Alice Qian
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    • Origin, Evolution, and Functional Impact of Short Insertion- Deletion Variants in Human Genomes: A Review
    • Locating Risk: Task Designers and the Challenge of Risk Disclosure in Crowdsourced RAI Content Work
    • Worker Discretion Advised: Co-designing Risk Disclosure in Crowdsourced Responsible AI (RAI) Content Work
    • An update on the Genetics, Cellular and Evolutionary Implications of X Chromosome Demasculinization
    • AURA: Amplifying Understanding, Resilience, and Awareness for Responsible AI Content Work
    • Family Screening in Relatives at Risk for Plakophilin-2–Associated Arrhythmogenic Right Ventricular Cardiomyopathy
    • Clinical Features and Outcomes of Pediatric MYH7‐Related Dilated Cardiomyopathy
    • Combined detrimental effect of male sex and GBA1 variants on cognitive decline in Parkinson's Disease
    • Genetic Liability to Higher Muscle Strength Associates with a Lower Risk of Cardiovascular Disease Mortality in Men Irrespective of Physical Activity in Adulthood: A Longitudinal Cohort Study
    • The Human Factor in AI Red Teaming: Perspectives from Social and Collaborative Computing
    • # Pragmatic or# Clinical: Analyzing TikTok Mental Health Videos
    • Cleaning Up the Streets: Understanding Motivations, Mental Models, and Concerns of Users Flagging Social Media Posts
    • Evinacumab for Pediatric Patients With Homozygous Familial Hypercholesterolemia
    • Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes
    • Personalizing content moderation on social media: User perspectives on moderation choices, interface design, and labor
    • Rare variant genetics and dilated cardiomyopathy severity: The DCM Precision Medicine Study
    • Hematological profile of Beta Thalassemia Trait
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    • Genetic Contributions to Early and Late Onset Ischemic Stroke
    • MicroRNA in the pathogenesis of glaucoma
    • Chronic Kidney Disease -A Forgotten Comorbidity in COPD
    • Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association.
    • The Clinical Outcome Study for dysferlinopathy
    • Incidence and risk factors of ventricular fibrillation before primary angioplasty in patients with first ST-elevation myocardial infarction a nationwide study in Denmark
    • Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy
    • A Gain-of-Function Mutation of the SCN5A Gene Causes Exercise-induced Polymorphic Ventricular Arrhythmias
    • Is BRAF V600E mutation a marker for central nodal metastasis in small papillary thyroid 2 carcinoma? 3
    • Society(cid:19)USA Panel Recommendations of the International AIDS Antiretroviral Treatment of Adult HIV Infection: 2010
    • Rectal cancer clinical practice guidelines in oncology.
    • Sural nerve T-cell receptor V b gene utilization in chronic inflammatory demyelinating polyneuropathy and vasculitic neuropathy
    • CLINICAL AND POPULATION SCIENCES Ticagrelor Added to Aspirin in Acute Nonsevere Ischemic Stroke or Transient Ischemic Attack of Atherosclerotic Origin
    • cres-Rituximab versus azathioprine for ANCA-associated vasculitis maintenance therapy: impact on global disability and health-related quality of life
    • Does Prehabilitation Improve Perioperative Outcomes When Compared to a Matched Cohort?
    • Early-Life Exposures, Neurodevelopment, and Health Outcomes: Protocol for a Birth Cohort Study
    • Impact of Initiating Biologics in Patients With Severe Asthma on Long-Term Oral Corticosteroids or Frequent Rescue Steroids (GLITTER): Data From the International Severe Asthma Registry
    • Influence of Cochlear Microanatomy on Hearing Preservation in Cochlear Implant Recipients
    • Optic Nerve Hypoplasia With Isolated Tortuosity of the Retinal Veins A Marker of Endocrinopathy
    • Preface for a Special Issue of AUDT with AI in Medical Ultrasound
    • REiNS: Genotype-Phenotype Correlations in Neurofibromatosis REiNS: Genotype-Phenotype Correlations in Neurofibromatosis and Their Potential Clinical use and Their Potential Clinical use
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REiNS: Genotype-Phenotype Correlations in Neurofibromatosis REiNS: Genotype-Phenotype Correlations in Neurofibromatosis and Their Potential Clinical use and Their Potential Clinical use

Jan 1, 0000·
MD Chetan Bettegowda
,
Prachi Upadhyaya
,
P. Evans
,
MD AeRang Kim
,
Priya Md
,
Michael Hanemann
,
MD D Gareth Evans
,
Genomic Medicine
· 0 min read
Cite
Type
Journal article
Last updated on Jan 1, 0000
← Preface for a Special Issue of AUDT with AI in Medical Ultrasound Jan 1, 0000

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