18 research outputs found
Monte Carlo methods for combining sample approximations of distributions
- Author
- Publication venue
- Publication date
- Field of study
Combining several (sample approximations of) distributions, which we term sub-posteriors, into a single distribution proportional to their product, is a common challenge in statistics and data science. For instance, this can occur in distributed `big data' problems, tempering problems, or when working under multi-party privacy constraints. Many existing approaches resort to approximating the individual sub-posteriors for practical necessity, then finding either an analytical approximation or sample approximation of the resulting (product-pooled) posterior. The quality of the posterior approximation for these approaches is poor when the sub-posteriors fall out-with a narrow range of distributional form, such as being approximately Gaussian. Recently, a Fusion approach has been proposed which finds a direct and exact Monte Carlo approximation of the posterior (as opposed to the sub-posteriors), circumventing the drawbacks of approximate approaches. Unfortunately, existing Fusion approaches have a number of computational limitations, particularly when unifying a large number of sub-posteriors or when the sub-posteriors exhibit large correlation. In this thesis, we generalise the theory underpinning existing Fusion approaches, and embed the resulting methodology within a recursive divide-and-conquer sequential Monte Carlo paradigm. This ultimately leads to a competitive Fusion approach, which is appreciably more robust and scalable in a variety of practical settings
How to Data in Datathons
- Author
- Publication venue
- Publication date
- 25/10/2023
- Field of study
The rise of datathons, also known as data or data science hackathons, has
provided a platform to collaborate, learn, and innovate in a short timeframe.
Despite their significant potential benefits, organizations often struggle to
effectively work with data due to a lack of clear guidelines and best practices
for potential issues that might arise. Drawing on our own experiences and
insights from organizing >80 datathon challenges with >60 partnership
organizations since 2016, we provide guidelines and recommendations that serve
as a resource for organizers to navigate the data-related complexities of
datathons. We apply our proposed framework to 10 case studies.Comment: 37th Conference on Neural Information Processing Systems (NeurIPS
2023) Track on Datasets and Benchmar
Robust estimation of bacterial cell count from optical density
- Author
- Aarnio Tiu
- Aaron Leow Chung Yong
- Abbas Anser
- Abduraimova Aiganym
- Abraham Doris
- Acar Beliz Leyla
- Acosta Joaquin
- Adler Nina
- Adulyanukosol Natthawut
- Agena Ejouan
- Agena Ethan
- Aggarwal Priya
- Aguirre Adriana Lizeth Rubio
- Ahlgren Christopher
- Ahuja Janvi
- Aizik Dror
- Akbary Mina
- Akinfenwa Akinwumi
- Akingbesote Ngozi D.
- Akova Umut
- Aldo Ferdinan
- Alexopoulos Ioannis
- Allen Lucy
- Alonso Alejandro
- Altarawneh Dina
- Alvarado Andres Benjamin Sanchez
- Ambre Sanika
- Ameziane Annissa
- Amheine Khadija
- Amin Ihya Fakhrurizal
- Amir Sayeda Sakina
- Amstel Chiel van
- An Yongyan
- Anand Nithishwer Mouroug
- Ananthakrishnan Sathvik
- Anderson Karl
- Angel Sagi
- Annem Vidhya
- Anson Chung Tsun Ho
- Anwar Mariam
- Appel Alana
- Araya Lucas
- Armstrong Alexander
- Arora Neha
- Arora Vasu
- Arruda Beck
- Ashwin F Amal Jude
- Astapenka Artur
- Astles Ben
- Astorino Gabe
- Aubry Celine
- Avileli Rebecca
- Azad Mahnaz Sabeta
- Babar Rehmat
- Babu Priyanka
- Badalli Turan
- Badash Lior
- Baichman-Kass Amichai
- Baldwin Geoff S.
- Baltensperger Oliver Andreas
- Bao Guanke
- Bao Minyue
- Baronaite Ugne
- Barrat Leon Michael
- Barrington Seth
- Barshap Alon
- Bartzoka Natalia
- Basu Anubhav
- Basulto Cynthia
- Bath Scott
- Battina Rohith
- Bauersachs Daniel
- Beal Jacob
- Beale Renee
- Beard Eleanor
- Beck Selina
- Becker Evan
- Benavides Samantha Ayde Pena
- Bennis Nicole
- Bete Anna
- Bhatt Darshak
- Bhowmick Shilpa
- Bian Weixin
- Bijman Eline Yafele
- Bindt Felix
- Blas Karla Soto
- Bo Tang
- Boada Yadira
- Boer Meine
- Bohner Ariel
- Borovko Irina
- Bott Amie
- Bouwmeester Susan
- Bowman Kyle
- Boxem Mike
- Boxuan Cheng
- Boyce Kira
- Boyer Jess
- Brasas Valentas
- Brewer Mathew
- Briand William
- Brink Matilda
- Browne Emily
- Buckley-Taylor Russell
- Budhan Stephanie
- Buller Lisa
- Burckhardt Nele
- Burgland Zachary
- Burns Frank
- Burridge Matt
- Burud Hanna Nedreberg
- Buson Felipe Xavier
- Butterfield Tom
- Byagathvalli Gaurav
- Byatt Gabriel
- Byun Sumin
- Caballero Amalia
- Cai Fu
- Cai Niangui
- Caldwell Sarah
- Camacho Yazmin
- Camille Monteil
- Campbell Robert
- Cao Qinhao
- Cao Yixin
- Cao Yuze
- Carrillo Leo
- Carter Jonah
- Casas Alexis
- Castillo Nora Esther Torres
- Castillo Sandra
- Cave John
- Chai Ruochen
- Chamiec-Case Elizabeth
- Chan Janice
- Chan Yuan-Yao
- Chandramouli Priyanka
- Chang Annabel
- Chang Catherine
- Chang Kevin
- Chang Thomas
- Chang Ting-Chen
- Chang Yu-Ci
- Chapman Tyler
- Chater Dounia
- Chau Anthony
- Chavez Benjamin
- Chavez Francisco
- Chehade Ibrahim
- Chen Carmen
- Chen Chih-Chiang
- Chen Ching-Wei
- Chen Janice
- Chen Junhong
- Chen Junyang
- Chen Junyu
- Chen Pei-Hong
- Chen Ryan
- Chen Weixuan
- Chen Yan
- Chen Yi-Cian
- Chen Yifei
- Chen Zhuoyang
- Cheng Cheng
- Cheng Haolun
- Cheng Hsuan
- Cheng Yu-Hong
- Cheng Yu-Hsuan
- Chenxi Liang
- Cherupalla Arjun
- Chi Jordi
- Chi Shumei
- Chiang Jason
- Chiang Woody
- Ching Lai Tsz
- Ching Lam Kai
- Ching Law Hiu
- Ching Luk Hau
- Chinnathambi Sathivel
- Cho Sungwoo
- Choi Lee Sze
- Choi Youngeun
- Chou Ryan
- Chou Ryan
- Chu Wai Yan
- Chua Yah Tse Sabrina
- Chuang Yi-Chien
- Chulkova Nadezhda
- Chun Cheung Man
- Chun Emily
- Chun Ng Tsz
- Cifuentes Rodrigo Hernandez
- Clapper Jude
- Clapper Jude
- Clark Brittany
- Clemente Borja Sanchez
- Clerc Valerian
- Clodomir Christina
- Coates Ryan
- Cohen Katherine
- Colant Noelle
- Coleman Sarah
- Colgan Cian
- Cone Eli
- Corre Christophe
- Costa Ben
- Cott Rachel Van
- Craw Darilyn
- Crispim Larissa de Souza
- Crone Michael Andrew
- Crooijmans Marjolein
- Crosby Laurel Constanti
- Crowley Peter
- Cruz Frida
- Cubukcu Hande
- Culfogienis Dylan
- Czekster Clarissa
- Dai Leijie
- Dalangin Rochelin
- Daniel Benjamin
- Daniels Lea
- Das Neves Laura
- Das Diptatanu
- Davis Christina
- De Silva Nimaya
- Deb Shalini S.
