المؤلفون: Iles, Mark M, Bishop, D Timothy, Taylor, John C, Hayward, Nicholas K, Brossard, Myriam, Cust, Anne E, Dunning, Alison M, Lee, Jeffrey E, Moses, Eric K, Akslen, Lars A, AMFS Investigators, Andresen, Per A, Avril, Marie-Françoise, Azizi, Esther, Scarrà, Giovanna Bianchi, Brown, Kevin M, Dębniak, Tadeusz, Elder, David E, Friedman, Eitan, Ghiorzo, Paola, Gillanders, Elizabeth M, Goldstein, Alisa M, Gruis, Nelleke A, Hansson, Johan, Harland, Mark, Helsing, Per, Hočevar, Marko, Höiom, Veronica, IBD investigators, Ingvar, Christian, Kanetsky, Peter A, Landi, Maria Teresa, Lang, Julie, Lathrop, G Mark, Lubiński, Jan, Mackie, Rona M, Martin, Nicholas G, Molven, Anders, Montgomery, Grant W, Novaković, Srdjan, Olsson, Håkan, Puig, Susana, Puig-Butille, Joan Anton, QMEGA and QTWIN Investigators, Radford-Smith, Graham L, Randerson-Moor, Juliette, SDH Study Group, van der Stoep, Nienke, van Doorn, Remco, Whiteman, David C, MacGregor, Stuart, Pooley, Karen A, Ward, Sarah V, Mann, Graham J, Amos, Christopher I, Pharoah, Paul DP, Demenais, Florence, Law, Matthew H, Newton Bishop, Julia A, Barrett, Jennifer H, GenoMEL Consortium

مصطلحات موضوعية: Australia, Confounding Factors, Epidemiologic, DNA Helicases, Europe, Germ-Line Mutation, Humans, Israel, Melanoma, Polymorphism, Single Nucleotide, Predictive Value of Tests, RNA, Research Design, Ribonucleoproteins, Skin Neoplasms, Telomerase, Telomere, Telomere-Binding Proteins, United States, Zinc Fingers

وصف الملف: application/pdf

العلاقة: https://www.repository.cam.ac.uk/handle/1810/245855Test

الإتاحة: https://www.repository.cam.ac.uk/handle/1810/245855Test

المؤلفون: Barrett, Jennifer H, Iles, Mark M, Harland, Mark, Taylor, John C, Aitken, Joanne F, Andresen, Per Arne, Akslen, Lars A, Armstrong, Bruce K, Avril, Marie-Francoise, Azizi, Esther, Bakker, Bert, Bergman, Wilma, Bianchi-Scarrà, Giovanna, Bressac-de Paillerets, Brigitte, Calista, Donato, Cannon-Albright, Lisa A, Corda, Eve, Cust, Anne E, Dębniak, Tadeusz, Duffy, David, Dunning, Alison M, Easton, Douglas F, Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Giles, Graham G, Hansson, Johan, Hocevar, Marko, Höiom, Veronica, Hopper, John L, Ingvar, Christian, Janssen, Bart, Jenkins, Mark A, Jönsson, Göran, Kefford, Richard F, Landi, Giorgio, Landi, Maria Teresa, Lang, Julie, Lubiński, Jan, Mackie, Rona, Malvehy, Josep, Martin, Nicholas G, Molven, Anders, Montgomery, Grant W, van Nieuwpoort, Frans A, Novakovic, Srdjan, Olsson, Håkan, Pastorino, Lorenza, Puig, Susana, Puig-Butille, Joan Anton, Randerson-Moor, Juliette, Snowden, Helen, Tuominen, Rainer, Van Belle, Patricia, van der Stoep, Nienke, Whiteman, David C, Zelenika, Diana, Han, Jiali, Fang, Shenying, Lee, Jeffrey E, Wei, Qingyi, Lathrop, G Mark, Gillanders, Elizabeth M, Brown, Kevin M, Goldstein, Alisa M, Kanetsky, Peter A, Mann, Graham J, Macgregor, Stuart, Elder, David E, Amos, Christopher I, Hayward, Nicholas K, Gruis, Nelleke A, Demenais, Florence, Bishop, Julia A Newton, Bishop, D Timothy, GenoMEL Consortium

مصطلحات موضوعية: GenoMEL Consortium, Humans, Melanoma, Skin Neoplasms, Genetic Predisposition to Disease, Case-Control Studies, Polymorphism, Single Nucleotide, Genome-Wide Association Study

