A myelin-related transcriptomic profile is shared by Pitt–Hopkins syndrome models and human autism spectrum disorder by Phan, BaDoi N., Bohlen, Joseph F., Davis, Brittany A., Ye, Zengyou, Chen, Huei-Ying, Mayfield, Brent, Sripathy, Srinidhi Rao, Cerceo Page, Stephanie, Campbell, Morganne N., Smith, Hannah L., Gallop, Danisha, Kim, Hyojin, Thaxton, Courtney L., Simon, Jeremy M., Burke, Emily E., Shin, Joo Heon, Kennedy, Andrew J., Sweatt, J. David, Philpot, Benjamin D., Jaffe, Andrew E., Maher, Brady J.

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Organization and maintenance of molecular domains in myelinated axons by Buttermore, Elizabeth D., Thaxton, Courtney L., Bhat, Manzoor A.

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Interpretable Clinical Genomics with a Likelihood Ratio Paradigm by Robinson, Peter N., Ravanmehr, Vida, Jacobsen, Julius O.B., Danis, Daniel, Zhang, Xingmin Aaron, Carmody, Leigh C., Gargano, Michael A., Thaxton, Courtney L., Karlebach, Guy, Reese, Justin, Holtgrewe, Manuel, Köhler, Sebastian, McMurry, Julie A., Haendel, Melissa A., Smedley, Damian

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Decreased Axon Caliber Underlies Loss of Fiber Tract Integrity, Disproportional Reductions in White Matter Volume, and Microcephaly in Angelman Syndrome Model Mice by Judson, Matthew C, Burette, Alain C, Thaxton, Courtney L, Pribisko, Alaine L, Shen, Mark D, Rumple, Ashley M, Del Cid, Wilmer A, Paniagua, Beatriz, Styner, Martin, Weinberg, Richard J, Philpot, Benjamin D

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Generating Clinical-Grade Gene–Disease Validity Classifications Through the ClinGen Data Platforms by Wright, Matt W, Thaxton, Courtney L, Nelson, Tristan, DiStefano, Marina T, Savatt, Juliann M, Brush, Matthew H, Cheung, Gloria, Mandell, Mark E, Wulf, Bryan, Ward, TJ, Goehringer, Scott, O'Neill, Terry, Weller, Phil, Preston, Christine G, Keseler, Ingrid M, Goldstein, Jennifer L, Strande, Natasha T, McGlaughon, Jennifer, Azzariti, Danielle R, Cordova, Ineke, Dziadzio, Hannah, Babb, Lawrence, Riehle, Kevin, Milosavljevic, Aleksandar, Martin, Christa Lese, Rehm, Heidi L, Plon, Sharon E, Berg, Jonathan S, Riggs, Erin R, Klein, Teri E

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A myelin-related transcriptomic profile is shared between Pitt Hopkins syndrome models and human autism spectrum disorder by Phan, BaDoi N., Bohlen, Joseph F., Davis, Brittany A., Ye, Zengyou, Chen, Huei-Ying, Mayfield, Brent, Sripathy, Srinidhi Rao, Page, Stephanie Cerceo, Campbell, Morganne N., Smith, Hannah L., Gallop, Danisha, Kim, Hyojin, Thaxton, Courtney L., Simon, Jeremy M., Burke, Emily E., Shin, Joo Heon, Kennedy, Andrew J., Sweatt, J. David, Philpot, Benjamin D., Jaffe, Andrew E., Maher, Brady J.