- Deepak Kumar S.
- Deibel Emilie
- Dejoie Julianne
- Dejoux Alice
- DeKloe Jackson
- Del Toro Mariano
- Delalez Nicolas
- Delgadillo Sabrina
- Delhomme Jean
- Demchuk Aubrey
- Deng Nian Ruei
- Deng Rui
- Denter Jennifer
- Deshmukh-Reeves Ed
- Despres Philippe C.
- Devi Velvizhi
- Dhaliwal Gurpreet
- Diaz Fernanda
- Ding Shizhi
- Ding Yiming
- Ding Zhipeng
- Dingyue Tang
- Dirven Yvette
- Dissmann Jil-Sophie
- Do Stephanie
- Dogra Arushi
- Dominguez Viana Isabel Perez
- Dong Dongyang
- Dong Haitao
- Dong Jason
- Dong Shan
- Dong Shan
- Dong Shan
- Dong Shangzhi
- Dong Shangzhi
- Doyle David
- Doyle Shannon
- Dube Alexandre
- Dubuc Emilien
- Dunstan Izzy
- Dusseaux Theodore A.
- Dvorkin Steve
- Edelmayer Marco
- Ehrenworth Amy
- Eidloth Franziska
- Eijkens Bruno
- Eilers Keno
- El Moubayed Yorgo
- Elcin Evrim
- Elias Noel
- Elikan Max
- Ellermeier Craig
- Elliott Hannah
- Elsa Yeung Hoi Lam
- Emilov Kristian
- Espinoza Diego
- Evans Rhys
- Faidh Mohammed
- Falgenhauer Elisabeth
- Fan Catherine
- Fang Chengzhu
- Fang Choco
- Fang Xiangyi
- Farhi Einan
- Farias Sebastian
- Farny Natalie
- Farny Natalie G.
- Farrell Jennifer
- Fassler Jan
- Faurdal David
- Faustova Ilona
- Feng Xinhua
- Fernandez Cesar Ibrahym Rodriguez
- Fierro Daniela Olono
- Figueroa Ana Cristina
- Figueroa Jose Arnulfo Juarez
- Fikry Clara
- Filzen Rachael
- Fischer Matthew
- Fitzgerald Kevin
- Fitzgerald Liza
- Flores Vinicius
- Foda Asmaa
- Fong Yuhui Deborah
- Forman Victor
- Frank Stefanie
- Frankel Eva
- Freire Paulo J. C.
- Friedman Yonatan
- Frohlich Lisa
- Fu Wenhan
- Fu Yousi
- Fuentes Ernie
- Fulton Leah
- Fung Ip Ning
- Fung Yam Shing
- Gabrielli Jacopo
- Gahagan Maddison
- Gaitt Tobias
- Gaizauskaite Aukse
- Gallegos Isabella
- Gamoneda Diego
- Gandhi Rishi
- Gao Cecily
- Garavito Paula
- Garcia Chrismar
- Garcia David
- Garrido Delia
- Garulli Elisa
- Gaspar Camila
- Gaudi Alex
- Ge Gao
- Ge Yubin
- George Stephan
- Gerard Antoine
- Gershater Markus
- Ghosh Souvik
- Giannopoulos Alexandros Dimitriou
- Giannoula Yvoni
- Gilman Daniel Barber James
- Glockner Eleanor
- Goenka Anushya
- Goetz Marley
- Gogineni Namrata
- Gokul [NO FIRST NAME IN SCOPUS]
- Gonzalo Gonzalo Saiz
- Goodson Michael
- Gopaul Deshmukh
- Gou Yanchen
- Govers Jolijn
- Graaf Floor de
- Grace Tsui Shing Yan
- Graves Daniel
- Grazulyte Inga
- Greenwald Matthew
- Gu Jiajun
- Gu Yiheng
- Gu Yining
- Guadagnino Brett
- Guenther James
- Guerassimoff Lea
- Guo Jintao
- Gupta Shreya
- Guptil Chris
- Guseva Anna
- Ha Jacqueline
- Haddock-Angelli Traci
- Haight Travis
- Hale Mitch
- Hamady Carla
- Han Wang
- Han Weitang
- Handal Paola
- Hanrong Zhu
- Hansen Cecilie
- Hao Junyao
- Hao Mei
- Hao Zhengguo
- Haoran Xu
- Haralsvik Anne Kristin
- Hariyani Imtiyaz
- Hartley Zach
- Hassan Sondoss
- Hau Sion
- He Fa
- He Hanker
- He Henry
- He Karen
- He Lindong
- He Menglan
- He Peixiang
- He Yuna
- He Zhien
- Healy Liam
- Heath Emily
- Heger Theresa
- Hei Chan Yick
- Heijningen Franca van
- Heintze Maxime
- Hemmings Sam
- Heng Heng
- Heng Mary
- Henras Anthony
- Herbert Heydy
- Hernandez Ivan Martin
- Hernandez Laura Armero
- Herrmann Max
- Heux Stephanie
- Hewitt Amy
- Hiesinger Marlene
- Hill Kurt
- Hin Chan Lok
- Hin Wong Chung
- Hin Yu Man
- Ho Anthony
- Ho Ng Sze
- Ho Tim
- Hodson Sophie
- Hofer Sebastian
- Holman Olivor
- Holmedal Ingebjorg
- Hong Lai Tsz
- Hong Lee Chi
- Hong Yiquan
- Hong Yirui
- Horz Philip
- Hoskan Mehmet Ali
- Hosseini Reza
- Hou Ali
- Houmani Moustafa
- Hsiao Chia-Yi
- Hsieh Yi Da
- Hsu Chia-Wei
- Hsu Yi-Hsuan
- Hu Miao
- Hu Shi
- Hu Vivian
- Hu Wenyue
- Hu Xinyi
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- Hu Zhaoqing
- Hu Zhiyuan
- Huang Fangliang
- Huang Jiaxi
- Huang Morris
- Huang Ray
- Huang William
- Huang Yansong
- Huang Yaohua
- Huang Yilin
- Huang Yinpin
- Huanying He
- HuaYue Zhang
- Huerta Ana Laura Torres
- Humphreys Christopher
- Hung Chia
- Husnatter Kai
- Huuki Liz
- Huynh Juilanne
- Hwang Michael
- Ibrahim Ahmed
- Ikagawa Yuichiro
- Ikhsan Muhammad
- Ikwuagwu Bon
- Imgold Markus
- Inanc Tugba
- Inckemann Rene
- Isaac Ashley
- Isaacs Farren
- Isogai Tatsuki
- Iwuogo Amanda
- Iyer Aditya
- Iyer Tvarita Shivakumar
- Izzati Nurul
- Jacq Annick
- Jain Rishabh
- Jain Shubham
- Jainarayanan Ashwin Kumar
- Jakutis Gabrielius
- Jaoui Samuel
- Japranata Valdi Ven
- Jaramillo Alfonso
- Jasiunas Simas
- Jasti Naveen
- Jay Leung Chung Yin
- Jayaraman Guhan
- Jayaraman Srimathi
- Jenakendran Jenaagan
- Jensen Joen Haahr
- Jesse Hayley
- Jha Aryaman
- Ji Peicheng
- Jiacheng Wu
- Jiahe Zhang
- Jiamiao Liu
- Jian Liu
- Jiang Nannan
- Jiang Zhenyu
- Jianzhao Yang
- Jiaqi Hu
- Jiaqi Xiao
- Jimenez Carlene
- Jin Kaifeng
- Jingjing Zhao
- Jinyu Zhu
- Jo Kyuhee
- Joe Lam Kai Ching
- Johnson Elizabeth
- Johnson Michael
- Jones Ari
- Jones Cara
- Jones Ethan
- Jones Megan
- Jones Melissa
- Jongkees Seino
- Jonsson Martin
- Jude Marcia Smiti
- Jung Younji
- Juskaite Ieva
- Justice Isaac
- Kabbara Ismat
- Kadimi Sricharan
- Kailash B.P.
