142 research outputs found
Quality Assurance and its impact on ovarian visualisation rates in the multicentre United Kingdom Collaborative Trial of Ovarian Cancer Screening (UKCTOCS)
- Author
- Publication venue
- Publication date
- 19/06/2015
- Field of study
OBJECTIVE: To describe the quality assurance (QA) processes and their impact on visualisation of postmenopausal ovaries in the ultrasound arm of a multicentre ovarian cancer screening trial. METHODS: In UKCTOCS, 50,640 women aged 50-74 at recruitment were randomised to the ultrasound arm and underwent annual transvaginal scans. QA processes were developed during the course of the trial and included regular monitoring of Visualisation Rate (VR) of right ovary. Non-subjective factors previously identified as impacting on VR of right ovary were included in a generalised estimating equation(GEE) model for binary outcomes to enable comparison of observed versus adjusted VR between individual sonographers who had undertaken >1000scans on trial /centres. Analysis of annual VR of sonographers / centres was undertaken. RESULTS: Between June 2001 and December 2010, across 13 centres, 48230 (of 50639) women attended for 270035 annual transvaginal scans. One or both ovaries were seen in 84.5% (228145/270035) of scans. The observed VR of the right ovary was 72.7% (196426/270035). For the 78 sonographers included in the model, the median difference between observed and adjusted VR was 2% (range 0-8%) and median change in rank was 3 (range 0-18). For the 13 centres, the median difference between observed versus adjusted VR was 0% (range 0-2%) with no change in ranking. The median adjusted VR for sonographers was 73% (IQR 65-82%) and for centres was 74.7% (IQR 67.1-79.0%). Despite increasing age of the cohort, there was a steady decrease in the number of sonographers with VR80% (14.3% in 2002 to 40.8 % in 2010). Median centre VR increased from 65.5% (range 55.7-81.0%) in 2001 to 80.3% (range74.5%-90.9%) in 2010. CONCLUSIONS: A robust QA programme can improve visualisation of postmenopausal ovaries and is an essential component of ultrasound-based ovarian cancer screening trials. While VR should be adjusted for non-subjective factors that impact on ovarian visualisation, subjective factors are likely to be the largest contributors to VR differences
The Manchester International Consensus Group recommendations for the management of gynecological cancers in Lynch syndrome.
- Author
- Arends MJ
- Bolton J
- Bosse T
- Burn J
- Church D
- Cornes JM
- Crawford R
- Crosbie EJ
- Donnelly K
- Eccles D
- Edmondson RJ
- Evans DG
- Frayling IM
- Ghaem-Maghami S
- Gollop P
- Goodman S
- Hampel H
- Hodgson S
- Kauff ND
- Kitchener HC
- Kitson SJ
- Lalloo F
- Lowry A
- Manchanda R
- McMahon RFT
- Mcvey RJ
- Menon U
- Miles T
- Moller P
- Monahan KJ
- Monahan KJ
- Moslein G
- Rosenthal A
- Ryan NAJ
- Sanchez AA
- Sasieni P
- Seif MW
- Singh N
- Skarrott P
- Snowsill TM
- Steele R
- Stormoken A
- Stringfellow H
- Tischkowitz M
- Wallace A
- Whyte L
- Wilkinson N
- Wilson G
- Wilson J
- Wood N
- Publication venue
- Genet Med
- Publication date
- 01/01/2019
- Field of study
PURPOSE: There are no internationally agreed upon clinical guidelines as to which women with gynecological cancer would benefit from Lynch syndrome screening or how best to manage the risk of gynecological cancer in women with Lynch syndrome. The Manchester International Consensus Group was convened in April 2017 to address this unmet need. The aim of the Group was to develop clear and comprehensive clinical guidance regarding the management of the gynecological sequelae of Lynch syndrome based on existing evidence and expert opinion from medical professionals and patients. METHODS: Stakeholders from Europe and North America worked together over a two-day workshop to achieve consensus on best practice. RESULTS: Guidance was developed in four key areas: (1) whether women with gynecological cancer should be screened for Lynch syndrome and (2) how this should be done, (3) whether there was a role for gynecological surveillance in women at risk of Lynch syndrome, and (4) what preventive measures should be recommended for women with Lynch syndrome to reduce their risk of gynecological cancer. CONCLUSION: This document provides comprehensive clinical guidance that can be referenced by both patients and clinicians so that women with Lynch syndrome can expect and receive appropriate standards of care
Ovarian cancer population screening and mortality after long-term follow-up in the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS): a randomised controlled trial
- Author
- Publication venue
- 'Elsevier BV'
- Publication date
- 12/05/2021
- Field of study
Background
Ovarian cancer continues to have a poor prognosis with the majority of women diagnosed with advanced disease. Therefore, we undertook the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS) to determine if population screening can reduce deaths due to the disease. We report on ovarian cancer mortality after long-term follow-up in UKCTOCS.
