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المؤلفون: Koettgen, Anna, Albrecht, Eva, Teumer, Alexander, Vitart, Veronique, Krumsiek, Jan, Hundertmark, Claudia, Pistis, Giorgio, Ruggiero, Daniela, O'Seaghdha, Conall M., Haller, Toomas, Yang, Qiong, Tanaka, Toshiko, Johnson, Andrew D., Kutalik, Zoltan, Smith, Albert V., Shi, Julia, Struchalin, Maksim, Middelberg, Rita P. S., Brown, Morris J., Gaffo, Angelo L., Pirastu, Nicola, Li, Guo, Hayward, Caroline, Zemunik, Tatijana, Huffman, Jennifer, Yengo, Loic, Zhao, Jing Hua, Demirkan, Ayse, Feitosa, Mary F., Liu, Xuan, Malerba, Giovanni, Lopez, Lorna M., van der Harst, Pim, Li, Xinzhong, Kleber, Marcus E., Hicks, Andrew A., Nolte, Ilja M., Johansson, Åsa, Murgia, Federico, Wild, Sarah H., Bakker, Stephan J. L., Peden, John F., Dehghan, Abbas, Steri, Maristella, Tenesa, Albert, Lagou, Vasiliki, Salo, Perttu, Mangino, Massimo, Rose, Lynda M., Lehtimaki, Terho, Woodward, Owen M., Okada, Yukinori, Tin, Adrienne, Mueller, Christian, Oldmeadow, Christopher, Putku, Margus, Czamara, Darina, Kraft, Peter, Frogheri, Laura, Thun, Gian Andri, Grotevendt, Anne, Gislason, Gauti Kjartan, Harris, Tamara B., Launer, Lenore J., McArdle, Patrick, Shuldiner, Alan R., Boerwinkle, Eric, Coresh, Josef, Schmidt, Helena, Schallert, Michael, Martin, Nicholas G., Montgomery, Grant W., Kubo, Michiaki, Nakamura, Yusuke, Tanaka, Toshihiro, Munroe, Patricia B., Samani, Nilesh J., Jacobs, David R., Jr., Liu, Kiang, D'Adamo, Pio, Ulivi, Sheila, Rotter, Jerome I., Psaty, Bruce M., Vollenweider, Peter, Waeber, Gerard, Campbell, Susan, Devuyst, Olivier, Navarro, Pau, Kolcic, Ivana, Hastie, Nicholas, Balkau, Beverley, Froguel, Philippe, Esko, Tonu, Salumets, Andres, Khaw, Kay Tee, Langenberg, Claudia, Wareham, Nicholas J., Isaacs, Aaron, Kraja, Aldi, Zhang, Qunyuan, Wild, Philipp S., Scott, Rodney J., Holliday, Elizabeth G., Org, Elin, Viigimaa, Margus, Bandinelli, Stefania, Metter, Jeffrey E., Lupo, Antonio, Trabetti, Elisabetta, Sorice, Rossella, Doering, Angela, Lattka, Eva, Strauch, Konstantin, Theis, Fabian, Waldenberger, Melanie, Wichmann, H-Erich, Davies, Gail, Gow, Alan J., Bruinenberg, Marcel, Stolk, Ronald P., Kooner, Jaspal S., Zhang, Weihua, Winkelmann, Bernhard R., Boehm, Bernhard O., Lucae, Susanne, Penninx, Brenda W., Smit, Johannes H., Curhan, Gary, Mudgal, Poorva, Plenge, Robert M., Portas, Laura, Persico, Ivana, Kirin, Mirna, Wilson, James F., Leach, Irene Mateo, van Gilst, Wiek H., Goel, Anuj, Ongen, Halit, Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G., Imboden, Medea, von Eckardstein, Arnold, Cucca, Francesco, Nagaraja, Ramaiah, Piras, Maria Grazia, Nauck, Matthias, Schurmann, Claudia, Budde, Kathrin, Ernst, Florian, Farrington, Susan M., Theodoratou, Evropi, Prokopenko, Inga, Stumvoll, Michael, Jula, Antti, Perola, Markus, Salomaa, Veikko, Shin, So-Youn, Spector, Tim D., Sala, Cinzia, Ridker, Paul M., Kaehoenen, Mika, Viikari, Jorma, Hengstenberg, Christian, Nelson, Christopher P., Meschia, James F., Nalls, Michael A., Sharma, Pankaj, Singleton, Andrew B., Kamatani, Naoyuki, Zeller, Tanja, Burnier, Michel, Attia, John, Laan, Maris, Klopp, Norman, Hillege, Hans L., Kloiber, Stefan, Choi, Hyon, Pirastu, Mario, Tore, Silvia, Probst-Hensch, Nicole M., Voelzke, Henry, Gudnason, Vilmundur, Parsa, Afshin, Schmidt, Reinhold, Whitfield, John B., Fornage, Myriam, Gasparini, Paolo, Siscovick, David S., Polasek, Ozren, Campbell, Harry, Rudan, Igor, Bouatia-Naji, Nabila, Metspalu, Andres, Loos, Ruth J. F., van Duijn, Cornelia M., Borecki, Ingrid B., Ferrucci, Luigi, Gambaro, Giovanni, Deary, Ian J., Wolffenbuttel, Bruce H. R., Chambers, John C., Maerz, Winfried, Pramstaller, Peter P., Snieder, Harold, Gyllensten, Ulf, Wright, Alan F., Navis, Gerjan, Watkins, Hugh, Witteman, Jacqueline C. M., Sanna, Serena, Schipf, Sabine, Dunlop, Malcolm G., Toenjes, Anke, Ripatti, Samuli, Soranzo, Nicole, Toniolo, Daniela, Chasman, Daniel I., Raitakari, Olli, Kao, W. H. Linda, Ciullo, Marina, Fox, Caroline S., Caulfield, Mark, Bochud, Murielle, Gieger, Christian

