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收藏GNNenrich: a novel method for pathway enrichment analysis based on graph neural networkGNNenrich：一种基于图神经网络通路富集分析的新方法
Mziou-Sallami, Mallek; Roger, Pierrick; Gloaguen, Arnaud; Dandine-Roulland, Claire; Ngaho, Thierry Jiogho; Brohard, Solene; Muret, Kevin; Sandron, Florian; Bonnet, Eric; Deleuze, Jean-Francois; Le Floch, Edith; Meyer, Vincent 分享 收藏 Human genetic structure in Northwest France provides new insights into West European historical demography法国西北部的人类遗传结构为西欧历史人口统计学提供了新的见解Alves, Isabel; Giemza, Joanna; Blum, Michael G. B.; Bernhardsson, Carolina; Chatel, Stephanie; Karakachoff, Matilde; Saint Pierre, Aude; Herzig, Anthony F.; Olaso, Robert; Monteil, Martial; Gallien, Veronique; Cabot, Elodie; Svensson, Emma; Bacq, Delphine; Baron, Estelle; Berthelier, Charlotte; Besse, Celine; Blanche, Helene; Bocher, Ozvan; Boland, Anne; Bonnaud, Stephanie; Charpentier, Eric; Dandine-Roulland, Claire; Ferec, Claude; Fruchet, Christine; Lecointe, Simon; Le Floch, Edith; Ludwig, Thomas E.; Marenne, Gaelle; Meyer, Vincent; Quellery, Elisabeth; Racimo, Fernando; Rouault, Karen; Sandron, Florian; Schott, Jean-Jacques; Velo-Suarez, Lourdes; Violleau, Jade; Willerslev, Eske; Coativy, Yves; Jezequel, Mael; Le Bris, Daniel; Nicolas, Clement; Pailler, Yvan; Goldberg, Marcel; Zins, Marie; Le Marec, Herve; Jakobsson, Mattias; Darlu, Pierre; Genin, Emmanuelle; Deleuze, Jean-Francois; Redon, Richard; Dina, Christian 分享 收藏 Shared Heritability of Blood Pressure and Pulse Wave Velocity: Insights From the STANISLAS CohortXhaard, Constance; de Villemereuil, Pierre; Benetos, Athanase; Bozec, Erwan; Dandine-Roulland, Claire; Le Floch, Edith; Regnault, Veronique; Lacolley, Patrick; Zannad, Faiez; Rossignol, Patrick; Girerd, Nicolas 分享 收藏 Layer myocardial strain is the most heritable echocardiographic traitHuttin, Olivier; Xhaard, Constance; Dandine-Roulland, Claire; Le Floch, Edith; Bacq-Daian, Delphine; Lamiral, Zohra; Bozec, Erwan; Deleuze, Jean-Francois; Zannad, Faiez; Rossignol, Patrick; Girerd, Nicolas 分享 收藏 Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease在法国女性中，乳腺癌的多基因风险评分的关联和表现是否具有该疾病的家族性易感性Jiao, Yue; Truong, Therese; Eon-Marchais, Severine; Mebirouk, Noura; Caputo, Sandrine M.; Dondon, Marie-Gabrielle; Karimi, Mojgan; Le Gal, Dorothee; Beauvallet, Juana; Le Floch, Edith; Dandine-Roulland, Claire; Bacq-Daian, Delphine; Olaso, Robert; Albuisson, Juliette; Audebert-Bellanger, Severine; Berthet, Pascaline; Bonadona, Valerie; Buecher, Bruno; Caron, Olivier; Cavaille, Mathias; Chiesa, Jean; Colas, Chrystelle; Collonge-Rame, Marie-Agnes; Coupier, Isabelle; Delnatte, Capucine; De Pauw, Antoine; Dreyfus, Helene; Fert-Ferrer, Sandra; Gauthier-Villars, Marion; Gesta, Paul; Giraud, Sophie; Gladieff, Laurence; Golmard, Lisa; Lasset, Christine; Lejeune-Dumoulin, Sophie; Leone, Melanie; Limacher, Jean-Marc; Lortholary, Alain; Luporsi, Elisabeth; Mari, Veronique; Maugard, Christine M.; Mortemousque, Isabelle; Mouret-Fourme, Emmanuelle; Nambot, Sophie; Nogues, Catherine; Popovici, Cornel; Prieur, Fabienne; Pujol, Pascal; Sevenet, Nicolas; Sobol, Hagay; Toulas, Christine; Uhrhammer, Nancy; Vaur, Dominique; Venat, Laurence; Boland-Auge, Anne; Guenel, Pascal; Deleuze, Jean-Francois; Stoppa-Lyonnet, Dominique; Andrieu, Nadine; Lesueur, Fabienne 分享 收藏 Identification of risk loci for primary aldosteronism in genome-wide association studies在全基因组关联研究中鉴定原发性醛固酮增多症的风险位点Le Floch, Edith; Cosentino, Teresa; Larsen, Casper K.; Beuschlein, Felix; Reincke, Martin; Amar, Laurence; Rossi, Gian-Paolo; De