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1 en than in women (P<0.0001, Cox proportional hazards model).
2 er (using the multivariable Cox proportional hazards model).
3  for a previously published Cox proportional hazards model.
4 imated with a multivariable Cox proportional hazards model.
5 splant-free survival with a Cox proportional hazards model.
6 l were examined using the Cox's proportional hazards model.
7 we further adjusted using a Cox proportional hazards model.
8 were estimated by using the Cox proportional hazards model.
9 s were investigated using a Cox proportional hazards model.
10 m standard analyses using a Cox proportional hazards model.
11 ly relevant covariates in a Cox proportional hazards model.
12 Rs) were estimated with the Cox proportional hazards model.
13  separately, using adjusted Cox proportional hazards models.
14 n-Meier curves and adjusted Cox proportional hazards models.
15 of a KT were examined using Cox proportional hazards models.
16 th mortality using adjusted Cox proportional hazards models.
17 ere defined in time-updated Cox proportional hazards models.
18 sing multivariable-adjusted Cox proportional hazards models.
19 a sequence of multivariable Cox proportional hazards models.
20 tervals were obtained using Cox proportional hazards models.
21 ociations were tested using Cox proportional hazards models.
22 xamined with time-dependent Cox proportional hazards models.
23 rtality were assessed using Cox proportional hazards models.
24 cases) were estimated using Cox proportional hazards models.
25 survival was performed with Cox proportional hazards models.
26 val (OS) were analyzed with Cox proportional hazards models.
27 ultivariate regression with Cox proportional hazards models.
28 valuated using log-rank and Cox proportional hazards models.
29  and linear regression, and Cox proportional hazards models.
30 onal multivariable-adjusted Cox proportional hazards models.
31 s estimated with the use of Cox proportional hazards models.
32 pilepsy were assessed using Cox proportional hazards models.
33 me to binary outcomes using Cox proportional hazards models.
34  mortality using univariate Cox proportional hazards models.
35 time-dependent covariate in Cox proportional hazards models.
36 k of MCI was investigated using proportional hazards models.
37 ons with death and MI using Cox proportional hazards models.
38 ion based on residuals from Cox proportional hazards models.
39 andom and fixed effects and Cox proportional hazards models.
40 vival analysis and adjusted Cox proportional hazards models.
41 ea-based deprivation) using Cox proportional hazards models.
42 eloping breast cancer using Cox proportional hazards models.
43  (CIs) were estimated using Cox proportional hazards models.
44 timated using multivariable Cox proportional hazards models.
45 ife tables and time-varying Cox proportional hazards models.
46 l after ALS diagnosis using Cox proportional hazards models.
47 nivariate and multivariable Cox proportional hazards models.
48 sed using Andersen-Gill and Cox proportional hazards models.
49 ident all-cause mortality using proportional hazards models.
50 using survival analyses and Cox proportional hazards models.
51 te Inpatient Database using Cox proportional hazards models.
52 lative hazards with conditional proportional hazards models.
53 n or KT were examined using Cox proportional hazards models.
54 -Meier survival curves, and Cox proportional-hazards models.
55 ction among vaccinees using Cox proportional hazards models.
56 nt AF was examined by using Cox proportional hazards models.
57  curves were measured using Cox-proportional hazards models.
58 lity was investigated using Cox proportional hazards models.
59 sing multivariable-adjusted Cox proportional hazards models.
60 d untreated groups by using Cox proportional hazards models.
61 alyses were performed using Cox-proportional hazards models.
62 e rates (IRs) and developed Cox proportional hazards models.
63 the Kaplan-Meier method and Cox proportional hazards modeling.
64 using step-up and step-down Cox proportional hazards modeling.
65 n-Meyer curves and adjusted Cox proportional hazards modeling.
66  factors were identified by Cox proportional hazards modeling.
67  rate curves and univariate Cox proportional hazards modeling.
68 ing Kaplan-Meier method and Cox proportional hazards modeling.
69 lan-Meier survival analysis and proportional hazards modeling.
70 ivariable and multivariable Cox proportional hazards modeling.
71 ariables as predictors with Cox proportional hazards modelling.
72                             Cox proportional hazards models accounting for competing risks were used
73                             Cox proportional hazards models, accounting for time under observation an
74  examined with the use of a Cox proportional hazards model adjusted for potential confounders.
