المؤلفون: Casula M., Paliogiannis P., Ayala F., De Giorgi V., Stanganelli I., Mandala M., Colombino M., Manca A., Sini M. C., Caraco C., Ascierto P. A., Satta R. R., Dedola M. F., Denti S., Fedeli M. A., Montesu M. A., Profili S., Scotto T., Sini G., Tanda F., Lissia A., Cossu A., Palmieri G., Ghiorzo P., Queirolo P., Quaglino P., Botti G., Sileni V. C., Di Giacomo A. M.

المساهمون: Casula, M., Paliogiannis, P., Ayala, F., De Giorgi, V., Stanganelli, I., Mandala, M., Colombino, M., Manca, A., Sini, M. C., Caraco, C., Ascierto, P. A., Satta, R. R., Dedola, M. F., Denti, S., Fedeli, M. A., Montesu, M. A., Profili, S., Scotto, T., Sini, G., Tanda, F., Lissia, A., Cossu, A., Palmieri, G., Ghiorzo, P., Queirolo, P., Quaglino, P., Botti, G., Sileni, V. C., Di Giacomo, A. M.

مصطلحات موضوعية: BRAF, Cancer, CDKN2A, Melanoma, Mutation, NGS, Skin, Adult, Aged, Carcinogenesi, Cyclin-Dependent Kinase Inhibitor p16, Female, Follow-Up Studie, Gene Amplification, Gene Frequency, Genetic Loci, Genetic Predisposition to Disease, Germ-Line Mutation, Human, Italy, Male, Middle Aged, Neoplasms, Multiple Primary, Skin Neoplasm, Tumor Suppressor Protein, Ubiquitin Thiolesterase, High-Throughput Nucleotide Sequencing

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31382929; info:eu-repo/semantics/altIdentifier/wos/WOS:000479241800002; volume:19; issue:1; firstpage:772; journal:BMC CANCER; http://hdl.handle.net/11365/1119639Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85070388191

الإتاحة: https://doi.org/10.1186/s12885-019-5984-7Test
http://hdl.handle.net/11365/1119639Test

المؤلفون: Gu, F, Chen, T-H, Pfeiffer, RM, Fargnoli, MC, Calista, D, Ghiorzo, P, Peris, K, Puig, S, Menin, C, De Nicolo, A, Rodolfo, M, Pellegrini, C, Pastorino, L, Evangelou, E, Zhang, T, Hua, X, DellaValle, CT, Timothy Bishop, D, MacGregor, S, Iles, MI, Law, MH, Cust, A, Brown, KM, Stratigos, AJ, Nagore, E, Chanock, S, Shi, J, Melanoma Meta-Analysis Consortium, MelaNostrum Consortium, Landi, MT

المصدر: 4156 ; 4145

مصطلحات موضوعية: Adult, Aged, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Italy, Male, Melanoma, Middle Aged, Multifactorial Inheritance, Nevus, Polymorphism, Single Nucleotide, Risk Assessment, Risk Factors, Skin Neoplasms, 06 Biological Sciences, 11 Medical and Health Sciences, Genetics & Heredity

جغرافية الموضوع: England

العلاقة: Human Molecular Genetics; http://hdl.handle.net/10044/1/62321Test; https://dx.doi.org/10.1093/hmg/ddy282Test

الإتاحة: https://doi.org/10.1093/hmg/ddy282Test
http://hdl.handle.net/10044/1/62321Test

المؤلفون: Taylor, N.J., Handorf, E.A., Mitra, N., Avril, M.F., Azizi, E., Bergman, W., Bianchi-Scarra, G., Bishop, D.T., Bressac-de Paillerets, B., Calista, D., Cannon-Albright, L.A., Cuellar, F., Cust, A.E., Demenais, F., Elder, D.E., Friedman, E., Gerdes, A.M., Ghiorzo, P., Goldstein, A.M., Grazziotin, T.C., Hansson, J., Hayward, N.K., Hocevar, M., Hoiom, V., Holland, E.A., Ingvar, C., Landi, M.T., Landman, G., Larre-Borges, A., Leachman, S.A., Mann, G.J., Nagore, E., Olsson, H., Palmer, J., Peric, B., Pjanova, D., Puig, S., Schmid, H., Stoep, N. van der, Tucker, M.A., Wadt, K.A.W., Whitaker, L., Yang, X.H.R., Bishop, J.A.N., Gruis, N.A., Kanetsky, P.A., GenoMEL Consortium

المصدر: Journal of Investigative Dermatology, 136(5), 1066-1069

مصطلحات موضوعية: Oncology, Adult, Male, CDKN2A Mutation, medicine.medical_specialty, Skin Neoplasms, Databases, Factual, Dermatology, Bioinformatics, Biochemistry, Risk Assessment, Article, Cohort Studies, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Molecular Biology, 2708, Cell Biology, CDKN2A, Internal medicine, medicine, Cyclin-Dependent Kinase Inhibitor p18, Humans, Genetic Predisposition to Disease, Melanoma, Cyclin-Dependent Kinase Inhibitor p16, Aged, business.industry, Incidence, Biopsy, Needle, Middle Aged, medicine.disease, Prognosis, Phenotype, Immunohistochemistry, Pedigree, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Mutation, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b97c3aa949b208844356c914f8333ed9Test
https://hdl.handle.net/1887/112521Test

