome Medicine
|
January 18, 2022
ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines
Christine G Preston, Matt W Wright, Rao Madhavrao, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
Journal of Translational Medicine
|
April 26, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
Page
of 16
Search research articles
Search
Showing results (151-160 of 157) with videos related to
Sort By:
Page
of 16
You have reached the last page of results.
This site can display upto 157 results.
Translational Oncology
|
January 10, 2025
Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications
Romy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 16, 2024
Adenomas from individuals with pathogenic biallelic variants in the <i>MUTYH</i> and <i>NTHL1</i> genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications
Romy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Cancers
|
October 28, 2023
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
Romy Walker, Khalid Mahmood, Julia Como, et al.
Annual Review of Biomedical Data Science
|
April 25, 2024
Generating Clinical-Grade Gene-Disease Validity Classifications Through the ClinGen Data Platforms
Matt W Wright, Courtney L Thaxton, Tristan Nelson, et al.
Genome Medicine
|
January 18, 2022
ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines
Christine G Preston, Matt W Wright, Rao Madhavrao, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
Journal of Translational Medicine
|
April 26, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
Page
of 16