Cancer Risks for BRCA1 and BRCA2 Mutation Carriers: Results From Prospective Analysis of EMBRACE by MAVADDAT, Nasim, PEOCK, Susan, DAVIDSON, Rosemarie, ECCLES, Diana, COLE, Trevor, COOK, Jackie, BREWER, Carole, TISCHKOWITZ, Marc, DOUGLAS, Fiona, HODGSON, Shirley, WALKER, Lisa, PORTEOUS, Mary E, FROST, Debra, MORRISON, Patrick J, SIDE, Lucy E, KENNEDY, M. John, HOUGHTON, Catherine, DONALDSON, Alan, ROGERS, Mark T, DORKINS, Huw, MIEDZYBRODZKA, Zosia, GREGORY, Helen, EASON, Jacqueline, ELLIS, Steve, BARWELL, Julian, MCCANN, Emma, MURRAY, Alex, ANTONIOU, Antonis C, EASTON, Douglas F, PLATTE, Radka, FINEBERG, Elena, EVANS, D. Gareth, IZATT, Louise, EELES, Rosalind A, ADLARD, Julian

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Prostate Cancer Risks for Male BRCA1▪ and BRCA2 Mutation Carriers: A Prospective Cohort Study by Nyberg, Tommy, Frost, Debra, Barrowdale, Daniel, Evans, D. Gareth, Bancroft, Elizabeth, Adlard, Julian, Ahmed, Munaza, Barwell, Julian, Brady, Angela F., Brewer, Carole, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Eason, Jacqueline, Gregory, Helen, Henderson, Alex, Izatt, Louise, Kennedy, M. John, Miller, Claire, Morrison, Patrick J., Murray, Alex, Ong, Kai-Ren, Porteous, Mary, Pottinger, Caroline, Rogers, Mark T., Side, Lucy, Snape, Katie, Walker, Lisa, Tischkowitz, Marc, Eeles, Rosalind, Easton, Douglas F., Antoniou, Antonis C.

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The Angelina Jolie effect: how high celebrity profile can have a major impact on provision of cancer related services by Evans, D Gareth, Barwell, Julian, Eccles, Diana M, Collins, Amanda, Izatt, Louise, Jacobs, Chris, Donaldson, Alan, Brady, Angela F, Cuthbert, Andrew, Harrison, Rachel, Thomas, Sue, Howell, Anthony, Miedzybrodzka, Zosia, Murray, Alex

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Assessing BRCA1 activity in DNA damage repair using human induced pluripotent stem cells as an approach to assist classification of BRCA1 variants of uncertain significance by Ozgencil, Meryem, Barwell, Julian, Tischkowitz, Marc, Izatt, Louise, Kesterton, Ian, Simpson, Michael, Sharpe, Paul, de Sepulveda, Paulo, Voisset, Edwige, Solomon, Ellen

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‘We have been in lockdown since he was born’: a mixed methods exploration of the experiences of families caring for children with intellectual disability during the COVID-19 pandem... by Wolstencroft, Jeanne, Hull, Laura, Warner, Lauren, Akhtar, Tooba Nadeem, Mandy, William, Skuse, David, Baker, Kate, Dewhurst, Eleanor, Lafont, Amy, Lucy Raymond, F, Shirley, Terry, Tilley, Hayley, Timur, Husne, Titterton, Catherine, Walker, Neil, Wallwork, Sarah, Wicks, Francesca, Ye, Zheng, Erwood, Marie, Andrews, Sophie, Birch, Philippa, Bowen, Samantha, Bradley, Karen, Challenger, Aimee, Chawner, Samuel, Cuthbert, Andrew, Hall, Jeremy, Holmans, Peter, Law, Sarah, Lewis, Nicola, Morrison, Sinead, Moss, Hayley, Owen, Michael, Ray, Sinead, Sopp, Matthew, Tong, Molly, Bree, Marianne van den, Coscini, Nadia, Davies, Sarah, Denaxas, Spiros, Denyer, Hayley, Fatih, Nasrtullah, Juj, Manoj, Kerry, Ellie, Lucock, Anna, Printzlau, Frida, Srinivasan, Ramya, Walker, Susan, Watkins, Alice, Searle, Beverly, Pelling, Anna, Dean, John, Robertson, Lisa, Alan, Denise Williams, Lucy, Donaldson, Procter, Annie, Berg, Jonathan, Lampe, Anne, Rankin, Julia, Joss, Shelagh, Chitty, Lyn, Flinter, Frances, Holder, Muriel, Kraus, Alison, Barwell, Julian, Vasudevan, Pradeep, Weber, Astrid, Newman, William, Splitt, Miranda, Clowes, Virginia, Dijk, Fleur van, Harrison, Rachel, Kini, Usha, Quarrell, Oliver, Baralle, Diana, Mansour, Sahar, Crow, Yanick

