229 research outputs found
COVID-19 Misinformation Trends in Australia: Prospective Longitudinal National Survey.
- Author
- Publication venue
- 'JMIR Publications Inc.'
- Publication date
- 01/01/2021
- Field of study
Background: Misinformation about COVID-19 is common and has been spreading rapidly across the globe through social media platforms and other information systems. Understanding what the public knows about COVID-19 and identifying beliefs based on misinformation can help shape effective public health communications to ensure efforts to reduce viral transmission are not undermined.
Objective: This study aimed to investigate the prevalence and factors associated with COVID-19 misinformation in Australia and their changes over time.
Methods: This prospective, longitudinal national survey was completed by adults (18 years and above) across April (n=4362), May (n=1882), and June (n=1369) 2020.
Results: Stronger agreement with misinformation was associated with younger age, male gender, lower education level, and language other than English spoken at home (P<.01 for all). After controlling for these variables, misinformation beliefs were significantly associated (P<.001) with lower levels of digital health literacy, perceived threat of COVID-19, confidence in government, and trust in scientific institutions. Analyses of specific government-identified misinformation revealed 3 clusters: prevention (associated with male gender and younger age), causation (associated with lower education level and greater social disadvantage), and cure (associated with younger age). Lower institutional trust and greater rejection of official government accounts were associated with stronger agreement with COVID-19 misinformation.
Conclusions: The findings of this study highlight important gaps in communication effectiveness, which must be addressed to ensure effective COVID-19 prevention
Search for new phenomena in final states with an energetic jet and large missing transverse momentum in pp collisions at √ s = 8 TeV with the ATLAS detector
- Author
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- Torres RET
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- Vaidya A
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- Vaniachine A
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- Vazquez CJB
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- Vukotic I
- Wagner P
- Wagner W
- Wagner-Kuhr J
- Wahdan S
- Wahlberg H
- Walbrecht VM
- Walder J
- Walker R
- Walker SD
- Walkowiak W
- Wallangen V
- Wang AM
- Wang AZ
- Wang C
- Wang F
- Wang H
- Wang J
- Wang P
- Wang Q
- Wang R
- Wang R-J
- Wang SM
- Wang W
- Wang WT
- Wang WX
- Wang Y
- Wang Z
- Wanotayaroj C
- Warburton A
- Ward CP
- Wardrope DR
- Warrack N
- Washbrook A
- Watson AT
- Watson MF
- Watts G
- Waugh BM
- Webb AF
- Webb S
- Weber C
- Weber MS
- Weber SA
- Weber SM
- Weidberg AR
- Weingarten J
- Weirich M
- Weiser C
- Wells PS
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- Wenig S
- Wermes N
- Werner MD
- Wessels M
- Weston TD
- Whalen K
- Whallon NL
- Wharton AM
- White A
- White AS
- White MJ
- Whiteson D
- Whitmore BW
- Wiedenmann W
- Wiel C
- Wielers M
- Wieseotte N
- Wiglesworth C
- Wiik-Fuchs LAM
- Wilkens HG
- Wilkins LJ
- Williams HH
- Williams S
- Willis C
- Willocq S
- Wingerter-Seez I
- Winkels E
- Winklmeier F
- Winston OJ
- Winter BT
- Wittgen M
- Wobisch M
- Wolf A
- Wolf TMH
- Wolff R
- Wolker R
- Wollrath J
- Wolter MW
- Wolters H
- Wong VWS
- Woods NL
- Worm SD
- Wosiek BK
- Wozniak KW
- Wraight K
- Wu SL
- Wu X
- Wu Y
- Wyatt TR
- Wynne BM
- Xella S
- Xi Z
- Xia L
- Xiao X
- Xiotidis I
- Xu D
- Xu H
- Xu L
- Xu T
- Xu W
- Xu Z
- Yabsley B
- Yacoob S
