5 research outputs found
Crystal growth, optical bandgap, thermal, mechanical, dielectric studies on NLO active semiorganic 4-dimethylaminopyridine sodium chloride crystal for frequency conversion
- Author
- BB Ivanova
- BB Koleva
- CR Raja
- D Xue
- D. Sivavishnu
- EM Onitsch
- G Varsanyi
- GJ Shanmuga Sundar
- IP Bincy
- J Chandrasekaran
- J Johnson
- J Johnson
- J Johnson
- J Ramajothi
- J. Johnson
- JH Joshi
- JH Joshi
- JH Joshi
- JH Joshi
- JH Joshi
- JH Joshi
- JH Joshi
- JJ Rodrigues Jr
- JS Pan
- K Thirupugalmani
- KD Parikh
- M Chao
- M Krishnakumar
- M Mahadevan
- M Packiya Raj
- M Rajkumar
- M Saravanan
- MA Kaid
- MA Rajkumar
- N Ennaceur
- N Horiuchi
- N Sundaraganesan
- O Sahin
- P Anandan
- P Justin
- P Karuppasamy
- P Karuppasamy
- P Karuppasamy
- P Pandey
- R Aarthi
- R Srineevasan
- R Srineevasan
- R. Srineevasan
- SE Allen Moses
- SK Kurtz
- SM Ravi Kumar
- T Dhanabal
- V Vasudevan
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Mapping the human genetic architecture of COVID-19
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2021
- Field of study
The genetic make-up of an individual contributes to the susceptibility and response to viral infection. Although environmental, clinical and social factors have a role in the chance of exposure to SARS-CoV-2 and the severity of COVID-191,2, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. Here we describe the results of three genome-wide association meta-analyses that consist of up to 49,562 patients with COVID-19 from 46 studies across 19 countries. We report 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases3–7. They also represent potentially actionable mechanisms in response to infection. Mendelian randomization analyses support a causal role for smoking and body-mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19 was made possible by the community of human genetics researchers coming together to prioritize the sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease
Ramucirumab with cisplatin and fluoropyrimidine as first-line therapy in patients with metastatic gastric or junctional adenocarcinoma (RAINFALL): a double-blind, randomised, placebo-controlled, phase 3 trial
- Author
- Acs Peter Istvan
- Al-Batran Salah-Eddin
- Alavez Alejandro Molina
- Alcindor Thierry
- Alfonso Pilar Garcia
- Alsina Maria
- Aprile Giuseppe
- Asmis Timothy R
- Ayala Hubert
- Bajaj Madhuri
- Barone Carlo
- Barrull Joana Vidal
- Bartoli Maria Alejandra
- Beck Joseph Thaddeus
- Bendell Johanna Chock
- Beny Alex
- Berry Scott
- Blasinska-Morawiec Maria
- Bodoky Gyorgy
- Bono Peter
- Brenner Baruch
- Brezden-Masley Christine
- Burkes Ronald L
- Cabanillas Fernando
- Carlesi Roberto
- Cats A
- Chau Ian
- Chua Cynthia Coo
- Csilla Andrs
- Csoszi Tibor
- Dammrich Daniel
- Das Mayukh
- De Vita Ferdinando
- Delgado Francisco Gutierrez
- Denlinger Crystal S
- Di Bartolomeo Maria
- Di Costanzo Francesco
- Dicarlo Brian Anthony
- Dichmann Robert Andrew
- Ducreux Michel
- Enzinger Peter C
- Erdkamp FLG
- Esaki Taito
- Escudero Miguel Angel
- Falcone Alfredo
- Fein Luis Enrique
- Ferry David
- Firdaus Irfan
- Folprecht Gunnar
- Ford Hugo
- Fuchs Charles S
- Fujitani Kazumasa
- Geboes Karen
- Gerardo Cardellino Giovanni
- Geva Ravit
- Godinez Francisco Javier Ramirez
