Katherina Walz

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Topics

Duchenne Muscular Dystrophy

Intellectual Disability

Top Venues

European journal of human genetics : EJHG

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Ozgul Alper, Ahmet Mutlu, Tahir Atik, Duygu Duman, Guney Bademci, Barbara Vona, Mahmut Tayyar Kalcioglu, Katherina Walz, Mustafa Tekin
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European journal of human genetics : EJHG (2024)
Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Ozgul Alper, Ahmet Mutlu, Tahir Atik, Duygu Duman, Guney Bademci, Barbara Vona, Mahmut Tayyar Kalcioglu, Katherina Walz, Mustafa Tekin
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European journal of human genetics : EJHG (2024)
Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Ozgul Alper, Ahmet Mutlu, Tahir Atik, Duygu Duman, Guney Bademci, Barbara Vona, Mahmut Tayyar Kalcioglu, Katherina Walz, Mustafa Tekin
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European journal of human genetics : EJHG 32 (6) (2024)
Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Ozgul Alper, Ahmet Mutlu, Tahir Atik, Duygu Duman, Guney Bademci, Barbara Vona, Mahmut Tayyar Kalcioglu, Katherina Walz, Mustafa Tekin
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European journal of human genetics : EJHG 32 (6) (2024)
Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Ozgul Alper, Ahmet Mutlu, Tahir Atik, Duygu Duman, Guney Bademci, Barbara Vona, Mahmut Tayyar Kalcioglu, Katherina Walz, Mustafa Tekin
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European journal of human genetics : EJHG 32 (6) (2024)
Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Ozgul Alper, Ahmet Mutlu, Tahir Atik, Duygu Duman, Guney Bademci, Barbara Vona, Mahmut Tayyar Kalcioglu, Katherina Walz, Mustafa Tekin
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European journal of human genetics : EJHG 32 (6) (2024)
Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, Shengru Guo, Daniel Owrang, Ozgul Alper, Ahmet Mutlu, Tahir Atik, Duygu Duman, Guney Bademci, Barbara Vona, Mahmut Tayyar Kalcioglu, Katherina Walz, Mustafa Tekin
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European journal of human genetics : EJHG (2024)
Alberto Varon, Zachary Whitt, Paige M Kalika, Lorraine Potocki, Deborah S Barbouth, Katherina Walz
Arnold-Chiari type 1 malformation in Potocki-Lupski syndrome. American journal of medical genetics. Part A 179 (7) (2019)