- Yajima K
- Yallup DP
- Yamaguchi N
- Yamaguchi Y
- Yamamoto A
- Yamatani M
- Yamazaki T
- Yamazaki Y
- Yan Z
- Yang HJ
- Yang HT
- Yang S
- Yang T
- Yang X
- Yang Y
- Yao W-M
- Yap YC
- Yasu Y
- Yatsenko E
- Ye H
- Ye J
- Ye S
- Yeletskikh I
- Yexley MR
- Yigitbasi E
- Yildiz HD
- Yorita K
- Yoshihara K
- Young C
- Young CJS
- Yu J
- Yuan R
- Yue X
- Zaazoua M
- Zabinski B
- Zacharis G
- Zaffaroni E
- Zahreddine J
- Zaitsev AM
- Zakareishvili T
- Zakharchuk N
- Zambito S
- Zanzi D
- Zaripovas DR
- Zeissner S
- Zeitnitz C
- Zemaityte G
- Zeng JC
- Zenin O
- Zenis T
- Zerwas D
- Zgubic M
- Zhang B
- Zhang DF
- Zhang G
- Zhang H
- Zhang J
- Zhang L
- Zhang M
- Zhang R
- Zhang S
- Zhang X
- Zhang Y
- Zhang Z
- Zhao P
- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
- Zhou B
- Zhou C
- Zhou M
- Zhou MS
- Zhou N
- Zhou Y
- Zhu C
- Zhu CG
- Zhu H
- Zhu HL
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine N
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zu Theenhausen HM
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Results of a search for new phenomena in final states with an energetic jet and large missing transverse momentum are reported. The search uses 20.3 fb−1 of √ s = 8 TeV data collected in 2012 with the ATLAS detector at the LHC. Events are required to have at least one jet with pT > 120 GeV and no leptons. Nine signal regions are considered with increasing missing transverse momentum requirements between Emiss T > 150 GeV and Emiss T > 700 GeV. Good agreement is observed between the number of events in data and Standard Model expectations. The results are translated into exclusion limits on models with either large extra spatial dimensions, pair production of weakly interacting dark matter candidates, or production of very light gravitinos in a gauge-mediated supersymmetric model. In addition, limits on the production of an invisibly decaying Higgs-like boson leading to similar topologies in the final state are presente
The molecular phylogeny of eph receptors and ephrin ligands
- Author
- A Barrios
- A Smith
- B Monschau
- BM Degnan
- C Larroux
- CE Krull
- DA Feldheim
- Dan O Mellott
- DM Brantley-Sieders
- Eph Nomenclature Committee
- F Delsuc
- F Helmbacher
- G Olivieri
- H Iwamasa
- H Suga
- H Suga
- HU Cheng
- HU Wang
- ID Chin-Sang
- J Eberhart
- J Eberhart
- J Gu
- J Walkenhorst
- JO Pickles
- JP Himanen
- K Patel
- KK Murai
- L Durbin
- LM Bianchi
- M Araujo
- M Araujo
- M Henkemeyer
- MA Nieto
- N Becker
- N Wada
- NW Gale
- P Ganju
- P Kury
- PM Helbling
- Q Xu
- Q Xu
- R Dearborn Jr
- R Hindges
- RH Adams
- Robert D Burke
- SE George
- SJ Bourlat
- SP Leys
- SS Gerety
- T Bossing
- U Drescher
- V Picco
- Y Satou
- Publication venue
- BioMed Central
- Publication date
- 01/01/2008
- Field of study
<p>Abstract</p> <p>Background</p> <p>The tissue distributions and functions of Eph receptors and their ephrin ligands have been well studied, however less is known about their evolutionary history. We have undertaken a phylogenetic analysis of Eph receptors and ephrins from a number of invertebrate and vertebrate species.</p> <p>Results</p> <p>Our findings indicate that Eph receptors form three major clades: one comprised of non-chordate and cephalochordate Eph receptors, a second comprised of urochordate Eph receptors, and a third comprised of vertebrate Eph receptors. Ephrins, on the other hand, fall into either a clade made up of the non-chordate and cephalochordate ephrins plus the urochordate and vertebrate ephrin-Bs or a clade made up of the urochordate and vertebrate ephrin-As.</p> <p>Conclusion</p> <p>We have concluded that Eph receptors and ephrins diverged into A and B-types at different points in their evolutionary history, such that primitive chordates likely possessed an ancestral ephrin-A and an ancestral ephrin-B, but only a single Eph receptor. Furthermore, ephrin-As appear to have arisen in the common ancestor of urochordates and vertebrates, whereas ephrin-Bs have a more ancient bilaterian origin. Ancestral ephrin-B-like ligands had transmembrane domains; as GPI anchors appear to have arisen or been lost at least 3 times.</p