- Gomez Christina Maria
- Gorbounova Vera
- Grootscholten M
- Hara Hiroki
- Hebbar Mohamed
- Hegewisch-Becker Susanna
- Hernandez Carlos Alberto
- Hironaka Shuichi
- Hofheinz Ralf-Dieter
- Hool Hugo
- Hussein Maen Abdelkarim
- Ilson David H
- Jaliffe Georgina Garnica
- Jang Raymond Woo-Jun
- Jr Reeves James A
- Kadowaki Shigenori
- Kaen Diego Lucas
- Kallio Raija
- Karaseva Nina A
- Kocsis Judit
- Kowalyszyn Rubn Dario
- Lacy Jill
- Lawler William E
- Leong Stephen
- Lim Howard J
- Lin Ji
- Lonardi Sara
- Lorenzen Sylvie
- Luft Alexander
- Machida Nozomu
- Madhusudan Srinivasan
- Madi Ayman
- Maisey Nicolas Robert
- Mansoor Wasat
- Melendez Fidel David Huitzil
- Melichar Bohuslav
- Mendez Guillermo Ariel
- Mineur Laurent
- Munoz Federico Longo
- Nechaeva Marina N
- Nordsmark Marianne
- Obermannova Radka
- Patel Ravindranath
- Peltola Katriina Johanna
- Petera Jiri
- Petty Russell
- Pezet Denis
- Pfeiffer Per
- Phelip Jean-Marc
- Pikiel Joanna
- Piko Bela
- Plazas Javier Gallego
- Prausova Jana
- Pribylova Jana
- Protsenko Svetlana
- Raj Moses Sundar
- Ruzsa Agnes
- Sakai Daisuke
- Samuel Leslie
- Sarosiek Tomasz
- Senellart Helene
- Shacham-Shmueli Einat
- Shah Manish A
- Shaib Walid
- Shitara Kohei
- Sinapi Isabelle
- Sugimoto Naotoshi
- Taieb Julien
- Takahari Daisuke
- Tehfe Moustapha
- Ten Tije AJ
- Tsuji Akihito
- Turmo Laura Visa
- Valencia Ricardo Villalobos
- Van Cutsem Eric
- Van den Eynde Marc
- Van Laarhoven HMW
- Velez-Cortez Hector
- Verma Udit
- Villanueva Angel Gomez
- Wadsley Jonathan
- Wainberg Zev A
- Wojcik Elzbieta
- Wojcik-Tomaszewska Joanna
- Won Elizabeth
- Yamaguchi Kensei
- Yilmaz Mette Karen Nytoft
- Yukisawa Seigo
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/03/2019
- Field of study
BACKGROUND: VEGF and VEGF receptor 2 (VEGFR-2)-mediated signalling and angiogenesis can contribute to the pathogenesis and progression of gastric cancer. We aimed to assess whether the addition of ramucirumab, a VEGFR-2 antagonist monoclonal antibody, to first-line chemotherapy improves outcomes in patients with metastatic gastric or gastro-oesophageal junction adenocarcinoma. METHODS: For this double-blind, randomised, placebo-controlled, phase 3 trial done at 126 centres in 20 countries, we recruited patients aged 18 years or older with metastatic, HER2-negative gastric or gastro-oesophageal junction adenocarcinoma, an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, and adequate organ function. Eligible patients were randomly assigned (1:1) with an interactive web response system to receive cisplatin (80 mg/m2, on the first day) plus capecitabine (1000 mg/m2, twice daily for 14 days), every 21 days, and either ramucirumab (8 mg/kg) or placebo on days 1 and 8, every 21 days. 5-Fluorouracil (800 mg/m2 intravenous infusion on days 1-5) was permitted in patients unable to take capecitabine. The primary endpoint was investigator-assessed progression-free survival, analysed by intention to treat in the first 508 patients. We did a sensitivity analysis of the primary endpoint, including a central review of CT scans. Overall survival was a key secondary endpoint. This study is registered with ClinicalTrials.gov, number NCT02314117. FINDINGS: Between Jan 28, 2015, and Sept 16, 2016, 645 patients were randomly assigned to receive ramucirumab