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Structural Heart : the Journal of the Heart Team|January 15, 2026
Impact of Measured and Predicted Patient-Prosthesis Mismatch on Quality of Life Following Transcatheter Aortic Valve ImplantationKarim Al-Azizi, Mohamad Bader Abo Hajar, Taylor Pickering, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|February 9, 2026
Five-Year Outcomes of Measured and Predicted Prosthesis-Patient Mismatch Following Valve-in-Valve Transcatheter Aortic Valve ImplantationKarim Al-Azizi, Ghadi Moubarak, Hajar Mohamad Bader Abo, et al.
Nature Chemical Biology|May 11, 2021
Sulfopin is a covalent inhibitor of Pin1 that blocks Myc-driven tumors in vivoChristian Dubiella, Benika J Pinch, Kazuhiro Koikawa, et al.
HGG Advances|February 20, 2026
Scaling Genomic Reanalysis to Unlock Diagnoses and Transform Rare Disease CareShira Rockowitz, Wanqing Shao, Courtney French, et al.
Annals of Neurology|May 10, 2014
Copy number variation plays an important role in clinical epilepsyHeather Olson, Yiping Shen, Jennifer Avallone, et al.
NPJ Genomic Medicine|August 23, 2018
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discoveryAlireza Haghighi, Joel B Krier, Agnes Toth-Petroczy, et al.
The Lancet. Oncology|July 24, 2009
TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studiesStefanie J Klug, Meike Ressing, Jochem Koenig, et al.
American Journal of Human Genetics|March 2, 2005
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutationsJennifer J Johnston, Isabelle Olivos-Glander, Christina Killoran, et al.
Human Genetics|March 12, 2017
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPUChristel Depienne, Caroline Nava, Boris Keren, et al.
European Journal of Human Genetics : EJHG|June 3, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndromeTheodore G Drivas, Dong Li, Divya Nair, et al.
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