Arcensus is now ISO/IEC 27001:2022 certified! This reaffirms our commitments to safeguard sensitive patient and genetic data. Do you want to learn more about our commitment to data security? Feel free to reach out! #ISO27001 #DataSecurity #GeneticDiagnostics

NEW EPISODE out now! Genetic Sounds, the ESHG Podcast. This month: Facilitating discussions about reproductive choices. eshg.buzzsprout.com

Feeling overwhelmed by the challenges of a genetic condition? Our helpline offers a compassionate ear and practical guidance to help you navigate this journey with confidence and resilience. You don't have to face it alone.

Don't miss out on the #Arcensus webinar this Wednesday! Discover the power of genetic testing in clinical settings as we delve into real-life patient cases with Dr. Eliane Chouery's. Register now and secure your spot! See you there! app.livestorm.co/p/0d295721-50d…

Scoping review of the recommendations and guidance for improving the quality of rare disease registries dlvr.it/T6XHl6

Join us at #ESHG2024in #Berlin! Looking forward to connect with genetic enthusiasts for discussions on genomics, collaborations, and research. Reach out if you would like to schedule a chat. Can't wait to meet you there! #genetics #networking #collaboration

#InvolveAustralia has released practical recommendations for health and medical research institutes and funders, urging them to play a stronger role in supporting #communityinvolvement in #research. View the recommendations here 👇 australiangenomics.org.au/projects/invol…

If you are attending #ESHG2024, stop by the poster presentation on "Nuclear Mitochondrial DNA disruption in KLHL10 gene causes Spermatogenic Failure" to explore new research on male infertility and reproductive health. See you there! #MaleInfertility #ReproductiveHealth

Genetic changes that leave newborns with little to no immune defence against infection have been pinpointed by scientists The discovery will help accelerate diagnosis and life-saving treatment for these high-risk #raredisease patients sanger.ac.uk/news_item/gene…

We are presenting new findings on Developmental and Epileptic Encephalopathies (DEE) at the #ESHG2024 conference! Three novel variants in the FZR1 gene shed light on the genetic basis and phenotype spectrum of this rare condition. #DEE #EpilepsyResearch

Excited to share another poster at #ESHG2024! Join us as we present our latest discovery: a novel missense variant in the SVBP gene causing neurodevelopmental disorders with microcephaly. #GeneticResearch #Microcephaly #SVBP #neurodevelopmentaldisorder

Have you seen the recent paper by Chi et al. (PMID: 38789118)? By re-evaluating existing WGS data with the latest techniques and knowledge, we can boost the diagnostic yield. This can lead to more accurate diagnoses, better-informed treatment plans, and improved patient outcomes.

Join our upcoming webinar on the clinical significance of cardiology-related secondary findings! 🗓️July 11th at 10 a.m. CET #GeneticsWebinar #Cardiology #GeneticTesting #ClinicalGuidelines #HealthcareEducation app.livestorm.co/p/394e9971-889…

We have launched our Arcensus monthly newsletter! Subscribe for educational resources, in-depth articles, expert opinions, case studies and more here: arcensus-diagnostics.com/en/newsletter/ #Arcensusnewsletter #genomicsnews

Don’t miss our webinar this Thursday to - Gain insights into secondary findings - Discover the value of secondary findings in cardiovascular disease - Learn to manage patients and relatives with CVD-related secondary findings: app.livestorm.co/p/394e9971-889… via Arcensus

We've worked with the RCGP to create a comprehensive toolkit of resources on #genomics for primary care practitioners. Check out the toolkit and find out what's on offer: buff.ly/3zXkHXT

We're relocating to a new office by the Baltic Sea in Warnemünde's Biotechnology Park! Our growth requires more space to expand our team and advance genomic insights. Visit our homepage to schedule a tour of our new office!

Duchenne Muscular Dystrophy (DMD) affects 1 in 5k boys and it often takes 2.5 years to diagnose. For #WorldDuchenneAwarenessDay, let's recognize the signs, advocate for early intervention, and promote early genetic testing. Great video @ DMD: lnkd.in/eNAb-zpK #WDAD2024

Repeat Expansion Disorders Likely Underdiagnosed A study led by UCL and Queen Mary University of London shows that repeat expansion disorders are a lot more common than previously thought meaning that many people with these conditions probably evade diagnosis. hubs.li/Q02RGj_10

Meet Dr. Alexandru Popa, the new CEO of Arcensus GmbH! With 20+ years in healthcare, he’ll strengthen our focus on delivering high-quality genomic data and comprehensive reports that empower patients and healthcare providers. arcensus-diagnostics.com #WGS #WES #Datadriven