plus fluoropyrimidine and cisplatin (n=326) or placebo plus fluoropyrimidine and cisplatin (n=319). Investigator-assessed progression-free survival was significantly longer in the ramucirumab group than the placebo group (hazard ratio [HR] 0·753, 95% CI 0·607-0·935, p=0·0106; median progression-free survival 5·7 months [5·5-6·5] vs 5·4 months [4·5-5·7]). A sensitivity analysis based on central independent review of the radiological images did not corroborate the investigator-assessed difference in progression-free survival (HR 0·961, 95% CI 0·768-1·203, p=0·74). There was no difference in overall survival between groups (0·962, 0·801-1·156, p=0·6757; median overall survival 11·2 months [9·9-11·9] in the ramucirumab group vs 10·7 months [9·5-11·9] in the placebo group). The most common grade 3-4 adverse events were neutropenia (85 [26%] of 323 patients in the ramucirumab group vs 85 [27%] of 315 in the placebo group), anaemia (39 [12%] vs 44 [14%]), and hypertension (32 [10%] vs 5 [2%]). The incidence of any-grade serious adverse events was 160 (50%) of 323 patients in the ramucirumab group and 149 (47%) of 315 patients in the placebo group. The most common serious adverse events were vomiting (14 [4%] in the ramucirumab group vs 21 [7%] in the placebo group) and diarrhoea (11 [3%] vs 19 [6%]). There were seven deaths in each group, either during study treatment or within 30 days of discontinuing study treatment, which were the result of treatment-related adverse events. In the ramucirumab group, these adverse events were acute kidney injury, cardiac arrest, gastric haemorrhage, peritonitis, pneumothorax, septic shock, and sudden death (n=1 of each). In the placebo group, these adverse events were cerebrovascular accident (n=1), multiple organ dysfunction syndrome (n=2), pulmonary embolism (n=2), sepsis (n=1), and small intestine perforation (n=1). INTERPRETATION: Although the primary analysis for progression-free survival was statistically significant, this outcome was not confirmed in a sensitivity analysis of progression-free survival by central independent review, and did not improve overall survival. Therefore, the addition of ramucirumab to cisplatin plus fluoropyrimidine chemotherapy is not recommended as first-line treatment for this patient population. FUNDING: Eli Lilly and Company.status: publishe
Ramucirumab with cisplatin and fluoropyrimidine as first-line therapy in patients with metastatic gastric or junctional adenocarcinoma (RAINFALL): a double-blind, randomised, placebo-controlled, phase 3 trial
- Author
- A. Cats
- A.J. Ten Tije
- Aaronson
- Agnes Ruzsa
- Ajani
- Akihito Tsuji
- Alejandro Molina Alavez
- Alex Beny
- Alexander V. Luft
- Alfredo Falcone
- Andràs Csilla
- Angel Gomez Villanueva
- Arnold
- Ayman Madi
- Bang
- Baruch Brenner
- Bela Piko
- Bohuslav Melichar
- Brian Anthony DiCarlo
- Cardellino Giovanni Gerardo
- Carlo Barone
- Carlos Alberto Hernandez
- Carmeliet
- Charles S Fuchs
- Chau
- Chau
- Christina Maria Gomez
- Christine Brezden-Masley
- Crystal S. Denlinger
- Cynthia Coo Chua
- Daisuke Sakai
- Daisuke Takahari
- Daniel Dammrich
- David Ferry
- David H Ilson
- Denis Pezet
- Diego Lucas Kaen
- Einat Shacham-Shmueli
- Elizabeth Won
- Elzbieta Wojcik
- Eric Van Cutsem
- F.L.G. Erdkamp
- Federico Longo Muñoz