75 mortality was assessed with Cox proportional hazards models adjusted for age, sex, AMD severity, VA,
76                          In Cox proportional hazards models adjusted for age, sex, race, clinical sit
77      Calculations were based on proportional hazards models adjusted for age, sex, race, HIV risk gro
78 ith SAR were analyzed using Cox proportional hazards models adjusted for clinicopathologic features a
79 e to death was studied with Cox proportional hazards models adjusted for demographic and clinical var
80  CRC-related survival using Cox proportional hazards models adjusted for demographic, tumor, and trea
81                  However, a Cox proportional hazards model, adjusted for age, sex, and genotype for t
82                   We fitted Cox proportional hazards models, adjusted for known confounders.
83 posure were estimated using Cox proportional hazards models, adjusted for potential confounders.
84 otype and OS is assessed by Cox proportional hazards model adjusting for age, sex, International stag
85 admission, we constructed a Cox proportional hazards model adjusting for age, sex, race, and comorbid
86 idence intervals (CIs) from Cox proportional hazards models adjusting for baseline prognostic factors
87 nd multiple sclerosis using Cox proportional hazards models, adjusting for individual and contextual
88                          In Cox proportional hazards models, ADT was associated with a decreased risk
89 rvival was assessed using a Cox proportional hazards model after adjusting for the propensity score f
90                                              Hazards models also suggested an association between low
91 d to receive an OLT using a Cox proportional hazards model and a generalized additive model with a lo
92                             Cox proportional hazards model and logistic regression were used to corre
93 al (DSS) were assessed with Cox proportional hazards modeling and a competing risk analysis, respecti
94 year after surgery by using Cox proportional hazards models and hazard ratios.
95 nical characteristics using Cox proportional hazards models and inverse probability weighting.
96                     We used Cox proportional hazards models and inverse probability-weighted estimate
97 al (RFS) were determined by Cox proportional hazards models and Kaplan-Meier method.
98                             Cox proportional hazards models and logistic regression were used to esti
99  derived using multivariate Cox proportional hazards models and standard clinical prediction rules.
100 ncy was assessed by using a Cox proportional hazards model, and a multiple variable model was examine
101 eier method, log-rank test, Cox proportional hazards models, and propensity score-matched analyses.
102  Kaplan-Meier analysis, and Cox proportional hazards models, as well, were developed to search for ri
103                             Cox proportional hazards modeling assessed the association between quarti
104                                 Proportional hazards models assessed differences in outcome reduction
105            The multivariate Cox proportional hazards model based on significant prognostic factors of
106 gnostic diet using adjusted Cox proportional hazards models based on follow-up until 2010.
107 fied multivariable-adjusted Cox proportional hazards models, black women and men were more likely to
108 ting for 34 covariates in a Cox proportional hazards model, borderline PH was associated with increas
109 e new Bayesian hierarchical Cox proportional hazards models, called the spike-and-slab lasso Cox, for
110                       Using Cox proportional hazards modeling, class 2 GEP was the prognostic factor
111    Using competing risk and Cox proportional hazards models, clinical factors at baseline and after t
112 cancer were estimated using Cox proportional hazards models, considering exposure as a time-varying v
113          In a multivariable Cox proportional hazards model controlling for sociodemographic, disease,
114              A multivariate Cox proportional hazards model demonstrated that multifocality, extrahepa
115            In multivariable Cox proportional hazards models, elevated HDGF levels predicted decreased
116                             Cox proportional hazards models estimated the risk of mortality associate
117        For accepted offers, Cox proportional hazards models estimated these probabilities using trans
118               Multivariable Cox proportional hazards models fit to individual patient data were perfo
119 n rehospitalization using a Cox proportional hazards model, following sequential adjustment for covar
120 ach outcome, we first ran a Cox proportional hazards model for each city, adjusting for prior cardiop
121 he hazard ratio, based on a Cox proportional hazards model for lisdexamfetamine vs placebo, was 0.09
122 ulness of extensions of the Cox proportional hazards model for repeated events in this context.
123                 Fits of the Cox proportional hazards model for the 2 sets of prognostic scores were c
124                By using the Cox proportional hazards model for univariate and multivariate analyses,
125            We fit multivariable proportional hazards models for baseline, time-updated and cumulative
126 ional Study, we constructed Cox proportional hazards models for CHD including age, pregnancy status,
127 ations, and biomarkers into Cox proportional hazards models for each outcome.
