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Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 5, 2019
The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning systemKenneth D Mandl, Tracy Glauser, Ian D Krantz, et al.
The American Journal of Cardiology|August 25, 2018
Physical Activity-Related Drivers of Perceived Health Status in Adults With Congenital Heart DiseaseJong Mi Ko, Kamila S White, Adrienne H Kovacs, et al.
Congenital Heart Disease|February 5, 2019
Education as important predictor for successful employment in adults with congenital heart disease worldwideMaayke A Sluman, Silke Apers, Judith K Sluiter, et al.
JGH Open : an Open Access Journal of Gastroenterology and Hepatology|December 12, 2025
Australian Real-World Effectiveness and Safety of Ustekinumab for the Treatment of Crohn's Disease: Results of the AURORA Study, Including the ANZIBD ConsortiumYoon-Kyo An, Niamh Lindsay, Natalie Allan, et al.
Nature Cell Biology|September 9, 2025
Durotaxis is a driver and potential therapeutic target in lung fibrosis and metastatic pancreatic cancerTaslim A Al-Hilal, Maria-Anna Chrysovergi, Paula E Grasberger, et al.
Implementation Science Communications|May 11, 2023
Data envelopment analysis to evaluate the efficiency of tobacco treatment programs in the NCI Moonshot Cancer Center Cessation InitiativeKathryn Pluta, Sarah D Hohl, Heather D'Angelo, et al.
Physical Review Letters|March 23, 2002
Observation of the decay K- --> pi(-)mu(+)mu(-) and measurements of the branching ratios for K+/- --> pi(+/-)mu(+)mu(-)H K Park, R A Burnstein, A Chakravorty, et al.
Leukemia|February 16, 2020
Multiple Myeloma DREAM Challenge reveals epigenetic regulator PHF19 as marker of aggressive diseaseMike J Mason, Carolina Schinke, Christine L P Eng, et al.
Nature Communications|August 27, 2024
Community assessment of methods to deconvolve cellular composition from bulk gene expressionBrian S White, Aurélien de Reyniès, Aaron M Newman, et al.
Genome Research|July 14, 2009
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applicationsTamim H Shaikh, Xiaowu Gai, Juan C Perin, et al.
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