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

by Stephens, Jonathan C., Darsley, Michael J., Turner, Arthur K.
Published 2006

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

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

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

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

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

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

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

by 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
Published 2013

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

by 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.
Published 2013

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

by 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.
Published 2006

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

by 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.
Published in Nat Commun (2020)

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

by 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.
Published in Nat Commun (2020)

Common genetic variants do not associate with CAD in familial hypercholesterolemia

by 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
Published 2014

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

by 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.
Published in Cell Rep (2015)

ADA2 deficiency complicated by EBV-driven lymphoproliferative disease

by 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.
Published in Clin Immunol (2020)

Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasia

by 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
Published in Blood (2020)

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

by 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
Published 2009

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

by 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
Published 2011

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

by 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.
Published in Genome Med (2018)

Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia

by 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
Published in Blood (2016)

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

by 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.
Published in Haematologica (2020)

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

by 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.
Published 2010

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

by 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.
Published 2009