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Clinical genetics: past, present and future by Tromans, Eva, Barwell, Julian

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Evaluating the Feasibility of Screening Relatives of Patients Affected by Nonsyndromic Thoracic Aortic Diseases: The REST Study by Abbasciano, Riccardo Giuseppe, Mariscalco, Giovanni, Barwell, Julian, Owens, Gareth, Zakkar, Mustafa, Joel-David, Lathishia, Pathak, Suraj, Adebayo, Adewale, Shannon, Nora, Haines, Rebecca Louise, Aujla, Hardeep, Eagle-Hemming, Bryony, Kumar, Tracy, Lai, Florence, Wozniak, Marcin, Murphy, Gavin

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Immunocytochemical detection of ERG expression in exfoliated urinary cells identifies with high specificity patients with prostate cancer by Pal, Raj P., Kockelbergh, Roger C., Pringle, John Howard, Cresswell, Lara, Hew, Roger, Dormer, John P., Cooper, Colin, Mellon, John Kilian, Barwell, Julian G., Hollox, Edward J.

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Telomere Instability in Lynch Syndrome Families Leads to Some Shorter Telomeres in MSH2+/- Carriers by Garrido-Navas, M Carmen, Tippins, Frances, Barwell, Julian, Hoffman, Jonathan, Codd, Veryan, Royle, Nicola J

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Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease by Grove, Jane I., Lo, Peggy C.K., Shrine, Nick, Barwell, Julian, Wain, Louise V., Tobin, Martin D., Salter, Andrew M., Borkar, Aditi N., Cuevas-Ocaña, Sara, Bennett, Neil, John, Catherine, Ntalla, Ioanna, Jones, Gabriela E., Neal, Christopher P., Thomas, Mervyn G., Kuht, Helen, Gupta, Pankaj, Vemala, Vishwaraj M., Grant, Allister, Adewoye, Adeolu B., Shenoy, Kotacherry T., Balakumaran, Leena K., Hollox, Edward J., Hannan, Nicholas R.F., Aithal, Guruprasad P.

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The new genomic medicine service and implications for patients by Snape, Katie, Wedderburn, Sarah, Barwell, Julian

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Association between single nucleotide polymorphisms in the DNA repair gene LIG3 and acute adverse skin reactions following radiotherapy by Murray, Robert J.S, Tanteles, George A, Mills, Jamie, Perry, Angus, Peat, Irene, Osman, Ahmed, Chan, Steve, Cheung, Kwok-Leung, Chakraborti, Prabir R, Woodings, Pamela L, Barwell, Julian G, Symonds, R. Paul, Talbot, Christopher J

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Letter comments on: Mainstreaming informed consent for genomic sequencing: A call for action by Dungey, Maurice, Dalby, Mark C., Moss, Esther L., Barwell, Julian

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What hinders minority ethnic access to cancer genetics services and what may help? by Allford, Anna, Qureshi, Nadeem, Barwell, Julian, Lewis, Celine, Kai, Joe

