Put your brand or message in front of ACMG members by being the exclusive annual sponsor of the ACMG’s high-quality member magazine, The ACMG Medical Geneticist. AS the sole, exclusive sponsor, you will receive a full-page color ad each issue – the only non-ACMG ad in each issue. Get the details: https://bit.ly/sponsormag The ACMG Medical Geneticist boasts a high level of readership, with 86% of members reporting they read at least some of each issue. Our members include MDs, PhDs, genetic counselors and other genetics professionals who work in a variety of settings including academic medical centers, private practice, labs, industry and the government. #medicalgenetics #genomics
ACMG - American College of Medical Genetics and Genomics’ Post
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Leukodystrophies manifest in approximately 1 in 7,000 live births, underscoring the critical role of genetic history in pediatric care. For healthcare professionals, this statistic highlights the importance of genetic consultation and testing in identifying potential risks and providing anticipatory guidance to families. By encouraging and facilitating access to genetic screening, medical professionals can empower families with actionable insights, enabling proactive management and care strategies for those at risk. - #Genetics #Genetictesting #Leukodystrophy
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From Sistemas Genómicos | member of SYNLAB we accompany professionals by offering personalised genetic counselling focused on the genomic understanding of the full range of human pathology for assertive and preventive decision-making. For more information: direcciondeservicios@sistemasgenomicos.com. #SistemasGenomicos #Genetic #Genetica #ConsejoGenetico #GeneticCounselling #Laboratorio #GeneBytesX #GeneBytes #NGS #Laboratory #MedicalExcellence #ExcelenciaMedica
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Eurofins Humangenetik welcomes you to booth #232 at #ESHG2024 in Berlin. Learn about our extensive range of human genetic diagnostic services designed to support your clinical practice. We look forward to discussing your needs and how our expertise in genetic diagnostics can contribute to enhanced patient care. #HumanGenetics #Genetics #Medicine #Diagnostics #GeneticTesting
Eurofins Humangenetik @ESHG 2024 Join us in Berlin from June 1st to 3rd and discover our comprehensive portfolio of human genetic diagnostic solutions designed to enhance patient care. Engage with our experts, exchange insights, and explore the evolving landscape of genetic medicine together. We look forward to connecting with you. #ESHG2024 #HumanGenetics #Genetics #Medicine #Diagnostics
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#ICYMI - Dr. Doron Behar, @Igentify’s CEO, spoke with Kira Dineen of DNA Today about the genetic counseling bottleneck and how innovative solutions are reshaping the landscape. Igentify’s #digitalhealth technology alleviates the workload of genetic counselors while ensuring more personalized and efficient patient care. “[Our] goal is to support genetic counselors, increase patient access to genomic content, and advance precision medicine.” – Dr. Doron Behar, CEO, Igentify Watch here: https://lnkd.in/e5EmCXP4 #GeneticCounseling #PrecisionMedicine #GeneticMedicine
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Experience Effortless Efficiency: With MAVEvidence, clinical geneticists, variant scientists, and genetic counselors streamline their workflow by avoiding the manual collection and analysis of large datasets. Our platform offers cutting-edge research at your fingertips, saving valuable time and enhancing the quality of variant interpretations. Elevate your genomic practices with MAVEvidence. Sign up for a free trial mavevidence.com #GenomicEfficiency #MAVEvidence #GeneticInterpretation #vus
Experience Effortless Efficiency: With MAVEvidence, clinical geneticists, variant scientists, and genetic counselors streamline their workflow by avoiding the manual collection and analysis of large datasets. Our platform offers cutting-edge research at your fingertips, saving valuable time and enhancing the quality of variant interpretations. Elevate your genomic practices with MAVEvidence. Sign up for a free trial mavevidence.com #GenomicEfficiency #MAVEvidence #GeneticInterpretation #vus
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Did you know that Carepoint Labs offers top-notch cytogenetic services? Whether you're in need of comprehensive genetic testing or exploring chromosomal abnormalities, Carepoint Labs has you covered. Learn more about our cytogenetic services and how we can assist you on our website. Trust Carepoint Labs for accurate results and expert care in genetic testing! #CarepointLab #GeneticTesting #Atlanta
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📢 Hot off the Press! New Research Findings and Insights Just Published 📚 The Journal of Clinical Genetics and Heredity has recently released a research article titled "A Comprehensive Review on Twin-twin Transfusion Syndrome Diagnosis and Treatment." Read the full-length article here: https://lnkd.in/gEgbMGmy Submissions are now open for the year 2024! Manuscripts can be directly submitted online via Clinicalgenetics@journalmapsci.org or through this link: https://lnkd.in/dvjH8PMv Don't miss out on the opportunity to contribute to the advancement of genetic research! #clinicalgenetics #heredityjournal #callforsubmissions #geneticresearch #geneticists #scientificdiscoveries #genomics #submitnow #submissionsopen #openaccess
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Establishing the association between a genetic variant and disease is critical for understanding disease etiology and clinical impact. However, our ability to assess pathogenicity under diverse circumstances is limited. A comment in npj Genomic Medicine explores the impact of genetic and environmental factors on variant penetrance and outcomes. https://lnkd.in/eSn42t2F #Genetics #Healthcare #Research
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Bioinformatician | Freelancer | NGS Data Analysis | Genomics | Computer aided Drug Discovery
"Unveiling the complexities and strategies in mosaic variant detection, a recent comprehensive study presents a robust benchmarking of 11 state-of-the-art detection approaches. This insightful research not only identifies best practices but also discusses the condition-dependent strengths, weaknesses, and potential improvements in detecting these intricate variants. An essential read for genomic researchers and bioinformaticians dedicated to enhancing the accuracy of variant detection and understanding genetic mosaicism." #Genomics #Bioinformatics #VariantDetection #Mosaicism
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ALSP is often inherited, but there are noteworthy occurrences of de novo mutations presenting without known familial precedent. For healthcare professionals, a comprehensive grasp of a patient's genetic history is indispensable. It informs the likelihood of conditions like ALSP and is integral to anticipatory healthcare strategies. Engagement in genetic testing is not just an individual health measure; it is an essential contribution to our collective understanding and management of ALSP, providing crucial data for ongoing research and clinical practice. 🧬 - #RareDisease #Genetics #BrainHealth
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