- Kalinowski Jorn
- Kalinowski Jorn
- Kalson Pranshu
- Kamble Yash Laxman
- Kanata Eleni
- Kanaya Toshihiro
- Kang Han
- Kang Xu
- Kang Ziqi
- Kantas Gamze
- Kantor Nicole
- Kapsokefalou Maria
- Karpauskaite Laura
- Karpus Laurynas
- Karshenas Arman
- Karumanchi Pranathi
- Katherine Lai Man Wai
- Katopodi Xanthi Leda
- Kawasaki Yusuke
- Kayihan Ceyhun
- Keating Collin
- Kehan Tao
- Keidar Nitzan
- Keij Sander
- Kelly Ellis
- Kelly Julia
- Kennedy Fiona
- Kenneth Ng Tsz Chun
- Khaimani Jatin
- Khalid Alizah
- Khenwar Arundhati
- Kiga Daisuke
- Kim Anna
- Kim Christine
- Kim Dong Ju
- Kim Ellie
- Kim Gloria
- Kim Goeun
- Kim Grace
- Kim Sean
- Kin-ning Wong Carol
- King Stefanie
- Kittur M. Sagar
- Kiu Lee Hong
- Kiu Wong Hoi
- Kivisto Samu
- Klaas Liz
- Klopprogge Bjarne
- Ko LiangYu
- Kofoed Selma
- Kohabir Kavish
- Kolosova Anastasia
- Kong Cheng Chak
- Kong Linzhen
- Kortus Drew
- Koski Jessica
- Kostadima Eleni
- Kostopoulos Ioannis V.
- Kotzastratis Stylianos
- Kou Senhao
- Koutelidakis Antonios E.
- Kozhevnikov Adrian
- Krabacher Rachel
- Krainer Birgit
- Krauss Elisha
- Kristy Brandon
- Krokos Vasilios
- Kruger Dustin
- Krusemann Jan Lukas
- Kryukova Jhanna
- Ku Chi-Yao
- Kuang Yi
- Kuangyi Wei
- Kuebler Nadine
- Kugathasan Luxcia
- Kumar Adarsh
- Kumar Vignesh
- Kumbhojkar Ninad
- Kurian Jacob
- Kwasniak Dominika
- Kyrpizidis Grigorios
- Labecka Nikol
- Lahad Divangana
- Lai Evelyn
- Lai Evelyn
- Lam Chan Wing
- Lam Kendrick
- Lam Kevin
- Lam Yiu Choi
- Lang Jacob
- Lang Yusen
- Lassel Nicole
- Latham Michael
- Laun Sarah
- Laurel Ralph
- Laurentius Andrea
- Laury Jessica
- Lautru Sylvie
- Lawrence Jack
- Leach Cass
- Leal Luis Mario
- Ledalla Karthik
- Lee James
- Lee Jordan
- Lee Matthew
- Lee Meixuan
- Lee Meng-Zhan
- Lee Yeonjae
- leelahakorn Nattawut
- Leeuw Monique de
- Lefevre Marine
- Lehtonen Leevi
- Leitner Karl
- Lekshmi Hema
- Lemieux Pascale
- Leon Karen De
- Lepetit Florian
- Levrier Antoine
- Li Caidian
- Li Changyu
- Li Hailong
- Li Haocong
- Li Jiadong
- Li Kevin
- Li Nuonan
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- Li Sophie Ruojia
- Li Tingting
- Li Tingting
- Li Tingyue
- Li Xuecheng
- Li Yanyan
- Li Yuanyuan
- Li Yuqi
- Li Zihao
- Li Zonghao
- Liang Tommy
- Liang Yuteng
- Liang Zhihan
- Liangjian Yang
- Liao Chin-Hsuan
- Liaoqi Du
- Lichi Fang
- Lim Sangwu
- Lim Yan Ping
- Lima Guilherme Meira
- Lin Beatrix Tung Xue
- Lin Chenyi
- Lin Junliang
- Lin Weifeng
- Lin Yasmin
- Lin Yu-Chun
- Lind Andrea Clausen
- Linke Dirk
- Litsa Maria
- Liu Fangqi
- Liu Huan
- Liu Jiangyuan
- Liu Jiezheng
- Liu Jingang
- Liu Ting
- Liu Wei-Ting
- Liu Weijia
- Liu Wukun
- Liu Xiaolong
- Liu Xutong
- Liu Yiheng
- Liu Yuansheng
- Liu Zhaoyu
- Liu Zhihao
- Liu Zhixiang
- Liu Zi
- Liya Devang Haresh
- Lo Natalie
- Lockwood Savannah
- Loeffler Frank
- Logel Dominic
- Loke Chun Kit
- Lombardero Francisco Javier Quero
- Longo Ylenia
- Loog Mart
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- Lorch Kevin
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- Lotz Thea
- Louis Simon
- Lu Chenyu
- Lu Yinjing
- Luan Lin
- Luo Chenfei
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- Luo Fang
- Luo Linda
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- Luo Zhi
- Luque Ana Cecilia
- Luzuriaga Juan Carlos
- Lykkegaard Magnus Ronne
- Ma Guanghui
- Ma Jiaxin
- Ma Liang
- Ma Lingling
- Ma Yingqi
- Ma Yuan
- Maddiboina Dhanyasri
- Madelenat Manon
- Madrid Micah
- Magzoub Mazin
- Mahapatra Nitish R.