The MAGIC trial: a pragmatic, multicentre, parallel, noninferiority, randomised trial of melatonin versus midazolam in the premedication of anxious children attending for elective surgery under general anaesthesia
- Author
- Albadri S
- Armstrong L
- Atkins S
- Babb M
- Biercamp C
- Biggs K
- Bolt R
- Bradburn M
- Buckley J
- Child-Cavill J
- Clarkson J
- Cope S
- Crawley S
- Deery C
- Dimairo M
- Duro E
- Eissa A
- Evans C
- Flight L
- Gath J
- Gavel G
- Geary T
- Gilchrist F
- Gopal P
- Hall J
- Herbert E
- Hutchence K
- Hyslop MC
- Ireland N
- Kettle J
- Khandelwal P
- Kukreja P
- Leeuwenberg I
- Limb J
- Loban A
- Marshman Z
- Masip N
- Mellor K
- Moores A
- Norrington AC
- Oshan V
- Papaioannou DE
- Paton RH
- Pickles E
- Ray J
- Rodd H
- Rolfe S
- Sheldon E
- Simmonds R
- Smith R
- Sundar A
- Thomason A
- Totton N
- Vernazza C
- Waterhouse S
- Wilson G
- Wilson MJ
- Yates J
- Young T
- Publication venue
- Elsevier Ltd
- Publication date
- 01/01/2023
- Field of study
\ua9 2023 The Author(s)Background: Child anxiety before general anaesthesia and surgery is common. Midazolam is a commonly used premedication to address this. Melatonin is an alternative anxiolytic, however trials evaluating its efficacy in children have delivered conflicting results. Methods: This multicentre, double-blind randomised trial was performed in 20 UK NHS Trusts. A sample size of 624 was required to declare noninferiority of melatonin. Anxious children, awaiting day case elective surgery under general anaesthesia, were randomly assigned 1:1 to midazolam or melatonin premedication (0.5 mg kg−1, maximum 20 mg) 30 min before transfer to the operating room. The primary outcome was the modified Yale Preoperative Anxiety Scale-Short Form (mYPAS-SF). Secondary outcomes included safety. Results are presented as n (%) and adjusted mean differences with 95% confidence intervals. Results: The trial was stopped prematurely (n=110; 55 per group) because of recruitment futility. Participants had a median age of 7 (6–10) yr, and 57 (52%) were female. Intention-to-treat and per-protocol modified Yale Preoperative Anxiety Scale-Short Form analyses showed adjusted mean differences of 13.1 (3.7–22.4) and 12.9 (3.1–22.6), respectively, in favour of midazolam. The upper 95% confidence interval limits exceeded the predefined margin of 4.3 in both cases, whereas the lower 95% confidence interval excluded zero, indicating that melatonin was inferior to midazolam, with a difference considered to be clinically relevant. No serious adverse events were seen in either arm. Conclusion: Melatonin was less effective than midazolam at reducing preoperative anxiety in children, although the early termination of the trial increases the likelihood of bias. Clinical trial registration: ISRCTN registry: ISRCTN18296119
Medical conditions in autism spectrum disorders
- Author
- A Bailey
- A Bailey
- A Battaglia
- A Goffin
- A Humphrey
- A Humphrey
- A Hunt
- A Kolevzon
- A Orrico
- A Pickles
- A Ronald
- A Ronald
- AE Silva
- AJ Wakefield
- AR Feinstein
- B Bakkaloglu
- BS Abrahams
- C Amiet
- C Dissanayake
- C Gillberg
- C Kato
- C Lord
- C Lord
- C Wolpert
- CM Durand
- CM Hultman
- CM Wolpert
- CR Marshall
- CS Loat
- D Stein
- DI Zafeiriou
- DS Wilkerson
