Items where Author is "Metcalfe, Alison"

ZUREK, Birte, ELLWANGER, Kornelia, VISSERS, Lisenka E. L. M., SCHÜLE, Rebecca, SYNOFZIK, Matthis, TÖPF, Ana, DE VOER, Richarda M., LAURIE, Steven, MATALONGA, Leslie, GILISSEN, Christian, OSSOWSKI, Stephan, ’T HOEN, Peter A. C., VITOBELLO, Antonio, SCHULZE-HENTRICH, Julia M., RIESS, Olaf, BRUNNER, Han G., BROOKES, Anthony J., RATH, Ana, BONNE, Gisèle, GUMUS, Gulcin, VERLOES, Alain, HOOGERBRUGGE, Nicoline, EVANGELISTA, Teresinha, HARMUTH, Tina, SWERTZ, Morris, SPALDING, Dylan, HOISCHEN, Alexander, BELTRAN, Sergi, GRAESSNER, Holm, HAACK, Tobias B., ZUREK, Birte, ELLWANGER, Kornelia, DEMIDOV, German, STURM, Marc, KESSLER, Christoph, WAYAND, Melanie, WILKE, Carlo, TRASCHÜTZ, Andreas, SCHÖLS, Ludger, HENGEL, Holger, HEUTINK, Peter, BRUNNER, Han, SCHEFFER, Hans, STEYAERT, Wouter, SABLAUSKAS, Karolis, DE VOER, Richarda M., KAMSTEEG, Erik-Jan, VAN DE WARRENBURG, Bart, VAN OS, Nienke, TE PASKE, Iris, JANSSEN, Erik, DE BOER, Elke, STEEHOUWER, Marloes, YALDIZ, Burcu, KLEEFSTRA, Tjitske, VEAL, Colin, GIBSON, Spencer, WADSLEY, Marc, MEHTARIZADEH, Mehdi, RIAZ, Umar, WARREN, Greg, DIZJIKAN, Farid Yavari, SHORTER, Thomas, STRAUB, Volker, BETTOLO, Chiara Marini, SPECHT, Sabine, CLAYTON-SMITH, Jill, BANKA, Siddharth, ALEXANDER, Elizabeth, JACKSON, Adam, FAIVRE, Laurence, THAUVIN, Christel, VITOBELLO, Antonio, DENOMMÉ-PICHON, Anne-Sophie, DUFFOURD, Yannis, TISSERANT, Emilie, BRUEL, Ange-Line, PEYRON, Christine, PÉLISSIER, Aurore, BELTRAN, Sergi, GUT, Ivo Glynne, LAURIE, Steven, PISCIA, Davide, MATALONGA, Leslie, PAPAKONSTANTINOU, Anastasios, BULLICH, Gemma, CORVO, Alberto, GARCIA, Carles, FERNANDEZ-CALLEJO, Marcos, HERNÁNDEZ, Carles, PICÓ, Daniel, PARAMONOV, Ida, LOCHMÜLLER, Hanns, GUMUS, Gulcin, BROS-FACER, Virginie, HANAUER, Marc, OLRY, Annie, LAGORCE, David, HAVRYLENKO, Svitlana, IZEM, Katia, RIGOUR, Fanny, STEVANIN, Giovanni, DURR, Alexandra, DAVOINE, Claire-Sophie, GUILLOT-NOEL, Léna, HEINZMANN, Anna, COARELLI, Giulia, ALLAMAND, Valérie, NELSON, Isabelle, YAOU, Rabah Ben, METAY, Corinne, EYMARD, Bruno, COHEN, Enzo, ATALAIA, Antonio, STOJKOVIC, Tanya, MACEK, Milan, TURNOVEC, Marek, THOMASOVÁ, Dana, KREMLIKOVÁ, Radka Pourová, FRANKOVÁ, Vera, HAVLOVICOVÁ, Markéta, KREMLIK, Vlastimil, PARKINSON, Helen, KEANE, Thomas, SENF, Alexander, ROBINSON, Peter, DANIS, Daniel, ROBERT, Glenn, COSTA, Alessia, PATCH, Christine, HANNA, Mike, HOULDEN, Henry, REILLY, Mary, VANDROVCOVA, Jana, MUNTONI, Francesco, ZAHARIEVA, Irina, SARKOZY, Anna, TIMMERMAN, Vincent, BAETS, Jonathan, VAN DE VONDEL, Liedewei, BEIJER, Danique, DE JONGHE, Peter, NIGRO, Vincenzo, BANFI, Sandro, TORELLA, Annalaura, MUSACCHIA, Francesco, PILUSO, Giulio, FERLINI, Alessandra, SELVATICI, Rita, ROSSI, Rachele, NERI, Marcella, ARETZ, Stefan, SPIER, Isabel, SOMMER, Anna Katharina, PETERS, Sophia, OLIVEIRA, Carla, PELAEZ, Jose Garcia, MATOS, Ana Rita, JOSÉ, Celina São, FERREIRA, Marta, GULLO, Irene, FERNANDES, Susana, GARRIDO, Luzia, FERREIRA, Pedro, CARNEIRO, Fátima, SWERTZ, Morris A., JOHANSSON, Lennart, VAN DER VELDE, Joeri K., VAN DER VRIES, Gerben, NEERINCX, Pieter B., ROELOFS-PRINS, Dieuwke, KÖHLER, Sebastian, METCALFE, Alison, VERLOES, Alain, DRUNAT, Séverine, ROORYCK, Caroline, TRIMOUILLE, Aurelien, CASTELLO, Raffaele, MORLEO, Manuela, PINELLI, Michele, VARAVALLO, Alessandra, DE LA PAZ, Manuel Posada, SÁNCHEZ, Eva Bermejo, MARTÍN, Estrella López, DELGADO, Beatriz Martínez, DE LA ROSA, F. Javier Alonso García, CIOLFI, Andrea, DALLAPICCOLA, Bruno, PIZZI, Simone, RADIO, Francesca Clementina, TARTAGLIA, Marco, RENIERI, Alessandra, BENETTI, Elisa, BALICZA, Peter, MOLNAR, Maria Judit, MAVER, Ales, PETERLIN, Borut, MÜNCHAU, Alexander, LOHMANN, Katja, HERZOG, Rebecca, PAULY, Martje, MACAYA, Alfons, MARCÉ-GRAU, Anna, OSORIO, Andres Nascimiento, DE BENITO, Daniel Natera, LOCHMÜLLER, Hanns, THOMPSON, Rachel, POLAVARAPU, Kiran, BEESON, David, COSSINS, Judith, CRUZ, Pedro M. Rodriguez, HACKMAN, Peter, JOHARI, Mridul, SAVARESE, Marco, UDD, Bjarne, HORVATH, Rita, CAPELLA, Gabriel, VALLE, Laura, HOLINSKI-FEDER, Elke, LANER, Andreas, STEINKE-LANGE, Verena, SCHRÖCK, Evelin and RUMP, Andreas (2021). Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. European Journal of Human Genetics, 29 (9), 1325-1331. [Article]

