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Alison Katz, PT, DPT, OCS
New Publication to Cancers Special Issue Time for a Paradigm Shift in Non-muscle-invasive Bladder Cancer (Volume II)
Thanks to the efforts of all involved, we have just published a paper, "Treatment Modalities for Non-Muscle Invasive Bladder Cancer: An Updated Review" to Cancers Special Issue Time for a Paradigm Shift in Non-muscle-invasive Bladder Cancer (Volume II). Read Here
Sleep Apnea Physiological Burdens and Cardiovascular Morbidity and Mortality.
Labarca, Gonzalo, Daniel Vena, Wen-Hsin Hu, Neda Esmaeili, Laura Gell, Hyung Chae Yang, Tsai-Yu Wang, et al. 2023. “Sleep Apnea Physiological Burdens and Cardiovascular Morbidity and Mortality.”. American Journal of Respiratory and Critical Care Medicine 208 (7): 802-13.
Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment.
Granot-Hershkovitz, Einat, Brian Spitzer, Yunju Yang, Wassim Tarraf, Bing Yu, Eric Boerwinkle, Myriam Fornage, et al. 2023. “Genetic Loci of Beta-Aminoisobutyric Acid Are Associated With Aging-Related Mild Cognitive Impairment.”. Translational Psychiatry 13 (1): 140.
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Mahajan, Anubha, Cassandra N Spracklen, Weihua Zhang, Maggie C Y Ng, Lauren E Petty, Hidetoshi Kitajima, Grace Z Yu, et al. 2022. “Multi-Ancestry Genetic Study of Type 2 Diabetes Highlights the Power of Diverse Populations for Discovery and Translation.”. Nature Genetics 54 (5): 560-72.
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.
Hu, Xiaowei, Dandi Qiao, Wonji Kim, Matthew Moll, Pallavi P Balte, Leslie A Lange, Traci M Bartz, et al. 2022. “Polygenic Transcriptome Risk Scores for COPD and Lung Function Improve Cross-Ethnic Portability of Prediction in the NHLBI TOPMed Program.”. American Journal of Human Genetics 109 (5): 857-70.
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.
Wainschtein, Pierrick, Deepti Jain, Zhili Zheng, TOPMed Anthropometry Working Group, NHLBI Trans-Omics for Precision Medicine Consortium, Adrienne Cupples, Aladdin H Shadyab, et al. 2022. “Assessing the Contribution of Rare Variants to Complex Trait Heritability from Whole-Genome Sequence Data.”. Nature Genetics 54 (3): 263-73.
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