- DZ Loesch
- E Bonora
- E Courchesne
- E Cryan
- E Fombonne
- E Redcay
- E Saemundsen
- E Saemundsen
- E Sponheim
- E Tierney
- E Tierney
- EA Varga
- EH Cook Jr
- EJ Glasson
- EM Dykens
- EY Deykin
- G Baird
- G Oliveira
- G Tripi
- GE Herman
- GM Repetto
- H Hara
- H Kakinuma
- H Stefansson
- HA Walker
- HG Kim
- HO Conn
- I Bukelis
- I Martin
- IC Gillberg
- J Feng
- J Gauthier
- J Loscalzo
- J Piven
- J Roohi
- J Sebat
- J Yan
- JA Finegan
- JA Thomas
- JA Vorstman
- JC Lewis
- JD Buxbaum
- JD Buxbaum
- JD Morrow
- JE Lainhart
- JE Roberts
- JH Miles
- JL Matson
- JL Nanson
- JN Levinson
- K Ouldim
- KI Goh
- KM Antshel
- KM Milner
- L Edelmann
- L Kayaalp
- L Potocki
- L Zwaigenbaum
- LA Weiss
- M Barton
- M Brimacombe
- M Kielinen
- M Koochek
- M Lauritsen
- M Rutter
- M Simic
- MA Sabry
- MA Sabry
- MC Phelan
- MF Lise
- MG Klug
- MW Veltman
- N Aa Van der
- N Juul-Dam
- NM Mukaddes
- NR Dennis
- O Mbarek
- P Bolton
- P Curatolo
- P Howlin
- P Szatmari
- Patrick F. Bolton
- PF Bolton
- PF Bolton
- PF Bolton
- PF Bolton
- PF Bolton
- PF Bolton
- PG Williams
- PJ Hagerman
- R Canitano
- R Moessner
- R Tuchman
- RA Muller
- RC Samaco
- RD Maimburg
- RH Mount
- RH Mount
- RJ Schroer
- S Barrett
- S Bishop
- S Bundey
- S Chakrabarti
- S Clifford
- S Deb
- S Jamain
- S Rineer
- S Smalley
- SE Mouridsen
- SL Christian
- SR Harris
- SW Harris
- T Deonna
- T Deonna
- T Martinsson
- T Marui
- T Sahoo
- T Sahoo
- TJ Ravel de
- TT MacDonald
- W Woodhouse
- WR Kates
- X Chen
- Y Nishimura
- Y Sugie
- Publication venue
- Springer US
- Publication date
- 01/01/2009
- Field of study
Autism spectrum disorder (ASD) is a behaviourally defined syndrome where the etiology and pathophysiology is only partially understood. In a small proportion of children with the condition, a specific medical disorder is identified, but the causal significance in many instances is unclear. Currently, the medical conditions that are best established as probable causes of ASD include Fragile X syndrome, Tuberous Sclerosis and abnormalities of chromosome 15 involving the 15q11-13 region. Various other single gene mutations, genetic syndromes, chromosomal abnormalities and rare de novo copy number variants have been reported as being possibly implicated in etiology, as have several ante and post natal exposures and complications. However, in most instances the evidence base for an association with ASD is very limited and largely derives from case reports or findings from small, highly selected and uncontrolled case series. Not only therefore, is there uncertainty over whether the condition is associated, but the potential basis for the association is very poorly understood. In some cases the medical condition may be a consequence of autism or simply represent an associated feature deriving from an underlying shared etiology. Nevertheless, it is clear that in a growing proportion of individuals potentially causal medical conditions are being identified and clarification of their role in etio-pathogenesis is necessary. Indeed, investigations into the causal mechanisms underlying the association between conditions such as tuberous sclerosis, Fragile X and chromosome 15 abnormalities are beginning to cast light on the molecular and neurobiological pathways involved in the pathophysiology of ASD. It is evident therefore, that much can be learnt from the study of probably causal medical disorders as they represent simpler and more tractable model systems in which to investigate causal mechanisms. Recent advances in genetics, molecular and systems biology and neuroscience now mean that there are unparalleled opportunities to test causal hypotheses and gain fundamental insights into the nature of autism and its development