MATALONGA, Leslie, HERNÁNDEZ-FERRER, Carles, PISCIA, Davide, SCHÜLE, Rebecca, SYNOFZIK, Matthis, TÖPF, Ana, VISSERS, Lisenka E. L. M., DE VOER, Richarda, TONDA, Raul, LAURIE, Steven, FERNANDEZ-CALLEJO, Marcos, PICÓ, Daniel, GARCIA-LINARES, Carles, PAPAKONSTANTINOU, Anastasios, CORVÓ, Alberto, JOSHI, Ricky, DIEZ, Hector, GUT, Ivo, HOISCHEN, Alexander, GRAESSNER, Holm, BELTRAN, Sergi, COHEN, Enzo, CUESTA, Isabel, DANIS, Daniel, DENOMMÉ-PICHON, Anne-Sophie, DUFFOURD, Yannis, GILISSEN, Christian, JOHARI, Mridul, LI, Shuang, NELSON, Isabelle, PETERS, Sophia, PARAMONOV, Ida, PRASANTH, Sivakumar, ROBINSON, Peter, SABLAUSKAS, Karolis, SAVARESE, Marco, STEYAERT, Wouter, VAN DER VELDE, Joeri K., VITOBELLO, Antonio, ARETZ, Stefan, CAPELLA, Gabriel, DE VOER, Richarda M., EVANS, Gareth, PELAEZ, Jose Garcia, HOLINSKI-FEDER, Elke, HOOGERBRUGGE, Nicoline, LANER, Andreas, OLIVEIRA, Carla, RUMP, Andreas, SCHRÖCK, Evelin, SOMMER, Anna Katharina, STEINKE-LANGE, Verena, PASKE, Iris te, TISCHKOWITZ, Marc, VALLE, Laura, BANKA, Siddharth, BENETTI, Elisa, CASARI, Giorgio, CIOLFI, Andrea, CLAYTON-SMITH, Jill, DALLAPICCOLA, Bruno, DE BOER, Elke, DENOMMÉ-PICHON, Anne-Sophie, ELLWANGER, Kornelia, FAIVRE, Laurence, GRAESSNER, Holm, HAACK, Tobias B., HAMMARSJÖ, Anna, HAVLOVICOVA, Marketa, HOISCHEN, Alexander, HUGON, Anne, JACKSON, Adam, KLEEFSTRA, Tjitske, LINDSTRAND, Anna, LÓPEZ-MARTÍN, Estrella, MACEK, Milan, MORLEO, Manuela, NIGRO, Vicenzo, NORDGREN, Ann, PETTERSSON, Maria, PINELLI, Michele, PIZZI, Simone, POSADA, Manuel, RADIO, Francesca Clementina, RENIERI, Alessandra, ROORYCK, Caroline, RYBA, Lukas, SCHWARZ, Martin, TARTAGLIA, Marco, THAUVIN, Christel, TORELLA, Annalaura, TRIMOUILLE, Aurélien, VERLOES, Alain, VISSERS, Lisenka, VITOBELLO, Antonio, VOTYPKA, Pavel, VYSHKA, Klea, ZUREK, Birte, BAETS, Jonathan, BEIJER, Danique, BONNE, Gisèle, COSSINS, Judith, EVANGELISTA, Teresinha, FERLINI, Alessandra, HACKMAN, Peter, HANNA, Michael G., HORVATH, Rita, HOULDEN, Henry, JOHARI, Mridul, LAU, Jarred, LOCHMÜLLER, Hanns, MACKEN, William L., MUSACCHIA, Francesco, NASCIMENTO, Andres, NATERA-DE BENITO, Daniel, NIGRO, Vincenzo, PILUSO, Giulio, PINI, Veronica, PITCEATHLY, Robert D. S., POLAVARAPU, Kiran, CRUZ, Pedro M. Rodriguez, SARKOZY, Anna, SAVARESE, Marco, SELVATICI, Rita, THOMPSON, Rachel, UDD, Bjarne, VAN DE VONDEL, Liedewei, VANDROVCOVA, Jana, ZAHARIEVA, Irina, BAETS, Jonathan, BALICZA, Peter, CHINNERY, Patrick, DÜRR, Alexandra, HAACK, Tobias, HENGEL, Holger, KAMSTEEG, Erik-Jan, KAMSTEEG, Christoph, LOHMANN, Katja, MACAYA, Alfons, MARCÉ-GRAU, Anna, MAVER, Ales, MOLNAR, Judit, MÜNCHAU, Alexander, PETERLIN, Borut, RIESS, Olaf, SCHÖLS, Ludger, SCHÜLE-FREYER, Rebecca, STEVANIN, Giovanni, SYNOFZIK, Matthis, TIMMERMAN, Vincent, VAN DE WARRENBURG, Bart, VAN OS, Nienke, WAYAND, Melanie, WILKE, Carlo, GRAESSNER, Holm, OSSOWSKI, Stephan, DEMIDOV, German, STURM, Marc, SCHULZE-HENTRICH, Julia