86 research outputs found
A study of a five horse-power single phase induction motor
- Publication venue
- Publication date
- 01/01/1915
- Field of study
Thesis (B.S.)--University of Illinois, 1915.Typescript
A novel formulation of inhaled sodium cromoglicate (PA101) in idiopathic pulmonary fibrosis and chronic cough: a randomised, double-blind, proof-of-concept, phase 2 trial
- Author
- Abel K.
- Adamali H.
- Adeloye D.
- Adeyemi F.
- Adeyemi O.
- Ahmad S.
- Ahmed R.
- Ainsworth M.
- Al-Sheklly B.
- Alamoudi A.
- Aljaroof M.
- Allan L.
- Allen R.
- Alli A.
- Altmann D.
- Anderson D.
- Andrews M.
- Angyal A.
- Antoniades C.
- Arbane G.
- Armour C.
- Armstrong L.
- Armstrong N.
- Arnold D.
- Arnold H.
- Ashworth A.
- Ashworth M.
- Assefa-Kebede H.
- Atkin P.
- Atkins A.
- Atkins H.
- Aul R.
- Avram C.
- Baggott R.
- Baguley D.
- Baillie J. Kenneth
- Baillie J.K.
- Bain S.
- Bakali M.
- Bakau M.
- Baldry E.
- Baldwin D.
- Ballard C.
- Bambrough J.
- Barker R.E.
- Barratt S.
- Barrett F.
- Basu N.
- Batterham R.
- Baxendale H.
- Bayes H.
- Bayley M.
- Beadsworth M
- Beirne P.
- Bell D.
- Bell R.
- Berry C.
- Betts S.
- Bhui K.
- Bishop L.
- Blaikely J.
- Bloomfield C.
- Bloss A.
- Bolger A.
- Bolton C.E.
- Bonnington J.
- Botkai A.
- Bourne C.
- Bourne M.
- Bradley E.
- Bramham K.
- Brear L.
- Breen G.
- Breeze J.
- Briggs A.
- Bright E.
- Brightling C.E.
- Brightling Christopher E.
- Brill S.
- Brindle K.
- Broad L.
- Broome M.
- Brown A
- Brown A
- Brown J.
- Brown J.
- Brown J.S.
- Brown Jeremy S.
- Brown M
- Brown M.
- Brown R.
- Brown V.
- Brugha T
- Brunskill N
- Buch M
- Bularga A
- Bullmore E
- Burn D
- Burns G
- Busby J
- Buttress A
- Byrne S
- Cairns P
- Calder P.C.
- Calvelo E
- Card B
- Carr L
- Carson G
- Carter P
- Cavanagh J
- Chalder T
- Chalder Trudie
- Chalmers J.D.
- Chalmers James D.
- Chambers R.C.
- Channon K
- Chapman K
- Charalambou A
- Chaudhuri N
- Checkley A
- Chen J
- Chetham L
- Chilvers E.R.
- Chinoy H
- Chong-James K
- Choudhury G
- Choudhury N
- Chowdhury P
- Chowienczyk P
- Christie C
- Clark C
- Clark D
- Clarke J
- Clift P
- Clohisey S
- Coburn Z
- Cole J
- Coleman C
- Connell D
- Connolly B
- Connor L
- Cook A
- Cooper B
- Coupland C
- Craig T
- Crisp P
- Cristiano D
- Crooks M.G.
- Cross A
- Cruz I
- Cullinan P
- Daines L
- Daines Luke
- Dalton M
- Dark P
- Dasgin J
- David A
- David C
- Davies F
- Davies G
- Davies G.A.
- Davies K
- Davies M
- Daynes E
- De Silva T
- De Soyza A
- De Soyza Anthony
- Deakin B
- Deans A
- Defres S
- Dell A
- Dempsey K
- Dennis J
- Dewar A
- Dharmagunawardena R
- Diar Bakerly N
- Diar Bakerly Nawar
- Dipper A
- Diver S
- Diwanji S.N.
- Dixon M
- Djukanovic R
- Dobson C
- Dobson H
- Dobson S.L.
- Docherty A.B.
- Docherty Annemarie B.
- Donaldson A
- Dong T
- Dormand N
- Dougherty A
- Dowling R
- Drain S
- Dulawan P
- Dunn S
- Dunn S
- Easom N
- Easom Nicholas
- Echevarria C
- Edwards S
- Edwardson C
- Elliott A
- Elliott B
- Ellis Y
- Elmer A
- Elneima O
- Elneima Omer
- Evans D
- Evans H
- Evans J
- Evans R
- Evans R.A.
- Evans R.I.
- Evans Rachael A.
- Evans T
- Fabbri L
- Fairbairn S
- Fairman A
- Fallon K
- Faluyi D
- Favager C
- Felton T
- Finch J
- Finney S
- Fisher H
- Fletcher S
- Flockton R
- Foote D
- Ford A
- Forton D
- Francis C
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- Frankel A
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- Free R
- French N
- Fuld J
- Furniss J
- Garner L
- Gautam N
- Geddes J.R.
- Geddes John R.
- George J
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- Glossop J
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- Gooptu B
- Gorsuch T
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- Greening N.J.
- Greening Neil J.
- Greenwood J
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- Gregory R
- Grieve D
- Gummadi M
- Gupta A
- Gurram S
- Guthrie E
- Hadley K
- Haggar A
- Hainey K
- Haldar P
- Hall I
- Hall L
- Halling-Brown M
- Hamil R
- Hanley N.A.
- Hardwick H
- Hardy E
- Hargadon B
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- Kamwa V
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- Kon S.S.
- Korszun A
- Kotanidis C
- Koychev I
- Kurupati P
- Kwan J
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- Leavy O.C.
- Leavy Olivia C.
- Lee D
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- Leitch K
- Lenagh R
- Lewis J
- Lewis K
- Lewis K.E.
- Lewis Keir
- Lewis V
- Lewis-Burke N
- Light T
- Lightstone L
- Lim L
- Linford S
- Lingford-Hughes A
- Lipman M
- Liyanage K
- Lloyd A
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- Lomas D
- Lone N.I.
- Lone Nazir I.
- Loosley R
- Lord J.M.
- Lord Janet M.
- Lota H
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- MacGowan G
- Macharia I
- Mackay C
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- Madathil S
- Madzamba G
- Magee N
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- Majeed N
- Major E
- Malim M
- Mallison G
- Man W
- Mandal S
- Mangion K
- Mansoori P
- Marciniak S
- Mariveles M
- Marks M
- Marks Michael
- Marshall B
- Martineau A
- Maskell N
- Matila D
- Matthews L
- Mayet J
- McAdoo S
- McAllister-Williams H
- McArdle A
- McArdle P
- McAulay D
- McAuley D.F.
- McAuley H
- McAuley Hamish
- McCafferty K
- McCann G.P.
- McCann Gerry P.
- McCauley H
- McCourt P
- Mcgarvey L
- McGinness J
- McGovern A
- McGuinness H
- McInnes I.B.
- McIvor E
- McIvor K
- McMahon A
- McMahon M.J.
- McMorrow L
- Mcnally T
- McNarry M
- McQueen A
- McShane H
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- Meiring J
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- Michael A
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- Monteiro W
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- Novotny P
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- Openshaw P.J.M.
- Openshaw Peter J. M.
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- Toshner Mark
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- Yousuf A
- Yousuf A.J.