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Letter comments on: Mainstreaming informed consent for genomic sequencing: A call for action: A single-centre comparison of mainstreamed genetic testing with a specialist genetics... by Dungey, Maurice, Dalby, Mark C., Moss, Esther L., Barwell, Julian

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Monozygotic twins and cholesteatomas: nature or nuture? by Brar, Sabrina, Wolf, Dennis M., Faoury, Morad, Barwell, Julian, Saggar, Anand, Daya, Hamid

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Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance by Wai, Htoo A, Lord, Jenny, Lyon, Matthew, Gunning, Adam, Kelly, Hugh, Cibin, Penelope, Seaby, Eleanor G, Spiers-Fitzgerald, Kerry, Lye, Jed, Ellard, Sian, Thomas, N Simon, Bunyan, David J, Douglas, Andrew G L, Baralle, Diana

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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer by Aittomäki, Kristiina, Anton-Culver, Hoda, Arndt, Volker, Aronson, Kristan J, Arun, Banu K, Azzollini, Jacopo, Barnes, Daniel R, Beckmann, Matthias W, Bermisheva, Marina, Białkowska, Katarzyna, Blomqvist, Carl, Bolla, Manjeet K, Borg, Ake, Campbell, Ian, Carter, Jonathan, Chang-Claude, Jenny, Chanock, Stephen J, Christiansen, Hans, Couch, Fergus J, Dennis, Joe, Diez, Orland, Dunning, Alison M, Ejlertsen, Bent, Fasching, Peter A, Fletcher, Olivia, Flyger, Henrik, Friedman, Eitan, Frost, Debra, Gago-Dominguez, Manuela, Glendon, Gord, Goldgar, David E, González-Neira, Anna, Greene, Mark H, Guénel, Pascal, Hollestelle, Antoinette, Hoover, Robert N, Hopper, John L, Imyanitov, Evgeny N, Isaacs, Claudine, Jakimovska, Milena, Janavicius, Ramunas, Joseph, Vijai, Khusnutdinova, Elza, Ko, Yon-Dschun, Konstantopoulou, Irene, Lambrechts, Diether, Lazaro, Conxi, Leslie, Goska, Lesueur, Fabienne, Long, Jirong, Lubiński, Jan, Makalic, Enes, Mannermaa, Arto, Margolin, Sara, Maurer, Tabea, Mavroudis, Dimitrios, Meindl, Alfons, Menon, Usha, Michailidou, Kyriaki, Montagna, Marco, Moserle, Lidia, Mulligan, Anna Marie, Nevanlinna, Heli, Nevelsteen, Ines, Olsson, Håkan, Osorio, Ana, Park-Simon, Tjoung-Won, Parsons, Michael T, Pedersen, Inge Sokilde, Peixoto, Ana, Plaseska-Karanfilska, Dijana, Poppe, Bruce, Radice, Paolo, Rantala, Johanna, Rennert, Gad, Saloustros, Emmanouil, Schmutzler, Rita K, Simard, Jacques, Spurdle, Amanda B, Stone, Jennifer, Swerdlow, Anthony J, Tapper, William J, Teixeira, Manuel R, Teulé, Alex, Thomassen, Mads, Thöne, Kathrin, Tischkowitz, Marc, Toland, Amanda E, Truong, Thérèse, Tung, Nadine, Vachon, Celine M, van Rensburg, Elizabeth J, Viel, Alessandra, Wang, Qin, Wappenschmidt, Barbara, Weitzel, Jeffrey N, Winqvist, Robert, Kraft, Peter, Milne, Roger L, Beesley, Jonathan

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Childhood intellectual disability and parents' mental health: integrating social, psychological and genetic influences by Baker, Kate, Devine, Rory T., Ng-Cordell, Elise, Raymond, F. Lucy, Hughes, Claire

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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants by Chawner, Samuel J.R.A, Doherty, Joanne L, Anney, Richard J. L, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B.M

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