Works by Gallon, Richard

Results: 21
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    Sequencing‐based microsatellite instability testing using as few as six markers for high‐throughput clinical diagnostics.

    Published in:
    Human Mutation, 2020, v. 41, n. 1, p. 332, doi. 10.1002/humu.23906
    By:
    • Gallon, Richard;
    • Sheth, Harsh;
    • Hayes, Christine;
    • Redford, Lisa;
    • Alhilal, Ghanim;
    • O'Brien, Ottilia;
    • Spiewak, Helena;
    • Waltham, Amanda;
    • McAnulty, Ciaron;
    • Izuogu, Osagie G.;
    • Arends, Mark J.;
    • Oniscu, Anca;
    • Alonso, Angel M.;
    • Laguna, Sira M.;
    • Borthwick, Gillian M.;
    • Santibanez‐Koref, Mauro;
    • Jackson, Michael S.;
    • Burn, John
    Publication type:
    Article
    4

    A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.

    Published in:
    Human Mutation, 2019, v. 40, n. 5, p. 649, doi. 10.1002/humu.23721
    By:
    • Gallon, Richard;
    • Mühlegger, Barbara;
    • Wenzel, Sören‐Sebastian;
    • Sheth, Harsh;
    • Hayes, Christine;
    • Aretz, Stefan;
    • Dahan, Karin;
    • Foulkes, William;
    • Kratz, Christian P.;
    • Ripperger, Tim;
    • Azizi, Amedeo A.;
    • Baris Feldman, Hagit;
    • Chong, Anne‐Laure;
    • Demirsoy, Ugur;
    • Florkin, Benoît;
    • Imschweiler, Thomas;
    • Januszkiewicz‐Lewandowska, Danuta;
    • Lobitz, Stephan;
    • Nathrath, Michaela;
    • Pander, Hans‐Jürgen
    Publication type:
    Article
    5

    Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.

    Published in:
    NPJ Precision Oncology, 2024, v. 8, n. 1, p. 1, doi. 10.1038/s41698-024-00603-z
    By:
    • Gallon, Richard;
    • Brekelmans, Carlijn;
    • Martin, Marie;
    • Bours, Vincent;
    • Schamschula, Esther;
    • Amberger, Albert;
    • Muleris, Martine;
    • Colas, Chrystelle;
    • Dekervel, Jeroen;
    • De Hertogh, Gert;
    • Coupier, Jérôme;
    • Colleye, Orphal;
    • Sepulchre, Edith;
    • Burn, John;
    • Brems, Hilde;
    • Legius, Eric;
    • Wimmer, Katharina
    Publication type:
    Article
    6

    A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumours.

    Published in:
    PLoS ONE, 2018, v. 13, n. 8, p. 1, doi. 10.1371/journal.pone.0203052
    By:
    • Redford, Lisa;
    • Alhilal, Ghanim;
    • Needham, Stephanie;
    • O’Brien, Ottie;
    • Coaker, Julie;
    • Tyson, John;
    • Amorim, Leonardo Maldaner;
    • Middleton, Iona;
    • Izuogu, Osagi;
    • Arends, Mark;
    • Oniscu, Anca;
    • Alonso, Ángel Miguel;
    • Laguna, Sira Moreno;
    • Gallon, Richard;
    • Sheth, Harsh;
    • Santibanez-Koref, Mauro;
    • Jackson, Michael S.;
    • Burn, John
    Publication type:
    Article
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    Mismatch repair deficiency testing in Lynch syndromeassociated urothelial tumors.

    Published in:
    Frontiers in Oncology, 2023, p. 1, doi. 10.3389/fonc.2023.1147591
    By:
    • Rasmussen, Maria;
    • Sowter, Peter;
    • Gallon, Richard;
    • Durhuus, Jon Ambæk;
    • Hayes, Christine;
    • Andersen, Ove;
    • Nilbert, Mef;
    • Schejbel, Lone;
    • Høgdall, Estrid;
    • Santibanez-Koref, Mauro;
    • Jackson, Michael S.;
    • Burn, John;
    • Therkildsen, Christina
    Publication type:
    Article
    9

    Three molecular pathways model colorectal carcinogenesis in Lynch syndrome.

    Published in:
    International Journal of Cancer, 2018, v. 143, n. 1, p. 139, doi. 10.1002/ijc.31300
    By:
    • Ahadova, Aysel;
    • Gallon, Richard;
    • Gebert, Johannes;
    • Ballhausen, Alexej;
    • Endris, Volker;
    • Kirchner, Martina;
    • Stenzinger, Albrecht;
    • Burn, John;
    • von Knebel Doeberitz, Magnus;
    • Bläker, Hendrik;
    • Kloor, Matthias
    Publication type:
    Article
    10

    Teenage-Onset Colorectal Cancers in a Digenic Cancer Predisposition Syndrome Provide Clues for the Interaction between Mismatch Repair and Polymerase δ Proofreading Deficiency in Tumorigenesis.

    Published in:
    Biomolecules (2218-273X), 2022, v. 12, n. 10, p. N.PAG, doi. 10.3390/biom12101350
    By:
    • Schamschula, Esther;
    • Kinzel, Miriam;
    • Wernstedt, Annekatrin;
    • Oberhuber, Klaus;
    • Gottschling, Hendrik;
    • Schnaiter, Simon;
    • Friedrichs, Nicolaus;
    • Merkelbach-Bruse, Sabine;
    • Zschocke, Johannes;
    • Gallon, Richard;
    • Wimmer, Katharina
    Publication type:
    Article
    11

    Detection of Mismatch Repair Deficiency in Endometrial Cancer: Assessment of IHC, Fragment Length Analysis, and Amplicon Sequencing Based MSI Testing.