- Zawia A
- Zhao B
- Zongo O
- Publication venue
- Elsevier
- Publication date
- 01/03/2013
- Field of study
Background Cough can be a debilitating symptom of idiopathic pulmonary fibrosis (IPF) and is difficult to treat. PA101 is a novel formulation of sodium cromoglicate delivered via a high-efficiency eFlow nebuliser that achieves significantly higher drug deposition in the lung compared with the existing formulations. We aimed to test the efficacy and safety of inhaled PA101 in patients with IPF and chronic cough and, to explore the antitussive mechanism of PA101, patients with chronic idiopathic cough (CIC) were also studied. Methods This pilot, proof-of-concept study consisted of a randomised, double-blind, placebo-controlled trial in patients with IPF and chronic cough and a parallel study of similar design in patients with CIC. Participants with IPF and chronic cough recruited from seven centres in the UK and the Netherlands were randomly assigned (1:1, using a computer-generated randomisation schedule) by site staff to receive PA101 (40 mg) or matching placebo three times a day via oral inhalation for 2 weeks, followed by a 2 week washout, and then crossed over to the other arm. Study participants, investigators, study staff, and the sponsor were masked to group assignment until all participants had completed the study. The primary efficacy endpoint was change from baseline in objective daytime cough frequency (from 24 h acoustic recording, Leicester Cough Monitor). The primary efficacy analysis included all participants who received at least one dose of study drug and had at least one post-baseline efficacy measurement. Safety analysis included all those who took at least one dose of study drug. In the second cohort, participants with CIC were randomly assigned in a study across four centres with similar design and endpoints. The study was registered with ClinicalTrials.gov (NCT02412020) and the EU Clinical Trials Register (EudraCT Number 2014-004025-40) and both cohorts are closed to new participants. Findings Between Feb 13, 2015, and Feb 2, 2016, 24 participants with IPF were randomly assigned to treatment groups. 28 participants with CIC were enrolled during the same period and 27 received study treatment. In patients with IPF, PA101 reduced daytime cough frequency by 31·1% at day 14 compared with placebo; daytime cough frequency decreased from a mean 55 (SD 55) coughs per h at baseline to 39 (29) coughs per h at day 14 following treatment with PA101, versus 51 (37) coughs per h at baseline to 52 (40) cough per h following placebo treatment (ratio of least-squares [LS] means 0·67, 95% CI 0·48–0·94, p=0·0241). By contrast, no treatment benefit for PA101 was observed in the CIC cohort; mean reduction of daytime cough frequency at day 14 for PA101 adjusted for placebo was 6·2% (ratio of LS means 1·27, 0·78–2·06, p=0·31). PA101 was well tolerated in both cohorts. The incidence of adverse events was similar between PA101 and placebo treatments, most adverse events were mild in severity, and no severe adverse events or serious adverse events were reported. Interpretation This study suggests that the mechanism of cough in IPF might be disease specific. Inhaled PA101 could be a treatment option for chronic cough in patients with IPF and warrants further investigation
Determinants of recovery from post-COVID-19 dyspnoea: analysis of UK prospective cohorts of hospitalised COVID-19 patients and community-based controls
- Author
- Abel K
- Adamali H
- Adeloye D
- Adeyemi O
- Adrego R
- Aguilar Jimenez LA
- Ahmad Haider N
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- Ahmed R
- Ahwireng N
- Ainsworth M
- Al-Sheklly B
- Alamoudi A
- Ali M
- Aljaroof M
- All AM
- Allan L
- Allen RJ
- Allerton L
- Allsop L
- Almeida P
- Altmann D
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- Amoils S
- Anderson D
- Antoniades C
- Arbane G
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- Ashish A
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- Aslani S
- Assefa-Kebede H
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- Baillie JK
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- Publication venue
- 'Elsevier BV'
- Publication date
- 27/03/2023
- Field of study
Background The risk factors for recovery from COVID-19 dyspnoea are poorly understood. We investigated determinants of recovery from dyspnoea in adults with COVID-19 and compared these to determinants of recovery from non-COVID-19 dyspnoea. Methods We used data from two prospective cohort studies: PHOSP-COVID (patients hospitalised between March 2020 and April 2021 with COVID-19) and COVIDENCE UK (community cohort studied over the same time period). PHOSP-COVID data were collected during hospitalisation and at 5-month and 1-year follow-up visits. COVIDENCE UK data were obtained through baseline and monthly online questionnaires. Dyspnoea was measured in both cohorts with the Medical Research Council Dyspnoea Scale. We used multivariable logistic regression to identify determinants associated with a reduction in dyspnoea between 5-month and 1-year follow-up. Findings We included 990 PHOSP-COVID and 3309 COVIDENCE UK participants. We observed higher odds of improvement between 5-month and 1-year follow-up among PHOSP-COVID participants who were younger (odds ratio 1.02 per year, 95% CI 1.01–1.03), male (1.54, 1.16–2.04), neither obese nor severely obese (1.82, 1.06–3.13 and 4.19, 2.14–8.19, respectively), had no pre-existing anxiety or depression (1.56, 1.09–2.22) or cardiovascular disease (1.33, 1.00–1.79), and shorter hospital admission (1.01 per day, 1.00–1.02). Similar associations were found in those recovering from non-COVID-19 dyspnoea, excluding age (and length of hospital admission). Interpretation Factors associated with dyspnoea recovery at 1-year post-discharge among patients hospitalised with COVID-19 were similar to those among community controls without COVID-19. Funding PHOSP-COVID is supported by a grant from the MRC-UK Research and Innovation and the Department of Health and Social Care through the National Institute for Health Research (NIHR) rapid response panel to tackle COVID-19. The views expressed in the publication are those of the author(s) and not necessarily those of the National Health Service (NHS), the NIHR or the Department of Health and Social Care. COVIDENCE UK is supported by the UK Research and Innovation, the National Institute for Health Research, and Barts Charity. The views expressed are those of the authors and not necessarily those of the funders
Genetic mechanisms of critical illness in COVID-19.
- Author
- A A Roger Thompson
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- A Agasou
- A Ahmed
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- A Allan
- A Altabaibeh
- A Alvaro
- A Aspinwall
- A Ayers
- A Bamford
- A Barron
- A Bashyal
- A Bellini
- A Bociek
- A Botello
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- A Gherman
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- Agnese Verzuri
- Agostino Ognibene
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- Ailsa Golightly
- Alan Maclean
- Alessandra
- Alessandra Stella
- Alessandra Vergori
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- Alexander J Mentzer
- Alice Donati
- Alison M Meynert
- Alistair Nichol
- Ana da Silva Filipe
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- Anjali J Shastri
- Anna Canaccini
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- Annarita Giliberti
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- Emmanuelle Marques
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- S Turki
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- S Wadd
- S Whiteley
- S Williams
- S Wood
- S Yussuf
- Sabino Scolletta
- Samreen Ijaz
- Sandro Mancarella
- Sandro Panese
- Sara Amitrano
- Sara McDonald
- Sarah Law
- Sarah McCafferty
- Saverio Giuseppe Parisi
- Saye Khoo
- Scott Richard
- Semple Malcolm G
- Serafina Valente
- Serena Ludovisi
- Sergio Daga
- Seán Keating
