43 research outputs found
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
- Author
- Abdalla Moustafa
- Adams F
- Adelman D
- Agardh E
- Ahlqvist E
- Ahlqvist Emma
- Ahluwalia Tarunveer S
- Ahola AJ
- Ahonen R
- Ahonen-Bishopp A
- Aiello L
- Aimolahti A
- Airas MA
- Aizawa K
- Ajanki T
- Akbar T
- Al Maghrabi N
- Albertini M
- Almgren P
- Almgren Peter
- Anderson S
- Ang Su Fen
- Apelqvist J
- Aranko S
- Arends V
- Asplund B
- Babu M
- Bain SC
- Ball C
- Bantle J
- Barbarini N
- Barnie A
- Bassi L
- Belch J
- Bellazzi R
- Bellenger N
- Bengtsson E
- Benigni A
- Bergenstal R
- Berglund L
- Bernal ML
- Betsholtz C
- Bhan A
- Björckbacka H
- Björkholm A
- Blodi B
- Blom-Nilsson U
- Bokvist K
- Boldrini B
- Boni E
- Borell M
- Boulton AJM
- Bourne P
- Boustany C
- Braffett B
- Brandslund Ivan
- Brennan EP
- Brosnan J
- Brosnan Mary Julia
- Bucalo M
- Burström A
- Byskata U
- Campbell C
- Canady J
- Casanova F
- Caulder S
- Chan JCN
- Chan KKH
- Chan TF
- Chan Juliana C N
- Chassin L
- Cheung GPY
- Christensen Cramer
- Cilio C
- Cimino L
- Cinthio M
- Clara Tan Si Hua
- Cleary P
- Clerin V
- Cobelli C
- Colhoun H
- Colhoun Helen M
- Colombo M
- Colson S
- Cowie C
- Crowther D
- Dagogo-Jack S
- Dahlström E
- Dallai A
- Dalton N
- Danis R
- Deanfield J
- Demaine AG
- Deshmukh H
- Deshmukh Harshal
- Di Camillo B
- Dijkstra M
- Donadelli R
- Dorajoo Rajkumar
- Dove F
- Dreja K
- Driscoll M
- Duffy Seamus
- Dunger D
- Dunger David
- Dunér P
- Ehlgen A
- Eliasson A
- Ellingford A
- Engelbertsen D
- Erola RM
- Ervasti S
- Fadista J
- Fagerholm E
- Fagerudd J
- Fahlstrom R
- Fan X
- Farran B
- Fauman E
- Fauman Eric
- Feodoroff M
- Ferguson M
- Ferrannini E
- Finotello F
- Flaherty N
- Florez JC
- Florez Jose C
- Formentini I
- Foroogh F
- Forsblom C
- Forsblom C
- Forsblom Carol
- Forsen M
- Forslund T
- Frayling T
- Gan LM
- Gassenhuber J
- Gatcomb P
- Gates P
- Genové G
- Gerl M
- Gertow K
- Gieger C
- Gigante B
- Godson C
- Golden E
- Goldstein D
- Gomez M
- Goncalves I
- Gooding K
- Gordin D
- Gordin D
- Grallert H
- Granlund H
- Grarup Niels
- Gregory NS
- Groop L
- Groop PH
- Groop PH
- Groop Leif C
- Groop Per-Henrik
- Groves C
- Gubitosi-Klug R
- Guidi F
- Guiducci C
- Gunyou K
- Gurzeler E
- Gyorgy Beata
- Haaga J
- Hadjadj Samy
- Hainsworth D
- Halonen A
- Hammarstedt A
- Hamsten A
- Hansen Torben
- Harjutsalo V
- Harjutsalo V
- Harjutsalo Valma
- Harth J
- Hattersley A
- Haukkala J
- Havulinna A
- He B
- Hedblad B
- Heikkilä O
- Heikkilä O
- Heinonen S
- Henderson G
- Hensley S
- Hentunen P
- Herman W
- Herrala T
- Hess S
- Hietala K
- Hietala K
- Hiraki
- Hirschhorn JN
- Hirschhorn Joel N
- Hitt S
- Horsford J
- Houston G
- Huang Y
- Huber J
- Hubschle T
- Hultgårdh A
- Huovinen E
- Huttunen E
- Huusko J
- Hyde C
- Hämäläinen A
- Häring H
- Igo Robert P
- Ikäheimo R
- Ilkka V
- Imamura Minako
- Isakova T
- Ivaska-Suomela M
- Jablonka B
- Jatkola E
- Jauhiainen A
- Jiang G
- Jiang Guozhi
- Johansson ME
- Johnson M
- Johnsonbaugh S
- Jokelainen KS
- Jones JK
- Jonsson AC
- Juliusdottir T
- Juretschke HP
- Jönsson-Rylander AC
- Kalliomäki FT
- Kananen K
- Kanninen T
- Kaprio SA
- Karhapää P
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- Karpe F
- Kauppinen-Mäkelin R
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- Koistinen A
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- Koskelainen J
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- Koskinen E
- Kozakova M
- Kravic J
- Kristiansson K
- Krolewski Andrzej S
- Kruger D
- Kubo Michiaki
- Kuusela M
- Kuusisto A
- Kyllönen L
- Kytö J
- Kytö J
- Kärkkäinen J
- Käräjämäki Annemari
- Kääriäinen TP
- Laakso J
- Laakso M
- Laakso M
- Lachin J
- Lackaye ME
- Ladenvall C
- Ladenvall Claes
- Lagerstam J
- Lagou V
- Laine MM
- Lajer Maria
- Lakka T
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- Lan HY
- Lansimaki HV
- Lappalainen A
- Larizza C
- Larkin M
- Laukkanen KH
- Laukkanen M
- Lawrence D
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- Lee Heung Man
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- Maxwell AP
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- McCarthy