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
- Author
- A Feher
- A Philippe
- AE Vine
- Agatino Battaglia
- AL Price
- Alexander Kolevzon
- Alison Merikangas
- Alistair T. Pagnamenta
- AM Persico
- Ana F. Sequeira
- Andrew Green
- Andrew Pickles
- Ann Le Couteur
- Ann P. Thompson
- Annemarie Poustka
- Annette Estes
- Anthony J. Bailey
- Anthony P. Monaco
- Astrid Vicente
- Barbara Parrini
- Bennett L. Leventhal
- Bernadette Roge
- Brett S. Abrahams
- Brian L. Yaspan
- Bridget A. Fernandez
- C Betancur
- Carine Mantoulan
- Catalina Betancur
- Catarina Correia
- Catherine Lord
- Cecilia Kim
- Christian R. Marshall
- Christina Corsello
- Christine M. Freitag
- Christopher Gillberg
- Christopher J. McDougle
- CM Durand
- CM Durand
- D Castermans
- D Pinto
- DA Kleinjan
- Dalila Pinto
- Daniel H. Geschwind
- David J. Posey
- DE Arking
- Denis C. Shields
- DV Zaykin
- Edwin H. Cook
- Eftichia Duketis
- Elena Bacchelli
- Elena Maestrini
- Ellen M. Wijsman
- Eric Fombonne
- F Dutheil
- F Hildebrandt
- FF Hamdan
- Fiorella Minopoli
- Fred Volkmar
- Frederico Duque
- Fritz Poustka
- Geraldine Dawson
- Gerard D. Schellenberg
- Ghazala K. Mirza
- Gillian Baird
- Gillian Hughes
- Gudrun Nygren
- Guiomar Oliveira
- GW Tam
- Hakon Hakonarson
- Helen McConachie
- Herman Van Engeland
- HG Kim
- Hilary Coon
- HY Zoghbi
- International Molecular Genetic Study of Autism Consortium (IMGSAC)
- Inês Sousa
- J Goudet
- J Hoshino
- JA Lamb
- Jacob A. S. Vorstman
- James S. Sutcliffe
- Jane McGrath
- Janine A. Lamb
- JC Barrett
- Jeff Munson
- Jeremy R. Parr
- Jiannis Ragoussis
- Jillian P. Casey
- Joachim Hallmayer
- Joana Almeida
- John B. Vincent
- John Gilbert
- John I. Nurnberger
- John Tsiantis
- Jonathan Green
- Jonathan L. Haines
- Joseph D. Buxbaum
- Joseph Piven
- Joseph T. Glessner
- Judith M. Conroy
- Judith Miller
- Kai Wang
- Katerina Papanikolaou
- Kathy White
- Kerstin Wittemeyer
- Kirsty Wing
- KP Lesch
- LA Thomas
- Latha Soorya
- LF Martin
- Lonnie Zwaigenbaum
- Louise Gallagher
- LR Cardon
- M Bahlo
- M Manchia
- M Nothnagel
- Marc Coutanche
- Maretha de Jonge
- Margaret A. Pericak-Vance
- Marion Leboyer
- Maïté Tauber
- MB Lauritsen
- MD Rubio
- MF Egan
- Michael Gill
- Michael L. Cuccaro
- Michael L. Rutter
- MJ Laan van der
- ML Sinkus
- MM Motazacker
- MS Yang
- Nadia Bolshakova
- Naisha Shah
- NP Shugalev
- Nuala Sykes
- Patrick F. Bolton
- Penny Farrar
- Peter Szatmari
- Phil Cali
- Raffaella Tancredi
- Regina Regan
- RH Flomen
- Richard Anney
- Richard Delorme
- Richard Holt
- Rita M. Cantor
- Roberta Igliozzi
- S Benko
- S Jamain
- S Purcell
- S Sahara
- SA Currenti
- Sabata C. Lund
- Sabine M. Klauck
- SB Gabriel
- Sean Brennan
- Sean Ennis
- Simon Wallace
- Stanley F. Nelson
- Stephen J. Guter
- Stephen W. Scherer
- Susan E. Folstein
- Susanne Thomson
- Suzanne Foley
- T Lencz
- TC Sudhof
- The International HapMap Consortium
- Thomas Bourgeron
- Thomas H. Wassink
- Tiago Magalhaes
- TL Yang
- Tom Berney
- Vanessa Hus
- Vera Stoppioni
- Veronica J. Vieland
- W Wong
- William M. McMahon
- XQ Liu
- Y Chen
- Y Jia
- Publication venue
- Springer-Verlag
- Publication date
- 01/01/2011
- Field of study
