Jaël Copier
@Jael_Copier
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PhD-candidate at Experimental Cardiology, Amsterdam UMC ~ Researching genetic cardiac arrythmias ~ Utrecht University alumni
Utrecht
Joined September 2020
Our editorial on emerging concepts and technologies in Cardiac Arrythmia Research is out in @JPhysiol! Thanks to all the talented early career co-authors: Ahmed Ramadam @EChleilat @HectorMartnezN2 @jaclynb_phd @JLCaldwellPhD @joa_gr @patymardi @vladimirsobota.
Check out our editorial in the @JPhysiol ! Inspired by @GordonConf on #GRC_Arrhythmia, we highlight some of the current hot topics in cardiac arrhythmia research
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Excited for this paper to be out! Was a great experience to be part of this team and research! @JLSanchezAlonso @lau_fed.
Sanchez-Alonso et al demonstrate functional coupling between #β2AR & #LTCC in cardiomyocytes & this is linked to #Cav3 & #CaMKII, present in rodents & humans & disrupted in #HF. .@lau_fed @JLSanchezAlonso @ImperiaNHLI
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RT @hmg_journal: Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance..
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RT @EML314: Our work on the complexity of a recurring variant in KCNH2 is now published! @Jael_Copier @cbezzina1 @GeneticAMS #CardioTwitte….
academic.oup.com
Abstract. Background: Variants in KCNH2, encoding the human ether a-go-go (hERG) channel that is responsible for the rapid component of the cardiac delayed
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Our paper, describing a new recurring variant in KCNH2 and the implications of reduced penetrance, just got published! @EML314 @cbezzina1 @GeneticAMS @DQCMBarge @VandenbergJamie @ArthurWilde5
academic.oup.com
Abstract. Background: Variants in KCNH2, encoding the human ether a-go-go (hERG) channel that is responsible for the rapid component of the cardiac delayed
Our study is out as pre-print. Describing eight families carrying KCNH2-p.(S906L), and its functional assessment. Emphasizing the complexity of the classification of variants with incomplete penetrance, and its consequences. @EML314 @ArthurWilde5 @VandenbergJamie @DQCMBarge.
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Our study is out as pre-print. Describing eight families carrying KCNH2-p.(S906L), and its functional assessment. Emphasizing the complexity of the classification of variants with incomplete penetrance, and its consequences. @EML314 @ArthurWilde5 @VandenbergJamie @DQCMBarge.
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance #bioRxiv.
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RT @MollyOReillyy: My favourite thing about conferences? .Networking with friends and colleagues, old and new! 🥂.@ICVS_UoB @amsterdamumc .@….
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RT @_CarolinePham: Spoiled ourselves with another day in beautiful Copenhagen! Cheers on attending and presenting our work at our first int….
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RT @cbezzina1: Fun times @ #EHRA2022. Great scientific sessions and a chance to catch up with friends at first in person conference in >2 y….
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My research regarding a variant in KCNH2 found in multiple patients with LQTS2 was part of today's e-posters at #EHRA2022. I am grateful for the opportunity to show these results at my first international congress.
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RT @EML314: Looking forward to #EHRA2022, exciting science and meeting everyone again. Very proud of the group: @_CarolinePham @Jael_Copier….
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RT @EML314: Collaboration and Communication in science: what would you like to hear about most? Scared of contacting that big shot? Will I….
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Very excited to join this amazing team!.
Really enjoyed the first meeting including the new team members today. Welcome @Jael_Copier and Karolina Andrzejczyk! Looking forward to all the exciting projects to come with @_CarolinePham and @Noelia_MuMar , #cardiac_arrhythmia_research, @amsterdamumc
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