Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx

<p>This work summarizes 15 years of genetic research on neutropenia in the Polish pediatric cohort, explores the distribution and spectrum of disease-causing genetic variants associated with congenital neutropenia in Poland, and demonstrates the impact of a nationwide information campaign on i...

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সংরক্ষণ করুন:
গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক: Katarzyna Bąbol-Pokora (11710986) (author)
অন্যান্য লেখক: Weronika Dobrewa (22687418) (author), Marta Bielska (22687421) (author), Szymon Janczar (14892591) (author), Joanna Madzio (22687424) (author), Aleksandra Jaworowska (22687427) (author), Sylwia Kołtan (8955506) (author), Marcin Hennig (22687430) (author), Joanna Renke (22687433) (author), Iwona Dachowska-Kałwak (22687436) (author), Magdalena Cienkusz (22687439) (author), Wojciech Młynarski (3404939) (author)
প্রকাশিত: 2025
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_version_ 1849927622783401984
author Katarzyna Bąbol-Pokora (11710986)
author2 Weronika Dobrewa (22687418)
Marta Bielska (22687421)
Szymon Janczar (14892591)
Joanna Madzio (22687424)
Aleksandra Jaworowska (22687427)
Sylwia Kołtan (8955506)
Marcin Hennig (22687430)
Joanna Renke (22687433)
Iwona Dachowska-Kałwak (22687436)
Magdalena Cienkusz (22687439)
Wojciech Młynarski (3404939)
author2_role author
author
author
author
author
author
author
author
author
author
author
author_facet Katarzyna Bąbol-Pokora (11710986)
Weronika Dobrewa (22687418)
Marta Bielska (22687421)
Szymon Janczar (14892591)
Joanna Madzio (22687424)
Aleksandra Jaworowska (22687427)
Sylwia Kołtan (8955506)
Marcin Hennig (22687430)
Joanna Renke (22687433)
Iwona Dachowska-Kałwak (22687436)
Magdalena Cienkusz (22687439)
Wojciech Młynarski (3404939)
author_role author
dc.creator.none.fl_str_mv Katarzyna Bąbol-Pokora (11710986)
Weronika Dobrewa (22687418)
Marta Bielska (22687421)
Szymon Janczar (14892591)
Joanna Madzio (22687424)
Aleksandra Jaworowska (22687427)
Sylwia Kołtan (8955506)
Marcin Hennig (22687430)
Joanna Renke (22687433)
Iwona Dachowska-Kałwak (22687436)
Magdalena Cienkusz (22687439)
Wojciech Młynarski (3404939)
dc.date.none.fl_str_mv 2025-11-26T06:33:42Z
dc.identifier.none.fl_str_mv 10.3389/fimmu.2025.1688208.s001
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/Table_1_The_genetic_landscape_of_congenital_neutropenia_in_Poland_summary_of_the_nationwide_screening_campaign_xlsx/30718682
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Genetic Immunology
ELANE
neutropenia
NGS
SBDs
immunodeficiencies
CYN
SCN
dc.title.none.fl_str_mv Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description <p>This work summarizes 15 years of genetic research on neutropenia in the Polish pediatric cohort, explores the distribution and spectrum of disease-causing genetic variants associated with congenital neutropenia in Poland, and demonstrates the impact of a nationwide information campaign on increasing the efficiency of patient recruitment. The study included 126 patients with suspected congenital neutropenia recruited in 2008–2019 and 291 patients recruited in 2020–2023 as part of the FixNet project, which featured a nationwide information campaign. Molecular analyses were performed using Sanger sequencing (91 patients) and targeted next-generation sequencing (NGS) (326 patients) in a panel of neutropenia-related genes. The information campaign significantly increased the number of referred patients from 10.5 per year to 72.75 per year. Based on the results obtained, 102 patients belonging to 80 different families were diagnosed with severe congenital neutropenia (SCN) and neutropenia-related syndromes, the majority (43%) of whom harbored variants in the ELANE gene, including 12 novel ones. Most of the remaining cases were SBDS, CLPB, SRP54, and CXCR4 gene defects. This work describes the largest cohort of genetic variations associated with suspected congenital neutropenia (CN) in Poland and is an important contribution to the international SCN registry.</p>
eu_rights_str_mv openAccess
id Manara_79e7470cca36c3db47be417fb647e93d
identifier_str_mv 10.3389/fimmu.2025.1688208.s001
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30718682
publishDate 2025
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsxKatarzyna Bąbol-Pokora (11710986)Weronika Dobrewa (22687418)Marta Bielska (22687421)Szymon Janczar (14892591)Joanna Madzio (22687424)Aleksandra Jaworowska (22687427)Sylwia Kołtan (8955506)Marcin Hennig (22687430)Joanna Renke (22687433)Iwona Dachowska-Kałwak (22687436)Magdalena Cienkusz (22687439)Wojciech Młynarski (3404939)Genetic ImmunologyELANEneutropeniaNGSSBDsimmunodeficienciesCYNSCN<p>This work summarizes 15 years of genetic research on neutropenia in the Polish pediatric cohort, explores the distribution and spectrum of disease-causing genetic variants associated with congenital neutropenia in Poland, and demonstrates the impact of a nationwide information campaign on increasing the efficiency of patient recruitment. The study included 126 patients with suspected congenital neutropenia recruited in 2008–2019 and 291 patients recruited in 2020–2023 as part of the FixNet project, which featured a nationwide information campaign. Molecular analyses were performed using Sanger sequencing (91 patients) and targeted next-generation sequencing (NGS) (326 patients) in a panel of neutropenia-related genes. The information campaign significantly increased the number of referred patients from 10.5 per year to 72.75 per year. Based on the results obtained, 102 patients belonging to 80 different families were diagnosed with severe congenital neutropenia (SCN) and neutropenia-related syndromes, the majority (43%) of whom harbored variants in the ELANE gene, including 12 novel ones. Most of the remaining cases were SBDS, CLPB, SRP54, and CXCR4 gene defects. This work describes the largest cohort of genetic variations associated with suspected congenital neutropenia (CN) in Poland and is an important contribution to the international SCN registry.</p>2025-11-26T06:33:42ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.3389/fimmu.2025.1688208.s001https://figshare.com/articles/dataset/Table_1_The_genetic_landscape_of_congenital_neutropenia_in_Poland_summary_of_the_nationwide_screening_campaign_xlsx/30718682CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/307186822025-11-26T06:33:42Z
spellingShingle Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx
Katarzyna Bąbol-Pokora (11710986)
Genetic Immunology
ELANE
neutropenia
NGS
SBDs
immunodeficiencies
CYN
SCN
status_str publishedVersion
title Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx
title_full Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx
title_fullStr Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx
title_full_unstemmed Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx
title_short Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx
title_sort Table 1_The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign.xlsx
topic Genetic Immunology
ELANE
neutropenia
NGS
SBDs
immunodeficiencies
CYN
SCN