Stabilization of a Plasmid Coding for a Heterologous Antigen in Salmonella enterica Serotype Typhi Vaccine Strain CVD908-htrA by Using Site-Specific Recombination

von Stephens, Jonathan C., Darsley, Michael J., Turner, Arthur K.
Veröffentlicht 2006

Generation and Characterization of a Live Attenuated Enterotoxigenic Escherichia coli Combination Vaccine Expressing Six Colonization Factors and Heat-Labile Toxin Subunit B

von Turner, Arthur K., Stephens, Jonathan C., Beavis, Juliet C., Greenwood, Judith, Gewert, Cornelia, Randall, Roger, Freeman, Donna, Darsley, Michael J.
Veröffentlicht 2011

Utility of the Leptospermum scoparium Compound Lepteridine as a Chemical Marker for Manuka Honey Authenticity

von Lin, Bin, Daniels, Benjamin J., Middleditch, Martin J., Furkert, Daniel P., Brimble, Margaret A., Bong, Jessie, Stephens, Jonathan M., Loomes, Kerry M.
Veröffentlicht in ACS Omega (2020)

Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes

von Ormondroyd, Elizabeth, Harper, Andrew R., Thomson, Kate L., Mackley, Michael P., Martin, Jennifer, Penkett, Christopher J., Salatino, Silvia, Stark, Hannah, Stephens, Jonathan, Watkins, Hugh
Veröffentlicht in Eur J Hum Genet (2020)

Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci

von Paul, Dirk S., Albers, Cornelis A., Rendon, Augusto, Voss, Katrin, Stephens, Jonathan, van der Harst, Pim, Chambers, John C., Soranzo, Nicole, Ouwehand, Willem H., Deloukas, Panos
Veröffentlicht 2013

The Effect of New Zealand Kanuka, Manuka and Clover Honeys on Bacterial Growth Dynamics and Cellular Morphology Varies According to the Species

von Lu, Jing, Carter, Dee A., Turnbull, Lynne, Rosendale, Douglas, Hedderley, Duncan, Stephens, Jonathan, Gannabathula, Swapna, Steinhorn, Gregor, Schlothauer, Ralf C., Whitchurch, Cynthia B., Harry, Elizabeth J.
Veröffentlicht 2013

Construction and Phase I Clinical Evaluation of the Safety and Immunogenicity of a Candidate Enterotoxigenic Escherichia coli Vaccine Strain Expressing Colonization Factor Antigen...

von Turner, Arthur K., Beavis, Juliet C., Stephens, Jonathan C., Greenwood, Judith, Gewert, Cornelia, Thomas, Nicola, Deary, Alison, Casula, Gabriella, Daley, Alexandra, Kelly, Paul, Randall, Roger, Darsley, Michael J.
Veröffentlicht 2006

Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans

von Wei, Wei, Pagnamenta, Alistair T., Gleadall, Nicholas, Sanchis-Juan, Alba, Stephens, Jonathan, Broxholme, John, Tuna, Salih, Odhams, Christopher A., Fratter, Carl, Turro, Ernest, Caulfield, Mark J., Taylor, Jenny C., Rahman, Shamima, Chinnery, Patrick F.
Veröffentlicht in Nat Commun (2020)

Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans

von Wei, Wei, Pagnamenta, Alistair T., Gleadall, Nicholas, Sanchis-Juan, Alba, Stephens, Jonathan, Broxholme, John, Tuna, Salih, Odhams, Christopher A., Fratter, Carl, Turro, Ernest, Caulfield, Mark J., Taylor, Jenny C., Rahman, Shamima, Chinnery, Patrick F.
Veröffentlicht in Nat Commun (2020)

Common genetic variants do not associate with CAD in familial hypercholesterolemia

von van Iperen, Erik P A, Sivapalaratnam, Suthesh, Boekholdt, S Matthijs, Hovingh, G Kees, Maiwald, Stephanie, Tanck, Michael W, Soranzo, Nicole, Stephens, Jonathan C, Sambrook, Jennifer G, Levi, Marcel, Ouwehand, Willem H, Kastelein, John JP, Trip, Mieke D, Zwinderman, Aeilko H
Veröffentlicht 2014

Leukemia-Associated Somatic Mutations Drive Distinct Patterns of Age-Related Clonal Hemopoiesis

von McKerrell, Thomas, Park, Naomi, Moreno, Thaidy, Grove, Carolyn S., Ponstingl, Hannes, Stephens, Jonathan, Crawley, Charles, Craig, Jenny, Scott, Mike A., Hodkinson, Clare, Baxter, Joanna, Rad, Roland, Forsyth, Duncan R., Quail, Michael A., Zeggini, Eleftheria, Ouwehand, Willem, Varela, Ignacio, Vassiliou, George S.
Veröffentlicht in Cell Rep (2015)

ADA2 deficiency complicated by EBV-driven lymphoproliferative disease

von Staples, Emily, Simeoni, Ilenia, Stephens, Jonathan C., Allen, Hana Lango, Wright, Penny, Davies, E. Graham, Javid, Babak, Gkrania-Klotsas, Effrossyni, Gattens, Michael, Firth, Helen, Shamardina, Olga, Deevi, Sri V.V., Prapa, Matina, Uttenthal, Ben, Kumararatne, Dinakantha, Thaventhiran, James E.D.
Veröffentlicht in Clin Immunol (2020)

Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasia

von Shovlin, Claire L., Simeoni, Ilenia, Downes, Kate, Frazer, Zoe C., Megy, Karyn, Bernabeu-Herrero, Maria E., Shurr, Abigail, Brimley, Jennifer, Patel, Dilipkumar, Kell, Loren, Stephens, Jonathan, Turbin, Isobel G., Aldred, Micheala A., Penkett, Christopher J., Ouwehand, Willem H., Jovine, Luca, Turro, Ernest
Veröffentlicht in Blood (2020)

A Genome-wide Association Study Identifies Three Loci Associated with Mean Platelet Volume

von Meisinger, Christa, Prokisch, Holger, Gieger, Christian, Soranzo, Nicole, Mehta, Divya, Rosskopf, Dieter, Lichtner, Peter, Klopp, Norman, Stephens, Jonathan, Watkins, Nicholas A., Deloukas, Panos, Greinacher, Andreas, Koenig, Wolfgang, Nauck, Matthias, Rimmbach, Christian, Völzke, Henry, Peters, Annette, Illig, Thomas, Ouwehand, Willem H., Meitinger, Thomas, Wichmann, H.-Erich, Döring, Angela
Veröffentlicht 2009

Exome sequencing identifies NBEAL2 as the causative gene for Gray Platelet Syndrome

von Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H
Veröffentlicht 2011

Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing

von Sanchis-Juan, Alba, Stephens, Jonathan, French, Courtney E., Gleadall, Nicholas, Mégy, Karyn, Penkett, Christopher, Shamardina, Olga, Stirrups, Kathleen, Delon, Isabelle, Dewhurst, Eleanor, Dolling, Helen, Erwood, Marie, Grozeva, Detelina, Stefanucci, Luca, Arno, Gavin, Webster, Andrew R., Cole, Trevor, Austin, Topun, Branco, Ricardo Garcia, Ouwehand, Willem H., Raymond, F. Lucy, Carss, Keren J.
Veröffentlicht in Genome Med (2018)

Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia

von Sivapalaratnam, Suthesh, Westbury, Sarah K., Stephens, Jonathan C., Greene, Daniel, Downes, Kate, Kelly, Anne M., Lentaigne, Claire, Astle, William J., Huizinga, Eric G., Nurden, Paquita, Papadia, Sofia, Peerlinck, Kathelijne, Penkett, Christopher J., Perry, David J., Roughley, Catherine, Simeoni, Ilenia, Stirrups, Kathleen, Hart, Daniel P., Tait, R Campbell, Mumford, Andrew D., Laffan, Michael A., Freson, Kathleen, Ouwehand, Willem H., Kunishima, Shinji, Turro, Ernest
Veröffentlicht in Blood (2016)

Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function

von Chan, Melissa V., Hayman, Melissa A., Sivapalaratnam, Suthesh, Crescente, Marilena, Allan, Harriet E., Edin, Matthew L., Zeldin, Darryl C., Milne, Ginger L., Stephens, Jonathan, Greene, Daniel, Hanif, Moghees, O’Donnell, Valerie B., Dong, Liang, Malkowski, Michael G., Lentaigne, Claire, Wedderburn, Katherine, Stubbs, Matthew, Downes, Kate, Ouwehand, Willem H., Turro, Ernest, Hart, Daniel P., Freson, Kathleen, Laffan, Michael A., Warner, Timothy D.
Veröffentlicht in Haematologica (2020)

Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function

von Goodall, Alison H., Burns, Philippa, Salles, Isabelle, Macaulay, Iain C., Jones, Chris I., Ardissino, Diego, de Bono, Bernard, Bray, Sarah L., Deckmyn, Hans, Dudbridge, Frank, Fitzgerald, Desmond J., Garner, Stephen F., Gusnanto, Arief, Koch, Kerstin, Langford, Cordelia, O'Connor, Marie N., Rice, Catherine M., Stemple, Derek, Stephens, Jonathan, Trip, Mieke D., Zwaginga, Jaap-Jan, Samani, Nilesh J., Watkins, Nicholas A., Maguire, Patricia B., Ouwehand, Willem H.
Veröffentlicht 2010

A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function

von Soranzo, Nicole, Rendon, Augusto, Gieger, Christian, Jones, Chris I., Watkins, Nicholas A., Menzel, Stephan, Döring, Angela, Stephens, Jonathan, Prokisch, Holger, Erber, Wendy, Potter, Simon C., Bray, Sarah L., Burns, Philippa, Jolley, Jennifer, Falchi, Mario, Kühnel, Brigitte, Erdmann, Jeanette, Schunkert, Heribert, Samani, Nilesh J., Illig, Thomas, Garner, Stephen F., Rankin, Angela, Meisinger, Christa, Bradley, John R., Thein, Swee Lay, Goodall, Alison H., Spector, Tim D., Deloukas, Panos, Ouwehand, Willem H.
Veröffentlicht 2009