Anthony D. Hill
Affiliations: | Harvard Medical School, Boston, MA, United States |
Area:
cortical developmentGoogle:
"Anthony Hill"Mean distance: 14.22 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentorSusan 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 |
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Publications
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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 |