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Anthony D. Hill - Publications

Affiliations: 
Harvard Medical School, Boston, MA, United States 
Area:
cortical development
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Walsh CA, Bolger JC, Byrne C, Cocchiglia S, Hao Y, Fagan A, Qin L, Cahalin A, McCartan D, McIlroy M, O'Gaora P, Xu J, Hill AD, Young LS. Global gene repression by the steroid receptor coactivator SRC-1 promotes oncogenesis. Cancer Research. 74: 2533-44. PMID 24648347 DOI: 10.1158/0008-5472.CAN-13-2133  0.398
2012 Mochida GH, Ganesh VS, de Michelena MI, Dias H, Atabay KD, Kathrein KL, Huang HT, Hill RS, Felie JM, Rakiec D, Gleason D, Hill AD, Malik AN, Barry BJ, Partlow JN, et al. CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development. Nature Genetics. 44: 1260-4. PMID 23023333 DOI: 10.1038/Ng.2425  0.637
2012 Poduri A, Evrony GD, Cai X, Elhosary PC, Beroukhim R, Lehtinen MK, Hills LB, Heinzen EL, Hill A, Hill RS, Barry BJ, Bourgeois BF, Riviello JJ, Barkovich AJ, Black PM, et al. Somatic activation of AKT3 causes hemispheric developmental brain malformations. Neuron. 74: 41-8. PMID 22500628 DOI: 10.1016/J.Neuron.2012.03.010  0.615
2011 Lehtinen MK, Zappaterra MW, Chen X, Yang YJ, Hill AD, Lun M, Maynard T, Gonzalez D, Kim S, Ye P, D'Ercole AJ, Wong ET, LaMantia AS, Walsh CA. The cerebrospinal fluid provides a proliferative niche for neural progenitor cells. Neuron. 69: 893-905. PMID 21382550 DOI: 10.1016/J.Neuron.2011.01.023  0.598
2009 Mochida GH, Mahajnah M, Hill AD, Basel-Vanagaite L, Gleason D, Hill RS, Bodell A, Crosier M, Straussberg R, Walsh CA. A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly. American Journal of Human Genetics. 85: 897-902. PMID 20004763 DOI: 10.1016/j.ajhg.2009.10.027  0.474
2007 Hill AD, Chang BS, Hill RS, Garraway LA, Bodell A, Sellers WR, Walsh CA. 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. PMID 17603806 DOI: 10.1002/Ajmg.A.31776  0.405
2007 Avila P, Hill A, Walsh C. Refining a locus for pontocerebellar hypoplasia 3; a human genetics linkage inquiry Developmental Biology. 306: 379. DOI: 10.1016/j.ydbio.2007.03.349  0.381
2003 Rajab A, Mochida GH, Hill A, Ganesh V, Bodell A, Riaz A, Grant PE, Shugart YY, Walsh CA. A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21. Neurology. 60: 1664-7. PMID 12771259 DOI: 10.1212/01.Wnl.0000068548.58498.41  0.624
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