Walz, Katherina

Datos académicos

PRODUCCION CIENTÍFICO TECNOLÓGICA

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Artículo ADAMTSL2 mutations determine the phenotypic severity in Geleophysic Dysplasia

Camarena, Vladimir; Williams, Monique M.; Morales, Alejo A.; Zafeer, Mohammad F.; Kilic, Okan V.; Kamiar, Ali; Abad, Clemer; Rasmussen, Monica A.; Briski, Laurence M.; Peart, LéShon; Bademci, Guney; Barbouth, Deborah S.; Smithson, Sarah; Wang, Gaofeng; Shehadeh, Lina A.; Walz, Katherina ; Tekin, Mustafa (American Society for Clinical Investigation, 2024-02)
Artículo Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning

Abad, Clemer; Robayo, Maria C.; Muñiz Moreno, Maria del Mar; Bernardi, Maria Trinidad ; Otero, Maria G.; Kosanovic, Christina; Griswold, Anthony J.; Pierson, Tyler Mark; Walz, Katherina ; Young, Juan (Nature Publishing Group, 2024-01)
Artículo Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America

De Rosa, Maria Agustina; Bernardi, Maria Trinidad ; Kleppe, Soledad; Walz, Katherina (MDPI, 2024-01)
Artículo Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice

Bademci, Guney; Lachgar Ruiz, María; Deokar, Mangesh; Zafeer, Mohammad Faraz; Abad, Clemer; Baylan, Muzeyyen Yildirim; Ingham, Neil J.; Chen, Jing; Sineni, Claire J.; Vadgama, Nirmal; Karakikes, Ioannis; Guo, Shengru; Duman, Duygu; Singh, Nitu; Harlalka, Gaurav; Jain, Shirish P.; Chioza, Barry A.; Walz, Katherina ; Steel, Karen P.; Nasir, Jamal; Tekin, Mustafa (National Academy of Sciences, 2022-06)
Artículo SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights

Rebelo, Adriana P.; Abad, Clemer; Dohrn, Maike F.; Li, Jian J.; Tieu, Ethan K.; Medina, Jessica; Yanick, Christopher; Huang, Jingyu; Zotter, Brendan; Young, Juan; Saporta, Mario; Scherer, Steven S.; Walz, Katherina ; Zuchner, Stephan (Oxford University Press, 2024-09)

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