Curriculum Vitae - National Human Genome Research Institute

contributes both causal and modifying alleles across the ciliopathy spectrum. Nat Genet
43:189-196, 2011. PMID: 21258341 [PMCID: PMC3071301]
Eric D. Green - 43
275. Hurle B, Marques-Bonet T, Antonacci F, Hughes I, Ryan JF, NISC Comparative
Sequencing Program, Eichler EE, Ornitz DM, and Green ED: Lineage-specific evolution
of the vertebrate Otopetrin gene family revealed by comparative genomic analyses. BMC
Evol Biol 11:23, 2011. PMID: 21261979 [PMCID: PMC3038909]
276. Mills RE, Walter K, Stewart C, Handsaker RE, Chen K, Alkan C, Abyzov A, Yoon SC, Ye
K, Cheetham RK, Chinwalla A, Conrad DF, Fu Y, Grubert F, Hajirasouliha I, Hormozdiari
F, Iakoucheva LM, Iqbal Z, Kang S, Kidd JM, Konkel MK, Korn J, Khurana E, Kural D,
Lam HY, Leng J, Li R, Li Y, Lin CY, Luo R, Mu XJ, Nemesh J, Peckham HE, Rausch T,
Scally A, Shi X, Stromberg MP, Stütz AM, Urban AE, Walker JA, Wu J, Zhang Y, Zhang
ZD, Batzer MA, Ding L, Marth GT, McVean G, Sebat J, Snyder M, Wang J, Ye K, Eichler
EE, Gerstein MB, Hurles ME, Lee C, McCarroll SA, Korbel JO, and 1000 Genomes
Project: Mapping copy number variation by population-scale genome sequencing. Nature
470:59-65, 2011. PMID: 21293372 [PMCID: PMC3077050]
277. Green ED, Guyer MS, and National Human Genome Research Institute: Charting a course
for genomic medicine from base pairs to bedside. Nature 470:204-213, 2011. PMID:
21307933
278. Sheridan MB, Hefferon TW, Wang N, Merlo C, Milla C, Borowitz D, Green ED, Mogayzel
Jr PJ, and Cutting GR: CFTR transcription defects in pancreatic sufficient cystic fibrosis
patients with only one mutation in the coding region of CFTR. J Med Genet 48:235-241,
2011. PMID: 21097845 [PMCID: PMC3065505]
279. Bookman EB, McAllister K, Gillanders E, Wanke K, Balshaw D, Rutter J, Reedy J,
Shaughnessy D, Agurs-Collins T, Paltoo D, Atienza A, Bierut L, Kraft P, Fallin MD, Perera
F, Turkheimer E, Boardman J, Marazita ML, Rappaport SM, Boerwinkle E, Suomi SJ,
Caporaso NE, Hertz-Picciotto I, Jacobson KC, Lowe WL, Goldman LR, Duggal P, Gunnar
MR, Manolio TA, Green ED, Olster DH, and Birnbaum LS (for the NIH G x E Interplay
Workshop participants): Gene-environment interplay in common complex diseases: forging
an integrative model— recommendations from an NIH workshop. Genet Epidemiol 35:217-
225, 2011. PMID: 21308768 [PMCID: PMC3228883]
280. Horvath JE, Sheedy CB, Merrett SL, Diallo AB, Swofford DL, NISC Comparative
Sequencing Program, Green ED, and Willard HF: Comparative analysis of the primate X-
inactivation center region and reconstruction of the ancestral primate XIST locus. Genome
Res 21:850-862, 2011. PMID: 21518738 [PMCID: PMC3106318]
281. The ENCODE Project Consortium: A user's guide to the Encyclopedia of DNA Elements
(ENCODE). PLoS Biol 9:e1001046, 2011. PMID: 21526222 [PMCID: PMC3079585]
282. Davis JK, Mittel LB, Lowman JJ, Thomas PJ, Maney DL, Martin CL, NISC Comparative
Sequencing Program, and Thomas JW: Haplotype-based genomic sequencing of a
chromosomal polymorphism in the white-throated sparrow (Zonotrichia albicollis). J
Hered 102:380-90, 2011. PMID: 21613376 [PMCID: PMC3113616]
283. Conrad DF, Keebler JEM, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl
CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone
EA, Hurles ME, and Awadalla P for The 1000 Genomes Project: Variation in genome-