Tarik F. Haydar
Affiliations: | Anatomy and Neurobiology | Boston University School of Medicine, Boston, MA |
Area:
Down syndrome, Forebrain DevelopmentGoogle:
"Tarik Haydar"Mean distance: 13.86 (cluster 6) | S | N | B | C | P |
Parents
Sign in to add mentorPat R. Levitt | grad student | 1992-1993 | Medical College of Pennsylvania |
Bruce K. Krueger | grad student | 1993-1997 | University of Maryland Medical School |
Pasko Rakic | post-doc | 1997-2002 | Yale School of Medicine |
Children
Sign in to add traineeJonathan Gal | research assistant | 2005-2006 | Children's National Medical Center |
Zeynep Atak | grad student | 2021- | Childrens National Medical Center |
Elizabeth K. Stancik | grad student | 2005-2011 | The George Washington University |
Bill Tyler | post-doc | 2009- | BU School of Medicine |
Luis Olmos | post-doc | 2011- | BU School of Medicine |
Houman Qadir | post-doc | 2023- | |
Ivan Navarro-Quiroga | post-doc | 2005-2007 | Children's National Medical Center |
Karine Loulier | post-doc | 2006-2009 | Children's National Medical Center |
Lina Chakrabarti | post-doc | 2004-2010 | Children's National Medical Center |
Kun Qian | research scientist | BU School of Medicine | |
Zhen Li | research scientist | 2020- | Children's National Hospital |
Allison R Horvath | research scientist | 2021- | Children's National Medical Center, Washington DC |
Collaborators
Sign in to add collaboratorZygmunt Galdzicki | collaborator | 2003- | Children's National Medical Center |
Joshua G. Corbin | collaborator | 2004- | Children's National Medical Center |
Scott M. Thompson | collaborator | 2009- | Children's National Medical Center |
Charles ffrench-Constant | collaborator | 2008-2009 | Children's National Medical Center |
BETA: Related publications
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Publications
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Sarić N, Atak Z, Sade CF, et al. (2024) Ciliopathy interacts with neonatal anesthesia to cause non-apoptotic caspase-mediated motor deficits. Biorxiv : the Preprint Server For Biology |
Li Z, Klein JA, Rampam S, et al. (2022) Asynchronous excitatory neuron development in an isogenic cortical spheroid model of Down syndrome. Frontiers in Neuroscience. 16: 932384 |
Jablonska B, Adams KL, Kratimenos P, et al. (2022) Sirt2 promotes white matter oligodendrogenesis during development and in models of neonatal hypoxia. Nature Communications. 13: 4771 |
Klein JA, Li Z, Rampam S, et al. (2021) Sonic Hedgehog Pathway Modulation Normalizes Expression of Olig2 in Rostrally Patterned NPCs With Trisomy 21. Frontiers in Cellular Neuroscience. 15: 794675 |
Li Z, Tyler WA, Zeldich E, et al. (2020) Transcriptional priming as a conserved mechanism of lineage diversification in the developing mouse and human neocortex. Science Advances. 6 |
Shaw PR, Klein JA, Aziz NM, et al. (2020) Longitudinal neuroanatomical and behavioral analyses show phenotypic drift and variability in the Ts65Dn mouse model of Down syndrome. Disease Models & Mechanisms |
Li Z, Tyler WA, Haydar TF. (2020) Lessons from single cell sequencing in CNS cell specification and function. Current Opinion in Genetics & Development. 65: 138-143 |
Haydar TF. (2020) Neurogenesis, Myelination, and Circuitry: The Case for a Distributed Therapeutic Regimen in Down Syndrome. American Journal On Intellectual and Developmental Disabilities. 125: 100-102 |
Aziz NM, Klein JA, Brady MR, et al. (2019) Spatiotemporal development of spinal neuronal and glial populations in the Ts65Dn mouse model of Down syndrome. Journal of Neurodevelopmental Disorders. 11: 35 |
Aziz NM, Guedj F, Pennings JLA, et al. (2018) Lifespan analysis of brain development, gene expression and behavioral phenotypes in the Ts1Cje, Ts65Dn and Dp(16)1/Yey mouse models of Down syndrome. Disease Models & Mechanisms |