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864 citation(s) found for "Jackson".

COMPARING REFRACTIVE OUTCOMES OF SECONDARY LENS SURGERY BETWEEN OPHTHALMOLOGY SUBSPECIALTIES IN PATIENTS WITH GOOD FINAL VISION
Sharma, Kannan , Israilevich, Rachel Naomi, Ross, Emily, Bloch, Jackson Frost, Murray, Isaiah, Pasa, Gokce Cinel, Starr, Matthew R , Israilevich, Rachel , Bloch, Jackson F. , Starr, Matthew R.

Retina | May 13, 2026 | Volume: 46 | Issue: 9 | Pages: 1578-1588

10.1097/iae.0000000000004879 | PMID 42132539 Get It

Purpose: The study compares refractive outcomes of secondary intraocular lens (SIOL) surgery performed by vitreoretinal, anterior segment, and both surgeons. Methods: Eyes included in this study underwent SIOL surgery from 2012 to 2024 and had a final postoperative visual acuity of 20/50 or better. Regression analysis compared refractive outcomes, and chi-squared analysis compared complications between subspecialty of SIOL surgeons. Results: A total of 94, 104, and 80 eyes were included in the retina surgeon, anterior segment surgeon, and combo surgeon cohorts, respectively. There was no significant difference in error between target and final postoperative spherical equivalence between retina and combo ( P = 0.079), retina and anterior segment ( P = 0.135), or anterior segment and combo cohorts ( P = 0.567). There was no significant difference in number of eyes with final spherical equivalence within 1 diopter of target spherical equivalence between retina and combo ( P = 0.136), retina and anterior segment ( P = 0.061), or anterior segment and combo cohorts ( P = 0.783). The retina cohort had higher postoperative corneal edema than the combo ( P = 0.017) and the anterior segment cohorts ( P = 0.035). The combo cohort had more postoperative retinal detachment than the anterior segment cohort ( P = 0.046). Conclusion: In eyes with good final vision, retina and anterior segment surgeons have similar refractive outcomes after SIOL surgery.
Crowdsourced educational resource to distinguish Translational Science (TS) from Translational Research (TR)
Hafer, Nathaniel , Cielo, Karen, Duguid, Paul , Dunn, Mendy , Gholami, Maryam , Hunt, Joe, Kane, Cathleen , Moussatche, Patricia , Navarro, Christy , Patterson, Brittney Jackson, Vitale, Alfred , Kane, Cathleen , Moussatche, Patricia , Vitale, Alfred , Croker, Jennifer A. , Hafer, Nathaniel , Duguid, Paul , Gholami, Maryam , Holmes, Kristi , Hunt, Joe

Journal of Clinical and Translational Science | May 6, 2026 | Volume: 10 | Issue: 1 | Pages: No page available

10.1017/cts.2026.10747 | PMID 42238987 Get It

Smarter FoCUS: AI-guided focused cardiac ultrasound enables novice detection of left ventricular dysfunction
Kane, Conor J. , Borgeson, Jordan, Greason, Christie, Malins, Jeffrey G. , Anisuzzaman, D M, Tsaban, Gal, Schonfeld, Daniel, Jackson, John I. , Wood, Julia, Lee, Eunjung, Friedman, P A, Kane, Garvan C, Oh, J, Pellikka, Patricia A, Poterucha, Timothy J. , Rosenbaum, Andrew, Attia, Zachi I, Thaden, Jeremy J. , Bird, Jared, Friedman, Paul A , Lopez-Jimenez, Francisco , Poterucha, Timothy Joseph , Bird, Jared G , Kane, Conor, Borgeson, Jordan, Greason, Christie, Anisuzzaman, DM , Tsaban, Gal , Schonfeld, Daniel Andres, Lee, E, Naser, Jwan A. , Friedman, Paul A. , López-Jiménez, Francisco , Kane, Garvan C. , Pellikka, Patricia A. , Attia, Zachi I. , Pislaru, Sorin V.

European Heart Journal - Digital Health | April 27, 2026 | Volume: 7 | Issue: 5 | Pages: No page available

