Tumor treating fields in neuro-oncology: integration of alternating electric fields therapy into promising treatment strategies von Berger, Tamar R., Wong, Eric T.

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Proteasome-mediated Proteolysis of the Polyglutamine-expanded Androgen Receptor Is a Late Event in Spinal and Bulbar Muscular Atrophy (SBMA) Pathogenesis von Heine, Erin M., Berger, Tamar R., Pluciennik, Anna, Orr, Christopher R., Zboray, Lori, Merry, Diane E.

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Identification of novel polyglutamine-expanded aggregation species in spinal and bulbar muscular atrophy von Berger, Tamar R, Montie, Heather L, Jain, Pranav, Legleiter, Justin, Merry, Diane E

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Effect of a Home-Based Exercise Intervention of Wearable Technology and Telephone Coaching on Walking Performance in Peripheral Artery Disease: The HONOR Randomized Clinical Trial von McDermott, Mary M, Spring, Bonnie, Berger, Jeffrey S, Treat-Jacobson, Diane, Conte, Michael S, Creager, Mark A, Criqui, Michael H, Ferrucci, Luigi, Gornik, Heather L, Guralnik, Jack M, Hahn, Elizabeth A, Henke, Peter, Kibbe, Melina R, Kohlman-Trigoboff, Debra, Li, Lingyu, Lloyd-Jones, Donald, McCarthy, Walter, Polonsky, Tamar S, Skelly, Christopher, Tian, Lu, Zhao, Lihui, Zhang, Dongxue, Rejeski, W. Jack

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Aggravation of fibrin deposition and microthrombus formation within the graft during kidney transplantation von van den Berg, Tamar A. J., van den Heuvel, Marius C., Wiersema-Buist, Janneke, Adelmeijer, Jelle, Nieuwenhuijs-Moeke, Gertrude J., Lisman, Ton, Bakker, Stephan J. L., van Goor, Harry, Pol, Robert A.

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COVID-19’s Impact on Genetics at One Medical Center in New York von Pereira, Elaine M., Chung, Wendy K.

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Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics von Cheung, Chloe, Berger, Sara M., Ross, Meredith, Kramer, Tamar, Li, Yuhuan, Andrews, Carli, Dergham, Katia R., Spitz, Elana, Florido, Michelle E., Ahimaz, Priyanka

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Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease−associated genes von de Bruijn, Suzanne E., Rodenburg, Kim, Corominas, Jordi, Ben-Yosef, Tamar, Reurink, Janine, Kremer, Hannie, Whelan, Laura, Plomp, Astrid S., Berger, Wolfgang, Farrar, G. Jane, Ferenc Kovács, Árpád, Fajardy, Isabelle, Hitti-Malin, Rebekkah J., Weisschuh, Nicole, Weener, Marianna E., Sharon, Dror, Pennings, Ronald J.E., Haer-Wigman, Lonneke, Hoyng, Carel B., Nelen, Marcel R., Vissers, Lisenka E.L.M., van den Born, L. Ingeborgh, Gilissen, Christian, Cremers, Frans P.M., Hoischen, Alexander, Neveling, Kornelia, Roosing, Susanne

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Critical role for Ser20 of human p53 in the negative regulation of p53 by Mdm2 von Unger, Tamar, Juven-Gershon, Tamar, Moallem, Eli, Berger, Michael, Vogt Sionov, Ronit, Lozano, Guillermina, Oren, Moshe, Haupt, Ygal

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Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination von Harel, Tamar, Quek, Debra Q. Y., Wong, Bernice H., Cazenave-Gassiot, Amaury, Wenk, Markus R., Fan, Hao, Berger, Itai, Shmueli, Dorit, Shaag, Avraham, Silver, David L., Elpeleg, Orly, Edvardson, Shimon

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Autologous Stem Cell Transplantation for Multiple Myeloma Patients Aged ≥ 75 Treated with Novel Agents von Vaxman, Iuliana, Visram, Alissa, Kumar, Shaji K., Dispenzieri, Angela, Buadi, Francis K., Dingli, David, Lacy, Martha Q., Muchtar, Eli, Kapoor, Prashant, Hogan, William J, Hayman, Suzanne R., Leung, Nelson, Gonsalves, Wilson I, Kourelis, Taxiarchis, Warsame, Rahma M, Berger, Tamar, Gertz, Morie A.

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