وصف الملف: application/pdf

العلاقة: Nature genetics; ng.959; https://hdl.handle.net/10161/17972Test

الإتاحة: https://hdl.handle.net/10161/17972Test

المؤلفون: Macgregor, Stuart, Montgomery, Grant W, Liu, Jimmy Z, Zhao, Zhen Zhen, Henders, Anjali K, Stark, Mitchell, Schmid, Helen, Holland, Elizabeth A, Duffy, David L, Zhang, Mingfeng, Painter, Jodie N, Nyholt, Dale R, Maskiell, Judith A, Jetann, Jodie, Ferguson, Megan, Cust, Anne E, Jenkins, Mark A, Whiteman, David C, Olsson, Håkan, Puig, Susana, Bianchi-Scarrà, Giovanna, Hansson, Johan, Demenais, Florence, Landi, Maria Teresa, Dębniak, Tadeusz, Mackie, Rona, Azizi, Esther, Bressac-de Paillerets, Brigitte, Goldstein, Alisa M, Kanetsky, Peter A, Gruis, Nelleke A, Elder, David E, Newton-Bishop, Julia A, Bishop, D Timothy, Iles, Mark M, Helsing, Per, Amos, Christopher I, Wei, Qingyi, Wang, Li-E, Lee, Jeffrey E, Qureshi, Abrar A, Kefford, Richard F, Giles, Graham G, Armstrong, Bruce K, Aitken, Joanne F, Han, Jiali, Hopper, John L, Trent, Jeffrey M, Brown, Kevin M, Martin, Nicholas G, Mann, Graham J, Hayward, Nicholas K

مصطلحات موضوعية: Chromosomes, Human, Pair 1, Humans, Melanoma, Polymorphism, Single Nucleotide, Genome-Wide Association Study

وصف الملف: application/pdf

العلاقة: Nature genetics; ng.958; https://hdl.handle.net/10161/17974Test

الإتاحة: https://hdl.handle.net/10161/17974Test

المؤلفون: Pellegrini, Cristina, Botta, Francesca, Massi, Daniela, Martorelli, Claudia, Facchetti, Fabio, Gandini, Sara, Maisonneuve, Patrick, Avril, Marie-Françoise, Demenais, Florence, Bressac-de Paillerets, Brigitte, Hoiom, Veronica, Cust, Anne E, Anton-Culver, Hoda, Gruber, Stephen B, Gallagher, Richard P, Marrett, Loraine, Zanetti, Roberto, Dwyer, Terence, Thomas, Nancy E, Begg, Colin B, Berwick, Marianne, Puig, Susana, Potrony, Miriam, Nagore, Eduardo, Ghiorzo, Paola, Menin, Chiara, Manganoni, Ausilia Maria, Rodolfo, Monica, Brugnara, Sonia, Passoni, Emanuela, Sekulovic, Lidija Kandolf, Baldini, Federica, Guida, Gabriella, Stratigos, Alexandros, Ozdemir, Fezal, Ayala, Fabrizio, Fernandez-de-Misa, Ricardo, Quaglino, Pietro, Ribas, Gloria, Romanini, Antonella, Migliano, Emilia, Stanganelli, Ignazio, Kanetsky, Peter A, Pizzichetta, Maria Antonietta, García-Borrón, Jose Carlos, Nan, Hongmei, Landi, Maria Teresa, Little, Julian, Newton-Bishop, Julia, Sera, Francesco, Fargnoli, Maria Concetta, Raimondi, Sara, Alaibac, Mauro, Ferrari, Andrea, Valeri, Barbara, Sicher, Mariacristina, Mangiola, Daniela, Nazzaro, Gianluca, Tosti, Giulio, Mazzarol, Giovanni, Giudice, Giuseppe, Ribero, Simone, Astrua, Chiara, Mazzoni, Laura, Orlow, Irene, Mujumdar, Urvi, Hummer, Amanda, Busam, Klaus, Roy, Pampa, Canchola, Rebecca, Clas, Brian, Cotignola, Javiar, Monroe, Yvette, Armstrong, Bruce, Kricker, Anne, Litchfield, Melisa, Tucker, Paul, Stephens, Nicola, Switzer, Teresa, Theis, Beth, From, Lynn, Chowdhury, Noori, Vanasse, Louise, Purdue, Mark, Northrup, David, Rosso, Stefano, Sacerdote, Carlotta, Leighton, Nancy, Gildea, Maureen, Bonner, Joe, Jeter, Joanne, Klotz, Judith, Wilcox, Homer, Weiss, Helen, Millikan, Robert, Mattingly, Dianne, Player, Jon, Tse, Chiu-Kit, Rebbeck, Timothy, Walker, Amy, Panossian, Saarene, Setlow, Richard, Mohrenweiser, Harvey, Autier, Philippe, Han, Jiali, Caini, Saverio, Hofman, Albert, Kayser, Manfred, Liu, Fan, Nijsten, Tamar, Uitterlinden, Andre G., Kumar, Rajiv, Bishop, Tim, Elliott, Faye, Lazovich, Deann, Polsky, David, Hansson, Johan, Pastorino, Lorenza, Gruis, Nelleke A., Bouwes Bavinck, Jan Nico, Aguilera, Paula, Badenas, Celia, Carrera, Cristina, Gimenez-Xavier, Pol, Malvehy, Josep, Puig-Butille, Joan Anton, Tell-Marti, Gemma, Blizzard, Leigh, Cochrane, Jennifer, Branicki, Wojciech, Debniak, Tadeusz, Morling, Niels, Johansen, Peter, Mayne, Susan, Bale, Allen, Cartmel, Brenda, Ferrucci, Leah, Pfeiffer, Ruth, Palmieri, Giuseppe, Kypreou, Katerina, Bowcock, Anne, Cornelius, Lynn, Council, M. Laurin, Motokawa, Tomonori, Anno, Sumiko, Helsing, Per, Andresen, Per Arne, Guida, Stefania, Wong, Collaborators (98): Alaibac M, Terence H., Ferrari, A, Valeri, B, Et, Al.

