{"id":1833,"date":"2017-03-19T13:25:09","date_gmt":"2017-03-19T12:25:09","guid":{"rendered":"https:\/\/2017.eshg.org\/?page_id=1833"},"modified":"2019-06-11T15:47:33","modified_gmt":"2019-06-11T14:47:33","slug":"tuesday","status":"publish","type":"page","link":"https:\/\/2019.eshg.org\/index.php\/programme\/tuesday\/","title":{"rendered":"Tuesday, June 18"},"content":{"rendered":"<div class=\"fusion-fullwidth fullwidth-box hundred-percent-fullwidth non-hundred-percent-height-scrolling\"  style='background-color: #ffffff;background-position: center center;background-repeat: no-repeat;padding-top:0px;padding-right:0px;padding-bottom:0px;padding-left:0px;'><div class=\"fusion-builder-row fusion-row \"><div  class=\"fusion-layout-column fusion_builder_column fusion_builder_column_1_2 fusion-builder-column-1 fusion-one-half fusion-column-first 1_2\"  style='margin-top:0px;margin-bottom:0px;'>\n\t\t\t\t\t<div class=\"fusion-column-wrapper\" style=\"padding: 0px 0px 0px 0px;background-position:left top;background-repeat:no-repeat;-webkit-background-size:cover;-moz-background-size:cover;-o-background-size:cover;background-size:cover;\"   data-bg-url=\"\">\n\t\t\t\t\t\t<div class=\"fusion-button-wrapper fusion-alignleft\"><style type=\"text\/css\" scoped=\"scoped\">.fusion-button.button-1{width:auto;}<\/style><a class=\"fusion-button button-flat fusion-button-square button-small button-lightgray button-1\" target=\"_self\" href=\"https:\/\/2019.eshg.org\/index.php\/programme\/monday\"><span class=\"fusion-button-icon-divider button-icon-divider-left\"><i class=\"fa-angle-double-left fas\"><\/i><\/span><span class=\"fusion-button-text fusion-button-text-left\">Monday<\/span><\/a><\/div><div class=\"fusion-clearfix\"><\/div>\n\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div><div  class=\"fusion-layout-column fusion_builder_column fusion_builder_column_1_2 fusion-builder-column-2 fusion-one-half fusion-column-last 1_2\"  style='margin-top:0px;margin-bottom:0px;'>\n\t\t\t\t\t<div class=\"fusion-column-wrapper\" style=\"padding: 0px 0px 0px 0px;background-position:left top;background-repeat:no-repeat;-webkit-background-size:cover;-moz-background-size:cover;-o-background-size:cover;background-size:cover;\"   data-bg-url=\"\">\n\t\t\t\t\t\t<div class=\"fusion-button-wrapper fusion-alignright\"><style type=\"text\/css\" scoped=\"scoped\">.fusion-button.button-2{width:auto;}<\/style><a class=\"fusion-button button-flat fusion-button-square button-small button-lightgray button-2\" target=\"_self\" href=\"https:\/\/2019.eshg.org\/index.php\/programme\/saturday\"><span class=\"fusion-button-text fusion-button-text-right\">back to Saturday<\/span><span class=\"fusion-button-icon-divider button-icon-divider-right\"><i class=\"fa-angle-double-right fas\"><\/i><\/span><\/a><\/div><div class=\"fusion-clearfix\"><\/div>\n\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div><div  class=\"fusion-layout-column fusion_builder_column fusion_builder_column_1_1 fusion-builder-column-3 fusion-one-full fusion-column-first fusion-column-last fusion-column-no-min-height 1_1\"  style='margin-top:0px;margin-bottom:0px;'>\n\t\t\t\t\t<div class=\"fusion-column-wrapper\" style=\"padding: 0px 0px 0px 0px;background-position:left top;background-repeat:no-repeat;-webkit-background-size:cover;-moz-background-size:cover;-o-background-size:cover;background-size:cover;\"   data-bg-url=\"\">\n\t\t\t\t\t\t<div class=\"fusion-menu-anchor\" id=\"PL3\"><\/div><div class=\"fusion-sep-clear\"><\/div><div class=\"fusion-separator fusion-full-width-sep sep-none\" style=\"margin-left: auto;margin-right: auto;margin-top:30px;\"><\/div><div class=\"fusion-title title fusion-title-1 fusion-title-size-four\" style=\"margin-top:0px;margin-bottom:31px;\"><h4 class=\"title-heading-left\" style=\"margin:0;\">09:00 &#8211; 10:30 hrs | <span style=\"color: #edb417;\">Concurrent Symposia S17-S20<\/span>\u00a0&amp; <span style=\"color: #e27cbd;\">Educational Sessions E13-E14<\/span><\/h4><div class=\"title-sep-container\"><div class=\"title-sep sep-double sep-solid\" style=\"border-color:#ffffff;\"><\/div><\/div><\/div><style type=\"text\/css\" scoped=\"scoped\">#accordion-1833-1 .fusion-panel:hover{ background-color: #f9f9f9 } #accordion-1833-1 .fusion-panel { border-color:#cccccc; border-width:1px; background-color:rgba(237,180,23,0.41); }.fusion-accordian  #accordion-1833-1 .panel-title a .fa-fusion-box{ color: #ffffff;}.fusion-accordian  #accordion-1833-1 .panel-title a .fa-fusion-box:before{ font-size: 13px; width: 13px;}.fusion-accordian  #accordion-1833-1 .panel-title a{font-size:21px;}.fusion-accordian  #accordion-1833-1 .fa-fusion-box { background-color: #333333;border-color: #333333;}.fusion-accordian  #accordion-1833-1 .panel-title a:hover, #accordion-1833-1 .fusion-toggle-boxed-mode:hover .panel-title a { color: #00529c;}.fusion-accordian  #accordion-1833-1 .panel-title .active .fa-fusion-box,.fusion-accordian  #accordion-1833-1 .panel-title a:hover .fa-fusion-box { background-color: #00529c!important;border-color: #00529c!important;}<\/style><div class=\"accordian fusion-accordian\"><div class=\"panel-group\" id=\"accordion-1833-1\"><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#8cd2e1a1adb7e250c\" href=\"#8cd2e1a1adb7e250c\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">S17 | ESHG-ASHG building bridges: Global collaboration to advance the use of genomics in health<\/div><\/a><\/h4><\/div><div id=\"8cd2e1a1adb7e250c\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chairs:\u00a0 Kiran Musunuru, Joris Veltman<br \/>\nRoom:\u00a0\u00a0 Hall C<\/p>\n<p class=\"PublishingTitle\">S17.1 Challenges and solutions to advance global collaboration to understand, diagnose, and develop therapies for rare diseases<\/p>\n<p class=\"AuthorBlock\"><b>Kym Boycott<\/b>;<br \/>\nCanada<\/p>\n<p class=\"PublishingTitle\">S17.2 EMBL-EBI and global data integration<\/p>\n<p class=\"AuthorBlock\"><b>Nick Goldman<\/b>;<br \/>\nUnited Kingdom<\/p>\n<p class=\"PublishingTitle\">S17.3 The NIH All of us program: Building a national research program of 1 million U.S. participants to advance precision medicine<\/p>\n<p class=\"AuthorBlock\"><b>Joshua Charles Denny<\/b>;<br \/>\nUnited States<\/p>\n<p class=\"PublishingTitle\">S17.4 Pulling the Strands Together: MEGA Steps to Drive European Genomics and Personalised Medicine<\/p>\n<p class=\"AuthorBlock\"><b>Denis Horgan<\/b>;<br \/>\nBrussels, Belgium<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#c97ba97c9ccbbb59a\" href=\"#c97ba97c9ccbbb59a\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">S18 | Our genetic history and its phenotypic consequences<\/div><\/a><\/h4><\/div><div id=\"c97ba97c9ccbbb59a\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chairs:\u00a0 Tord Jonson, Matti Pirinen<br \/>\nRoom:\u00a0\u00a0 K2+K3<\/p>\n<p class=\"PublishingTitle\">S18.1 Tales of Early Humans, Admixture, and Adaptation<\/p>\n<p class=\"AuthorBlock\"><b>Mattias Jakobsson<\/b>;<br \/>\nSweden<\/p>\n<p class=\"PublishingTitle\">S18.2 Timing past admixture events and characterizing their consequences in contemporary human populations<\/p>\n<p class=\"AuthorBlock\"><b>Garrett Hellenthal<\/b>;<br \/>\nUnited Kingdom<\/p>\n<p class=\"PublishingTitle\">S18.3 Consequences of population genetic differences in genetic risk prediction across diverse human populations<\/p>\n<p class=\"AuthorBlock\"><b>Alicia Martin<\/b>;<br \/>\nUnited States<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#75f5bdc939cf581e5\" href=\"#75f5bdc939cf581e5\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">S19 | Treating rare genetic disease<\/div><\/a><\/h4><\/div><div id=\"75f5bdc939cf581e5\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chairs:\u00a0 Brunella Franco, Asbj\u00f8rg Stray-Pedersen<br \/>\nRoom:\u00a0\u00a0 F1+F2+F3<\/p>\n<p class=\"PublishingTitle\">S19.1 Regeneration of the entire human epidermis using transgenic stem cells<\/p>\n<p class=\"AuthorBlock\"><b>Laura De Rosa<\/b>;<br \/>\nItaly<\/p>\n<p class=\"PublishingTitle\">S19.2 Gene therapy for inherited neuromuscular disorders<\/p>\n<p class=\"AuthorBlock\"><b>Francesco Muntoni<\/b>;<br \/>\nUnited Kingdom<\/p>\n<p class=\"PublishingTitle\">S19.3 Gene therapy for hemoglobinopathies<\/p>\n<p class=\"AuthorBlock\"><b>Giuliana Ferrari<\/b>;<br \/>\nItaly<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#5dd8d75bd11015791\" href=\"#5dd8d75bd11015791\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">S20 | Epigenetics and early development<\/div><\/a><\/h4><\/div><div id=\"5dd8d75bd11015791\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chairs:\u00a0 Siren Berland, Lucy Raymond<br \/>\nRoom:\u00a0\u00a0 G2+G3<\/p>\n<p class=\"PublishingTitle\">S20.1 Single Cell Epigenomic Analysis of the Anatomy and Neuronal Circuitry of the Brain<\/p>\n<p class=\"AuthorBlock\"><b>Joseph R. Ecker<\/b>;<br \/>\nUnited States<\/p>\n<p class=\"PublishingTitle\">S20.2 Genetic-epigenetic interactions: mechanistic insights and practical applications<\/p>\n<p class=\"AuthorBlock\"><b>Benjamin Tycko<\/b>;<br \/>\nUnited