Dina Manaa

Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer

V. Jobanputra, Anne-Katrin Emde, K. Wrzeszczynski, 2018, The Journal of molecular diagnostics : JMD.

Localisation of Fault Using Travelling Wave Theory Based on Multi-End System

Dina Manaa, Dr. M. A. Baseer, P. Dr.PraveenR., 2017 .

Whole genome error-corrected sequencing for sensitive circulating tumor DNA cancer monitoring

A. Cheng, M. Zody, Dennie T. Frederick, 2022, bioRxiv.

Cardiac Iron Overload: Correlation between MRI T2* & Two Dimensional Strain Echocardiography in Children with b-Thalassemia Major

Dina Manaa, M. El-Shanshory, Osama Abd Rab El-Rassol, 2018 .

Most genetic risk for autism resides with common variation

Kathryn Roeder, Ann B. Lee, Stephan Ripke, 2014, Nature Genetics.

Identification of targetable BRAF ΔN486_P490 variant by whole-genome sequencing leading to dabrafenib-induced remission of a BRAF-mutant pancreatic adenocarcinoma

Vanessa V. Michelini, V. Jobanputra, R. Darnell, 2019, Cold Spring Harbor molecular case studies.

Machine learning guided signal enrichment for ultrasensitive plasma tumor burden monitoring

A. Cheng, M. Berger, C. Andersen, 2022, bioRxiv.

Ultrasensitive plasma-based monitoring of tumor burden using machine learning-guided signal enrichment

Dennie T. Frederick, M. Imieliński, A. Mungall, 2024, Nature medicine.