Every study, searchable

How sensitive is evidence for recent global warming acceleration to the final years included and the model of natural variability? A registered audit uses a frozen NASA global annual temperature series. A fixed-breakpoint model estimates a warming-rate increase of 0.232 °C per decade, with a confidence interval from 0.106 to 0.358. A search over possible breakpoints gives p = 0.0271 with fitted autocorrelation, but p = 0.4078 when the recent endpoint years are excluded. Stronger assumed autocorrelation also weakens the test. These are conditional statistical results about an unadjusted series, with limited simulated power for smaller slope changes.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In the frozen NASA GISTEMP annual series for 1970-2025, a fixed-2015-knot model estimates a warming-rate increase of 0.232 degrees Celsius per decade with a 95% HAC interval of 0.106 to 0.358, while the registered breakpoint-search p-value is 0.0271 through 2025, 0.4078 through 2022, and 0.1726 through 2025 when the AR(1) lag coefficient is fixed at 0.6.

Why did United States heart-disease deaths increase between 2018 and 2024? An updated analysis of final national death counts and published population estimates averages all six orders of a demographic decomposition. Known-age deaths increase by 28135. Population size contributes 25981.4 deaths, age composition 26512.2, and age-specific rates -24358.5. Demographic contributions outweigh the negative rate contribution. These are arithmetic contributions conditional on the source denominators, which change estimation methods during the period, rather than causal effects or individual mortality risks.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In the bundled CDC WONDER D158 final snapshot for United States residents with known age, 2018-2024 heart-disease deaths increase by 28,135. Averaging all six orders of the population-size, age-share-vector, and age-specific-rate-vector decomposition yields contributions of +25,981.4, +26,512.2, and -24,358.5 deaths, respectively (display-rounded), so positive demographic contributions outweigh the negative rate contribution. The statement is conditional on the published population denominators and specified age bins, and is arithmetic rather than causal or an individual clinical-risk estimate.

How much false-positive error can arise when a nominally exact test treats clustered subsamples as independent? An exact finite benchmark enumerates null distributions for 75 balanced designs. In the selected beta-binomial design, the cell-level Fisher test rejects with probability 0.21567065919813758, compared with 0.0436374106894531 for a test using the known clustered null. With a single observation per donor, the Fisher rejection probability is 0.021484375. These are exact probabilities conditional on the specified toy model. They demonstrate calibration failure from ignoring dependence, without evaluating real biological pipelines or ranking practical alternatives.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: For the specified null of five independent donors per arm and twenty conditionally independent Bernoulli observations per donor with latent Beta(5,5) success probabilities (within-donor correlation 1/11), the cell-level two-sided probability-ordering Fisher test at nominal alpha=0.05 rejects with exact-model probability 0.215670659198, versus 0.043637410689 for the known-clustered-null absolute-difference-tail oracle. The finite 75-design grid has 31 cell-level Fisher probabilities above nominal, while all 75 oracle probabilities and all 15 independent-observation controls are at or below nominal. These are conditional toy-model calibration results, not evaluations of real biological analysis methods.

Can repeated rounding hide escape even when a Mandelbrot parameter is exactly representable? We construct the first binary floating-point successor of the real cusp and give an elementary invariant argument: both separate rounding and single-round evaluation keep its computed critical orbit below an absorbing boundary, although its exact orbit is unbounded. An exact rational simulator and directed integer enclosures check 22 precisions. At single precision, the stationary transitions occur at 8999 and 9532, while the exact orbit first escapes at 18196. This supplies an adversarial numerical test family; it does not claim discovery of rounding artifacts or slow escape.

• Published, Reviewed.Published, Reviewed: For every binary significand precision p >= 3, the exactly representable parameter c_p = 1/4 + 2^(-(p+1)) has an unbounded exact critical orbit, while both nearest-even recurrences RN_p(RN_p(x_n^2)+c_p) and RN_p(x_n^2+c_p), starting at zero, stay in [0,1/2] for every iterate, with 1/2 absorbing.
• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: For all 22 precisions p from 3 through 24, the supplied exact-dyadic benchmark reaches the stationary value 1/2 under both rounding models and certifies finite exact first escapes, with first stationary transitions 8999 and 9532 and exact first escape 18196 at p=24.

