Alicia Guemez-Gamboa
Affiliations: | Rockefeller University, New York, NY, United States |
Area:
Neurodevelopment, human genetics, neural circuitsGoogle:
"Alicia Guemez-Gamboa"Mean distance: (not calculated yet)
Parents
Sign in to add mentorJulio Moran | grad student | UNAM IFC | |
Nicholas C. Spitzer | post-doc | ||
Joseph G. Gleeson | post-doc | 2013-2016 | Northwestern Univ Medical School |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Rakotomamonjy J, Rylaarsdam L, Guemez-Gamboa A. (2020) PYRC2-Related Hypomyelinating Leukodystrophy: More to This Than Meets the Eye. Neuron. 107: 3-5 |
Li H, Saucedo-Cuevas L, Yuan L, et al. (2019) Zika Virus Protease Cleavage of Host Protein Septin-2 Mediates Mitotic Defects in Neural Progenitors. Neuron |
Guemez-Gamboa A, Çağlayan AO, Stanley V, et al. (2018) Loss of protocadherin-12 leads to Diencephalic-Mesencephalic Junction Dysplasia syndrome. Annals of Neurology |
Marin-Valencia I, Gerondopoulos A, Zaki MS, et al. (2017) Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. American Journal of Human Genetics |
Lardelli RM, Schaffer AE, Eggens VR, et al. (2017) Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing. Nature Genetics |
Baek ST, Copeland B, Yun EJ, et al. (2015) An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development. Nature Medicine |
Guemez-Gamboa A, Nguyen LN, Yang H, et al. (2015) Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome. Nature Genetics. 47: 809-13 |
Guemez-Gamboa A, Xu L, Meng D, et al. (2014) Non-cell-autonomous mechanism of activity-dependent neurotransmitter switching. Neuron. 82: 1004-16 |
Guemez-Gamboa A, Coufal NG, Gleeson JG. (2014) Primary cilia in the developing and mature brain. Neuron. 82: 511-21 |
Akizu N, Silhavy JL, Rosti RO, et al. (2014) Mutations in CSPP1 lead to classical Joubert syndrome. American Journal of Human Genetics. 94: 80-6 |