Autism spectrum disorder (ASD) is a highly heritable disorder of complex and heterogeneous aetiology. It is primarily characterized by altered cognitive ability including impaired language and communication skills and fundamental deficits in social reciprocity. Despite some notable successes in neuropsychiatric genetics, overall, the high heritability of ASD (~90%) remains poorly explained by common genetic risk variants. However, recent studies suggest that rare genomic variation, in particular copy number variation, may account for a significant proportion of the genetic basis of ASD. We present a large scale analysis to identify candidate genes which may contain low-frequency recessive variation contributing to ASD while taking into account the potential contribution of population differences to the genetic heterogeneity of ASD. Our strategy, homozygous haplotype (HH) mapping, aims to detect homozygous segments of identical haplotype structure that are shared at a higher frequency amongst ASD patients compared to parental controls. The analysis was performed on 1,402 Autism Genome Project trios genotyped for 1 million single nucleotide polymorphisms (SNPs). We identified 25 known and 1,218 novel ASD candidate genes in the discovery analysis including CADM2, ABHD14A, CHRFAM7A, GRIK2, GRM3, EPHA3, FGF10, KCND2, PDZK1, IMMP2L and FOXP2. Furthermore, 10 of the previously reported ASD genes and 300 of the novel candidates identified in the discovery analysis were replicated in an independent sample of 1,182 trios. Our results demonstrate that regions of HH are significantly enriched for previously reported ASD candidate genes and the observed association is independent of gene size (odds ratio 2.10). Our findings highlight the applicability of HH mapping in complex disorders such as ASD and offer an alternative approach to the analysis of genome-wide association data
Measurement of VH, H → b b ¯ production as a function of the vector-boson transverse momentum in 13 TeV pp collisions with the ATLAS detector
- Author
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- Zorbas TG
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- Zu Theenhausen HM
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2019
- Field of study
Cross-sections of associated production of a Higgs boson decaying into bottom-quark pairs and an electroweak gauge boson, W or Z, decaying into leptons are measured as a function of the gauge boson transverse momentum. The measurements are performed in kinematic fiducial volumes defined in the `simplified template cross-section' framework. The results are obtained using 79.8 fb-1 of proton-proton collisions recorded by the ATLAS detector at the Large Hadron Collider at a centre-of-mass energy of 13 TeV. All measurements are found to be in agreement with the Standard Model predictions, and limits are set on the parameters of an effective Lagrangian sensitive to modifications of the Higgs boson couplings to the electroweak gauge bosons
Measurement of the t¯tZ and t¯tW cross sections in proton-proton collisions at √s=13 TeV with the ATLAS detector
- Author
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- Aad G
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- Abbott DC
- Abdinov O
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- Zemaityte G
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- Zeng Q
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- Zhemchugov A
- Zheng Z
- Zhong D
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- Zhu CG
- Zhu H
- Zhu HL
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- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zur Nedden M
- Zwalinski L
- Álvarez Piqueras D
- Åkesson TPA
- Šfiligoj T
- Ženiš T
- Živković L
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2019
- Field of study
