Safety and Effectiveness of a Nurse-Led Outreach Program for Assessment and Treatment of Chronic Hepatitis C in the Custodial Setting
Lloyd, Andrew R., Clegg, Jac, Lange, Jens, Stevenson, Aleta, Post, Jeffrey J., Lloyd, David, Rudge, Giulia, Boonwaat, Leng, Forrest, Gary, Douglas, Jenny, Monkley, Denise
Published in Clinical infectious diseases (15.04.2013)
Published in Clinical infectious diseases (15.04.2013)
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Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B
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
Published in Nature genetics (01.11.2004)
Published in Nature genetics (01.11.2004)
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Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype
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
Published in American journal of medical genetics. Part A (01.12.2013)
Published in American journal of medical genetics. Part A (01.12.2013)
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A national cohort study and confidential enquiry to investigate ethnic disparities in maternal mortality
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.
Published in EClinicalMedicine (01.01.2022)
Published in EClinicalMedicine (01.01.2022)
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Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height
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
Published in Oncotarget (01.12.2011)
Published in Oncotarget (01.12.2011)
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Stratification of Wilms tumor by genetic and epigenetic analysis
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
Published in Oncotarget (31.03.2012)
Published in Oncotarget (31.03.2012)
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Journal Article
Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor
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
Published in Nature genetics (01.11.2008)
Published in Nature genetics (01.11.2008)
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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
Douglas, Jenny, Hanks, Sandra, Temple, I. Karen, Davies, Sally, Murray, Alexandra, Upadhyaya, Meena, Tomkins, Susan, Hughes, Helen E., Trevor Cole, R.P., Rahman, Nazneen
Published in American journal of human genetics (01.01.2003)
Published in American journal of human genetics (01.01.2003)
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Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma
Slade, Ingrid, Murray, Anne, Hanks, Sandra, Kumar, Ajith, Walker, Lisa, Hargrave, Darren, Douglas, Jenny, Stiller, Charles, Izatt, Louise, Rahman, Nazneen
Published in Familial cancer (01.06.2011)
Published in Familial cancer (01.06.2011)
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Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
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
Published in American journal of human genetics (01.10.2003)
Published in American journal of human genetics (01.10.2003)
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Mutations in RNF135 , a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth
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
Published in Nature genetics (01.08.2007)
Published in Nature genetics (01.08.2007)
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Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24
McEntagart, Meriel E., Reid, Sarah L., Irtthum, Alexandre, Douglas, Jenny B., Eyre, Keith E. D., Donaghy, Michael J., Anderson, Neil E., Rahman, Nazneen
Published in Annals of neurology (01.02.2005)
Published in Annals of neurology (01.02.2005)
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Editorial: Special edition 'Race and Ethnicity'
Douglas, Jenny, Butcher, John
Published in Widening participation and lifelong learning (09.12.2021)
Published in Widening participation and lifelong learning (09.12.2021)
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Evaluation of NSD2 and NSD3 in overgrowth syndromes
Douglas, Jenny, Coleman, Kim, Tatton-Brown, Katrina, Hughes, Helen E, Temple, I Karen, Cole, Trevor R P, Rahman, Nazneen
Published in European journal of human genetics : EJHG (01.02.2005)
Published in European journal of human genetics : EJHG (01.02.2005)
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Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer
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, Ansari Pour, Naser, 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
Published in Nature (London) (17.01.2013)
Published in Nature (London) (17.01.2013)
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Homozygous deletions at 3p12 in breast and lung cancer
SUNDARESAN, V, CHUNG, G, MINNA, J, SEKIDO, Y, LERMAN, M, LATIF, F, BERGH, J, HUA LI, LOWE, N, OGILVIE, D, RABBITTS, P, HEPPELL-PARTON, A, XIONG, J, GRUNDY, C, ROBERTS, I, JAMES, L, CAHN, A, BENCH, A, DOUGLAS, J
Published in Oncogene (01.10.1998)
Published in Oncogene (01.10.1998)
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DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome
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
Published in Journal of medical genetics (01.04.2011)
Published in Journal of medical genetics (01.04.2011)
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Poor transmission of seasonal cold viruses in a British Antarctic Survey base
Everett, Tom, Douglas, Jenny, May, Shoshanna, Horne, Simon, Marquis, Peter, Cunningham, Richard, Tang, Julian W
Published in The Journal of infection (01.06.2019)
Published in The Journal of infection (01.06.2019)
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