Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease: Serum Urate and Dyslipidemia von Wallace, Chris, Newhouse, Stephen J., Braund, Peter, Zhang, Feng, Tobin, Martin, Falchi, Mario, Ahmadi, Kourosh, Dobson, Richard J., Marçano, Ana Carolina B., Hajat, Cother, Burton, Paul, Deloukas, Panagiotis, Brown, Morris, Connell, John M., Dominiczak, Anna, Lathrop, G. Mark, Webster, John, Farrall, Martin, Spector, Tim, Samani, Nilesh J., Caulfield, Mark J., Munroe, Patricia B.

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The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia von Arnason, Alfred, Marçano, Ana Carolina B, Braybrook, Claire, Goodfellow, Paul J, Doudney, Kit, Moore, Gudrun E, Patton, Michael A, Stanier, Philip, Bjornsson, Arni

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Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients von Braybrook, Claire, Lisgo, Steven, Doudney, Kit, Henderson, Deborah, Marçano, Ana Carolina B., Strachan, Tom, Patton, Michael A., Villard, Laurent, Moore, Gudrun E., Stanier, Philip, Lindsay, Susan

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Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study von Munroe, Patricia B, Wallace, Chris, Xue, Ming-Zhan, Marçano, Ana Carolina B, Dobson, Richard J, Onipinla, Abiodun K, Burke, Beverley, Gungadoo, Johannie, Newhouse, Stephen J, Pembroke, Janine, Brown, Morris, Dominiczak, Anna F, Samani, Nilesh J, Lathrop, Mark, Connell, John, Webster, John, Clayton, David, Farrall, Martin, Mein, Charles A, Caulfield, Mark

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Linkage Analysis Using Co-Phenotypes in the BRIGHT Study Reveals Novel Potential Susceptibility Loci for Hypertension von Wallace, Chris, Xue, Ming-Zhan, Newhouse, Stephen J., Marçano, Ana Carolina B., Onipinla, Abiodun K., Burke, Beverley, Gungadoo, Johannie, Dobson, Richard J., Brown, Morris, Connell, John M., Dominiczak, Anna, Lathrop, G. Mark, Webster, John, Farrall, Martin, Mein, Charles, Samani, Nilesh J., Caulfield, Mark J., Clayton, David G., Munroe, Patricia B.

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Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension von Marçano, Ana Carolina Braga, Burke, Beverley, Gungadoo, Johannie, Wallace, Chris, Kaisaki, Pamela J, Woon, Peng Y, Farrall, Martin, Clayton, David, Brown, Morris, Dominiczak, Anna, Connell, John M, Webster, John, Lathrop, Mark, Caulfield, Mark, Samani, Nilesh, Gauguier, Dominique, Munroe, Patricia B

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