Methods
In this randomised controlled trial, postmenopausal women aged 50–74 years were recruited from 13 centres in National Health Service trusts in England, Wales, and Northern Ireland. Exclusion criteria were bilateral oophorectomy, previous ovarian or active non-ovarian malignancy, or increased familial ovarian cancer risk. The trial management system confirmed eligibility and randomly allocated participants in blocks of 32 using computer generated random numbers to annual multimodal screening (MMS), annual transvaginal ultrasound screening (USS), or no screening, in a 1:1:2 ratio. Follow-up was through national registries. The primary outcome was death due to ovarian or tubal cancer (WHO 2014 criteria) by June 30, 2020. Analyses were by intention to screen, comparing MMS and USS separately with no screening using the versatile test. Investigators and participants were aware of screening type, whereas the outcomes review committee were masked to randomisation group. This study is registered with ISRCTN, 22488978, and ClinicalTrials.gov, NCT00058032.
Findings
Between April 17, 2001, and Sept 29, 2005, of 1 243 282 women invited, 202 638 were recruited and randomly assigned, and 202 562 were included in the analysis: 50 625 (25·0%) in the MMS group, 50 623 (25·0%) in the USS group, and 101 314 (50·0%) in the no screening group. At a median follow-up of 16·3 years (IQR 15·1–17·3), 2055 women were diagnosed with tubal or ovarian cancer: 522 (1·0%) of 50 625 in the MMS group, 517 (1·0%) of 50 623 in the USS group, and 1016 (1·0%) of 101 314 in the no screening group. Compared with no screening, there was a 47·2% (95% CI 19·7 to 81·1) increase in stage I and 24·5% (−41·8 to –2·0) decrease in stage IV disease incidence in the MMS group. Overall the incidence of stage I or II disease was 39·2% (95% CI 16·1 to 66·9) higher in the MMS group than in the no screening group, whereas the incidence of stage III or IV disease was 10·2% (−21·3 to 2·4) lower. 1206 women died of the disease: 296 (0·6%) of 50 625 in the MMS group, 291 (0·6%) of 50 623 in the USS group, and 619 (0·6%) of 101 314 in the no screening group. No significant reduction in ovarian and tubal cancer deaths was observed in the MMS (p=0·58) or USS (p=0·36) groups compared with the no screening group.
Interpretation
The reduction in stage III or IV disease incidence in the MMS group was not sufficient to translate into lives saved, illustrating the importance of specifying cancer mortality as the primary outcome in screening trials. Given that screening did not significantly reduce ovarian and tubal cancer deaths, general population screening cannot be recommended.
