138 research outputs found
A unified approach to quantifying algorithmic unfairness: Measuring individual & group unfairness via inequality indices
- Publication venue
- Proceedings of the ACM SIGKDD International Conference on Knowledge Discovery and Data Mining
- Publication date
- 01/01/2018
- Field of study
Discrimination via algorithmic decision making has received considerable
attention. Prior work largely focuses on defining conditions for fairness, but
does not define satisfactory measures of algorithmic unfairness. In this paper,
we focus on the following question: Given two unfair algorithms, how should we
determine which of the two is more unfair? Our core idea is to use existing
inequality indices from economics to measure how unequally the outcomes of an
algorithm benefit different individuals or groups in a population. Our work
offers a justified and general framework to compare and contrast the
(un)fairness of algorithmic predictors. This unifying approach enables us to
quantify unfairness both at the individual and the group level. Further, our
work reveals overlooked tradeoffs between different fairness notions: using our
proposed measures, the overall individual-level unfairness of an algorithm can
be decomposed into a between-group and a within-group component. Earlier
methods are typically designed to tackle only between-group unfairness, which
may be justified for legal or other reasons. However, we demonstrate that
minimizing exclusively the between-group component may, in fact, increase the
within-group, and hence the overall unfairness. We characterize and illustrate
the tradeoffs between our measures of (un)fairness and the prediction accuracy
IL-4 as a Repurposed Biological Drug for Myocardial Infarction through Augmentation of Reparative Cardiac Macrophages: Proof-of-Concept Data in Mice.
- Author
- A Saggini
- AR Pinto
- AV Shinde
- D RĂŒckerl
- DK Singla
- FD Finkelman
- HB Cohen
- I-CC Ho
- JM Lambert
- K Miyasato
- M Kaneko
- M Nahrendorf
- M Shiraishi
- M Singh
- MB Atkins
- MH Gilleece
- N Briceno
- N Tano
- NG Frangogiannis
- PH Wiernik
- R Kleemann
- RP Whitehead
- RP Whitehead
- S Epelman
- SJ Jenkins
- T Ben-Mordechai
- T Harel-Adar
- T Heidt
- T Satoh
- T Weinberger
- TT Braga
- V Barbay
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 23/06/2017
- Field of study
Recent research has shown that reparative (alternatively activated or M2) macrophages play a role in repair of damaged tissues, including the infarcted hearts. Administration of IL-4 is known to augment M2 macrophages. This translational study thus aimed to investigate whether IL-4 administration is useful for the treatment of myocardial infarction. Long-acting IL-4 complex (IL-4c; recombinant IL-4 mixed with anti-IL-4 monoclonal antibody as a stabilizer) was administered after coronary artery ligation in mice. It was observed that IL-4c administration increased accumulation of CD206+F4/80+ M2-like macrophages predominantly in the injured myocardium, compared to the control. Sorted cardiac M2-like macrophages highly expressed wide-ranging tissue repair-related genes. Indeed, IL-4c administration enhanced cardiac function in association with reduced infarct size and enhanced tissue repair (strengthened connective tissue formation, improved microvascular formation and attenuated cardiomyocyte hypertrophy). Experiments using Trib1 -/- mice that had a depleted ability to develop M2 macrophages and other in-vitro studies supported that these IL-4-mediated effects were induced via M2-like macrophages. On the other hand, when administered at Day 28 post-MI, the effects of IL-4c were diminished, suggesting a time-frame for IL-4 treatment to be effective. These data represent proof-of-concept of efficacy of IL-4 treatment for acute myocardial infarction, encouraging its further development.This project was funded by the Heart Research UK Translational Research Grant
