“. . . If You’re Not Part of the Institution You Fall by the Wayside”: Service Providers’ Perspectives on Moving Young Men From Disconnection and Isolation to Connection and Belong...

per Grace, Billy, Richardson, Noel, Carroll, Paula
Publicat a Am J Mens Health (2016)

Recruiting men from across the socioeconomic spectrum via GP registers and community outreach to a weight management feasibility randomised controlled trial

per McDonald, Matthew D., Dombrowski, Stephan U., Skinner, Rebecca, Calveley, Eileen, Carroll, Paula, Elders, Andrew, Gray, Cindy M., Grindle, Mark, Harris, Fiona M., Jones, Claire, Hoddinott, Pat
Publicat a BMC Med Res Methodol (2020)

Systematic reviews of and integrated report on the quantitative, qualitative and economic evidence base for the management of obesity in men.

per Robertson, Clare, Archibald, Daryll, Avenell, Alison, Douglas, Flora, Hoddinott, Pat, van Teijlingen, Edwin, Boyers, Dwayne, Stewart, Fiona, Boachie, Charles, Fioratou, Evie, Wilkins, David, Street, Tim, Carroll, Paula, Fowler, Colin
Publicat a Health Technol Assess (2014)

Ribonuclease H2 mutations induce a cGAS/STING‐dependent innate immune response

per Mackenzie, Karen J, Carroll, Paula, Lettice, Laura, Tarnauskaitė, Žygimantė, Reddy, Kaalak, Dix, Flora, Revuelta, Ailsa, Abbondati, Erika, Rigby, Rachel E, Rabe, Björn, Kilanowski, Fiona, Grimes, Graeme, Fluteau, Adeline, Devenney, Paul S, Hill, Robert E, Reijns, Martin AM, Jackson, Andrew P
Publicat a EMBO J (2016)

cGAS surveillance of micronuclei links genome instability to innate immunity

per Mackenzie, Karen J., Carroll, Paula, Martin, Carol-Anne, Murina, Olga, Fluteau, Adeline, Simpson, Daniel, Olova, Nelly, Sutcliffe, Hannah, Rainger, Jacqueline, Robertson, Andrea, Osborn, Ruby, Wheeler, Ann, Nowotny, Marcin, Gilbert, Nick, Chandra, Tamir, Reijns, Martin A. M., Jackson, Andrew P.
Publicat a Nature (2017)

A Unique Protein Phosphatase with Kelch-Like Domains (PPKL) in Plasmodium Modulates Ookinete Differentiation, Motility and Invasion

per Guttery, David S., Poulin, Benoit, Ferguson, David J. P., Szöőr, Balázs, Wickstead, Bill, Carroll, Paula L., Ramakrishnan, Chandra, Brady, Declan, Patzewitz, Eva-Maria, Straschil, Ursula, Solyakov, Lev, Green, Judith L., Sinden, Robert E., Tobin, Andrew B., Holder, Anthony A., Tewari, Rita
Publicat 2012

Game of Stones: feasibility randomised controlled trial of how to engage men with obesity in text message and incentive interventions for weight loss

per Dombrowski, Stephan U, McDonald, Matthew, van der Pol, Marjon, Grindle, Mark, Avenell, Alison, Carroll, Paula, Calveley, Eileen, Elders, Andrew, Glennie, Nicola, Gray, Cindy M, Harris, Fiona M, Hapca, Adrian, Jones, Claire, Kee, Frank, McKinley, Michelle C, Skinner, Rebecca, Tod, Martin, Hoddinott, Pat
Publicat a BMJ Open (2020)

PRIM1 deficiency causes a distinctive primordial dwarfism syndrome

per Parry, David A., Tamayo-Orrego, Lukas, Carroll, Paula, Marsh, Joseph A., Greene, Philip, Murina, Olga, Uggenti, Carolina, Leitch, Andrea, Káposzta, Rita, Merő, Gabriella, Nagy, Andrea, Orlik, Brigitta, Kovács-Pászthy, Balázs, Quigley, Alan J., Riszter, Magdolna, Rankin, Julia, Reijns, Martin A.M., Szakszon, Katalin, Jackson, Andrew P.
Publicat a Genes Dev (2020)

