Ali Fatemi

2022

Corrigendum to: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform (Human Mutation, (2020), 41, 6, (1131-1137), 10.1002/humu.24008)

Helman, G., Takanohashi, A., Hagemann, T. L., Perng, M. D., Walkiewicz, M., Woidill, S., Sase, S., Cross, Z., Du, Y., Zhao, L., Waldman, A., Haake, B. C., Fatemi, A., Brenner, M., Sherbini, O., Messing, A., Vanderver, A. & Simons, C., Sep 2022, In: Human mutation. 43, 9, p. 1344 1 p.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2021

Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy (Nature Genetics, (2020), 52, 10, (1046-1056), 10.1038/s41588-020-0695-1)

Jin, S. C., Lewis, S. A., Bakhtiari, S., Zeng, X., Sierant, M. C., Shetty, S., Nordlie, S. M., Elie, A., Corbett, M. A., Norton, B. Y., van Eyk, C. L., Haider, S., Guida, B. S., Magee, H., Liu, J., Pastore, S., Vincent, J. B., Brunstrom-Hernandez, J., Papavasileiou, A. & Fahey, M. C. & 57 others, Berry, J. G., Harper, K., Zhou, C., Zhang, J., Li, B., Zhao, H., Heim, J., Webber, D. L., Frank, M. S. B., Xia, L., Xu, Y., Zhu, D., Zhang, B., Sheth, A. H., Knight, J. R., Castaldi, C., Tikhonova, I. R., López-Giráldez, F., Keren, B., Whalen, S., Buratti, J., Doummar, D., Cho, M., Retterer, K., Millan, F., Wang, Y., Waugh, J. L., Rodan, L., Cohen, J. S., Fatemi, A., Lin, A. E., Phillips, J. P., Feyma, T., MacLennan, S. C., Vaughan, S., Crompton, K. E., Reid, S. M., Reddihough, D. S., Shang, Q., Gao, C., Novak, I., Badawi, N., Wilson, Y. A., McIntyre, S. J., Mane, S. M., Wang, X., Amor, D. J., Zarnescu, D. C., Lu, Q., Xing, Q., Zhu, C., Bilguvar, K., Padilla-Lopez, S., Lifton, R. P., Gecz, J., MacLennan, A. H. & Kruer, M. C., Mar 2021, In: Nature genetics. 53, 3, p. 412 1 p.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2020

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

The SPARK Consortium, Dec 1 2020, In: Nature communications. 11, 1, 5398.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2019

Erratum: De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia (The American Journal of Human Genetics (2019) 105(2) (413–424), (S0002929719302393), (10.1016/j.ajhg.2019.06.014))

Undiagnosed Diseases Network, Sep 5 2019, In: American journal of human genetics. 105, 3, p. 672-674 3 p.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

2018

Newborn Screening and Emerging Therapies for X-Linked Adrenoleukodystrophy

Moser, A. B. & Fatemi, A., Oct 1 2018, In: JAMA Neurology. 75, 10, p. 1175-1176 2 p.

Research output: Contribution to journal › Comment/debate › peer-review

8 Scopus citations

2015

Correction: Systemic Injection of CD34⁺ -Enriched Human Cord Blood Cells Modulates Poststroke Neural and Glial Response in a Sex-Dependent Manner in CD1 Mice (Stem Cells and Development (2015) 24, 1 (51-66))

Kadam, S., Chen, H. G., Markowitz, G. J., Raja, S., George, S., Verina, T., Shotwell, E., Loechelt, B., Johnston, M. V., Kamani, N., Fatemi, A. & Comi, A. M., Apr 1 2015, In: Stem Cells and Development. 24, 7, p. 916 1 p.

Research output: Contribution to journal › Comment/debate › peer-review

Ali Fatemi

Research output

Search results

Corrigendum to: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform (Human Mutation, (2020), 41, 6, (1131-1137), 10.1002/humu.24008)

Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy (Nature Genetics, (2020), 52, 10, (1046-1056), 10.1038/s41588-020-0695-1)

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

Erratum: De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia (The American Journal of Human Genetics (2019) 105(2) (413–424), (S0002929719302393), (10.1016/j.ajhg.2019.06.014))

Newborn Screening and Emerging Therapies for X-Linked Adrenoleukodystrophy

Correction: Systemic Injection of CD34+ -Enriched Human Cord Blood Cells Modulates Poststroke Neural and Glial Response in a Sex-Dependent Manner in CD1 Mice (Stem Cells and Development (2015) 24, 1 (51-66))

Correction: Systemic Injection of CD34⁺ -Enriched Human Cord Blood Cells Modulates Poststroke Neural and Glial Response in a Sex-Dependent Manner in CD1 Mice (Stem Cells and Development (2015) 24, 1 (51-66))