This HTML5 document contains 43 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Subject Item

n2:id

marcrel:aut

n4:id n5:id n6:id n8:id n9:id n10:id n12:id n13:id n14:id n15:id n16:id n17:id n18:id n19:id n20:id n21:id n22:id n23:id n24:id n25:id n26:id n27:id n28:id n29:id n30:id n31:id n32:id n33:id n34:id n36:id n37:id n38:id n39:id n40:id

dcterms:bibliographicCitation

Courraud Jeremie, Chater-Diehl Eric, Durand Benjamin, Vincent Marie, Muniz Moreno Maria del Mar, Boujelbene Imène, Drouot Nathalie, Genschik Lauréline, Schaefer Elise, Nizon Mathilde, Gerard Bénédicte, Abramowicz Marc, Cogné Benjamin, Bronicki Lucas, Burglen Lydie, Barth Magalie, Charles Perrine, Colin Estelle, Coubes Christine, David Albert, Delobel Bruno, Demurger Florence, Passemard Sandrine, Denommé Anne-Sophie, Faivre Laurence, Feger Claire, Fradin Melanie, Francannet Christine, Genevieve David, Goldenberg Alice, Guerrot Anne-Marie, Isidor Bertrand, Johannesen Katrine M., Keren Boris, Kibæk Maria, Kuentz Paul, Mathieu-Dramard Michele, Demeer Bénédicte, Metreau Julia, Steensbjerre Møller Rikke, Moutton Sébastien, Pasquier Laurent, Pilekær Sørensen Kristina, Perrin Laurence, Renaud Mathilde, Saugier Pascale, Rio Marlene, Svane Joane, Thevenon Julien, Tran Mau Them Frederic, Tronhjem Cathrine Elisabeth, Vitobello Antonio, Layet Valerie, Birling Marie-Christine, Drunat Severine, Bayat Allan, Dubourg Christèle, El Chehadeh Salima, Fagerberg Christina, Mignot Cyril, Guipponi Michel, Bienvenu Thierry, Herault Yann, Thompson Julie, Willems Marjolaine, Mandel Jean-Louis, Weksberg Rosanna . Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder . Genetics in Medicine, 2021, 23 (11), pp.2150-2159 . ⟨10.1038/s41436-021-01263-1⟩ Courraud Jeremie, Chater-Diehl Eric, Durand Benjamin, Vincent Marie, Muniz Moreno Maria Del Mar, Boujelbene Imène, Drouot Nathalie, Genschik Lauréline, Schaefer Elise, Nizon Mathilde, Gerard Bénédicte, Abramowicz Marc, Cogné Benjamin, Bronicki Lucas, Burglen Lydie, Barth Magalie, Charles Perrine, Colin Estelle, Coubes Christine, David Albert, Delobel Bruno, Demurger Florence, Passemard Sandrine, Denommé Anne-Sophie, Faivre Laurence, Feger Claire, Fradin Melanie, Francannet Christine, Genevieve David, Goldenberg Alice, Guerrot Anne-Marie, Isidor Bertrand, Johannesen Katrine M., Keren Boris, Kibæk Maria, Kuentz Paul, Mathieu-Dramard Michele, Demeer Bénédicte, Metreau Julia, Steensbjerre Møller Rikke, Moutton Sébastien, Pasquier Laurent, Pilekær Sørensen Kristina, Perrin Laurence, Renaud Mathilde, Saugier Pascale, Rio Marlene, Svane Joane, Thevenon Julien, Tran Mau Them Frederic, Tronhjem Cathrine Elisabeth, Vitobello Antonio, Layet Valerie, Birling Marie-christine, Drunat Severine, Bayat Allan, Dubourg Christèle, El Chehadeh Salima, Fagerberg Christina, Mignot Cyril, Guipponi Michel, Bienvenu Thierry, Herault Yann, Thompson Julie, Willems Marjolaine, Mandel Jean-louis, Weksberg Rosanna. Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder. Genetics in Medicine, Nature Publishing Group, 2021, pp.e1008500. ⟨10.1038/s41436-021-01263-1⟩ Courraud Jeremie, Chater-Diehl Eric, Durand Benjamin, Vincent Marie, Muniz Moreno Maria del Mar, Boujelbene Imène, Drouot Nathalie, Genschik Lauréline, Schaefer Elise, Nizon Mathilde, Gerard Bénédicte, Cogné Benjamin, David Albert, Denommé Anne-Sophie, Faivre Laurence, Fradin Melanie, Genevieve David, Goldenberg Alice, Guerrot Anne-Marie, Isidor Bertrand, Kuentz Paul, Moutton Sébastien, Pasquier Laurent, Saugier Pascale, Rio Marlene, Birling Marie-Christine, Dubourg Christèle, Bienvenu Thierry, Herault Yann, Thompson Julie, Willems Marjolaine, Mandel Jean-Louis, Weksberg Rosanna . Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder . Genetics in Medicine, 2021, 23 (11), pp.2150-2159 . ⟨10.1038/s41436-021-01263-1⟩ Courraud Jeremie, Chater-Diehl Eric, Durand Benjamin, Vincent Marie, Muniz Moreno Maria Del Mar, Boujelbene Imène, Drouot Nathalie, Genschik Lauréline, Schaefer Elise, Nizon Mathilde, Gerard Bénédicte, Abramowicz Marc, Cogné Benjamin, Bronicki Lucas, Burglen Lydie, Barth Magalie, Charles Perrine, Colin Estelle, Coubes Christine, David Albert, Delobel Bruno, Demurger Florence, Passemard Sandrine, Denommé Anne-Sophie, Faivre Laurence, Feger Claire, Fradin Melanie, Francannet Christine, Genevieve David, Goldenberg Alice, Guerrot Anne-Marie, Isidor Bertrand, Johannesen Katrine M., Keren Boris, Kibæk Maria, Kuentz Paul, Mathieu-Dramard Michele, Demeer Bénédicte, Metreau Julia, Steensbjerre Møller Rikke, Moutton Sébastien, Pasquier Laurent, Pilekær Sørensen Kristina, Perrin Laurence, Renaud Mathilde, Saugier Pascale, Rio Marlene, Svane Joane, Thevenon Julien, Tran Mau Them Frederic, Tronhjem Cathrine Elisabeth, Vitobello Antonio, Layet Valerie, Birling Marie-christine, Drunat Severine, Bayat Allan, Dubourg Christèle, El Chehadeh Salima, Fagerberg Christina, Mignot Cyril, Guipponi Michel, Bienvenu Thierry, Herault Yann, Thompson Julie, Willems Marjolaine, Mandel Jean-louis, Weksberg Rosanna. Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder. Genetics in Medicine, Nature Publishing Group, 2021, 23, pp.2150-2159. ⟨10.1038/s41436-021-01263-1⟩ CourraudJeremie, Chater-DiehlEric, DurandBenjamin, VincentMarie, Muniz MorenoMaria del Mar, BoujelbeneImène, DrouotNathalie, GenschikLauréline, SchaeferElise, NizonMathilde, GerardBénédicte, AbramowiczMarc, CognéBenjamin, BronickiLucas, BurglenLydie, BarthMagalie, CharlesPerrine, ColinEstelle, CoubesChristine, DavidAlbert, DelobelBruno, DemurgerFlorence, PassemardSandrine, DenomméAnne-Sophie, FaivreLaurence, FegerClaire, FradinMelanie, FrancannetChristine, GenevieveDavid, GoldenbergAlice, GuerrotAnne-Marie, IsidorBertrand, JohannesenKatrine M., KerenBoris, KibækMaria, KuentzPaul, Mathieu-DramardMichele, DemeerBénédicte, MetreauJulia, Steensbjerre MøllerRikke, MouttonSébastien, PasquierLaurent, Pilekær SørensenKristina, PerrinLaurence, RenaudMathilde, SaugierPascale, RioMarlene, SvaneJoane, ThevenonJulien, Tran Mau ThemFrederic, TronhjemCathrine Elisabeth, VitobelloAntonio, LayetValerie, BirlingMarie-Christine, DrunatSeverine, BayatAllan, DubourgChristèle, El ChehadehSalima, FagerbergChristina, MignotCyril, GuipponiMichel, BienvenuThierry, HeraultYann, ThompsonJulie, WillemsMarjolaine, MandelJean-Louis, WeksbergRosanna . Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder . Genetics in Medicine, 2021, 23 (11), pp.2150-2159 . ⟨10.1038/s41436-021-01263-1⟩ Courraud Jeremie, Chater-Diehl Eric, Durand Benjamin, Vincent Marie, Muniz Moreno Maria del Mar, Boujelbene Imène, Drouot Nathalie, Genschik Lauréline, Schaefer Elise, Nizon Mathilde, Gerard Bénédicte, Cogné Benjamin, David Albert, Denommé Anne-Sophie, Faivre Laurence, Fradin Melanie, Genevieve David, Goldenberg Alice, Guerrot Anne-Marie, Isidor Bertrand, Kuentz Paul, Moutton Sébastien, Pasquier Laurent, Saugier Pascale, Rio Marlene, Birling Marie-Christine, Dubourg Christèle, Bienvenu Thierry, Herault Yann, Thompson Julie, Willems Marjolaine, Mandel Jean-Louis, Weksberg Rosanna. Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder. Genetics in Medicine, 2021, 23 (11), pp.2150-2159. ⟨10.1038/s41436-021-01263-1⟩

dcterms:title

Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder

dc:date

2021

bibo:doi

10.1038/s41436-021-01263-1