Mutations in the NHEJ Component XRCC4 Cause Primordial Dwarfism

per Murray, Jennie E., van der Burg, Mirjam, IJspeert, Hanna, Carroll, Paula, Wu, Qian, Ochi, Takashi, Leitch, Andrea, Miller, Edward S., Kysela, Boris, Jawad, Alireza, Bottani, Armand, Brancati, Francesco, Cappa, Marco, Cormier-Daire, Valerie, Deshpande, Charu, Faqeih, Eissa A., Graham, Gail E., Ranza, Emmanuelle, Blundell, Tom L., Jackson, Andrew P., Stewart, Grant S., Bicknell, Louise S.
Publicat a Am J Hum Genet (2015)

Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis

per Martin, Carol-Anne, Murray, Jennie E., Carroll, Paula, Leitch, Andrea, Mackenzie, Karen J., Halachev, Mihail, Fetit, Ahmed E., Keith, Charlotte, Bicknell, Louise S., Fluteau, Adeline, Gautier, Philippe, Hall, Emma A., Joss, Shelagh, Soares, Gabriela, Silva, João, Bober, Michael B., Duker, Angela, Wise, Carol A., Quigley, Alan J., Phadke, Shubha R., Wood, Andrew J., Vagnarelli, Paola, Jackson, Andrew P.
Publicat a Genes Dev (2016)

Corrigendum: Mutations in genes encoding condensins cause microcephaly through decatenation failure at mitosis

per Martin, Carol-Anne, Murray, Jennie E., Carroll, Paula, Leitch, Andrea, MacKenzie, Karen J., Halachev, Mihail, Fetit, Ahmed E., Keith, Charlotte, Bicknell, Louise S., Fluteau, Adeline, Gautier, Philippe, Hall, Emma A., Joss, Shelagh, Soares, Gabriela, Silva, João, Bober, Michael B., Duker, Angela, Wise, Carol A., Quigley, Alan J., Phadke, Shubha R., Wood, Andrew J., Vagnarelli, Paola, Jackson, Andrew P.
Publicat a Genes Dev (2017)

The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes

per Waters, Aoife M, Asfahani, Rowan, Carroll, Paula, Bicknell, Louise, Lescai, Francesco, Bright, Alison, Chanudet, Estelle, Brooks, Anthony, Christou-Savina, Sonja, Osman, Guled, Walsh, Patrick, Bacchelli, Chiara, Chapgier, Ariane, Vernay, Bertrand, Bader, David M, Deshpande, Charu, O’ Sullivan, Mary, Ocaka, Louise, Stanescu, Horia, Stewart, Helen S, Hildebrandt, Friedhelm, Otto, Edgar, Johnson, Colin A, Szymanska, Katarzyna, Katsanis, Nicholas, Davis, Erica, Kleta, Robert, Hubank, Mike, Doxsey, Stephen, Jackson, Andrew, Stupka, Elia, Winey, Mark, Beales, Philip L
Publicat a J Med Genet (2015)

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

per Reynolds, John J, Bicknell, Louise S, Carroll, Paula, Higgs, Martin R, Shaheen, Ranad, Murray, Jennie E, Papadopoulos, Dimitrios K, Leitch, Andrea, Murina, Olga, Tarnauskaitė, Žygimantė, Wessel, Sarah R, Zlatanou, Anastasia, Vernet, Audrey, von Kriegsheim, Alex, Mottram, Rachel MA, Logan, Clare V, Bye, Hannah, Li, Yun, Brean, Alexander, Maddirevula, Sateesh, Challis, Rachel C, Skouloudaki, Kassiani, Almoisheer, Agaadir, Alsaif, Hessa S, Amar, Ariella, Prescott, Natalie J, Bober, Michael B, Duker, Angela, Faqeih, Eissa, Seidahmed, Mohammed Zain, Al Tala, Saeed, Alswaid, Abdulrahman, Ahmed, Saleem, Al-Aama, Jumana Yousuf, Altmüller, Janine, Al Balwi, Mohammed, Brady, Angela F, Chessa, Luciana, Cox, Helen, Fischetto, Rita, Heller, Raoul, Henderson, Bertram D, Hobson, Emma, Nürnberg, Peter, Percin, E Ferda, Peron, Angela, Spaccini, Luigina, Quigley, Alan J, Thakur, Seema, Wise, Carol A, Yoon, Grace, Alnemer, Maha, Tomancak, Pavel, Yigit, Gökhan, Taylor, A Malcolm R, Reijns, Martin AM, Simpson, Michael A, Cortez, David, Alkuraya, Fowzan S, Mathew, Christopher G, Jackson, Andrew P, Stewart, Grant S
Publicat a Nat Genet (2017)