Works by Rajan, Deepa S.

Results: 6

Survival of a male patient harboring CASK Arg27Ter mutation to adolescence.
Published in:
Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1426
By:
- Mukherjee, Konark;
- Patel, Paras A.;
- Rajan, Deepa S.;
- LaConte, Leslie E. W.;
- Srivastava, Sarika
Publication type:
Article
Evolving therapies in neuronopathic LSDs: opportunities and challenges.
Published in:
2022
By:
- Rajan, Deepa S;
- Escolar, Maria L
Publication type:
Literature Review
Functional and structural deficiencies of Gemin5 variants associated with neurological disorders.
Published in:
Life Science Alliance, 2022, v. 5, n. 7, p. 1, doi. 10.26508/lsa.202201403
By:
- Francisco-Velilla, Rosario;
- Embarc-Buh, Azman;
- del Caño-Ochoa, Francisco;
- Abellan, Salvador;
- Vilar, Marçal;
- Alvarez, Sara;
- Fernandez-Jaen, Alberto;
- Kour, Sukhleen;
- Rajan, Deepa S.;
- Pandey, Udai Bhan;
- Ramón-Maiques, Santiago;
- Martinez-Salas, Encarnacion
Publication type:
Article
Adults with Cerebral Palsy Require Ongoing Neurologic Care: A Systematic Review.
Published in:
2021
By:
- Smith, Sarah E.;
- Gannotti, Mary;
- Hurvitz, Edward A.;
- Jensen, Frances E.;
- Krach, Linda E.;
- Kruer, Michael C.;
- Msall, Michael E.;
- Noritz, Garey;
- Rajan, Deepa S.;
- Aravamuthan, Bhooma R.
Publication type:
journal article
SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration.
Published in:
Acta Neuropathologica, 2023, v. 146, n. 3, p. 477, doi. 10.1007/s00401-023-02607-8
By:
- Fortuna, Tyler R.;
- Kour, Sukhleen;
- Chimata, Anuradha Venkatakrishnan;
- Muiños-Bühl, Anixa;
- Anderson, Eric N.;
- Nelson IV, Charlie H.;
- Ward, Caroline;
- Chauhan, Om;
- O'Brien, Casey;
- Rajasundaram, Dhivyaa;
- Rajan, Deepa S.;
- Wirth, Brunhilde;
- Singh, Amit;
- Pandey, Udai Bhan
Publication type:
Article
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
Published in:
Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22627-w
By:
- Kour, Sukhleen;
- Rajan, Deepa S.;
- Fortuna, Tyler R.;
- Anderson, Eric N.;
- Ward, Caroline;
- Lee, Youngha;
- Lee, Sangmoon;
- Shin, Yong Beom;
- Chae, Jong-Hee;
- Choi, Murim;
- Siquier, Karine;
- Cantagrel, Vincent;
- Amiel, Jeanne;
- Stolerman, Elliot S.;
- Barnett, Sarah S.;
- Cousin, Margot A.;
- Castro, Diana;
- McDonald, Kimberly;
- Kirmse, Brian;
- Nemeth, Andrea H.
Publication type:
Article

Works by Rajan, Deepa S.

Survival of a male patient harboring CASK Arg27Ter mutation to adolescence.

Evolving therapies in neuronopathic LSDs: opportunities and challenges.

Functional and structural deficiencies of Gemin5 variants associated with neurological disorders.

Adults with Cerebral Palsy Require Ongoing Neurologic Care: A Systematic Review.

SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration.

Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.