Examining the neurodevelopmental and motor phenotypes of Bohring-Opitz syndrome (ASXL1) and Bainbridge-Ropers syndrome (ASXL3) by Maya C. Ayoub, Jeffrey T. Anderson, Bianca E. Russell, Rujuta B. Wilson

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Complex genomic rearrangements of the Y chromosome in a premature infant by Stephanie A. Balow, Alyxis G. Coyan, Nicki Smith, Bianca E. Russell, Danielle Monteil, Robert J. Hopkin, Teresa A. Smolarek

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ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3 by Isabella Lin, Zain Awamleh, Mili Sinvhal, Andrew Wan, Leroy Bondhus, Angela Wei, Bianca E. Russell, Rosanna Weksberg, Valerie A. Arboleda

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Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation by Isabella Lin, Angela Wei, Zain Awamleh, Meghna Singh, Aileen Ning, Analeyla Herrera, REACH Biobank and Registry, Bianca E. Russell, Rosanna Weksberg, Valerie A. Arboleda

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Homozygous missense variant in BMPR1A resulting in BMPR signaling disruption and syndromic features by Bianca E. Russell, Diana Rigueur, Kathryn N. Weaver, Kristen Sund, Janet S. Basil, Robert B. Hufnagel, Cynthia A. Prows, Alan Oestreich, Lihadh Al‐Gazali, Robert J Hopkin, Howard M. Saal, Karen Lyons, Andrew Dauber

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