المساهمون: Pellegrini, C., Botta, F., Massi, D., Martorelli, C., Facchetti, F., Gandini, S., Maisonneuve, P., Avril, M. -F., Demenais, F., Bressac-de Paillerets, B., Hoiom, V., Cust, A. E., Anton-Culver, H., Gruber, S. B., Gallagher, R. P., Marrett, L., Zanetti, R., Dwyer, T., Thomas, N. E., Begg, C. B., Berwick, M., Puig, S., Potrony, M., Nagore, E., Ghiorzo, P., Menin, C., Manganoni, A. M., Rodolfo, M., Brugnara, S., Passoni, E., Sekulovic, L. K., Baldini, F., Guida, G., Stratigos, A., Ozdemir, F., Ayala, F., Fernandez-de-Misa, R., Quaglino, P., Ribas, G., Romanini, A., Migliano, E., Stanganelli, I., Kanetsky, P. A., Pizzichetta, M. A., Garcia-Borron, J. C., Nan, H., Landi, M. T., Little, J., Newton-Bishop, J., Sera, F., Fargnoli, M. C., Raimondi, S., Alaibac, M., Ferrari, A., Valeri, B., Sicher, M., Mangiola, D., Nazzaro, G., Tosti, G., Mazzarol, G., Giudice, G., Ribero, S., Astrua, C., Mazzoni, L., Orlow, I., Mujumdar, U., Hummer, A., Busam, K., Roy, P., Canchola, R., Clas, B., Cotignola, J., Monroe, Y., Armstrong, B., Kricker, A., Litchfield, M., Tucker, P., Stephens, N., Switzer, T., Theis, B., From, L., Chowdhury, N., Vanasse, L., Purdue, M., Northrup, D., Rosso, S., Sacerdote, C., Leighton, N., Gildea, M., Bonner, J., Jeter, J., Klotz, J., Wilcox, H., Weiss, H., Millikan, R., Mattingly, D., Player, J., Tse, C. -K., Rebbeck, T., Walker, A., Panossian, S., Setlow, R., Mohrenweiser, H., Autier, P., Han, J., Caini, S., Hofman, A., Kayser, M., Liu, F., Nijsten, T., Uitterlinden, A. G., Kumar, R., Bishop, T., Elliott, F., Lazovich, D., Polsky, D., Hansson, J., Pastorino, L., Gruis, N. A., Bouwes Bavinck, J. N., Aguilera, P., Badenas, C., Carrera, C., Gimenez-Xavier, P., Malvehy, J., Puig-Butille, J. A., Tell-Marti, G., Blizzard, L., Cochrane, J., Branicki, W., Debniak, T., Morling, N., Johansen, P., Mayne, S., Bale, A., Cartmel, B., Ferrucci, L., Pfeiffer, R., Palmieri, G., Kypreou, K., Bowcock, A., Cornelius, L., Council, M. L., Motokawa, T., Anno, S., Helsing, P., Andresen, P. A., Guida, S., Wong, T. H., Ege Üniversitesi, Epidemiology, Genetic Identification, Dermatology

