Ngā hua rapu - Rehm, Heidi L.

Disease-targeted sequencing: a cornerstone in the clinic mā Rehm, Heidi L.

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Rapid access to genetic discoveries underlying human disease mā Rehm, Heidi L.

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Evolving health care through personal genomics mā Rehm, Heidi L.

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A new era in the interpretation of human genomic variation mā Rehm, Heidi L.

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Time to make rare disease diagnosis accessible to all mā Rehm, Heidi L.

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Building the foundation for genomics in precision medicine mā Aronson, Samuel J., Rehm, Heidi L.

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Association of Racial/Ethnic Categories With the Ability of Genetic Tests to Detect a Cause of Cardiomyopathy mā Landry, Latrice G., Rehm, Heidi L.

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The Ancestral Pace of Variant Reclassification mā Plon, Sharon E, Rehm, Heidi L

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Is ‘likely pathogenic’ really 90% likely? Reclassification data in ClinVar mā Harrison, Steven M., Rehm, Heidi L.

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Keeping up with the genomes: scaling genomic variant interpretation mā Rehm, Heidi L., Fowler, Douglas M.

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Genetic variation in the Middle East—an opportunity to advance the human genetics field mā Abou Tayoun, Ahmad N., Rehm, Heidi L.

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The Changing Landscape of Molecular Diagnostic Testing: Implications for Academic Medical Centers mā Rehm, Heidi L., Hynes, Elizabeth, Funke, Birgit H.

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Targeted Sequencing Using Affymetrix CustomSeq Arrays mā Teekakirikul, Polakit, Cox, Stephanie, Funke, Birgit, Rehm, Heidi L.

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ClinVar Is a Critical Resource to Advance Variant Interpretation mā Rehm, Heidi L., Harrison, Steven M., Martin, Christa L.

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Overview of specifications to the ACMG/AMP variant interpretation guidelines mā Harrison, Steven M., Biesecker, Leslie G., Rehm, Heidi L.

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Strategies to Uplift Novel Mendelian Gene Discovery for Improved Clinical Outcomes mā Seaby, Eleanor G., Rehm, Heidi L., O’Donnell-Luria, Anne

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Seven years since the launch of the Matchmaker Exchange: the evolution of genomic matchmaking mā Boycott, Kym M., Azzariti, Danielle R., Hamosh, Ada, Rehm, Heidi L.

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Reclassification of the BRAF p.Ile208Val variant by case-level data sharing mā Grant, Andrew R., Hemphill, Sarah E., Vincent, Lisa M., Rehm, Heidi L.

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TMPRSS3 Gene Variants With Implications for Auditory Treatment and Counseling mā Moon, In Seok, Grant, Andrew R., Sagi, Varun, Rehm, Heidi L., Stankovic, Konstantina M.

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TEMPORAL BONE ABNORMALITIES IN CHILDREN WITH GJB2 MUTATIONS mā Kenna, Margaret A., Rehm, Heidi L., Frangulov, Anna, Feldman, Henry A., Robson, Caroline D.

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