Funding
National Institute for Health Research, Cancer Research UK, and The Eve Appeal
The Development of Therapeutic Antibodies That Neutralize Homologous and Heterologous Genotypes of Dengue Virus Type 1
- Author
- AJ Johnson
- AJ McCoy
- AP Goncalvez
- AP Goncalvez
- AP Goncalvez
- AP Goncalvez
- B Lin
- B Tassaneetrithep
- Bimmi Shrestha
- BM Kaufman
- Christopher A. Nelson
- CJ Lai
- D Ben-Nathan
- D Ben-Nathan
- D Cecilia
- Daved H. Fremont
- DE Volk
- DS Burke
- DW Beasley
- DW Beasley
- DW Vaughn
- E Harlow
- E Mehlhop
- E Navarro-Sanchez
- E Pokidysheva
- E Simantini
- EA Gould
- EC Holmes
- ET Boder
- ET Boder
- EY Jones
- F Megret
- FA Rey
- G Nybakken
- GD Gromowski
- GD Gromowski
- GJ Barton
- H Sultana
- I Valdes
- IL Serafin
- IM Yu
- IN Shindyalov
- J Kimura-Kuroda
- JA Mondotte
- James D. Brien
- JD Morrey
- JD Morrey
- JH Chu
- JJ Schlesinger
- JT Roehrig
- JT Roehrig
- JT Roehrig
- K Hiramatsu
- K Matsui
- Katie M. O'Brien
- KC Leitmeyer
- L Hermida
- L Li
- L Potterton
- LH Gould
- M Engle
- M Throsby
- MD Sanchez
- MD Winn
- Melissa A. Edeling
- Michael S. Diamond
- MJ Zhang
- MR Vogt
- MS Diamond
- MS Diamond
- MS Diamond
- MV Cherrier
- MW Brandriss
- O Lisova
- P Thullier
- PJ Klasse
- PM Armstrong
- R Rajamanonmani
- R Rico-Hesse
- R Rico-Hesse
- R Rico-Hesse
- R Rico-Hesse
- Ralph S. Baric
- RJ Kuhn
- S Bhardwaj
- S Chen
- S Gollins
- S Sukupolvi-Petty
- S Yu
- S. Kyle Austin
- SA Seif
- SB Halstead
- SB Halstead
- SB Halstead
- SC Wu
- SJ Balsitis
- SM Lok
- Soila Sukupolvi-Petty
- SY Xiao
- Syd Johnson
- T Oliphant
- T Oliphant
- T Oliphant
- T Trirawatanapong
- Taekyung Kim
- TC Pierson
- TC Pierson
- TJ Chambers
- TP Monath
- TR Kreil
- V Nayak
- W Kabsch
- W Minor
- W Zhang
- WD Crill
- WD Crill
- WD Crill
- WD Crill
- WM Wahala
- Y Modis
- Y Modis
- Y Zhang
- YC Chen
- Z Chen
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
Antibody protection against flaviviruses is associated with the development of neutralizing antibodies against the viral envelope (E) protein. Prior studies with West Nile virus (WNV) identified therapeutic mouse and human monoclonal antibodies (MAbs) that recognized epitopes on domain III (DIII) of the E protein. To identify an analogous panel of neutralizing antibodies against DENV type-1 (DENV-1), we immunized mice with a genotype 2 strain of DENV-1 virus and generated 79 new MAbs, 16 of which strongly inhibited infection by the homologous virus and localized to DIII. Surprisingly, only two MAbs, DENV1-E105 and DENV1-E106, retained strong binding and neutralizing activity against all five DENV-1 genotypes. In an immunocompromised mouse model of infection, DENV1-E105 and DENV1-E106 exhibited therapeutic activity even when administered as a single dose four days after inoculation with a heterologous genotype 4 strain of DENV-1. Using epitope mapping and X-ray crystallographic analyses, we localized the neutralizing determinants for the strongly inhibitory MAbs to distinct regions on DIII. Interestingly, sequence variation in DIII alone failed to explain disparities in neutralizing potential of MAbs among different genotypes. Overall, our experiments define a complex structural epitope on DIII of DENV-1 that can be recognized by protective antibodies with therapeutic potential
Precise determination of the mass of the Higgs boson and tests of compatibility of its couplings with the standard model predictions using proton collisions at 7 and 8 TeV
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abdulsalam A
- Acosta D
- Acosta JG
- Adair A
- Adam W
- Adams JR
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adzic P
- Afanasiev S
- Agapitos A
- Agram JL
- Ahmad A
- Ahmad M
- Ahuja S
- Akchurin N
- Akgun B
- Akin IV
- Albajar C
- Albayrak EA
- Albergo S
- Albrow M
- Alcaraz Maestre J
- Aldaya Martin M
- Alderweireldt S
- Aleksandrov A
- Alexander J
- Alimena J
- Alverson G
