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Mashup Score: 28Improved Access to Genetics Care is Needed to Address Health Inequities in ATTRv Amyloidosis | Circulation - 3 month(s) ago
View all available purchase options and get full access to this article. Kittleson MM, Ruberg FL, Ambardekar AV, Brannagan TH, Cheng RK, Clark JO, Dember LM, Frantz JG, Hershberger RE, et al; Writing Committee. 2023 ACC Expert Consensus Decision Pathway on Comprehensive Multidisciplinary Care for the Patient With Cardiac Amyloidosis: A Report of the American College of Cardiology Solution Set Oversight Committee. J Am Coll Cardiol. 2023;81:1076–1126. doi: 10.1016/j.jacc.2022.11.022 Longoni M, Bhasin K,
Source: www.ahajournals.orgCategories: General Medicine News, CardiologistsTweet
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Mashup Score: 25Genomic Classification of Tumors - 4 month(s) ago
While it is current practice today to molecularly characterize tumors based on their genetic fingerprints, CCR investigators were among the first to classify tumors based on genetics. As a result, treatments are now being tailored to an individual’s specific cancer subtype, and new therapies are being developed to target the vulnerabilities of different types of cancer cells. Major CCR successes in this area have improved the classification of kidney cancers and lymphomas and have laid the foundation for what is now called precision medicine.
Source: ccr.cancer.govCategories: General Medicine News, Oncologists1Tweet
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Mashup Score: 4
Analysis of high-quality, haplotype-resolved primate genomes provides a more complete understanding of lineage-specific, recurrent mutations and structurally divergent regions associated with primate adaptive evolution and human diseases.
Source: www.cell.comCategories: General Medicine News, General Journals & SocietTweet
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Mashup Score: 5
Analysis of high-quality, haplotype-resolved primate genomes provides a more complete understanding of lineage-specific, recurrent mutations and structurally divergent regions associated with primate adaptive evolution and human diseases.
Source: www.cell.comCategories: General Medicine News, General Journals & SocietTweet
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Mashup Score: 5
From a genetic perspective, modern humans are best defined as a combination of genetic features of archaic humans where each individual carries most but not necessarily all genetic features. This review examines the genetic features of modern humans, Neandertals, and Denisovans and how gene flow among them affected their physiology.
Source: www.cell.comCategories: General Medicine News, General Journals & SocietTweet
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Mashup Score: 0Building Efficiency and Scaling With a Remote Genetic Counseling Program - 12 month(s) ago
Smita K. Rao, MBBS, MS, et al gave an overview of implementing genetic counseling into oncology practices through telemedicine.
Source: www.cancernetwork.comCategories: General Medicine News, Onc News and JournalsTweet
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Mashup Score: 0
Original Article from The New England Journal of Medicine — Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child
Source: www.nejm.orgCategories: General Medicine News, Cardiologists1Tweet
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Mashup Score: 0
Cheryl VerStrate, DNP, AGPCNP-BC, OCN, discusses why nurses should be prepared to discuss direct-to-consumer genomic testing with their patients.
Source: www.oncnursingnews.comCategories: Hem/Onc News and Journals, Latest HeadlinesTweet
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Mashup Score: 0A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities - 1 year(s) ago
Rationale: In addition to rare genetic variants and the MUC5B locus, common genetic variants contribute to idiopathic pulmonary fibrosis (IPF) risk. The predictive power of common variants outside …
Source: www.atsjournals.orgCategories: Latest Headlines, RheumatologyTweet-
#BWHRheumatology studied role of common genetic variants in identifying idiopathic pulmonary fibrosis (IPF) and interstitial lung abnormalities (ILA) risk. Polygenic risk scores (PRS) w/o MUC5B region associated w/ IPF, ILA, and ILA progression. https://t.co/3DUSXZnU4I #genetics https://t.co/Aaloi2FmBx
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Mashup Score: 1
In a study reported in JAMA Oncology, Darst et al identified germline genetic variants that were associated with increased risk of aggressive vs nonaggressive prostate cancer. As stated by the investigators, “Germline gene panel testing is recommended for men with advanced prostate cancer or a family history of cancer. While evidence is limited for some genes currently included in panel testing, gene panels are also likely to be incomplete and missing genes that influence p rostate cancer risk and
Source: ascopost.comCategories: Hem/Onc News and Journals, Latest HeadlinesTweet
🧬New editorial w/ @MathewMaurer @LathanLiou: current inadequacies in access to #genetics care in the US hinder ATTRv detection/treatment, disproportionately so in minority communities; solutions proposed! @GeneticCouns @MountSinaiHeart @GeneticsSociety https://t.co/ZKEzEBQJCg