- Shankar-Hari Manu
- Shen Xia
- Shih Barbara
- Shiranee Sriskandan
- Shona C Moore
- Silvia Cappelli
- Simona Marcantonio
- Simone Furini
- Sophie Halpin
- Sophie Venturelli
- Stefania Mantovani
- Stefano Baratti
- Stefano Ceri
- Stefano Rusconi
- Stella Aslibekyan
- Stephanie Roberts
- Stephen R Knight
- Summers Charlotte
- Susanna Croci
- Susanna Guerrini
- T Anderson
- T Arden
- T Baird
- T Behan
- T Bemand
- T Cosier
- T Coventry
- T Duncan
- T Felton
- T Geary
- T Hazleton
- T Joefield
- T Kannan
- T Lawton
- T Marsden
- T Martin
- T McHugh
- T Newman
- T Nortcliffe
- T O Jones
- T Pogreban
- T Rees
- T Samakomva
- T Smith
- T Smith
- T Szakmany
- T Varghes
- T Williams
- T Wood
- Tammy Gilchrist
- Tenesa Albert
- Teresa Filshtein-Sonmez
- Thomas M Drake
- Thushan de Silva
- Tim Walsh
- Tom Fletcher
- Tom Solomon
- Tony Wackett
- Trevor Paterson
- Tullio Trotta
- Turtle Lance
- U Poultney
- V Amin
- V Anumakonda
- V Bastion
- V Cannons
- V Crickmore
- V Gopal
- V Irvine
- V Kasipandian
- V Krishnamurthy
- V Lake
- V Linnett
- V Martinson
- V Nagarajan
- V Page
- V Parris
- V Parris
- V Pristopan
- V Ratnam
- V Rivers
- V Sarathy
- V Thomas
- V Thwaites
- V Tuckey
- V Turner
- V Wagstaff
- V Waugh
- Valentina Anemoli
- Vanessa Sancho-Shimizu
- Victoria Shaw
- Vitart Veronique
- W Harrison
- W Khaliq
- W Khaliq
- W McCormick
- W Woodyatt
- Walker Susan
- Walsh Timothy
- Wang Bo
- Wei Shen Lim
- Wendy S Barclay
- William A Paxton
- William Greenhalf
- Wilson James F
- Wrobel Nicola
- Wu Yang
- X Qiu
- Y Baird
- Y Choudhury
- Y Hussain
- Y Jackson
- Y Thirlwall
- Yang Jian
- Yang Zhijian
- Z Alldis
- Z Belagodu
- Z Bradshaw
- Z Coton
- Z Daly
- Z Farzad
- Z Fernandez
- Z Garland
- Z Maqsood
- Z Omar
- Z Prime
- Z Scott
- Zechner Marie
- Zhai Ranran
- Zheng Chenqing
- Publication venue
- Nature
- Publication date
- 01/01/2020
- Field of study
Host-mediated lung inflammation is present1, and drives mortality2, in the critical illness caused by coronavirus disease 2019 (COVID-19). Host genetic variants associated with critical illness may identify mechanistic targets for therapeutic development3. Here we report the results of the GenOMICC (Genetics Of Mortality In Critical Care) genome-wide association study in 2,244 critically ill patients with COVID-19 from 208 UK intensive care units. We have identified and replicated the following new genome-wide significant associations: on chromosome 12q24.13 (rs10735079, P = 1.65 × 10-8) in a gene cluster that encodes antiviral restriction enzyme activators (OAS1, OAS2 and OAS3); on chromosome 19p13.2 (rs74956615, P = 2.3 × 10-8) near the gene that encodes tyrosine kinase 2 (TYK2); on chromosome 19p13.3 (rs2109069, P = 3.98 × 10-12) within the gene that encodes dipeptidyl peptidase 9 (DPP9); and on chromosome 21q22.1 (rs2236757, P = 4.99 × 10-8) in the interferon receptor gene IFNAR2. We identified potential targets for repurposing of licensed medications: using Mendelian randomization, we found evidence that low expression of IFNAR2, or high expression of TYK2, are associated with life-threatening disease; and transcriptome-wide association in lung tissue revealed that high expression of the monocyte-macrophage chemotactic receptor CCR2 is associated with severe COVID-19. Our results identify robust genetic signals relating to key host antiviral defence mechanisms and mediators of inflammatory organ damage in COVID-19. Both mechanisms may be amenable to targeted treatment with existing drugs. However, large-scale randomized clinical trials will be essential before any change to clinical practice
Circulating microRNAs in sera correlate with soluble biomarkers of immune activation but do not predict mortality in ART treated individuals with HIV-1 infection: A case control study
- Author
- Aagaard B.
- Abel S.
- Abeli C.
- Abgrall S.
- Aboulker J. P.
- Abrams D. I.
- Abusamra L.
- Acosta E. A.
- Adam A.
- Adams S.
- Adams S.
- Adamski A.
- Agmon-Levin N.
- Agrawal S.
- Aichelburg A.
- Aichelburg A.
- Ainsworth J. G.
- Aiuti F.
- Alcázar-Caballero R.
- Aldir M.
- Alexander I.
- Allegra D.
- Allworth A. M.
- Almeida M. M. T. B.
- Amat K.
- Ambrose P.
- Ampunpong U.
- Andersen P Lehm
- Andersen Å. Bengaard
- Anderson C.
- Anderson J.
- Anderson J.
- Anderson J. S. C.
- Andrews L.
- Andrews L.
- Aneja B.
- Angel E.
- Angel J.
- Angus B.
- Angus B. J.
- Anstead G.
- Antoniadou A.
- Antoniskis D.
- Antunes F.
- Antunes F.
- Aouba A.
- Aquilia S.
- Aquilia S.
- Aragon D. R.
- Aragon E.
- Aragon E.
- Arastéh K.
- Araujo F.
- Arduino R.
- Arduino R.
- Armishaw J.
- Arnaiz J.
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- Arnaiz J. A.
- Arribas J.
- Arrizabalaga J.
- Arsenault M.
- Artz R.
- Artz R.
- Auchieng C.
- Auperin L.
- Baadegaard B.
- Babiker A.
- Babiker G.
- Bahia F.
- Bailowitz J.
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- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2015
- Field of study
Introduction: The use of anti-retroviral therapy (ART) has dramatically reduced HIV-1 associated morbidity and mortality. However, HIV-1 infected individuals have increased rates of morbidity and mortality compared to the non-HIV-1 infected population and this appears to be related to end-organ diseases collectively referred to as Serious Non-AIDS Events (SNAEs). Circulating miRNAs are reported as promising biomarkers for a number of human disease conditions including those that constitute SNAEs. Our study sought to investigate the potential of selected miRNAs in predicting mortality in HIV-1 infected ART treated individuals. Materials and Methods: A set of miRNAs was chosen based on published associations with human disease conditions that constitute SNAEs. This case: control study compared 126 cases (individuals who died whilst on therapy), and 247 matched controls (individuals who remained alive). Cases and controls were ART treated participants of two pivotal HIV-1 trials. The relative abundance of each miRNA in serum was measured, by RTqPCR. Associations with mortality (all-cause, cardiovascular and malignancy) were assessed by logistic regression analysis. Correlations between miRNAs and CD4+ T cell count, hs-CRP, IL-6 and D-dimer were also assessed. Results: None of the selected miRNAs was associated with all-cause, cardiovascular or malignancy mortality. The levels of three miRNAs (miRs -21, -122 and -200a) correlated with IL-6 while miR-21 also correlated with D-dimer. Additionally, the abundance of miRs -31, -150 and -223, correlated with baseline CD4+ T cell count while the same three miRNAs plus miR- 145 correlated with nadir CD4+ T cell count. Discussion: No associations with mortality were found with any circulating miRNA studied. These results cast doubt onto the effectiveness of circulating miRNA as early predictors of mortality or the major underlying diseases that contribute to mortality in participants treated for HIV-1 infection
Cohort Profile: Post-Hospitalisation COVID-19 (PHOSP-COVID) study
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- Linford S
- Lingford-Hughes A
- Lipman M
- Liyanage K
- Lloyd A
- Logan S
- Lomas D
- Lomas D
- Lone NI
- Lone NI
- Lone NI
- Lone NI
- Loosley R
- Lord JM
- Lord JM
- Lord JM
- Lord JM
- Lota H
- Lovegrove W
- Lucey A
- Lukaschuk E
- Lukaschuk E
- Lye A
- Lynch C
- MacDonald S
- MacGowan G
- Macharia I
- Mackie J
- Macliver L
- Madathil S
- Madzamba G
- Magee N
- Magtoto MM
- Mairs N
- Majeed N
- Major E
- Malein F
- Malim M
- Mallison G
- Man WD-C
- Man WD-C
- Man WD-C
- Mandal S
- Mangion K
- Manisty C
- Manisty C
- Manley R
- Mansoori P
- March K
- Marciniak S
- Marino P
- Mariveles M
- Marks M
- Marks M
- Marks M
- Marks M
- Marouzet E
- Marsh S
- Marshall B
- Marshall M
- Martin J
- Martineau A
- Martinez LM
- Maskell N
- Maskell N
- Matila D
- Matimba-Mupaya W
- Matthews L
- Mbuyisa A
- McAdoo S
- McAllister-Williams H
- McArdle A
- McArdle P
- McAulay D
- McAuley DF
- McAuley HJC
- McAuley HJC
- McAuley HJC
- McAuley HJC
- McAuley HJC
- McCafferty K
- McCall JW
- McCall JW
- McCann GP
