المؤلفون: Deuker M., Stolzenbach L. F., Pecoraro A., Rosiello G., Luzzago S., Tian Z., Saad F., Chun F. K. -H., Karakiewicz P. I.

المساهمون: M. Deuker, L.F. Stolzenbach, A. Pecoraro, G. Rosiello, S. Luzzago, Z. Tian, F. Saad, F.K.-. Chun, P.I. Karakiewicz

مصطلحات موضوعية: AANHPI, AAPI, Native Hawaiian, NHOPI, Pacific Islander, Prostate cancer survival, Racial disparitie, SEER, Aged, Asian American, Censuse, European Continental Ancestry Group, Human, Male, Middle Aged, Neoplasm Grading, Neoplasm Staging, Prognosi, Prostate-Specific Antigen, Prostatic Neoplasm, Retrospective Studie, United States, Settore MED/24 - Urologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32458094; info:eu-repo/semantics/altIdentifier/wos/WOS:000553590000001; volume:39; issue:3; firstpage:787; lastpage:796; numberofpages:10; journal:WORLD JOURNAL OF UROLOGY; http://hdl.handle.net/2434/881545Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085510373

الإتاحة: https://doi.org/10.1007/s00345-020-03242-8Test
http://hdl.handle.net/2434/881545Test

المؤلفون: Labreche, K, Kinnersley, B, Berzero, G, Di Stefano, AL, Rahimian, A, Detrait, I, Marie, Y, Grenier-Boley, B, Hoang-Xuan, K, Delattre, J-Y, Idbaih, A, Houlston, RS, Sanson, M

المساهمون: Kinnersley, Benjamin, Houlston, Richard

مصطلحات موضوعية: Chromosomes, Human, Pair 1, Pair 19, Humans, Glioma, Brain Neoplasms, Genetic Predisposition to Disease, Isocitrate Dehydrogenase, Telomerase, Proto-Oncogene Proteins c-myc, RNA, Messenger, Case-Control Studies, Mutation, Polymorphism, Single Nucleotide, European Continental Ancestry Group, Stathmin, Promoter Regions, Genetic, Genetic Loci, Genetic Association Studies, Preliminary Data

وصف الملف: Print-Electronic; 755; application/pdf

العلاقة: Acta neuropathologica, 2018, 135 (5), pp. 743 - 755; https://repository.icr.ac.uk/handle/internal/1624Test

الإتاحة: https://doi.org/10.1007/s00401-018-1825-zTest
https://repository.icr.ac.uk/handle/internal/1624Test

المؤلفون: Liu, Fan, Duffy, David L., Hysi, Pirro G., Jacobs, Leonie C., Lao, Oscar, Zhong, Kaiyin, Walsh, Susan, Chaitanya, Lakshmi, Wollstein, Andreas, Zhu, Gu, Montgomery, Grant W., Henders, Anjali K., Mangino, Massimo, Glass, Daniel, Bataille, Veronique, Sturm, Richard A., Rivadeneira, Fernando, Hofman, Albert, van IJcken, Wilfred F. J., Uitterlinden, André G., Palstra, Robert‑Jan T. S., Spector, Timothy D.

المساهمون: Department of Biology, School of Science

المصدر: PMC

مصطلحات موضوعية: Agouti Signaling Protein -- genetics, Antigens, Neoplasm -- genetics, Chromosomes, Human -- genetics, European Continental Ancestry Group -- genetics, Guanine Nucleotide Exchange Factors -- genetics, Interferon Regulatory Factors -- genetics, Membrane Transport Proteins -- genetics, Polymorphism, Single Nucleotide

وصف الملف: application/pdf

العلاقة: Human Genetics; Liu, F., Visser, M., Duffy, D. L., Hysi, P. G., Jacobs, L. C., Lao, O., … Kayser, M. (2015). Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. Human Genetics, 134(8), 823–835. http://doi.org/10.1007/s00439-015-1559-0Test; https://hdl.handle.net/1805/8073Test

الإتاحة: https://doi.org/10.1007/s00439-015-1559-0Test
https://hdl.handle.net/1805/8073Test

المؤلفون: Duca L., Nava I., Tavazzi D., Marcon A., Motta I., Graziadei G.