States<\/p>\n<p class=\"PublishingTitle\">S20.3 Functional genomics approaches for uncovering the role of regulatory sequences in developmental abnormalities and disease<\/p>\n<p class=\"AuthorBlock\"><b>Justin L. Cotney<\/b>;<br \/>\nUnited States<\/p>\n<\/div><\/div><\/div><\/div><\/div><style type=\"text\/css\" scoped=\"scoped\">#accordion-1833-2 .fusion-panel:hover{ background-color: #f9f9f9 } #accordion-1833-2 .fusion-panel { border-color:#cccccc; border-width:1px; background-color:rgba(226,124,189,0.39); }.fusion-accordian  #accordion-1833-2 .panel-title a .fa-fusion-box{ color: #ffffff;}.fusion-accordian  #accordion-1833-2 .panel-title a .fa-fusion-box:before{ font-size: 13px; width: 13px;}.fusion-accordian  #accordion-1833-2 .panel-title a{font-size:21px;}.fusion-accordian  #accordion-1833-2 .fa-fusion-box { background-color: #333333;border-color: #333333;}.fusion-accordian  #accordion-1833-2 .panel-title a:hover, #accordion-1833-2 .fusion-toggle-boxed-mode:hover .panel-title a { color: #00529c;}.fusion-accordian  #accordion-1833-2 .panel-title .active .fa-fusion-box,.fusion-accordian  #accordion-1833-2 .panel-title a:hover .fa-fusion-box { background-color: #00529c!important;border-color: #00529c!important;}<\/style><div class=\"accordian fusion-accordian\"><div class=\"panel-group\" id=\"accordion-1833-2\"><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#8b242c812d1a102c2\" href=\"#8b242c812d1a102c2\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">E13 | Genetic innovations in reproductive medicine<\/div><\/a><\/h4><\/div><div id=\"8b242c812d1a102c2\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chair:\u00a0\u00a0 Maris Laan<br \/>\nRoom:\u00a0 F4+F5<\/p>\n<p class=\"PublishingTitle\">E13.1 Novel discoveries of genes implicated in male and female infertility<\/p>\n<p class=\"AuthorBlock\"><b>Christophe Arnoult <\/b>;<br \/>\nFrance<\/p>\n<p class=\"PublishingTitle\">E13.2 Population genetic carrier screening programs for reproductive purposes<\/p>\n<p class=\"AuthorBlock\"><b>Jo\u00ebl Zlotogora<\/b>;<br \/>\nIsrael<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#7f07066d50330af3a\" href=\"#7f07066d50330af3a\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">E14 | Understanding human disease through animal models<\/div><\/a><\/h4><\/div><div id=\"7f07066d50330af3a\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chair:\u00a0\u00a0 Jose Luis Costa<br \/>\nRoom:\u00a0 K1<\/p>\n<p class=\"PublishingTitle\">E14.1 Animal models of Machado-Joseph disease<\/p>\n<p class=\"AuthorBlock\"><b>Luis Pereira de Almeida<\/b>;<br \/>\nPortugal<\/p>\n<p class=\"PublishingTitle\">E14.2 CRISPR\/Cas9 and TALENs fuel genetically engineered clinically relevant Xenopus tropicalis models.<\/p>\n<p class=\"AuthorBlock\"><b>Kris Vleminckx<\/b>;<br \/>\nBelgium<\/p>\n<\/div><\/div><\/div><\/div><\/div><div class=\"fusion-title title fusion-title-2 fusion-title-size-four\" style=\"margin-top:0px;margin-bottom:31px;\"><h4 class=\"title-heading-left\" style=\"margin:0;\"><h4><span style=\"color: #000000;\">10:30 &#8211; 11:00 hrs | Coffee Break<br \/>\n<\/span><\/h4><\/h4><div class=\"title-sep-container\"><div class=\"title-sep sep-double sep-solid\" style=\"border-color:#ffffff;\"><\/div><\/div><\/div><div class=\"fusion-menu-anchor\" id=\"C24\"><\/div><div class=\"fusion-title title fusion-title-3 fusion-title-size-four\" style=\"margin-top:0px;margin-bottom:31px;\"><h4 class=\"title-heading-left\" style=\"margin:0;\"><h4>11:00 &#8211; 12:30 hrs |\u00a0<span style=\"color: #a7d189;\">Concurrent Sessions C24-C29<\/span> from submitted abstracts<\/h4><\/h4><div class=\"title-sep-container\"><div class=\"title-sep sep-double sep-solid\" style=\"border-color:#ffffff;\"><\/div><\/div><\/div><style type=\"text\/css\" scoped=\"scoped\">#accordion-1833-3 .fusion-panel:hover{ background-color: #f9f9f9 } #accordion-1833-3 .fusion-panel { border-color:#cccccc; border-width:1px; background-color:rgba(167,209,137,0.79); }.fusion-accordian  #accordion-1833-3 .panel-title a .fa-fusion-box{ color: #ffffff;}.fusion-accordian  #accordion-1833-3 .panel-title a .fa-fusion-box:before{ font-size: 13px; width: 13px;}.fusion-accordian  #accordion-1833-3 .panel-title a{font-size:21px;}.fusion-accordian  #accordion-1833-3 .fa-fusion-box { background-color: #333333;border-color: #333333;}.fusion-accordian  #accordion-1833-3 .panel-title a:hover, #accordion-1833-3 .fusion-toggle-boxed-mode:hover .panel-title a { color: #00529c;}.fusion-accordian  #accordion-1833-3 .panel-title .active .fa-fusion-box,.fusion-accordian  #accordion-1833-3 .panel-title a:hover .fa-fusion-box { background-color: #00529c!important;border-color: #00529c!important;}<\/style><div class=\"accordian fusion-accordian\"><div class=\"panel-group\" id=\"accordion-1833-3\"><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#e5283a22eb9fce05b\" href=\"#e5283a22eb9fce05b\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">C24 | Mosaicisms<\/div><\/a><\/h4><\/div><div id=\"e5283a22eb9fce05b\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p class=\"LocationName\">Chairs:\u00a0\u00a0 Jill Clayton-Smith, Feliciano Ramos<br \/>\nRoom:\u00a0\u00a0 Hall C<\/p>\n<p class=\"PresentationNumber\">C24.1 Analysis of Mosaicism for Sequence and Copy Number Variants in a Broad Diversity of Hereditary Disorders in a Large Clinical Cohort<\/p>\n<p class=\"AuthorBlock\"><b>SWAROOP ARADHYA<\/b>, R. Truty, C. Kautzer, M. Kennemer, S. Lincoln, J. Rhees, A. Stafford, R. Nussbaum;<br \/>\nSan Francisco, United States<\/p>\n<p class=\"PresentationNumber\">C24.2 Uniparental disomy in the Rare Disease Programme of the UK\u2019s 100,000 Genomes Project<\/p>\n<p class=\"AuthorBlock\"><b>Katherine R. Smith<\/b>, M. Bleda, D. Kasperaviciute, K. Ibanez, A. Rueda Martin, E. Thomas, E. Baple, A. Tucci, M.J. Caulfield, A. Rendon;<br \/>\nLondon, United Kingdom<\/p>\n<p class=\"PresentationNumber\">C24.3 Somatic mutation cell lineage analysis reveals progressive clonal determination in human embryo<\/p>\n<p class=\"AuthorBlock\"><b>Sara Bizzotto*<\/b>, J. Ganz, Y. Dou, R.N. Doan, E. Maury, M. Kwon, T. Bae, A. Abyzov, P.J. Park, C.A. Walsh;<br \/>\nBoston, United States<\/p>\n<p class=\"PresentationNumber\">C24.4 Basal and mutagen-driven somatic mutagenesis shape the genome of healthy human cells<b><\/b><\/p>\n<p class=\"AuthorBlock\"><b>Irene Franco*<\/b>, H. Helgadottir, A. Moggio, M. Larsson, P. Vrtacnik, A. Johansson, N. Norgren, P. Lundin, D. Mas-Ponte, J. Nordstr\u00f6m, T. Lundgren, P. Stenvinkel, L. Wennberg, F. Supek, M. Eriksson;<br \/>\nHUDDINGE, Sweden<\/p>\n<p class=\"PresentationNumber\">C24.5 Genetic basis of mosaic pigmentary disorders of the skin and how to detect them: the M.U.S.T.A.R.D. cohort\u2019s experience<\/p>\n<p class=\"AuthorBlock\"><b>Arthur SORLIN*<\/b>, V. Carmignac, P. Kuentz, \u00c9. Tisserant, Y. Duffourd, M.U.S.T.A.R.D. cohort\u2019s investigators, J. Rivi\u00e8re, P. Callier, C. Philippe, C. Thauvin, L. Faivre, P. Vabres;<br \/>\nDijon, France<\/p>\n<p class=\"PresentationNumber\">C24.6 The Hutchinson-Gilford progeria syndrome mutation is a somatic mutation in chronic kidney disease<\/p>\n<p class=\"AuthorBlock\"><b>Maria Eriksson<\/b>, H.T. Helgadottir, N. Viceconte, A. Witasp, E. Wall\u00e9n Arzt, A. Sola Carvajal, G. Revechon, A. Thorell, D. McGuinness, P.G. Shiels, A. Wernerson, P. Stenvinkel;<br \/>\nHuddinge, Sweden<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#0b92e2afe393e2016\" href=\"#0b92e2afe393e2016\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">C25 | Bioinformatics and multiomics<\/div><\/a><\/h4><\/div><div id=\"0b92e2afe393e2016\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p class=\"LocationName\">Chairs:\u00a0\u00a0 Christian Gillisen, Daniel Nilsson<br \/>\nRoom:\u00a0\u00a0 K2+K3<\/p>\n<p class=\"PresentationNumber\">C25.1 A transcriptome-wide Mendelian randomization study to uncover tissue-dependent regulatory mechanisms across the human phenome<\/p>\n<p class=\"AuthorBlock\"><b>Tom G. Richardson*<\/b>, G. Hemani, T.R. Gaunt, C.L. Relton, G. Davey Smith;<br \/>\nBristol, United Kingdom<\/p>\n<p class=\"PresentationNumber\">C25.2 Multivariate GWAS of inflammatory markers reveals novel disease associations<\/p>\n<p class=\"AuthorBlock\"><b>Sanni E. Ruotsalainen*<\/b>, J. Partanen, I. Surakka, M. Pirinen, V. Salomaa, M. Salmi, S. Jalkanen, M.J. Daly, S. Ripatti, J. Koskela;<br \/>\nHelsinki, Finland<\/p>\n<p class=\"PresentationNumber\">C25.3 Analysis of genetic variants through aggregation of homologous human protein domains via MetaDome strongly improves diagnostic prediction of missense variants<\/p>\n<p class=\"AuthorBlock\"><b>Laurens Wiel*<\/b>, C. Baakman, D. Gilissen, H. Venselaar, J.A. Veltman, G. Vriend, C. Gilissen;<br \/>\nNijmegen, Netherlands<\/p>\n<p class=\"PresentationNumber\">C25.4 reg2gene: predicting enhancer-gene associations using ensemble learning approaches<\/p>\n<p class=\"AuthorBlock\"><b>Inga Patarcic*<\/b>, V. Franke, A. Akalin;<br \/>\nBerlin, Germany<\/p>\n<p class=\"PresentationNumber\">C25.5 A GWAS on data-driven 3D facial