    Published in:
    Cancers, 2024, v. 16, n. 23, p. 3970, doi. 10.3390/cancers16233970
    By:
    • Sowter, Peter;
    • Gallon, Richard;
    • Hayes, Christine;
    • Phelps, Rachel;
    • Borthwick, Gillian;
    • Prior, Shaun;
    • Combe, Jenny;
    • Buist, Holly;
    • Pearlman, Rachel;
    • Hampel, Heather;
    • Goodfellow, Paul;
    • Evans, D. Gareth;
    • Crosbie, Emma J.;
    • Ryan, Neil;
    • Burn, John;
    • Santibanez-Koref, Mauro;
    • Jackson, Michael S.
    Publication type:
    Article
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    Is HLA type a possible cancer risk modifier in Lynch syndrome?

    Published in:
    International Journal of Cancer, 2023, v. 152, n. 10, p. 2024, doi. 10.1002/ijc.34312
    By:
    • Ahadova, Aysel;
    • Witt, Johannes;
    • Haupt, Saskia;
    • Gallon, Richard;
    • Hüneburg, Robert;
    • Nattermann, Jacob;
    • ten Broeke, Sanne;
    • Bohaumilitzky, Lena;
    • Hernandez‐Sanchez, Alejandro;
    • Santibanez‐Koref, Mauro;
    • Jackson, Michael S.;
    • Ahtiainen, Maarit;
    • Pylvänäinen, Kirsi;
    • Andini, Katarina;
    • Grolmusz, Vince Kornel;
    • Möslein, Gabriela;
    • Dominguez‐Valentin, Mev;
    • Møller, Pål;
    • Fürst, Daniel;
    • Sijmons, Rolf
    Publication type:
    Article
    15

    The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance.

    Published in:
    International Journal of Cancer, 2021, v. 148, n. 4, p. 800, doi. 10.1002/ijc.33224
    By:
    • Ahadova, Aysel;
    • Seppälä, Toni T.;
    • Engel, Christoph;
    • Gallon, Richard;
    • Burn, John;
    • Holinski‐Feder, Elke;
    • Steinke‐Lange, Verena;
    • Möslein, Gabriela;
    • Nielsen, Maartje;
    • Broeke, Sanne W.;
    • Laghi, Luigi;
    • Dominguez‐Valentin, Mev;
    • Capella, Gabriel;
    • Macrae, Finlay;
    • Scott, Rodney;
    • Hüneburg, Robert;
    • Nattermann, Jacob;
    • Hoffmeister, Michael;
    • Brenner, Hermann;
    • Bläker, Hendrik
    Publication type:
    Article
    16

    Report of the sixth meeting of the European Consortium 'Care for CMMRD' (C<sub>4</sub>CMMRD), Paris, France, November 16th 2022.

    Published in:
    Familial Cancer, 2024, v. 23, n. 4, p. 447, doi. 10.1007/s10689-024-00403-1
    By:
    • Guerrini-Rousseau, Léa;
    • Gallon, Richard;
    • Pineda, Marta;
    • Brugières, Laurence;
    • Baert-Desurmont, Stéphanie;
    • Corsini, Carole;
    • Dangouloff-Ros, Volodia;
    • Gorris, Mark A. J.;
    • Haberler, Christine;
    • Hoarau, Pauline;
    • Jongmans, Marjolijn C.;
    • Kloor, Matthias;
    • Loeffen, Jan;
    • Rigaud, Charlotte;
    • Robbe, Julie;
    • Vibert, Roseline;
    • Weijers, Dilys;
    • Wimmer, Katharina;
    • Colas, Chrystelle
    Publication type:
    Article
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    O09 Microsatellite-unstable sporadic sebaceous and duodenal tumours are associated with loss of mismatch protein expression.

    Published in:
    British Journal of Dermatology, 2024, v. 190, n. 6, p. e72, doi. 10.1093/bjd/ljae105.009
    By:
    • Holt, Georgie;
    • Alfailakawi, Waleed;
    • Cook, Sam;
    • Ness, Thomas;
    • Coulthard, Rowen;
    • Jones, Claire;
    • Hayes, Christine;
    • Phelps, Rachel;
    • Kist, Ralf;
    • Jackson, Mike;
    • Santibanez-Koref, Mauro;
    • Burn, John;
    • Burt, Alastair;
    • Husain, Akhtar;
    • Lamb, Chris;
    • Gallon, Richard;
    • Rajan, Neil
    Publication type:
    Article
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    Detection of constitutional mismatch repair deficiency in children and adolescents with acute lymphoblastic leukemia.

    Published in:
    Leukemia & Lymphoma, 2023, v. 64, n. 1, p. 217, doi. 10.1080/10428194.2022.2131412
    By:
    • Gallon, Richard;
    • Phelps, Rachel;
    • Betts, Leigh;
    • Hayes, Christine;
    • Masic, Dino;
    • Irving, Julie A. E.;
    • McAnulty, Ciaron;
    • Saha, Vaskar;
    • Vora, Ajay;
    • Wimmer, Katharina;
    • Motwani, Jayashree;
    • Macartney, Christine;
    • Burn, John;
    • Jackson, Michael S.;
    • Moorman, Anthony V.;
    • Santibanez-Koref, Mauro
    Publication type:
    Article