Choice of Statistical Tools for Outlier Removal Causes Substantial Changes in Analyte Reference Intervals in Healthy Populations von Hickman, Peter E, Koerbin, Gus, Potter, Julia M, Glasgow, Nicholas, Cavanaugh, Juleen A, Abhayaratna, Walter P, West, Nic P, Glasziou, Paul

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Deleterious GRM1 mutations in schizophrenia von Ayoub, Mohammed Akli, Angelicheva, Dora, Vile, David, Chandler, David, Morar, Bharti, Cavanaugh, Juleen A, Visscher, Peter M, Jablensky, Assen, Pfleger, Kevin D G, Kalaydjieva, Luba

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Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters von Bröer, Stefan, Bailey, Charles G, Kowalczuk, Sonja, Ng, Cynthia, Vanslambrouck, Jessica M, Rodgers, Helen, Auray-Blais, Christiane, Cavanaugh, Juleen A, Bröer, Angelika, Rasko, John E J

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Genetics of inflammatory bowel disease: The state of play von Cavanaugh, Juleen A

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Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19 von Seow, Heng F, Bröer, Stefan, Bröer, Angelika, Bailey, Charles G, Potter, Simon J, Cavanaugh, Juleen A, Rasko, John E J

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Characterization of the monomethylarsonate reductase and dehydroascorbate reductase activities of Omega class glutathione transferase variants: implications for arsenic metabolism... von Schmuck, Erica M, Board, Philip G, Whitbread, Astrid K, Tetlow, Natasha, Cavanaugh, Juleen A, Blackburn, Anneke C, Masoumi, Amir

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The histone demethylase Jhdm1a regulates hepatic gluconeogenesis von Pan, Dongning, Mao, Chunxiao, Zou, Tie, Yao, Annie Y, Cooper, Marcus P, Boyartchuk, Victor, Wang, Yong-Xu

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The Clinical Relevance of Compound Heterozygosity for the C282Y and H63D Substitutions in Hemochromatosis von Walsh, Alissa, Dixon, Jeannette L., Ramm, Grant A., Hewett, David G., Lincoln, Douglas J., Anderson, Gregory J., Subramaniam, V. Nathan, Dodemaide, Julian, Cavanaugh, Juleen A., Bassett, Mark L., Powell, Lawrie W.

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Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial von Frishberg, Yaacov, Deschênes, Georges, Groothoff, Jaap W, Hulton, Sally-Anne, Magen, Daniella, Harambat, Jérôme, Van't Hoff, William G, Lorch, Ulrike, Milliner, Dawn S, Lieske, John C, Haslett, Patrick, Garg, Pushkal P, Vaishnaw, Akshay K, Talamudupula, Sandeep, Lu, Jiandong, Habtemariam, Bahru A, Erbe, David V, McGregor, Tracy L, Cochat, Pierre

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The molecular basis of neutral aminoacidurias von Bröer, Angelika, Cavanaugh, Juleen A, Rasko, John E J, Bröer, Stefan

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Further evidence for allelic heterogeneity in Hartnup disorder von Azmanov, Dimitar N, Kowalczuk, Sonja, Rodgers, Helen, Auray-Blais, Christiane, Giguère, Robert, Rasko, John E.J, Bröer, Stefan, Cavanaugh, Juleen A

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Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugs von Schmuck, Erica, Cappello, Jean, Coggan, Marjorie, Brew, Jenny, Cavanaugh, Juleen A., Blackburn, Anneke C., Baker, Rohan T., Eyre, Helen J., Sutherland, Grant R., Board, Philip G.

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The IBD international genetics consortium provides further evidence for linkage to IBD4 and shows gene‐environment interaction von Pierik, Marie, Yang, Huiying, Barmada, Michael M., Cavanaugh, Juleen A., Annese, Vito, Brant, Steven R., Cho, Judy H., Duerr, Richard H., Hugot, Jean‐Pierre, McGovern, Dermot P., Paavola‐Sakki, Paulina, Radford‐Smith, Graham L., Pavli, P., Silverberg, Mark S., Schreiber, Stephan, Taylor, Kent D., Vlietinck, Robert

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IBD international genetics consortium: International cooperation making sense of complex disease von Cavanaugh, Juleen A.

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Persistence of the Common Hartnup Disease D173N Allele in Populations of European Origin von Azmanov, Dimitar N., Rodgers, Helen, Auray‐Blais, Christiane, Giguère, Robert, Bailey, Charles, Bröer, Stefan, Rasko, John E. J., Cavanaugh, Juleen A.

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Statement of Principle von Seaquist, Elizabeth R, Boulton, Andrew J.M, Harrell, R. Mack, Grunberger, George, Santen, Richard J

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Statement of Principle von Seaquist, Elizabeth R, Boulton, Andrew J.M, Harrell, R. Mack, Grunberger, George, Santen, Richard J

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Statement of Principle von Seaquist, Elizabeth R, Boulton, Andrew J.M, Harrell, R. Mack, Grunberger, George, Santen, Richard J

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Statement of Principle von Seaquist, Elizabeth R, Boulton, Andrew J.M, Harrell, R. Mack, Grunberger, George, Santen, Richard J

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Lack of association of the CD14 promoter polymorphism −159C/T with Caucasian inflammatory bowel disease von Peters, Kirsten E., O'Callaghan, Nathan J., Cavanaugh, Juleen A.

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