☰

Anthony D. Hill

Affiliations: 
Harvard Medical School, Boston, MA, United States 
Area:
cortical development
Google:
"Anthony Hill"
Mean distance: 14.22 (cluster 11)
 		SNBCP
Tree Publications Grants Similar researchers PubMed Report error

Parents

Sign in to add mentor
Susan K. McConnell grad student 2002 Stanford
 (Notch signaling and the control of cell fate in the developing cerebral cortex.)
Chris A. Walsh post-doc Harvard Medical School
Chinfei Chen research scientist Harvard - Boston Children's Hospital

Children

Sign in to add trainee

Collaborators

Sign in to add collaborator
BETA: Related publications

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.

Walsh CA, Bolger JC, Byrne C, et al. (2014) Global gene repression by the steroid receptor coactivator SRC-1 promotes oncogenesis. Cancer Research. 74: 2533-44
Mochida GH, Ganesh VS, de Michelena MI, et al. (2012) CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development. Nature Genetics. 44: 1260-4
Poduri A, Evrony GD, Cai X, et al. (2012) Somatic activation of AKT3 causes hemispheric developmental brain malformations. Neuron. 74: 41-8
Lehtinen MK, Zappaterra MW, Chen X, et al. (2011) The cerebrospinal fluid provides a proliferative niche for neural progenitor cells. Neuron. 69: 893-905
Mochida GH, Mahajnah M, Hill AD, et al. (2009) A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly. American Journal of Human Genetics. 85: 897-902
Hill AD, Chang BS, Hill RS, et al. (2007) A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome. American Journal of Medical Genetics. Part A. 143: 1692-8
Avila P, Hill A, Walsh C. (2007) Refining a locus for pontocerebellar hypoplasia 3; a human genetics linkage inquiry Developmental Biology. 306: 379
Rajab A, Mochida GH, Hill A, et al. (2003) A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21. Neurology. 60: 1664-7
See more...