PCDH19‐related epilepsy is associated with a broad neurodevelopmental spectrum by Smith, Lacey, Singhal, Nilika, El Achkar, Christelle M., Truglio, Gessica, Rosen Sheidley, Beth, Sullivan, Joseph, Poduri, Annapurna

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Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort by Rochtus, Anne, Olson, Heather E., Smith, Lacey, Keith, Louisa G., El Achkar, Christelle, Taylor, Alan, Mahida, Sonal, Park, Meredith, Kelly, McKenna, Shain, Catherine, Rockowitz, Shira, Rosen Sheidley, Beth, Poduri, Annapurna

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Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors by Smith, Lacey, Malinowski, Jennifer, Ceulemans, Sophia, Peck, Katlin, Walton, Nephi, Sheidley, Beth Rosen, Lippa, Natalie

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Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy by Koh, Hyun Yong, Smith, Lacey, Wiltrout, Kimberly N, Podury, Archana, Chourasia, Nitish, D'Gama, Alissa M, Park, Meredith, Knight, Devon, Sexton, Emma L, Koh, Julia J, Oby, Brandon, Pinsky, Rebecca, Shao, Diane D, French, Courtney E, Shao, Wanqing, Rockowitz, Shira, Sliz, Piotr, Zhang, Bo, Mahida, Sonal, Moufawad El Achkar, Christelle, Yuskaitis, Christopher J, Olson, Heather E, Sheidley, Beth Rosen, Poduri, Annapurna H

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Genetics of Epilepsy in the Era of Precision Medicine: Implications for Testing, Treatment, and Genetic Counseling by Sheidley, Beth Rosen, Smith, Lacey A., Helbig, Katherine L.

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Compound heterozygosity with PRRT2 : Pushing the phenotypic envelope in genetic epilepsies by El Achkar, Christelle Moufawad, Rosen Sheidley, Beth, O'Rourke, Declan, Takeoka, Masanori, Poduri, Annapurna

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Psychiatric Disorders in Clinical Genetics II: Individualizing Recurrence Risks by Austin, Jehannine C., Palmer, Christina G. S., Rosen-Sheidley, Beth, Veach, Patricia McCarthy, Gettig, Elizabeth, Peay, Holly L.

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Psychiatric Disorders in Clinical Genetics I: Addressing Family Histories of Psychiatric Illness by Peay, Holly L., Veach, Patricia McCarthy, Palmer, Christina G. S., Rosen-Sheidley, Beth, Gettig, Elizabeth, Austin, Jehannine C.

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PCDH 19 ‐related epilepsy is associated with a broad neurodevelopmental spectrum by Smith, Lacey, Singhal, Nilika, El Achkar, Christelle M., Truglio, Gessica, Rosen Sheidley, Beth, Sullivan, Joseph, Poduri, Annapurna

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Genetics and genotype–phenotype correlations in early onset epileptic encephalopathy with burst suppression by Olson, Heather E., Kelly, McKenna, LaCoursiere, Christopher M., Pinsky, Rebecca, Tambunan, Dimira, Shain, Catherine, Ramgopal, Sriram, Takeoka, Masanori, Libenson, Mark H., Julich, Kristina, Loddenkemper, Tobias, Marsh, Eric D., Segal, Devorah, Koh, Susan, Salman, Michael S., Paciorkowski, Alex R., Yang, Edward, Bergin, Ann M., Sheidley, Beth Rosen, Poduri, Annapurna

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Parental Interest in a Genetic Risk Assessment Test for Autism Spectrum Disorders by Narcisa, Vivien, Discenza, Marie, Vaccari, Erica, Rosen-Sheidley, Beth, Hardan, Antonio Y., Couchon, Elizabeth

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Autism-related language, personality, and cognition in people with absolute pitch: results of a preliminary study by Brown, Walter A, Cammuso, Karen, Sachs, Henry, Winklosky, Brian, Mullane, Julie, Bernier, Raphael, Svenson, Sarah, Arin, Deborah, Rosen-Sheidley, Beth, Folstein, Susan E

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Communicative Competence in Parents of Children with Autism and Parents of Children with Specific Language Impairment by Ruser, Tilla F, Arin, Deborah, Dowd, Michael, Putnam, Sara, Winklosky, Brian, Rosen-Sheidley, Beth, Piven, Joseph, Tomblin, Bruce, Tager-Flusberg, Helen, Folstein, Susan

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A Model Program for Translational Medicine in Epilepsy Genetics by Smith, Lacey A., Ullmann, Jeremy F. P., Olson, Heather E., Achkar, Christelle M. El, Truglio, Gessica, Kelly, McKenna, Rosen-Sheidley, Beth, Poduri, Annapurna

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Mutations in NRXN1 and NRXN2 in a patient with early-onset epileptic encephalopathy and respiratory depression by Rochtus, Anne M, Trowbridge, Sara, Goldstein, Richard D, Sheidley, Beth Rosen, Prabhu, Sanjay P, Haynes, Robin, Kinney, Hannah C, Poduri, Annapurna H

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Autism-related language, personality, and cognition in people with absolute pitch: Results of a preliminary study. Commentary by BROWN, Walter A, CAMMUSO, Karen, RIMLAND, Bernard A, SACHS, Henry, WINKLOSKY, Brian, MULLANE, Julie, BERNIER, Raphael, SVENSON, Sarah, ARIN, Deborah, ROSEN-SHEIDLEY, Beth, FOLSTEIN, Susan E

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Compound heterozygosity with PRRT2: Pushing the phenotypic envelope in genetic epilepsies by El Achkar, Christelle Moufawad, Rosen Sheidley, Beth, O'Rourke, Declan, Takeoka, Masanori, Poduri, Annapurna

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Genetic Counseling for Autism Spectrum Disorders by Rosen-Sheidley, Beth, Wolpert, Chantelle, Folstein, Susan

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