Molecular pathology of Lynch syndrome von Cerretelli, Guia, Ager, Ann, Arends, Mark J, Frayling, Ian M

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The NF1 somatic mutational landscape in sporadic human cancers von Philpott, Charlotte, Tovell, Hannah, Frayling, Ian M, Cooper, David N, Upadhyaya, Meena

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Molecular testing for Lynch syndrome in people with colorectal cancer: systematic reviews and economic evaluation von Snowsill, Tristan, Coelho, Helen, Huxley, Nicola, Jones-Hughes, Tracey, Briscoe, Simon, Frayling, Ian M, Hyde, Chris

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Lynch syndrome – cancer pathways, heterogeneity and immune escape von Seth, Sidhant, Ager, Ann, Arends, Mark J, Frayling, Ian M

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DNA mismatch repair deficiency in sporadic colorectal cancer and Lynch syndrome von Poulogiannis, George, Frayling, Ian M, Arends, Mark J

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The proportion of endometrial tumours associated with Lynch syndrome (PETALS): A prospective cross-sectional study von Ryan, Neil A. J., McMahon, Raymond, Tobi, Simon, Snowsill, Tristan, Esquibel, Shona, Wallace, Andrew J., Bunstone, Sancha, Bowers, Naomi, Mosneag, Ioana E., Kitson, Sarah J., O'Flynn, Helena, Ramchander, Neal C., Sivalingam, Vanitha N., Frayling, Ian M., Bolton, James, McVey, Rhona J., Evans, D. Gareth, Crosbie, Emma J.

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Cost-effectiveness analysis of reflex testing for Lynch syndrome in women with endometrial cancer in the UK setting von Snowsill, Tristan M, Ryan, Neil A J, Crosbie, Emma J, Frayling, Ian M, Evans, D Gareth, Hyde, Chris J

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High-Resolution DNA Copy Number Profiling of Malignant Peripheral Nerve Sheath Tumors Using Targeted Microarray-Based Comparative Genomic Hybridization von MANTRIPRAGADA, Kiran K, SPURLOCK, Gillian, KLUWE, Lan, CHUZHANOVA, Nadia, FERNER, Rosalie E, FRAYLING, Lan M, DUMANSKI, Jan P, GUHA, Abhijit, MAUTNER, Victor, UPADHYAYA, Meena

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A systematic review of test accuracy studies evaluating molecular micro-satellite instability testing for the detection of individuals with lynch syndrome von Coelho, Helen, Jones-Hughes, Tracey, Snowsill, Tristan, Briscoe, Simon, Huxley, Nicola, Frayling, Ian M, Hyde, Chris

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Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database von Møller, Pål, Seppälä, Toni, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paola, Evans, D Gareth, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf, Jeffries, Jacqueline, Vasen, Hans, Burn, John, Nakken, Sigve, Hovig, Eivind, Rødland, Einar Andreas, Tharmaratnam, Kukatharmini, de Vos tot Nederveen Cappel, Wouter H, Hill, James, Wijnen, Juul, Green, Kate, Lalloo, Fiona, Sunde, Lone, Mints, Miriam, Bertario, Lucio, Pineda, Marta, Navarro, Matilde, Morak, Monika, Renkonen-Sinisalo, Laura, Frayling, Ian M, Plazzer, John-Paul, Pylvanainen, Kirsi, Sampson, Julian R, Capella, Gabriel, Mecklin, Jukka-Pekka, Möslein, Gabriela

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A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/Afghanistan von Sethi, Mieran, Haque, Shaheen, Fawcett, Heather, Wing, Jonathan F., Chandler, Natalie, Mohammed, Shehla, Frayling, Ian M., Norris, Paul G., McGibbon, David, Young, Antony R., Sarkany, Robert P.E., Lehmann, Alan R., Fassihi, Hiva

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Pathways to a cancer-free future: a protocol for modelled evaluations to minimise the future burden of colorectal cancer in Australia von Feletto, Eleonora, Lew, Jie-Bin, Worthington, Joachim, He, Emily, Caruana, Michael, Butler, Katherine, Hui, Harriet, Taylor, Natalie, Banks, Emily, Barclay, Karen, Broun, Kate, Butt, Alison, Carter, Rob, Cuff, Jeff, Dessaix, Anita, Ee, Hooi, Emery, Jon, Frayling, Ian M, Grogan, Paul, Holden, Carol, Horn, Christopher, Jenkins, Mark A, Kench, James G, Laaksonen, Maarit A, Leggett, Barbara, Mitchell, Gillian, Morris, Susan, Parkinson, Bonny, St John, D James, Taoube, Linda, Tucker, Katherine, Wakefield, Melanie A, Ward, Robyn L, Win, Aung Ko, Worthley, Daniel L, Armstrong, Bruce K, Macrae, Finlay A, Canfell, Karen