(RG2653/15/16), British Heart Foundation Programme Grant (RG/15/31236), and Queen
Mary Innovation Proof of Concept Grant (2015). The National Institute for Health Researchfunded
Barts Cardiovascular Biomedical Research Unit also supported this project.This project was funded by the Heart Research UK Translational Research Grant (RG2653/15/16), British Heart Foundation Programme Grant (RG/15/31236), and Queen Mary Innovation Proof of Concept Grant (2015). The National Institute for Health Research-funded Barts Cardiovascular Biomedical Research Unit also supported this project
Induction of neurotoxicity by organophosphate pesticide chlorpyrifos and modulating role of cow urine
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Identifying a Window of Vulnerability during Fetal Development in a Maternal Iron Restriction Model
- Author
- A Ece
- AC Looker
- AD Legatt
- AE Kurekci
- AF Lukowski
- AL Love
- AM Siega-Riz
- AN Eden
- Anne E. Luebke
- AT Schmidt
- B Lozoff
- B Lozoff
- B Lozoff
- B Lozoff
- B Lozoff
- B Lozoff
- B Lozoff
- B Lozoff
- B Zhou
- BT Felt
- C Algarin
- C Munoz
- C Tanaka
- Camelia Mihaila
- CL Kwik-Uribe
- CL Kwik-Uribe
- CW Ponton
- D Brigham
- Dawn L. Lee
- DG Sweet
- DJ Morath
- DJ Morath
- DS Hartfield
- DS Hartfield
- E Casanueva
- E Dillman
- EL Unger
- ES Carlson
- ES Carlson
- F Banhidy
- F Corapci
- F Emamghorashi
- F Tang
- Frederick G. Strathmann
- GD Zhou
- H Cankaya
- HJ Park
- HP Wu
- HS Lee
- J Beard
- J Beard
- J Beard
- J Beard
- J Beard
- JC Jaime-Perez
- JL Beard
- JL Beard
- JL Beard
- Jordan Schramm
- JS Halterman
- JW Hall 3rd
- K Noben-Trauth
- KE Brunette
- KM Erikson
- L Gambling
- L Gambling
- L-l Wu
- M Knipper
- M Roncagliolo
- Margot Mayer-Pröschel
- MB Zimmermann
- ME Badaracco
- ME Conrad
- ME Conrad
- MK Georgieff
- MK Georgieff
- MR Naghii
- MS Burhans
- MW Church
- N Gregori
- N Melamed
- NA Shaw
- P Nguyen
- PG Reeves
- PN Singla
- PR Dallman
- RA deRegnier
- RD Baynes
- RF Florentino
- RJ Stoltzfus
- RM Angulo-Kinzler
- RM Angulo-Kinzler
- Robert M. Gelein
- S De Pee
- S Grantham-McGregor
- SA Xanthakos
- SB Amin
- SF Maison
- SJ Focht
- SL Bourque
- SU Sarici
- T Ito
- T Shafir
- T Walter
- TD Wachs
- Thomas Burne
- TO Scholl
- TR Cutmore
- VF Fairbanks
- W El Guindi
- W van Gelder
- W van Gelder
- WS Chong
- Y Wang
- Publication venue
- Public Library of Science
- Publication date
- 01/03/2011
- Field of study
It is well acknowledged from observations in humans that iron deficiency during pregnancy can be associated with a number of developmental problems in the newborn and developing child. Due to the obvious limitations of human studies, the stage during gestation at which maternal iron deficiency causes an apparent impairment in the offspring remains elusive. In order to begin to understand the time window(s) during pregnancy that is/are especially susceptible to suboptimal iron levels, which may result in negative effects on the development of the fetus, we developed a rat model in which we were able to manipulate and monitor the dietary iron intake during specific stages of pregnancy and analyzed the developing fetuses. We established four different dietary-feeding protocols that were designed to render the fetuses iron deficient at different gestational stages. Based on a functional analysis that employed Auditory Brainstem Response measurements, we found that maternal iron restriction initiated prior to conception and during the first trimester were associated with profound changes in the developing fetus compared to iron restriction initiated later in pregnancy. We also showed that the presence of iron deficiency anemia, low body weight, and changes in core body temperature were not defining factors in the establishment of neural impairment in the rodent offspring
Associations of maternal iron intake and hemoglobin in pregnancy with offspring vascular phenotypes and adiposity at age 10: findings from the avon longitudinal study of parents and children.