- Alves GA
- Amapane N
- Amsler C
- Anagnostou G
- Anderson I
- Anderson J
- Andrea J
- Andreev V
- Andreev Y
- Androsov K
- Antonelli L
- Antunovic Z
- Apanasevich L
- Apollinari G
- Appelt E
- Apresyan A
- Apyan A
- Arcidiacono R
- Arenton MW
- Argiro S
- Arneodo M
- Arora S
- Asavapibhop B
- Asawatangtrakuldee C
- Asin I
- Askew A
- Aslanoglou X
- Assran Y
- Ata M
- Attikis A
- Aubin A
- Auffray E
- Autermann C
- Auzinger G
- Avdeeva E
- Avery P
- Avetisyan A
- Avila C
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzolini V
- Azzurri P
- Baarmand MM
- Baber M
- Bacchetta N
- Bachmair F
- Bachtis M
- Baden A
- Baffioni S
- Bagliesi G
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Bakirci MN
- Ball AH
- Ban Y
- Banerjee S
- Banerjee S
- Bansal S
- Barbagli G
- Barberis E
- Barbieri R
- Bargassa P
- Barge D
- Baringer P
- Barker A
- Barnes VE
- Barnett BA
- Barney D
- Barone L
- Barth C
- Bartosik N
- Basegmez S
- Battilana C
- Bauerdick LA
- Baumgartel D
- Baus C
- Bayshev I
- Bean A
- Beauceron S
- Beaudette F
- Beaupere N
- Beernaert K
- Behnamian H
- Behr J
- Behrens U
- Beirão Da Cruz E Silva C
- Belforte S
- Beliy N
- Belknap DA
- Bell AJ
- Bell KW
- Bellan R
- Belloni A
- Beluffi C
- Belyaev A
- Belyaev A
- Benaglia A
- Bencze G
- Bendavid J
- Benedetti D
- Benelli G
- Benhabib L
- Beni N
- Benitez JF
- Benucci L
- Benussi L
- Benvenuti AC
- Beranek S
- Beretvas A
- Bergauer T
- Berger J
- Beri SB
- Bernardes CA
- Bernardini J
- Bernet C
- Berry D
- Berry E
- Berryhill J
- Bertl W
- Besancon M
- Betchart B
- Bethani A
- Betts RR
- Bhardwaj A
- Bhat PC
- Bhatnagar V
- Bhattacharya S
- Bhattacharya S
- Bhawandeep U
- Bhowmik S
- Bialkowska H
- Bian JG
- Bianchini L
- Bianco S
- Biasini M
- Bierwagen K
- Biino C
- Bilei GM
- Bilin B
- Bilki B
- Bilmis S
- Biselloa D
- Bitioukov S
- Blekman F
- Blobel V
- Bloch D
- Bloch P
- Bloom K
- Bluj M
- Blumenfeld B
- Blyweert S
- Boccali T
- Bocci A
- Bochenek J
- Bodek A
- Bodlak M
- Boimska B
- Bolla G
- Bolognesi S
- Bonacorsi D
- Bonato A
- Bondu O
- Bontenackels M
- Boos E
- Bornheim A
- Borras K
- Bortignon P
- Bortoletto D
- Bose S
- Bose T
- Botta C
- Boudoul G
- Bouhali O
- Bourilkov D
- Boutle S
- Bouvier E
- Bradmiller-Feld J
- Braibant-Giacomelli S
- Branca A
- Branson JG
- Breedon R
- Breto G
- Breuker H
- Brew C
- Brigliadori L
- Brigljevic V
- Brinkerhoff A
- Brinson J
- Brito L
- Broccolo G
- Brochero Cifuentes JA
- Brochet S
- Brodski M
- Brom JM
- Brona G
- Brooke JJ
- Brown RM
- Brownson E
- Brun H
- Bruner C
- Bruno G
- Buchmann MA
- Buchmuller O
- Bucinskaite I
- Bunichev V
- Bunin P
- Bunkowski K
- Bunn J
- Buontempo S
- Burgmeier A
- Burkett K
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- Busson P
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- Butler JN
- Butler PH
- Butz E
- Bylsma B
- Bäni L
- Böser C
- Cabrera A
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- Caebergs T
- Caillol C
- Cakir A
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- Calamba A
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- Calligaris L
- Calvert B
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- Campagnari C
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- Candelise V
- Canelli MF
- Cankocak K
- Capiluppi P
- Cappello G
- Cardaci M
- Carlin R
- Carlsmith D
- Carlson B
- Carrillo Montoya CA
- Carrillo Moreno S
- Cartiglia N
- Carvalho W
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- Casal B
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- Casimiro Linares E
- Castaldi R
- Castaneda Hernandez A
- Castello R
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- Castro A
- Caudron A
- Cavallari F
- Cavallo FR
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- Centis Vignali M
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- Cerati GB
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- Ciesielski R