المساهمون: L. Duca, I. Nava, D. Tavazzi, A. Marcon, I. Motta, G. Graziadei

مصطلحات موضوعية: epidemiology, favism, G6PD deficiency, G6PD mutation, G6PD variant, hemolytic anemia, adolescent, adult, Africa South of the Sahara, aged, allele, Asian Continental Ancestry Group, child, preschool, China, emigrants and immigrant, European Continental Ancestry Group, female, gene frequency, genetic variation, genotype, glucosephosphate dehydrogenase, glucosephosphate dehydrogenase deficiency, human, Italy, male, Mediterranean region, middle aged, retrospective studie, young adult

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34533603; info:eu-repo/semantics/altIdentifier/wos/WOS:000696807400002; volume:100; issue:11; firstpage:2683; lastpage:2688; numberofpages:6; journal:ANNALS OF HEMATOLOGY; http://hdl.handle.net/2434/879270Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85115055126

الإتاحة: https://doi.org/10.1007/s00277-021-04630-9Test
http://hdl.handle.net/2434/879270Test

المؤلفون: Pastor-Barriuso, Roberto, Ascunce, Nieves, Ederra, María, Erdozáin, Nieves, Murillo, Alberto, Alés-Martínez, Jose Enrique, Pollan-Santamaria, Marina

المساهمون: Eli Lilly

مصطلحات موضوعية: European Continental Ancestry Group, Models, Statistical, Risk, Age Factors, Breast Neoplasms, Cohort Studies, Female, Humans, Incidence, Neoplasm Invasiveness, Population Surveillance, Proportional Hazards Models, Spain

العلاقة: Publisher's version; https://doi.org/10.1007/s10549-013-2428-yTest; info:eu_repo/grantAgreement/ES/EV1 1082/08; Breast Cancer Res Treat . 2013 Feb;138(1):249-59.; http://hdl.handle.net/20.500.12105/10265Test; Breast cancer research and treatment

الإتاحة: https://doi.org/20.500.12105/10265Test
https://doi.org/10.1007/s10549-013-2428-yTest
https://hdl.handle.net/20.500.12105/10265Test

المؤلفون: Pierre I. Karakiewicz, Emanuele Montanari, Angela Pecoraro, Stefano Luzzago, Alberto Briganti, Sophie Knipper, Zhe Tian, Shahrokh F. Shariat, Sebastiano Nazzani, Giuseppe Rosiello, Carlotta Palumbo, Fred Saad, Ottavio De Cobelli, Gennaro Musi

المساهمون: Luzzago, S., Palumbo, C., Rosiello, G., Knipper, S., Pecoraro, A., Nazzani, S., Tian, Z., Musi, G., Montanari, E., Shariat, S. F., Saad, F., Briganti, A., de Cobelli, O., Karakiewicz, P. I.

مصطلحات موضوعية: Male, Cancer Research, medicine.medical_specialty, medicine.medical_treatment, Metastatic renal cell carcinoma, European Continental Ancestry Group, Hispanic, Caucasian, Kidney, Gastroenterology, White People, 03 medical and health sciences, 0302 clinical medicine, Renal cell carcinoma, Cytoreductive nephrectomy, Internal medicine, Epidemiology, medicine, Humans, 030212 general & internal medicine, Neoplasm Metastasis, Survival rate, Carcinoma, Renal Cell, Cancer staging, Aged, Proportional Hazards Models, African-American, African Americans, Systemic therapy, Proportional hazards model, business.industry, Combination chemotherapy, Hispanic or Latino, Middle Aged, medicine.disease, Nephrectomy, Kidney Neoplasms, Cancer registry, Black or African American, Survival Rate, Oncology, Italy, 030220 oncology & carcinogenesis, Female, Hispanic Americans, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::938c490eba4603337536bf299fd123c4Test