- McCarthy M
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- McKay GJ
- McKeague P
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- McKnight AJ
- McKnight AJ
- McKnight Amy-Jayne
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- Merentie M
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- Moilanen L
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- Orho-Melander Marju
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- Ostling G
- Ottoson-Laakso E
- Oukko-Ruponen SE
- Pacheco GD
- Pagliaccia F
- Paldanius KR
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- Parkkonen M
- Parta JA
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- Pedersen O
- Pedersen Oluf
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- Perico N
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- Perna A
- Perna Annalisa
- Perola M
- Persson A
- Persson M
- Persson MÅ
- Pettersson-Fernholm K
- Pezzolesi Marcus G
- Pietilä A
- Pietiläinen AL
- Piras R
- Pirttiniemi I
- Pittman C
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- Rosengård-Bärlund M
- Rossing Peter
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- Silveira A
- Sim Xueling
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- Sipilä V
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- So Wing Yee
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- Syreeni A
- Szeto CC
- Szeto Cheuk Chun
- Söderlund J
- Tai E Shyong
- Taimi M
- Takahashi Atsushi
- Tam CHT
- Tam Claudia H T
- Tamborlane W
- Tang N
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- Taylor A
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- Toivonen KR
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- Toppila I
- Tortoli P
- Tregouet David
- Trifoglio E
- Tryggvason K
- Tsui SKW
- Tuomi Tiinamaija
- Tuomikangas J
- Tuovinen U
- Tuthill T
- Uggeldahl T
- Unwin R
- Valo E
- Valo Erkka
- Valtonen E
- van Dam Rob M
- van Zuydam N
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- Vangjeli C
- Vanhanen A
- Vauhkonen I
- Venturi E
- Vesisenaho T
- Viberti GC
- Vikström M
- Virkkala T
- Virtanen T
- Vitali F
- Viti J
- Vittetoe B
- Voutilainen E
- Vähänen A
- Wabers H
- Wadén J
- Wadén J
- Walentinsson A
- Walker J
- Walker M
- Walker N
- Wang Ling
- Wang-Sattler R
- Weng M
- Whatling C
- White N
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- Wigley C
- Wigren M
- Williams WW
- Witte Daniel R
- Wohlfart P
- Wong M
- Xie F
- Xie F
- Yeung MW
- Yip KYL
- Ylä-Herttuala S
- Yu P
- Yu W
- Zetterqvist A
- Zhang S
- Zhang ZM
- Ziegler G
- Ziemek D. Linda T
- Ziemek Daniel
- Zierer A
- Zimdahl-Gelling H
- Zinman B
- Zinman B
- Åkerlund M
- Österholm AM
- Publication venue
- Publication date
- 01/01/2018
- Field of study
dentification of sequence variants robustly associated with predisposition to diabetic kidney disease (DKD) has the potential to provide insights into the pathophysiological mechanisms responsible. We conducted a genome-wide association study (GWAS) of DKD in type 2 diabetes (T2D) using eight complementary dichotomous and quantitative DKD phenotypes: the principal dichotomous analysis involved 5,717 T2D subjects, 3,345 with DKD. Promising association signals were evaluated in up to 26,827 subjects with T2D (12,710 with DKD). A combined T1D+T2D GWAS was performed using complementary data available for subjects with T1D, which, with replication samples, involved up to 40,340 subjects with diabetes (18,582 with DKD). Analysis of specific DKD phenotypes identified a novel signal near GABRR1 (rs9942471, P = 4.5 x 10(-8)) associated with microalbuminuria in European T2D case subjects. However, no replication of this signal was observed in Asian subjects with T2D or in the equivalent T1D analysis. There was only limited support, in this substantially enlarged analysis, for association at previously reported DKD signals, except for those at UMOD and PRKAG2, both associated with estimated glomerular filtration rate. We conclude that, despite challenges in addressing phenotypic heterogeneity, access to increased sample sizes will continue to provide more robust inference regarding risk variant discovery for DKD.Peer reviewe