- Ferdinando De Vita
- Ferlay
- Fernando Cabanillas
- Fidel David Huitzil Melendez
- Francesco Di Costanzo
- Francisco Gutiérrez Delgado
- Francisco Javier Ramirez Godinez
- Fuchs
- Fukumura
- Georgina Garnica Jaliffe
- Giuseppe Aprile
- Guillermo Ariel Mendez
- Gunnar Folprecht
- Gyorgy Bodoky
- H.M.W. Van Laarhoven
- Hector Velez-Cortez
- Herbst
- Hiroki Hara
- Howard J. Lim
- Hubert Ayala
- Hugo Ford
- Hugo Hool
- Hélène Senellart
- Ian Chau
- Irfan Firdaus
- Isabelle Sinapi
- James A. Jr Reeves
- Jana Prausova
- Jana Pribylova
- Javier Gallego Plazas
- Jean-Marc Phelip
- Ji Lin
- Jill Lacy
- Jiri Petera
- Joana Vidal Barrull
- Joanna Pikiel
- Joanna Wojcik-Tomaszewska
- Johanna Chock Bendell
- Jonathan Wadsley
- Joseph Thaddeus Beck
- Judit Kocsis
- Julien Taieb
- Karen Geboes
- Katriina Johanna Peltola
- Kazumasa Fujitani
- Kensei Yamaguchi
- Kim
- Kohei Shitara
- Laura Visa Turmo
- Laurent Mineur
- Leslie Samuel
- Lieto
- Luis Enrique Fein
- M.I. Grootscholten
- Madhuri Bajaj
- Maeda
- Maen Abdelkarim Hussein
- Manish A Shah
- Marc Van den Eynde
- Maria Alejandra Bartoli
- Maria Alsina
- Maria Błasińska-Morawiec
- Maria Di Bartolomeo
- Marianne Nordsmark
- Marina N. Nechaeva
- Mayukh Das
- Mette Karen Nytoft Yilmaz
- Michel Ducreux
- Miguel Angel Escudero
- Mohamed Hebbar
- Moses Sundar Raj
- Moustapha Tehfe
- Muro
- Naotoshi Sugimoto
- Nicolas Robert Maisey
- Nina A. Karaseva
- Nozomu Machida
- Ohtsu
- Ohtsu
- Per Pfeiffer
- Peter Bono
- Peter C Enzinger
- Peter Istvan Acs
- Pilar García Alfonso
- Radka Obermannova
- Raija Kallio
- Ralf-Dieter Hofheinz
- Ravindranath Patel
- Ravit Geva
- Raymond Woo-Jun Jang
- Ricardo Villalobos Valencia
- Robert Andrew Dichmann
- Roberto Carlesi
- Ronald L. Burkes
- Rubén Dario Kowalyszyn
- Russell Petty
- Salah-Eddin Al-Batran
- Sara Lonardi
- Scott Berry
- Seigo Yukisawa
- Shen
- Shen
- Shigenori Kadowaki
- Shuichi Hironaka
- Smyth
- Song
- Spratlin
- Srinivasan Madhusudan
- Stephen Leong
- Susanna Hegewisch-Becker
- Svetlana Protsenko
- Sylvie Lorenzen
- Tabenero
- Taito Esaki
- Takahari
- Thierry Alcindor
- Tibor Csoszi
- Timothy R. Asmis
- Tomasz Sarosiek
- Torre
- Udit Verma
- Van Cutsem
- Vera Gorbounova
- Wagner
- Walid Shaib
- Wasat Mansoor
- Wilke
- William E. Lawler
- Witte
- Yang
- Yoon
- Zev A Wainberg
- Publication venue
- 'Elsevier BV'
- Publication date
- Field of study
Mapping the human genetic architecture of COVID-19
- Author
- Abdelrazik M
- Abdullah T
- Abe R
- Abe S
- Abecasis GR
- Abel L
- Abernathy C
- Abraheem A
- Abul-Husn NS
- Acosta-Herrera M
- Acquilini D
- Acquilini D
- Adachi T
- Adachi Y
- Adams C
- Adams K
- Adanini O
- Adeleye O
- Adeniji K
- Adra D
- Afifi N
- Afilalo J
- Afilalo M
- Afolabi D
- Afrasiabi Z
- Afset JE
- Agasou A
- Aghemo A
- Agranoff D
- Agrawal S
- Aguirre LA
- Agwuh K
- Ahmad HF
- Ahmad N
- Ahmed A
- Ahmed C
- Ahmed KA
- Ai M
- Ail D
- Akeroyd L
- Akhtar MN
- Akhtar S
- Akinkugbe O
- Aksentijevich A
- Al Thani A
- Al-Muftah W
- Al-Sarraj Y
- Alarcon C
- Alarcon-Riquelme ME
- Alasdair F
- Alaverdian D
- Alavere H
- Albertos R
- Albillos A
- Albrecht W
- Albrich W
- Albrich WC
- Aldera EL
- Aldridge J
- Alegria A
- Alex B
- Alexander P
- Alfonso J
- Algera AG
- Ali A
- Ali IMA
- Ali S
- Aliberti S
- Allan A
- Allan E
- Allan J
- Alldis Z