M., SCHÜLE, Rebecca, KESSLER, Christoph, HEUTINK, Peter, BRUNNER, Han, SCHEFFER, Hans, ’T HOEN, Peter A. C., SABLAUSKAS, Karolis, VAN DE WARRENBURG, Bart, TE PASKE, Iris, JANSSEN, Erik, STEEHOUWER, Marloes, YALDIZ, Burcu, BROOKES, Anthony J., VEAL, Colin, GIBSON, Spencer, WADSLEY, Marc, MEHTARIZADEH, Mehdi, RIAZ, Umar, WARREN, Greg, DIZJIKAN, Farid Yavari, SHORTER, Thomas, STRAUB, Volker, BETTOLO, Chiara Marini, SPECHT, Sabine, CLAYTON-SMITH, Jill, BANKA, Siddharth, ALEXANDER, Elizabeth, JACKSON, Adam, FAIVRE, Laurence, THAUVIN, Christel, TISSERANT, Emilie, BRUEL, Ange-Line, PEYRON, Christine, PÉLISSIER, Aurore, BELTRAN, Sergi, GUT, Ivo Glynne, LAURIE, Steven, PISCIA, Davide, MATALONGA, Leslie, PAPAKONSTANTINOU, Anastasios, BULLICH, Gemma, CORVO, Alberto, GARCIA, Carles, FERNANDEZ-CALLEJO, Marcos, HERNÁNDEZ, Carles, PICÓ, Daniel, PARAMONOV, Ida, LOCHMÜLLER, Hanns, GUMUS, Gulcin, BROS-FACER, Virginie, RATH, Ana, HANAUER, Marc, OLRY, Annie, LAGORCE, David, HAVRYLENKO, Svitlana, IZEM, Katia, RIGOUR, Fanny, DURR, Alexandra, DAVOINE, Claire-Sophie, GUILLOT-NOEL, Léna, HEINZMANN, Anna, COARELLI, Giulia, ALLAMAND, Valérie, YAOU, Rabah Ben, METAY, Corinne, EYMARD, Bruno, ATALAIA, Antonio, STOJKOVIC, Tanya, MACEK, Milan, TURNOVEC, Marek, THOMASOVÁ, Dana, KREMLIKOVÁ, Radka Pourová, FRANKOVÁ, Vera, HAVLOVICOVÁ, Markéta, KREMLIK, Vlastimil, PARKINSON, Helen, KEANE, Thomas, SPALDING, Dylan, SENF, Alexander, ROBERT, Glenn, COSTA, Alessia, PATCH, Christine, HANNA, Mike, HOULDEN, Henry, REILLY, Mary, VANDROVCOVA, Jana, MUNTONI, Francesco, VAN DE VONDEL, Liedewei, BEIJER, Danique, DE JONGHE, Peter, BANFI, Sandro, TORELLA, Annalaura, ROSSI, Rachele, NERI, Marcella, SPIER, Isabel, MATOS, Ana Rita, JOSÉ, Celina São, FERREIRA, Marta, GULLO, Irene, FERNANDES, Susana, GARRIDO, Luzia, FERREIRA, Pedro, CARNEIRO, Fátima, SWERTZ, Morris A., JOHANSSON, Lennart, VAN DER VRIES, Gerben, NEERINCX, Pieter B., ROELOFS-PRINS, Dieuwke, KÖHLER, Sebastian, METCALFE, Alison, TRIMOUILLE, Aurelien, CASTELLO, Raffaele, VARAVALLO, Alessandra, DE LA PAZ, Manuel Posada, SÁNCHEZ, Eva Bermejo, MARTÍN, Estrella López, DELGADO, Beatriz Martínez, DE LA ROSA, F. Javier Alonso García, RADIO, Francesca Clementina, BALICZA, Peter, MOLNAR, Maria Judit, MAVER, Ales, PETERLIN, Borut, MÜNCHAU, Alexander, LOHMANN, Katja, HERZOG, Rebecca, PAULY, Martje, MACAYA, Alfons, MARCÉ-GRAU, Anna, OSORIO, Andres Nascimiento, DE BENITO, Daniel Natera, LOCHMÜLLER, Hanns, THOMPSON, Rachel, POLAVARAPU, Kiran, BEESON, David, COSSINS, Judith, CRUZ, Pedro M. Rodriguez, HACKMAN, Peter, JOHARI, Mridul, SAVARESE, Marco, UDD, Bjarne, HORVATH, Rita, CAPELLA, Gabriel, VALLE, Laura, HOLINSKI-FEDER, Elke, LANER, Andreas, STEINKE-LANGE, Verena, SCHRÖCK, Evelin and RUMP, Andreas (2021). Solving patients with rare diseases through programmatic reanalysis of genome-phenome data. European Journal of Human Genetics, 29 (9), 1337-1347. [Article]