- McCann GP
- McCann GP
- McCann GP
- McCormick J
- McCormick W
- McCourt P
- McCracken C
- McGarvey L
- McGarvey L
- Mcgee K
- McGhee C
- McGinness J
- McGlynn K
- McGlynn K
- McGovern A
- McGuinness H
- McInnes IB
- McIntosh J
- McIvor E
- McIvor K
- McLeavey L
- McMahon A
- McMahon MJ
- McMorrow L
- Mcnally T
- McNarry M
- McNeill J
- McQueen A
- McShane H
- McShane H
- Mears C
- Megson C
- Megson S
- Mehta P
- Meiring J
- Melling L
- Mencias M
- Menke R
- Menzies D
- Michael A
- Michael B
- Miller CA
- Miller CA
- Milligan L
- Mills C
- Mills G
- Mills G
- Mills NL
- Milner L
- Misra S
- Mitchell J
- Mitchell J
- Mohamed A
- Mohamed N
- Mohammed S
- Molyneaux PL
- Molyneaux PL
- Monteiro W
- Moriera S
- Morillas MM
- Morley A
- Morrison L
- Morriss R
- Morrow A
- Moss A
- Moss AJ
- Moss AJ
- Moss P
- Motohashi K
- Msimanga N
- Mukaetova-Ladinska E
- Munawar U
- Munro K
- Murira J
- Nanda U
- Nassa H
- Nasseri M
- Nathu R
- Neal A
- Needham R
- Neill P
- Neubauer S
- Neubauer S
- Neubauer S
- Neubauer S
- Nevado-Holgado A
- Newby DE
- Newell H
- Newman J
- Newman T
- Nichols TE
- Nicholson T
- Nicolaou C
- Nicolaou C
- Nicoll D
- Nikolaidis A
- Nikolaidou C
- Nolan C
- Nolan CM
- Noonan MJ
- Norman C
- Novotny P
- Nunag J
- Nwafor L
- Nwanguma U
- Nyaboko J
- O'Brien C
- O'Brien C
- O'Brien C
- O'Brien L
- O'Donnell K
- O'Regan DP
- O'Regan DP
- Odell N
- Ogbole G
- Ogg G
- Olaosebikan O
- Oliver C
- Omar Z
- Openshaw PJ
- Openshaw PJM
- Osborne L
- Osbourne R
- Ostermann M
- Ostermann M
- Overton C
- Owen J
- Oxton J
- Pack J
- Pacpaco E
- Paddick S
- Painter S
- Pakzad A
- Pakzad A
- Palmer S
- Papineni P
- Paques K
- Paradowski K
- Pareek M
- Parekh D
- Parekh D
- Parekh D
- Parekh D
- Parekh D
- Parekh D
- Parfrey H
- Pariante C
- Parker S
- Parkes M
- Parkes M
- Parmar J
- Patale S
- Patel B
- Patel M
- Patel S
- Pattenadk D
- Pavlides M
- Payne S
- Pearce L
- Pearl J
- Pearl JE
- Peckham D
- Peckham D
- Pendlebury J
- Peng Y
- Pennington C
- Peralta I
- Perkins E
- Peterkin Z
- Peto T
- Petousi N
- Petrie J
- Pfeffer P
- Pfeffer P
- Pfeffer P
- Pfeffer P
- Phipps J
- Piechnik S
- Pimm
- Pimm J
- Pius R
- Plant H
- Plein S
- Plein S
- Plekhanova T
- Plowright M
- Poinasamy K
- Poinasamy K
- Poinasamy K
- Poinasamy K
- Poinasamy K
- Polgar O
- Poll L
- Porter J
- Porter J
- Porter JC
- Porter JC
- Portukhay S
- Powell N
- Prabhu A
- Pratt J
- Price A
- Price C
- Price C
- Price D
- Price L
- Prickett A
- Propescu I
- Propescu J
- Prosper S
- Pugmire S
- Quaid S
- Quigley J
- Quint J
- Quint J
- Quint JK
- Quint JK
- Quint JK
- Qureshi H
- Qureshi IN
- Radhakrishnan K
- Rahman N
- Rahman NM
- Rahman NM
- Ralser M
- Raman B
- Raman B
- Raman B
- Raman B
- Raman B
- Ramos A
- Ramos H
- Rangeley J
- Rangelov B
- Rangelov B
- Ratcliffe L
- Ravencroft P
- Reddington A
- Reddy A
- Reddy R
- Redfearn H
- Redwood D
- Reed A
- Rees M
- Rees T
- Regan K
- Reynolds W
- Ribeiro C
- Richards A
- Richardson E
- Richardson M
- Richardson M
- Rivera-Ortega P
- Roberts K
- Robertson E
- Robinson E
- Robinson L
- Roche L
- Roddis C
- Rodger J
- Rogers N
- Ross A
- Ross G
- Rossdale J
- Rossdale J
- Rostron A
- Rostron A
- Rowe A
- Rowland A
- Rowland J
- Rowland MJ
- Rowland MJ
- Rowland MJ
- Rowland-Jones SL
- Rowland-Jones SL
- Rowland-Jones SL
- Roy K
- Roy M
- Rudan I
- Russell E
- Russell RJ
- Saalmink G
- Sabit R
- Sage EK
- Samakomva T
- Samani N
- Samat AA
- Sampson C
- Samuel K
- Samuel R
- Sanders ZB
- Sanderson A
- Sapey E
- Sapey E
- Sapey E
- Saralaya D
- Sargent J
- Sarginson C
- Sass T
- Sattar AN
- Sattar N
- Sattar N
- Sattar N
- Saunders K
- Saunders K
- Saunders L
- Saunders LC
- Saunders P
- Saunders RM
- Saunders RM
- Saunders RM
- Saunders RM
- Savill H
- Saxon W
- Sayer A
- Sayer A
- Schronce J
- Schwaeble W
- Scott JT
- Scott JT
- Scott JT
- Scott K
- Selby N
- Semple MG
- Semple MG
- Semple MG
- Semple MG
- Semple MG
- Sereno M
- Sereno M
- Sereno M
- Sereno M
- Sereno M
- Sewell TA
- Shah AM
- Shah AM
- Shah K
- Shah P
- Shankar-Hari M
- Sharma M
- Sharpe C
- Sharpe M
- Sharpe M
- Shashaa S
- Shaw A
- Shaw K
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- Shaw V
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- Sheikh A
- Sheikh A
- Sheikh A
- Sheikh A
- Sheikh A
- Shelton S
- Shenton L
- Shevket K
- Shikotra A
- Shikotra A
- Shikotra A
- Shikotra A
- Shikotra A
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- Siddiqui S
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- Sidebottom J
- Sigfrid L
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- Singapuri A
- Singapuri A
- Singapuri A
- Singapuri A
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- Singh C
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- Singh SJ
- Singh SJ
- Singh SJ
- Sissons D
- Skeemer J
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- Smith A
- Smith D
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- Smith L
- Smith N
- Smith N
- Smith S
- Soares M
- Solano TS
- Solly R
- Solstice AR
- Soulsby T
- Southern D
- Sowter D
- Spears M
- Spencer LG
- Speranza F
- Stadon L
- Stanel S
- Steeds R
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- Steele N
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- Stewart I
- Stimpson R
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- Stoker W
- Stone R
- Storrar W
- Storrie A
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- Stringer E
- Strong-Sheldrake S
- Stroud N
- Subbe C
- Sudlow C
- Sudlow CL
- Suleiman Z
- Summers C
- Summersgill C
- Sutherland D
- Sykes DL
- Sykes R
- Talbot N
- Tan AL
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- Tarusan L
- Tavoukjian V
- Taylor A
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- Te A
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- Tee CJ
- Teixeira J
- Tench H
- Terry S
- Thackray-Nocera S
- Thaivalappil F
- Thamu B
- Thickett D
- Thomas AK
- Thomas C
- Thomas D
- Thomas D
- Thomas DC
- Thomas DC
- Thomas S
- Thomas-Woods T
- Thompson AAR
- Thompson AAR
- Thompson AAR
- Thompson AAR
- Thompson AR
- Thompson T
- Thornton T
- Thorpe M
- Thorpe M
- Thwaites R
- Thwaites RS
- Tilley J
- Tinker N
- Tiongson GF
- Tobin M
- Tomlinson J
- Tong C
- Toshner M
- Toshner M
- Toshner M
- Toshner M
- Toshner M
- Touyz R
- Treibel T
- Tripp KA
- Tunnicliffe E
- Tunnicliffe EM
- Turnbull A
- Turner E
- Turner K
- Turner S
- Turner V
- Turney S
- Turtle L
- Turtle L
- Turton H
- Ugoji J
- Ugwuoke R
- Upthegrove R
- Valabhji J
- Venson B
- Ventura M
- Vere J
- Vickers C
- Vinson B
- Vogiatzis I
- Wade E
- Wade P
- Wain LV
- Wain LV
- Wain LV
- Wain LV
- Wain LV
- Wain LV
- Wain LV
- Wain LV
- Wain LV
- Wainwright T
- Wajero LO
- Walder S
- Walker S
- Walker S
- Walker S
- Walker S
- Wall E
- Wallis T
- Walmsley S
- Walsh JA
- Walsh S
- Warburton L
- Ward TJC
- Warwick K
- Wassall H
- Waterson S
- Watson E
- Watson J
- Watson L
- Webster M
- Welch C
- Welch H
- Welsh B
- Wessely S
- West S
- Weston H
- Wheeler H
- White S
- Whitehead V
- Whitney J
- Whittaker S
- Whittam B
- Whitworth V
- Wight A
- Wild JM
- Wild JM
- Wild JM
- Wild JM
- Wilkins M
- Wilkinson D
- Wilkinson D
- Williams B
- Williams J
- Williams N
- Williams N
- Williams N
- Williams-Howard SA
- Willicombe M
- Willis G
- Willoughby J
- Wilson A
- Wilson D
- Wilson D
- Wilson I
- Window N
- Witham M
- Witham M
- Wolf-Roberts R
- Wood C
- Woodhead F
- Woods J
- Wootton DG
- Wootton DG
- Wootton DG
- Wootton DG
- Wormleighton J
- Worsley J
- Wraith D
- Wright C
- Wright L
- Wright S
- Wyles J
- Wynn E
- Wynter I
- Xie C
- Xu M
- Xu M
- Yasmin N
- Yasmin S
- Yates T
- Yates T
- Yip KP
- Young A
- Young B
- Young S
- Yousuf A
- Zawia A
- Zeidan L
- Zhao B
- Zheng B
- Zongo O
- Publication venue
- Oxford University Press (OUP)
- Publication date
- 18/12/2023
- Field of study
Finishing the euchromatic sequence of the human genome
- Author
- . Haifeng
- . Magner
- . Yin
- Abbott Scott
- Abbott-Ozersky Amanda
- Abdellah Zahra
- Abouelleil Amr
- Abrajano Anne
- Adachi Tamami
- Adam Catherine
- Adams Charles Q.