128 r probability estimates and Cox proportional hazards models for post-HCT outcomes based on recipient
129                             Cox proportional hazards models for recurrent gap-time data were used to
130 he primary analysis using a Cox proportional hazards model gave a mortality reduction over years 0-14
131 d all-cause mortality using Cox proportional hazards models; hazard ratios with 95% confidence interv
132                          In Cox proportional hazards models, higher levels of miR-124-3p were signifi
133                         The Cox proportional hazards model identified RFA as an independent predictor
134  constructed a multivariate Cox proportional hazards model in which the impact of each covariate was
135 ng an age- and sex-adjusted Cox proportional-hazards model, in all participants and also after restri
136 or covariates, results from Cox proportional hazards models, including SBP and DBP, jointly suggested
137   In multivariable-adjusted Cox proportional hazards models, increasing years of baseline rotating ni
138                              In proportional hazards model, insurance and tumor characteristics match
139         Marginal structural Cox proportional hazards modeling investigated the relationships between
140             In time-varying Cox proportional hazards models, liver transplantation (hazard ratio [HR]
141                           A Cox proportional hazards model of survival outcome indicated that a CMR w
142 Survival was analyzed using Cox proportional hazards models of time to death.
143 re enables analyses under a Cox proportional hazards model or Weibull regression model, and can accou
144                          On Cox proportional hazards modeling, patients achieving recovery of total c
145         In a time-dependent Cox proportional-hazards model, picobirnaviruses were predictive of the o
146                     Data was analyzed in Cox hazards models providing mortality rate ratios (MRRs).
147 lyzed using a multivariable Cox proportional hazards model, providing hazard ratios (HRs) with 95% co
148             In the adjusted Cox proportional hazards model, reinfection with a heterologous HCV genot
149 Meier survival analyses and Cox proportional hazards modeling, respectively.
150               Multivariable Cox proportional hazards modeling revealed no effect of repeated mismatch
151  0.10-mg/m3 exposure level, Cox proportional hazards models showed significantly increased risk of mo
152 nly through a multivariable Cox proportional hazards model stratified by trial.
153 ation were calculated using Cox proportional hazards models stratified by cohort.
154 ere evaluated with weighted Cox proportional hazards models stratified by race/ethnicity.
155                             Cox proportional hazards models, stratified according to birth-year cohor
156                             Cox proportional hazards models, stratified by age, were used to estimate
157 ozone using a two-pollutant Cox proportional-hazards model that controlled for demographic characteri
158  disability worsening by use of proportional hazards models that included OCT metrics and age, diseas
159 were tested with the use of Cox proportional hazards models that were adjusted for age, sex, body mas
160        The results were analysed using a Cox hazards model, the log-rank test, Kaplan-Meier curves, c
161                      In the Cox-proportional hazards model, the use of induction of was not associate
162       We used a proportional subdistribution hazards model to estimate the 10-year risk of developing
163           We first fitted a Cox proportional hazards model to examine the relation of knee SxOA to th
164 actorial analysis using the Cox proportional hazards model to identify factors affecting survival (as
165                   We used a Cox proportional hazards model to identify index case, contact, and house
166                     We used Cox proportional hazards modeling to assess sequentially adding baseline
167 l adult population and used Cox proportional hazards modeling to estimate determinants of death.
168                     We used Cox proportional hazards modeling to estimate hazard ratios (HRs) of chil
169                     We used Cox proportional hazards modeling to examine the association between nitr
170                     We used Cox proportional hazards models to assess associations of the biomarkers
171                      We fit Cox proportional hazards models to assess the association of diabetes wit
172                   We used Cox's proportional hazards models to calculate hazard ratios (HRs) for pote
173 rst developed multivariable Cox proportional hazards models to determine predictors of developing dep
174            We used adjusted Cox proportional hazards models to determine risks of death or death-cens
175 panic-CRIC Studies, we used Cox proportional hazards models to determine the association between race
176                     We used Cox proportional hazards models to estimate age- and multivariable-adjust
177                     We used Cox proportional hazards models to estimate associations between resident
178                         We used proportional hazards models to estimate associations.
179            The authors used Cox proportional hazards models to estimate hazard ratios of mortality fo
180                     We used Cox proportional hazards models to estimate HRs and 95% CIs.
181                     We used Cox proportional hazards models to estimate HRs and their 95% CIs for tim
182 vascular Health Study using Cox proportional hazards models to examine the association between FGF23
183                     We used Cox proportional hazards models to examine the association between risk o
184                   We fitted Cox proportional hazards models to examine the association of remission s
185       We used multivariable Cox proportional hazards models to examine the associations between Weste
186 ier survival and univariate Cox proportional hazards models to examine the effect of LSF on survival
187 for bankruptcy, we then fit Cox proportional hazards models to examine the relationship between bankr
188 stimate 5-year survival and Cox proportional hazards models to generate hazard ratios.
