HLA-DQB1 Haplotypes and their Relation to Oral Signs Linked to Celiac Disease Diagnosis

por Erriu, Matteo, Sanna, Serena, Nucaro, Annalisa, Orrù, Germano, Garau, Valentino, Montaldo, Caterina
Publicado 2011

Mendelian randomization while jointly modeling cis genetics identifies causal relationships between gene expression and lipids

por van der Graaf, Adriaan, Claringbould, Annique, Rimbert, Antoine, Westra, Harm-Jan, Li, Yang, Wijmenga, Cisca, Sanna, Serena
Publicado 2020

A Likelihood-Based Framework for Variant Calling and De Novo Mutation Detection in Families

por Li, Bingshan, Chen, Wei, Zhan, Xiaowei, Busonero, Fabio, Sanna, Serena, Sidore, Carlo, Cucca, Francesco, Kang, Hyun M., Abecasis, Gonçalo R.
Publicado 2012

Genotype calling and haplotyping in parent-offspring trios

por Chen, Wei, Li, Bingshan, Zeng, Zhen, Sanna, Serena, Sidore, Carlo, Busonero, Fabio, Kang, Hyun Min, Li, Yun, Abecasis, Gonçalo R.
Publicado 2013

SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits

por Meirelles, Osorio D, Ding, Jun, Tanaka, Toshiko, Sanna, Serena, Yang, Hsih-Te, Dudekula, Dawood B, Cucca, Francesco, Ferrucci, Luigi, Abecasis, Goncalo, Schlessinger, David
Publicado 2013

LocusZoom: regional visualization of genome-wide association scan results

por Pruim, Randall J., Welch, Ryan P., Sanna, Serena, Teslovich, Tanya M., Chines, Peter S., Gliedt, Terry P., Boehnke, Michael, Abecasis, Gonçalo R., Willer, Cristen J.
Publicado 2010

Sex-Specific Parental Effects on Offspring Lipid Levels

por Predazzi, Irene M, Sobota, Rafal S, Sanna, Serena, Bush, William S, Bartlett, Jacquelaine, Lilley, Jessica S, Linton, MacRae F, Schlessinger, David, Cucca, Francesco, Fazio, Sergio, Williams, Scott M
Publicado 2015

Lack of Association Between Genetic Variants at ACE2 and TMPRSS2 Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes

por Lopera Maya, Esteban A., van der Graaf, Adriaan, Lanting, Pauline, van der Geest, Marije, Fu, Jingyuan, Swertz, Morris, Franke, Lude, Wijmenga, Cisca, Deelen, Patrick, Zhernakova, Alexandra, Sanna, Serena
Publicado 2020

Association of protein function-altering variants with cardiometabolic traits: the strong heart study

por Shan, Yue, Cole, Shelley A., Haack, Karin, Melton, Phillip E., Best, Lyle G., Bizon, Christopher, Kobes, Sayuko, Köroğlu, Çiğdem, Baier, Leslie J., Hanson, Robert L., Sanna, Serena, Li, Yun, Franceschini, Nora
Publicado 2022

Common Variants at 10 Genomic Loci Influence Hemoglobin A(1C) Levels via Glycemic and Nonglycemic Pathways

por Soranzo, Nicole, Sanna, Serena, Wheeler, Eleanor, Gieger, Christian, Radke, Dörte, Dupuis, Josée, Bouatia-Naji, Nabila, Langenberg, Claudia, Prokopenko, Inga, Stolerman, Elliot, Sandhu, Manjinder S., Heeney, Matthew M., Devaney, Joseph M., Reilly, Muredach P., Ricketts, Sally L.
Publicado 2010

Impact of commonly used drugs on the composition and metabolic function of the gut microbiota

por Vich Vila, Arnau, Collij, Valerie, Sanna, Serena, Sinha, Trishla, Imhann, Floris, Bourgonje, Arno R., Mujagic, Zlatan, Jonkers, Daisy M. A. E., Masclee, Ad A. M., Fu, Jingyuan, Kurilshikov, Alexander, Wijmenga, Cisca, Zhernakova, Alexandra, Weersma, Rinse K.
Publicado 2020

Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability

por Matzaraki, Vasiliki, Le, Kieu T. T., Jaeger, Martin, Aguirre-Gamboa, Raúl, Johnson, Melissa D., Sanna, Serena, Rosati, Diletta, Franke, Lude, Zhernakova, Alexandra, Fu, Jingyuan, Withoff, Sebo, Jonkers, Iris, Li, Yang, Joosten, Leo A. B., Netea, Mihai G., Wijmenga, Cisca, Kumar, Vinod
Publicado 2021

Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome

por Zhernakova, Daria V., Le, Trang H., Kurilshikov, Alexander, Atanasovska, Biljana, Bonder, Marc Jan, Sanna, Serena, Claringbould, Annique, Võsa, Urmo, Deelen, Patrick, Franke, Lude, de Boer, Rudolf A., Kuipers, Folkert, Netea, Mihai G., Hofker, Marten H., Wijmenga, Cisca, Zhernakova, Alexandra, Fu, Jingyuan
Publicado 2018