- Maljavin Artemi
- Mancinotti Davide
- Mangkusaputra Venda
- Mansfield Laura
- Mao Jiangjiao
- Marcoleta Andres
- Marinovic Adrian
- Marken John
- Markiv Anatoliy
- Marquina D.
- Marta Britany
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- Martinez Victor Javier Robledo
- Maruo Tatuya
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- Matthew Cheah
- Maupu Clemence
- Mayer Julia
- Mazelis Ignas
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- McDonough Matt
- McShane Evie
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- Meerbrei Tanja
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- Milano Fiona
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- Ming Shaw Kar
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- Mishler Dennis M.
- Mishra Vibhu
- Mitropoulos Alex
- Mo Yilin
- Mohan Kumar B.S.
- Moncayo Eduardo
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- Ong June
- Oropeza Carlos Javier Cordero
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- Otto Matthias
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- Parab Komal
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- Park Mikyung
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- Parmar Jasmeen
- Parmentier Mathieu
- Parr Lillian
- Parry Geraint
- Partridge Daniel
- Pasi Mor
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- Patel Abhilash
- Patel Bhargav
- Patel Jaymin
- Patel Vainav
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- Patil Mitali
- Pattiradjawane Lorenzo
- Paul Ahavi
- Pavelek Tucker
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- Pedamallu Havisha
- Pedersen Hege Hetland
- Pedrolli Danielle Biscaro
- Pehlivan Meryem
- Pei Yifei
- Pei Yuanzhe
- Peiyao Fan
- Pena Thevenet Esteban de la
- Peng Jiarong
- Peng Jiarong
- Peng Yue
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- Penny Leo
- Peras Marie
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- Pezzutto Denise
- Phelan Cam
- Pinheiro Vitor
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- Pitaliya Madhav
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- Prakash Satya
- Prakash Supriya
- Pratama Muhammad Iqbal Adi
- Preetha R.
- Premo Jacob
- Prins Rianne
- Pruneski James
- Ptak Jeffrey
- Putthoff Lisa
- Qi Ariel
- Qian Ling
- Qiang Ye
- Qiaochu Jiang
- Qin Zichen
- Qipeng Zhang
- Qiu Hao
- Qu Jingting
- Qu Mingbo
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- Raadam Morten
- Rai Hrishika
- Rajagopal Varshni
- Raju Deeksha
- Rajurkar Aishwarya
- Rakhimov Jennifer
- Rambhatla Rahul
- Ramstrom Elin
- Ramzeen Aaron
- Ran Guozheng
- Ran Yuncong
- Rana Yash
- Rao Achala
- Rao Xichen
- Rasheed Moiz
- Rashid Khadija
- Rasmussen Tenna
- Rasmussen Victoria Svaerke
- Rastogi Tashi
- Raut Sandeep
- Rautanen Pauliina
- Reaney Bethany
- Rebello Alex
- Rege Mayuri
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- Ren Wenan
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- Resendiz Armando Cortes
- Reshamwala Shamlan M. S.
- Rettedal Neil
- Ribeiro Nathan Vinicius
- Ries Anna
- Rigon Luca
- Ripp Steven
- Ritmejeris Justas
- Rivas Paula
- Rivera Mario Loya
- Roberts Luc
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- Rodriguez Guillermo Fernandez
- Roige Biel Badia
- Rokaitis Irmantas
- Rolfsnes Rebekka Rekkedal
- Romeo Yves
- Rong Ziyue
- Rosa Caio Gomes Tavares
- Rouleau Francois D.
- Ruhnau Johannes
- Ruhnau Johannes
- Run Zhouyan
- Ruscher David
- Ruzic Robert
- Ruzicka Alex
- Ryan Sean
- Ryu Bo Sun
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- Sabuwala Burhanuddin
- Sackey Juliana
- Saha Margaret
- Saini Karandip
- Sanchania Vishal
- Sanchez Magaly Aguirre
- Sande Amanda
- Sander Edward
- Sang Jonathan Cheng Hon
- Sans Laura
- Santamaria Stefanie
- Santos Ana
- Saragliadis Athanasios
- Satoh Takehito
- Sauter Antoni Planas
- Sauvageau Dominic
- Saville Luke
- Saville Luke
- Sawant Maithili
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- Schaaf Kaitlin
- Schacht Makayla
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- Schmidtchen Lisbeth
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- Schwarz Dominic
- Scott Allison
- Secen Mert
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- Selvarajah Vinoo
- Senes Carolina
- Senyuz Ilayda
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- Zhao Peng
- Zhao Tianyan
- Zhao Wenxue
- Zhao Yihang
- Zhaoting Li
- Zhecheng Huang
- Zheng Daniel
- Zheng Jiyang
- Zhiwei Song
- Zhong Yanling
- Zhou Hanmi
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- Zhou Jianan
- Zhou Rui
- Zhou Shuyao
- Zhou Xuanhao
- Zhou Yanjun
- Zhou Yi
- Zhou Yinchi
- Zhou Yineng
- Zhou Yuezhang
- Zhou Yuxin
- Zhou Zhiyu
- Zhu Chushu
- Zhu Ke
- Zhu Xueqian
- Zi Lihan
- Zilinskaite Nemira
- Zimmermann Andreas
- Zimmermann Jennifer
- Zirong Zeng
- Ziwei Zhou
- Ziyi Zhao
- Zorrilla Francisco
- Zou Jiahua
- Zukauskaite Kristina
- Zulueta Patricia
- Zvirblyte Justina
- Publication venue
- Publication date
- 01/01/2020
- Field of study
Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data
Impact of COVID-19 on cardiovascular testing in the United States versus the rest of the world
- Author
- Abad Pedro
- Abbara Suhny
- Abbasi Taimur
- Abbott Brian
- Abdel Aziz Islam Shawky
- Abdulla Jawdat
- Abikhzer Gad
- Abohashem Shady
- Abougabal Mahasen
- Abramson Sandra
- Abrihan Paz
- Acuña Arturo Romero
- Affandi Erwin
- Afzal Muhammad Shehzad
- Agolti Mariela
- Agranovich Svetlana
- Aguadé-Bruix Santiago
- Aguero Roberto Nicolas
- Ahmed Hassan Mohamed Ismail
- Ahmed Taghreed
- Akhter Afroza
- Al Dhuhli Humoud
- Al Kindi Faiza
- Al-Abboud Tarek
- Al-Bulushi Naeema
- Al-Mallah Mouaz
- Alak Maria del Carmen
- Alam Edison
- Alaoui Nadia Ismaili
- Alasnag Mirvat
- Albadr Amjed
- Albalooshi Batool
- Albano Domenico
- Alberguina Lucia Graciela
- Albernaz Siqueira Maria Helena
- Alexanderson-Rosas Erick
- Alfaro Ana
- Ali Mohamed Mandour
- Alkadhi Hatem
- Alkandari Faridah
- Allam Adel
- Allarakha Mohammad Aaftaab
- Almeida Augusto
- Almousalli Omar
- Alongi Pierpaolo
- Alonso Omar
- Alves Togni Paulo Henrique
- Alves Wilson Furlan
- Ananthasubramaniam Karthikeyan
- Anderson Jill
- Andrade Jose Henrique
- Andrade Luciana
- Angelidis George
- Anselmi Carlos
- Ansheles Alexey
- Araújo Roberta
- Archontaki Aikaterini
- Arnone Gaspare
- Arnous Samer
- Arnson Yoav
- Arroñada Guillermo
- Arturo Harold
- Asano Hiroshi
- Ascani Sebastian Perez
- Asfour Ahmed
- Askew Jeffrey
- Assadi Majid
- Astesiano Alfredo
- Astesiano Andrea
- Attanasio Lea
- Atyani Said
- Ayala Sandra
- Ayetey Harold
- Ayodele Tolulope
- Azevedo Guilherme
- Bagatin Elisa
- Bailly Matthieu
- Baldari Sergio
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- Bang Ji-In
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- Nijjar Prabhjot
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- Otsuka Hideki
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- Pabon Luz
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- Ussov Wladimir Yurievich
- Uusitalo Valtteri
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- Valiullina Nailya
- Vallejo Enrique
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- Vallée Jean-Paul
- Valsamaki Pipitsa
- Vamadevan Shankar
- Van Asperen Erik-Jan
- Van De Heyning Caroline M.