SCHÜLE, Rebecca, TIMMANN, Dagmar, ERASMUS, Corrie E., REICHBAUER, Jennifer, WAYAND, Melanie, VAN DE WARRENBURG, Bart, SCHÖLS, Ludger, WILKE, Carlo, BEVOT, Andrea, ZUCHNER, Stephan, BELTRAN, Sergi, LAURIE, Steven, MATALONGA, Leslie, GRAESSNER, Holm, SYNOFZIK, Matthis, BAETS, Jonathan, BALICZA, Peter, CHINNERY, Patrick, DÜRR, Alexandra, HAACK, Tobias, HENGEL, Holger, HORVATH, Rita, HOULDEN, Henry, KAMSTEEG, Erik-Jan, KAMSTEEG, Christoph, LOHMANN, Katja, MACAYA, Alfons, MARCÉ-GRAU, Anna, MAVER, Ales, MOLNAR, Judit, MÜNCHAU, Alexander, PETERLIN, Borut, RIESS, Olaf, SCHÖLS, Ludger, SCHÜLE, Rebecca, STEVANIN, Giovanni, SYNOFZIK, Matthis, TIMMERMAN, Vincent, VAN DE WARRENBURG, Bart, VAN OS, Nienke, VANDROVCOVA, Jana, WAYAND, Melanie, WILKE, Carlo, GRAESSNER, Holm, ZUREK, Birte, ELLWANGER, Kornelia, OSSOWSKI, Stephan, DEMIDOV, German, STURM, Marc, SCHULZE-HENTRICH, Julia M., HEUTINK, Peter, BRUNNER, Han, SCHEFFER, Hans, HOOGERBRUGGE, Nicoline, HOISCHEN, Alexander, ’T HOEN, Peter A. C., VISSERS, Lisenka E. L. M., GILISSEN, Christian, STEYAERT, Wouter, SABLAUSKAS, Karolis, DE VOER, Richarda M., JANSSEN, Erik, DE BOER, Elke, STEEHOUWER, Marloes, YALDIZ, Burcu, KLEEFSTRA, Tjitske, BROOKES, Anthony J., VEAL, Colin, GIBSON, Spencer, WADSLEY, Marc, MEHTARIZADEH, Mehdi, RIAZ, Umar, WARREN, Greg, DIZJIKAN, Farid Yavari, SHORTER, Thomas, TÖPF, Ana, STRAUB, Volker, BETTOLO, Chiara Marini, SPECHT, Sabine, CLAYTON-SMITH, Jill, BANKA, Siddharth, ALEXANDER, Elizabeth, JACKSON, Adam, FAIVRE, Laurence, THAUVIN, Christel, VITOBELLO, Antonio, DENOMMÉ-PICHON, Anne-Sophie, DUFFOURD, Yannis, TISSERANT, Emilie, BRUEL, Ange-Line, PEYRON, Christine, PÉLISSIER, Aurore, BELTRAN, Sergi, GUT, Ivo Glynne, LAURIE, Steven, PISCIA, Davide, MATALONGA, Leslie, PAPAKONSTANTINOU, Anastasios, BULLICH, Gemma, CORVO, Alberto, GARCIA, Carles, FERNANDEZ-CALLEJO, Marcos, HERNÁNDEZ, Carles, PICÓ, Daniel, PARAMONOV, Ida, LOCHMÜLLER, Hanns, GUMUS, Gulcin, BROS-FACER, Virginie, RATH, Ana, HANAUER, Marc, OLRY, Annie, LAGORCE, David, HAVRYLENKO, Svitlana, IZEM, Katia, RIGOUR, Fanny, DURR, Alexandra, DAVOINE, Claire-Sophie, GUILLOT-NOEL, Léna, HEINZMANN, Anna, COARELLI, Giulia, BONNE, Gisèle, EVANGELISTA, Teresinha, ALLAMAND, Valérie, NELSON, Isabelle, YAOU, Rabah