- Adamson Aaron
- Adekoya Emmanuel
- Adio-Oduola Babajide
- Aerts Andrea
- Aggarwal Arun
- Ahmadi Alireza
- Ahmed Shahana
- Aimable Matthew
- Ainscough Rachael
- Ait-Zahra Mostafa
- Aizu Tomoyuki
- Alcivare Dana
- Alegria Michelle
- Ali Alla
- Ali Johar
- Allegria-hartmann Michelle
- Alleman Jennifer
- Allen Carlana C.
- Allen Heather
- Allen Nicole R.
- Allen Susan
- Allen Thaddeus
- Almeida Jeff
- Almond Claire
- Alsbrooks Stephen L.
- Altherr Michael R.
- Amaratunge Harshinie C.
- Ambler Andrew
- Ambrose Karen
- Ambrose Kerrie
- Amemiya Chris
- Amico-Keller Gina
- Amin Amita G.
- Anderson Mechele
- Anderson Scott
- Anderson Scott
- Andora Janice
- Andredesz Carol
- Andrew Robert
- Andrews Dan
- Andrews Daniel
- Andrews Neil
- Andrews Stephanie
- Andriese Tim
- Anthouard Véronique
- Antonarakis Stylianos E.
- Anyalebechi Vivian
- Aoki Norie
- Apostolou Sinoula
- Apweiler Eva
- Arachchi Harindra
- Arai Rie
- Arbery Hazel
- Arcaina Marlon
- Arcaina Terisita
- Archer Beth
- Arellano Andre
- Arellano-Jones Perry
- Armbruster Jeff
- Armstrong Jon
- Arredondo Dilrukshi P.
- Arredondo Heather Hope
- Artiguenave François
- Asakawa Shuichi
- Asakawa Teruyo
- Ash Gareth
- Ashcroft Kevin
- Ashurst Jennifer
- Ashwell Robert
- Ashworth Linda K.
- Aslanidis Cara
- Asomugha Chinwe O.
- Asuncion Lawreen
- Atkin Deborah
- Atkinson Andrea
- Atkinson Barry
- Attix Cristina
- Attwood John
- Aubin Keith
- Auger Katherine
- Austin Shannon Michelle
- Avila Aaron
- Avis Terry
- Ayele Mulu
- Babayan Primo
- Babbage Anne
- Babbage Sarah
- Bach Phil
- Bachatsang Pasang
- Bacon Joanne
- Badri Hummy
- Baertsch Robert
- Bagguley Claire
- Bailey Jonathan
- Bajorek Eva
- Baker Andrew
- Baker Dan
- Baker M.
- Baker Richard
- Bakis Michele
- Baldwin Jennifer
- Banda Michael
- Banerjee Ruby
- Bao Jingyue
- Bao Qiyu
- Bao Weidong
- Bao Weidong
- Baptiste Pertrice
- Barbaria Joseph A.
- Barbe Valérie
- Bardill Simon
- Barker Daniel
- Barker Darren
- Barker Gary
- Barlow Karen
- Baron Laurent
- Barrett Anika
- Bartlett Rebecca
- Basham Victoria
- Bashman David
- Basu Suba
- Bateman Alex
- Bates Karen
- Battles John
- Batzer Mark
- Baumgart Cornelia
- Baumohl Jason
- Baynes Caroline
- Bayul Tashi
- Beall Keith
- Beard Lisa
- Beard Susan
- Beare David
- Beasley Alastair
- Beasley Helen
- Beasley Oliver
- Beaucham Leslie
- Beaudet Arthur
- Beck Alfred
- Beck Stephen
- Becker Michael
- Bell Emma
- Bell George I.
- Bellard Terell M.
- Bellerby Damian
- Bellerby Tristram
- Belter Edward A., Jr.
- Bemrose Richard
- Benard Michael Anthony
- BenKahla Alia
- Benke J
- Benner William
- Bennett James
- Bensasson Douda
- Bentley Andrew
- Bentley Dan
- Bentley David
- Berardinis Véronique de
- Bercovitz John
- Berghoff Amy
- Bergmann Anne
- Berkowicz Nicolas
- Berks Mary
- Berks Michael
- Bethel Graeme
- Beugelsdijk Tony J.
- Bhakta Rita
- Bhuchar Venita
- Bi Shihua
- Bian Xuemeng
- Bieri Tamberlyn
- Bimage Kesha E.
- Bird Christine
- Birditt Brian
- Birney Ewan
- Birney Ewan
- Birren Bruce
- Bissell Helen
- Biswalo Kaneza
- Bituin Aleksandr
- Black Stacey
- Blackburne-Maze Suzanne
- Blair Jessica Anne
- Blakey Sarah
- Blanks Tia
- Blasiar Darin
- Blazej Robert
- Blitshsteyn Berta
- Blomstrom David B.
- Bloom Scott
- Bloom Toby
- Blumer Heather
- Blye Jason
- Blyth Peter R.
- Blöcker Helmut
- Boatright Elizabeth
- Boehm John
- Boen Juanan
- Boguslavskiy Leonid
- Bolton Christel
- Bolund Lars
- Bondoc Marnel
- Bonfield James
- Bonnett Ralph
- Bonnin David
- Border Richard
- Borowsky Mark
- Borzym Katja
- Boukhgalter Boris
- Bowen Eric
- Bradley Amanda
- Bradshaw-Cordum Holly
- Brady Nicola
- Brandriff Brigitte F.
- Brannon Wade
- Branscomb Elbert
- Bray Jason
- Bray-Allen Sarah
- Brettin Thomas
- Bridgeman Anne
- Bridgers Michael
- Brimhall Angela K.
- Brokstein Peter
- Brook Jonathan
- Brooking Shane
- Brottier Philippe
- Brown Andrew
- Brown Clive
- Brown Jacqui
- Brown Margaret
- Brown Mary
- Brown Mary J.
- Brown Michael
- Brown Nancy C.
- Bruce David D.
- Bruce Robert
- Bruno William J.
