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The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022

The European Society of Human Genetics—Young Committee (ESHG-Y) aims to support young human geneticists by developing strategies and programs for better education and creating a strong network in all European countries. In this report, we present the ESHG-Y projects conducted since its conception. W...

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Detalles Bibliográficos
Autores principales: Avram, Elena, Ding, Can, de Miranda Cerqueira, Juliana Xavier, Johari, Mridul, da Silva, Ana Raquel Gouveia Freitas, Săbău, Ileana-Delia, Noor, Nuru, Kalantari, Silvia, Dore, Rhys, Barbosa-Matos, Rita, Mroczek, Magdalena, Tonini, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133236/
https://www.ncbi.nlm.nih.gov/pubmed/36755105
http://dx.doi.org/10.1038/s41431-023-01300-4
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author Avram, Elena
Ding, Can
de Miranda Cerqueira, Juliana Xavier
Johari, Mridul
da Silva, Ana Raquel Gouveia Freitas
Săbău, Ileana-Delia
Noor, Nuru
Kalantari, Silvia
Dore, Rhys
Barbosa-Matos, Rita
Mroczek, Magdalena
Tonini, Francesca
author_facet Avram, Elena
Ding, Can
de Miranda Cerqueira, Juliana Xavier
Johari, Mridul
da Silva, Ana Raquel Gouveia Freitas
Săbău, Ileana-Delia
Noor, Nuru
Kalantari, Silvia
Dore, Rhys
Barbosa-Matos, Rita
Mroczek, Magdalena
Tonini, Francesca
author_sort Avram, Elena
collection PubMed
description The European Society of Human Genetics—Young Committee (ESHG-Y) aims to support young human geneticists by developing strategies and programs for better education and creating a strong network in all European countries. In this report, we present the ESHG-Y projects conducted since its conception. We organized the educational sessions at the ESHG Annual Conference, the European Dysmorphology Meetings, and a virtual session in collaboration with the European Board of Medical Genetics (EBMG). Also, the ESHG-Y regularly promotes relevant activities and succeeded in creating an active network of young geneticists. Our representatives have a supportive role in well-known organizations such as: ESHG Board, ESHG Scientific Program Committee, ESHG Education Committee, EBMG, ERN-Ithaca, Unique - Rare Chromosome Disorder Support group, Orphanet, EuroGEMS, MOOC BIG and more. Taking into consideration all activities and ongoing projects, we can state that the ESHG-Y successfully achieves its objectives and brings young professionals together.
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spelling pubmed-101332362023-04-28 The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022 Avram, Elena Ding, Can de Miranda Cerqueira, Juliana Xavier Johari, Mridul da Silva, Ana Raquel Gouveia Freitas Săbău, Ileana-Delia Noor, Nuru Kalantari, Silvia Dore, Rhys Barbosa-Matos, Rita Mroczek, Magdalena Tonini, Francesca Eur J Hum Genet Correspondence The European Society of Human Genetics—Young Committee (ESHG-Y) aims to support young human geneticists by developing strategies and programs for better education and creating a strong network in all European countries. In this report, we present the ESHG-Y projects conducted since its conception. We organized the educational sessions at the ESHG Annual Conference, the European Dysmorphology Meetings, and a virtual session in collaboration with the European Board of Medical Genetics (EBMG). Also, the ESHG-Y regularly promotes relevant activities and succeeded in creating an active network of young geneticists. Our representatives have a supportive role in well-known organizations such as: ESHG Board, ESHG Scientific Program Committee, ESHG Education Committee, EBMG, ERN-Ithaca, Unique - Rare Chromosome Disorder Support group, Orphanet, EuroGEMS, MOOC BIG and more. Taking into consideration all activities and ongoing projects, we can state that the ESHG-Y successfully achieves its objectives and brings young professionals together. Springer International Publishing 2023-02-09 2023-04 /pmc/articles/PMC10133236/ /pubmed/36755105 http://dx.doi.org/10.1038/s41431-023-01300-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Correspondence
Avram, Elena
Ding, Can
de Miranda Cerqueira, Juliana Xavier
Johari, Mridul
da Silva, Ana Raquel Gouveia Freitas
Săbău, Ileana-Delia
Noor, Nuru
Kalantari, Silvia
Dore, Rhys
Barbosa-Matos, Rita
Mroczek, Magdalena
Tonini, Francesca
The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022
title The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022
title_full The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022
title_fullStr The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022
title_full_unstemmed The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022
title_short The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022
title_sort european society of human genetics—young committee- activities and achievements between 2019–2022
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133236/
https://www.ncbi.nlm.nih.gov/pubmed/36755105
http://dx.doi.org/10.1038/s41431-023-01300-4
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