Ben, METAY, Corinne, EYMARD, Bruno, COHEN, Enzo, ATALAIA, Antonio, STOJKOVIC, Tanya, MACEK, Milan, TURNOVEC, Marek, THOMASOVÁ, Dana, KREMLIKOVÁ, Radka Pourová, FRANKOVÁ, Vera, HAVLOVICOVÁ, Markéta, KREMLIK, Vlastimil, PARKINSON, Helen, KEANE, Thomas, SPALDING, Dylan, SENF, Alexander, ROBINSON, Peter, DANIS, Daniel, ROBERT, Glenn, COSTA, Alessia, PATCH, Christine, HANNA, Mike, HOULDEN, Henry, REILLY, Mary, VANDROVCOVA, Jana, MUNTONI, Francesco, ZAHARIEVA, Irina, SARKOZY, Anna, DE JONGHE, Peter, NIGRO, Vincenzo, BANFI, Sandro, TORELLA, Annalaura, MUSACCHIA, Francesco, PILUSO, Giulio, FERLINI, Alessandra, SELVATICI, Rita, ROSSI, Rachele, NERI, Marcella, ARETZ, Stefan, SPIER, Isabel, SOMMER, Anna Katharina, PETERS, Sophia, OLIVEIRA, Carla, PELAEZ, Jose Garcia, MATOS, Ana Rita, JOSÉ, Celina São, FERREIRA, Marta, GULLO, Irene, FERNANDES, Susana, GARRIDO, Luzia, FERREIRA, Pedro, CARNEIRO, Fátima, SWERTZ, Morris A., JOHANSSON, Lennart, VAN DER VELDE, Joeri K., VAN DER VRIES, Gerben, NEERINCX, Pieter B., ROELOFS-PRINS, Dieuwke, KÖHLER, Sebastian, METCALFE, Alison, VERLOES, Alain, DRUNAT, Séverine, ROORYCK, Caroline, TRIMOUILLE, Aurelien, CASTELLO, Raffaele, MORLEO, Manuela, PINELLI, Michele, VARAVALLO, Alessandra, DE LA PAZ, Manuel Posada, SÁNCHEZ, Eva Bermejo, MARTÍN, Estrella López, DELGADO, Beatriz Martínez, DE LA ROSA, F. Javier Alonso García, CIOLFI, Andrea, DALLAPICCOLA, Bruno, PIZZI, Simone, RADIO, Francesca Clementina, TARTAGLIA, Marco, RENIERI, Alessandra, BENETTI, Elisa, BALICZA, Peter, MOLNAR, Maria Judit, MAVER, Ales, PETERLIN, Borut, MÜNCHAU, Alexander, LOHMANN, Katja, HERZOG, Rebecca, PAULY, Martje, MACAYA, Alfons, MARCÉ-GRAU, Anna, OSORIO, Andres Nascimiento, DE BENITO, Daniel Natera, LOCHMÜLLER, Hanns, THOMPSON, Rachel, POLAVARAPU, Kiran, BEESON, David, COSSINS, Judith, CRUZ, Pedro M. Rodriguez, HACKMAN, Peter, JOHARI, Mridul, SAVARESE, Marco, UDD, Bjarne, HORVATH, Rita, CAPELLA, Gabriel, VALLE, Laura, HOLINSKI-FEDER, Elke, LANER, Andreas, STEINKE-LANGE, Verena, SCHRÖCK, Evelin and RUMP, Andreas (2021). Solving unsolved rare neurological diseases—a Solve-RD viewpoint. European Journal of Human Genetics, 29 (9), 1332-1336. [Article]