- Van Gaal William
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- Vitola Joao V.
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- Várady Edit
- Vázquez Manuel Castillo
- Wagenaar Nils
- Wakabayashi Yasushi
- Waller Alfonso
- Waltrick Roberto
- Wang Ellen
- Wang Jian
- Wang Ximing
- Wang Yifan
- Wang Yining
- Wang Zhao-Qian
- Ward Parker
- Wayne Victor
- Weihmuller Juan Sebastian
- Weir-Mccall Jonathan
- Weiss Konrad
- Weissman Gaby
- Wesbey George
- White James
- White Kelly
- Williams Michelle C.
- Williams Michelle C.
- Wilson Peter
- Winchester David
- Winchester David
- Wolcan Juan
- Wolinsky David
- Won Kyoung Sook
- Wong David
- Wong Kirby
- Wu Jiang
- Wu Zhifang
- Xia Liming
- Xiao Jiangxi
- Xu Lei
- Xu Zhuoran
- Yamada Shinichiro
- Yamazaki Shinya
- Yang Youyou
- Yew Min Sen
- Yin Wu
- Yoneyama Tatsuya
- Yost Sandra
- Young Calum
- Younger John
- Younis Muhammad Numair
- Yu Jianqun
- Yuan Li
- Zaid Eed Abu
- Zakavi Seyed Rasoul
- Zapparoli Marcello
- Zavadovsky Konstantin
- Zeffiro Susana
- Zeidán Nahla
- Zerahn Bo
- Zgaljardic Michael
- Zhang Longjiang
- Zhang Tong
- Zhang Xiaoli
- Zhang Yong-Gao
- Zhu Li
- Zhuravlev Kirill
- Zoboli Stefania
- Zukotynski Katherine
- Zuluaga Alejandro
- Øvrehus Kristian Altern
- Štalc Monika
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2021
- Field of study
Objectives: This study sought to quantify and compare the decline in volumes of cardiovascular procedures between the United States and non-US institutions during the early phase of the coronavirus disease-2019 (COVID-19) pandemic.
Background: The COVID-19 pandemic has disrupted the care of many non-COVID-19 illnesses. Reductions in diagnostic cardiovascular testing around the world have led to concerns over the implications of reduced testing for cardiovascular disease (CVD) morbidity and mortality.
Methods: Data were submitted to the INCAPS-COVID (International Atomic Energy Agency Non-Invasive Cardiology Protocols Study of COVID-19), a multinational registry comprising 909 institutions in 108 countries (including 155 facilities in 40 U.S. states), assessing the impact of the COVID-19 pandemic on volumes of diagnostic cardiovascular procedures. Data were obtained for April 2020 and compared with volumes of baseline procedures from March 2019. We compared laboratory characteristics, practices, and procedure volumes between U.S. and non-U.S. facilities and between U.S. geographic regions and identified factors associated with volume reduction in the United States.
Results: Reductions in the volumes of procedures in the United States were similar to those in non-U.S. facilities (68% vs. 63%, respectively; p = 0.237), although U.S. facilities reported greater reductions in invasive coronary angiography (69% vs. 53%, respectively; p < 0.001). Significantly more U.S. facilities reported increased use of telehealth and patient screening measures than non-U.S. facilities, such as temperature checks, symptom screenings, and COVID-19 testing. Reductions in volumes of procedures differed between U.S. regions, with larger declines observed in the Northeast (76%) and Midwest (74%) than in the South (62%) and West (44%). Prevalence of COVID-19, staff redeployments, outpatient centers, and urban centers were associated with greater reductions in volume in U.S. facilities in a multivariable analysis.
Conclusions: We observed marked reductions in U.S. cardiovascular testing in the early phase of the pandemic and significant variability between U.S. regions. The association between reductions of volumes and COVID-19 prevalence in the United States highlighted the need for proactive efforts to maintain access to cardiovascular testing in areas most affected by outbreaks of COVID-19 infection
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- Chu CT
- Chua JJE
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- Chung H
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- Comincini S
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- Consiglio A
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- Zwerschke W
- Álvarez ÉMC
- Ávalos Y
- Önal G
- Üstün S
- Čolić M
- Đokić J
- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
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- A. -G. Wu
- A. C. Ma
- A. K. Au
- Abdel-Aziz A. K.
- Abdelfatah S.
- Abdellatif M.
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- Zhuang H.
- Zhuang X.
- Zientara-Rytter K.
- Zimmermann C. M.
- Ziviani E.
- Zoladek T.
- Zong W. -X.
- Zorov D. B.
- Zorzano A.
- Zou W.
- Zou Z.
- Zou Z.
- Zuryn S.
- Zwerschke W.