- Author
- A Boyd
- AE Donald
- C Crowe
- CM Law
- Darren C. Greenwood
- Debbie A. Lawlor
- E Bergel
- E Kaneshige
- F Lone
- François Blachier
- HJ McArdle
- I Rogers
- Janet E. Cade
- JK Cruickshank
- John Deanfield
- JPJ Halcox
- JPJ Halcox
- KM Godfrey
- L Allen
- L Gambling
- L Gambling
- L Gambling
- L Gambling
- L Gambling
- L Gambling
- LM Zhou
- M Brion
- M Zimmermann
- MB Belfort
- MJA Brion
- N Milman
- NA Alwan
- Nisreen A. Alwan
- P Royston
- P Whincup
- PN Baker
- PN Singla
- R Collings
- RL Bergmann
- RMD Agrawal
- S Lisle
- SL Kelleher
- T Tamura
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2014
- Field of study
Iron deficiency is common during pregnancy. Experimental animal studies suggest that it increases cardiovascular risk in the offspring
Analgesic exposure in pregnant rats affects fetal germ cell development with inter-generational reproductive consequences
- Author
- A Aminoshariae
- A Dean
- AD Krentz
- AJ Childs
- BJ Anderson
- C Chalmey
- CA Snijder
- CE Aiken
- D Dewailly
- DM Kristensen
- DM Kristensen
- DM Walker
- DR Xia
- F Champagne
- GR Hutchison
- GS Berkowitz
- H Lim
- H Sasaki
- H Wermann
- JA Arosh
- JA West
- JB Kerr
- JR Vane
- JV Jeppesen
- KA McClellan
- M Abe
- M Scarola
- M Zeybel
- MA Naga Rani
- MB Frungieri
- MJ Warner
- MM Werler
- MS Jensen
- MS Jobling
- N Kalfa
- N Lei
- NK Singla
- P Reddy
- PG Thorpe
- RA Bayne
- RA Black
- RE Brandlistuen
- RT Mitchell
- S Jerabek
- S Mazaud-Guittot
- S van den Driesche
- S van den Driesche
- S Yamaguchi
- SK Huang
- T Fullston
- V King
- W Rayburn
- X Liao
- Y Seki
- Y Sugimoto
- Y Wei
- Z Hochberg
- Z Liew
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 27/01/2016
- Field of study
Analgesics which affect prostaglandin (PG) pathways are used by most pregnant women. As germ cells (GC) undergo developmental and epigenetic changes in fetal life and are PG targets, we investigated if exposure of pregnant rats to analgesics (indomethacin or acetaminophen) affected GC development and reproductive function in resulting offspring (F1) or in the F2 generation. Exposure to either analgesic reduced F1 fetal GC number in both sexes and altered the tempo of fetal GC development sex-dependently, with delayed meiotic entry in oogonia but accelerated GC differentiation in males. These effects persisted in adult F1 females as reduced ovarian and litter size, whereas F1 males recovered normal GC numbers and fertility by adulthood. F2 offspring deriving from an analgesic-exposed F1 parent also exhibited sex-specific changes. F2 males exhibited normal reproductive development whereas F2 females had smaller ovaries and reduced follicle numbers during puberty/adulthood; as similar changes were found for F2 offspring of analgesic-exposed F1 fathers or mothers, we interpret this as potentially indicating an analgesic-induced change to GC in F1. Assuming our results are translatable to humans, they raise concerns that analgesic use in pregnancy could potentially affect fertility of resulting daughters and grand-daughters
International Consensus Statement on Rhinology and Allergy: Rhinosinusitis
- Author
- Aanaes K
- Abadie WM
- Abi Najm S
- Abigail P
- Abrahams JJ
- Abrass LJ
- Abreu CB
- Abreu NA
- Abshirini H
- Abuzeid WM
- Abuzeid WM
- Achar P
- Ackerhans M
- Adam P
- Adappa ND
- Adappa ND
- Adappa ND
- Adappa ND
- Adriaensen G
- Agache I
- Aghamohammadi A