MASTERSON, Abigail, LEE, Geraldine, KHAN, Ehsan, TITCHENER, Karen, DOYLE-BLUNDEN, Janet, METCALFE, Alison, TEE, Stephen and BLISS, Miss Julie (2020). Redefining the role of the NURSE academic in practice: A PILOT STUDY. Nurse Education in Practice, p. 102750. [Article]

MACHIRORI, Mavis, PATCH, Christine and METCALFE, Alison (2019). Black and Minority Ethnic women's decision-making for risk reduction strategies after BRCA testing: Use of context and knowledge. European journal of medical genetics, 62 (5), 376-384. [Article]

GIMPEL, Charlotte, BERGMANN, Carsten, BOCKENHAUER, Detlef, BREYSEM, Luc, CADNAPAPHORNCHAI, Melissa A, CETINER, Metin, DUDLEY, Jan, EMMA, Francesco, KONRAD, Martin, HARRIS, Tess, HARRIS, Peter C, KÖNIG, Jens, LIEBAU, Max C, MARLAIS, Matko, MEKAHLI, Djalila, METCALFE, Alison, OH, Jun, PERRONE, Ronald D, SINHA, Manish D, TITIENI, Andrea, TORRA, Roser, WEBER, Stefanie, WINYARD, Paul JD and SCHAEFER, Franz (2019). International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people. Nature Reviews Nephrology. [Article]

EFSTATHIOU, Nikolaos, WALKER, Wendy, METCALFE, Alison and VANDERSPANK-WRIGHT, Brandi (2018). The state of bereavement support in adult intensive care: A systematic review and narrative synthesis. Journal of critical care, 50, 177-187. [Article]

GOLDMAN, Amy, METCALFE, Alison and MACLEOD, Rhona (2018). The process of disclosure: Mothers' experiences of communicating X-Linked carrier risk information to at-risk daughters. Journal of genetic counseling, 27 (5), 1265-1274. [Article]

MENDES, Álvaro, METCALFE, Alison, PANEQUE, Milena, SOUSA, Liliana, CLARKE, Angus J. and SEQUEIROS, Jorge (2018). Communication of information about genetic risks: putting families at the center. Family Process, 57 (3), 836-846. [Article]

JACKSON, Jennifer, GETTINGS, Sheryl and METCALFE, Alison (2018). “The power of Twitter”: using social media at a conference with nursing students. Nurse Education Today, 68, 188-191. [Article]

VETSCH, Janine, WAKEFIELD, Claire E, WARBY, Meera, TUCKER, Katherine, PATTERSON, Pandora, MCGILL, Brittany C, METCALFE, Alison, COHN, Richard J and FARDELL, Joanna E (2018). Cancer-Related Genetic Testing and Personalized Medicine for Adolescents: A narrative review of impact and understanding. Journal of Adolescent and Young Adult Oncology, 7 (3). [Article]