Sousa, Kelly; Baron, Stephanie; Chantalat, Sophie; Saintpierre, Benjamin; Lenzini, Livia; Frouin, Arthur; Giscos-Douriez, Isabelle; Ferey, Matthis; Abdellatif, Alaa B.; Meatchi, Tchao; Empana, Jean-Philippe; Jouven, Xavier; Gieger, Christian; Waldenberger, Melanie; Peters, Annette; Cusi, Daniele; Salvi, Erika; Meneton, Pierre; Touvier, Mathilde; Deschasaux, Melanie; Druesne-Pecollo, Nathalie; Boulkroun, Sheerazed; Fernandes-Rosa, Fabio L.; Deleuze, Jean-Francois; Jeunemaitre, Xavier; Zennaro, Maria-Christina 分享 收藏 Weak Association Between Genetic Markers of Hyperuricemia and Cardiorenal Outcomes: Insights From the STANISLAS Study Cohort With a 20-Year Follow-UpKanbay, Mehmet; Xhaard, Constance; Le Floch, Edith; Dandine-Roulland, Claire; Girerd, Nicolas; Ferreira, Joao Pedro; Boivin, Jean-Marc; Wagner, Sandra; Bacq-Daian, Delphine; Deleuze, Jean-Francois; Zannad, Faiez; Rossignol, Patrick 分享 收藏 Impact of natriuretic peptide polymorphisms on diastolic and metabolic function in a populational cohort: insights from the STANISLAS cohortXhaard, Constance; Rouget, Raphael; Vodovar, Nicolas; Le Floch, Edith; Dandine-Roulland, Claire; Wagner, Sandra; Bacq-Daian, Delphine; Thuillier, Quentin; Boivin, Jean-Marc; Branlant, Christiane; Deleuze, Jean-Francois; Behm-Ansmant, Isabelle; Zannad, Faiez; Rossignol, Patrick; Girerd, Nicolas 分享 收藏 Genome-wide haplotype association study in imaging genetics using whole-brain sulcal openings of 16,304 UK Biobank subjectsKarkar, Slim; Dandine-Roulland, Claire; Mangin, Jean-Francois; Le Guen, Yann; Philippe, Cathy; Deleuze, Jean-Francois; Pierre-Jean, Morgane; Le Floch, Edith; Frouin, Vincent 分享 收藏 Circulating plasma proteins and new-onset diabetes in a population-based study: proteomic and genomic insights from the STANISLAS cohortFerreira, Joao Pedro; Lamiral, Zohra; Xhaard, Constance; Duarte, Kevin; Bresso, Emmanuel; Devignes, Marie-Dominique; Le Floch, Edith; Roulland, Claire Dandine; Deleuze, Jean-Francois; Wagner, Sandra; Guerci, Bruno; Girerd, Nicolas; Zannad, Faiez; Boivin, Jean-Marc; Rossignol, Patrick 分享 收藏 Heritability of a resting heart rate in a 20-year follow-up family cohort with GWAS data: Insights from the STANISLAS cohortXhaard, Constance; Dandine-Roulland, Claire; de Villemereuil, Pierre; Le Floch, Edith; Bacq-Daian, Delphine; Machu, Jean-Loup; Ferreira, Joao Pedro; Deleuze, Jean-Francois; Zannad, Faiez; Rossignol, Patrick; Girerd, Nicolas 分享 收藏 分享 收藏 Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders遗传性视网膜疾病中缺失的基因缺陷在哪里？内含子和同义变体至少与4% 种CACNA1F-mediated遗传性视网膜疾病有关Zeitz, Christina; Michiels, Christelle; Neuille, Marion; Friedburg, Christoph; Condroyer, Christel; Boyard, Fiona; Antonio, Aline; Bouzidi, Nassima; Milicevic, Diana; Veaux, Robin; Tourville, Aurore; Zoumba, Axelle; Seneina, Imene; Foussard, Marine; Andrieu, Camille; Preising, Markus N.; Blanchard, Steven; Saraiva, Jean-Paul; Mesrob, Lilia; Le Floch, Edith; Jubin, Claire; Meyer, Vincent; Blanche, Helene; Boland, Anne; Deleuze, Jean-Francois; Sharon, Dror; Drumare, Isabelle; Defoort-Dhellemmes, Sabine; De Baere, Elfride; Leroy, Bart P.; Zanlonghi, Xavier; Casteels, Ingele; de Ravel, Thorny J.; Balikova, Irina; Koenekoop, Rob K.; Laffargue, Fanny; McLean, Rebecca; Gottlob, Irene; Bonneau, Dominique; Schorderet, Daniel F.; Munier, Francis L.; McKibbin, Martin; Prescott, Katrina; Pelletier, Valerie; Dollfus, Helene; Perdomo-Trujillo, Yaumara; Faure, Celine; Reiff, Charlotte; Wissinger, Bernd; Meunier, Isabelle; Kohl, Susanne; Banin, Eyal; Zrenner, Eberhart; Jurklies, Bernhard; Lorenz, Birgit; Sahel, Jose-Alain; Audo, Isabelle 分享 收藏 
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