المصدر: Nature Genetics. 45(2):145-154

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-196032

المؤلفون: Tore, Silvia

مصطلحات موضوعية: BIO/18 Genetica

وصف الملف: 1014436/application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1389::f5d90b9e2728ce02c99d6b769fb34d2b
http://eprints.uniss.it/1035/

المؤلفون: Casula, Milena, Ascierto, Paolo A., Cossu, Antonio, Sini, Maria C., Tore, Silvia, Colombino, Maria, Satta, Maria P., Manca, Antonella, Rozzo, Carla, Satriano, Sabrina M R, Castello, Giuseppe, Lissia, Amelia, Tanda, Francesco, Palmieri, Giuseppe

المصدر: Melanoma research 13 (2003): 571–579. doi:10.1097/00008390-200312000-00006
info:cnr-pdr/source/autori:Casula, Milena; Ascierto, Paolo A.; Cossu, Antonio; Sini, Maria C.; Tore, Silvia; Colombino, Maria; Satta, Maria P.; Manca, Antonella; Rozzo, Carla; Satriano, Sabrina M R; Castello, Giuseppe; Lissia, Amelia; Tanda, Francesco; Palmieri, Giuseppe; Palmieri, Giuseppe/titolo:Mutation analysis of candidate genes in melanoma-prone families: Evidence of different pathogenetic mechanisms at chromosome 9P21/doi:10.1097%2F00008390-200312000-00006/rivista:Melanoma research/anno:2003/pagina_da:571/pagina_a:579/intervallo_pagine:571–579/volume:13

مصطلحات موضوعية: Male, Cancer Research, Candidate gene, DNA Mutational Analysis, Locus (genetics), Dermatology, Biology, Germline mutation, FISH, CDKN2A, CDKN2B, medicine, melanoma, Humans, Genetic Predisposition to Disease, Chromosome 9p21, Gene, Germ-Line Mutation, In Situ Hybridization, Fluorescence, locus CDKN, Family Health, Genetics, Polymorphism, Genetic, medicine.diagnostic_test, Malignant melanoma, analisi mutazionale, Fluorescence in situ hybridization, Haplotype, Exons, Sequence Analysis, DNA, Molecular biology, Introns, Pedigree, Mutation analysis, Haplotypes, Italy, Oncology, Mutation, gene oncosopressore, Female, Chromosomes, Human, Pair 9

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9614d8a7ff79b1359a552eb96ef05fa

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المؤلفون: Paolo Usai, Mario Pirastu, Ivo Deiana, Alessandro Sassu, Silvia Tore, Paola Forabosco, Giovanni Battista Maestrale, Maria Rosa Caruso, Caterina Mele, Ivana Persico, Bibiana Bonerba, Timothy A. Thornton, Maria Pina Concas, Giuseppina Casu, Paola Pistidda, Stefania Casula

المساهمون: Tore, Silvia, Casula, Stefania, Casu, Giuseppina, Concas, MARIA PINA, Pistidda, Paola, Persico, Ivana, Sassu, Alessandro, Maestrale, Giovanni Battista, Mele, Caterina, Caruso, Maria Rosa, Bonerba, Bibiana, Usai, Paolo, Deiana, Ivo, Thornton, Timothy, Pirastu, Mario, Forabosco, Paola

المصدر: PLoS Genetics
PLoS Genetics, Vol 7, Iss 1, p e1001281 (2011)

مصطلحات موضوعية: Cancer Research, Data Interpretation, Gout, 030232 urology & nephrology, Genome-wide association study, Cohort Studies, 0302 clinical medicine, Genotype, Carrier Proteins, Case-Control Studies, Data Interpretation, Statistical, Genetic Loci, Genome-Wide Association Study, Humans, Italy, Microfilament Proteins, Nephrolithiasis, Pedigree, Polymorphism, Single Nucleotide, Uric Acid, Genetic Predisposition to Disease, Ecology, Evolution, Behavior and Systematics, Molecular Biology, Genetics, Genetics (clinical), Genetics and Genomics/Genetics of Disease, 0303 health sciences, education.field_of_study, Ecology, Single Nucleotide, Statistical, 3. Good health, Cohort, Case-Control Studie, Inbreeding, Genetic isolate, Human, Research Article, medicine.medical_specialty, lcsh:QH426-470, Evolution, Population, Locus (genetics), MED/03 Genetica medica, Genetics and Genomics/Complex Traits, Biology, 03 medical and health sciences, Genetic, Behavior and Systematics, Molecular genetics, Nephrolithiasi, Genetics and Genomics/Population Genetics, medicine, Polymorphism, education, 030304 developmental biology, Genetics and Genomics, Microfilament Protein, Ecology, Evolution, Behavior and Systematic, lcsh:Genetics, Cohort Studie, Carrier Protein