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Evidence-Based Assessment of Genes in Dilated Cardiomyopathy by Jordan, Elizabeth, Peterson, Laiken, Ai, Tomohiko, Asatryan, Babken, Bronicki, Lucas, Brown, Emily, Celeghin, Rudy, Edwards, Matthew, Fan, Judy, Ingles, Jodie, James, Cynthia A., Jarinova, Olga, Johnson, Renee, Judge, Daniel P., Lahrouchi, Najim, Lekanne Deprez, Ronald H., Lumbers, R. Thomas, Mazzarotto, Francesco, Medeiros Domingo, Argelia, Miller, Rebecca L., Morales, Ana, Murray, Brittney, Peters, Stacey, Pilichou, Kalliopi, Protonotarios, Alexandros, Semsarian, Christopher, Shah, Palak, Syrris, Petros, Thaxton, Courtney, van Tintelen, J. Peter, Walsh, Roddy, Wang, Jessica, Ware, James, Hershberger, Ray E.

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Spatiotemporal ablation of myelinating glia-specific neurofascin (NfascNF155) in mice reveals gradual loss of paranodal axoglial junctions and concomitant disorganization of axonal... by Pillai, Anilkumar M., Thaxton, Courtney, Pribisko, Alaine L., Cheng, Jr-Gang, Dupree, Jeffrey L., Bhat, Manzoor A.

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Nodes of Ranvier Act as Barriers to Restrict Invasion of Flanking Paranodal Domains in Myelinated Axons by Thaxton, Courtney, Pillai, Anilkumar M., Pribisko, Alaine L., Dupree, Jeffrey L., Bhat, Manzoor A.

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Variant classification for Pompe disease; ACMG/AMP specifications from the ClinGen lysosomal diseases variant curation expert panel by Goldstein, Jennifer L., McGlaughon, Jennifer, Kanavy, Dona, Goomber, Shelly, Pan, Yinghong, Deml, Brett, Donti, Taraka, Kearns, Liz, Seifert, Bryce A., Schachter, Miriam, Son, Rachel G., Thaxton, Courtney, Udani, Rupa, Bali, Deeksha, Baudet, Heather, Caggana, Michele, Hung, Christina, Kyriakopoulou, Lianna, Rosenblum, Lynne, Steiner, Robert, Pinto e Vairo, Filippo, Wang, Yang, Watson, Michael, Fernandez, Raquel, Weaver, Meredith, Clarke, Lorne, Rehder, Catherine

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Lumping versus splitting: How to approach defining a disease to enable accurate genomic curation by Thaxton, Courtney, Goldstein, Jennifer, DiStefano, Marina, Wallace, Kathleen, Witmer, P. Dane, Haendel, Melissa A., Hamosh, Ada, Rehm, Heidi L., Berg, Jonathan S.

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An Evidence-Based Assessment of Genes in Dilated Cardiomyopathy by Jordan, Elizabeth, Peterson, Laiken, Ai, Tomohiko, Asatryan, Babken, Bronicki, Lucas, Brown, Emily, Celeghin, Rudy, Edwards, Matthew, Fan, Judy, Ingles, Jodie, James, Cynthia A., Jarinova, Olga, Johnson, Renee, Judge, Daniel P., Lahrouchi, Najim, Lekanne Deprez, Ronald H., Lumbers, R. Thomas, Mazzarotto, Francesco, Domingo, Argelia Medeiros, Miller, Rebecca L., Morales, Ana, Murray, Brittney, Peters, Stacey, Pilichou, Kalliopi, Protonotarios, Alexandros, Semsarian, Christopher, Shah, Palak, Syrris, Petros, Thaxton, Courtney, van Tintelen, J. Peter, Walsh, Roddy, Wang, Jessica, Ware, James, Hershberger, Ray E.

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In Vivo Deletion of Immunoglobulin Domains 5 and 6 in Neurofascin (Nfasc) Reveals Domain-Specific Requirements in Myelinated Axons by Thaxton, Courtney, Pillai, Anilkumar M, Pribisko, Alaine L, Labasque, Marilyne, Dupree, Jeffrey L, Faivre-Sarrailh, Catherine, Bhat, Manzoor A

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The Nursing Dimension of Providing Palliative Care to Children and Adolescents with Cancer by Docherty, Sharron L., Thaxton, Cheryl, Allison, Courtney, Barfield, Raymond C., Tamburro, Robert F.

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