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Cell-Free RNA Profiles in Maternal Blood May Predict Preeclampsia

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cfRNA signatures from maternal blood draw may identify women at risk for developing preeclampsia prior to clinical presentation

In Utero Hormone Levels May Affect Migraine Risk in Adulthood

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Sex differences in migraine prevalence may not be entirely accounted for by genetic factors

Genetic Diagnosis May Aid Management of Pediatric Epilepsy

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Establishing a genetic diagnosis for patients with unexplained infantile or childhood-onset epilepsy can help individualize treatment

Genetic Diagnosis of Rare Diseases Up With Genome Sequencing

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Diagnostic yields were higher for disorders likely to have a monogenic cause versus those with a complex cause

AAV Gene Transfer Feasible for the Treatment of Hemophilia A

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In a phase 1-2 trial, 16 of 18 men had sustained expression of factor VIII after gene transfer with adeno-associated viral vector (SPK-8011)

Conventional IVF Noninferior to PGT-A for Live-Birth Rate

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Cumulative live-birth rate with use of conventional IVF noninferior to that for embryo selection with preimplantation genetic testing for aneuploidy

Protocol Examined for Returning Results in Genomic Research

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Among participants in a biobank found to be carrying pathogenic or likely pathogenic variants, 76.3 percent unaware of these research results

Black Women With Breast Cancer Face Barriers to Genetic Counseling

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In nationwide survey, a majority of U.S. breast oncologists report that Black women encounter more barriers to genetic counseling, testing

Cascade Testing Proposed for Siblings of Newborns With Cancer Genes

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Surveillance for siblings of newborns with pathogenic variants in cancer genes could reduce rare child cancer deaths

Gene Variant Tied to Risk for Interstitial Lung Disease in RA

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For patients with rheumatoid arthritis, lifetime risks for ILD were 16.8 percent for MUC5B carriers, 6.1 percent for noncarriers