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
Evaluation of an Automated High-Throughput Liquid-Based RNA Extraction Platform on Pooled Nasopharyngeal or Saliva Specimens for SARS-CoV-2 RT-PCR
- Author
- Publication venue
- 'MDPI AG'
- Publication date
- 02/04/2021
- Field of study
SARS-CoV-2 RT-PCR with pooled specimens has been implemented during the COVID-19 pandemic as a cost- and manpower-saving strategy for large-scale testing. However, there is a paucity of data on the efficiency of different nucleic acid extraction platforms on pooled specimens. This study compared a novel automated high-throughput liquid-based RNA extraction (LRE) platform (PHASIFY™) with a widely used magnetic bead-based total nucleic acid extraction (MBTE) platform (NucliSENS® easyMAG®). A total of 60 pools of nasopharyngeal swab and 60 pools of posterior oropharyngeal saliva specimens, each consisting of 1 SARS-CoV-2 positive and 9 SARS-CoV-2 negative specimens, were included for the comparison. Real-time RT-PCR targeting the SARS-CoV-2 RdRp/Hel gene was performed, and GAPDH RT-PCR was used to detect RT-PCR inhibitors. No significant differences were observed in the Ct values and overall RT-PCR positive rates between LRE and MBTE platforms (92.5% (111/120] vs. 90% (108/120]), but there was a slightly higher positive rate for LRE (88.3% (53/60]) than MBTE (81.7% (49/60]) among pooled saliva. The automated LRE method is comparable to a standard MBTE method for the detection of SAR-CoV-2 in pooled specimens, providing a suitable alternative automated extraction platform. Furthermore, LRE may be better suited for pooled saliva specimens due to more efficient removal of RT-PCR inhibitors
PTEN-L is a novel protein phosphatase for ubiquitin dephosphorylation to inhibit PINK1–Parkin-mediated mitophagy
- Author
- A Eiyama
- A Kazlauskaite
- A Kazlauskaite
- A Kumar
- A Ordureau
- A Ordureau
- A Tanaka
- AM Pickrell
- B Bingol
- BD Hopkins
- BJ Ryan
- Boon-Huat Bay
- C Kondapalli
- C Vives-Bauza
- CA Worby
- Celestial T. Yap
- Chunxin Wang
- D Narendra
- DP Narendra
- F Koyano
- GR Masson
- Grace Gui-Yin Lim
- Guang Lu
- H Liang
- H Vais
- H Wang
- Han-Ming Shen
- Hanry Yu
- Hayden Weng-Siong Tan
- Hui-Ying Chan
- I Garcia-Cao
- JD Aguirre
- Jianbin Zhang
- Jigang Wang
- Jingzi Zhang
- JJ Lemasters
- Jung-Eun Park
- JW Harper
- K Okatsu
- K Shiba-Fukushima
- K Shiba-Fukushima
- Kah-Leong Lim
- LA Kane
- LC Cantley
- Lei Fang
- Liming Wang
- M Gersch
- M Iguchi
- M Lazarou
- Mallilankaraman Karthik
- MS Song
- N Matsuda
- N Matsuda
- Pornteera Pawijit
- R Pulido
- Ritu Chawla
- S Callegari
- S Pickles
- SB Johnston
- Shuo Deng
- Siu-Kwan Sze
- SJ Ham
- SM Jin
- SR Yoshii
- T Cornelissen
- T Gu
- T Wauer
- T Wauer
- TM Durcan
- TN Nguyen
- V Sauve
- V Stambolic
- Yajun Wu
- Yan Tong
- Yancheng Tang
- Yih-Cherng Liou
- Yihua Wu
- Yik-Lam Cho
- Yin Shi
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
Mitophagy is an important type of selective autophagy for specific elimination of damaged mitochondria. PTEN-induced putative kinase protein 1 (PINK1)-catalyzed phosphorylation of ubiquitin (Ub) plays a critical role in the onset of PINK1-Parkin-mediated mitophagy. Phosphatase and tensin homolog (PTEN)-long (PTEN-L) is a newly identified isoform of PTEN, with addition of 173 amino acids to its N-terminus. Here we report that PTEN-L is a novel negative regulator of mitophagy via its protein phosphatase activity against phosphorylated ubiquitin. We found that PTEN-L localizes at the outer mitochondrial membrane (OMM) and overexpression of PTEN-L inhibits, whereas deletion of PTEN-L promotes, mitophagy induced by various mitochondria-damaging agents. Mechanistically, PTEN-L is capable of effectively preventing Parkin mitochondrial translocation, reducing Parkin phosphorylation, maintaining its closed inactive conformation, and inhibiting its E3 ligase activity. More importantly, PTEN-L reduces the level of phosphorylated ubiquitin (pSer65-Ub) in vivo, and in vitro phosphatase assay confirms that PTEN-L dephosphorylates pSer65-Ub via its protein phosphatase activity, independently of its lipid phosphatase function. Taken together, our findings demonstrate a novel function of PTEN-L as a protein phosphatase for ubiquitin, which counteracts PINK1-mediated ubiquitin phosphorylation leading to blockage of the feedforward mechanisms in mitophagy induction and eventual suppression of mitophagy. Thus, understanding this novel function of PTEN-L provides a key missing piece in the molecular puzzle controlling mitophagy, a critical process in many important human diseases including neurodegenerative disorders such as Parkinson's disease.NMRC (Natl Medical Research Council, S’pore)Published versio
Proceedings of The HKIE Geotechnical Division 42nd Annual Seminar: A New Era of Metropolis and Infrastructure Developments in Hong Kong, Challenges and Opportunities to Geotechnical Engineering
- Author
- A Cunningham
- A K H Kwan
- A W Y Chan
- A Y F Leung
- Alan K L Kwong
- Alan Ng
- Alex Chan
- Alvin K M Lam
- Andrew K W Seto
- Andrew K W Seto
- Andrew T F Wong
- Andy LEUNG Yat Fai
- Anthony Hui
- Anthony Wong
- Anthony Wong
- C C J Wong
- C H Yan
- C H Yan
- C Ng
- C Ng
- Carrie Cheung
- Chris C W Chan
- Chris Cheung
- Chris Cheung
- Clayton Y K Chan
- Cloud Lo
- Collette Tse
- D Remus
- D Voss
- D Y Tan
- D Y Tan
- Daman Lee
- Dazhong Li
- Dennis K F Lau
- Derek Yung
- Dominic O K Lo
- Dora Shum
- E H Y Sze
- E Y M Chan
- Elton M Y Ko
- Endicott L John
- Eric X R Chen
- F L C Lo
- F L C Lo
- Florence Chu
- Florence L F Chu
- Francis Lee
- Franklin K L To
- Freda Chu
- G Ma
- G X Guan
- Gavin S H Toh
- Gavin S H Toh
- Geoffrey Pook
- Geoffrey Pook
- Gintaras Žaržojus
- Gisela Domej
- Goman Ho
- H G Zhu
- H W M Li
- Henry Cheung
- Henry Cheung
- I Li
- Ieva Lekstutytė
- Ivan H H Chan
- Ivan H H Chan
- Ivan M L Sham
- J Chen
- J Chin
- J Chin
- J Gaudon
- J H Yin
- J R Hart
- Joel Y F Wong
- Jonathan Hart
- K M Chiang
- K M Chiang
- K P Chan
- K Sevecek
- K T Hung
- Kathy Lau
- Kevin Chan
- Kevin Styles
- Kian Y K Chiu
- L Jeanne
- L Liu
- L Liu
- L M Zhang
- L W Wong
- Leo Man
- M K Chong
- M K Chong
- M S K Hassan
- Martin M K Kwong
- Michael Chak
- Michael Chak
- Michael Wright
- Mindaugas Zakarka
- Ming Kwok
- N Taylor
- Norman M H Lee
- P C Wu
- P K K Wu
- P K K Wu
- P L Ng
- Paul Tsui
- Petra Lee
- Philip Chung
- Philip W K Chung
- Q Xu
- Q Zhao
- R B Storry
- R B Storry
- R H L Li
- R Tsui
- R Tsui
- R Tsui
- Raymond S L Ng
- Raymond W M Cheung
- Raymond W M Cheung
- Regine Tsui
- Ricky Pang
- Ryan Yan
- S N Goh
- S Q Lin
- S T G Ng
- S Y N Cheng
- Sam H S Liu
- Sam H S Liu
- Samson Leung
- Samuel Lee
- Saulius Gadeikis
- Simon Leung
- Simon Leung
- Songye Zhu
- Steven Jenkins
- Steven Jenkins
- T C W Wong
- T M S Sacadura
- T Xiao
- Thomas S K Lam
- V H Loo
- V Tricot
- Victon W L Wong
- Victor Li
- Victor Shea
- Vincent Leung
- W B Chen
- W H Tsang
- W Hou
- W Hou
- Wei LEE Siew
- Wenzhu Hou
- Weyman C T Ngai
- X Monin
- X Wang
- Y Chen
- Y Chen
- Y K Ho
- Y K Ho
- Y M T Yong
- Y Sitanggang
- Y T A Chan
- Y.B Liu
- Yassine Bennani Braouli
- Z X Cao
- Zhang Zhen
- Šarūnas Skuodis
- Šarūnas Skuodis
- Publication venue
- AIJR Books
- Publication date
- 17/09/2022
- Field of study
This seminar proceedings contain articles on the various research ideas of the academic community and practitioners presented at The HKIE Geotechnical Division 42nd Annual Seminar (GDAS2022). GDAS2022 was organized by the Geotechnical Division, The Hong Kong Institution of Engineers on 13th May 2022.