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- Cimmino A
- Ciocci MA
- Cittolin S
- Ciulli V
- Civinini C
- Claes DR
- Clare R
- Clarida W
- Clarke C
- Clement E
- Clerbaux B
- CMS Collaboration
- Cockerill DJ
- Codispoti G
- Colafranceschi S
- Colaleo A
- Cole JE
- Colino N
- Collard C
- Colling D
- Contardo D
- Conte E
- Contreras-Campana C
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- Conway J
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- Cooper SI
- Cornelis T
- Correa Martins Junior M
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- Costantini S
- Costanza F
- Couderc F
- Coughlan JA
- Courbon B
- Cousins R
- Covarelli R
- Cowden C
- Cox B
- Cox PT
- Creanza D
- Cripps N
- Cristella L
- Crucy S
- Cuevas J
- Cuffiani M
- Cumalat JP
- Curry D
- Cussans D
- Custódio A
- Cutts D
- Cwiok M
- Czellar S
- D'Agnolo RT
- D'Alessandro R
- D'Alfonso M
- d'Enterria D
- D'Hondt J
- D'imperio G
- Da Costa EM
- Da Silveira GG
- Dabrowski A
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- Dahmes B
- Dahms T
- Dalchenko M
- Dall'Osso M
- Dallavalle GM
- Damgov J
- Danielson T
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- Daskalakis G
- Dasu S
- Daubie E
- Dauncey P
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- de Barbaro P
- De Boer W
- De Cosa A
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- De Jesus Damiao D
- De La Barca Sanchez MC
- De La Cruz B
- De La Cruz-Burelo E
- De Lentdecker G
- De Mattia M
- De Oliveira Martins C
- De Palma M
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- de Trocóniz JF
- De Visscher S
- De Wolf EA
- Degano A
- Deiters K
- Dejardin M
- Del Re D
- Delaere C
- Delannoy AG
- Delgado Peris A
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- Domínguez Vázquez D
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- Draeger AR
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- Field RD
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- Fiori F
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- Flacher H
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- Flix J
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- Flouris G
- Flowers K
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- Flucke G
- Flügge G
- Focardi E
- Folgueras S
- Fonseca De Souza S
- Fontaine JC
- Ford WT
- Forthomme L
- Foudas C
- Fouz MC
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- Frensch F
- Friedl M
- Friis E
- Frueboes T
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- Ganguly S
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- Garutti E
- Gary JW
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- Gasparini F
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- Genchev V
- Gennai S
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- Geralis T
- Gerber CE
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- Gershtein Y
- Geurts FJ
- Ghete VM
- Ghezzi A
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- Giacomelli P
- Giakoumopoulou VA
- Giammanco A
- Giassi A
- Giffels M
- Gigi D
- Gilbert A
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- Gilmore J
- Giordano D
- Giordano F
- Girgis S
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- Givernaud A
- Gizhko A
- Glege F
- Glushkov I
- Gninenko S
- Gobbo B
- Godinovic N
- Godshalk A
- Goebel K
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- Goldenzweig P
- Goldouzian R
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- Golovtsov V
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- Golutvin I
- Gomber B
- Gomez Ceballos G
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- Publication venue
- Publication date
- 01/01/2014
- Field of study
Peer reviewe
Search for Dark Matter and Supersymmetry with a Compressed Mass Spectrum in the Vector Boson Fusion Topology in Proton-Proton Collisions at root s=8 TeV
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abdulsalam A
