Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation von Finucane, Brenda M, Ledbetter, David H, Vorstman, Jacob AS

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A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk von Berry, Alexander S. F., Finucane, Brenda M., Myers, Scott M., Walsh, Lauren K., Seibert, John M., Martin, Christa Lese, Ledbetter, David H., Oetjens, Matthew T.

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Long overdue: including adults with brain disorders in precision health initiatives von Finucane, Brenda M, Myers, Scott M, Martin, Christa L, Ledbetter, David H

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Response to van Riel et al von Savatt, Juliann M, Oetjens, Matthew T, Myers, Scott M, Finucane, Brenda M

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Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System Population von Shimelis, Hermela, Oetjens, Matthew T., Walsh, Lauren K., Wain, Karen E., Znidarsic, Masa, Myers, Scott M., Finucane, Brenda M., Ledbetter, David H., Martin, Christa Lese

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Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome von Taylor, Cora M., Finucane, Brenda M., Moreno-De-Luca, Andres, Walsh, Lauren K., Martin, Christa Lese, Ledbetter, David H.

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Association of Supernumerary Sex Chromosome Aneuploidies With Venous Thromboembolism von Berry, Alexander S. F, Finucane, Brenda M, Myers, Scott M, Abril, Angela, Kirchner, H. Lester, Ledbetter, David H, Martin, Christa Lese, Oetjens, Matthew T

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Frequency of truncating FLCN variants and Birt-Hogg-Dubé-associated phenotypes in a health care system population von Savatt, Juliann M, Shimelis, Hermela, Moreno-De-Luca, Andres, Strande, Natasha T, Oetjens, Matthew T, Ledbetter, David H, Martin, Christa Lese, Myers, Scott M, Finucane, Brenda M

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A survey of seizures and current treatments in 15q duplication syndrome von Conant, Kerry D., Finucane, Brenda, Cleary, Nicole, Martin, Ashley, Muss, Candace, Delany, Mary, Murphy, Erin K., Rabe, Olivia, Luchsinger, Kadi, Spence, Sarah J., Schanen, Carolyn, Devinsky, Orrin, Cook, Edwin H., LaSalle, Janine, Reiter, Lawrence T., Thibert, Ronald L.

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Fragile X-associated tremor/ataxia syndrome: Clinical features, genetics, and testing guidelines von Berry-Kravis, Elizabeth, Abrams, Liane, Coffey, Sarah M., Hall, Deborah A., Greco, Claudia, Gane, Louise W., Grigsby, Jim, Bourgeois, James A., Finucane, Brenda, Jacquemont, Sebastien, Brunberg, James A., Zhang, Lin, Lin, Janet, Tassone, Flora, Hagerman, Paul J., Hagerman, Randi J., Leehey, Maureen A.

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The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variants von Wain, Karen E., Palen, Emily, Savatt, Juliann M., Shuman, Devin, Finucane, Brenda, Seeley, Andrea, Challman, Thomas D., Myers, Scott M., Martin, Christa Lese

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AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission von Yrigollen, Carolyn M, Martorell, Loreto, Durbin-Johnson, Blythe, Naudo, Montserrat, Genoves, Jordi, Murgia, Alessandra, Polli, Roberta, Zhou, Lili, Barbouth, Deborah, Rupchock, Abigail, Finucane, Brenda, Latham, Gary J, Hadd, Andrew, Berry-Kravis, Elizabeth, Tassone, Flora

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Auditory Phenotype of Smith-Magenis Syndrome von Brendal, Megan A, King, Kelly A, Zalewski, Christopher K, Finucane, Brenda M, Introne, Wendy, Brewer, Carmen C, Smith, Ann C. M

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Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia von Feuk, Lars, Kalervo, Aino, Lipsanen-Nyman, Marita, Skaug, Jennifer, Nakabayashi, Kazuhiko, Finucane, Brenda, Hartung, Danielle, Innes, Micheil, Kerem, Batsheva, Nowaczyk, Małgorzata J., Rivlin, Joseph, Roberts, Wendy, Senman, Lili, Summers, Anne, Szatmari, Peter, Wong, Virginia, Vincent, John B., Zeesman, Susan, Osborne, Lucy R., Cardy, Janis Oram, Kere, Juha, Scherer, Stephen W., Hannula-Jouppi, Katariina

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Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: Cast a wide FISHing net von Mcdonald-Mcginn, Donna M, Tonnesen, Melissa K, Laufer-Cahana, Ayala, Finucane, Brenda, Driscoll, Deborah A, Emanuel, Beverly S, Zackai, Elaine H

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2012 National Society of Genetic Counselors Presidential Address: Maintaining Our Professional Identity in an Ever-Expanding Genetics Universe von Finucane, Brenda

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Introduction to the Special Issue on Developmental Disabilities von Finucane, Brenda

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BEYOND MEDICAL ACTIONABILITY: PERSONAL UTILITY OF KNOWING A GENETIC ETIOLOGY von Finucane, Brenda, Martin, Christa, Wain, Karen, Palen, Emily, Ledbetter, David

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DELETERIOUS “SHIFT” IN FUNCTIONAL PERFORMANCE EXPLAINS CLINICAL VARIABILITY IN RARE GENETIC NEURODEVELOPMENTAL PSYCHIATRIC DISORDERS von Ledbetter, David, Finucane, Brenda, Taylor, Cora, de Luca, Andres Morena, Myers, Scott, Martin, Christa

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Letter to the editor von Finucane, Brenda, Myers, Scott M, Challman, Thomas D, Martin, Christa Lese, Ledbetter, David H

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