eprintid: 10206115
rev_number: 9
eprint_status: archive
userid: 699
dir: disk0/10/20/61/15
datestamp: 2025-03-14 10:52:48
lastmod: 2025-03-14 10:52:48
status_changed: 2025-03-14 10:52:48
type: article
metadata_visibility: show
sword_depositor: 699
creators_name: Howell, KB
creators_name: White, SM
creators_name: McTague, A
creators_name: D’Gama, AM
creators_name: Costain, G
creators_name: Poduri, A
creators_name: Scheffer, IE
creators_name: Chau, V
creators_name: Smith, LD
creators_name: Stephenson, SEM
creators_name: Wojcik, M
creators_name: Davidson, A
creators_name: Sebire, N
creators_name: Sliz, P
creators_name: Beggs, AH
creators_name: Chitty, LS
creators_name: Cohn, RD
creators_name: Marshall, CR
creators_name: Andrews, NC
creators_name: North, KN
creators_name: Cross, JH
creators_name: Christodoulou, J
creators_name: Scherer, SW
title: International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
ispublished: pub
divisions: UCL
divisions: B02
divisions: D13
divisions: G28
divisions: G26
divisions: G23
divisions: G25
note: This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
abstract: Advances in genomic technologies have revolutionized the diagnosis of rare genetic diseases, leading to the emergence of precision therapies. However, there remains significant effort ahead to ensure the promise of precision medicine translates to improved outcomes. Here, we discuss the challenges in advancing precision child health and highlight how international collaborations such as the International Precision Child Health Partnership, which embed research into clinical care, can maximize benefits for children globally.
date: 2025-02-27
date_type: published
publisher: Springer Science and Business Media LLC
official_url: https://doi.org/10.1038/s41525-025-00474-8
oa_status: green
full_text_type: pub
language: eng
primo: open
primo_central: open_green
verified: verified_manual
elements_id: 2365795
doi: 10.1038/s41525-025-00474-8
medium: Electronic
pii: 10.1038/s41525-025-00474-8
lyricists_name: Chitty, Lyn
lyricists_name: Sebire, Neil
lyricists_name: Cross, Judith
lyricists_name: McTague, Amy
lyricists_id: LCHIT39
lyricists_id: NJSEB45
lyricists_id: JHCRO62
lyricists_id: AMCTA71
actors_name: McTague, Amy
actors_id: AMCTA71
actors_role: owner
funding_acknowledgements: P50 HD105351 [NICHD NIH HHS]; T32 HD098061 [NICHD NIH HHS]
full_text_status: public
publication: npj Genomic Medicine
volume: 10
article_number: 13
event_location: England
issn: 2056-7944
citation:        Howell, KB;    White, SM;    McTague, A;    D’Gama, AM;    Costain, G;    Poduri, A;    Scheffer, IE;                                                                 ... Scherer, SW; + view all <#>        Howell, KB;  White, SM;  McTague, A;  D’Gama, AM;  Costain, G;  Poduri, A;  Scheffer, IE;  Chau, V;  Smith, LD;  Stephenson, SEM;  Wojcik, M;  Davidson, A;  Sebire, N;  Sliz, P;  Beggs, AH;  Chitty, LS;  Cohn, RD;  Marshall, CR;  Andrews, NC;  North, KN;  Cross, JH;  Christodoulou, J;  Scherer, SW;   - view fewer <#>    (2025)    International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease.                   npj Genomic Medicine , 10     , Article 13.  10.1038/s41525-025-00474-8 <https://doi.org/10.1038/s41525-025-00474-8>.       Green open access   
 
document_url: https://discovery.ucl.ac.uk/id/eprint/10206115/1/McTague_s41525-025-00474-8.pdf