- Bruskiewich Richard
- Bryant Jackie
- Bryant Jennifer E.
- Bryant Nathaniel P.
- Brüls Thomas
- Buatsi Delali
- Buck David
- Buckingham Judith M.
- Buckle Veronica
- Buczek Donald
- Budd Claire
- Buhay Christian J.
- Bulbul Kerem
- Buller Sarah
- Bunker Nathan
- Burberry Jill
- Burch Paula Ellen
- Burford Deborah
- Burgess Joanne
- Burgin Matt
- Burkett Carrie E.
- Burkhart-Schultz Karolyn
- Burrell Kevin L.
- Burrill Wayne
- Burrows Christine
- Burton Christine
- Burton John
- Butcher Phil
- Butler Adam
- Butler Jon
- Butler Paul
- Caenepeel Sean
- Cahill Patrick
- Cai Tianjing
- Cai Zhen
- Cairns Murray
- Calderon Eliana
- Callen David F.
- Camarata Jody
- Camire David
- Camm Nick
- Campbell Christopher
- Campbell Connie S.
- Campbell Evelyn W.
- Campbell Mary I.
- Campbell Mary L.
- Campo Kevin
- Canning Bruno
- Cao Ting
- Cao Yuzhu
- Caoile Chenier
- Cardenas Faviola
- Cardenas Lolo
- Cardenas Veronica
- Carder Carol
- Carder Paul
- Carpenter Kelly
- Carrano Anthony V.
- Carriere Jason
- Carter Jason
- Carter Kelvin
- Carter Nigel
- Caruso Lauren
- Casias Kristal
- Cattolico Laurence
- Cavanna Tamara
- Cavazos Iracema
- Cavazos Sandra R.
- Ceasar Heather
- Cedroni Maria
- Cepeda Mario
- Chacko Joseph
- Chain Patrick
- Chalk Shani
- Challacombe Jean F.
- Chan Ka
- Chan Sheryl N.
- Chan Yee Man
- Chang Jean L.
- Chapman Jarrod
- Chapman Joanna
- Chapple Jeffrey
- Charles Rachel
- Chasteen Leslie A.
- Chavarria Simeon
- Chazaro Bruno
- Chen Baoxian
- Chen Bin
- Chen Chira
- Chen Chong
- Chen Chong
- Chen Chun-Nan
- Chen Cong
- Chen Ellson
- Chen Hsiu-Chuan
- Chen Jianlong
- Chen Jie
- Chen Jin
- Chen Junbao
- Chen Lihong
- Chen Lixia
- Chen Ray
- Chen Shu
- Chen Tong
- Chen Xiaoyun
- Chen Xinyi
- Chen Yanjiong
- Chen Yiyu
- Chen Zhu
- Chen Zhu
- Chen Zhu
- Cheng Jan-Fang
- Cheng Zhihua
- Chertkov Olga
- Cheshatsang Yama
- Chi Cheng
- Chi Han C.
- Chillingworth Neil
- Chin Sylvia
- Chinn Corey
- Chinwalla Asif
- Chissoe Stephanie
- Chiu Sally
- Chothia Tom
- Christensen Mari
- Christopoulos Constantine
- Chu Joseph
- Chui Connie
- Chung A
- Cinkowsky Michael J.
- Citroen Mieke
- Clack Rob
- Clamp Michele
- Clark Anthea
- Clark Graham
- Clark Kevin
- Clark Lynn
- Clark Lynn M.
- Clark Richard
- Clark Sarah
- Clark Sue
- Clarke Adrian
- Clarke Betty
- Clarke Eddie
- Clarke Kay
- Clarke Laura
- Clawson Hiram
- Clee Chris
- Clegg Shelia
- Clerc Blankenburg Kerstin Petra
- Cleveland David
- Clifford Karen
- Clifton Sandra W.
- Coates Julia
- Cobley Victoria
- Cockrell Raynard
- Coffey Alison
- Cofield Jackie
- Coggill Penelope
- Cohn Judith D.
- Colayco Rick
- Cole Lotte
- Collier Rachael
- Collings Simon
- Collins Francis S.
- Collins John
- Collins Philip
- Collymore Al
- Colman Louise
- Combs Jessie
- Comstock Robin
- Cong Bin
- Conner Richard
- Connolly Anthony
- Connolly Karen
- Conquer Jennie
- Conrad Ansgar
- Conroy Donald
- Considine Tony
- Constance Doug
- Cook April
- Cook Leanna
- Cooke Patrick
- Cooper Jonathan
- Cooper Rachel
- Cooper Robert
- Copeland Alex
- Coppola Maria
- Copsey Teresa
- Corby Nicole
- Cordes Matt
- Cordray Rebecca
- Cornell Christine
- Cornell Earl
- Cornell Linda
- Cornell Ruth
- Corum Ben
- Cottage Amanda
- Cotton Sara
- Coulson Alan
- Couronne Olivier
- Courtney Laura P.
- Coville Gez
- Cox Anthony
- Cox Caroline D.
- Cox Tony
- Coxhill Robert
- Coyle Marcus D.
- Craig Matthew
- Crane Tom
- Crawford Amanda L.
- Crawley Matt
- Cree Andrew
- Crespeau Hervé
- Crew Victor
- Critchlow Terrance
- Critz Paul
- Cruaud Corinne
- Cuff James
- Cui Hongjuan
- Cui Jinhui
- Cui Peng
- Cui Peng
- Culley Karl
- Cummings Auli
- Cummings Kirsti
- Cummings Paul
- Cummings Stephanie
- Cuomo Christina A.
- Curran Adam
- Curwen Valery
- Cutts Jeffrey
- Czubayko Martin
- D\u27Souza Lisa Marie
- Da Silva Corinne
- Dai Li
- Dalin Eillen
- Dang Michelle
- Danganan Linda
- Daniels Rachael
- Dathorne Stephanie R.
- Daum Christopher
- David Robert
- Davidson Lucy
- Davidson Stuart
- Davies Jonathon
- Davies Joy
- Davies Nicholas
- Davies Robert
- Davila Mary Louise
- Davis Candi Mon\u27et
- Davis Cheryl
- Davis Clay
- Davis Jayne
- Davis John
- Davis Matthew
- Davy-Carroll Latarsha
- Dawoe Tenzin
- Dawson Elisabeth
- De Anda Claudia
- De Latorre Andrea
- Deadman Rebecca
- Dean Peter
- Dear Simon
- Dearden Frances
- DeArellano Kurt
- Deaven Larry I.
- Deaven Larry L.
- Deere Kerry
- DeGray Stewart
- Degusta David
- Deguzman Maria
- Dehal Paramvir
- Delgado Marcos
- Delgado Oliver
- Delhaunty Kimberley
- Deloukas Panos
- Deng Yajun
- Dennis Janet
- Denson Shawn
- Denys Mirian
- Deramo Christine
- Desai Anu
- Detter John C.
- Devlin Laurie
- Dewar Ken
- Dhami Pawandeep
- Dhongsar Chemey
- Dias Jennifer
- Dias Victoria
- Dibartolo Genevieve
- Dibling Catherine
- Dickson Mark
- Diekhans Mark
- Dietz-Band Jeanne
- Digennaro Richard
- Dilts Karen
- Dimitrijevic-Bussod Mira
- Ding Hao
- Ding Keyue
- Ding Li
- Ding Yan
- Dinh Huyen H.
- Dixon Kami
- Do Long
- Dobbs Ruth
- Dobson Richard
- Dockree Catherine
- Doddington Daniel
- Dodsworth Steven
- Doggett Norman
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- Dong Hui
- Dong Kimberly
- Dong Wei
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- Dong Xiaojia
- Donlin Jeremy E.
- Dooley Kathy
- Dooling David
- Dorje Passang
- Dorjee Kunsang
- Dorris Lester
- Dorsett Victor
- Doucette-Stamm Lynn
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- Draper Heather
- Du Feiyu
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- Dubchak Inna
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- Dunwell Erin
- Dupes Alan
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- Durham Jillian
- Dutta Ireena
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- Eckenberg Ralph
- Edgar Darren
- Edionwe Susan Omwanghe Osayanro
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- Edwards Jennifer
- Edwards Karen
- Egan Amy
- Eichler Evan
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- Ejima Fumio
- Elkin Chris
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- Elliot Jeffrey
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- Emelianenko Natalia
- Emery-Cohen Alexandra J.
