Dr Catherine Mercer

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Publications

5 publications

Page 1 of 1

A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

Elizabeth K. Bancroft, Elizabeth C. Page, Mark N. Brook, Sarah Thomas, Natalie Taylor, Jennifer Pope, Jana McHugh, Ann Britt Jones, Questa Karlsson, Susan Merson, Kai Ren Ong, Jonathan Hoffman, Camilla Huber, Lovise Maehle, Eli Marie Grindedal, Astrid Stormorken, D. Gareth Evans, Jeanette Rothwell, Fiona Lalloo, Angela F. Brady, Marion Bartlett, Katie Snape, Helen Hanson, Paul James, Joanne McKinley, Lyon Mascarenhas, Sapna Syngal, Chinedu Ukaegbu, Lucy Side, Tessy Thomas, Julian Barwell, Manuel R. Teixeira, Louise Izatt, Mohnish Suri, Finlay A. Macrae, Nicola Poplawski, Rakefet Chen-Shtoyerman, Munaza Ahmed, Hannah Musgrave, Nicola Nicolai, Lynn Greenhalgh, Carole Brewer, Nicholas Pachter, Allan D. Spigelman, Ashraf Azzabi, Brian T. Helfand, Dorothy Halliday, Diana M. Eccles, Darran Ball & Catherine Mercer, 2021, The Lancet Oncology, 22(11), 1618-1631

DOI: 10.1016/S1470-2045(21)00522-2

Type: article

Partnered intimate activities in early adolescence — findings from the UK millennium cohort study

Yvonne Kelly, Afshin Zilanawala, Clare Tanton, Ruth Lewis & Catherine H. Mercer, 2019, Journal of Adolescent Health, 65(3), 397-404

DOI: 10.1016/j.jadohealth.2019.04.028

Type: article

The Tatton-Brown-Rahman Syndrome:

Katrina Tatton-Brown, Anna Zachariou, Chey Loveday, Lise Aksglaede, Diana Baralle, Daniela Barge-Schaapveld, Moira Blyth, Mieke Bouma, Jeroen Breckpot, Tabib Dabir, Valerie Cormier-Daire, Marie-Ange Delrue, Christine Fauth, Richard Fisher, Blanca Gener, David Goudie, Tessa Homfray, Matthew Hunter, Agnete Jorgensen, Sarina G Kant, Cathy Kiraly-Borri, David A. Koolen, Ajith Kumar, Anatalia Labilloy, Carlo Mercelis, Catherine Mercer, Cyril Mignot, Kathryn Miller, Katherine Neas, Ruth Newbury-Ecob, Daniela T Pilz, Renata Posmyk, Carlos Prada, Keri Ramsey, Linda Randolph, Lisa Read, Angelo Selicorni, Debbie Shears, Mohnish Suri, Isabel Temple, Peter Turnpenny, Lionel van Maldergem, Vinod Varghese, Irma Veenstra-Knol, Naomi Yachelevich, Laura Yates & Nazneen Rahman, 2018, Wellcome Open Research , 3, 46

DOI: 10.12688/wellcomeopenres.14430.1

Type: article

Familial Ebstein’s anomaly

Catherine Mercer, Gaia Andreoletti, Aisling Carroll, Anthony P. Salmon, I. Karen Temple & Sarah Ennis, 2017, Circulation: Cardiovascular Genetics, 10(6)

DOI: 10.1161/circgenetics.116.001683

Type: article

Unexpected Findings in a Child with Atypical Hemolytic Uremic Syndrome: An Example of How Genomics Is Changing the Clinical Diagnostic Paradigm

Eleanor G. Seaby, Rodney D. Gilbert, Gaia Andreoletti, Reuben J Pengelly, Catherine Mercer, David Hunt & Sarah Ennis, 2017, Frontiers in Pediatrics, 5

DOI: 10.3389/fped.2017.00113

Type: article

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