No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study by Rebbeck, Timothy R., Antoniou, Antonis C., Llopis, Trinidad Caldes, Nevanlinna, Heli, Aittomäki, Kristiina, Simard, Jacques, Spurdle, Amanda B., Couch, Fergus J., Pereira, Lutecia H. Mateus, Greene, Mark H., Andrulis, Irene L., Pasche, Boris, Kaklamani, Virginia, Hamann, Ute, Szabo, Csilla, Peock, Susan, Cook, Margaret, Harrington, Patricia A., Donaldson, Alan, Male, Allison M., Gardiner, Carol Anne, Gregory, Helen, Side, Lucy E., Robinson, Anne C., Emmerson, Louise, Ellis, Ian, Peyrat, Jean-Philippe, Fournier, Joëlle, Vennin, Philippe, Adenis, Claude, Muller, Danièle, Fricker, Jean-Pierre, Longy, Michel, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Schmutzler, Rita K., Versmold, Beatrix, Engel, Christoph, Meindl, Alfons, Kast, Karin, Schaefer, Dieter, Froster, Ursula G., Chenevix-Trench, Georgia, Easton, Douglas F.

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The mutation spectrum in Holt-Oram syndrome by CROSS, STEPHEN J, CHING, YUNG-HAO, LI, QUAN YI, ARMSTRONG-BUISSERET, LINDSAY, SPRANGER, STEPHANIE, LYONNET, STANISLAW, BONNET, DAMIEN, PENTTINEN, MAILA, JONVEAUX, PHILIPPE, LEHEUP, BRUNO, MORTIER, GEERT, VAN RAVENSWAAIJ, CONNY, GARDINER, CAROL-ANNE, BROOK, J DAVID, NEWBURY-ECOB, RUTH

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Effect of candesartan on prevention (DIRECT-Prevent 1) and progression (DIRECT-Protect 1) of retinopathy in type 1 diabetes: randomised, placebo-controlled trials by Chaturvedi, Nish, Prof, Porta, Massimo, Prof, Klein, Ronald, Prof, Orchard, Trevor, Prof, Fuller, John, Prof, Parving, Hans Henrik, Prof, Bilous, Rudy, Prof, Sjølie, Anne Katrin, Prof

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Effect of candesartan on progression and regression of retinopathy in type 2 diabetes (DIRECT-Protect 2): a randomised placebo-controlled trial by Sjølie, Anne Katrin, Prof, Klein, Ronald, Prof, Porta, Massimo, Prof, Orchard, Trevor, Prof, Fuller, John, Prof, Parving, Hans Henrik, Prof, Bilous, Rudy, Prof, Chaturvedi, Nish, Prof

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Structural analysis of pathogenic mutations in the DYRK1A gene in patients with developmental disorders by Evers, Jochem M G, Laskowski, Roman A, Bertolli, Marta, Clayton-Smith, Jill, Deshpande, Charu, Eason, Jacqueline, Elmslie, Frances, Flinter, Frances, Gardiner, Carol, Hurst, Jane A, Kingston, Helen, Kini, Usha, Lampe, Anne K, Lim, Derek, Male, Alison, Naik, Swati, Parker, Michael J, Price, Sue, Robert, Leema, Sarkar, Ajoy, Straub, Volker, Woods, Geoff, Thornton, Janet M, Wright, Caroline F

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Characterization of renal cell carcinoma‐associated constitutional chromosome abnormalities by genome sequencing by Smith, Philip S., Whitworth, James, West, Hannah, Cook, Jacqueline, Gardiner, Carol, Lim, Derek H. K., Morrison, Patrick J., Hislop, R. Gordon, Murray, Emily, Tischkowitz, Marc, Warren, Anne Y., Woodward, Emma R., Maher, Eamonn R.

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Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing by Hocking, Lynne J, Andrews, Claire, Armstrong, Christine, Ansari, Morad, Baty, David, Berg, Jonathan, Bradley, Therese, Clark, Caroline, Diamond, Austin, Doherty, Jill, Lampe, Anne, McGowan, Ruth, Moore, David J, O'Sullivan, Dawn, Purvis, Andrew, Santoyo-Lopez, Javier, Westwood, Paul, Abbott, Michael, Williams, Nicola, Aitman, Timothy J, Miedzybrodzka, Zosia

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Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height by Tatton-Brown, Katrina, Hanks, Sandra, Ruark, Elise, Zachariou, Anna, Duarte, Silvana Del Vecchio, Ramsay, Emma, Snape, Katie, Murray, Anne, Perdeaux, Elizabeth R, Seal, Sheila, Loveday, Chey, Banka, Siddharth, Clericuzio, Carol, Flinter, Frances, Magee, Alex, McConnell, Vivienne, Patton, Michael, Raith, Wolfgang, Rankin, Julia, Splitt, Miranda, Strenger, Volker, Taylor, Clare, Wheeler, Patricia, Temple, Karen I, Cole, Trevor, Douglas, Jenny, Rahman, Nazneen

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From opera buffa to opera seria: anniversaries of Royal College of Surgeons of England research initiatives by Hutchinson, Peter J, Pinkney, Thomas, Mohan, Midhun, Cromwell, David, van der Meulen, Jan, Coomer, Martyn, Tomlinson, Ralph, King, Sarah, Akkulak, Murat, Hinchliffe, Robert, Beard, David J, Morton, Dion, Orr, Linda

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Earliest functional declines in Huntington disease by Beglinger, Leigh J, O'Rourke, Justin J.F, Wang, Chiachi, Langbehn, Douglas R, Duff, Kevin, Paulsen, Jane S

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Suicidal ideation in Huntington disease: The role of comorbidity by Wetzel, Heather H, Gehl, Carissa R, Dellefave–Castillo, Lisa, Schiffman, Judith F, Shannon, Kathleen M, Paulsen, Jane S

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No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers by Spurdle, Amanda B., Deans, Andrew J., Duffy, David, Goldgar, David E., Chen, Xiaoqing, Beesley, Jonathan, Easton, Douglas F., Antoniou, Antonis C., Peock, Susan, Cook, Margaret, Nathanson, Katherine L., Domchek, Susan M., MacArthur, Grant A., Chenevix-Trench, Georgia

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