- Abu Zeid S
- Ackert A
- Acosta D
- Acosta JG
- Adair A
- Adam W
- Adams JR
- Adams MR
- Adams T
- Adiguzel A
- Adzic P
- Agapitos A
- Aggleton R
- Agram J-L
- Ahmad A
- Ahmad M
- Ahmad M
- Ahmed I
- Ahuja S
- Akchurin N
- Akgun B
- Al-bataineh A
- Albergo S
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- Alcaraz Maestre J
- Aldaya Martin M
- Alderweireldt S
- Aldá Júnior WL
- Aleksandrov A
- Alexander J
- Alimena J
- Almond J
- Alunni Solestizi L
- Alverson G
- Alves FL
- Alves GA
- Alyari M
- Amapane N
- Amsler C
- Anagnostou G
- Anderson D
- Anderson I
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- Andreev V
- Andreev Yu
- Andrews MB
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- Apollinari G
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- Publication venue
- Publication date
- 01/01/2016
- Field of study
Peer reviewe
Search for strongly interacting massive particles generating trackless jets in proton-proton collisions at s = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abercrombie D
- Acharya H
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- Zenaiev O
- Zeuner WD
- Zghiche A
- Zhang F
- Zhang H
- Zhang J
- Zhang S
- Zhang W
- Zhang Y
- Zhang Z
- Zhao J
- Zhokin A
- Zhu DH
- Zhu RY
- Zich J
- Zielinski K
- Ziemons T
- Zientek M
- Zlebcik R
- Zoi I
- Zolkapli Z
- Zorbakir IS
- Zorbilmez C
- Zotto P
- Zou D
- Zucchetta A
- Zumerle G
- Zuo X
- Zuolo D
- Zygala L
- Álvarez Fernández A
- Österberg K
- Özçelik Ö
- Široký J
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
A search for dark matter in the form of strongly interacting massive particles (SIMPs) using the CMS detector at the LHC is presented. The SIMPs would be produced in pairs that manifest themselves as pairs of jets without tracks. The energy fraction of jets carried by charged particles is used as a key discriminator to suppress efficiently the large multijet background, and the remaining background is estimated directly from data. The search is performed using proton-proton collision data corresponding to an integrated luminosity of 16.1 fb - 1 , collected with the CMS detector in 2016. No significant excess of events is observed above the expected background. For the simplified dark matter model under consideration, SIMPs with masses up to 100 GeV are excluded and further sensitivity is explored towards higher masses
Combination of CMS searches for heavy resonances decaying to pairs of bosons or leptons
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullah WAT Wan
- Abdullin S
- Abercrombie D
- Acharya H
- Acosta D
- Acosta JG
- Adam W
- Adams MR
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- Ahmad W Haj
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- Xiao R
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- Yang UK
- Yang YC
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- Yazgan E
- Yetkin EA
- Yohay R
- Yoo HD
- Yoo J
- Yoon I
- Yu D
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- Yu I
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- Yumiceva F
- Yusli MN
- Zabi A
- Zaganidis N
- Zahid S
- Zaleski S
- Zalewski P
- Zanetti A
- Zanetti M
- Zarubin A
- Zarucki M
- Zecchinelli AG
- Zenaiev O
- Zenz SC
- Zeuner WD
- Zghiche A
- Zhang A
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- Zhokin A
- Zhu DH
- Zhu RY
- Zientek M
- Zlebcik R
- Zobec J
- Zoi I
- Zolkapli Z
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- Zuo X
- Zuolo D
- Publication venue
- Elsevier
- Publication date
- 01/01/2019
- Field of study
