Brain apolipoprotein E levels in mice challenged by a Western diet increase in an allele-dependent manner von Liemisa, Braison, Newbury, Samantha F, Novy, Mariah J, Pasato, Jonathan A, Morales-Corraliza, Jose, Peng, Katherine Y, Mathews, Paul M

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Expression and proteolytic processing of the amyloid precursor protein is unaffected by the expression of the three human apolipoprotein E alleles in the brains of mice von Novy, Mariah J., Newbury, Samantha F., Liemisa, Braison, Morales-Corraliza, Jose, Alldred, Melissa J., Ginsberg, Stephen D., Mathews, Paul M.

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A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures von Martinelli, Angela, Rice, Mabel L, Talcott, Joel B, Diaz, Rebeca, Smith, Shelley, Raza, Muhammad Hashim, Snowling, Margaret J, Hulme, Charles, Stein, John, Hayiou-Thomas, Marianna E, Hawi, Ziarih, Kent, Lindsey, Pitt, Samantha J, Newbury, Dianne F, Paracchini, Silvia

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Expanding the phenotype of ASXL3‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3 von Schirwani, Schaida, Albaba, Shadi, Carere, Deanna Alexis, Guillen Sacoto, Maria J., Milan Zamora, Francisca, Si, Yue, Rabin, Rachel, Pappas, John, Renaud, Deborah L., Hauser, Natalie, Reid, Evan, Blanchet, Patricia, Foulds, Nichola, Dixit, Abhijit, Fisher, Richard, Armstrong, Ruth, Isidor, Bertrand, Cogne, Benjamin, Schrier Vergano, Samantha, Demirdas, Serwet, Dykzeul, Natalie, Cohen, Julie S., Grand, Katheryn, Morel, Dayna, Slavotinek, Anne, Albassam, Hessa F., Naik, Swati, Dean, John, Ragge, Nicola, Cinzia, Costa, Tedesco, Maria Giovanna, Harrison, Rachel E., Bouman, Arjan, Palen, Emily, Challman, Thomas D., Willemsen, Marjolein H., Vogt, Julie, Cunniff, Christopher, Bergstrom, Katherine, Walia, Jagdeep S., Bruel, Ange‐Line, Kini, Usha, Alkuraya, Fowzan S., Slegesky, Valerie, Meeks, Naomi, Girotto, Paula, Johnson, Diana, Newbury‐Ecob, Ruth, Ockeloen, Charlotte W., Prontera, Paolo, Lynch, Sally Ann, Li, Dong, Graham, John M., Balasubramanian, Meena

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Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder von Newbury, Dianne F, Mari, Francesca, Sadighi Akha, Elham, Macdermot, Kay D, Canitano, Roberto, Monaco, Anthony P, Taylor, Jenny C, Renieri, Alessandra, Fisher, Simon E, Knight, Samantha J L

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A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures von Martinelli, Angela, Rice, Mabel L, Talcott, Joel B, Diaz, Rebeca, Smith, Shelley, Raza, Muhammad Hashim, Snowling, Margaret J, Hulme, Charles, Stein, John, Hayiou-Thomas, Marianna E, Hawi, Ziarih, Kent, Lindsey, Pitt, Samantha J, Newbury, Dianne F, Paracchini, Silvia

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