Author

Magdalena A. Walkiewicz

Baylor College of Medicine

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Undiagnosed Diseases Network· 2 shared Achim A WerneriD· 1 shared Adam W. HanseniD· 1 shared Adekunle M. AdesinaiD· 1 shared Alper GezdiriciiD· 1 shared Anne Michele SlavotinekiD· 1 shared Anthony J. AsmariD· 1 shared Apratim MitraiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetics

Undiagnosed Diseases Network

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2 papers

Recent·Most cited

Regulation of human development by ubiquitin chain editing of chromatin remodelers

David B. Beck, Mohammed Abul Basar, Anthony J. Asmar, Joyce J. Thompson, Hirotsugu Oda, Daniela Tiaki Uehara, Ken Saida, Precilla D’Souza, Joann Norma Bodurtha, Weiyi Mu, Kristin W. Baranano, Noriko Miyake, Raymond Wang, Marlies J. E. Kempers, Yutaka Nishimura, , Achim A Werner

This study identifies OTUD5 as essential for chromatin remodeling during development, showing its role in preventing degradation of chromatin regulators and maintaining proper gene expression networks.

bioRxiv · Jan 23, 2020 · PreprintGenetics

Phenotypic expansion in DDX3X -- a common cause of intellectual disability in females

Xia Wang, Jennifer Ellen Posey, Jill Anne Rosenfeld, Carlos A. Bacino, Fernando Scaglia, LaDonna L. Immken, Jill M. Harris, Scott E. Hickey, Theresa Mihalic Mosher, Anne Michele Slavotinek, Jing Zhang, Joke Beuten, Magalie S. Leduc, Weimin He, Francesco Vetrini, , Paolo M. Moretti

The paper identifies additional DDX3X variants in individuals with intellectual disability and expands the known phenotypic spectrum of DDX3X disorders.

Annals of Clinical and Translational Neurology · Sep 15, 2018Peer-reviewedGenetics