المؤلفون: Adhikari, K., Mendoza-Revilla, J., Sohail, A., Fuentes-Guajardo, M., Lampert, J., Chacón-Duque, J.C., Hurtado, M., Villegas, V., Granja, V., Acuña-Alonzo, V., Jaramillo, C., Arias, W., Lozano, R.B., Everardo, P., Gómez-Valdés, J., Villamil-Ramírez, H., Silva de Cerqueira, C.C., Hunemeier, T., Ramallo, V., Schuler-Faccini, L., Salzano, F.M., Gonzalez-José, R., Bortolini, M.-C., Canizales-Quinteros, S., Gallo, C., Poletti, G., Bedoya, G., Rothhammer, F., Tobin, D.J., Fumagalli, M., Balding, D., Ruiz-Linares, A.

مصطلحات موضوعية: allele, Alleles, amino acid substitution, Article, Asian continental ancestry group, binding site, Biological Evolution, carrier protein, Caucasian, chromosome 1q, chromosome 20q, chromosome 22q, controlled study, convergent evolution, epistasis, Genetic, ethnic group, Ethnic Groups, European Continental Ancestry Group, evolution, exon, eye color, female, gene expression, gene frequency, gene linkage disequilibrium, gene locus, genetic association, genetics, Population

العلاقة: urn:issn:2041-1723; https://hdl.handle.net/20.500.12866/7500Test; https://doi.org/10.1038/s41467-018-08147-0Test

الإتاحة: https://doi.org/20.500.12866/7500Test
https://doi.org/10.1038/s41467-018-08147-0Test
https://hdl.handle.net/20.500.12866/7500Test

المؤلفون: Anna C. Need, Katri Räikkönen, Edythe D. London, Jari Lahti, Aiden Corvin, Antony Payton, Russell A. Poldrack, Nikolaos Smyrnis, Matthew C. Keller, Ian J. Deary, Aarno Palotie, Deborah K. Attix, Srdjan Djurovic, Elisabeth Widen, John M. Starr, Fred W. Sabb, Kjetil Sundet, Stella G. Giakoumaki, David C. Liewald, Daniel R. Weinberger, Neil Pendleton, Panos Bitsios, Jin Yu, Ole A. Andreassen, Bettina Konte, Alex Hatzimanolis, William E R Ollier, Johan G. Eriksson, Ina Giegling, Emma Knowles, Dwight Dickinson, Elizabeth T. Cirulli, David C. Glahn, Nelson A. Freimer, Panos Roussos, Aristotle N. Voineskos, Thomas Espeseth, Joey W. Trampush, Dan E. Arking, Gary Davies, Nicholas C. Stefanis, Dan Rujescu, Derek W. Morris, Gary Donohoe, Vidar M. Steen, S. Le Hellard, Anil K. Malhotra, Astri J. Lundervold, Todd Lencz, Ornit Chiba-Falek, Andrea Christoforou, Matthew A. Scult, Emily Drabant Conley, Michael A Horan, Ingrid Melle, M. Gill, Robert M. Bilder, Katherine E. Burdick, Ivar Reinvang, M. L. Z. Yang, Eliza Congdon, Tyrone D. Cannon, Richard E. Straub, Pamela DeRosse, Ahmad R. Hariri, Dimitrios Avramopoulos

المساهمون: Medicum, Behavioural Sciences, Institute for Molecular Medicine Finland, Elisabeth Ingrid Maria Widen / Principal Investigator, Clinicum, Aarno Palotie / Principal Investigator, Department of Medical and Clinical Genetics, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Helsinki Collegium for Advanced Studies, Developmental Psychology Research Group, Genomics of Neurological and Neuropsychiatric Disorders, Genomic Discoveries and Clinical Translation

