Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Dis... by Ho, Karen S, Wassman, E Robert, Baxter, Adrianne L, Hensel, Charles H, Martin, Megan M, Prasad, Aparna, Twede, Hope, Vanzo, Rena J, Butler, Merlin G

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Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis by Prasad, Aparna, Sdano, Matthew A, Vanzo, Rena J, Mowery-Rushton, Patricia A, Serrano, Moises A, Hensel, Charles H, Wassman, E Robert

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MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways by Paciorkowski, Alex R., Traylor, Ryan N., Rosenfeld, Jill A., Hoover, Jacqueline M., Harris, Catharine J., Winter, Susan, Lacassie, Yves, Bialer, Martin, Lamb, Allen N., Schultz, Roger A., Berry-Kravis, Elizabeth, Porter, Brenda E., Falk, Marni, Venkat, Anu, Vanzo, Rena J., Cohen, Julie S., Fatemi, Ali, Dobyns, William B., Shaffer, Lisa G., Ballif, Blake C., Marsh, Eric D.

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Glutaric acidemia Type 1: Outcomes before and after expanded newborn screening by Viau, Krista, Ernst, Sharon L., Vanzo, Rena J., Botto, Lorenzo D., Pasquali, Marzia, Longo, Nicola

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Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing by Hensel, Charles H., Vanzo, Rena J., Martin, Megan M., Ling, Ling, Aliaga, Solange M., Bui, Minh, Francis, David I., Twede, Hope, Field, Michael H., Morison, Jonathon W., Amor, David J., Godler, David E.

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Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders by Vanzo, Rena J., Twede, Hope, Ho, Karen S., Prasad, Aparna, Martin, Megan M., South, Sarah T., Wassman, E. Robert

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The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism by Vanzo, Rena J, Prasad, Aparna, Staunch, Lauren, Hensel, Charles H, Serrano, Moises A, Wassman, E Robert, Kaplun, Alexander, Grandin, Temple, Boles, Richard G

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Mosaic deletion of 20pter due to rescue by somatic recombination by Martin, Megan M., Vanzo, Rena J., Sdano, Mallory R., Baxter, Adrianne L., South, Sarah T.

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SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot by Vanzo, Rena J., Martin, Megan M., Sdano, Mallory R., Teta, Kathie, Aggarwal, Vimla, South, Sarah T.

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A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome by Baxter, Adrianne L., Vivian, Jay L., Hagelstrom, R. Tanner, Hossain, Waheeda, Golden, Wendy L., Wassman, E. Robert, Vanzo, Rena J., Butler, Merlin G.

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Familial KANK1 deletion that does not follow expected imprinting pattern by Vanzo, Rena J, Martin, Megan M, Sdano, Mallory R, South, Sarah T

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Correspondence regarding SNX8 haploinsufficiency and its potential for cardiac anomalies including tetralogy of Fallot by Vanzo, Rena J., Martin, Megan M., Sdano, Mallory R., Teta, Kathie, South, Sarah T.

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Academia, advocacy, and industry: A collaborative method for clinical research advancement by Vanzo, Rena J., Lortz, Amanda, Calhoun, Amy R. U. L., Carey, John C.

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Clinical Utility of Chromosomal Microarray Analysis of DNA from Buccal Cells: Detection of Mosaicism in Three Patients by Sdano, Mallory R., Vanzo, Rena J., Martin, Megan M., Baldwin, Erin E., South, Sarah T., Rope, Alan F., Allen, William P., Kearney, Hutton

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Altered gene expression in mice selected for high maternal aggression by Gammie, S. C., Auger, A. P., Jessen, H. M., Vanzo, R. J., Awad, T. A., Stevenson, S. A.

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The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism by Vanzo, Rena J, Prasad, Aparna, Staunch, Lauren, Hensel, Charles H, Serrano, Moises A, Wassman, E Robert, Kaplun, Alexander, Grandin, Temple, Boles, Richard G

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GRIN2B encephalopathy: Novel findings on phenotype, variant clustering, functional consequences and treatment aspects by Platzer, Konrad, Yuan, Hongjie, Schütz, Hannah, Winschel, Alexander, Chen, Wenjuan, Hu, Chun, Kusumoto, Hirofumi, Heyne, Henrike O, Helbig, Katherine L, Tang, Sha, Willing, Marcia C, Tinkle, Brad T, Adams, Darius J, Depienne, Christel, Keren, Boris, Mignot, Cyril, Frengen, Eirik, Strømme, Petter, Biskup, Saskia, Docker, Dennis, Strom, Tim M, Mefford, Heather C, Myers, Candace T, Muir, Alison M, LaCroix, Amy, Sadleir, Lynette, Scheffer, Ingrid E, Brilstra, Eva, van Haelst, Mieke M, van der Smagt, Jasper J, Bok, Levinus A, Møller, Rikke S, Jensen, Uffe B, Millichap, John J, Berg, Anne T, Goldberg, Ethan M, De Bie, Isabelle, Fox, Stephanie, Major, Philippe, Jones, Julie R, Zackai, Elaine H, Abou Jamra, Rami, Rolfs, Arndt, Leventer, Richard J, Lawson, John A, Roscioli, Tony, Jansen, Floor E, Ranza, Emmanuelle, Korff, Christian M, Lehesjoki, Anna-Elina, Courage, Carolina, Linnankivi, Tarja, Smith, Douglas R, Stanley, Christine, Mintz, Mark, McKnight, Dianalee, Decker, Amy, Tan, Wen-Hann, Tarnopolsky, Mark A, Brady, Lauren I, Wolff, Markus, Dondit, Lutz, Pedro, Helio F, Parisotto, Sarah E, Jones, Kelly L, Patel, Anup D, Franz, David N, Vanzo, Rena, Marco, Elysa, Ranells, Judith D, Di Donato, Nataliya, Dobyns, William B, Laube, Bodo, Traynelis, Stephen F, Lemke, Johannes R

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Limitations of exome sequencing in detecting rare and undiagnosed diseases by Burdick, Kendall J., Cogan, Joy D., Rives, Lynette C., Robertson, Amy K., Koziura, Mary E., Brokamp, Elly, Duncan, Laura, Hannig, Vickie, Pfotenhauer, Jean, Vanzo, Rena, Paul, Michael S., Bican, Anna, Morgan, Thomas, Duis, Jessica, Newman, John H., Hamid, Rizwan, Phillips, John A.

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