Safety and Effectiveness of a Nurse-Led Outreach Program for Assessment and Treatment of Chronic Hepatitis C in the Custodial Setting von Lloyd, Andrew R., Clegg, Jac, Lange, Jens, Stevenson, Aleta, Post, Jeffrey J., Lloyd, David, Rudge, Giulia, Boonwaat, Leng, Forrest, Gary, Douglas, Jenny, Monkley, Denise

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Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B von Méhes, Károly, Shannon, Nora, FitzPatrick, David, Reid, Sarah, Douglas, Jenny, Firth, Helen, Plaja, Alberto, Robin, Nathanial, Irrthum, Alexandre, Nash, Richard, Tolmie, John, Kidd, Alexa, Swansbury, John, Coleman, Kim, Hanks, Sandra, Rahman, Nazneen

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Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype von Tatton-Brown, Katrina, Murray, Anne, Hanks, Sandra, Douglas, Jenny, Armstrong, Ruth, Banka, Siddharth, Bird, Lynne M., Clericuzio, Carol L., Cormier-Daire, Valerie, Cushing, Tom, Flinter, Frances, Jacquemont, Marie-Line, Joss, Shelagh, Kinning, Esther, Lynch, Sally Ann, Magee, Alex, McConnell, Vivienne, Medeira, Ana, Ozono, Keiichi, Patton, Michael, Rankin, Julia, Shears, Debbie, Simon, Marleen, Splitt, Miranda, Strenger, Volker, Stuurman, Kyra, Taylor, Clare, Titheradge, Hannah, Van Maldergem, Lionel, Temple, I. Karen, Cole, Trevor, Seal, Sheila, Rahman, Nazneen

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A national cohort study and confidential enquiry to investigate ethnic disparities in maternal mortality von Knight, Marian, Bunch, Kathryn, Vousden, Nicola, Banerjee, Anita, Cox, Philippa, Cross-Sudworth, Fiona, Dhanjal, Mandish K., Douglas, Jenny, Girling, Joanna, Kenyon, Sara, Kotnis, Rohit, Patel, Roshni, Shakespeare, Judy, Tuffnell, Derek, Wilkinson, Meg, Kurinczuk, Jennifer J.

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Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height von 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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Stratification of Wilms tumor by genetic and epigenetic analysis von Scott, Richard H, Murray, Anne, Baskcomb, Linda, Turnbull, Clare, Loveday, Chey, Al-Saadi, Reem, Williams, Richard, Breatnach, Fin, Gerrard, Mary, Hale, Juliet, Kohler, Janice, Lapunzina, Pablo, Levitt, Gill A, Picton, Sue, Pizer, Barry, Ronghe, Milind D, Traunecker, Heidi, Williams, Denise, Kelsey, Anna, Vujanic, Gordan M, Sebire, Neil J, Grundy, Paul, Stiller, Charles A, Pritchard-Jones, Kathy, Douglas, Jenny, Rahman, Nazneen

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Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor von Douglas, Jenny, Maher, Eamonn R, Cook, Jackie A, Barker, Karen, Craft, Alan, Baskcomb, Linda, Gerrard, Mary, Rahman, Nazneen, Scott, Richard H, Levitt, Gill A, Hanks, Sandra, Picton, Sue, Huxter, Nikki, Williams, Denise, Stiller, Charles A, Pritchard-Jones, Kathy, Kohler, Janice A, Ronghe, Milind D, Pizer, Barry, Pujol, Pascal, Birch, Jillian M

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NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes von Douglas, Jenny, Hanks, Sandra, Temple, I. Karen, Davies, Sally, Murray, Alexandra, Upadhyaya, Meena, Tomkins, Susan, Hughes, Helen E., Trevor Cole, R.P., Rahman, Nazneen

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Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma von Slade, Ingrid, Murray, Anne, Hanks, Sandra, Kumar, Ajith, Walker, Lisa, Hargrave, Darren, Douglas, Jenny, Stiller, Charles, Izatt, Louise, Rahman, Nazneen

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Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis von Hanks, Sandra, Adams, Sarah, Douglas, Jenny, Arbour, Laura, Atherton, David J., Balci, Sevim, Bode, Harald, Campbell, Mary E., Feingold, Murray, Keser, Gökhan, Kleijer, Wim, Mancini, Grazia, McGrath, John A., Muntoni, Francesco, Nanda, Arti, Teare, M. Dawn, Warman, Matthew, Pope, F. Michael, Superti-Furga, Andrea, Futreal, P. Andrew, Rahman, Nazneen