CMS Collaboration: et al.A statistical combination of searches for heavy resonances decaying to pairs of bosons or leptons is presented. The data correspond to an integrated luminosity of 35.9 fb collected during 2016 by the CMS experiment at the LHC in proton-proton collisions at a center-of-mass energy of 13 TeV. The data are found to be consistent with expectations from the standard model background. Exclusion limits are set in the context of models of spin-1 heavy vector triplets and of spin-2 bulk gravitons. For mass-degenerate W′ and Z′ resonances that predominantly couple to the standard model gauge bosons, the mass exclusion at 95% confidence level of heavy vector bosons is extended to 4.5 TeV as compared to 3.8 TeV determined from the best individual channel. This excluded mass increases to 5.0 TeV if the resonances couple predominantly to fermions.Individuals have received support from the Marie-Curie program and the European Research Council and Horizon 2020 Grant, contract Nos. 675440, 752730, and 765710 (European Union); the Programa Estatal de Fomento de la Investigación Científica y Técnica de Excelencia María de Maeztu, grant MDM-2015-0509 and the Programa Severo Ochoa del Principado de Asturias
Search for Higgs boson pair production in the gamma gamma b(b)over-bar final state in pp collisions at root s=13 TeV
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullah WAT Wan
- Abdullin S
- Abdulsalam A
- Abercrombie D
- Abu Zeid S
- Ackert A
- Acosta D
- Acosta JG
- Acosta M Vazquez
- Adam W
- Adams MR
- Adams T
- Adzic P
- Afanasiev S
- Agapitos A
- Agaras MN
- Aggarwal A
- Aggleton R
- Agram J-L
- Ahmad A
- Ahmad M
- Ahmad M
- Ahmed I
- Ahuja S
- Akbiyik M
- Akchurin N
- Akgun B
- Al-bataineh A
- Albajar C
- Albergo S
- Albert A
- Albrow M
- Alcaraz Maestre J
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- Publication venue
- Publication date
- 01/01/2018
- Field of study
A search is presented for the production of a pair of Higgs bosons, where one decays into two photons and the other one into a bottom quark-antiquark pair. The analysis is performed using proton-proton collision data at root s = 13 TeV recorded in 2016 by the CMS detector at the LHC, corresponding to an integrated luminosity of 35.9 fb(-1) . The results are in agreement with standard model (SM) predictions. In a search for resonant production, upper limits are set on the cross section for new spin-0 or spin-2 particles. For the SM-like nonresonant production hypothesis, the data exclude a product of cross section and branching fraction larger than 2.0 fb at 95% confidence level (CL), corresponding to about 24 times the SM prediction. Values of the effective Higgs boson self-coupling K X are constrained to be within the range -11 < K-lambda < 17 at 95% CL, assuming all other Higgs boson couplings are at their SM value. The constraints on K-lambda, are the most restrictive to date. (C) 2018 The Author(s). Published by Elsevier B.V.Peer reviewe
Measurement of the Zγ production cross section in pp collisions at 8 TeV and search for anomalous triple gauge boson couplings
- Author
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- Abbiendi G
- Abbrescia M
- Abdullin S
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- Acosta JG
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Open Access, Copyright CERN, for the benefit of the CMS Collaboration. Article funded by SCOAP3.Abstract: The cross section for the production of Zγ in proton-proton collisions at 8 TeV is measured based on data collected by the CMS experiment at the LHC corresponding to an integrated luminosity of 19.5 fb−1. Events with an oppositely-charged pair of muons or electrons together with an isolated photon are selected. The differential cross section as a function of the photon transverse momentum is measured inclusively and exclusively, where the exclusive selection applies a veto on central jets. The observed cross sections are compatible with the expectations of next-to-next-to-leading-order quantum chromodynamics. Limits on anomalous triple gauge couplings of ZZγ and Zγγ are set that improve on previous experimental results obtained with the charged lepton decay modes of the Z boson
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