phenotypes selected by matching siblings reveals 310 genetic loci<\/p>\n<p class=\"AuthorBlock\"><b>Hanne Hoskens*<\/b>, K. Indencleef, J. Li, J.D. White, A. Ortega-Castrillon, J. Wysocka, S. Walsh, S. Richmond, J.R. Shaffer, S.M. Weinberg, M.D. Shriver, H. Peeters, P. Claes;<br \/>\nLeuven, Belgium<\/p>\n<p class=\"PresentationNumber\">C25.6 GestaltMatcher: Identifying the second patient of its kind in the phenotype space<\/p>\n<p class=\"AuthorBlock\"><b>Tzung-Chien Hsieh*<\/b>, A. Bar-Haim, D. Duki\u0107, T.J. Pantel, M. Mensah, Y. Gurovich, N. Fleischer, Y. Hanani, G. Nadav, T. Kamphans, P. Krawitz;<br \/>\nBonn, Germany<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#85cb4d76c56bbbd5a\" href=\"#85cb4d76c56bbbd5a\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">C26 | Mitochondrial disorder<\/div><\/a><\/h4><\/div><div id=\"85cb4d76c56bbbd5a\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p class=\"LocationName\">Chairs:\u00a0 Olaf Bodamer, Elsebet \u00d8stergaard<br \/>\nRoom:\u00a0\u00a0 F1+F2+F3<\/p>\n<p class=\"PresentationNumber\">C26.1 Mutations in LIG3 are a novel cause of mitochondrial neurogastrointestinal encephalomyopathy<\/p>\n<p class=\"AuthorBlock\"><b>ELENA BONORA<\/b>, F. Bianco, C. Bergamini, G. Kellaris, F. Ullah, F. Isidori, I. Liparulo, C. Diquigiovanni, L. Masin, M.G. Cratere, E. Boschetti, V. Papa, A. Maresca, G. Cenacchi, R. Casadio, P. Martelli, I. Matera, I. Ceccherini, R. Fato, G. Raiola, S. Arrigo, S. Signa, M.S. Severino, P. Striano, C. Fiorillo, P. Picco, V. Carelli, N. Katsanis, M. Seri, R. De Giorgio;<br \/>\nBOLOGNA, Italy<\/p>\n<p class=\"PresentationNumber\">C26.2 Mutations in <i>POLRMT <\/i>impair mitochondrial transcription and are associated with a spectrum ofmitochondrial disease presentations<\/p>\n<p class=\"AuthorBlock\">M. Ol\u00e1hov\u00e1, B. Peter, H. Diaz, Z. Szilagyi, E.W. Sommerville, E.L. Blakely, J. Collier, V. Str\u00e1neck\u00fd, H. Hartmannov\u00e1, A.J. Bleyer, K.L. McBride, S.A. Bowden, Z. Korandov\u00e1, A. Pecinov\u00e1, H. Ropers, K. Kimia, H. Najmabadi, M. Tarnopolsky, L.I. Brady, N. Weaver, C.E. Prada, T. Mr\u00e1\u010dek, S. Kmoch, G.S. Gorman, M. Falkenberg, C. Gustafsson, <b>Robert W. Taylor<\/b>;<br \/>\nNewcastle upon Tyne, United Kingdom<\/p>\n<p class=\"PresentationNumber\">C26.3 Mutations in the <i>MRPS28<\/i> gene encoding the small mitoribosomal subunit protein bS1m in a patient with intrauterine growth retardation, craniofacial dysmorphism and multisystemic involvement<\/p>\n<p class=\"AuthorBlock\"><b>Juliette Pulman*<\/b>, B. Ruzzenente, L. Bianchi, M. Rio, N. Boddaert, A. Munnich, A. R\u00f6tig, M. Metodiev;<br \/>\nParis, France<\/p>\n<p class=\"PresentationNumber\">C26.4 Brain-on-a-chip &#8211; a neurophysiological model of MELAS disease and comorbid psychopathology<\/p>\n<p class=\"AuthorBlock\"><b>Tamas Kozicz<\/b>, T. Klein-Gunnewiek, D. Cassiman, T. Nelson, R. Rodenburg, E. Perales-Clemente, E. Morava, N. Nadif Kasri;<br \/>\nRochester, United States<\/p>\n<p class=\"PresentationNumber\">C26.5 The homozygous variant c.797G&gt;A\/p.(Cys266Tyr) in <i>PISD <\/i>is associated with a spondyloepimetaphyseal dysplasia with large epiphyses and disturbed mitochondrial function<\/p>\n<p class=\"AuthorBlock\"><b>Leonie von Elsner*<\/b>, K.M. Girisha, K. Neethukrishna, M. Muranjan, A. Shukla, G.S. Bhavani, G. Nishimura, K. Kutsche, G. Mortier;<br \/>\nHamburg, Germany<\/p>\n<p class=\"PresentationNumber\">C26.6 SSBP1 mutations cause a complex optic atrophy spectrum disorder with mitochondrial DNA depletion<b><\/b><\/p>\n<p class=\"AuthorBlock\"><b>Tommaso Pippucci<\/b>, V. Del Dotto, F. Ullah, I. Di Meo, P. Magini, M. Gusic, A. Maresca, L. Caporali, F. Palombo, F. Tagliavini, E.H. Baugh, C. La Morgia, P. Barboni, M. Carbonelli, M.L. Valentino, R. Liguori, V. Shashi, J. Sullivan, S. Nagaraj, E. Bertini, R. Carrozzo, F. Emma, I. Cutcutache, M. Armstrong, M. Page, N. Stong, E. Davies, D. Karall, S. Boesch, M. Seri, M. Falkenberg, H. Prokisch, N. Katsanis, V. Tiranti, V. Carelli;<br \/>\nBologna, Italy<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#d5c285b25c67c6268\" href=\"#d5c285b25c67c6268\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">C27 | Developmental disorders 2<\/div><\/a><\/h4><\/div><div id=\"d5c285b25c67c6268\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p class=\"LocationName\">Chairs:\u00a0 Marta Bertoli, Trine Prescott<br \/>\nRoom:\u00a0\u00a0 F4+F5<\/p>\n<p class=\"PresentationNumber\">C27.1 Diagnostic utility of genome-wide DNA methylation testing in genetically