Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

200 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[A front-of-pack labelling system for food and beverages for Mexico: a strategy of healthy decision-making.].
Kaufer-Horwitz M, Tolentino-Mayo L, Jáuregui A, Sánchez-Bazán K, Bourges H, Martínez S, Perichart O, Rojas-Russell M, Moreno L, Hunot C, Nava E, Ríos-Cortázar V, Palos-Lucio G, González L, González-de Cossio T, Pérez M, Borja Aburto VH, González A, Apolinar E, Pale LE, Colín E, Barriguete A, López O, López S, Aguilar-Salinas CA, Hernández-Ávila M, Martínez-Duncker D, de León F, Kershenobich D, Rivera J, Barquera S. Kaufer-Horwitz M, et al. Among authors: colin e. Salud Publica Mex. 2018 Jul-Ago;60(4):479-486. doi: 10.21149/9615. Salud Publica Mex. 2018. PMID: 30137950 Spanish.
Loss of CTLH component MAEA impairs DNA repair and replication and leads to developmental delay.
Hough SH, Jhujh SS, Awwad SW, Lewis OE, Lam S, Thomas JC, Mosler T, Bader A, Bartik L, McKee S, Amudhavalli S, Colin E, Damseh N, Clement E, Cacheiro P, Majumdar A, Smedley D, Fluss J, Giannini R, Thiffault I, Zagnoli Vieira G, Belotserkovskaya R, Smerdon SJ, Beli P, Galanty Y, Carnie CJ, Stewart GS, Jackson SP. Hough SH, et al. Among authors: colin e. EMBO Mol Med. 2025 Dec 19. doi: 10.1038/s44321-025-00352-x. Online ahead of print. EMBO Mol Med. 2025. PMID: 41420108 Free article.
Exome sequencing in severe non-syndromic specific learning and language disorders in a French cohort.
Viora-Dupont E, Delanne J, Garde A, Nambot S, Colin E, Bournez M, Fauconnier-Fatus C, Racine C, Simao De Souza C, Bernard C, Maurer A, Espitalier A, Binquet C, Bouctot M, Humbert ML, Briffaut AS, Darmency V, Plumet P, Cotinaud-Ricou A, Relin N, Callier P, Mosca-Boidron AL, Marle N, Tran Mau-Them F, Denommé-Pichon AS, Safraou H, Vitobello A, Philippe C, Duffourd Y, Bruel AL, Thauvin-Robinet C, Faivre L. Viora-Dupont E, et al. Among authors: colin e. Mol Autism. 2025 Oct 30;16(1):54. doi: 10.1186/s13229-025-00688-8. Mol Autism. 2025. PMID: 41168819 Free PMC article.
PERIGENOMED-CLINICS 1-the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in France.
Level C, Thauvin-Robinet C, Binquet C, Duffourd Y, Davoine E, Chevarin M, Tran-Mau-Them F, Lemaitre M, Bruel AL, Safraou H, Salvi D, Tisserant E, Lecommandeur E, Charreton A, Hassine A, de Tayrac M, Redon R, Barc J, Schmitt S, Piard J, Kuentz P, Cormier C, Malbos M, Racine C, Chabrol B, Cheillan D, Tardy V, Colin E, Bris C, Mercier S, Nizon M, Gaudillat L, Loizeau V, Lenelle C, Mottet N, Simon E, Arnoux JB, Carpentier M, Renaud C, Ziegler A, Lejeune C, Jannot AS, Asensio ML, Rollier P, Odent S, Bezieau S, Pasquier L, Huet F, Faivre L. Level C, et al. Among authors: colin e. BMJ Open. 2025 Oct 23;15(10):e105752. doi: 10.1136/bmjopen-2025-105752. BMJ Open. 2025. PMID: 41130699 Free PMC article.
Genome sequencing for the diagnosis of intellectual disability as a paradigm for rare diseases in the French healthcare setting: the prospective DEFIDIAG study.
El Chehadeh S, Heide S, Quélin C, Rio M, Margot H, Geneviève D, Isidor B, Goldenberg A, Guégan C, Lesca G, Willems M, Ormières C, Caumes R, Busa T, Bonneau D, Guerrot AM, Marey I, Vera G, Marzin P, Philippe A, Garde A, Coubes C, Vincent M, Michaud V, Mignot C, Charles P, Sigaudy S, Edery P, Lacombe D, Boland A, Nowak F, Bouctot M, Humbert-Asensio ML, Simon A, Chennen K, Sabour N, Delmas C, Nicolas G, Saugier-Veber P, Lecoquierre F, Cassinari K, Keren B, Courtin T, De Sainte Agathe JM, Malan V, Barcia G, Tran Mau-Them F, Safraou H, Philippe C, Thévenon J, Chatron N, Januel L, Piton A, Haushalter V, Gérard B, Lejeune C, Faivre L, Sanlaville D, Héron D, Odent S, Nitschké P, Schluth-Bolard C, Lyonnet S, Deleuze JF, Binquet C, Dollfus H; DEFIDIAG study group. El Chehadeh S, et al. Genome Med. 2025 Oct 3;17(1):110. doi: 10.1186/s13073-025-01527-4. Genome Med. 2025. PMID: 41044778 Free PMC article.
Further phenotypical delineation of DLG3-related neurodevelopmental disorders.
Malbos M, Gautier T, Shillington A, Colin E, Le Guillou X, Caluseriu O, Isidor B, Cogné B, Mignot C, Keren B, Weber S, Jacquin C, Dudding T, Calame D, Piard J, Levy J, Latypova X, Verloes A, Niclass T, Jacquette A, White L, Moizard MP, Dollfus H, Moutton S, Delanne J, Racine C, Thomas Q, Denommé-Pichon AS, Tran Mau-Them F, Bruel AL, Safraou H, Philippe C, Duffourd Y, Thauvin-Robinet C, Govin J, Vitobello A, Faivre L. Malbos M, et al. Among authors: colin e. Eur J Hum Genet. 2025 Dec;33(12):1585-1595. doi: 10.1038/s41431-025-01937-3. Epub 2025 Sep 22. Eur J Hum Genet. 2025. PMID: 40983642
200 results