189       We used multivariable Cox proportional hazards models to independently estimate the risk of PD
190                     We used Cox proportional hazards models to investigate whether associations of br
191                     We used Cox proportional hazards models to obtain adjusted hazard ratios and 95%
192 dividual patient level with Cox proportional hazards models to quantify associations of creatinine-ba
193                         We used proportional hazards models to test the association between cardiogen
194                  We applied Cox proportional hazards models to test the potential HTEs on the remaini
195                     We used Cox proportional hazards models to test whether biomarker concentrations
196 ix exposure metrics and fit Cox proportional hazards models to the simulated data using the six metri
197         In a time-dependent Cox proportional hazards model, transmissions with 80% to 98% RVP were as
198 a propensity score-weighted Cox proportional hazards model using data from the British Association of
199                Multivariate Cox proportional hazards models using time-dependent endocrine drug use v
200                             Cox proportional hazards models using time-updated covariates were constr
201 or disengagement based on a Cox proportional hazards model, using multiple imputation for missing dat
202 with multivariable adjusted Cox proportional hazards models, using the 120-129 mm Hg systolic blood p
203                   Multivariable proportional hazards modeling utilizing several flexible smoothing ap
204             A multivariable Cox proportional hazards model was developed to determine predictors of t
205  all-cause mortality, and a Cox proportional hazards model was developed.
206                    A stratified proportional hazards model was used in an intention-to-treat analysis
207                             Cox-proportional hazards model was used to assess PFS in patient subgroup
208                The marginal Cox proportional hazards model was used to assess the factors associated
209                             Cox proportional hazards model was used to calculate hazard ratios with 9
210                A univariate Cox proportional hazards model was used to correlate disease-specific sur
211                  A multivariate proportional hazards model was used to determine the association of i
212                Multivariate Cox proportional hazards model was used to generate the nomogram from tum
213                           A Cox proportional hazards model was used to investigate first live birth a
214                 Conditional Cox proportional hazards modeling was used to compare the groups for the
215 treatment failure rates and Cox proportional hazards modeling was used to identify risk factors.
216 l variables and a penalised Cox proportional-hazards model, was used to compare method performance.
217                     Using a Cox proportional hazards model, we identified predictors of waitlist mort
218         Using multivariable Cox proportional hazards models, we compared cumulative incidence of all-
219  Using covariate-adjustment Cox proportional hazards models, we estimated associations of mean annual
220         Using multivariable Cox proportional hazards models, we estimated hazard ratios (HRs) for all
221                       Using Cox proportional hazards models, we estimated hazard ratios and confidenc
222                       Using Cox proportional hazards models, we evaluated both metrics as predictors
223 and death calculated by the Cox proportional hazards model were compared with those of age-matched co
224                             Cox proportional hazards models were adjusted for demographic and cardiov
225                             Cox proportional hazards models were applied to determine the effects of
226 Kaplan-Meier estimation and Cox proportional hazards models were conducted to identify risk factors f
227        Cosinor analysis and Cox proportional-hazards models were employed to analyze seasonality of i
228                             Cox proportional hazards models were fitted to assess associations of ast
229                             Cox proportional hazards models were fitted to calculate hazard ratios fo
230               Multivariable Cox proportional hazards models were fitted to evaluate the risk of NODAT
231     Unadjusted and adjusted Cox proportional hazards models were performed to compare outcomes by pat
232               Multivariable Cox proportional hazards models were performed to evaluate survival by Un
233                             Cox proportional hazards models were performed to examine associations.
234 ed at 130 SELECT sites, and Cox proportional hazards models were used in a modified intent-to-treat a
235                             Cox proportional hazards models were used to adjust for relevant demograp
236                             Cox proportional hazards models were used to analyze the association betw
237  204 serum metabolites, and Cox proportional hazards models were used to analyze the longitudinal ass