المصدر: Lancet Child & Adolescent Health
LANCET CHILD & ADOLESCENT HEALTH
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
Lancet Child & Adolescent Health, 3(5), 332-342. Elsevier
The Lancet. Child & adolescent health, vol 3, iss 5
Lancet Child Adolesc Health

مصطلحات موضوعية: Male, Skin Neoplasms, Pediatrics, Cohort Studies, 0302 clinical medicine, Odds Ratio, Developmental and Educational Psychology, Pediatrics, Perinatology and Child Health, 030212 general & internal medicine, Child, Cancer, Pediatric, Tumor, childhood disease, Middle Aged, Perinatology and Child Health, cohort analysis, Meta-analysis, Melanocortin, Cohort, Female, MC1R gene, Receptor, Melanocortin, Type 1, Receptor, Type 1, Cohort study, Adult, medicine.medical_specialty, adolescent, melanoma, cohort analysi, Subgroup analysis, Article, 03 medical and health sciences, Genetic, Clinical Research, 030225 pediatrics, Internal medicine, Genetics, Biomarkers, Tumor, medicine, Humans, Genetic Predisposition to Disease, Polymorphism, Germ-Line Mutation, Aged, Retrospective Studies, Polymorphism, Genetic, business.industry, Prevention, Case-control study, Retrospective cohort study, GEM Study Group, Odds ratio, Logistic Models, M-SKIP Study Group, Case-Control Studies, Cutaneous melanoma, IMI Study Group, business, Biomarkers

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4be7fb7756edb069e5b275b25e38ef3cTest
https://researchonline.lshtm.ac.uk/id/eprint/4652504/1/Sera_etal_2019_mc1r_variants_childhood_adolescent_melanoma.pdfTest

المؤلفون: Law, Matthew H, Bishop, D Timothy, Lee, Jeffrey E, Brossard, Myriam, Martin, Nicholas G, Moses, Eric K, Song, Fengju, Barrett, Jennifer H, Kumar, Rajiv, Easton, Douglas F, Pharoah, Paul DP, Swerdlow, Anthony J, Kypreou, Katerina P, Taylor, John C, Harland, Mark, Randerson-Moor, Juliette, Akslen, Lars A, Andresen, Per A, Avril, Marie-Françoise, Azizi, Esther, Scarrà, Giovanna Bianchi, Brown, Kevin M, Dębniak, Tadeusz, Duffy, David L, Elder, David E, Fang, Shenying, Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Gillanders, Elizabeth M, Goldstein, Alisa M, Gruis, Nelleke A, Hansson, Johan, Helsing, Per, Hočevar, Marko, Höiom, Veronica, Ingvar, Christian, Kanetsky, Peter A, Chen, Wei V, GenoMEL Consortium, Essen-Heidelberg Investigators, SDH Study Group, Q-MEGA and QTWIN Investigators, AMFS Investigators, ATHENS Melanoma Study Group, Landi, Maria Teresa, Lang, Julie, Lathrop, G Mark, Lubiński, Jan, Mackie, Rona M, Mann, Graham J, Molven, Anders, Montgomery, Grant W, Novaković, Srdjan, Olsson, Håkan, Puig, Susana, Puig-Butille, Joan Anton, Qureshi, Abrar A, Radford-Smith, Graham L, van der Stoep, Nienke, van Doorn, Remco, Whiteman, David C, Craig, Jamie E, Schadendorf, Dirk, Simms, Lisa A, Burdon, Kathryn P, Nyholt, Dale R, Pooley, Karen A, Orr, Nick, Stratigos, Alexander J, Cust, Anne E, Ward, Sarah V, Hayward, Nicholas K, Han, Jiali, Schulze, Hans-Joachim, Dunning, Alison M, Bishop, Julia A Newton, Demenais, Florence, Amos, Christopher I, MacGregor, Stuart, Iles, Mark M

مصطلحات موضوعية: Case-Control Studies, Chromosomes, Human, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Melanoma, Polymorphism, Single Nucleotide, Skin Neoplasms, Cutaneous Malignant

