{"id":3319,"date":"2023-10-25T16:59:20","date_gmt":"2023-10-25T14:59:20","guid":{"rendered":"https:\/\/ern-ithaca.eu\/?post_type=news&p=3319"},"modified":"2023-11-14T19:06:23","modified_gmt":"2023-11-14T18:06:23","slug":"ern-ithaca-webinar-10-incidental-and-secondary-findings-from-exome-genome-sequencing-the-views-of-various-european-countries-and-eshg","status":"publish","type":"news","link":"https:\/\/ern-ithaca.eu\/es\/events-news\/news\/ern-ithaca-webinar-10-incidental-and-secondary-findings-from-exome-genome-sequencing-the-views-of-various-european-countries-and-eshg\/","title":{"rendered":"ERN-ITHACA webinar 10 “Incidental and secondary findings from exome\/genome sequencing : The views of various European countries and ESHG”"},"content":{"rendered":"

The issue of incidental data<\/strong>, which has always existed in genetics, is becoming exponential with the advent of genomic medicine. The issue of secondary data<\/strong>, involving an active search for variants in a list of so-called actionable genes, is very popular in the USA, whereas Europeans are urging caution. 
In this webinar, we would like to take a look at the evolution of recommendations made by certain European countries, as well as those of the ESHG.<\/p>\n\n\n\n

<\/div>\n\n\n\n

Program:<\/strong><\/p>\n\n\n\n

Bienvenida e introducci\u00f3n <\/strong>
Speaker : Laurence Faivre
From : CHU Dijon-Bourgogne, Dijon, France<\/p>\n\n\n\n

ESHG recommendations on Opportunistic genomic screening<\/strong>
Speaker : Dr Francesca Forzano
From : King’s College, London, UK<\/p>\n\n\n\n

Secondary findings in exome sequencing. Experience in a tertiary public hospital in Spain<\/strong>
Speaker : Dr Marta Codina Sol\u00e0 and Dr Anna Abuli
From : Hospital Universitari Vall d\u2019Hebron, Barcelona, Spain<\/p>\n\n\n\n

Management of unexpected findings in the NHS England Genomic Medicine Service<\/strong>
Speaker : Rachael Mein\u00a0
From : NHS England Genomics Unit Senior Laboratory Advisor (Rare Disease), UK\u00a0<\/p>\n\n\n\n

Studies for exploring the expectations of patients\/families regarding additional findings from exome sequencing in France<\/strong>
Speaker : Laurence Faivre
From : CHU Dijon-Bourgogne, Dijon, France<\/p>\n\n\n\n

<\/div>\n\n\n\n

Fecha<\/strong>: 28 November, 05:00 – 06:30 PM, French time<\/p>\n\n\n\n

Formulario de inscripci\u00f3n: https:\/\/forms.office.com\/e\/cUU3JXMYTt<\/a><\/strong><\/p>\n\n\n\n

Link to connect:<\/strong> Rejoindre la conversation (microsoft.com)<\/a>Rejoindre la conversation (microsoft.com)<\/a><\/a><\/p>","protected":false},"excerpt":{"rendered":"

The issue of incidental data, which has always existed in genetics, is becoming exponential with the advent of genomic medicine. The issue of secondary data, involving an active search for variants in a list of so-called actionable genes, is very popular in the USA, whereas Europeans are urging caution. In this webinar, we would like to take […]<\/p>\n","protected":false},"featured_media":0,"template":"","categories":[150],"tags":[],"class_list":["post-3319","news","type-news","status-publish","hentry","category-ern-ithaca-event"],"acf":[],"yoast_head":"\nERN-ITHACA webinar 10 "Incidental and secondary findings from exome\/genome sequencing : The views of various European countries and ESHG" - ERN ITHACA<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/ern-ithaca.eu\/es\/news\/ern-ithaca-webinar-10-incidental-and-secondary-findings-from-exome-genome-sequencing-the-views-of-various-european-countries-and-eshg\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"ERN-ITHACA webinar 10 "Incidental and secondary findings from exome\/genome sequencing : The views of various European countries and ESHG" - ERN ITHACA\" \/>\n<meta property=\"og:description\" content=\"The issue of incidental data, which has always existed in genetics, is becoming exponential with the advent of genomic medicine. 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