238            Kaplan-Meier and Cox proportional hazards models were used to analyze the outcome.
239                             Cox proportional hazards models were used to analyze variables associated
240               Multivariable Cox proportional hazards models were used to assess effects on noncancer
241               Multivariable Cox proportional hazards models were used to assess the association betwe
242               Multivariable Cox proportional hazards models were used to assess the relationship betw
243                             Cox proportional hazards models were used to calculate hazard ratios (HRs
244                             Cox proportional-hazards models were used to calculate life expectancy.
245                                 Proportional hazards models were used to calculate risk for all-cause
246                             Cox proportional hazards models were used to calculate the hazard ratios
247                             Cox proportional hazards models were used to compare incidences of stunti
248          Survival rates and Cox proportional hazards models were used to compare stage-specific 5-yea
249                             Cox proportional hazards models were used to compare survival between pat
250                             Cox proportional hazards models were used to compare the risk of developi
251                             Cox proportional hazards models were used to compute hazard ratios and ac
252               Multivariable Cox proportional hazards models were used to compute HRs for breast cance
253                             Cox proportional hazards models were used to compute the associations wit
254                             Cox proportional hazards models were used to determine whether risk facto
255                             Cox proportional hazards models were used to estimate adjusted hazard rat
256              Time-dependent Cox proportional hazards models were used to estimate adjusted hazard rat
257                                 Proportional hazards models were used to estimate adjusted HRs and 95
258                             Cox proportional hazards models were used to estimate adjusted HRs and 95
259                             Cox proportional hazards models were used to estimate associations per ea
260                             Cox proportional hazards models were used to estimate hazard ratios (HRs)
261                                 Proportional hazards models were used to estimate hazard ratios and 9
262                             Cox proportional hazards models were used to estimate hazard ratios and 9
263                             Cox proportional hazards models were used to estimate hazard ratios(HRs)
264                             Cox proportional hazards models were used to estimate hazard ratios.
265               Multivariable Cox proportional-hazards models were used to estimate hazards ratios (HRs
266 B, hazard ratios (HRs) from Cox proportional hazards models were used to estimate incident exfoliatio
267               Multivariable Cox proportional hazards models were used to estimate T2D HRs and 95% CIs
268                             Cox proportional hazards models were used to estimate the association of
269                             Cox proportional hazards models were used to estimate the relative mortal
270                             Cox proportional hazards models were used to estimate the relative mortal
271                             Cox proportional hazards models were used to evaluate body size and risk
272                             Cox proportional hazards models were used to evaluate factors associated
273                             Cox proportional hazards models were used to evaluate the association bet
274 s used to estimate DSS, and Cox proportional hazards models were used to evaluate the association bet
275 ses and marginal structural Cox proportional hazards models were used to evaluate the relationship be
276                 Proportional subdistribution hazards models were used to examine the association betw
277                             Cox proportional hazards models were used to examine the associations bet
278                             Cox proportional hazards models were used to identify independent risk fa
279              Time-dependent Cox proportional hazards models were used to investigate repeated measure
280 ial logistic regression and Cox proportional hazards models were used to model progression, CKD remis
281                             Cox proportional hazards models were used to model time to first MACCE ev
282                             Cox proportional hazards models were used to test predictors of disease p
283                             Cox proportional hazards models were used, with an incident case of HBV i
284                             Cox proportional-hazards models were used.
285 ersen-Gill extension to the Cox proportional hazards model while accounting for the competing risk of
286 eled using a multivariable subdistributional hazards model while treating any other cause of death as
287 s were determined using the Cox proportional hazards model with a significance level set at P <0.05.
288              We performed a Cox proportional hazards model with propensity score weighting to evaluat
289        The performance of a Cox proportional hazards model with the SPC analysis predictor was assess
290 = .0075, respectively) and in a proportional hazards model with time-dependent covariates (adjusted h
291 and then performed a piece-wise proportional hazards modeling with 2 time periods: discharge to 90 da
292         We applied extended Cox proportional hazards modeling with time-dependent covariates to total
293 tality was determined using Cox proportional hazards models with backward stepwise selection and incl
294      Multivariable-adjusted Cox proportional hazards models with cumulative updating of exposures wer
295            In multivariable Cox proportional hazards models with follow-up through 2012, a higher fet
296                     We used Cox proportional-hazards models with incident coronary heart disease and
297  hierarchical multivariable Cox proportional hazards models with occurrence of depression as a time-v
298 vember 2013, analyzed using Cox proportional hazards models with time-varying covariates.
299 fied multivariable-adjusted Cox proportional hazards modeling, with adjustment for time-updated covar
300 os (HRs) for death by using Cox proportional hazards models, with adjustment for age, sex, race/ethni

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