CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients von Romanelli, V, Belinchón, A, Campos-Barros, A, Heath, K.E, García-Miñaur, S, Martínez-Glez, V, Palomo, R, Mercado, G, Gracia, R, Lapunzina, P

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Broadening the phenotypic spectrum of POP1‐skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia von Barraza‐García, J., Rivera‐Pedroza, C.I., Hisado‐Oliva, A., Belinchón‐Martínez, A., Sentchordi‐Montané, L., Duncan, E.L., Clark, G.R., del Pozo, A., Ibáñez‐Garikano, K., Offiah, A., Prieto‐Matos, P., Cormier‐Daire, V., Heath, K.E.

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A non-pathogenic pseudoautosomal region 1 copy number variant downstream of SHOX von Benito-Sanz, S., Aragones, A., Gracia, R., Campos-Barros, A., Heath, K.E.

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Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats von Aitman, T.J. (Royal Postgraduate Medical School, London, UK.), Gotoda, T, Evans, A.L, Imrie, H, Heath, K.E, Trembling, P.M, Truman, H, Wallace, C.A, Rahman, A, Dore, C

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Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2 von Dijk, F.S. van, Semler, O., Etich, J., Kohler, A., Jimenez-Estrada, J.A., Bravenboer, N., Claeys, L., Riesebos, E., Gegic, S., Piersma, S.R., Jimenez, C.R., Waisfisz, Q., Flores, C.L., Nevado, J., Harsevoort, A.J., Janus, G.J.M., Franken, A.A.M., Sar, A.M. van der, Meijers-Heijboer, H., Heath, K.E., Lapunzina, P., Nikkels, P.G.J., Santen, G.W.E., Nuchel, J., Plomann, M., Wagener, R., Rehberg, M., Hoyer-Kuhn, H., Eekhoff, E.M.W., Pals, G., Morgelin, M., Newstead, S., Wilson, B.T., Ruiz-Perez, V.L., Maugeri, A., Netzer, C., Zaucke, F., Micha, D.

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Heterozygous aggrecan variants are associated with short stature and brachydactyly: Description of 16 probands and a review of the literature von Sentchordi-Montané, L, Aza-Carmona, M, Benito-Sanz, S, Barreda-Bonis, A.C, Sánchez-Garre, C, Prieto-Matos, P, Ruiz-Ocaña, P, Lechuga-Sancho, A, Carcavilla-Urquí, A, Mulero-Collantes, I, Martos-Moreno, G.A, Del Pozo, A, Vallespín, E, Offiah, A, Parrón-Pajares, M, Dinis, I, Sousa, S.B, Ros-Pérez, P, González-Casado, I, Heath, K.E

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Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia von Barraza-García, J, Rivera-Pedroza, C.I, Hisado-Oliva, A, Belinchón-Martínez, A, Sentchordi-Montané, L, Duncan, E.L, Clark, G.R, Del Pozo, A, Ibáñez-Garikano, K, Offiah, A, Prieto-Matos, P, Cormier-Daire, V, Heath, K.E

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Supplementary Material for: Chromosome 1p31.1p31.3 Deletion in a Patient with Craniosynostosis, Central Nervous System and Renal Malformation: Case Report and Review of the Literat... von Rivera-Pedroza, C.I., Barraza-García, J., Paumard-Hernández, B., Nevado, J., Orbea-Gallardo, C., Sánchez Del Pozo, J., Heath, K.E.

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Using a rule-based envelope model to predict the expansion of habitat suitability within New Zealand for the tick Haemaphysalis longicornis, with future projections based on two cl... von Lawrence, K.E., Summers, S.R., Heath, A.C.G., McFadden, A.M.J., Pulford, D.J., Tait, A.B., Pomroy, W.E.