وصف الملف: 766273/application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ceb62e23080a3b690ed793e959b7b746
http://eprints.uniss.it/6244/

المؤلفون: Köttgen A; Renal Division, Freiburg University Hospital, Freiburg, Germany. anna.koettgen@uniklinik-freiburg.de, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, Shi J, Struchalin M, Middelberg RP, Brown MJ, Gaffo AL, Pirastu N, Li G, Hayward C, Zemunik T, Huffman J, Yengo L, Zhao JH, Demirkan A, Feitosa MF, Liu X, Malerba G, Lopez LM, van der Harst P, Li X, Kleber ME, Hicks AA, Nolte IM, Johansson A, Murgia F, Wild SH, Bakker SJ, Peden JF, Dehghan A, Steri M, Tenesa A, Lagou V, Salo P, Mangino M, Rose LM, Lehtimäki T, Woodward OM, Okada Y, Tin A, Müller C, Oldmeadow C, Putku M, Czamara D, Kraft P, Frogheri L, Thun GA, Grotevendt A, Gislason GK, Harris TB, Launer LJ, McArdle P, Shuldiner AR, Boerwinkle E, Coresh J, Schmidt H, Schallert M, Martin NG, Montgomery GW, Kubo M, Nakamura Y, Tanaka T, Munroe PB, Samani NJ, Jacobs DR Jr, Liu K, D'Adamo P, Ulivi S, Rotter JI, Psaty BM, Vollenweider P, Waeber G, Campbell S, Devuyst O, Navarro P, Kolcic I, Hastie N, Balkau B, Froguel P, Esko T, Salumets A, Khaw KT, Langenberg C, Wareham NJ, Isaacs A, Kraja A, Zhang Q, Wild PS, Scott RJ, Holliday EG, Org E, Viigimaa M, Bandinelli S, Metter JE, Lupo A, Trabetti E, Sorice R, Döring A, Lattka E, Strauch K, Theis F, Waldenberger M, Wichmann HE, Davies G, Gow AJ, Bruinenberg M, Stolk RP, Kooner JS, Zhang W, Winkelmann BR, Boehm BO, Lucae S, Penninx BW, Smit JH, Curhan G, Mudgal P, Plenge RM, Portas L, Persico I, Kirin M, Wilson JF, Mateo Leach I, van Gilst WH, Goel A, Ongen H, Hofman A, Rivadeneira F, Uitterlinden AG, Imboden M, von Eckardstein A, Cucca F, Nagaraja R, Piras MG, Nauck M, Schurmann C, Budde K, Ernst F, Farrington SM, Theodoratou E, Prokopenko I, Stumvoll M, Jula A, Perola M, Salomaa V, Shin SY, Spector TD, Sala C, Ridker PM, Kähönen M, Viikari J, Hengstenberg C, Nelson CP, Meschia JF, Nalls MA, Sharma P, Singleton AB, Kamatani N, Zeller T, Burnier M, Attia J, Laan M, Klopp N, Hillege HL, Kloiber S, Choi H, Pirastu M, Tore S, Probst-Hensch NM, Völzke H, Gudnason V, Parsa A, Schmidt R, Whitfield JB, Fornage M, Gasparini P, Siscovick DS, Polašek O, Campbell H, Rudan I, Bouatia-Naji N, Metspalu A, Loos RJ, van Duijn CM, Borecki IB, Ferrucci L, Gambaro G, Deary IJ, Wolffenbuttel BH, Chambers JC, März W, Pramstaller PP, Snieder H, Gyllensten U, Wright AF, Navis G, Watkins H, Witteman JC, Sanna S, Schipf S, Dunlop MG, Tönjes A, Ripatti S, Soranzo N, Toniolo D, Chasman DI, Raitakari O, Kao WH, Ciullo M, Fox CS, Caulfield M, Bochud M, Gieger C

مؤلفون مشاركون: LifeLines Cohort Study, CARDIoGRAM Consortium, DIAGRAM Consortium, ICBP Consortium, MAGIC Consortium

المصدر: Nature genetics [Nat Genet] 2013 Feb; Vol. 45 (2), pp. 145-54. Date of Electronic Publication: 2012 Dec 23.

نوع المنشور: Comparative Study; Journal Article; Meta-Analysis

بيانات الدورية: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Loci/*genetics , Gout/*genetics , Signal Transduction/*genetics , Uric Acid/*blood, Analysis of Variance ; Gene Frequency ; Genome-Wide Association Study ; Glucose/metabolism ; Gout/blood ; Humans ; Inhibins/genetics ; Inhibins/metabolism ; Polymorphism, Single Nucleotide/genetics ; White People