Hao Hu

ORCID

Publication Activity (10 Years)

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

Top Venues

eLife

Brain : a journal of neurology

Clinical genetics

Development (Cambridge, England)

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

Publications

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)
Hao Hu, Kaishou Xu
Reply: Is it time to rename hereditary cases of cerebral palsy? Brain : a journal of neurology 145 (10) (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)
Xiang Fang, Yaser Gamallat, Zhiheng Chen, Hanran Mai, Pei Zhou, Chuanbo Sun, Xiaoliang Li, Hong Li, Shuxin Zheng, Caihua Liao, Miaomiao Yang, Yan Li, Zeyu Yang, Caiqi Ma, Dingding Han, Liandong Zuo, Wenming Xu, Hao Hu, Ling Sun, Na Li
Hypomorphic and hypermorphic mouse models of Fsip2 indicate its dosage-dependent roles in sperm tail and acrosome formation. Development (Cambridge, England) 148 (11) (2021)
Na Li, Pei Zhou, Miaomiao Yang, Xiang Fang, Nadine Krämer, Tauqeer Ahmed Mughal, Ansar Ahmed Abbasi, Ye Yang, Angela M Kaindl, Hao Hu
Zebrafish modeling mimics developmental phenotype of patients with RAPGEF1 mutation. Clinical genetics 100 (2) (2021)

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Publication Activity (10 Years)

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Hao Hu