Seminar Title: The HKIE Geotechnical Division 42nd Annual SeminarSeminar Acronym: GDAS2022Seminar Date: 13 May 2022Seminar Location: Hong KongSeminar Organizers: Geotechnical Division, The Hong Kong Institution of Engineers
Link to the GDAS2021 Proceedings: Proceedings of The HKIE Geotechnical Division 41st Annual Semina
Cerebral microbleeds and stroke risk after ischaemic stroke or transient ischaemic attack:a pooled analysis of individual patient data from cohort studies
- Author
- Abrigo Jill
- Aghoram Prasanna
- Akijian Layan
- Al-Shahi Salman Rustam
- Algra Ale
- Ambler Gareth
- Anwar Ijaz
- Armitage Paul
- Arsava Ethem Murat
- Assayag Einor Ben
- Ay Hakan
- Bae Hee-Joon
- Bakker Stef
- Banerjee Gargi
- Barbato Carmen
- Barry Adrian
- Beigneux Ysoline
- Berntsen Paul
- Birns Jonathan
- Bonati Leo
- Bordet Régis
- Bornstein Natan M.
- Bracoub Luc
- Brouwers Paul
- Brown Martin
- Browning Simone
- Burger Ilse
- Burn Mathew
- Caine Sarah
- Calvet David
- Camps-Renom Pol
- Carty Fiona
- Chabriat Hugues
- Chadha Dinesh
- Chan Chung Yan
- Chan Koon Ho
- Chan Oi Ling
- Chandra Ronil
- Chang Richard
- Chappell Francesca
- Charidimou Andreas
- Chen Christopher
- Cheung Raymond Tak Fai
- Cheung Ryan Hoi Kit
- Choy Lillian
- Christ Nicolas
- Chu Winnie
- Cohen David
- Cohen Hannah
- Cooper Martin
- Corrigan John
- Coutts Shelagh B.
- Coyle John
- Cullen Claire
- Dani Krishna
- Darawil Khaled
- Datta Prabel
- Davis Michelle
- de Leeuw Frank-Erik
- De Schryver Els
- Delgado Mederos
- Delmaire Christine
- Demirelli Derya Selcuk
- Dennis Martin
- Douste-Blazy Marie-Yvonne
- Douven Elles
- El-Koussy Marwan
- Elmarim Abduelbaset
- Emsley Hedley
- Engelter Stefan T.
- England Timothy
- Eppinger Sebastian
- Escudero Raquel
- Esisi Bernard
- Fazekas Franz
- Fladt Joachim
- Flossman Enrico
- Flossmann Enrico
- Fluri Felix
- Fong Wing Chi
- Fratacci Marie Dominique
- Fujita Kyohei
- Gass Achim
- Gattringer Thomas
- Gensicke Henrik
- Giallombardo Elio
- Gomez-Anson Beatriz
- Gratz Pascal
- Guevarra Christine
- Guisado-Alonso Daniel
- Gunathilagan Gunaratam
- Gunkel Sarah
- Guyler Paul
- Gyanwali Bibek
- Hallevi Hen
- Han Moon-Ku
- Hara Hideo
- Hargroves David
- Harkness Kirsty
- Harrington Frances
- Hassan Ahamad
- Hayden Derek
- Hendrikse Jeroen
- Hennerici Michael
- Heo Ji Hoe
- Hernández Maria Valdés
- Hert Lisa
- Hertzberger Leopold
- Heye Anna
- Hilal Saima
- Ho Shu Leung
- Hoi Chu Peng
- Horstmann Solveig
- Houlden Henry
- Hui Edward
- Ide Toshihiro
- Iida Kotaro
- Ikeda Syuhei
- Imaizumi Toshio
- Inamura Shigeru
- Ip Hing Lung
- Irie Hiroyuki
- Ispoglou Sissi
- Jang Myung Suk
- Jouvent Eric
- Jung Simon
- Jäger Hans R.
- Jöbsis Joost
- Kandiah Nagaendran
- Kang Jihoon
- Kappelle Jaap
- Karayiannis Christopher
- Kelly Deborah
- Kelly Peter J.
- Kim Beom Joon
- Kim Young Dae
- Kliper Efrat
- Ko Eunbin
- Koga Masatoshi
- Kooi M. Eline
- Korczyn Amos
- Koudstaal Peter
- Krishnamurthy Vinodh
- Kwa Vincent I. H.
- Kwan Joseph Shiu Kwong
- Köhler Sebastian
- Lam Bonnie Yin Ka
- Lau Kui Kai
- Lawrence Enas
- Leach Simon
- Lee Keon-Joo
- Leff Alexander
- Legrand Laurence
- Lemmens Robin
- Leung Kam Tat
- Leung Thomas
- Li Linxin
- Li Richard
- Li Siu Hung
- Lim Jae-Sung
- Linn Cisca
- Lip Gregory Y. H.
- Liu Wenyan
- Lou Min
- Lovelock Caroline
- Luder Robert
- Ly John
- Lyrer Philippe
- Ma Henry
- Ma Karen
- Ma Sze Ho
- Maaijwee Noortje
- Maeder Philippe
- Mahawish Karim
- Mak Henry Ka Fung
- Makin Stephen
- Mamun Maam
- Manawadu Dulka
- Mangion David
- Manoj Aravindakshan
- Mansoor Syed
- Marsh Rachel
- Marti-Fabregas Joan
- Martínez-Domeño Alejandro
- Marín Rebeca
- Mas Jean-Louis
- Mattle Heinrich P.