10.1093/ehjdh/ztag066 | PMID 42169733 Get It

Abstract Aims Heart failure is prevalent; however, there is no cost-effective screening option. Against formal echocardiography, we assessed the diagnostic performance of focused cardiac ultrasound (FoCUS), performed by novice users guided and interpreted by artificial intelligence (AI) for the assessment of left ventricular ejection fraction (LVEF). Methods and results We prospectively enrolled 496 adults referred for diagnostic echocardiography. Novice operators (without clinical or imaging experience) underwent a 4-h imaging workshop, then performed FoCUS using a point-of-care device (Philips Lumify) utilizing real-time AI-image guidance (UltraSight). Images were assessed by AI-image interpretation software (Mayo Clinic), and two expert blinded echocardiologists. Median age was 67, 39% female, and body mass index range 17–56 kg/m2. Forty-one subjects (8.3%) exhibited moderate or greater LV dilatation and 28 (5.6%) had LVEF <40%. The median scan time was 4 min (IQR 3–5). Adequate views were achieved in 95.0% and 97.4% of subjects for AI interpretation and expert analysis, respectively. A two-step diagnostic screening process for low EF in which only abnormal AI reads or uninterpretable scans were reviewed by experts (15.1%) had a sensitivity 96.2%, specificity 95.4%, PPV 54.3%, and NPV 99.8%. A subsequent prospective validation study of 344 subjects demonstrated similar results (sensitivity 100%, specificity 99.4%). Conclusion In this early feasibility investigation, AI-guidance technology embedded on a handheld device, enabled novice users without clinical or imaging experience to acquire sufficient quality images to accurately assess LVEF with minimal training. The technology evaluated in this study may hold promise for AI-guidance and interpretation to facilitate low-cost screening for cardiac dysfunction.
Seizure recurrence after hemispheric disconnection—An EEG false lateralization trap
Natteru, Prashant , Gupta, Ajay , Alzahrany, Majed , Bingaman, William , Valappil, Ahsan Moosa Naduvil , Moosa, Ahsan N. , Natteru, Prashant A

Epileptic Disorders | April 22, 2026 | Volume: 28 | Issue: 4 | Pages: 1309-1312

10.1002/epd2.70253 | PMID 42017341 Get It

Associations of State Mandatory Paid Sick Leave Policies With Cancer Outcomes in the United States
Kohut-Jackson, Abigail , Barnes, Justin M. , Chino, Fumiko , Zheng, Zhiyuan , Han, Xuesong, Johnson, Kimberly , Yabroff, K. Robin , Johnston, Kenton J. , Han, Xuesong , Zheng, Jason , Han, Xuesong , Johnson, Kimberly J , Yabroff, K Robin

JCO Oncology Practice | April 10, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1200/op-25-00596 | PMID 41962062 Get It

PURPOSE Since 2012, several states have implemented mandatory paid sick leave (PSL) policies. PSL can provide patients time and income continuity to undergo screening and/or timely diagnostic workup for new cancer-related symptoms and complete lengthy and expensive cancer treatment courses. This study aimed to examine the association between mandatory PSL policies and cancer stage at diagnosis and overall survival (OS). METHODS Adults age 18-64 years diagnosed with cancer were identified from the Surveillance, Epidemiology, and End Results program registries between 2010 and 2019. Difference-in-differences (DID) analyses were used to compare absolute changes in stage I and stage IV diagnoses and 1-year OS before and after policy implementation in states that enacted mandatory PSL relative to states that did not enact such policies. RESULTS A total of 1,052,307 patients with cancer were included. In adjusted DID analyses, there were a 0.83 (95% CI = –1.49 to –0.16, P = .014) PP decrease in stage IV diagnoses and a 0.63 (95% CI = 0.10 to 1.17, P = .021) PP increase in 1-year OS associated with implementation of mandatory PSL policies. In exploratory analyses, males and individuals with lung cancer experienced the greatest shifts in policy-associated changes in stage at diagnosis and OS. CONCLUSION PSL policy implementation is associated with decreased late-stage diagnoses and improved OS in patients with cancer. Policies that improve opportunities to receive medical care may facilitate earlier cancer detection and ultimately contribute to better patient outcomes.
Abstract 6831: Virtual clinical trials of BMP4 differentiation therapy.
Harbour, Nicholas , Michaelides, Loizos , Hubbard, M.E. , Rani, Vinitha , Kenchappa, Rajappa S., Farias, Virginea, Carrano, Anna , Quinones-Hinojosa, Alfredo, Swanson, Kristin R. , Swanson, Kristin R , Curtin, Lee , Jackson, Pamela , Farias, Virgínea , Owen, Markus R. , Quiñones‐Hinojosa, Alfredo

Cancer Research | April 3, 2026 | Volume: 86 | Issue: 7_Supplement | Pages: 6831-6831