unsolved patients with suspected hereditary conditions<\/p>\n<p class=\"AuthorBlock\"><b>bekim sadikovic<\/b>;<br \/>\nLondon, Canada<\/p>\n<p class=\"PresentationNumber\">C27.2 Multiomics Approach to Diagnosing Undiagnosed Patients<\/p>\n<p class=\"AuthorBlock\"><b>Matthew T. Wheeler<\/b>, J.N. Kohler, D.E. Bonner, D.B. Zastrow, C. Reuter, M. Majcherska, L. Fernandez, C. McCormack, S. Marwaha, C. Curnin, A. Dries, M. Ruzhnikov, J. Hom, J. Sampson, P.G. Fisher, Undiagnosed Diseases Network, E.A. Ashley, J.A. Bernstein;<br \/>\nPalo Alto, United States<\/p>\n<p class=\"PresentationNumber\">C27.3 Mutated epigenetic modifiers in CYLD cutaneous syndrome<\/p>\n<p class=\"AuthorBlock\">H.R. Davies, K. Hodgson, E. Schwalbe, J. Coxhead, N. Sinclair, X. Zou, S. Cockell, A. Husain, S. Nik-Zainal, <b>Neil Rajan<\/b>;<br \/>\nNewcastle upon Tyne, United Kingdom<\/p>\n<p class=\"PresentationNumber\">C27.4 Identification and characterization of NEPRO-related skeletal dysplasia resembling cartilage hair hypoplasia<\/p>\n<p class=\"AuthorBlock\"><b>Dhanya Lakshmi Narayanan*<\/b>, N. Kausthubham, G.S. Bhavani, H. Shah, A. Shukla, G. Mortier, K.M. Girisha;<br \/>\nManipal, India<\/p>\n<p class=\"PresentationNumber\">C27.5 Impact of <i>ALPK1<\/i> causative variant in ROSAH syndrome, a newly characterised retinal and multisystem autosomal dominant disorder<\/p>\n<p class=\"AuthorBlock\"><b>Robyn V. Jamieson<\/b>, A. Sabri, J.R. Grigg, A. Cheng, T.H. Loi;<br \/>\nSydney, Australia<\/p>\n<p class=\"PresentationNumber\">C27.6 New mechanism for retinal degeneration on chrXq27.1<\/p>\n<p class=\"AuthorBlock\"><b>Jessica C. Gardner<\/b>, K. Jovanovich, D. Ottaviani, J. Jackson, A.T. Moore, K. Ziaka, K. Hau, A. Lane, M. Michaelides, M.E. Cheetham, A.J. Hardcastle;<br \/>\nLondon, United Kingdom<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#c2e18ee2a4dab3b3b\" href=\"#c2e18ee2a4dab3b3b\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">C28 | Breaking Abstracts<\/div><\/a><\/h4><\/div><div id=\"c2e18ee2a4dab3b3b\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p class=\"LocationName\">Chairs:\u00a0 Inga Prokopenko, Anna Lindstrand<br \/>\nRoom:\u00a0\u00a0 G2+G3<\/p>\n<p class=\"NoPresentations\">More information will follow in May.<\/p>\n<\/div><\/div><\/div><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#c355f0b97692512ce\" href=\"#c355f0b97692512ce\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">C29 | Stakeholder perspectives in cancer genetics<\/div><\/a><\/h4><\/div><div id=\"c355f0b97692512ce\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p><img loading=\"lazy\" class=\"alignnone wp-image-6695 \" src=\"https:\/\/2019.eshg.org\/wp-content\/uploads\/2019\/06\/ELPAGNew.png\" alt=\"\" width=\"46\" height=\"28\" srcset=\"https:\/\/2019.eshg.org\/wp-content\/uploads\/2019\/06\/ELPAGNew-200x120.png 200w, https:\/\/2019.eshg.org\/wp-content\/uploads\/2019\/06\/ELPAGNew-320x202.png 320w, https:\/\/2019.eshg.org\/wp-content\/uploads\/2019\/06\/ELPAGNew.png 350w\" sizes=\"(max-width: 46px) 100vw, 46px\" \/><br \/>\nChairs:\u00a0 Luzia Garrido, Ulf Kristoffersson<br \/>\nRoom:\u00a0\u00a0 K1<\/p>\n<p class=\"PresentationNumber\">C29.1 The public favours healthcare-mediated disclosure of hereditary cancer risk to at-risk relatives: a population-based survey in Sweden<b><\/b><\/p>\n<p class=\"AuthorBlock\">A. Andersson,<strong> C. Hawranek<\/strong>, A. \u00d6fverholm, H. Ehrencrona, K. Grill, S. Hajdarevic, B. Melin, E. Tham, B. Numan Hellquist, Anna Ros\u00e9n;<br \/>\nUme\u00e5, Sweden<\/p>\n<p class=\"PresentationNumber\">C29.2 Communication across generations: disclosure of BRCA cancer risk with young adults<\/p>\n<p class=\"AuthorBlock\"><b>Alison L. Young*<\/b>, P.N. Butow, P. Rhodes, K.M. Tucker, R. Williams, E. Healey, C.E. Wakefield;<br \/>\nSydney, Australia<\/p>\n<p class=\"PresentationNumber\">C29.3 High-Risk Women\u2019s Responses and Understanding of Polygenic Breast Cancer Risk Information<\/p>\n<p class=\"AuthorBlock\"><b>Tatiane Yanes*<\/b>, R. Kaur, B. Meiser, M. Scheepers-Joynt, S. McInerny, K. Barlow-Stewart, Y. Antill, L. Salmon, C. Smyth, J. Halliday, P. James, M. Young;<br \/>\nSydney, Australia<\/p>\n<p class=\"PresentationNumber\">C29.4 Families\u2019 and healthcare professionals\u2019 uncertainties in the era of cancer precision medicine: results from PRISM<b><\/b><\/p>\n<p class=\"AuthorBlock\"><b>Janine Vetsch*<\/b>, C.E. Wakefield, M. Warby, K. Tucker, E. Duve, G. Marshall, T. Trahair, T. O&#8217;Brien, L. Lau, D. Ziegler;<br \/>\nRandwick, Australia<\/p>\n<p