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1 y was higher in men than in women (P<0.0001, Cox proportional hazards model).
2 (HR+) breast cancer (using the multivariable Cox proportional hazards model).
3 52 and SE of 0.02 for a previously published Cox proportional hazards model.
4 sk model and transplant-free survival with a Cox proportional hazards model.
5 ncidence were estimated with a multivariable Cox proportional hazards model.
6 men who did not; we further adjusted using a Cox proportional hazards model.
7 Rs) with 95% CIs were estimated by using the Cox proportional hazards model.
8 among DMT stoppers were investigated using a Cox proportional hazards model.
9 ed with those from standard analyses using a Cox proportional hazards model.
10 bsolute Shrinkage and Selection Operator for Cox proportional hazards model.
11 ting for clinically relevant covariates in a Cox proportional hazards model.
12 Hazard ratios (HRs) were estimated with the Cox proportional hazards model.
13 type of dementia, separately, using adjusted Cox proportional hazards models.
14 is employed Kaplan-Meier curves and adjusted Cox proportional hazards models.
15 ation or receipt of a KT were examined using Cox proportional hazards models.
16 ere associated with mortality using adjusted Cox proportional hazards models.
17 study follow-up were defined in time-updated Cox proportional hazards models.
18 was determined using multivariable-adjusted Cox proportional hazards models.
19 s estimated from a sequence of multivariable Cox proportional hazards models.
20 to 90 days was examined with time-dependent Cox proportional hazards models.
21 95% confidence intervals were obtained using Cox proportional hazards models.
22 Associations were tested using Cox proportional hazards models.
23 cardiovascular mortality were assessed using Cox proportional hazards models.
24 (2,636 incident cases) were estimated using Cox proportional hazards models.
25 free and overall survival was performed with Cox proportional hazards models.
26 and overall survival (OS) were analyzed with Cox proportional hazards models.
27 scription using multivariate regression with Cox proportional hazards models.
28 ranslation were evaluated using log-rank and Cox proportional hazards models.
29 ed using logistic and linear regression, and Cox proportional hazards models.
30 tched and traditional multivariable-adjusted Cox proportional hazards models.
31 auses of death was estimated with the use of Cox proportional hazards models.
32 isk factors for epilepsy were assessed using Cox proportional hazards models.
33 ion models and time to binary outcomes using Cox proportional hazards models.
34 ts, and all-cause mortality using univariate Cox proportional hazards models.
35 s evaluated as a time-dependent covariate in Cox proportional hazards models.
36 ted hospitalizations with death and MI using Cox proportional hazards models.
37 ng a smooth function based on residuals from Cox proportional hazards models.
38 ted using mixed random and fixed effects and Cox proportional hazards models.
39 Kaplan-Meier survival analysis and adjusted Cox proportional hazards models.
40 and all-cause mortality were examined using Cox proportional hazards models.
41 ciation of CAC with ASCVD was examined using Cox proportional hazards models.
42 ld income, and area-based deprivation) using Cox proportional hazards models.
43 Adjusted hazard ratios were estimated using Cox proportional hazards models.
44 ts are expressed as hazard ratios (HRs) from Cox proportional hazards models.
45 Associations were tested via multivariate Cox proportional hazards models.
46 r the risk of developing breast cancer using Cox proportional hazards models.
47 fidence intervals (CIs) were estimated using Cox proportional hazards models.
48 analyzed using life tables and time-varying Cox proportional hazards models.
49 s) and 95% CIs estimated using multivariable Cox proportional hazards models.
50 and with survival after ALS diagnosis using Cox proportional hazards models.
51 en groups using univariate and multivariable Cox proportional hazards models.
52 tality were assessed using Andersen-Gill and Cox proportional hazards models.
53 or hemorrhagic), using survival analyses and Cox proportional hazards models.
54 11 California State Inpatient Database using Cox proportional hazards models.
55 l to WU completion or KT were examined using Cox proportional hazards models.
56 ors of HIV-1 infection among vaccinees using Cox proportional hazards models.
57 range with incident AF was examined by using Cox proportional hazards models.
58 s index and mortality was investigated using Cox proportional hazards models.
59 rostate cancer, using multivariable-adjusted Cox proportional hazards models.
60 etween treated and untreated groups by using Cox proportional hazards models.
61 ed crude incidence rates (IRs) and developed Cox proportional hazards models.
62 are tests, Kaplan-Meier survival curves, and Cox proportional-hazards models.
63 itis and survival curves were measured using Cox-proportional hazards models.
64 riate survival analyses were performed using Cox-proportional hazards models.
65 evaluated using the Kaplan-Meier method and Cox proportional hazards modeling.
66 is was performed using step-up and step-down Cox proportional hazards modeling.
67 uated using Kaplan-Meyer curves and adjusted Cox proportional hazards modeling.
68 inical prognostic factors were identified by Cox proportional hazards modeling.
69 aplan-Meier event rate curves and univariate Cox proportional hazards modeling.
70 d without RVAD using Kaplan-Meier method and Cox proportional hazards modeling.
71 assessed using univariable and multivariable Cox proportional hazards modeling.
72 d we assessed covariables as predictors with Cox proportional hazards modelling.
