Suchergebnisse - "Mehta, Nikita"

PubPharm (11)

1

The clinical and genomic landscape of patients with DDX41 variants identified during diagnostic sequencing

enthalten in: Blood advances | 2023

von Maierhofer, A. | Mehta, N. | Chisholm, R. | +11

2

Prevalence and Clinical Implications of Mismatch Repair-Proficient Colorectal Cancer in Patients With Lynch Syndrome

enthalten in: JCO precision oncology | 2023

von Ranganathan, M. | Sacca, R. | Trottier, M. | +27

3

Disparities in cancer genetics care by race/ethnicity among pan-cancer patients with pathogenic germline variants

enthalten in: Cancer | 2022

von Liu, Y. | Maio, A. | Kemel, Y. | +24

4

Revision of RUNX1 variant curation rules

enthalten in: Blood advances | 2022

von Feurstein, S. | Luo, X. | Shah, M. | +4

5

Diagnostic yield and clinical relevance of expanded genetic testing for cancer patients

enthalten in: Genome medicine | 2022

von Ceyhan-Birsoy, O. | Jayakumaran, G. | Kemel, Y. | +22

6

Substance Use Treatment Engagement among Men Who Have Sex with Men Who Use Stimulants in the Northeastern United States

enthalten in: Substance use & misuse | 2022

von Viera, A. | Sosnowy, C. | van den Berg, J. | +4

7

Somatic intronic TP53 c.375+5G mutations are a recurrent but under-recognized mode of TP53 inactivation

enthalten in: The journal of pathology. Clinical research | 2022

von Chui, M. | Yang, C. | Mehta, N. | +5

8

Germline Variants Identified in Patients with Early-onset Renal Cell Carcinoma Referred for Germline Genetic Testing

enthalten in: European urology oncology | 2021

von Truong, H. | Sheikh, R. | Kotecha, R. | +24

CommentIn: J Urol. 2022 May;207(5):1151-1153. - PMID 35152713

9

Paired Tumor-Normal Sequencing Provides Insights Into the TP53-Related Cancer Spectrum in Patients With Li-Fraumeni Syndrome

enthalten in: Journal of the National Cancer Institute | 2021

von Ceyhan-Birsoy, O. | Selenica, P. | Chui, M. | +22

CommentIn: J Natl Cancer Inst. 2021 Nov 29;113(12):1615-1617. - PMID 34240211

10

ATP Synthase c-Subunit Leak Causes Aberrant Cellular Metabolism in Fragile X Syndrome

enthalten in: Cell | 2020

von Licznerski, P. | Park, H. | Rolyan, H. | +18

CommentIn: Mol Cell. 2020 Nov 5;80(3):381-383. - PMID 33157013