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113 results

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Page 1
An automatic facial landmarking for children with rare diseases.
Hennocq Q, Bongibault T, Bizière M, Delassus O, Douillet M, Cormier-Daire V, Amiel J, Lyonnet S, Marlin S, Rio M, Picard A, Khonsari RH, Garcelon N. Hennocq Q, et al. Among authors: garcelon n. Am J Med Genet A. 2023 May;191(5):1210-1221. doi: 10.1002/ajmg.a.63126. Epub 2023 Jan 30. Am J Med Genet A. 2023. PMID: 36714960
Pediatric Tumors and Developmental Anomalies: A French Nationwide Cohort Study.
Semeraro M, Fouquet C, Vial Y, Amiel J, Galmiche L, Cretolle C, Blanc T, Jolaine V, Garcelon N, Entz-Werle N, Pellier I, Vérité C, Sophie Taque, Coulomb A, Petit A, Corradini N, Bouazza N, Lacour B, Clavel J, Brugières L, Bourdeaut F, Sarnacki S; members of the TED Consortium. Semeraro M, et al. Among authors: garcelon n. J Pediatr. 2023 Aug;259:113451. doi: 10.1016/j.jpeds.2023.113451. Epub 2023 May 9. J Pediatr. 2023. PMID: 37169337
Association of Antihypertensive Agents with the Risk of In-Hospital Death in Patients with Covid-19.
Chouchana L, Beeker N, Garcelon N, Rance B, Paris N, Salamanca E, Polard E, Burgun A, Treluyer JM, Neuraz A; AP-HP/Universities/Inserm COVID-19 research collaboration, AP-HP Covid CDR Initiative, and “Entrepôt de Données de Santé” AP-HP Consortium”. Chouchana L, et al. Among authors: garcelon n. Cardiovasc Drugs Ther. 2022 Jun;36(3):483-488. doi: 10.1007/s10557-021-07155-5. Epub 2021 Feb 17. Cardiovasc Drugs Ther. 2022. PMID: 33595761 Free PMC article.
Deep Learning on Bone Scintigraphy to Detect Abnormal Cardiac Uptake at Risk of Cardiac Amyloidosis.
Delbarre MA, Girardon F, Roquette L, Blanc-Durand P, Hubaut MA, Hachulla É, Semah F, Huglo D, Garcelon N, Marchal E, El Esper I, Tribouilloy C, Lamblin N, Duhaut P, Schmidt J, Itti E, Damy T. Delbarre MA, et al. Among authors: garcelon n. JACC Cardiovasc Imaging. 2023 Aug;16(8):1085-1095. doi: 10.1016/j.jcmg.2023.01.014. Epub 2023 Apr 12. JACC Cardiovasc Imaging. 2023. PMID: 37227330 Free article.
Next Generation Phenotyping and Synthetic Faces in Coffin Siris Syndrome.
Hennocq Q, Lienhard O, Rao D, Amiel J, Benichou L, Bongibault T, Hidalgo AB, Cormier-Daire V, Lyonnet S, Picard A, Rio M, Zaiter A, Garcelon N, Tkemaladze T, Khonsari RH. Hennocq Q, et al. Among authors: garcelon n. Clin Genet. 2024 Dec 26. doi: 10.1111/cge.14682. Online ahead of print. Clin Genet. 2024. PMID: 39726094
Facilitating phenotyping from clinical texts: the medkit library.
Neuraz A, Vaillant G, Arias C, Birot O, Huynh KT, Fabacher T, Rogier A, Garcelon N, Lerner I, Rance B, Coulet A. Neuraz A, et al. Among authors: garcelon n. Bioinformatics. 2024 Nov 28;40(12):btae681. doi: 10.1093/bioinformatics/btae681. Bioinformatics. 2024. PMID: 39546377 Free PMC article.
113 results