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
- Author
- Abdel-Aziz AK
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- Mukherjee A
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- Shravage BV
- Shridhar V
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- Shutt TE
- Sica V
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- Silva-Pavez E
- Silvente-Poirot S
- Simmonds RE
- Simon AK
- Simon H-U
- Simons M
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- Skirycz A
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- Sluimer JC
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- Srinivas Bharath MM
- St Clair D
- Stagni V
- Staiano L
- Stallings CL
- Stalnecker CA
- Stankov MV
- Stathopulos PB
- Stefan K
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- Steffan JS
- Steinkasserer A
- Stenmark H
- Sterneckert J
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- Strohecker AM
- Stupack DG
- Su H
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- Subauste CS
- Subbian S
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- Sue CM
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- Titorenko VI
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- Tomaipitinca L
- Tomar D
- Tomas-Zapico C
- Tomić S
- Tong BC-K
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- Torgersen ML
- Torii S
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- Torriglia A
- Towers CG
- Towns R
- Toyokuni S
- Trajkovic V
- Tramontano D
- Tran Q-G
- Travassos LH
- Trelford CB
- Tremel S
- Trougakos IP
- Tsao BP
- Tschan MP
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- Tsugawa H
- Tsvetkov AS
- Tumbarello DA
- Tumtas Y
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- Tuxworth RI
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- Valko A
- Vallee RB
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- van der Veen S
- Van Kaer L
- van Loosdregt J
- van Wijk SJL
- Vandenberghe W
- Vanhorebeek I
- Vannier-Santos MA
- Vannini N
- Vanrell MC
- Vantaggiato C
- Varano G
- Varela-Nieto I
- Varga M
- Vasconcelos MH
- Vats S
- Vavvas DG
- Vega-Naredo I
- Vega-Rubin-de-Celis S
- Velasco G
- Vellai T
- Vellenga E
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- Velázquez AP
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- Waguri S
- Waite KA
- Wakatsuki S
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- Wang B
- Wang C
- Wang C
- Wang C
- Wang C-Y
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- Wang W
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- Wang X
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- Wang Y
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- Warnes G
- Warnsmann V
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- Weaver TE
- Wegrzyn G
- Wehman AM
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- Wei L
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- Wei Y
- Weiergräber OH
- Weihl CC
- Weindl G
- Weiskirchen R
- Wells A
- Wen RH
- Wen X
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- Weykopf B
- Wheatley SP
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- Whitworth AJ
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- Wildenberg ME
- Wileman T
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- Witkin SS
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- Woehlbier U
- Wollert T
- Wong E
- Wong JH
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- Wu A-G
- Wu C
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- Wu KK
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- Wu S
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- Wu S-Y
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- Xavier RJ
- Xia H
- Xia L
- Xia Z
- Xiang G
- Xiang J
- Xiang M
- Xiang W
- Xiao B
- Xiao G
- Xiao H
- Xiao H-T
- Xiao J
- Xiao L
- Xiao S
- Xiao Y
- Xie B
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- Xu C
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- Yakhine-Diop SMS
- Yamaguchi M
- Yamaguchi O
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- Yamashina S
- Yan S