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Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium von Power, Robert A, Tansey, Katherine E, Buttenschøn, Henriette Nørmølle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S, Kutalik, Zoltán, Lee, S. Hong, Ripke, Stephan, Steinberg, Stacy, Teumer, Alexander, Viktorin, Alexander, Wray, Naomi R, Arolt, Volker, Baune, Bernard T, Boomsma, Dorret I, Børglum, Anders D, Byrne, Enda M, Castelao, Enrique, Craddock, Nick, Craig, Ian W, Dannlowski, Udo, Deary, Ian J, Degenhardt, Franziska, Forstner, Andreas J, Gordon, Scott D, Grabe, Hans J, Grove, Jakob, Hamilton, Steven P, Hayward, Caroline, Heath, Andrew C, Hocking, Lynne J, Homuth, Georg, Hottenga, Jouke J, Kloiber, Stefan, Krogh, Jesper, Landén, Mikael, Lang, Maren, Levinson, Douglas F, Lichtenstein, Paul, Lucae, Susanne, MacIntyre, Donald J, Madden, Pamela, Magnusson, Patrik K.E, Martin, Nicholas G, McIntosh, Andrew M, Middeldorp, Christel M, Milaneschi, Yuri, Montgomery, Grant W, Mors, Ole, Müller-Myhsok, Bertram, Nyholt, Dale R, Oskarsson, Hogni, Owen, Michael J, Padmanabhan, Sandosh, Penninx, Brenda W.J.H, Pergadia, Michele L, Porteous, David J, Potash, James B, Preisig, Martin, Rivera, Margarita, Shi, Jianxin, Shyn, Stanley I, Sigurdsson, Engilbert, Smit, Johannes H, Smith, Blair H, Stefansson, Hreinn, Stefansson, Kari, Strohmaier, Jana, Sullivan, Patrick F, Thomson, Pippa, Thorgeirsson, Thorgeir E, Van der Auwera, Sandra, Weissman, Myrna M, Breen, Gerome, Lewis, Cathryn M

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Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs von Hemani, Gibran, Yang, Jian, Vinkhuyzen, Anna, Powell, Joseph E., Willemsen, Gonneke, Hottenga, Jouke-Jan, Abdellaoui, Abdel, Mangino, Massimo, Valdes, Ana M., Medland, Sarah E., Madden, Pamela A., Heath, Andrew C., Henders, Anjali K., Nyholt, Dale R., de Geus, Eco J.C., Magnusson, Patrik K.E., Ingelsson, Erik, Montgomery, Grant W., Spector, Timothy D., Boomsma, Dorret I., Pedersen, Nancy L., Martin, Nicholas G., Visscher, Peter M.

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Predicting the potential environmental suitability for Theileria orientalis transmission in New Zealand cattle using maximum entropy niche modelling von Lawrence, K.E., Summers, S.R., Heath, A.C.G., McFadden, A.M.J., Pulford, D.J., Pomroy, W.E.

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Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion von Vinkhuyzen, A A E, Pedersen, N L, Yang, J, Lee, S H, Magnusson, P K E, Iacono, W G, McGue, M, Madden, P A F, Heath, A C, Luciano, M, Payton, A, Horan, M, Ollier, W, Pendleton, N, Deary, I J, Montgomery, G W, Martin, N G, Visscher, P M, Wray, N R

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Characterization of selective laser-sintered hydroxyapatite-based biocomposite structures for bone replacement von Hao, L, Savalani, M.M, Zhang, Y, Tanner, K.E, Heath, R.J, Harris, R.A

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Applying polygenic risk scores to postpartum depression von Byrne, Enda M., Carrillo-Roa, Tania, Penninx, Brenda W. J. H., Sallis, Hannah M., Viktorin, Alexander, Chapman, Brett, Henders, Anjali K., Pergadia, Michele L., Heath, Andrew C., Madden, Pamela A. F., Sullivan, Patrick F., Boschloo, Lynn, van Grootheest, Gerard, McMahon, George, Lawlor, Debbie A., Landén, Mikael, Lichtenstein, Paul, Magnusson, Patrik K. E., Evans, David M., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G., Meltzer-Brody, Samantha, Wray, Naomi R.

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Neuropathology and behavioural features of transgenic murine models of Alzheimer's disease von Ameen-Ali, K.E, Wharton, S.B, Simpson, J.E, Heath, P.R, Sharp, P, Berwick, J

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Acid and aluminum effects on freshwater zooplankton: An in situ Mesocosm study von Havens, K.E., Heath, R.T.

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Translating SOD1 gene silencing towards the clinic: A highly efficacious, off-target free and biomarker-supported strategy for familial ALS von Iannitti, T, Scarrott, J, Likhite, S, Coldicott, I.R.P, Lewis, K.E, Heath, P.R, Higginbottom, A, Myszczynska, M.A, Milo, M, Hautbergue, G.M, Meyer, K, Kaspar, B.K, Ferraiuolo, L, Shaw, P.J, Azzouz, M

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Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis von Cooper-Knock, J, Moll, T, Ramesh, T, Castelli, L, Beer, A, Robins, H, Fox, I, Niedermoser, I, Van Damme, P, Moisse, M, Robberecht, W, Hardiman, O, Panades, M.P, Assialioui, A, Mora, J.S, Basak, A.N, Morrison, K.E, Shaw, C.E, Al-Chalabi, A, Landers, J.E, Wyles, M, Heath, P.R, Higginbottom, A, Walsh, T, Kazoka, M, McDermott, C.J, Hautbergue, G.M, Kirby, J, Shaw, P.J

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Phytoplankton succession during acidification with and without increasing aluminum levels von Havens, K.E., Heath, R.T.

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