المؤلفون: Ghiorzo, P., Pensotti, V., Fornarini, G., Sciallero, S., Battistuzzi, L., Belli, F., BONELLI, Luigi Salvatore, Borgonovo, G., Bruno, W., Gozza, A., Gargiulo, S., Mastracci, L., Nasti, S., PALMIERI, GIOVANNI, Papadia, F., Pastorino, L., Russo, A., Savarino, V., Varesco, L., Bernard, L., Bianchi Scarrà, G.

المساهمون: Ghiorzo, P.*, Pensotti, V., Fornarini, G., Sciallero, S., Battistuzzi, L., Belli, F., Bonelli, L., Borgonovo, G., Bruno, W., Gozza, A., Gargiulo, S., Mastracci, L., Nasti, S., Palmieri, G., Papadia, F., Pastorino, L., Russo, A., Savarino, V., Varesco, L., Bernard, L., Bianchi Scarrà, G.

مصطلحات موضوعية: BRCA, Germline mutation, Hereditary breast ovarian cancer syndrome (HBOC), PALB2, Pancreatic cancer susceptibility, Adenocarcinoma, Adult, Aged, 80 and over, BRCA1 Protein, BRCA2 Protein, Breast Neoplasm, Case-Control Studie, Fanconi Anemia Complementation Group N Protein, Female, Genetic Predisposition to Disease, Germ-Line Mutation, Human, Italy, Male, Middle Aged, Nuclear Protein, Ovarian Neoplasm, Pancreatic Neoplasm, Pedigree, Tumor Suppressor Protein, Gene Deletion, Genetic, Oncology, Genetics (clinical)

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21989927; info:eu-repo/semantics/altIdentifier/wos/WOS:000301508300007; volume:11; issue:1; firstpage:41; lastpage:47; numberofpages:7; journal:FAMILIAL CANCER; http://hdl.handle.net/10447/291851Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84858293392

الإتاحة: https://doi.org/10.1007/s10689-011-9483-5Test
http://hdl.handle.net/10447/291851Test

المؤلفون: Pastorino L., BONELLI, Loredana, Ghiorzo P., Queirolo P., Battistuzzi L., Balleari E., NASTI, Simona, Gargiulo S., Gliori S., Savoia P., Abate Osella S., Bernengo M. G., Bianchi Scarra G.

المساهمون: Pastorino, L., Bonelli, Loredana, Ghiorzo, P., Queirolo, P., Battistuzzi, L., Balleari, E., Nasti, Simona, Gargiulo, S., Gliori, S., Savoia, P., Abate Osella, S., Bernengo, M. G., Bianchi Scarra, G.

مصطلحات موضوعية: CDKN2A, Familial melanoma, Germline mutation, MC1R, Multiple melanoma, Adolescent, Adult, Aged, 80 and over, Cyclin-Dependent Kinase 4, Cyclin-Dependent Kinase Inhibitor p16, Female, Genetic Variation, Germ-Line Mutation, Human, Male, Melanoma, Middle Aged, Receptor, Melanocortin, Type 1, Risk Factor, Skin Neoplasm, Young Adult

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/18983535; info:eu-repo/semantics/altIdentifier/wos/WOS:000261079800013; volume:21; issue:6; firstpage:700; lastpage:709; numberofpages:10; journal:PIGMENT CELL & MELANOMA RESEARCH; http://hdl.handle.net/11579/105208Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-56249147495

الإتاحة: https://doi.org/10.1111/j.1755-148X.2008.00512.xTest
http://hdl.handle.net/11579/105208Test

المؤلفون: Zebary, A., Omholt, K., Doorn, R. van, Ghiorzo, P., Harbst, K., Johansson, C.H., Hoiom, V., Jonsson, G., Pjanova, D., Puig, S., Scarra, G.B., Harland, M., Olsson, H., Brage, S.E., Palmer, J., Kanter-Lewensohn, L., Vassilaki, I., Hayward, N.K., Newton-Bishop, J., Gruis, N.A., Hansson, J., Melanoma Genetics Consortium GenoM

المصدر: Journal of Investigative Dermatology
Journal of Investigative Dermatology, 134(1), 287-290

مصطلحات موضوعية: Adult, Male, Proto-Oncogene Proteins B-raf, Neuroblastoma RAS viral oncogene homolog, Skin Neoplasms, Adolescent, Somatic cell, Dermatology, Biochemistry, Germline, GTP Phosphohydrolases, Young Adult, Germline mutation, CDKN2A, Humans, Medicine, Young adult, Melanoma, Molecular Biology, Cyclin-Dependent Kinase Inhibitor p16, Germ-Line Mutation, Aged, Aged, 80 and over, business.industry, Membrane Proteins, Cell Biology, Middle Aged, Cancer research, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e138464d40dad058a05ba18766d1dd3Test
https://hdl.handle.net/1887/103912Test