class=\"PresentationNumber\">C29.5 Advanced cancer patient perspectives on consenting to molecular tumour profiling<\/p>\n<p class=\"AuthorBlock\"><b>Megan Best*<\/b>, P. Butow, N. Bartley, C. Jacobs, I. Juraskova, A. Newson, D. Goldstein, J. Savard, B. Meiser, M. Ballinger, B. Biesecker, D. Thomas;<br \/>\nSydney, Australia<\/p>\n<p class=\"PresentationNumber\">C29.6 Dimensions of grief and loss for families living with Li Fraumeni Syndrome<\/p>\n<p class=\"AuthorBlock\"><b>Allison Werner-Lin<\/b>, S.L. Merrill, J.L. Young, C.D. Wilsnack, V. Groner, J.T. Loud, R.C. Bremer, J.A. Peters, M.H. Greene, S.A. Savage, P.P. Khincha;<br \/>\nPhiladelphia, United States<\/p>\n<\/div><\/div><\/div><\/div><\/div><div class=\"fusion-menu-anchor\" id=\"PL3\"><\/div><div class=\"fusion-title title fusion-title-4 fusion-title-size-four\" style=\"margin-top:0px;margin-bottom:31px;\"><h4 class=\"title-heading-left\" style=\"margin:0;\"><h4><span style=\"color: #000000;\">12:30 &#8211; 13:30 hrs |\u00a0Lunch\u00a0Break<br \/>\n<\/span><\/h4><\/h4><div class=\"title-sep-container\"><div class=\"title-sep sep-double sep-solid\" style=\"border-color:#ffffff;\"><\/div><\/div><\/div><div class=\"fusion-title title fusion-title-5 fusion-title-size-four\" style=\"margin-top:0px;margin-bottom:31px;\"><h4 class=\"title-heading-left\" style=\"margin:0;\"><p>13:30 &#8211; 14:15 hrs | <span style=\"color: #80c8f3;\">Plenary Session PL3<br \/>\n<\/span><\/p><\/h4><div class=\"title-sep-container\"><div class=\"title-sep sep-double sep-solid\" style=\"border-color:#ffffff;\"><\/div><\/div><\/div><style type=\"text\/css\" scoped=\"scoped\">#accordion-1833-4 .fusion-panel:hover{ background-color: #f9f9f9 } #accordion-1833-4 .fusion-panel { border-color:#cccccc; border-width:1px; background-color:rgba(128,200,243,0.63); }.fusion-accordian  #accordion-1833-4 .panel-title a .fa-fusion-box{ color: #ffffff;}.fusion-accordian  #accordion-1833-4 .panel-title a .fa-fusion-box:before{ font-size: 13px; width: 13px;}.fusion-accordian  #accordion-1833-4 .panel-title a{font-size:21px;}.fusion-accordian  #accordion-1833-4 .fa-fusion-box { background-color: #333333;border-color: #333333;}.fusion-accordian  #accordion-1833-4 .panel-title a:hover, #accordion-1833-4 .fusion-toggle-boxed-mode:hover .panel-title a { color: #00529c;}.fusion-accordian  #accordion-1833-4 .panel-title .active .fa-fusion-box,.fusion-accordian  #accordion-1833-4 .panel-title a:hover .fa-fusion-box { background-color: #00529c!important;border-color: #00529c!important;}<\/style><div class=\"accordian fusion-accordian\"><div class=\"panel-group\" id=\"accordion-1833-4\"><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#2a53a3dceb9e1469d\" href=\"#2a53a3dceb9e1469d\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">PL3 | Mendel Lecture<\/div><\/a><\/h4><\/div><div id=\"2a53a3dceb9e1469d\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chairs:\u00a0 Alexandre Reymond, Joris Veltman<br \/>\nRoom:\u00a0\u00a0 Hall C<\/p>\n<p class=\"PublishingTitle\">PL3.1 Mendel Lecture: A 25 Year Genomic Odyssey<\/p>\n<p class=\"AuthorBlock\"><b>Craig Venter;<br \/>\n<\/b>La Jolla, United States<b><br \/>\n<\/b><\/p>\n<div id=\"selenium-highlight\"><\/div>\n<\/div><\/div><\/div><\/div><\/div><div class=\"fusion-menu-anchor\" id=\"PL4\"><\/div><div class=\"fusion-title title fusion-title-6 fusion-title-size-four\" style=\"margin-top:0px;margin-bottom:31px;\"><h4 class=\"title-heading-left\" style=\"margin:0;\"><p>14:15 &#8211; 15:00 hrs | <span style=\"color: #80c8f3;\">Plenary Session PL4<br \/>\n<\/span><\/p><\/h4><div class=\"title-sep-container\"><div class=\"title-sep sep-double sep-solid\" style=\"border-color:#ffffff;\"><\/div><\/div><\/div><style type=\"text\/css\" scoped=\"scoped\">#accordion-1833-5 .fusion-panel:hover{ background-color: #f9f9f9 } #accordion-1833-5 .fusion-panel { border-color:#cccccc; border-width:1px; background-color:rgba(128,200,243,0.63); }.fusion-accordian  #accordion-1833-5 .panel-title a .fa-fusion-box{ color: #ffffff;}.fusion-accordian  #accordion-1833-5 .panel-title a .fa-fusion-box:before{ font-size: 13px; width: 13px;}.fusion-accordian  #accordion-1833-5 .panel-title a{font-size:21px;}.fusion-accordian  #accordion-1833-5 .fa-fusion-box { background-color: #333333;border-color: #333333;}.fusion-accordian  #accordion-1833-5 .panel-title a:hover, #accordion-1833-5 .fusion-toggle-boxed-mode:hover .panel-title a { color: #00529c;}.fusion-accordian  #accordion-1833-5 .panel-title .active .fa-fusion-box,.fusion-accordian  #accordion-1833-5 .panel-title a:hover .fa-fusion-box { background-color: #00529c!important;border-color: #00529c!important;}<\/style><div class=\"accordian fusion-accordian\"><div class=\"panel-group\" id=\"accordion-1833-5\"><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#a9005c72573d44687\" href=\"#a9005c72573d44687\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">PL4 | ESHG Award Lecture<\/div><\/a><\/h4><\/div><div id=\"a9005c72573d44687\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chairs:\u00a0 Alexandre Reymond, Joris Veltman<br \/>\nRoom:\u00a0\u00a0 Hall C<\/p>\n<p class=\"PublishingTitle\">PL4.1 ESHG Award Lecture: We and our second genome: two key players in common complex diseases<\/p>\n<p class=\"AuthorBlock\"><b>Cisca Wijmenga<\/b>;<br \/>\nGroningen, The Netherlands<\/p>\n<div id=\"selenium-highlight\"><\/div>\n<\/div><\/div><\/div><\/div><\/div><div class=\"fusion-menu-anchor\" id=\"PL5\"><\/div><div class=\"fusion-title title fusion-title-7 fusion-title-size-four\" style=\"margin-top:0px;margin-bottom:31px;\"><h4 class=\"title-heading-left\" style=\"margin:0;\"><p>15:00 &#8211; 16:00 hrs | <span style=\"color: #80c8f3;\">Plenary Session PL5<br \/>\n<\/span><\/p><\/h4><div class=\"title-sep-container\"><div class=\"title-sep sep-double sep-solid\" style=\"border-color:#ffffff;\"><\/div><\/div><\/div><style type=\"text\/css\" scoped=\"scoped\">#accordion-1833-6 .fusion-panel:hover{ background-color: #f9f9f9 } #accordion-1833-6 .fusion-panel { border-color:#cccccc; border-width:1px; background-color:rgba(128,200,243,0.63); }.fusion-accordian  #accordion-1833-6 .panel-title a .fa-fusion-box{ color: #ffffff;}.fusion-accordian  #accordion-1833-6 .panel-title a .fa-fusion-box:before{ font-size: 13px; width: 13px;}.fusion-accordian  #accordion-1833-6 .panel-title a{font-size:21px;}.fusion-accordian  #accordion-1833-6 .fa-fusion-box { background-color: #333333;border-color: #333333;}.fusion-accordian  #accordion-1833-6 .panel-title a:hover, #accordion-1833-6 .fusion-toggle-boxed-mode:hover .panel-title a { color: #00529c;}.fusion-accordian  #accordion-1833-6 .panel-title .active .fa-fusion-box,.fusion-accordian  #accordion-1833-6 .panel-title a:hover .fa-fusion-box { background-color: #00529c!important;border-color: #00529c!important;}<\/style><div class=\"accordian fusion-accordian\"><div class=\"panel-group\" id=\"accordion-1833-6\"><div class=\"fusion-panel panel-default fusion-toggle-no-divider fusion-toggle-boxed-mode\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\"><a data-toggle=\"collapse\" data-target=\"#7fb28fdd5680f3bc3\" href=\"#7fb28fdd5680f3bc3\"><div class=\"fusion-toggle-icon-wrapper\"><i class=\"fa-fusion-box\"><\/i><\/div><div class=\"fusion-toggle-heading\">PL5 | Awards Session<\/div><\/a><\/h4><\/div><div id=\"7fb28fdd5680f3bc3\" class=\"panel-collapse collapse \"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p>Chairs:\u00a0 Alexandre Reymond, Joris Veltman<br \/>\nRoom:\u00a0\u00a0 Hall C<\/p>\n<p class=\" PublishingTitle\">EJHG-SN Citation Awards<\/p>\n<p class=\" PublishingTitle\">ESHG Awards for Best Presentations by Young Investigators<\/p>\n<p class=\" PublishingTitle\">European DNA Day Contest<\/p>\n<p class=\" PublishingTitle\">Closing Address<\/p>\n<\/div><\/div><\/div><\/div><\/div><div class=\"fusion-clearfix\"><\/div>\n\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div><div  class=\"fusion-layout-column fusion_builder_column fusion_builder_column_1_2 fusion-builder-column-4 fusion-one-half fusion-column-first 1_2\"  style='margin-top:0px;margin-bottom:0px;'>\n\t\t\t\t\t<div class=\"fusion-column-wrapper\" style=\"padding: 0px 0px 0px 0px;background-position:left top;background-repeat:no-repeat;-webkit-background-size:cover;-moz-background-size:cover;-o-background-size:cover;background-size:cover;\"   data-bg-url=\"\">\n\t\t\t\t\t\t<div class=\"fusion-button-wrapper fusion-alignleft\"><style type=\"text\/css\" scoped=\"scoped\">.fusion-button.button-3{width:auto;}<\/style><a class=\"fusion-button button-flat fusion-button-square button-small button-lightgray button-3\" target=\"_self\" href=\"https:\/\/2019.eshg.org\/index.php\/programme\/monday\"><span class=\"fusion-button-icon-divider button-icon-divider-left\"><i class=\"fa-angle-double-left fas\"><\/i><\/span><span class=\"fusion-button-text fusion-button-text-left\">Monday<\/span><\/a><\/div><div class=\"fusion-clearfix\"><\/div>\n\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div><div  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