Ethiraj Ravindran

ORCID

Publication Activity (10 Years)

Years Active: 2021-2022
Publications (10 Years): 10

Top Venues

eLife

Journal of medical genetics

Human molecular genetics

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

Publications

Ethiraj Ravindran, Ramona Jühlen, Carlos H Vieira-Vieira, Thuong Ha, Yuval Salzberg, Boris Fichtman, Lena Luise-Becker, Nuno Martins, Sylvie Picker-Minh, Paraskevi Bessa, Peer Arts, Matilda R Jackson, Ajay Taranath, Benjamin Kamien, Christopher Barnett, Na Li, Victor Tarabykin, Gisela Stoltenburg-Didinger, Amnon Harel, Matthias Selbach, Achim Dickmanns, Birthe Fahrenkrog, Hao Hu, Hamish Scott, Angela M Kaindl
Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders. Human molecular genetics 30 (22) (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Cynthia Gutierrez de Velazco, Ali Ghazanfar, Nadine Kraemer, Sami Zaqout, Abdul Waheed, Mohsan Hanif, Sadia Mughal, Alessandro Prigione, Na Li, Xiang Fang, Hao Hu, Angela M Kaindl
Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability. Journal of medical genetics (2021)

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Publication Activity (10 Years)

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Ethiraj Ravindran