المؤلفون: Kerstann, Kf, Bradford, Pt, Steighner, R, Calista, D, Fargnoli, Mc, Peris, Ketty, Scaini, Mc, Menin, C, Ghiorzo, P, Bianchi Scarra', G, Goldstein, Am, Landi, Mt

المساهمون: Kerstann, Kf, Bradford, Pt, Steighner, R, Calista, D, Fargnoli, Mc, Peris, Ketty, Scaini, Mc, Menin, C, Ghiorzo, P, Bianchi Scarra', G, Goldstein, Am, Landi, Mt

مصطلحات موضوعية: Family, Genes, p16, Genetic Linkage, Adolescent, Adult, Aged, 80 and over, Cyclin-Dependent Kinase 4, DNA, Neoplasm, Female, Genetic Predisposition to Disease, Humans, Incidence, Italy, Male, Melanoma, Middle Aged, Odds Ratio, Polymerase Chain Reaction, Young Adult, Settore MED/35 - MALATTIE CUTANEE E VENEREE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/18628440; volume:17; issue:7; firstpage:1838; lastpage:1840; numberofpages:3; issueyear:2008; journal:CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION; http://hdl.handle.net/10807/57526Test

الإتاحة: https://doi.org/10.1158/1055-9965.EPI-08-0264Test
http://hdl.handle.net/10807/57526Test

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: Fargnoli M. C., Peris K.

المساهمون: Kim, J., Luo, W., Wang, M., Wegman-Ostrosky, T., Frone, M. N., Johnston, J. J., Nickerson, M. L., Rotunno, M., Li, S. A., Achatz, M. I., Brodie, S. A., Dean, M., De Andrade, K. C., Fortes, F. P., Gianferante, M., Khincha, P., Mcmaster, M. L., Mcreynolds, L. J., Pemov, A., Pinheiro, M., Santiago, K. M., Alter, B. P., Caporaso, N. E., Gadalla, S. M., Goldin, L. R., Greene, M. H., Loud, J., Yang, X. R., Freedman, N. D., Gapstur, S. M., Gaudet, M. M., Calista, D., Ghiorzo, P., Fargnoli, Maria Concetta, Nagore, E., Peris, Ketty, Puig, S., Landi, M. T., Hicks, B., Zhu, B., Liu, J., Sampson, J. N., Chanock, S. J., Mirabello, L. J., Morton, L. M., Biesecker, L. G., Tucker, M. A., Savage, S. A., Goldstein, A. M., Stewart, D. R.

مصطلحات موضوعية: ACMG secondary findings, Familial cancer exome, Population study, Variant classification, Aged, Cohort Studies, DNA Mutational Analysis, Ethnic Groups, Female, Genes, Neoplasm, Humans, Male, Neoplasms, Genetic Predisposition to Disease, Mutation, Polymorphism, Single Nucleotide, Settore MED/35 - MALATTIE CUTANEE E VENEREE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30583724; info:eu-repo/semantics/altIdentifier/wos/WOS:000454254400001; volume:10; issue:1; firstpage:99; lastpage:N/A; issueyear:2018; journal:GENOME MEDICINE; http://hdl.handle.net/10807/167432Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85058913898

الإتاحة: https://doi.org/10.1186/s13073-018-0607-5Test
http://hdl.handle.net/10807/167432Test

المؤلفون: Peris, Ketty

المساهمون: Bodelon, C, Pfeiffer, Rm, Bollati, V, Debbache, J, Calista, D, Ghiorzo, P, Fargnoli, Mc, Bianchi Scarra, G, Peris, Ketty, Hoxha, M, Hutchinson, A, Burdette, L, Burke, L, Fang, S, Tucker, Ma, Goldstein, Am, Lee, Je, Wei, Q, Savage, Sa, Yang, Xr, Amos, C, Landi, Mt

مصطلحات موضوعية: Adolescent, Adult, Aged, Case-Control Studies, Disease Progression, Dysplastic Nevus Syndrome, Environmental Exposure, Female, Genetic Predisposition to Disease, Humans, Male, Melanoma, Middle Aged, Nevus, Pigmentation, Polymorphism, Single Nucleotide, Risk Factors, Skin Neoplasms, Sunlight, Telomere, Young Adult, Settore MED/35 - MALATTIE CUTANEE E VENEREE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23300679; info:eu-repo/semantics/altIdentifier/wos/WOS:000312829100052; volume:7; issue:12; firstpage:e52466; lastpage:e52466; issueyear:2012; journal:PLOS ONE; http://hdl.handle.net/10807/56390Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84871668613

الإتاحة: https://doi.org/10.1371/journal.pone.0052466Test
http://hdl.handle.net/10807/56390Test