- Agius AM
- Agyeman AA
- Ahn CN
- Ahn HJ
- Ahn JC
- Ahn SH
- AhovuoâSaloranta A
- Aitken M
- Ajaiyeoba A
- Akbari E
- Akdis CA
- Akira S
- Akiyama K
- Akiyama K
- Akiyama K
- Al Komser MK
- Alam ES
- Alandejani T
- Alanin MC
- Albritton FDT
- Albu S
- Albu S
- Albu S
- Aldini G
- Alexander NS
- Aljebab F
- Alkire BC
- Allen EK
- Alobid I
- Alobid I
- Alobid I
- Aloulah M
- Alqudah M
- Alromaih S
- Alsaleh S
- Alsharif S
- Alt JA
- Alt JA
- Alt JA
- Alt JA
- Alt JA
- Alves MP
- AlâQudah M
- AlâQudah M.
- AlâQudah M.
- AlâRawi MM
- AlâShaikh S
- AlâShemari H
- AlâSwiahb JN
- Amali A
- Amar YG
- Amble FR
- American Academy of Pediatrics Steering Committee on Quality Improvement and Management (AAP SCQIM)
- Amin MR
- Amine M
- Amodu EJ
- Anamika A
- Anand V
- Anderson DE
- Anderson WC
- Andhale S
- Ankichetty SP
- Annamalai S
- Anon JB
- AnselmoâLima WT
- Antisdel JL
- Antisdel JL
- Antunes MB
- Antunes MB
- Anushiravani M
- Anzai Y
- AnziÄ SA
- Aramani A
- Arden KE
- Arild Danielsen K
- Aring AM
- Arjomandi H
- Armenaka M
- Arnstead N
- Arslan H
- Arslan HH
- Asaka D
- Asero R
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- Atighechi S
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- Aukema AA
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- Autio TJ
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- Avdeeva K
- Awad OG
- Awad OGA
- Ayers CM
- Ayoub N
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- Ayoub N
- Azbell C
- Azila A
- Baba S
- Baba S
- Baba S
- Babela R
- Babinski D
- Bachert C
- Bachert C
- Bachert C
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- Bachert C
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- Bachert C
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- Bachmann G
- Badia L
- Bae JS
- Bagheri SHR
- Baguley C
- Baguley CJ
- Bahtouee M
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- Bakhshaee M
- Balikci HH
- Balikci HH
- Balk EM
- Bang YJ
- Banhiran W
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- Baraniuk JN
- Barham HP
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- Bednarski KA
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- Beswick DM
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- Beyea JA
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- Biedlingmaier JF
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- Biel MA
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- Chandler JR
- Chandra RK
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- Chandra RK
- Chandy Z
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- Chang HS
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- Chang YâS
- Chaudhary N
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- Chong LY
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- Christensen DN
- Christensen JM
- Chu DK
- Chung BJ
- Chung SD
- Church CA
- Cirkovic I
- Citardi MJ
- Citardi MJ
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- Clarhed UKE
- Clark DW
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- Clayman GL
- Cleland EJ
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- Clement PA
- Clinger JD
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- Dwyhalo KM
- Dykewicz MS
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- Ebbens FA
- Ebbens FA
- Ebell MH
- Ebell MH
- Eberhart LH
- Ebert CS
- Ecevit MC
- Eckhoff A
- Ediriweera ER
- Eggesbo HB.