- Allen L
- Allen S
- Allibone S
- Allison KS
- Allos R
- Ally SM
- Almaden-Boyle C
- Altabaibeh A
- Altmueller J
- Alvaro A
- Amar D
- Amin V
- Amitrano S
- Amiya S
- Ampuero J
- Anan R
- Anania S
- Anastasescu E
- Anderson F
- Anderson J
- Anderson M
- Anderson P
- Anderson S
- Anderson S
- Anderson T
- Ando A
- Andolfo I
- Andrade V
- Andretta F
- Andreucci E
- Andreucci E
- Andrew A
- Andrew B
- Andrew G
- Andrews E
- Andrews SJ
- Andrews SJ
- Andrews SJ
- Andrews SJ
- Andrikopoulos P
- Anedda F
- Aneli S
- Anemoli V
- Angelini C
- Angus B
- Annis A
- Antcliffe D
- Antinori A
- Antoni MD
- Anumakonda V
- Anwar M
- Anzai T
- Apetri E
- Arai D
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- Archer K
- Arciero E
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- Armstrong J
- Armstrong JA
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- Armstrong R
- Arning N
- Arnold S
- Arora J
- Artuso R
- Arumugam P
- Asakura T
- Asano K
- Aschard H
- Ascolillo S
- Ashish A
- Ashley E
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- Asiimwe IG
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- Asselta R
- Atanasovska B
- Atkinson D
- Atkinson EG
- Attwood B
- Aucella F
- Augustin M
- Auld D
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- Auton A
- Auton A
- Avendano-Ortiz J
- Awano N
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- Azuure C
- Azzolini E
- Baba R
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- Badia JR
- Badji RM
- Bahmer T
- Baikady RR
- Baillie JK
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- Baines B
- Baines D
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- Bakshi S
- Bakthavatsalam D
- Balaconis MK
- Baldassarri M
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- Ball CA
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- Bamford A
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- Bancroft H
- Band G
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- Baptista D
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- Barber R
- Barbieri C
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- Barbour A
- Barclay L
- Barclay WS
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- Zanelli G
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- zu Bentrup FM
- Zucchi P
- Zwinderman AHK
- Zyndorf M
- Publication venue
- Publication date
- 01/01/2021
- Field of study
The genetic make-up of an individual contributes to the susceptibility and response to viral infection. Although environmental, clinical and social factors have a role in the chance of exposure to SARS-CoV-2 and the severity of COVID-191,2, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. Here we describe the results of three genome-wide association meta-analyses that consist of up to 49,562 patients with COVID-19 from 46 studies across 19 countries. We report 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases3,4,5,6,7. They also represent potentially actionable mechanisms in response to infection. Mendelian randomization analyses support a causal role for smoking and body-mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19 was made possible by the community of human genetics researchers coming together to prioritize the sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease