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Genomic medicine

Genetic yield of next-generation sequencing for detecting monogenic familial hypercholesterolemia in uzbek patients with coronary artery disease

Rano B. Alieva, Aleksandr B. Shek, [ ... ], Dilnora B. Yusupalieva

A clinical pilot study for personalized risk-based breast cancer screening utilizing a polygenic risk score

Tone Hovda, Siim Sober, [ ... ], Kristine Kleivi Sahlberg

Awareness, attitudes, and barriers toward Transthyretin Amyloid Cardiomyopathy in Latin America: A questionnaire-based cross-sectional study

Cecilia Camacho-Hubner, Marcia Waddington-Cruz, [ ... ], Guilherme Silva Julian

Benchmark of biomarker identification and prognostic modeling methods on diverse censored data

Wesley Fletcher, Samiran Sinha

A fusion-deletion genomic-event underlies poor prognosis in young patients with luminal breast cancer

Le-Wei Zheng, Yi-Ming Liu, Ke-Da Yu, Cui-Cui Liu

Cost-effectiveness of pre-emptive pharmacogenetic testing: An umbrella review

Taichi Ochi, Manon G. den Uil, [ ... ], Talitha L. Feenstra

Parental acceptability of newborn screening expansion in the genomic era: A nationwide French survey informed by the Theoretical Framework of Acceptability (SeDeN-p3)

Camille Level, Laurence Faivre, [ ... ], Christine Peyron

Cardiologists’ perspectives on pharmacogenomics implementation in a hybrid health system: A qualitative study from the United Arab Emirates

Maram O. Abbas, Azhar T. Rahma, [ ... ], Fatma Al-Maskari

Tumor hypoxia is associated with global copy-number alteration burden and subtype-dependent overall survival in breast cancer: Evidence from TCGA and METABRIC

Wenhan Yang

Pharmacogenomics knowledge and implementation readiness among community pharmacists in Jordan: A national cross-sectional study

Khalid Awad Al-Kubaisi, Derar H. Abdel-Qader, [ ... ], Ahmed Alhusban

Factors that influence care for second and third trimester termination of pregnancy for medical reasons in Canada: A qualitative investigation

Madeleine Ennis, Elise Lavoie-Lebel, [ ... ], Jessica Liauw

The impact of uncertainty on disclosure of prenatal exome sequencing results: A vignette study among medical students

Jasmijn E. Klapwijk, Vyne Van der Schoot, [ ... ], Sam R. Riedijk

WGS identifies Lynch syndrome (LS) patients and uncovers a large family with MSH2-related LS in Southern Thailand

Worrawit Wanitsuwan, Kanet Kanjanapradit, [ ... ], Sukanya Horpaopan

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