Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG) von Gregg, Anthony R., Aarabi, Mahmoud, Klugman, Susan, Leach, Natalia T., Bashford, Michael T., Goldwaser, Tamar, Chen, Emily, Sparks, Teresa N., Reddi, Honey V., Rajkovic, Aleksandar, Dungan, Jeffrey S.

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Analysis of Circulating MicroRNA: Preanalytical and Analytical Challenges von MCDONALD, Jennifer S, MILOSEVIC, Dragana, REDDI, Honey V, GREBE, Stefan K, ALGECIRAS-SCHIMNICH, Alicia

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The clinical application of polygenic risk scores: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG) von Abu-El-Haija, Aya, Reddi, Honey V., Wand, Hannah, Rose, Nancy C., Mori, Mari, Qian, Emily, Murray, Michael F.

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Editorial: Emerging talents in genomic assay technology von Reddi, Honey V., Pavlov, Youri I.

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The 2019 medical genetics workforce: A focus on laboratory geneticists von Maiese, Deborah R., Lyon, Megan, Reddi, Honey V., Blitzer, Miriam G., Bodurtha, Joann N., Muenke, Maximilian

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KIF11 Variants Associated With Novel Renal System Involvement-Two Cases That Expand the Phenotypic Spectrum of Microcephaly With or Without Chorioretinopathy, Lymphedema, or Impair... von Gonzalez, Tessa, Tyler, Rebecca C, Schilter, Kala F, McCarrier, Julie, Muriello, Michael, Basel, Donald, Reddi, Honey V

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CUP-AI-Dx: A tool for inferring cancer tissue of origin and molecular subtype using RNA gene-expression data and artificial intelligence von Zhao, Yue, Pan, Ziwei, Namburi, Sandeep, Pattison, Andrew, Posner, Atara, Balachander, Shiva, Paisie, Carolyn A., Reddi, Honey V, Rueter, Jens, Gill, Anthony J, Fox, Stephen, Raghav, Kanwal P.S., Flynn, William F, Tothill, Richard W., Li, Sheng, Karuturi, R. Krishna Murthy, George, Joshy

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Retrospective genotype-phenotype analysis in a 305 patient cohort referred for testing of a targeted epilepsy panel von Hesse, Andrew N., Bevilacqua, Jennifer, Shankar, Kritika, Reddi, Honey V.

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Incidental detection of acquired variants in germline genetic and genomic testing: a points to consider statement of the American College of Medical Genetics and Genomics (ACMG) von Chao, Elizabeth C., Astbury, Caroline, Deignan, Joshua L., Pronold, Melissa, Reddi, Honey V., Weitzel, Jeffrey N.

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Reduction in ACE2 expression in peripheral blood mononuclear cells during COVID-19 - implications for post COVID-19 conditions von Ahmed, Gulrayz, Abdelgadir, Yasir, Abdelghani, Amro, Simpson, Pippa, Barbeau, Jody, Basel, Donald, Barrios, Christy S, Smith, Brandon A, Schilter, Kala F, Udani, Rupa, Reddi, Honey V, Willoughby, Rodney E

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Novel CTNND2‐TERT fusion in a spindle cell liposarcoma von Occidental, Michael, Shen, Guomiao, Feng, Xiaojun, Zhu, Kelsey, Kelly, Kevin, Nie, Qian, Reddi, Honey V., Lakiotaki, Eleftheria, Viniou, Nora Athina, Korkolopoulou, Penelope, Linos, Konstantinos, Jour, George

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Implementation of a Customized Tertiary Analysis Platform for the Reporting of Somatic Variants von Schilter, Kala F, Dubay, Sarah, Stachowiak, Matt, Kaplan, Alysia, Stauffenger, Abby, Reddi, Honey V

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Analytical validation and implementation of a pan cancer next-generation sequencing panel, CANSeqTMKids for molecular profiling of childhood malignancies von Schilter, Kala F., Smith, Brandon A., Nie, Qian, Stoll, Kathryn, Felix, Juan C., Jarzembowski, Jason A., Reddi, Honey V.

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ASPYRE-Lung: validation of a simple, fast, robust and novel method for multi-variant genomic analysis of actionable NSCLC variants in FFPE tissue von Evans, Ryan T, Gillon-Zhang, Elizabeth, Brown, Julia N, Knudsen, Katherine E, King, Candace, Green, Amanda S, Silva, Ana-Luisa, Mordaka, Justyna M, Palmer, Rebecca N, Tomassini, Alessandro, Collazos, Alejandra, Xyrafaki, Christina, Turner, Iyelola, Ho, Chau Ha, Nugent, Dilyara, Jose, Jinsy, Andreazza, Simonetta, Potts, Nicola D, von Bargen, Kristine, Gray, Eleanor R, Stolarek-Januszkiewicz, Magdalena, Cooke, Aishling, Reddi, Honey V, Balmforth, Barnaby W, Osborne, Robert J

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RNA Sequencing Identifies Multiple Fusion Transcripts, Differentially Expressed Genes, and Reduced Expression of Immune Function Genes in BRAF (V600E) Mutant vs BRAF Wild-Type Papi... von Smallridge, Robert C, Chindris, Ana-Maria, Asmann, Yan W, Casler, John D, Serie, Daniel J, Reddi, Honey V, Cradic, Kendall W, Rivera, Michael, Grebe, Stefan K, Necela, Brian M, Eberhardt, Norman L, Carr, Jennifer M, McIver, Bryan, Copland, John A, Thompson, E. Aubrey

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A novel variant of TNNC1 associated with severe dilated cardiomyopathy causing infant mortality and stillbirth: a case of germline mosaicism von Udani, Rupa, Schilter, Kala F., Tyler, Rebecca C., Smith, Brandon A., Wendt-Andrae, Jaime L., Kappes, Ulrike P., Scharer, Gunter, Lehman, Anna, Steinraths, Michelle, Reddi, Honey V.

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Long-term retinal imaging of a case of suspected congenital rubella infection von Langlo, Christopher S., Trotter, Alana, Reddi, Honey V., Schilter, Kala F., Tyler, Rebecca C., Udani, Rupa, Neitz, Maureen, Carroll, Joseph, Connor, Thomas B.

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Laboratory testing for preconception/prenatal carrier screening: A technical standard of the American College of Medical Genetics and Genomics (ACMG) von Guha, Saurav, Reddi, Honey V., Aarabi, Mahmoud, DiStefano, Marina, Wakeling, Erin, Dungan, Jeffrey S., Gregg, Anthony R.

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Mutations in TP53 , PIK3CA , PTEN and other genes in EGFR mutated lung cancers: correlation with clinical outcomes von VanderLaan, Paul A, Rangachari, Deepa, Mockus, Susan M, Spotlow, Vanessa, Reddi, Honey V, Malcolm, Joan, Huberman, Mark S, Joseph, Loren J, Kobayashi, Susumu S, Costa, Daniel B

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Laboratory testing for fragile X, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG) von Spector, Elaine, Behlmann, Andrea, Kronquist, Kathryn, Rose, Nancy C., Lyon, Elaine, Reddi, Honey V.

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