Curriculum Vitae - National Human Genome Research Institute

Eric D. Green - 34
186. Emison ES, McCallion AS, Kashuk CS, Bush RT, Grice E, Lin S, Portnoy ME, Cutler DJ,
Green ED, and Chakravarti A: A common sex-dependent mutation in a RET enhancer
underlies Hirschsprung disease risk. Nature 434:857-863, 2005.
187. Curtiss NP, Bonifas JM, Lauchle JO, Balkman JD, Kratz CP, Emerling BM, Green ED, Le
Beau MM, and Shannon KM: Isolation and analysis of candidate myeloid tumor suppressor
genes from a commonly deleted segment of 7q22. Genomics 85:600-607, 2005. PMID:
15820312
188. Kashuk CS, Stone EA, Grice EA, Portnoy ME, Green ED, Sidow A, Chakravarti A, and
McCallion AS: Phenotype-genotype correlation in Hirschsprung disease is illuminated by
comparative analysis of the RET protein sequence. Proc Natl Acad Sci USA 102:8949-8954,
2005. PMID: 15956201 [PMCID: PMC1157046]
189. Cooper GM, Stone EA, Asimenos G, NISC Comparative Sequencing Program, Green ED,
Batzoglou S, and Sidow A: Distribution and intensity of constraint in mammalian genomic
sequence. Genome Res 15:901-913, 2005. PMID: 15965027 [PMCID: PMC1172034]
190. Schueler MG, Dunn JM, Bird CP, Ross MT, Viggiano L, NISC Comparative Sequencing
Program, Rocchi M, Willard HF, and Green ED: Progressive proximal expansion of the
primate X chromosome centromere. Proc Natl Acad Sci USA 102:10563-10568, 2005.
PMID: 16030148 [PMCID: PMC1180780]
191. Portnoy ME, McDermott KJ, Antonellis A, Margulies EH, Prasad AB, NISC Comparative
Sequencing Program, Kingsley DM, Green ED, and Mortlock DP: Detection of potential
GDF6 regulatory elements by multispecies sequence comparisons and identification of a
skeletal joint enhancer. Genomics 86:295-305, 2005. PMID: 15979840
192. Sivakumar K, Kyriakides T, Puls I, Nicholson GA, Funalot B, Antonellis A, Sambuughin N,
Christodoulou K, Beggs JL, Zamba-Papanicolaou E, Ionasescu V, Dalakas MC, Green ED,
Fischbeck KH, and Goldfarb LG: Phenotypic spectrum of disorders associated with glycyltRNA
synthetase mutations. Brain 128:2304-2314, 2005. PMID: 16014653
193. Portnoy ME and Green ED: Comparative sequencing of vertebrate genomes. In
Encyclopedia of Genetics, Genomics, Proteomics, and Bioinformatics (LB Jorde, PFR Little,
KJ Dunn, and S Subramaniam, eds; John Wiley & Sons Ltd), pp. 1239-1248, 2005.
194. Kim Y-H, Verlander JW, Matthews SW, Kurtz I, Shin W, Weiner ID, Everett LA, Green ED,
Nielsen S, and Wall SM: Intercalated cell H + /OH - transporter expression is reduced in Slc26a4
null mice. Am J Physiol Renal Physiol 289:F1262-F1272, 2005. PMID: 16144965
195. Grice EA, Rochelle ES, Green ED, Chakravarti A, and McCallion AS: Evaluation of the RET
regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer. Hum Mol
Genet 14:3837-3845, 2005. PMID: 16269442
196. Riazuddin S, Khan SN, Ahmed ZM, Ghosh M, Caution K, Nazli S, Kabra M, Zafar AU, Chen
K, Naz S, Antonellis A, Pavan WJ, Green ED, Wilcox ER, Friedman PL, Morell, RJ,
Riazuddin S, and Friedman TB: Mutations in TRIOBP, which encodes a putative cytoskeletalorganizing
protein, are associated with nonsyndromic recessive deafness. Am J Hum Genet
78:137-143, 2006. PMID: 16385457 [PMCID: PMC1380211]
197. Antonellis A, Bennett WR, Menheniott TR, Prasad AB, Lee-Lin S-Q, NISC Comparative
Sequencing Program, Green ED, Paisley D, Kelsh RN, Pavan WJ, and Ward A: Deletion of
long-range sequences at Sox10 compromises developmental expression in a mouse model of
Waardenburg-Shah (WS4) syndrome. Hum Molec Genet 15:259-271, 2006. PMID: 16330480