10.1158/1538-7445.am2026-6831 Get It

Abstract Glioma stem cells (GSCs) are considered a major driver of glioblastoma (GBM) progression and are highly resistant to standard cytotoxic treatments. BMP4 has been shown to promote GSC differentiation, enhance radiosensitivity, slow tumor growth, and extend survival in animal models. Despite this promise, BMP4 has yet to achieve clinical impact, owing largely to heterogeneous and nonlinear responses across preclinical experimental systems. To elucidate how BMP4 could function as an effective targeted differentiation therapy in GBM, we develop a mathematical model that describes the growth of a GBM tumor via a hierarchy of GSCs, progenitor and terminally differentiated cells. We parameterize our model using new radiotherapy and proliferation assay data (with and without BMP4 exposure) from twelve patient-derived GSC lines. This integration of model and data allows us, for the first time, to quantitatively capture patient-specific heterogeneity in BMP4 sensitivity. We perform global sensitivity analysis on the model, identifying proliferation rate and GSC self-renewal sensitivity as key determinants of BMP4 efficacy. These parameters act as model-derived biomarkers that distinguish BMP4-responsive tumors from non-responsive ones. In an in silico analysis across a broad cohort of virtual patients, we find that continuous BMP4 delivery from surgical resection through radiotherapy consistently outperforms a single-dose strategy. Virtual clinical trials further show that, without stratification using these model-derived biomarkers, BMP4 yields little observable therapeutic benefit. In contrast, selecting patients with more proliferative, BMP4-responsive GSCs markedly increases the likelihood of observing a significant treatment effect. Citation Format: Nicholas Harbour, Lee Curtin, Loizos Michaelides, Matthew E. Hubbard, Pamela Jackson, Vinitha Rani, Rajappa Kenchappa, Virginea Farias, Anna Carrano, Markus Owen, Alfredo Quinones-Hinojosa, Kristin Swanson. Virtual clinical trials of BMP4 differentiation therapy [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6831.
Neurodegeneration risk variants promote lysosomal TMEM106B fibril accumulation
Replogle, John, Marks, Jordan D. , Fernandez, Martin G , Yu, Dahyun , Winters, Elizabeth, Jawahar, Vidhya Maheswari, Deshmukh, Rishi, Sutanto, Renaldo, Kowal, Isabelle, Frankenfield, Ashley M. , Shi, Rachel , Carlomagno, Yari , Jansen-West, Karen, Kopach, Andrii , Ndayambaje, I. Sandra , Qi, Yue Andy, Shantaraman, Ananth, Pozo-Cabanell, Ignacio, Sheth, Udit , Yue, Mei, Duong, Duc, Bennett, David A, Damme, Markus, Boeve, Brad F, Day, Gregory S, Skarnes, William C, Petersen, Ronald C, Josephs, K., Graff-Radford, Neill, Barmada, Sami J. , Zhang, Yongjie, Hao, Ling , DeTure, Michael , Rawlinson, Bailey, Cook, Erica Engelberg, Casey, Monica Castanedes, Perez, Nathan M, Dickson, Dennis, Liu, Yue, Seyfried, Nicholas T., Wingo, Thomas S, Mosalaganti, Shyamal , Petrucelli, Leonard, Ward, Michael E, Ward, Michael E. , Replogle, John Michael , Todd, Tiffany W. , Engelberg-Cook, Erica , Perez, Nathan, Ward, Michael E , Barmada, Sami , Sheth, Udit , Yuan, Hebao , Kowal, Isabelle , Jansen‐West, Karen , Qi, Yue , Shantaraman, Anantharaman , Duong, Duc, Ferguson, Shawn M. , Bennett, David A. , Daμμe, Markus , Day, Gregory S. , Kellman, Benjamin P. , Skarnes, William C. , Petersen, Ronald C. , Graff‐Radford, Neill R. , McDonough, Justin A. , Prudencio, Mercedes , Dickson, Dennis W. , Wingo, Aliza P. , Liu, Yue, Seyfried, Nicholas T. , Wingo, Thomas S , Petrucelli, Leonard

No container title available | March 28, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.64898/2026.03.26.714634 | PMID 41929000 Get It

Variants in TMEM106B and GRN , which encode lysosomal proteins, interact through unknown mechanisms to increase the risk of age-related cognitive decline and neurodegeneration. Here, we show that these variants converge on a single molecular intermediate: the cleaved intra-lysosomal fibril core of TMEM106B, a precursor to amyloid fibrils that accumulate in the aging brain. A protein-coding TMEM106B risk variant (p.T185) drives fibril core accumulation by impairing its degradation and GRN risk variants amplify this effect. Mice over-expressing the fibril core develop hallmarks of neurodegeneration, and cryo-electron tomography reveals intra-lysosomal fibrils in cultured neurons, mice, and diseased human brain. In GRN -mutation carriers, in whom fibril burden is greatest, fibrils extrude through ruptured lysosomal membranes. These findings identify intra-lysosomal TMEM106B fibrillization as a convergent neurodegeneration mechanism and potential therapeutic target.