The GLUT9 Gene Is Associated with Serum Uric Acid Levels in Sardinia and Chianti Cohorts

por Li, Siguang, Sanna, Serena, Maschio, Andrea, Busonero, Fabio, Usala, Gianluca, Mulas, Antonella, Lai, Sandra, Dei, Mariano, Orrù, Marco, Albai, Giuseppe, Bandinelli, Stefania, Schlessinger, David, Lakatta, Edward, Scuteri, Angelo, Najjar, Samer S, Guralnik, Jack, Naitza, Silvia, Crisponi, Laura, Cao, Antonio, Abecasis, Gonçalo, Ferrucci, Luigi, Uda, Manuela, Chen, Wei-Min, Nagaraja, Ramaiah
Publicado 2007

Integration of multi-omics data and deep phenotyping enables prediction of cytokine responses

por Bakker, Olivier B., Aguirre-Gamboa, Raul, Sanna, Serena, Oosting, Marije, Smeekens, Sanne P., Jaeger, Martin, Zorro, Maria, Võsa, Urmo, Withoff, Sebo, Netea-Maier, Romana T., Koenen, Hans J.P.M., Joosten, Irma, Xavier, Ramnik J., Franke, Lude, Joosten, Leo A.B., Kumar, Vinod, Wijmenga, Cisca, Netea, Mihai G., Li, Yang
Publicado 2018

Systematic Prioritization of Candidate Genes in Disease Loci Identifies TRAFD1 as a Master Regulator of IFNγ Signaling in Celiac Disease

por van der Graaf, Adriaan, Zorro, Maria M., Claringbould, Annique, Võsa, Urmo, Aguirre-Gamboa, Raúl, Li, Chan, Mooiweer, Joram, Ricaño-Ponce, Isis, Borek, Zuzanna, Koning, Frits, Kooy-Winkelaar, Yvonne, Sollid, Ludvig M., Qiao, Shuo-Wang, Kumar, Vinod, Li, Yang, Franke, Lude, Withoff, Sebo, Wijmenga, Cisca, Sanna, Serena, Jonkers, Iris
Publicado 2021

Genome-Wide Association Study of Multiple Sclerosis Confirms a Novel Locus at 5p13.1

por Matesanz, Fuencisla, González-Pérez, Antonio, Lucas, Miguel, Sanna, Serena, Gayán, Javier, Urcelay, Elena, Zara, Ilenia, Pitzalis, Maristella, Cavanillas, María L., Arroyo, Rafael, Zoledziewska, Magdalena, Marrosu, Marisa, Fernández, Oscar, Leyva, Laura, Alcina, Antonio, Fedetz, Maria, Moreno-Rey, Concha, Velasco, Juan, Real, Luis M., Ruiz-Peña, Juan Luis, Cucca, Francesco, Ruiz, Agustín, Izquierdo, Guillermo
Publicado 2012

Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits

por Scuteri, Angelo, Sanna, Serena, Chen, Wei-Min, Uda, Manuela, Albai, Giuseppe, Strait, James, Najjar, Samer, Nagaraja, Ramaiah, Orrú, Marco, Usala, Gianluca, Dei, Mariano, Lai, Sandra, Maschio, Andrea, Busonero, Fabio, Mulas, Antonella, Ehret, Georg B, Fink, Ashley A, Weder, Alan B, Cooper, Richard S, Galan, Pilar, Chakravarti, Aravinda, Schlessinger, David, Cao, Antonio, Lakatta, Edward, Abecasis, Gonçalo R
Publicado 2007

GENOME-WIDE ASSOCIATION ANALYSES BASED ON WHOLE-GENOME SEQUENCING IN SARDINIA PROVIDE INSIGHTS INTO REGULATION OF HEMOGLOBIN LEVELS

por Danjou, Fabrice, Zoledziewska, Magdalena, Sidore, Carlo, Steri, Maristella, Busonero, Fabio, Maschio, Andrea, Mulas, Antonella, Perseu, Lucia, Barella, Susanna, Porcu, Eleonora, Pistis, Giorgio, Pitzalis, Maristella, Pala, Mauro, Menzel, Stephan, Metrustry, Sarah, Spector, Timothy D., Leoni, Lidia, Angius, Andrea, Uda, Manuela, Moi, Paolo, Thein, Swee Lay, Galanello, Renzo, Abecasis, Gonçalo R., Schlessinger, David, Sanna, Serena, Cucca, Francesco
Publicado 2015

Fine Mapping of Five Loci Associated with Low-Density Lipoprotein Cholesterol Detects Variants That Double the Explained Heritability

por Sanna, Serena, Li, Bingshan, Mulas, Antonella, Sidore, Carlo, Kang, Hyun M., Jackson, Anne U., Piras, Maria Grazia, Usala, Gianluca, Maninchedda, Giuseppe, Sassu, Alessandro, Serra, Fabrizio, Palmas, Maria Antonietta, Wood, William H., Njølstad, Inger, Laakso, Markku, Hveem, Kristian, Tuomilehto, Jaakko, Lakka, Timo A., Rauramaa, Rainer, Boehnke, Michael, Cucca, Francesco, Uda, Manuela, Schlessinger, David, Nagaraja, Ramaiah, Abecasis, Gonçalo R.
Publicado 2011