وصف الملف: application/pdf

العلاقة: https://www.repository.cam.ac.uk/handle/1810/251343Test

الإتاحة: https://www.repository.cam.ac.uk/handle/1810/251343Test

المؤلفون: Pasquali, Elena, García Borrón, José C., Fargnoli, Maria Concetta, Gandini, Sara, Maisonneuve, Patrick, Bagnardi, Vincenzo, Specchia, Claudia, Liu, Fan, Kayser, Manfred, Nijsten, Tamar, Nagore, Eduardo, Kumar, Rajiv, Hansson, Johan, Kanetsky, Peter A., Ghiorzo, Paola, Debniak, Tadeusz, Branicki, Wojciech, Gruis, Nelleke A., Han, Jiali, Dwyer, Terry, Blizzard, Leigh, Landi, Maria Teresa, Palmieri, Giuseppe, Ribas, Gloria, Stratigos, Alexander, Council, M. Laurin, Autier, Philippe, Little, Julian, Newton Bishop, Julia, Sera, Francesco, Raimondi, Sara, Caini, Saverio, Hofman, Albert, Uitterlinden, Andre G., Scherer, Dominique, Hoiom, Veronica, Pastorino, Lorenza, Cochrane, Jennifer, Fernandez De Misa, Ricardo, Morling, Niels, Johansen, Peter, Pfeiffer, Ruth, Kypreou, Katerina, Bowcock, Anne, Cornelius, Lynn, Motokawa, Tomonori, Anno, Sumiko, Helsing, Per, Andresen, Per Arne, Wong, Terence H.

المساهمون: International Prevention Research Institute (IPRI), Strathclyde Institute of Global Public Health at iPRI (SIGPH@iPRI), Pasquali, E, García Borrón, J, Fargnoli, M, Gandini, S, Maisonneuve, P, Bagnardi, V, Specchia, C, Liu, F, Kayser, M, Nijsten, T, Nagore, E, Kumar, R, Hansson, J, Kanetsky, P, Ghiorzo, P, Debniak, T, Branicki, W, Gruis, N, Han, J, Dwyer, T, Blizzard, L, Landi, M, Palmieri, G, Ribas, G, Stratigos, A, Council, M, Autier, P, Little, J, Newton Bishop, J, Sera, F, Raimondi, S, Caini, S, Hofman, A, Uitterlinden, A, Scherer, D, Hoiom, V, Pastorino, L, Cochrane, J, Fernandez De Misa, R, Morling, N, Johansen, P, Pfeiffer, R, Kypreou, K, Bowcock, A, Cornelius, L, Motokawa, T, Anno, S, Helsing, P, Andresen, P, Wong, T, Genetic Identification, Dermatology

المصدر: International Journal of Cancer
International Journal of Cancer, Wiley, 2015, 136 (3), pp.618-31. ⟨10.1002/ijc.29018⟩
INTERNATIONAL JOURNAL OF CANCER
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
International Journal of Cancer, 136(3), 618-631
International journal of cancer (Online) 136 (2015): 618–31. doi:10.1002/ijc.29018
info:cnr-pdr/source/autori:Pasquali, Elena; Garcia-Borron, Jose C; Fargnoli, Maria Concetta; Gandini, Sara; Maisonneuve, Patrick; Bagnardi, Vincenzo; Specchia, Claudia; Liu, Fan; Kayser, Manfred; Nijsten, Tamar; Nagore, Eduardo; Kumar, Rajiv; Hansson, Johan; Kanetsky, Peter A; Ghiorzo, Paola; Debniak, Tadeusz; Branicki, Wojciech; Gruis, Nelleke A; Han, Jiali; Dwyer, Terry; Blizzard, Leigh; Landi, Maria Teresa; Palmieri, Giuseppe; Ribas, Gloria; Stratigos, Alexander; Council, M Laurin; Autier, Philippe; Little, Julian; Newton-Bishop, Julia; Sera, Francesco; Raimondi, Sara/titolo:MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: A pooled-analysis from the M-SKIP project./doi:10.1002%2Fijc.29018/rivista:International journal of cancer (Online)/anno:2015/pagina_da:618/pagina_a:31/intervallo_pagine:618–31/volume:136
International Journal of Cancer, 136(3), 618-631. Wiley-Liss Inc.

مصطلحات موضوعية: Risk, Cancer Research, genetic epidemiology, Skin Neoplasms, European Continental Ancestry Group, Skin Pigmentation, Type 1/*genetics Risk Skin Neoplasms/etiology/*genetics Skin Pigmentation genetic epidemiology melanocortin-1 receptor melanoma meta-analysis, Article, White People, SDG 3 - Good Health and Well-being, Melanocortin-1 receptor, European Continental Ancestry Group *Genetic Predisposition to Disease Humans Melanoma/etiology/*genetics Middle Aged Phenotype Receptor, melanoma, Humans, Genetic epidemiology, Meta-analysi, Genetic Predisposition to Disease, Melanoma, melanocortin-1 receptor, Middle Aged, meta-analysis, Phenotype, Oncology, Melanocortin, Meta-analysis, Receptor, Melanocortin, Type 1, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Receptor, Type 1

