Search Results - "Howard, Eleanor"

Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder by Frank, René A W, McRae, Allan F, Pocklington, Andrew J, van de Lagemaat, Louie N, Navarro, Pau, Croning, Mike D R, Komiyama, Noboru H, Bradley, Sophie J, Challiss, R A John, Armstrong, J Douglas, Finn, Robert D, Malloy, Mary P, MacLean, Alan W, Harris, Sarah E, Starr, John M, Bhaskar, Sanjeev S, Howard, Eleanor K, Hunt, Sarah E, Coffey, Alison J, Ranganath, Venkatesh, Deloukas, Panos, Rogers, Jane, Muir, Walter J, Deary, Ian J, Blackwood, Douglas H, Visscher, Peter M, Grant, Seth G N

“…Current models of schizophrenia and bipolar disorder implicate multiple genes, however their biological relationships remain elusive. To test the genetic role…”
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Target-enrichment strategies for next-generation sequencing by Shendure, Jay, Turner, Daniel J, Mamanova, Lira, Coffey, Alison J, Scott, Carol E, Kozarewa, Iwanka, Turner, Emily H, Kumar, Akash, Howard, Eleanor

“…We have not yet reached a point at which routine sequencing of large numbers of whole eukaryotic genomes is feasible, and so it is often necessary to select…”
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Seven newly identified loci for autoimmune thyroid disease by COOPER, Jason D, SIMMONDS, Matthew J, TODD, John A, GOUGH, Stephen C. L, WALKER, Neil M, BURREN, Oliver, BRAND, Oliver J, HUI GUO, WALLACE, Chris, STEVENS, Helen, COLEMAN, Gillian, FRANKLYN, Jayne A

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Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease by Huertas-Vazquez, Adriana, Nelson, Christopher P, Guo, Xiuqing, Reinier, Kyndaron, Uy-Evanado, Audrey, Teodorescu, Carmen, Ayala, Jo, Jerger, Katherine, Chugh, Harpriya, Braund, Peter S, Deloukas, Panos, Hall, Alistair S, Balmforth, Anthony J, Jones, Michelle, Taylor, Kent D, Pulit, Sara L, Newton-Cheh, Christopher, Gunson, Karen, Jui, Jonathan, Rotter, Jerome I, Albert, Christine M, Samani, Nilesh J, Chugh, Sumeet S

“…Recent genome-wide association studies (GWAS) have identified novel loci associated with sudden cardiac death (SCD). Despite this progress, identified DNA…”
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Erratum: Target-enrichment strategies for next-generation sequencing by Mamanova, Lira, Coffey, Alison J, Scott, Carol E, Kozarewa, Iwanka, Turner, Emily H, Kumar, Akash, Howard, Eleanor, Shendure, Jay, Turner, Daniel J

“…Nat. Methods 7, 111–118 (2010); published online 28 January 2010; corrected after print 12 April 2010. In the version of this article initially published, the…”
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Target-enrichment strategies for next-generation sequencing by Mamanova, Lira, Coffey, Alison J, Scott, Carol E, Kozarewa, Iwanka, Turner, Emily H, Kumar, Akash, Howard, Eleanor, Shendure, Jay, Turner, Daniel J

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Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation-New MCA/MR syndrome in two affected sibs and a mildly affected mother? by Wieczorek, Dagmar, Shaw-Smith, Charles, Kohlhase, Jürgen, Schmitt, Wolfgang, Buiting, Karin, Coffey, Alison, Howard, Eleanor, Hehr, Ute, Gillessen-Kaesbach, Gabriele

“…The previously undescribed combination of esophageal atresia, hypoplasia of the zygomatic complex, microcephaly, cup‐shaped ears, congenital heart defect, and…”
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Using ThinkVantage Technologies: Volume 2 Maintaining and Recovering Client Systems by Byron Braswell, Chris Holland, David Kohler, Dudley Miller, Eleanor Howard, Goran Wibran, Guy Varendonck, Håkon Fosshaug, Ive Mattheessens, Jamel Lynch, James Cowles, Johan Freidlitz, John Zywicki, Keith Gedrose, Lucas Biggers, Syed Irfan, Yossi Soberano

“…ThinkVantage Technologies bring your PCs one step closer to being self-configured, self-optimizing, self-protecting, and self-healing, to help save you time…”
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Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient by Raffan, Eleanor, Hurst, Liam A, Turki, Saeed Al, Carpenter, Gillian, Scott, Carol, Daly, Allan, Coffey, Alison, Bhaskar, Sanjeev, Howard, Eleanor, Khan, Naz, Kingston, Helen, Palotie, Aarno, Savage, David B, O'Driscoll, Mark, Smith, Claire, O'Rahilly, Stephen, Barroso, Inês, Semple, Robert K

“…Genetic diagnosis of inherited metabolic disease is conventionally achieved through syndrome recognition and targeted gene sequencing, but many patients…”
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