Does maintaining normal tissue mechanics prevent cancer initiation? A focused evidence map separates the endpoints of 4 selected papers and reanalyzes an available tumor-count table. The selected contrasts occupy 4 classes, with 0 papers testing incident cancer after a mechanical intervention in humans. The table concerns already malignant cells: blocking-antibody pretreatment gives risk ratios of 0.4667 and 0.5 against its controls. These endpoints answer different questions; neither a smaller transplantation risk nor a human biomarker change establishes primary prevention. This is a bounded, exploratory source audit, not a systematic review or a new biological experiment.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In a purposively selected four-paper evidence map, the coded contrasts occupy four distinct endpoint classes, only one paper starts its reprogramming program with normal primary cells, and none measures incident cancer after a mechanical intervention in humans, with all counts restricted to this selected set rather than the literature.
• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: Reanalysis of Weaver et al. (1997) Table II gives 7/16 tumor-bearing mice after blocking-antibody pretreatment of already malignant cells versus 15/16 untreated and 14/16 control-antibody mice, risk ratios 0.4667 and 0.5000, with two-sided Fisher p-values 0.005923 and 0.023333 (Holm-adjusted 0.011846 and 0.023333), while conservative simultaneous 95% risk-ratio intervals are 0.1612 to 1.1614 and 0.1625 to 1.3304 under independent-binomial sampling.

We provide an explicit rational parameter for every finite iteration cutoff. Its critical orbit remains uniformly below the usual escape radius throughout the cutoff, although an elementary growth argument proves that it eventually escapes. The contribution is a deterministic adversarial test family, a short uniform proof, and a certified finite benchmark. Integer enclosures and Arb ball arithmetic agree on 7 cases, with first-escape counts [23,61,212,815,3228,12879,51482]. Slow escape near the real parabolic cusp is established in the literature; we claim no discovery of that phenomenon or of its asymptotic law.

• Published, Reviewed.Published, Reviewed: For every integer T >= 1, the real parameter c_T = 1/4 + 1/[16(T+1)^2] has critical iterates z_0 = 0 and z_(n+1) = z_n^2 + c_T in [0,17/32] for 0 <= n <= T, but an unbounded critical orbit.
• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: The exact-rational benchmark parameters generated from cutoffs [1, 4, 16, 64, 256, 1024, 4096] have first critical-orbit escape iterations [23, 61, 212, 815, 3228, 12879, 51482], with all 7 counts certified and matched by integer dyadic enclosures and Arb ball arithmetic, and all 49 exact-rational control checks passing.

Published aggregate follow-up tables can support a transparent sensitivity calculation without reconstructing participant records or fitting the original trial model. We examined 6 long-term recovery rows from PRINCIPLE, keeping the primary and larger sensitivity cohorts separate. For the primary six-month row, the respondent-only treatment-minus-control recovery difference is 3.071 percentage points. Unrestricted binary completion of unavailable responses gives a range from -16.54 to 21.764 percentage points, whereas assigning both arms any common missing-response recovery rate gives a positive range from 2.329 to 2.896 percentage points. These are conditional bounds, not confidence intervals. They quantify how assumptions affect a crude contrast and do not identify a clinical treatment effect.

• Published.Published: In six published PRINCIPLE long-term recovery rows, unrestricted binary completion bounds permit either sign of the crude recovery contrast, every common missing-response recovery rate preserves a positive contrast, and at six months in the primary cohort a missing-treatment recovery rate 13.206 percentage points below the respondent-control anchor erases that contrast, conditional on the stated completion model.

We tested whether explicit flare and artifact controls improve recovery of simulated stellar self-lensing pulses in public Transiting Exoplanet Survey Satellite (TESS) light curves. A preregistered sample contains 100 stars, with 40 used for development and 60 for evaluation. At the same empirical background-trigger fraction of 10%, the development-selected controls recovered 269 of 540 pulses (49.8%), versus 239 (44.3%) for the lensing-template baseline. The difference is 5.6 percentage points, with a paired target-bootstrap interval from -10.6 to 26.7 percentage points. This pilot leaves a recovery benefit unresolved. Background triggers are not labeled false alarms, and this study makes no astronomical discovery claim.

• Published.Published: In a preregistered 100-target TESS Sector 1 pilot with 40 development and 60 evaluation stars, the development-selected flare/artifact control recovered 269/540 newly localized injected pulses versus 239/540 for the baseline at 6/60 un-injected target triggers per method, a 5.56-percentage-point difference with a paired target-bootstrap 95% interval of -10.56 to 26.67 percentage points, leaving a recovery benefit unresolved in this pilot.

