Many extensions of the Standard Model predict the production of dark matter particles at the LHC. Sufficiently light dark matter particles may be produced in decays of the Higgs boson that would appear invisible to th...
A search for new phenomena giving rise to pairs of opposite electrically charged muons with impact parameters in the millimeter range is presented, using 139 fb−1 of s=13 TeV pp collision data from the ATLAS detector ...
The ATLAS detector at the Large Hadron Collider has been used to measure jet substructure modification and suppression in Pb+Pb collisions at a nucleon–nucleon center-of-mass energy sNN=5.02TeV in comparison with pro...
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The ATLAS detector at the Large Hadron Collider has been used to measure jet substructure modification and suppression in Pb+Pb collisions at a nucleon–nucleon center-of-mass energy sNN=5.02TeV in comparison with proton–proton (pp) collisions at s=5.02TeV. The Pb+Pb data, collected in 2018, have an integrated luminosity of 1.72nb−1, while the pp data, collected in 2017, have an integrated luminosity of 260pb−1. Jets used in this analysis are clustered using the anti-kt algorithm with a radius parameter R=0.4. The jet constituents, defined by both tracking and calorimeter information, are used to determine the angular scale rg of the first hard splitting inside the jet by reclustering them using the Cambridge–Aachen algorithm and employing the soft-drop grooming technique. The nuclear modification factor, RAA, used to characterize jet suppression in Pb+Pb collisions, is presented differentially in rg, jet transverse momentum, and in intervals of collision centrality. The RAA value is observed to depend significantly on jet rg. Jets produced with the largest measured rg are found to be twice as suppressed as those with the smallest rg in central Pb+Pb collisions. The RAA values do not exhibit a strong variation with jet pT in any of the rg intervals. The rg and pT dependence of jet RAA is qualitatively consistent with a picture of jet quenching arising from coherence and provides the most direct evidence in support of this approach.
Measurements of joint-polarisation states of W and Z gauge bosons in W±Z production are presented. The data set used corresponds to an integrated luminosity of 139 fb−1 of proton–proton collisions at a centre-of...
A search for nonresonant Higgs boson pair production in the bb¯bb¯ final state is presented. The analysis uses 126 fb−1 of pp collision data at s=13 TeV collected with the ATLAS detector at the Large Hadro...
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A search for nonresonant Higgs boson pair production in the bb¯bb¯ final state is presented. The analysis uses 126 fb−1 of pp collision data at s=13 TeV collected with the ATLAS detector at the Large Hadron Collider, and targets both the gluon-gluon fusion and vector-boson fusion production modes. No evidence of the signal is found and the observed (expected) upper limit on the cross section for nonresonant Higgs boson pair production is determined to be 5.4 (8.1) times the Standard Model predicted cross section at 95% confidence level. Constraints are placed on modifiers to the HHH and HHVV couplings. The observed (expected) 2σ constraints on the HHH coupling modifier, κλ, are determined to be [−3.5,11.3] ([−5.4,11.4]), while the corresponding constraints for the HHVV coupling modifier, κ2V, are [−0.0,2.1] ([−0.1,2.1]). In addition, constraints on relevant coefficients are derived in the context of the Standard Model effective field theory and Higgs effective field theory, and upper limits on the HH production cross section are placed in seven Higgs effective field theory benchmark scenarios.
Searches for the exclusive decays of the Higgs boson to an ω meson and a photon or a K⁎ meson and a photon can probe flavour-conserving and flavour-violating Higgs boson couplings to light quarks, respectively. Searc...
To investigate the genetic basis of type 2 diabetes (T2D) to high resolution, the GoT2D and T2D-GENES consortia catalogued variation from whole-genome sequencing of 2,657 European individuals and exome sequencing of 1...
To investigate the genetic basis of type 2 diabetes (T2D) to high resolution, the GoT2D and T2D-GENES consortia catalogued variation from whole-genome sequencing of 2,657 European individuals and exome sequencing of 12,940 individuals of multiple ancestries. Over 27M SNPs, indels, and structural variants were identified, including 99% of low-frequency (minor allele frequency [MAF] 0.1-5%) non-coding variants in the whole-genome sequenced individuals and 99.7% of low-frequency coding variants in the whole-exome sequenced individuals. Each variant was tested for association with T2D in the sequenced individuals, and, to increase power, most were tested in larger numbers of individuals (>80% of low-frequency coding variants in ~82 K Europeans via the exome chip, and ~90% of low-frequency non-coding variants in ~44 K Europeans via genotype imputation). The variants, genotypes, and association statistics from these analyses provide the largest reference to date of human genetic information relevant to T2D, for use in activities such as T2D-focused genotype imputation, functional characterization of variants or genes, and other novel analyses to detect associations between sequence variation and T2D.
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