- Ehnhage A
- Ehnhage A
- El Mograbi A
- Elborn JS
- Elhakim M
- Eliashar R
- Elkins MR
- Elkins MR
- Ellis CN
- Eloy JA
- Eloy JA
- Eloy JA
- Eloy JA
- Eloy P
- Eluecque H
- elâFiky LM
- ElâHennawi DM
- ElâShmaa NS
- Emre IE
- Endam LM
- Endo Y
- Erbek SS
- Erbek SS
- Ernst FR
- Error M
- Esmaeilzadeh H
- Esposito S
- Esposito S
- EssaidiâLaziosi M
- Eviatar E
- Eweiss AZ
- Expert Panel on Neurologic I
- Eyigor H
- Ezzat W
- Fabre C
- Faghih Habibi A
- Falagas ME
- Falco JJ
- Fan Y
- Fandino M
- Farag AA
- Farrell PM
- Farzal Z
- Farzanegan B
- Fastenberg JH
- Feazel LM
- Federspil PA
- Feldman C
- Ference EH
- Ference EH
- Ference EH
- Ferguson BJ
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- Ferguson BJ
- Ferguson BJ
- Ferguson JL
- Fernandez IJ
- Ferrara A
- Filiaci F
- Filiaci F
- Flam JO
- Fleissig E
- Flyman S
- Fokkens W
- Fokkens WJ
- Fokkens WJ
- Fokkens WJ
- Fokkens WJ
- Fokkens WJ
- Fong SA
- Food Organization A, Organization WH
- Foreman A
- Foreman A
- Fortune DS
- Forwith KD
- Forwith KD
- Fowler K
- Fraczek M
- Fraczek M. RâNB
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- Frank S
- Franklin JH
- Freeman SB
- Frenkiel S
- Frerichs KA
- Fried M
- Fried M
- Fried M
- Fried M
- Friedman M
- Friedman M
- Friedman M
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- ZielinskaâBlizniewska H
- Zou L
- Zuckerman JD
- Zurlo JJ
- Zuskin E
- Äulig J
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2021
- Field of study
Background: The 5 years since the publication of the first International Consensus Statement on Allergy and Rhinology: Rhinosinusitis (ICARâRS) has witnessed foundational progress in our understanding and treatment of rhinologic disease. These advances are reflected within the more than 40 new topics covered within the ICARâRSâ2021 as well as updates to the original 140 topics. This executive summary consolidates the evidenceâbased findings of the document. Methods: ICARâRS presents over 180 topics in the forms of evidenceâbased reviews with recommendations (EBRRs), evidenceâbased reviews, and literature reviews. The highest grade structured recommendations of the EBRR sections are summarized in this executive summary. Results: ICARâRSâ2021 covers 22 topics regarding the medical management of RS, which are grade A/B and are presented in the executive summary. Additionally, 4 topics regarding the surgical management of RS are grade A/B and are presented in the executive summary. Finally, a comprehensive evidenceâbased management algorithm is provided. Conclusion: This ICARâRSâ2021 executive summary provides a compilation of the evidenceâbased recommendations for medical and surgical treatment of the most common forms of RS
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- Ălvarez FernĂĄndez A
- Ăzçelik Ă
- Publication venue
- Springer Nature on behalf of SISSA
- Publication date
- 09/10/2022
- Field of study
A preprint version of the article is available at arXiv:2206.09466v2 [hep-ex], https://arxiv.org/abs/2206.09466v2 . Comments: Replaced with the published version. Added the journal reference and the DOI. All the figures and tables can be found at httpS://cms-results.web.cern.ch/cms-results/public-results/publications/HIG-20-013 (CMS Public Pages). Report number: CMS-HIG-20-013, CERN-EP-2022-120.Production cross sections of the standard model Higgs boson decaying to a pair of W bosons are measured in proton-proton collisions at a center-of-mass energy of 13 TeV. The analysis targets Higgs bosons produced via gluon fusion, vector boson fusion, and in association with a W or Z boson. Candidate events are required to have at least two charged leptons and moderate missing transverse momentum, targeting events with at least one leptonically decaying W boson originating from the Higgs boson. Results are presented in the form of inclusive and differential cross sections in the simplified template cross section framework, as well as couplings of the Higgs boson to vector bosons and fermions. The data set collected by the CMS detector during 2016-2018 is used, corresponding to an integrated luminosity of 138 fb^â1. The signal strength modifier ÎŒ, defined as the ratio of the observed production rate in a given decay channel to the standard model expectation, is measured to be ÎŒ = 0.95 +0.10â0.09. All results are found to be compatible with the standard model within the uncertainties.SCOAP3