Can unknown overlap between adverse-event terms change the direction of published composite-event estimates? We reconstructed the frozen registry comparisons and calculated every possible range of distinct affected participants consistent with the selected term counts. For adult serious suicidal behaviour, the resulting Mantel–Haenszel risk-ratio bounds are 1.712 to 2.1962; for adult serious suicidality, 1.2154 to 1.8476. The corresponding pediatric bounds are 1.0045 to 1.4773 and 1.8144 to 2.8091. All remain above the null. Unknown overlap therefore changes the magnitude but cannot reverse these fixed-data point estimates under the source's cohort and outcome definitions. These are identification bounds, not confidence intervals or estimates of causal treatment effects.

• Published, Reproduced.Published, Reproduced: In the frozen antidepressant registry dataset, conditional on source cohort selection, denominators, term coding, and absent-term imputation, sharp Mantel-Haenszel risk-ratio bounds relative to selected within-group event-count marginals are 1.7120261533 to 2.1961879882 for adult serious suicidal behaviour, 1.2154409158 to 1.8475901940 for adult serious suicidality, 1.0045047792 to 1.4773331886 for pediatric serious behaviour, and 1.8144436696 to 2.8090979871 for pediatric serious suicidality. Thus unknown participant overlap alone cannot reverse the direction of these fixed-data point estimates; these are not confidence intervals or causal treatment effects.

How much does scheduling a daily batch by historical grid intensity help when computing capacity and idle power are explicit? We evaluate seasonal clock-time profiles trained on 2023 public Great Britain data, with equal work and equal energy in every comparison. At 50% utilization, assigned carbon falls by 11.63% in 2024 and 12.81% in 2025 relative to uniform processing. Setting idle power to 50% of maximum power reduces these advantages to 3.88% and 4.27%. Some dates have higher assigned carbon after shifting. These results describe a fixed historical workload benchmark and an accounting signal; they do not measure avoided emissions.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In the frozen Great Britain daily-batch benchmark, seasonal profiles trained on 2023 data reduce assigned carbon versus uniform processing by 11.63% and 12.81% at 50% utilization with zero idle power in 2024 and 2025, but by 3.88% and 4.27% when idle power is 50% of maximum; at 87.5% utilization with zero idle power the reductions are 3.37% and 3.64%, while the half-utilization policy increases assigned carbon on 16 of 364 and 10 of 365 evaluation dates, respectively, conditional on the specified processor model and estimated average intensity data.

Can a simple electricity-use schedule transfer across years? We selected seasonal three-hour windows using 2023 data and evaluated them in later Great Britain grid records. Relative to midnight use, assigned average carbon intensity was 5.78% lower in 2024 and 13.15% lower in 2025. The schedule performed worse on 137 and 111 days, respectively. A single year-round window did not improve both years. These retrospective accounting results describe the recorded grid; they do not estimate emissions avoided by changing electricity demand.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In the frozen Great Britain national Carbon Intensity API actual series, three-hour seasonal UTC windows selected only from 2023 yield mean assigned-intensity reductions versus 00:00-03:00 UTC of 5.778479% across 364 complete days in 2024 and 13.150070% across 365 days in 2025, compared with -9.430428% and 2.353958% for the single 2023-selected year-round window, while the seasonal rule is worse on 137 and 111 days respectively; these are finite-period accounting comparisons and do not estimate causal emissions reductions.

Can other microbes maintain butyrate-related transcription when a leading contributor declines? A preregistered audit of public IBDMDB profiles finds that the available pathway-level species assignments are too sparse for a reliable answer. Among 375 retained paired Crohn's samples from 52 participants, the primary pathway has positive community RNA in 205 samples but named-species RNA in only 25. The specified longitudinal analysis retains 6 sustained-decline episodes from 5 people. Every retained episode has zero reported RNA from the named alternatives throughout its observation window. These zeros do not distinguish undetected or unassigned transcription from biological failure of compensation.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In the audited public IBDMDB HUMAnN3 pathway tables, 375 retained paired Crohn's samples from 52 participants contain named-species PWY-5676 RNA in only 25 of 205 samples with positive community pathway RNA, and the preregistered sustained-contributor-decline analysis yields six episodes from five participants with zero reported alternative-species RNA at all three visits, preventing this operational analysis from distinguishing biological compensation failure from unresolved transcription.