المصدر: Molecular Psychiatry
Trampush, J W, Zhan Yang, M L, Knowles, E, Davies, G, Liewald, D, Starr, J, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, Derosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N B, Cannon, T D, London, E, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I, Glahn, D C, Malhotra, A K & Lencz, T 2017, ' GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function : A report from the COGENT consortium ', Molecular Psychiatry, vol. 22, pp. 336-345 . https://doi.org/10.1038/mp.2016.244Test
Molecular psychiatry, vol 22, iss 3
Trampush, J W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, D C, Starr, J M, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, DeRosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N A, Cannon, T D, London, E D, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I J, Glahn, D C, Malhotra, A K & Lencz, T 2017, ' GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function : a report from the COGENT consortium ', Molecular psychiatry, vol. 22, no. 3, pp. 336-345 . https://doi.org/10.1038/mp.2016.244Test, https://doi.org/10.1038/mp.2016.244Test
Molecular psychiatry, vol 22, iss 11

مصطلحات موضوعية: 0301 basic medicine, Male, Multifactorial Inheritance, Genome-wide association study, Cathie Marsh Institute, Medical and Health Sciences, 3124 Neurology and psychiatry, 0302 clinical medicine, Cognition, Gene Frequency, 2.1 Biological and endogenous factors, provides insights, Aetiology, Genetics, Psychiatry, scottish mental survey, 11 Medical And Health Sciences, Single Nucleotide, Biological Sciences, Middle Aged, educational-attainment, developmental delay, Psychiatry and Mental health, uk biobank n=112151, Mental Health, intellectual disability, Female, Psychology, Corrigendum, Biotechnology, Adult, ability, 515 Psychology, human intelligence, European Continental Ancestry Group, Neurocognitive Disorders, Single-nucleotide polymorphism, Basic Behavioral and Social Science, Polymorphism, Single Nucleotide, White People, 17 Psychology And Cognitive Sciences, 03 medical and health sciences, Cellular and Molecular Neuroscience, Clinical Research, Behavioral and Social Science, Journal Article, SNP, Humans, Genetic Predisposition to Disease, Allele, Polymorphism, Molecular Biology, Allele frequency, Alleles, Genetic Association Studies, Genetic association, Prevention, Human Genome, Psychology and Cognitive Sciences, Genetic Variation, 06 Biological Sciences, Minor allele frequency, 030104 developmental biology, executive function, Genetic Loci, ResearchInstitutes_Networks_Beacons/cathie_marsh_institute, genome-wide association, 1182 Biochemistry, cell and molecular biology, Immediate Communication, Neurocognitive, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dec26100056b46b727e48a65987866d2Test
https://hdl.handle.net/1956/19271Test

المؤلفون: Zhao, Z, Wen, W, Michailidou, K, Bolla, MK, Wang, Q, Zhang, B, Long, J, Shu, X-O, Schmidt, MK, Milne, RL, García-Closas, M, Chang-Claude, J, Lindstrom, S, Bojesen, SE, Ahsan, H, Aittomäki, K, Andrulis, IL, Anton-Culver, H, Arndt, V, Beckmann, MW, Beeghly-Fadiel, A, Benitez, J, Blomqvist, C, Bogdanova, NV, Børresen-Dale, A-L, Brand, J, Brauch, H, Brenner, H, Burwinkel, B, Cai, Q, Casey, G, Chenevix-Trench, G, Couch, FJ, Cox, A, Cross, SS, Czene, K, Dörk, T, Dumont, M, Fasching, PA, Figueroa, J, Flesch-Janys, D, Fletcher, O, Flyger, H, Fostira, F, Gammon, M, Giles, GG, Guénel, P, Haiman, CA, Hamann, U, Harrington, P, Hartman, M, Hooning, MJ, Hopper, JL, Jakubowska, A, Jasmine, F, John, EM, Johnson, N, Kabisch, M, Khan, S, Kibriya, M, Knight, JA, Kosma, V-M, Kriege, M, Kristensen, V, Le Marchand, L, Lee, E, Li, J, Lindblom, A, Lophatananon, A, Luben, R, Lubinski, J, Malone, KE, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, McLean, C, Meijers-Heijboer, H, Meindl, A, Miao, H, Muir, K, Neuhausen, SL, Nevanlinna, H, Neven, P, Olson, JE, Perkins, B, Peterlongo, P, Phillips, K-A, Pylkäs, K, Rudolph, A, Santella, R, Sawyer, EJ, Schmutzler, RK, Schoemaker, M, Shah, M, Shrubsole, M, Southey, MC, Swerdlow, AJ, Toland, AE, Tomlinson, I, Torres, D, Truong, T, Ursin, G, Van Der Luijt, RB, Verhoef, S, Wang-Gohrke, S, Whittemore, AS, Winqvist, R, Pilar Zamora, M, Zhao, H, Dunning, AM, Simard, J, Hall, P, Kraft, P, Pharoah, P, Hunter, D, Easton, DF, Zheng, W