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Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database von Møller, Pål, Seppälä, Toni, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paola, Evans, D Gareth, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf, Jeffries, Jacqueline, Vasen, Hans, Burn, John, Nakken, Sigve, Hovig, Eivind, Rødland, Einar Andreas, Tharmaratnam, Kukatharmini, de Vos tot Nederveen Cappel, Wouter H, Hill, James, Wijnen, Juul, Jenkins, Mark, Green, Kate, Lalloo, Fiona, Sunde, Lone, Mints, Miriam, Bertario, Lucio, Pineda, Marta, Navarro, Matilde, Morak, Monika, Renkonen-Sinisalo, Laura, Frayling, Ian M, Plazzer, John-Paul, Pylvanainen, Kirsi, Genuardi, Maurizio, Mecklin, Jukka-Pekka, Möslein, Gabriela, Sampson, Julian R, Capella, Gabriel

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Gastric tumours in FAP von Walton, Sarah-Jane, Frayling, Ian M., Clark, Susan K., Latchford, Andrew

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Getting It Right with Lynch Syndrome Genetic and Phenotypic Diagnosis von Frayling, Ian M.

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From doctors as patients: a manifesto for tackling persisting symptoms of covid-19 von Alwan, Nisreen A, Attree, Emily, Blair, Jennifer Mary, Bogaert, Debby, Bowen, Mary-Ann, Boyle, John, Bradman, Madeleine, Briggs, Tracy Ann, Burns, Sarah, Campion, Daniel, Cushing, Katherine, Delaney, Brendan, Dixon, Chris, Dolman, Grace E, Dynan, Caitriona, Frayling, Ian M, Freeman-Romilly, Nell, Hammond, Iulia, Judge, Jenny, Järte, Linn, Lokugamage, Amali, MacDermott, Nathalie, MacKinnon, Mairi, Majithia, Visita, Northridge, Tanya, Powell, Laura, Rayner, Clare, Read, Ginevra, Sahu, Ekta, Shand, Claudia, Small, Amy, Strachan, Cara, Suett, Jake, Sykes, Becky, Taylor, Sharon, Thomas, Kevin, Thomson, Margarita, Wiltshire, Alexis, Woods, Victoria

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High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correla... von Rojnueangnit, Kitiwan, Xie, Jing, Gomes, Alicia, Sharp, Angela, Callens, Tom, Chen, Yunjia, Liu, Ying, Cochran, Meagan, Abbott, Mary-Alice, Atkin, Joan, Babovic-Vuksanovic, Dusica, Barnett, Christopher P., Crenshaw, Melissa, Bartholomew, Dennis W., Basel, Lina, Bellus, Gary, Ben-Shachar, Shay, Bialer, Martin G., Bick, David, Blumberg, Bruce, Cortes, Fanny, David, Karen L., Destree, Anne, Duat-Rodriguez, Anna, Earl, Dawn, Escobar, Luis, Eswara, Marthanda, Ezquieta, Begona, Frayling, Ian M., Frydman, Moshe, Gardner, Kathy, Gripp, Karen W., Hernández-Chico, Concepcion, Heyrman, Kurt, Ibrahim, Jennifer, Janssens, Sandra, Keena, Beth A, Llano-Rivas, Isabel, Leppig, Kathy, McDonald, Marie, Misra, Vinod K., Mulbury, Jennifer, Narayanan, Vinodh, Orenstein, Naama, Galvin-Parton, Patricia, Pedro, Helio, Pivnick, Eniko K., Powell, Cynthia M., Randolph, Linda, Raskin, Salmo, Rosell, Jordi, Rubin, Karol, Seashore, Margretta, Schaaf, Christian P., Scheuerle, Angela, Schultz, Meredith, Schorry, Elizabeth, Schnur, Rhonda, Siqveland, Elizabeth, Tkachuk, Amanda, Tonsgard, James, Upadhyaya, Meena, Verma, Ishwar C., Wallace, Stephanie, Williams, Charles, Zackai, Elaine, Zonana, Jonathan, Lazaro, Conxi, Claes, Kathleen, Korf, Bruce, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine

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Identification of people with Lynch syndrome from those presenting with colorectal cancer in England: baseline analysis of the diagnostic pathway von McRonald, Fiona E, Pethick, Joanna, Santaniello, Francesco, Shand, Brian, Tyson, Adele, Tulloch, Oliver, Goel, Shilpi, Lüchtenborg, Margreet, Borthwick, Gillian M, Turnbull, Clare, Shaw, Adam C, Monahan, Kevin J, Frayling, Ian M, Hardy, Steven, Burn, John

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Mainstreaming cancer genetics: feasibility of an advanced nurse practitioner-led service diagnosing Lynch syndrome from colorectal cancer in Ireland von Loughrey, Mechelle, O’Connell, Lauren V., McSorley, Lynda, Martin, Sean, Hanly, Ann, Winter, Des C., Frayling, Ian M., Sheahan, Kieran, Kennelly, Rory

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The predicted impact and cost‐effectiveness of systematic testing of people with incident colorectal cancer for Lynch syndrome von Kang, Yoon‐Jung, Killen, James, Caruana, Michael, Simms, Kate, Taylor, Natalie, Frayling, Ian M, Snowsill, Tristan, Huxley, Nicola, Coupe, Veerle MH, Hughes, Suzanne, Freeman, Victoria, Boussioutas, Alex, Trainer, Alison H, Ward, Robyn L, Mitchell, Gillian, Macrae, Finlay A, Canfell, Karen

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