MACHIRORI, Mavis, PATCH, Christine and METCALFE, Alison (2018). Study of the relationship between Black men, culture and prostate cancer beliefs. Cogent Medicine, 5, p. 1442636. [Article]

METCALFE, Alison (2018). Sharing Genetic Risk Information: Implications for family nurses across the life span. Journal of Family Nursing, 24 (1), 86-105. [Article]

OAKLEY, Catherine, TAYLOR, Cath, REAM, Emma and METCALFE, Alison (2016). Avoidant conversations about death by clinicians causes delays in reporting of neutropenic sepsis: Grounded theory study. Psycho-Oncology, 26 (10), 1505-1512. [Article]

EISLER, Ivan, FLINTER, Frances, GREY, Jo, HUTCHISON, Suzanne, JACKSON, Carole, LONGWORTH, Louise, MACLEOD, Rhona, MCALLISTER, Marion, METCALFE, Alison, PATCH, Christine, COPE, Buddug, ROBERT, Glenn Brian, ROWLAND, Emma and ULPH, Fiona (2016). Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their views and experience of facilitating multi-family discussion groups. Journal of Genetic Counseling, 26 (2), 199-214. [Article]

ROWLAND, Emma, PLUMRIDGE, Gill, CONSIDINE, Anne-Marie and METCALFE, Alison (2016). Preparing young people for future decision-making about cancer risk in families affected or at risk from hereditary breast cancer: A qualitative interview study. European Journal of Oncology Nursing, 25, 9-15. [Article]

WALDBOTH, Veronika, PATCH, Christine, MAHRER-IMHOF, Romy and METCALFE, Alison (2016). Living a normal life in an extraordinary way: A systematic review investigating experiences of families of young people's transition into adulthood when affected by a genetic and chronic childhood condition. International Journal of Nursing Studies, 62, 44-59. [Article]

CHUDLEIGH, Jane, BUCKINGHAM, Sarah, DIGNAN, Jo, O'DRISCOLL, Sandra, JOHNSON, Kemi, REES, David, WYATT, Hilary and METCALFE, Alison (2016). Parents' Experiences of Receiving the Initial Positive Newborn Screening (NBS) Result for Cystic Fibrosis and Sickle Cell Disease. Journal of Genetic Counseling, 25 (6), 1215-1226. [Article]

EISLER, Ivan, ELLISON, Matthew, FLINTER, Frances, GREY, Jo, HUTCHISON, Suzanne, JACKSON, Carole, LONGWORTH, Louise, MACLEOD, Rhona, MCALLISTER, Marion, METCALFE, Alison, MURRELLS, Trevor John, PATCH, Christine, PRITCHARD, Stuart, ROBERT, Glenn Brian, ROWLAND, Emma Janette and ULPH, Fiona (2015). Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery. European Journal of Human Genetics, 24, 794-802. [Article]

DHEENSA, Sandi, METCALFE, Alison and WILLIAMS, Robert (2015). What do men want from antenatal screening? Findings from an interview study in England. Midwifery, 31 (1), 208-214. [Article]

ROWLAND, Emma and METCALFE, Alison (2014). A systematic review of men's experiences of their partner's mastectomy: coping with altered bodies. Psycho-Oncology, 23 (9), 963-974. [Article]

NEWINGTON, Lisa and METCALFE, Alison (2014). Researchers' and clinicians' perceptions of recruiting participants to clinical research: a thematic meta-synthesis. Journal of Clinical Medicine Research, 6 (3), 162-172. [Article]

NEWINGTON, Lisa and METCALFE, Alison (2014). Factors influencing recruitment to research: qualitative study of the experiences and perceptions of research teams. BMC Medical Research Methodology, 14, p. 10. [Article]

ROWLAND, E. and METCALFE, Alison (2013). Communicating inherited genetic risk between parent and child: A meta-thematic synthesis. International Journal of Nursing Studies, 50 (6), 870-880. [Article]

DHEENSA, Sandi, METCALFE, Alison and WILLIAMS, Robert Alan (2013). Men's experiences of antenatal screening: A metasynthesis of the qualitative research. International Journal of Nursing Studies, 50 (1), 121-133. [Article]

BENCH, Suzanne, DAY, Tina and METCALFE, Alison (2013). Randomised controlled trials: an introduction for nurse researchers. Nurse Researcher, 20 (5), 38-44. [Article]

DHEENSA, Sandi, WILLIAMS, Bob and METCALFE, Alison (2013). Shattered Schemata and Fragmented Identities: Men's experiences of antenatal genetic screening in Great Britain. Journal of Family Issues, 34 (8), 1081-1103. [Article]