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- Yang Q
- Yang S
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- Yang S-F
- Yang W
- Yang WY
- Yang X
- Yang X
- Yang Y
- Yang Y
- Yao H
- Yao S
- Yao X
- Yao Y-G
- Yao Y-M
- Yasui T
- Yazdankhah M
- Yen PM
- Yi C
- Yi-Ren Hong C-WH
- Yin X-M
- Yin Y
- Yin Z
- Yin Z
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- Ying Z
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- Yiu SPT
- Yoo YH
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- Yoshii SR
- Yoshimori T
- Yousefi B
- Yu B
- Yu H
- Yu J
- Yu J
- Yu L
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- Yu WH
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- Yuan S-SF
- Yuan Y
- Yuan Z
- Yue J
- Yue Z
- Yun J
- Yung RL
- Zacks DN
- Zaffagnini G
- Zambelli VO
- Zanella I
- Zang QS
- Zanivan S
- Zappavigna S
- Zaragoza P
- Zarbalis KS
- Zarebkohan A
- Zarrouk A
- Zeitlin SO
- Zeng J
- Zeng J-D
- Zhan L
- Zhang B
- Zhang DD
- Zhang H
- Zhang H
- Zhang H
- Zhang H
- Zhang H
- Zhang H
- Zhang H
- Zhang H-L
- Zhang J
- Zhang J
- Zhang J-P
- Zhang KYB
- Zhang L
- Zhang L
- Zhang L
- Zhang L
- Zhang LW
- Zhang M
- Zhang P
- Zhang S
- Zhang W
- Zhang X
- Zhang X
- Zhang X
- Zhang X
- Zhang X
- Zhang X-W
- Zhang XD
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y-D
- Zhang Y-Y
- Zhang Z
- Zhang Z
- Zhang Z
- Zhang Z
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- Zhao H
- Zhao L
- Zhao S
- Zhao T
- Zhao X-F
- Zhao Y
- Zhao Y
- Zhao Y
- Zhao Y
- Zheng G
- Zheng K
- Zheng L
- Zheng S
- Zheng X-L
- Zheng Y
- Zheng Z-G
- Zhivotovsky B
- Zhong Q
- Zhou A
- Zhou B
- Zhou C
- Zhou G
- Zhou H
- Zhou H
- Zhou H
- Zhou J
- Zhou J
- Zhou J
- Zhou J
- Zhou K
- Zhou R
- Zhou X-J
- Zhou Y
- Zhou Y
- Zhou Y
- Zhou Z
- Zhou Z-Y
- Zhu B
- Zhu C
- Zhu G-Q
- Zhu H
- Zhu H
- Zhu H
- Zhu W-G
- Zhu Y
- Zhu Y
- Zhuang H
- Zhuang X
- Zientara-Rytter K
- Zimmermann CM
- Ziviani E
- Zoladek T
- Zong W-X
- Zorov DB
- Zorzano A
- Zou W
- Zou Z
- Zou Z
- Zuryn S
- 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
Search for gravitational waves associated with gamma-ray bursts detected by Fermi and Swift during the LIGO–Virgo run O3b
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- Zimmerman AB
- Zucker ME
- Zweizig J
- Publication venue
- 'American Astronomical Society'
- Publication date
- 01/01/2022
- Field of study
We search for gravitational-wave signals associated with gamma-ray bursts (GRBs) detected by the Fermi and Swift satellites during the second half of the third observing run of Advanced LIGO and Advanced Virgo (2019 November 1 15:00 UTC–2020 March 27 17:00 UTC). We conduct two independent searches: a generic gravitational-wave transients search to analyze 86 GRBs and an analysis to target binary mergers with at least one neutron star as short GRB progenitors for 17 events. We find no significant evidence for gravitational-wave signals associated with any of these GRBs. A weighted binomial test of the combined results finds no evidence for subthreshold gravitational-wave signals associated with this GRB ensemble either. We use several source types and signal morphologies during the searches, resulting in lower bounds on the estimated distance to each GRB. Finally, we constrain the population of low-luminosity short GRBs using results from the first to the third observing runs of Advanced LIGO and Advanced Virgo. The resulting population is in accordance with the local binary neutron star merger rate
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- A Horuzsko
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- D Roopenian
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- Diego Fraidenraich
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- E Wylegala
- G Opelz
- G Pellegrini
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- A Celzard
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- AS Mayorov
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- N Funakoshi
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- T Aasen
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- T Zhou
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