Curriculum Vitae - National Human Genome Research Institute
Curriculum Vitae - National Human Genome Research Institute
Curriculum Vitae - National Human Genome Research Institute
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Eric D. Green - 25<br />
112. Lai CSL, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison<br />
DC, Green ED, Vargha-Khadem F, and Monaco AP: The SPCH1 region on human 7q31:<br />
genomic characterization of the critical interval and localization of translocations<br />
associated with speech and language disorder. Am J Hum Genet 67:357-368, 2000. PMID:<br />
10880297 [PMCID: PMC1287211]<br />
113. DeSilva U, Miller E, Gorlach A, Foster CB, Green ED, and Chanock SJ: Molecular<br />
characterization of the mouse p47-phox (Ncf1) gene and comparative analysis of the mouse<br />
p47-phox (Ncf1) gene to the human NCF1 gene. Molec Cell Biol Res Commun 3:224-230,<br />
2000. PMID: 10891396<br />
114. Jamison DC, Thomas JW, and Green ED: ComboScreen facilitates the multiplex<br />
hybridization-based screening of high-density clone arrays. Bioinformatics 16:678-684,<br />
2000. PMID: 11099254<br />
115. Yan W, Guan X-Y, Green ED, Nicolson R, Yap TK, Zhang J, Jacobsen LK, Krasnewich<br />
DM, Kumra S, Lenane MC, Gochman P, Damschroder-Williams PJ, Esterling LE, Long,<br />
RT, Martin BM, Sidransky E, Rapoport JL, and Ginns EI: Childhood-onset<br />
schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC<br />
contig spanning the translocation breakpoint at 7q21. Am J Med Genet 96:749-753, 2000.<br />
PMID: 11121174<br />
116. Doyle JL, DeSilva U, Miller W, and Green ED: Divergent human and mouse orthologs of a<br />
novel gene (WBSCR15/Wbscr15) reside within the genomic interval commonly deleted in<br />
Williams syndrome. Cytogenet Cell Genet 90:285-290, 2000. PMID: 11124535<br />
117. Green ED: The <strong>Human</strong> <strong>Genome</strong> Project and its impact on the study of human disease. In The<br />
Metabolic and Molecular Bases of Inherited Disease, 8th Edition (CR Scriver, AL Beaudet,<br />
WS Sly, D Valle, B Childs, KW Kinzler, and B Vogelstein, eds; McGraw-Hill, Inc.), pp.<br />
259-298, 2001.<br />
118. Everett LA, Belyantseva IA, Noben-Trauth K, Cantos R, Chen A, Thakkar SI, Hoogstraten-<br />
Miller SL, Kachar B, Wu DK, and Green ED: Targeted disruption of mouse Pds provides<br />
insight about the inner-ear defects encountered in Pendred syndrome. Hum Molec Genet<br />
10:153-161, 2001. PMID: 11152663<br />
119. Kohn LD, Suzuki K, Nakazato M, Royaux I, and Green ED: Effects of thyroglobulin and<br />
pendrin on iodide flux through the thyrocyte. Trends Endocrinol Metab 12:10-16, 2001.<br />
PMID: 11137035<br />
120. Sahoo T, Goenaga-Dias E, Serebriiskii IG, Thomas JW, Kotova E, Cuellar JG, Peloquin JM,<br />
Golemis E, Beitinjaneh F, Green ED, Johnson EW, and Marchuk DA: Computational and<br />
experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) gene.<br />
Genomics 71:123-126, 2001. PMID:11161805<br />
121. Green ED: The <strong>Human</strong> <strong>Genome</strong> Project: elucidating our genetic blueprint. Frontiers of<br />
Engineering: Reports on Leading-Edge Engineering from the 2000 NAE Symposium on<br />
Frontiers of Engineering (<strong>National</strong> Academy of Engineering), pp. 47-53, 2001.
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