A measurement of the associated production of a top-quark pair (t¯t) with a vector boson (W, Z) in proton-proton collisions at a center-of-mass energy of 13 TeV is presented, using 36.1 fb−1 of integrated luminosity collected by the ATLAS detector at the Large Hadron Collider. Events are selected in channels with two same- or opposite-sign leptons (electrons or muons), three leptons or four leptons, and each channel is further divided into multiple regions to maximize the sensitivity of the measurement. The t¯tZ and t¯tW production cross sections are simultaneously measured using a combined fit to all regions. The best-fit values of the production cross sections are σt¯tZ=0.95±0.08stat±0.10syst pb and σt¯tW=0.87±0.13stat±0.14syst pb in agreement with the Standard Model predictions. The measurement of the t¯tZ cross section is used to set constraints on effective field theory operators which modify the t¯tZ vertex
Search for heavy neutral Higgs bosons produced in association with b-quarks and decaying into b-quarks at root s=13 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abbott DC
- Abdinov O
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abud AA
- Abulaiti Y
- Acharya BS
- Achkar B
- Adachi S
- Adam L
- Adamczyk L
- Adamek L
- Adelman J
- Adersberger M
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahmadov F
- Ahmed WS
- Ai X
- Aielli G
- Akatsuka S
- Akesson TPA
- Akilli E
- Akimov A
- Al Khoury K
- Alberghi GL
- Albert J
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexandre D
- Alexopoulos T
- Alfonsi A
- Alhroob M
- Ali B
- Alimonti G
- Alison J
- Alkire SP
- Allaire C
- Allbrooke BMM
- Allen BW
- Allport PP
- Aloisio A
- Alonso A
- Alonso F
- Alpigiani C
- Alshehri AA
- Alvarez Estevez M
- Alvarez Piqueras D
- Alviggi MG
- Amaral Coutinho Y
- Ambler A
- Ambroz L
- Amelung C
- Amidei D
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- Zhemchugov A
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- Zu Theenhausen HM
- Zwalinski L
- Publication venue
- AMER PHYSICAL SOC
- Publication date
- 13/08/2020
- Field of study
A search for heavy neutral Higgs bosons produced in association with one or two
b
-quarks and decaying to
b
-quark pairs is presented using
27.8
fb
−
1
of
√
s
=
13
TeV
proton-proton collision data recorded by the ATLAS detector at the Large Hadron Collider during 2015 and 2016. No evidence of a signal is found. Upper limits on the heavy neutral Higgs boson production cross section times its branching ratio to
b
¯
b
are set, ranging from 4.0 to 0.6 pb at 95% confidence level over a Higgs boson mass range of 450 to 1400 GeV. Results are interpreted within the two-Higgs-doublet model and the minimal supersymmetric Standard Model
Measurement of single top-quark production in association with a W boson in the single-lepton channel at \sqrt{s} = 8\,\text {TeV} with the ATLAS detector
- Author
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- Zimmermann S
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- Publication venue
- 'Springer Fachmedien Wiesbaden GmbH'
- Publication date
- 01/01/2021
- Field of study
The production cross-section of a top quark in association with a W boson is measured using proton–proton collisions at \sqrt{s} = 8\,\text {TeV}. The dataset corresponds to an integrated luminosity of 20.2\,\text {fb}^{-1}, and was collected in 2012 by the ATLAS detector at the Large Hadron Collider at CERN. The analysis is performed in the single-lepton channel. Events are selected by requiring one isolated lepton (electron or muon) and at least three jets. A neural network is trained to separate the tW signal from the dominant t{\bar{t}} background. The cross-section is extracted from a binned profile maximum-likelihood fit to a two-dimensional discriminant built from the neural-network output and the invariant mass of the hadronically decaying W boson. The measured cross-section is \sigma _{tW} = 26 \pm 7\,\text {pb}, in good agreement with the Standard Model expectation
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