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Measurement of the differential ttÂŻ production cross section as a function of the jet mass and extraction of the top quark mass in hadronic decays of boosted top quarks
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- Zuolo D
- Zygala L
- Ălvarez CR
- Publication venue
- Springer Nature
- Publication date
- 03/07/2023
- Field of study
Data Availability:
This manuscript has no associated data or the data will not be deposited. [Authorsâ comment: Release and preservation of data used by the CMS Collaboration as the basis for publications is guided by the CMS policy as stated in https://cms-docdb.cern.ch/cgibin/PublicDocDB/RetrieveFile?docid=6032 &filename=CMSDataPolicyV1.2.pdf &version=2.]A measurement of the jet mass distribution in hadronic decays of Lorentz-boosted top quarks is presented. The measurement is performed in the lepton + jets channel of top quark pair production (ttÂŻ
) events, where the lepton is an electron or muon. The products of the hadronic top quark decay are reconstructed using a single large-radius jet with transverse momentum greater than 400GeV
. The data were collected with the CMS detector at the LHC in proton-proton collisions and correspond to an integrated luminosity of 138fbâ1
. The differential ttÂŻ
production cross section as a function of the jet mass is unfolded to the particle level and is used to extract the top quark mass. The jet mass scale is calibrated using the hadronic W boson decay within the large-radius jet. The uncertainties in the modelling of the final state radiation are reduced by studying angular correlations in the jet substructure. These developments lead to a significant increase in precision, and a top quark mass of 173.06±0.84GeV.SCOAP
Recommended from our members
Measurement of the Higgs boson production via vector boson fusion and its decay into bottom quarks in proton-proton collisions at sâ = 13 TeV
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- Publication venue
- Springer Nature on behalf of SISSA
- Publication date
- 30/01/2024
- Field of study
A preprint version of the article is available at arXiv:2308.01253v2 [hep-ex], https://arxiv.org/abs/2308.01253v2 . Comments: Replaced with the published version. Added the journal reference and the DOI. All the figures and tables can be found at https://cms-results.web.cern.ch/cms-results/public-results/publications/HIG-22-009 (CMS Public Pages). Report number: CMS-HIG-22-009, CERN-EP-2023-110.A measurement of the Higgs boson (H) production via vector boson fusion (VBF) and its decay into a bottom quark-antiquark pair (bbÂŻ) is presented using proton-proton collision data recorded by the CMS experiment at sâ = 13 TeV and corresponding to an integrated luminosity of 90.8 fbâ1. Treating the gluon-gluon fusion process as a background and constraining its rate to the value expected in the standard model (SM) within uncertainties, the signal strength of the VBF process, defined as the ratio of the observed signal rate to that predicted by the SM, is measured to be ÎŒqqHHbbÂŻ = 1.01 +0.55â0.46. The VBF signal is observed with a significance of 2.4 standard deviations relative to the background prediction, while the expected significance is 2.7 standard deviations. Considering inclusive Higgs boson production and decay into bottom quarks, the signal strength is measured to be ÎŒincl.HbbÂŻ = 0.99 +0.48â0.41, corresponding to an observed (expected) significance of 2.6 (2.9) standard deviations.SCOAP3, STFC; Marie-Curie program and the European Research Council and Horizon 2020 Gran
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