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3fbe2d51774a677533fee3c6a23fa444Test
https://hal.archives-ouvertes.fr/hal-01262211Test

المؤلفون: Ramus, Susan J, Kartsonaki, Christiana, Gayther, Simon A, Pharoah, Paul D P, Sinilnikova, Olga M, Beesley, Jonathan, Chen, Xiaoqing, McGuffog, Lesley, Healey, Sue, Couch, Fergus J, Wang, Xianshu, Fredericksen, Zachary, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Roversi, Gaia, Barile, Monica, Viel, Alessandra, Allavena, Anna, Ottini, Laura, Papi, Laura, Gismondi, Viviana, Capra, Fabio, Radice, Paolo, Greene, Mark H, Mai, Phuong L, Andrulis, Irene L, Glendon, Gord, Ozcelik, Hilmi, Thomassen, Mads, Gerdes, Anne-Marie, Kruse, Torben A, Cruger, Dorthe, Jensen, Uffe Birk, Caligo, Maria Adelaide, Olsson, Håkan, Kristoffersson, Ulf, Lindblom, Annika, Arver, Brita, Karlsson, Per, Stenmark Askmalm, Marie, Borg, Ake, Neuhausen, Susan L, Ding, Yuan Chun, Nathanson, Katherine L, Domchek, Susan M, Jakubowska, Anna, Lubiński, Jan, Huzarski, Tomasz, Byrski, Tomasz, Gronwald, Jacek, Górski, Bohdan, Cybulski, Cezary, Dębniak, Tadeusz, Osorio, Ana, Durán, Mercedes, Tejada, Maria-Isabel, Benítez, Javier, Hamann, Ute, Rookus, Matti A, Verhoef, Senno, Tilanus-Linthorst, Madeleine A, Vreeswijk, Maaike P, Bodmer, Danielle, Ausems, Margreet G E M, van Os, Theo A, Asperen, Christi J, Blok, Marinus J, Meijers-Heijboer, Hanne E J, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Dunning, Alison M, Evans, D Gareth, Eeles, Ros, Pichert, Gabriella, Cole, Trevor, Hodgson, Shirley, Brewer, Carole, Morrison, Patrick J, Porteous, Mary, Kennedy, M John, Rogers, Mark T, Side, Lucy E, Donaldson, Alan, Gregory, Helen, Godwin, Andrew, Stoppa-Lyonnet, Dominique, Moncoutier, Virginie, Castera, Laurent, Mazoyer, Sylvie, Barjhoux, Laure, Bonadona, Valérie, Leroux, Dominique, Faivre, Laurence, Lidereau, Rosette, Nogues, Catherine, Bignon, Yves-Jean, Prieur, Fabienne, Collonge-Rame, Marie-Agnès, Venat-Bouvet, Laurence, Fert-Ferrer, Sandra, Miron, Alex, Buys, Saundra S, Hopper, John L, Daly, Mary B, John, Esther M, Terry, Mary Beth, Goldgar, David, Hansen, Thomas v O, Jønson, Lars, Ejlertsen, Bent, Agnarsson, Bjarni A, Offit, Kenneth, Kirchhoff, Tomas, Vijai, Joseph, Dutra-Clarke, Ana V C, Przybylo, Jennifer A, Montagna, Marco, Casella, Cinzia, Imyanitov, Evgeny N, Janavicius, Ramunas, Blanco, Ignacio, Lázaro, Conxi, Moysich, Kirsten B, Karlan, Beth Y, Gross, Jenny, Beattie, Mary S, Schmutzler, Rita, Wappenschmidt, Barbara, Meindl, Alfons, Ruehl, Ina, Fiebig, Britta, Sutter, Christian, Arnold, Norbert, Deissler, Helmut, Varon-Mateeva, Raymonda, Kast, Karin, Niederacher, Dieter, Gadzicki, Dorothea, Caldes, Trinidad, de la Hoya, Miguel, Nevanlinna, Heli, Aittomäki, Kristiina, Simard, Jacques, Soucy, Penny, Spurdle, Amanda B, Holland, Helene, Chenevix-Trench, Georgia, Easton, Douglas F, Antoniou, Antonis C

المساهمون: Department of Gynaecological Oncology, UCL EGA Institute for Women's Health, University College London, London, UK. sramus@usc.edu

