Emrah Gecili
Overview
Explore the profile of Emrah Gecili including associated specialties, affiliations and a list of published articles.
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21
Citations
80
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Recent Articles
1.
Gelir F, Akan T, Alp S, Gecili E, Bhuiyan M, Disbrow E, et al.
J Med Biol Eng
. 2025 Mar;
45(1):63-83.
PMID: 40046733
Purpose: Alzheimer's disease (AD), a neurodegenerative disorder, is a condition that impairs cognition, memory, and behavior. Mild cognitive impairment (MCI), a transitional stage before AD, urgently needs the development of...
2.
Gelir F, Chatla S, Bhuiyan M, Disbrow E, Conrad S, Vanchiere J, et al.
Sci Rep
. 2025 Mar;
15(1):7660.
PMID: 40038506
The progression of Alzheimer's disease (AD), a leading cause of dementia worldwide, is known for its variability and complexity, challenging the conventional methods of monitoring and predicting disease trajectories. This...
3.
Colegate S, Palipana A, Gecili E, Szczesniak R, Brokamp C
J Clin Transl Sci
. 2024 Sep;
8(1):e94.
PMID: 39220818
Introduction: Patients with cystic fibrosis (CF) experience frequent episodes of acute decline in lung function called pulmonary exacerbations (PEx). An existing clinical and place-based precision medicine algorithm that accurately predicts...
4.
Peterson C, Rao M, Palipana A, Manning E, Vancil A, Ryan P, et al.
Sci Total Environ
. 2024 Aug;
950:175348.
PMID: 39117222
Environmental exposures and community characteristics have been linked to accelerated lung function decline in people with cystic fibrosis (CF), but geomarkers, the measurements of these exposures, have not been comprehensively...
5.
Zhou G, Wang Z, Palipana A, Andrinopoulou E, Afonso P, McPhail G, et al.
Respir Res
. 2024 Apr;
25(1):187.
PMID: 38678203
Background: Modulator therapies that seek to correct the underlying defect in cystic fibrosis (CF) have revolutionized the clinical landscape. Given the heterogeneous nature of lung disease progression in the post-modulator...
6.
Palipana A, Vancil A, Gecili E, Rasnick E, Ehrlich D, Pestian T, et al.
Environ Adv
. 2023 Dec;
14.
PMID: 38094913
Background: Cystic fibrosis (CF) is a genetic disease but is greatly impacted by non-genetic (social/environmental and stochastic) influences. Some people with CF experience rapid decline, a precipitous drop in lung...
7.
Reifenberg J, Gecili E, Pestian T, Andrinopoulou E, Ryan P, Brokamp C, et al.
J Cyst Fibros
. 2023 May;
22(4):694-701.
PMID: 37142525
Background: Secondhand smoke exposure, an important environmental health factor in cystic fibrosis (CF), remains uniquely challenging to children with CF as they strive to maintain pulmonary function during early stages...
8.
Szczesniak R, Andrinopoulou E, Su W, Afonso P, Burgel P, Cromwell E, et al.
Ann Am Thorac Soc
. 2023 Mar;
20(7):958-968.
PMID: 36884219
Studies estimating the rate of lung function decline in cystic fibrosis have been inconsistent regarding the methods used. How the methodology used impacts the validity of the results and comparability...
9.
Gecili E, Brokamp C, Rasnick E, Afonso P, Andrinopoulou E, Dexheimer J, et al.
Pediatr Pulmonol
. 2023 Feb;
58(5):1501-1513.
PMID: 36775890
Background: The extent to which environmental exposures and community characteristics of the built environment collectively predict rapid lung function decline, during adolescence and early adulthood in cystic fibrosis (CF), has...
10.
Palipana A, Gecili E, Song S, Johnson S, Szczesniak R, Gupta N
Chest
. 2023 Jan;
163(6):1458-1470.
PMID: 36610667
Background: Lung function decline varies significantly in patients with lymphangioleiomyomatosis (LAM), impeding individualized clinical decision-making. Research Question: Can we aid individualized decision-making in LAM by developing a dynamic prediction model...