PLUMRIDGE, G., METCALFE, Alison, COAD, J. and GILL, P. (2012). The role of support groups in facilitating families in coping with a genetic condition and in discussion of genetic risk information. Health expectations : an international journal of public participation in health care and health policy, Health expectations : an international journal of public participation in health care and health policy, 15 (3), 255-266. [Article]

ALBADA, Akke, WERRETT, Julie, VAN DULMEN, Sandra, BENSING, Jozien, CHAPMAN, C, AUSEMS, MG and METCALFE, Alison (2011). Breast cancer genetic counselling referrals: how comparable are the findings between the UK and the Netherlands? Journal of Community Genetics, 2 (4), 233-247. [Article]

WILLIAMS, Robert Alan, DHEENSA, Sandi and METCALFE, Alison (2011). Men's involvement in antenatal screening: A qualitative pilot study using email. Midwifery, 27 (6), 861-866. [Article]

METCALFE, Alison and CLIFFORD, Collette (2011). Response to Ingleton C & Green E (2010) Commentary on Metcalfe A, Pumphrey R & Clifford C (2009) Hospice nurses' and genetics: implications for end-of-life care. Journal of Clinical Nursing 19, 192-207. Journal Of Clinical Nursing, 20 (23-24), 3584-3586. [Article]

LILLIE, A.K., CLIFFORD, C. and METCALFE, Alison (2011). Caring for families with a family history of cancer: why concerns about genetic predisposition are missing from the palliative agenda. Palliative Medicine, 25 (2), 117-124. [Article]

PLUMRIDGE, Gillian, METCALFE, Alison, COAD, Jane and GILL, Paramjit (2011). Parents' Communication with Siblings of Children Affected by an Inherited Genetic Condition. Journal of Genetic Counseling, 20 (4), 374-383. [Article]

METCALFE, Alison, PLUMRIDGE, Gill, COAD, Jane, SHANKS, Andrew and GILL, Paramjit (2011). Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiences. European Journal of Human Genetics, 19 (6), 640-646. [Article]

PLUMRIDGE, G., METCALFE, Alison, COAD, J. and GILL, Paramjit (2010). Family communication about genetic risk information: Particular issues for Duchenne muscular dystrophy. American Journal of Medical Genetics. Part A, 152A (5), 1225-1232. [Article]

MATHERS, J, GREENFIELD, S, METCALFE, Alison, COLE, T, FLANANGAN, S and WILSON, S (2010). Family history in primary care: understanding GPs' resistance to clinical genetics - qualitative study. British Journal of General Practice (BJGP), 60 (574), 221-230. [Article]

METCALFE, Alison, PUMPHREY, R. and CLIFFORD, C. (2010). Hospice nurses and genetics: Implications for end-of-life care. Journal Of Clinical Nursing, 19 (1-2), 192-207. [Article]

METCALFE, Alison, WERRETT, J., BURGESS, L., CHAPMAN, C. and CLIFFORD, C. (2009). Cancer genetic predisposition: information needs of patients irrespective of risk level. Familial Cancer, 8 (4), 403-412. [Article]

METCALFE, Alison, PUMPHREY, R. and CLIFFORD, C. (2009). Children affected by genetic conditions in end-of-life care. Part 2: findings and discussion. International journal of Palliative Nursing, 15 (1), 22-28. [Article]

METCALFE, Alison, WILSON, Sue, MCCAHON, Deborah, SLEIGHTHOLME, Helen, GILL, Paramjit and COLE, Trevor (2009). Integrating genetic risk assessment for multi-factorial conditions into primary care. Primary Health Care Research and Development, 10 (03), 200-209. [Article]

COAD, J., PLUMRIDGE, G. and METCALFE, Alison (2009). Involving children and young people in the development of art-based research tools. Nurse Researcher, 16 (4), 56-64. [Article]

METCALFE, Alison, PUMPHREY, R. and CLIFFORD, C. (2008). Children affected by genetic conditions in end-of-life care. Part 1: Development of a study. International Journal of Palliative Nursing, 14 (12), 596-601. [Article]

METCALFE, Alison, COAD, J., PLUMRIDGE, G.M., GILL, P. and FARNDON, P. (2008). Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research. European Journal of Human Genetics, 16 (10), 1193-1200. [Article]

METCALFE, Alison, HAYDON, Jo, BENNETT, Catherine and FARNDON, Peter (2008). Midwives' views of the importance of genetics and their confidence with genetic activities in clinical practice: implications for the delivery of genetics education. Journal Of Clinical Nursing, 17 (4), 519-530. [Article]