مصطلحات موضوعية: Adult, Aged, 80 and over, Alleles, Chromosomes, Human, Pair 9, Female, Genes, BRCA1, BRCA2, Genotype, Germ-Line Mutation, Heterozygote, Humans, Likelihood Functions, Middle Aged, Odds Ratio, Ovarian Neoplasms, Polymorphism, Single Nucleotide, Retrospective Studies, Risk Factors

العلاقة: http://dx.doi.org/10.1093/jnci/djq494Test; J. Natl. Cancer Inst. 2011, 103(2):105-16; http://hdl.handle.net/2336/227832Test; Journal of the National Cancer Institute

الإتاحة: https://doi.org/10.1093/jnci/djq494Test
http://hdl.handle.net/2336/227832Test

المؤلفون: Raimondi, Sara, Gandini, Sara, Fargnoli, Maria Concetta, Bagnardi, Vincenzo, Maisonneuve, Patrick, Specchia, Claudia, Kumar, Rajiv, Nagore, Eduardo, Han, Jiali, Hansson, Johan, Kanetsky, Peter A., Ghiorzo, Paola, Gruis, Nelleke A., Dwyer, Terry, Blizzard, Leigh, Fernandez-De-Misa, Ricardo, Branicki, Wojciech, Debniak, Tadeusz, Morling, Niels, Landi, Maria Teresa, Palmieri, Giuseppe, Ribas, Gloria, Stratigos, Alexander, Cornelius, Lynn, Motokawa, Tomonori, Anno, Sumiko, Helsing, Per, Wong, Terence H., Autier, Philippe, García-Borrón, José C., Little, Julian, Newton-Bishop, Julia, Sera, Francesco, Liu, Fan, Kayser, Manfred, Nijsten, Tamar

المساهمون: Genetic Identification, Dermatology, International Prevention Research Institute (IPRI), Raimondi, S, Gandini, S, Fargnoli, M, Bagnardi, V, Maisonneuve, P, Specchia, C, Kumar, R, Nagore, E, Han, J, Hansson, J, Kanetsky, P, Ghiorzo, P, Gruis, N, Dwyer, T, Blizzard, L, Fernandez de Misa, R, Branicki, W, Debniak, T, Morling, N, Landi, M, Palmieri, G, Ribas, G, Stratigos, A, Cornelius, L, Motokawa, T, Anno, S, Helsing, P, Wong, T, Autier, P, García Borrón, J, Little, J, Newton Bishop, J, Sera, F, Liu, F, Kayser, M, Nijsten, T, Study Group, G

المصدر: BMC Medical Research Methodology, 12
BMC Medical research methodology (Online) 12 (2012): 1–13. doi:10.1186/1471-2288-12-116
info:cnr-pdr/source/autori:Raimondi, Sara; Raimondi, Sara; Gandini, Sara; Fargnoli, Maria Concetta; Bagnardi, Vincenzo; Bagnardi, Vincenzo; Maisonneuve, Patrick; Specchia, Claudia; Kumar, Rajiv; Nagore, Eduardo; Han, Jiali; Han, Jiali; Han, Jiali; Hansson, Johan; Kanetsky, Peter A.; Ghiorzo, Paola; Gruis, Nelleke A.; Dwyer, Terry; Blizzard, Leigh; Fernandez-De-Misa, Ricardo; Branicki, Wojciech; Debniak, Tadeusz; Morling, Niels; Landi, Maria Teresa; Palmieri, Giuseppe; Ribas, Gloria; Stratigos, Alexander; Cornelius, Lynn; Motokawa, Tomonori; Anno, Sumiko; Helsing, Per; Wong, Terence H.; Autier, Philippe; García-Borrón, José C.; Little, Julian; Newton-Bishop, Julia; Sera, Francesco; Liu, Fan; Kayser, Manfred; Nijsten, Tamar/titolo:Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: Study design and methods for pooling results of genetic epidemiological studies/doi:10.1186%2F1471-2288-12-116/rivista:BMC Medical research methodology (Online)/anno:2012/pagina_da:1/pagina_a:13/intervallo_pagine:1–13/volume:12
BMC Medical Research Methodology, 12. BioMed Central Ltd.
BMC Medical Research Methodology
BMC Medical Research Methodology, BioMed Central, 2012, 12, pp.116. ⟨10.1186/1471-2288-12-116⟩
BMC Medical Research Methodology, Vol 12, Iss 1, p 116 (2012)

