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B

Bryndis Birnir

swedish institute for infectious disease control
H指数:36
被引数:4,430

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GABA-mediated inhibition of human CD4
EBIOMEDICINE
IF10.8
2024-07-011
OAAI
Jin, Zhe; Hammoud, Hayma; Bhandage, Amol Keshavasa; Korol, Sergiy Vasylyovych; Trujeque-Ramos, Olivia; Koreli, Stasini; Gong, Zhitao; Chowdhury, Azasul Islam; Sandbaumhueter, Friederike Andrea; Jansson, Erik Tomas; Lindsay, Robin Sean; Christoffersson, Gustaf; Andren, Per Erik; Carlsson, Per-Ola; Bergsten, Peter; Kamali-Moghaddam, Masood; Birnir, Bryndis
Discovery and Hit-to-Lead Optimization of Benzothiazole Scaffold- Based DNA Gyrase Inhibitors with Potent Activity against Acinetobacter baumannii and Pseudomonas aeruginosa
JOURNAL OF MEDICINAL CHEMISTRY
IF6.8
2023-01-1221
OAAI
Cotman, Andrej Emanuel; Durcik, Martina; Tiz, Davide Benedetto; Fulgheri, Federica; Secci, Daniela; Sterle, Masa; Mozina, Stefan; Skok, Ziga; Zidar, Nace; Zega, Anamarija; Ilas, Janez; Masic, Lucija Peterlin; Tomasic, Tihomir; Hughes, Diarmaid; Huseby, Douglas L.; Cao, Sha; Garoff, Linnea; Fernandez, Talia Berruga; Giachou, Paraskevi; Crone, Lisa; Simoff, Ivailo; Svensson, Richard; Birnir, Bryndis; Korol, Sergiy V.; Jin, Zhe; Vicente, Francisca; Ramos, Maria C.; de la Cruz, Mercedes; Glinghammar, Bjorn; Lenhammar, Lena; Henderson, Sara R.; Mundy, Julia E. A.; Maxwell, Anthony; Stevenson, Clare E. M.; Lawson, David M.; Janssen, Guido V.; Sterk, Geert Jan; Kikelj, Danijel
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (vol 108, pg 739, 2021)
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2022-03-010
OAAI
Fatima, Ambrin; Hoeber, Jan; Schuster, Jens; Koshimizu, Eriko; Maya-Gonzalez, Carolina; Keren, Boris; Mignot, Cyril; Akram, Talia; Ali, Zafar; Miyatake, Satoko; Tanigawa, Junpei; Koike, Takayoshi; Kato, Mitsuhiro; Murakami, Yoshiko; Abdullah, Uzma; Ali, Muhammad Akhtar; Fadoul, Rein; Laan, Loora; Castillejo-Lopez, Casimiro; Liik, Maarika; Jin, Zhe; Birnir, Bryndis; Matsumoto, Naomichi; Baig, Shahid M.; Klar, Joakim; Dahl, Niklas
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2021-04-0116
OAAI
Fatima, Ambrin; Hoeber, Jan; Schuster, Jens; Koshimizu, Eriko; Maya-Gonzalez, Carolina; Keren, Boris; Mignot, Cyril; Akram, Talia; Ali, Zafar; Miyatake, Satoko; Tanigawa, Junpei; Koike, Takayoshi; Kato, Mitsuhiro; Murakami, Yoshiko; Abdullah, Uzma; Ali, Muhammad Akhtar; Fadoul, Rein; Laan, Loora; Castillejo-Lopez, Casimiro; Liik, Maarika; Jin, Zhe; Birnir, Bryndis; Matsumoto, Naomichi; Baig, Shahid M.; Klar, Joakim; Dahl, Niklas

研究方向

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Z
Zhe Jin
H 指数:31论文数:177被引数:3,795
S
Sergiy V. Korol
H 指数:17论文数:46被引数:889
A
Amol K. Bhandage
H 指数:18论文数:47被引数:1,072
P
Peter W. Gage
H 指数:60论文数:226被引数:1.1万
E
Esa R. Korpi
H 指数:62论文数:359被引数:1.3万
N
Niklas Dahl
H 指数:62论文数:354被引数:1.5万
J
Joakim Klar
H 指数:32论文数:131被引数:4,237
G
Georgy Bakalkin
H 指数:41论文数:226被引数:5,802
D
Daniel Espes
H 指数:23论文数:92被引数:1,817
I
Igor Bazov
H 指数:26论文数:63被引数:1,809