المساهمون: Fletcher, Olivia, Schoemaker, Minouk, Swerdlow, Anthony

مصطلحات موضوعية: Humans, Breast Neoplasms, Diabetes Mellitus, Type 2, Genetic Predisposition to Disease, Odds Ratio, Risk Factors, Case-Control Studies, Polymorphism, Single Nucleotide, Middle Aged, European Continental Ancestry Group, Ethnic Groups, Female, Genetic Variation

وصف الملف: Print-Electronic; 693; application/pdf

العلاقة: Cancer causes & control : CCC, 2016, 27 (5), pp. 679 - 693; https://repository.icr.ac.uk/handle/internal/147Test

الإتاحة: https://doi.org/10.1007/s10552-016-0741-6Test
https://repository.icr.ac.uk/handle/internal/147Test

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Genel Cerrahi Anabilim Dalı., orcid:0000-0002-3820-424X, orcid:0000-0002-2088-9914, orcid:0000-0002-1619-6680, orcid:0000-0001-7904-883X, Çeçener, Gülşah, Eskiler, Gamze Güney, Egeli, Ünal, Tunca, Berrin, Alemdar, Adem, Gökgöz, Şehsuvar, Taşdelen, İsmet, AAP-9988-2020, AAB-6011-2022, ABI-6078-2020, HIZ-7332-2022, AAH-1420-2021, 6508156530, 57190947987, 55665145000, 6602965754, 57190943001, 6603238737, 9637821500

مصطلحات موضوعية: Biochemistry & molecular biology, Early-onset breast cancer, Moderate-penetrance genes, PALB2 gene, Turkish population, And/or ovarian-cancer, Germline mutations, Fanconi-anemia, Susceptibility alleles, Truncating mutations, BRCA2 mutations, Families, Women, Identification, Relatives, Adult, Age of onset, BRCA1 protein, BRCA2 protein, Breast neoplasms, DNA mutational analysis, European continental ancestry group, Female, Genetic association studies, Genetic predisposition to disease, Germ-line mutation, Humans, Middle aged, Nuclear proteins, Polymorphism

العلاقة: Makale - Uluslararası Hakemli Dergi; UAP(T)-2015/3; Molecular Biology Reports; Çeçener, G. vd. (2016). "Association of PALB2 sequence variants with the risk of early-onset breast cancer in patients from Turkey". Molecular Biology Reports, 43(11), 1273-1284.; https://doi.org/10.1007/s11033-016-4061-4Test; https://linkTest.springer.com/article/10.1007/s11033-016-4061-4; http://hdl.handle.net/11452/32250Test; 000387671100010; 2-s2.0-84984647071; 1273; 1284; 43; 11

الإتاحة: https://doi.org/10.1007/s11033-016-4061-4Test
http://hdl.handle.net/11452/32250Test