☰ Neurotree

Tarik F. Haydar

Affiliations:

Anatomy and Neurobiology

Boston University School of Medicine, Boston, MA

Area:

Down syndrome, Forebrain Development

Google:

Mean distance: 13.86 (cluster 6)

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Parents

Pat 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

Jonathan 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

Zygmunt 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

Publications

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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
Guillamon-Vivancos T, Tyler WA, Medalla M, et al. (2018) Distinct Neocortical Progenitor Lineages Fine-tune Neuronal Diversity in a Layer-specific Manner. Cerebral Cortex (New York, N.Y. : 1991)

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