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Mutations in RNF135 , a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth von Rahman, Nazneen, Douglas, Jenny, Cilliers, Deirdre, Coleman, Kim, Tatton-Brown, Katrina, Barker, Karen, Bernhard, Brigitte, Burn, John, Huson, Susan, Josifova, Dragana, Lacombe, Didier, Malik, Mohsin, Mansour, Sahar, Reid, Evan, Cormier-Daire, Valerie, Cole, Trevor, Childhood Overgrowth Collaboration, The

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Editorial: Special edition 'Race and Ethnicity' von Douglas, Jenny, Butcher, John

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PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations von McConville, Carmel, Reid, Sarah, Baskcomb, Linda, Douglas, Jenny, Rahman, Nazneen

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Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer von Ruark, Elise, Snape, Katie, Humburg, Peter, Loveday, Chey, Bajrami, Ilirjana, Brough, Rachel, Rodrigues, Daniel Nava, Renwick, Anthony, Seal, Sheila, Ramsay, Emma, Duarte, Silvana Del Vecchio, Rivas, Manuel A., Warren-Perry, Margaret, Zachariou, Anna, Campion-Flora, Adriana, Hanks, Sandra, Murray, Anne, Pour, Naser Ansari, Douglas, Jenny, Gregory, Lorna, Rimmer, Andrew, Walker, Neil M., Yang, Tsun-Po, Adlard, Julian W., Barwell, Julian, Berg, Jonathan, Brady, Angela F., Brewer, Carole, Brice, Glen, Chapman, Cyril, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Douglas, Fiona, Eccles, Diana, Evans, D. Gareth, Greenhalgh, Lynn, Henderson, Alex, Izatt, Louise, Kumar, Ajith, Lalloo, Fiona, Miedzybrodzka, Zosia, Morrison, Patrick J., Paterson, Joan, Porteous, Mary, Rogers, Mark T., Shanley, Susan, Walker, Lisa, Gore, Martin, Houlston, Richard, Brown, Matthew A., Caufield, Mark J., Deloukas, Panagiotis, McCarthy, Mark I., Todd, John A., Turnbull, Clare, Reis-Filho, Jorge S., Ashworth, Alan, Antoniou, Antonis C., Lord, Christopher J., Donnelly, Peter, Rahman, Nazneen

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DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome von Slade, Ingrid, Bacchelli, Chiara, Davies, Helen, Murray, Anne, Abbaszadeh, Fatemeh, Hanks, Sandra, Barfoot, Rita, Burke, Amos, Chisholm, Julia, Hewitt, Martin, Jenkinson, Helen, King, Derek, Morland, Bruce, Pizer, Barry, Prescott, Katrina, Saggar, Anand, Side, Lucy, Traunecker, Heidi, Vaidya, Sucheta, Ward, Paul, Futreal, P Andrew, Vujanic, Gordan, Nicholson, Andrew G, Sebire, Neil, Turnbull, Clare, Priest, John R, Pritchard-Jones, Kathryn, Houlston, Richard, Stiller, Charles, Stratton, Michael R, Douglas, Jenny, Rahman, Nazneen

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Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24 von McEntagart, Meriel E., Reid, Sarah L., Irtthum, Alexandre, Douglas, Jenny B., Eyre, Keith E. D., Donaghy, Michael J., Anderson, Neil E., Rahman, Nazneen

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Evaluation of NSD2 and NSD3 in overgrowth syndromes von Douglas, Jenny, Coleman, Kim, Tatton-Brown, Katrina, Hughes, Helen E, Temple, I Karen, Cole, Trevor R P, Rahman, Nazneen

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Poor transmission of seasonal cold viruses in a British Antarctic Survey base von Everett, Tom, Douglas, Jenny, May, Shoshanna, Horne, Simon, Marquis, Peter, Cunningham, Richard, Tang, Julian W

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Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations von Tatton-Brown, Katrina, Douglas, Jenny, Coleman, Kim, Baujat, Geneviève, Cole, Trevor R.P., Das, Soma, Horn, Denise, Hughes, Helen E., Temple, I. Karen, Faravelli, Francesca, Waggoner, Darrel, Türkmen, Seval, Cormier-Daire, Valérie, Irrthum, Alexandre, Rahman, Nazneen

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Mutations in CEP57 cause mosaic variegated aneuploidy syndrome von Snape, Katie, Hanks, Sandra, Ruark, Elise, Barros-Núñez, Patricio, Elliott, Anna, Murray, Anne, Lane, Andrew H, Shannon, Nora, Callier, Patrick, Chitayat, David, Clayton-Smith, Jill, FitzPatrick, David R, Gisselsson, David, Jacquemont, Sebastien, Asakura-Hay, Keiko, Micale, Mark A, Tolmie, John, Turnpenny, Peter D, Wright, Michael, Douglas, Jenny, Rahman, Nazneen

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