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- Erickson Jeffery
- Erler Anne Marie
- Errington Helen
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- Evans Gareth
- Evans John
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- Evans Richard
- Eveleth Gerald
- Eyras Eduardo
- Fan Hongyuan
- Fan Keke
- Fang Jianqiu
- Farina Abderrahim
- Faro Susan
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- Fawcett Joseph J.
- Fechtel Kim
- Fellingham Charlotte
- Felming Claire
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- Fernando Pushpa Ranjani
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- Footman Simon
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- Fujiyama Asao
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- Fuller Liam
- Fuller Sharin
- Fullerton Kathryn
- Fulton Lucinda A.
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- Furey Terrence S.
- Furuhashi Mie
- Förste Silke
- Gabisi Abdul M.
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- Garcia Ricardo M, III
- Garcia-Martinez Antonio
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- Gardner Alison
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- Gardyna Steph
- Garner Patrick
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- Garnett Jane
- Garza Melissa
- Gatewood Joseph M.
- Gatland Leigh
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- Geng Jianing
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- Gibbs Ben
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- Grant Michael
- Grant Susan
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- Gribble Susan
- Griffith Jeffrey K.
- Griffiths Coline
- Griffiths Ed
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- Grimwood Jane
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- Gu Wenyi
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- Guel Metzalli
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- Guevara Whitney V.
- Gui Qi
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- Gunning Kate
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- Hamilton Matt
- Hamlett John
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- Hammon Nancy
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- Hammond Sian
- Hamza Khalid
- Han Guiqing
- Han Shunsheng
- Han Xurong
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- Hancock Julie
- Harbes Brandy A.
- Harding Adam
- Harkins C. Richard
- Harley Joanne
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- Haugen Eric
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- Hawes Alicia C.
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- Hawkins Natalie
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- Heyen Joshua
- Higgs Douglas
- Hildebrand Carl E.
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- Hillyard Guy
- Hines Sandra
- Hinkins Russell
- Hinrichs Angela S.
- Hitchens Matthew Edward
- Ho Issac
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- Hodgson Anne V.
- Hodgson David
- Hoffman Susan M.G.
- Hoffs Michael
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- Honan Tracy
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- Howard Philip
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- Howden Philip
- Howe Kevin
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- Huang Fang
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- Huang Wei
- Huang Zhengping
- Hubbard Timothy
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- Huckle Elizabeth
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- Hupman Matt
- Huynh Sandy
- Hyde David
- Hynds Christopher
- Idlebird Devincent G.
- Iliev Ilian
- Imbro Paula
- Imo Kelvin C.
- Inacio Nicole
- Inagaki Naomi
- Ince Michael
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- Inoue Shuuji
- Isak Amber
- Isherwood Judith
- Ishibashi Akiko
- Ishikawa Sabine K.
- Ishizaki Hinako
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- Jaklevic Joseph
- Jaklevic Michael
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- Jareborg Niclas
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- Jia Jia
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- Keenan Stephen
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- Kosiura Anna
- Kou Zhaohui
- Kovar Christie L.
- Krawczyk Marie-Claude
- Kremitzki Colin
- Kremmidiotis Gabriel
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- Kruchowski Scott S.
- Kube Michael
- Kubischta Duane
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- Loulseged Hermela
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- Lu Lingfeng
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- Lu Yongxiang
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- Lu Yue
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- Ludeman Thom
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- Madabhushi Ramki
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- Mungall Andy
- Munidasa Mala
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- Murayama Yuji
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- Nair Seema R.
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- Nakagawa Masayo
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- Nwaokelemeh Ogechi O.
- Nwokenkwo Stanley
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- O\u27Donovan Daniel
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- Olson Maynard V.
- Omotosho Bamidele
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- Yadav Shailendra
- Yakub Syed
- Yamamoto Lynn
- Yamamoto Noriko
- Yamamoto Yuko
- Yamashita Yasue
- Yamazaki Satoru
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- Yang Huanming
- Yang Huanming
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- Yao Zhijian
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- Yeager Shane
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- Zainoun Joanne
- Zembeck Lisa
- Zeng Yixin
- Zhai Dong
- Zhan Guoping
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- Zhang Guangyu
- Zhang Guohua
- Zhang Guohua
- Zhang Haiqing
- Zhang Haiqing
- Zhang Haiqing
- Zhang Hongbo
- Zhang Hongbo
- Zhang Jingjing
- Zhang Jingjing
- Zhang Jingkun
- Zhang Jiuchun
- Zhang Jiuchun
- Zhang Lanzhi
- Zhang Li
- Zhang Li
- Zhang Meihua
- Zhang Meng
- Zhang Ming
- Zhang Qing
- Zhang Ruhua
- Zhang Shaojie
- Zhang Tiezhen
- Zhang Wei
- Zhang Wei
- Zhang Xianglin
- Zhang Xianglin
- Zhang Xiaoliang
- Zhang Xiuqing
- Zhang Yan
- Zhang Yi
- Zhang Yilin
- Zhang Yilin
- Zhang Ying
- Zhang Yuansen
- Zhang Yuzhi
- Zhang Zhengdong
- Zhao Hongmei
- Zhao Lijian
- Zhao Shenru
- Zhao Zhijing
- Zhen Zhicheng
- Zheng Haibo
- Zhong Ming
- Zhou Carol
- Zhou Haixia
- Zhou Jianling
- Zhou Nannan
- Zhou Xinfeng
- Zhou Yan
- Zhou Yang
- Zhou Yi
- Zhu Bingying
- Zhu Bofeng
- Zhu Fenghua
- Zhu Genfeng
- Zhu Genfeng
- Zhu Miao
- Zhu Ning
- Zhu Yongge
- Zhu Zhen
- Zhuang Shitao
- Zierten Deborah
- Zimmer Andrew
- Zody Michael C.
- Zollo Massimo
- Zorrilla Sara E.