75 al infarction was examined with the use of a Cox proportional hazards model adjusted for potential co
76 d cause-specific mortality was assessed with Cox proportional hazards models adjusted for age, sex, A
79 s of biomarkers with SAR were analyzed using Cox proportional hazards models adjusted for clinicopath
81 with overall and CRC-related survival using Cox proportional hazards models adjusted for demographic
82 05 persons 60 years of age or older, we used Cox proportional-hazards models adjusted for age and sex
85 ls for lithium exposure were estimated using Cox proportional hazards models, adjusted for potential
86 ation between genotype and OS is assessed by Cox proportional hazards model adjusting for age, sex, I
87 ates of 30-day readmission, we constructed a Cox proportional hazards model adjusting for age, sex, r
88 isks and 95% confidence intervals (CIs) from Cox proportional hazards models adjusting for baseline p
89 nson's disease, and multiple sclerosis using Cox proportional hazards models, adjusting for individua
92 and the likelihood to receive an OLT using a Cox proportional hazards model and a generalized additiv
93 nd analyzed for predictors of outcome with a Cox proportional hazards model and linear regression.
95 e-specific survival (DSS) were assessed with Cox proportional hazards modeling and a competing risk a
96 ath and aortic dissection were identified by Cox proportional hazards modeling and a mortality risk s
98 mographic and clinical characteristics using Cox proportional hazards models and inverse probability
100 rence free survival (RFS) were determined by Cox proportional hazards models and Kaplan-Meier method.
102 A risk score was derived using multivariate Cox proportional hazards models and standard clinical pr
103 k of loss of patency was assessed by using a Cox proportional hazards model, and a multiple variable
104 sing the Kaplan-Meier method, log-rank test, Cox proportional hazards models, and propensity score-ma
105 istic regression, Kaplan-Meier analysis, and Cox proportional hazards models, as well, were developed
108 f updated postdiagnostic diet using adjusted Cox proportional hazards models based on follow-up until
109 Using sex-stratified multivariable-adjusted Cox proportional hazards models, black women and men wer
114 (HRs) of breast cancer were estimated using Cox proportional hazards models, considering exposure as
121 sex differences in rehospitalization using a Cox proportional hazards model, following sequential adj
123 ime to relapse; the hazard ratio, based on a Cox proportional hazards model for lisdexamfetamine vs p
124 o assess the usefulness of extensions of the Cox proportional hazards model for repeated events in th
127 itiative Observational Study, we constructed Cox proportional hazards models for CHD including age, p
129 lated Kaplan-Meier probability estimates and Cox proportional hazards models for post-HCT outcomes ba
135 level of P < .10 constructed a multivariate Cox proportional hazards model in which the impact of ea
136 isk of SCD by using an age- and sex-adjusted Cox proportional-hazards model, in all participants and
137 ith adjustments for covariates, results from Cox proportional hazards models, including SBP and DBP,
139 acute kidney injury [AKI]) was studied using Cox proportional hazards models (intention-to-treat and
144 tios for mortality censored at 14 days using Cox proportional hazards models on an IPW-adjusted cohor
148 mortality was analyzed using a multivariable Cox proportional hazards model, providing hazard ratios
155 ence of BMPR2 mutation were calculated using Cox proportional hazards models stratified by cohort.
156 Associations were evaluated with weighted Cox proportional hazards models stratified by race/ethni
159 eese, and butter were tested with the use of Cox proportional hazards models that were adjusted for a
160 illion (ppb) for ozone using a two-pollutant Cox proportional-hazards model that controlled for demog
163 ndertook a multifactorial analysis using the Cox proportional hazards model to identify factors affec
166 ose in the general adult population and used Cox proportional hazards modeling to estimate determinan
173 rt (CRIC) and Hispanic-CRIC Studies, we used Cox proportional hazards models to determine the associa
180 ine in the Cardiovascular Health Study using Cox proportional hazards models to examine the associati
183 y using Kaplan-Meier survival and univariate Cox proportional hazards models to examine the effect of
184 and did not file for bankruptcy, we then fit Cox proportional hazards models to examine the relations
185 Meier method to estimate 5-year survival and Cox proportional hazards models to generate hazard ratio
190 aseline at the individual patient level with Cox proportional hazards models to quantify associations
193 t to create the six exposure metrics and fit Cox proportional hazards models to the simulated data us
194 ording to the Kaplan-Meier method and used a Cox proportional-hazards model to adjust for significant
198 mic therapies in a propensity score-weighted Cox proportional hazards model using data from the Briti
201 ed risk factors for disengagement based on a Cox proportional hazards model, using multiple imputatio
202 ) were estimated with multivariable adjusted Cox proportional hazards models, using the 120-129 mm Hg
212 sed to determine treatment failure rates and Cox proportional hazards modeling was used to identify r
214 on eight clinical variables and a penalised Cox proportional-hazards model, was used to compare meth
222 os (HRs) for SMN and death calculated by the Cox proportional hazards model were compared with those
235 y and were enrolled at 130 SELECT sites, and Cox proportional hazards models were used in a modified
238 d and quantitated 204 serum metabolites, and Cox proportional hazards models were used to analyze the
265 In substudy B, hazard ratios (HRs) from Cox proportional hazards models were used to estimate in
274 n-Meier method was used to estimate DSS, and Cox proportional hazards models were used to evaluate th
275 al landmark analyses and marginal structural Cox proportional hazards models were used to evaluate th
288 red using the Andersen-Gill extension to the Cox proportional hazards model while accounting for the
289 with the outcomes were determined using the Cox proportional hazards model with a significance level
293 prediction of mortality was determined using Cox proportional hazards models with backward stepwise s
297 April 2002 and November 2013, analyzed using Cox proportional hazards models with time-varying covari
300 mated hazard ratios (HRs) for death by using Cox proportional hazards models, with adjustment for age
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