- McCormick Michael
- Medanta Jayesh Modi
- Medrano-Martorell Santiago
- Meenakishundaram Sanjeevikumar
- Mendyk Anne-Marie
- Merino Elisa
- Mess Werner
- Mitchell John
- Miwa Kaori
- Mohd Nor Azlisham
- Mok Vincent
- Molad Jeremy
- Moran Christopher
- Muir Keith
- Murphy Sean
- Muñoz-Maniega Susana
- Nachev Parashkev
- Nallasivam Arumug
- Nederkoorn Paul
- Ng Ping Wing
- Nishihara Masashi
- Nuñez Fidel
- O'Connell Janice
- O'Mahony Paul
- Okwera James
- Orken Dilek Necioglu
- Ozkan Hatice
- Pachai Chahin
- Panos Leonidas D.
- Parry Anthea
- Parry-Jones Adrian
- Pasco Kath
- Patterson Chris
- Perry Richard
- Peters Nils
- Phan Thanh
- Polymeris Alexandros
- Power Michael
- Prabhakaran Mathuri
- Prats-Sánchez Luis
- Price Christopher
- Proschel Harald
- Purrucker Jan
- Putterill Janet
- Ramos Lino
- Randall Marc
- Roffe Christine
- Roos Yvo
- Rothwell Peter M.
- Saastamoinen Kari
- Sajid Mahmud
- Sakka Eleni
- Sato Shoichiro
- Schembri Mark
- Schoonewille Wouter
- Schrooten Maarten
- Scott Jon
- Seiffge David J.
- Sekaran Lakshmanan
- Shakeshaft Clare
- Sharma Pankaj
- Shaw Louise
- Shiozawa Masayuki
- Silva Mauro
- Simister Robert
- Singhal Shahoo
- Slater Lee-Anne
- Smith Eric E.
- Smith Matthew
- Smyth Nigel
- Song Tae-Jin
- Soo Yannie
- Soufan Cathy
- Sprigg Nikola
- Srikanth Velandai
- Staals Julie
- Stam Jan
- Suman Appu
- Sword Jane
- Tanaka Jun
- Tanriverdi Zeynep
- Teo Kay Cheong
- Thijs Vincent
- Thilemann Sebastian
- Thornton John
- Thrippleton Michael
- Toyoda Kazunori
- Traenka Christopher
- Tsang Suk Fung
- Tse Man Yu
- Tuladhar Anil M.
- Uysal Ender
- Vahidassr Djamil
- van Dam-Nolen Dianne H. K.
- van der Lugt Aad
- van der Sande Jaap
- van Gemert Maarten
- van Oostenbrugge Robert
- Veltkamp Roland
- Venketasubramanian Narayanaswamy
- Verbiest Henk
- Vicaut Eric
- Warburton Elizabeth
- Ward Nicholas
- Wardlaw Joanna M.
- Werring David J.
- White Mark
- Wiegertjes Kim
- Wilkinson Peter
- Williams David J.
- Wilson Duncan
- Wong Adrian
- Wong Edmund Ka Ming
- Wong Kwok Kui
- Wong Lawrence
- Wong Yuen Kwun
- Xu Chao
- Yakushiji Yusuke
- Yang Mi Hwa
- Yatawara Chathuri
- Yoshifuji Kazuhisa
- Yousry Tarek
- Zerna Charlotte
- Zhou Ying
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2019
- Field of study
BACKGROUND
Cerebral microbleeds are a neuroimaging biomarker of stroke risk. A crucial clinical question is whether cerebral microbleeds indicate patients with recent ischaemic stroke or transient ischaemic attack in whom the rate of future intracranial haemorrhage is likely to exceed that of recurrent ischaemic stroke when treated with antithrombotic drugs. We therefore aimed to establish whether a large burden of cerebral microbleeds or particular anatomical patterns of cerebral microbleeds can identify ischaemic stroke or transient ischaemic attack patients at higher absolute risk of intracranial haemorrhage than ischaemic stroke.
METHODS
We did a pooled analysis of individual patient data from cohort studies in adults with recent ischaemic stroke or transient ischaemic attack. Cohorts were eligible for inclusion if they prospectively recruited adult participants with ischaemic stroke or transient ischaemic attack; included at least 50 participants; collected data on stroke events over at least 3 months follow-up; used an appropriate MRI sequence that is sensitive to magnetic susceptibility; and documented the number and anatomical distribution of cerebral microbleeds reliably using consensus criteria and validated scales. Our prespecified primary outcomes were a composite of any symptomatic intracranial haemorrhage or ischaemic stroke, symptomatic intracranial haemorrhage, and symptomatic ischaemic stroke. We registered this study with the PROSPERO international prospective register of systematic reviews, number CRD42016036602.
FINDINGS
Between Jan 1, 1996, and Dec 1, 2018, we identified 344 studies. After exclusions for ineligibility or declined requests for inclusion, 20 322 patients from 38 cohorts (over 35 225 patient-years of follow-up; median 1·34 years [IQR 0·19-2·44]) were included in our analyses. The adjusted hazard ratio [aHR] comparing patients with cerebral microbleeds to those without was 1·35 (95% CI 1·20-1·50) for the composite outcome of intracranial haemorrhage and ischaemic stroke; 2·45 (1·82-3·29) for intracranial haemorrhage and 1·23 (1·08-1·40) for ischaemic stroke. The aHR increased with increasing cerebral microbleed burden for intracranial haemorrhage but this effect was less marked for ischaemic stroke (for five or more cerebral microbleeds, aHR 4·55 [95% CI 3·08-6·72] for intracranial haemorrhage vs 1·47 [1·19-1·80] for ischaemic stroke; for ten or more cerebral microbleeds, aHR 5·52 [3·36-9·05] vs 1·43 [1·07-1·91]; and for ≥20 cerebral microbleeds, aHR 8·61 [4·69-15·81] vs 1·86 [1·23-1·82]). However, irrespective of cerebral microbleed anatomical distribution or burden, the rate of ischaemic stroke exceeded that of intracranial haemorrhage (for ten or more cerebral microbleeds, 64 ischaemic strokes [95% CI 48-84] per 1000 patient-years vs 27 intracranial haemorrhages [17-41] per 1000 patient-years; and for ≥20 cerebral microbleeds, 73 ischaemic strokes [46-108] per 1000 patient-years vs 39 intracranial haemorrhages [21-67] per 1000 patient-years).
INTERPRETATION
In patients with recent ischaemic stroke or transient ischaemic attack, cerebral microbleeds are associated with a greater relative hazard (aHR) for subsequent intracranial haemorrhage than for ischaemic stroke, but the absolute risk of ischaemic stroke is higher than that of intracranial haemorrhage, regardless of cerebral microbleed presence, antomical distribution, or burden.
FUNDING
British Heart Foundation and UK Stroke Association