- Zuo Lin
- Publication venue
- LSU Digital Commons
- Publication date
- 21/10/2004
- Field of study
The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead
Brazilian Consensus on Photoprotection
- Author
- Abarca J
- Abdel-Malek Z
- Abel E
- Acosta LR
- Adam J
- Ahmed AM
- Alaluf S
- Almutawa F
- Aloai JF
- Aloia JF
- Aloia JF
- Alonso-Lebrero JL
- Alves LM
- Anderson RR
- Andersson-Willman B
- Andrés-Lacueva C
- Aripuanã Cobério Terena
- Armstrong AW
- Avenel-Audran M
- Avenel-Audran M
- Bachrach S
- Bais AF
- Balk SJ
- Balk SJ
- Ball Arefiev KL
- Balogh TS
- Batista T
- Battie C
- Bauer A
- Bauer J
- Baumann L
- Bech-Thomsen N
- Becker JA
- Benvenuto-Andrade C
- Berneburg M
- Bernstein EF
- Biesalski HK
- Binkley N
- Binkley N
- Bischoff-Ferrari HA
- Bodekaer M
- Boisen AM
- Bouilly-Gauthier D
- Boyd AS
- Bradford PT
- Broekmans WM
- Bucay VW
- Buendía Eisman A
- Buendía-Eisman A
- Buller DB
- Buller DB
- Caccialanza M
- Camera E
- Capote R
- Carolina Reato Marçon
- Castanedo-Cazares JP
- Cestari T
- Chan AC
- Chen AC
- Chen L
- Chen T
- Chesney RW
- Chiu YE
- Cho HS
- Cho S
- Clemens TL
- Corrêa MP
- Corrêa MP
- Corrêa MP
- Costa FB
- Crane LA
- Crane LA
- Criado P
- Cross SE
- Cusack C
- D'Orazio J
- Dain SJ
- Darlington S
- Darvin ME
- Dattani JT
- Davis A
- Day AK
- de Gruijl FR
- de Laat A
- de Paula Corrêa M
- de Paula Corrêa M
- de Paula Corrêa M
- Denise Steiner
- Dennis LK
- Diffey BL
- Diffey BL
- Diffey BL
- Diffey BL
- Dlugos DJ
- Dobs AS
- Dominguez AR
- Draelos ZD
- Draelos ZD
- Draelos ZD
- Draelos ZD
- Duarte I
- Dumay O
- Dunnigan MG
- Dusza SW
- Eadie E
- Eberlein-König B
- Edwards Jr EK
- Eicker J
- Eloisa Leis Ayres
- Engelsen O
- English DR
- Erden Inal M
- Erden Inal M
- Fabris MR
- Falk M
- Farrerons J
- Farrerons J
- Fartasch M
- Fioletov VE
- Fitzpatrick TB
- Flávia Alvim Sant'anna Addor
- Flávia Naranjo Ravelli
- Fonseca V
- Fryer MJ
- Fuller R
- Gambichler T
- Gambichler T
- Garcia F
- Gaspar LR
- Geller AC
- Ghazi S
- Gies P
- Gilaberte Y
- Gilchrest BA
- Ginde AA
- Glanz K
- Glanz K
- Glanz K
- Glass D
- Glazebrook C
- Glazer JL
- Godar DE
- Godar DE
- Gonzales S
- Gonzalez S
- Gonzalez S
- Grant WB
- Greul AK
- Groves GA
- Grune T
- Guevara IL
- Guinot C
- Gupta AK
- Guéniche A
- Guéniche A
- Hackenberg S
- Halder RM
- Halliwell B
- Haluza D
- Harms J
- Harris SS
- Hatch KL
- Hatua P
- Haywood R
- Heinrich U
- Helio Amante Miot
- Hercogova J
- Hexsel CL
- Heydenreich J
- Higuera-Ciapara I
- Hillhouse J
- Hodgkin P
- Holick MF
- Holick MF
- Holick MF
- Holick MF
- Holick MF
- Hollis BW
- Holloway L
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- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Clinical characteristics with inflammation profiling of long COVID and association with 1-year recovery following hospitalisation in the UK: a prospective observational study
- Author
- Abel K
- Adamali H
- Adeloye D
- Adeyemi O
- Adrego R
- Ahmad S
- Ahmed R
- Ahwireng N
- Ainsworth M
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- Wyles J
- Wynter I
- Xu M
- Yasmin N
- Yasmin S
- Yates T
- Yip KP
- Young A
- Young B
- Young S
- Yousuf AJ
- Zawia A
- Zeidan L
- Zhao B
- Zheng B
- Zongo O
- Publication venue
- Elsevier
- Publication date
- 01/04/2022
- Field of study
Background
No effective pharmacological or non-pharmacological interventions exist for patients with long COVID. We aimed to describe recovery 1 year after hospital discharge for COVID-19, identify factors associated with patient-perceived recovery, and identify potential therapeutic targets by describing the underlying inflammatory profiles of the previously described recovery clusters at 5 months after hospital discharge.
Methods
The Post-hospitalisation COVID-19 study (PHOSP-COVID) is a prospective, longitudinal cohort study recruiting adults (aged ≥18 years) discharged from hospital with COVID-19 across the UK. Recovery was assessed using patient-reported outcome measures, physical performance, and organ function at 5 months and 1 year after hospital discharge, and stratified by both patient-perceived recovery and recovery cluster. Hierarchical logistic regression modelling was performed for patient-perceived recovery at 1 year. Cluster analysis was done using the clustering large applications k-medoids approach using clinical outcomes at 5 months. Inflammatory protein profiling was analysed from plasma at the 5-month visit. This study is registered on the ISRCTN Registry, ISRCTN10980107, and recruitment is ongoing.
Findings
2320 participants discharged from hospital between March 7, 2020, and April 18, 2021, were assessed at 5 months after discharge and 807 (32·7%) participants completed both the 5-month and 1-year visits. 279 (35·6%) of these 807 patients were women and 505 (64·4%) were men, with a mean age of 58·7 (SD 12·5) years, and 224 (27·8%) had received invasive mechanical ventilation (WHO class 7–9). The proportion of patients reporting full recovery was unchanged between 5 months (501 [25·5%] of 1965) and 1 year (232 [28·9%] of 804). Factors associated with being less likely to report full recovery at 1 year were female sex (odds ratio 0·68 [95% CI 0·46–0·99]), obesity (0·50 [0·34–0·74]) and invasive mechanical ventilation (0·42 [0·23–0·76]). Cluster analysis (n=1636) corroborated the previously reported four clusters: very severe, severe, moderate with cognitive impairment, and mild, relating to the severity of physical health, mental health, and cognitive impairment at 5 months. We found increased inflammatory mediators of tissue damage and repair in both the very severe and the moderate with cognitive impairment clusters compared with the mild cluster, including IL-6 concentration, which was increased in both comparisons (n=626 participants). We found a substantial deficit in median EQ-5D-5L utility index from before COVID-19 (retrospective assessment; 0·88 [IQR 0·74–1·00]), at 5 months (0·74 [0·64–0·88]) to 1 year (0·75 [0·62–0·88]), with minimal improvements across all outcome measures at 1 year after discharge in the whole cohort and within each of the four clusters.
Interpretation
The sequelae of a hospital admission with COVID-19 were substantial 1 year after discharge across a range of health domains, with the minority in our cohort feeling fully recovered. Patient-perceived health-related quality of life was reduced at 1 year compared with before hospital admission. Systematic inflammation and obesity are potential treatable traits that warrant further investigation in clinical trials.
Funding
UK Research and Innovation and National Institute for Health Research
Accelarated immune ageing is associated with COVID-19 disease severity
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- Woodhead F.
- Woods J.
- Wootton D.G.
- Wormleighton J.
- Worsley J.
- Wraith D.
- Wrey Brown C.
- Wright C.
- Wright L.
- Wright S.
- Wyles J.
- Wynter I.
- Xu M.
- Yasmin N.
- Yasmin S.
- Yates T.
- Yip K.P.
- Young A.
- Young B.
- Young S.
- Yousuf A.J.
- Zawia A.
- Zeidan L.
- Zhao B.
- Zheng B.
- Zongo O.
- Publication venue
- BMC
- Publication date
- 11/01/2024
- Field of study
Background
The striking increase in COVID-19 severity in older adults provides a clear example of immunesenescence, the age-related remodelling of the immune system. To better characterise the association between convalescent immunesenescence and acute disease severity, we determined the immune phenotype of COVID-19 survivors and non-infected controls.
Results
We performed detailed immune phenotyping of peripheral blood mononuclear cells isolated from 103 COVID-19 survivors 3–5 months post recovery who were classified as having had severe (n = 56; age 53.12 ± 11.30 years), moderate (n = 32; age 52.28 ± 11.43 years) or mild (n = 15; age 49.67 ± 7.30 years) disease and compared with age and sex-matched healthy adults (n = 59; age 50.49 ± 10.68 years). We assessed a broad range of immune cell phenotypes to generate a composite score, IMM-AGE, to determine the degree of immune senescence. We found increased immunesenescence features in severe COVID-19 survivors compared to controls including: a reduced frequency and number of naïve CD4 and CD8 T cells (p < 0.0001); increased frequency of EMRA CD4 (p < 0.003) and CD8 T cells (p < 0.001); a higher frequency (p < 0.0001) and absolute numbers (p < 0.001) of CD28−ve CD57+ve senescent CD4 and CD8 T cells; higher frequency (p < 0.003) and absolute numbers (p < 0.02) of PD-1 expressing exhausted CD8 T cells; a two-fold increase in Th17 polarisation (p < 0.0001); higher frequency of memory B cells (p < 0.001) and increased frequency (p < 0.0001) and numbers (p < 0.001) of CD57+ve senescent NK cells. As a result, the IMM-AGE score was significantly higher in severe COVID-19 survivors than in controls (p < 0.001). Few differences were seen for those with moderate disease and none for mild disease. Regression analysis revealed the only pre-existing variable influencing the IMM-AGE score was South Asian ethnicity (
= 0.174, p = 0.043), with a major influence being disease severity (
= 0.188, p = 0.01).
Conclusions
Our analyses reveal a state of enhanced immune ageing in survivors of severe COVID-19 and suggest this could be related to SARS-Cov-2 infection. Our data support the rationale for trials of anti-immune ageing interventions for improving clinical outcomes in these patients with severe disease
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