مصطلحات موضوعية: Male, Skin Neoplasms, Standardization, Epidemiology, Pooling, Disease, Bioinformatics, Logistic regression, Study Protocol, 0302 clinical medicine, Statistical Analysis Plan, Adult Case-Control Studies Data Collection/standards Data Interpretation, Skin cancer, Genetic epidemiology, Statistical *Epidemiologic Research Design Female *Genetic Predisposition to Disease Hospitalization Humans Logistic Models Male Meta-Analysis as Topic Phenotype *Receptor, Melanoma, lcsh:R5-920, 0303 health sciences, Data Collection, Smoking, Pooled-analysis, 3. Good health, Hospitalization, Phenotype, 030220 oncology & carcinogenesis, Meta-analysis, Data Interpretation, Statistical, Genetic epidemiology, Melanoma, Meta-analysis, Pooled-analysis, Skin cancer, Study design, Melanocortin, Sunlight, Female, lcsh:Medicine (General), Receptor, Melanocortin, Type 1, Adult, Health Informatics, Computational biology, 03 medical and health sciences, Meta-Analysis as Topic, SDG 3 - Good Health and Well-being, medicine, Humans, Genetic Predisposition to Disease, MED/01 - STATISTICA MEDICA, 030304 developmental biology, business.industry, Study design, medicine.disease, Logistic Models, Case-Control Studies, Epidemiologic Research Design, Type 1 Skin Neoplasms/*genetics/physiopathology/secondary Smoking Sunlight/*adverse effects, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::065f519f0b33d73c755a7653d17b59c6Test
https://hdl.handle.net/1887/106313Test

المؤلفون: Fargnoli, Maria Concetta, Peris, Ketty

المساهمون: Landi, Maria Teresa, Bishop, D Timothy, MacGregor, Stuart, Machiela, Mitchell J, Stratigos, Alexander J, Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Choi, Jiyeon, Fargnoli, Maria Concetta, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J, Menin, Chiara, Martinez, Jacobo, Hadjisavvas, Andrea, Song, Lei, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Goldstein, Alisa M, Potrony, Miriam, Kypreou, Katerina P, Pastorino, Lorenza, Queirolo, Paola, Pellegrini, Cristina, Cattaneo, Laura, Zawistowski, Matthew, Gimenez-Xavier, Pol, Rodriguez, Arantxa, Elefanti, Lisa, Manoukian, Siranoush, Rivoltini, Licia, Smith, Blair H, Loizidou, Maria A, Del Regno, Laura, Massi, Daniela, Mandala, Mario, Khosrotehrani, Kiarash, Akslen, Lars A, Amos, Christopher I, Andresen, Per A, Avril, Marie-Françoise, Azizi, Esther, Soyer, H Peter, Bataille, Veronique, Dalmasso, Bruna, Bowdler, Lisa M, Burdon, Kathryn P, Chen, Wei V, Codd, Veryan, Craig, Jamie E, Dębniak, Tadeusz, Falchi, Mario, Fang, Shenying, Friedman, Eitan, Simi, Sarah, Galan, Pilar, Garcia-Casado, Zaida, Gillanders, Elizabeth M, Gordon, Scott, Green, Adele, Gruis, Nelleke A, Hansson, Johan, Harland, Mark, Harris, Jessica, Helsing, Per, Henders, Anjali, Hočevar, Marko, Höiom, Veronica, Hunter, David, Ingvar, Christian, Kumar, Rajiv, Lang, Julie, Lathrop, G Mark, Lee, Jeffrey E, Li, Xin, Lubiński, Jan, Mackie, Rona M, Malt, Maryrose, Malvehy, Josep, McAloney, Kerrie, Mohamdi, Hamida, Molven, Ander, Moses, Eric K, Neale, Rachel E, Novaković, Srdjan, Nyholt, Dale R, Olsson, Håkan, Orr, Nichola, Fritsche, Lars G, Puig-Butille, Joan Anton, Qureshi, Abrar A, Radford-Smith, Graham L, Randerson-Moor, Juliette, Requena, Celia, Rowe, Casey, Samani, Nilesh J, Sanna, Marianna, Schadendorf, Dirk

مصطلحات موضوعية: Female, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Male, Melanoma, Phenotype, Pigmentation, Polymorphism, Single Nucleotide, Skin Neoplasms, Settore MED/35 - MALATTIE CUTANEE E VENEREE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32341527; info:eu-repo/semantics/altIdentifier/wos/WOS:000529000400001; volume:52; issue:5; firstpage:494-504; lastpage:504; issueyear:2020; journal:NATURE GENETICS; http://hdl.handle.net/10807/167440Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85084007486

الإتاحة: https://doi.org/10.1038/s41588-020-0611-8Test
http://hdl.handle.net/10807/167440Test