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

4,903 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism.
Poulter JA, Al-Araimi M, Conte I, van Genderen MM, Sheridan E, Carr IM, Parry DA, Shires M, Carrella S, Bradbury J, Khan K, Lakeman P, Sergouniotis PI, Webster AR, Moore AT, Pal B, Mohamed MD, Venkataramana A, Ramprasad V, Shetty R, Saktivel M, Kumaramanickavel G, Tan A, Mackey DA, Hewitt AW, Banfi S, Ali M, Inglehearn CF, Toomes C. Poulter JA, et al. Among authors: tan a. Am J Hum Genet. 2013 Dec 5;93(6):1143-50. doi: 10.1016/j.ajhg.2013.11.002. Epub 2013 Nov 27. Am J Hum Genet. 2013. PMID: 24290379 Free PMC article. Review.
Infants' Social Evaluation of Helpers and Hinderers: A Large-Scale, Multi-Lab, Coordinated Replication Study.
Lucca K, Yuen F, Wang Y, Alessandroni N, Allison O, Alvarez M, Axelsson EL, Baumer J, Baumgartner HA, Bertels J, Bhavsar M, Byers-Heinlein K, Capelier-Mourguy A, Chijiiwa H, Chin CS, Christner N, Cirelli LK, Corbit J, Daum MM, Doan T, Dresel M, Exner A, Fei W, Forbes SH, Franchin L, Frank MC, Geraci A, Giraud M, Gornik ME, Wiesmann CG, Grossmann T, Hadley IM, Havron N, Henderson AME, Matzner EH, Immel BA, Jankiewicz G, Jędryczka W, Kanakogi Y, Kominsky JF, Lew-Williams C, Liberman Z, Liu L, Liu Y, Loeffler MT, Martin A, Mayor J, Meng X, Misiak M, Moreau D, Nencheva ML, Oña LS, Otálora Y, Paulus M, Pepe B, Pickron CB, Powell LJ, Proft M, Quinn AA, Rakoczy H, Reschke PJ, Roth-Hanania R, Rothmaler K, Schlegelmilch K, Schlingloff-Nemecz L, Schmuckler MA, Schuwerk T, Seehagen S, Şen HH, Shainy MR, Silvestri V, Soderstrom M, Sommerville J, Song HJ, Sorokowski P, Stutz SE, Su Y, Taborda-Osorio H, Tan AWM, Tatone D, Taylor-Partridge T, Tsang CKA, Urbanek A, Uzefovsky F, Visser I, Wertz AE, Williams M, Wolsey K, Wong TT, Woodward AM, Wu Y, Zeng Z, Zimmer L, Hamlin JK. Lucca K, et al. Among authors: tan awm. Dev Sci. 2025 Jan;28(1):e13581. doi: 10.1111/desc.13581. Dev Sci. 2025. PMID: 39600132
Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk.
Chew EG, Liu Z, Li Z, Chung SJ, Lian MM, Tandiono M, Heng YJ, Ng EY, Tan LC, Chng WL, Tan TJ, Peh EK, Ho YS, Chen XY, Lim EY, Chang CH, Leong JJ, Peh TX, Chan LL, Chao Y, Au WL, Prakash KM, Lim JL, Tay YW, Mok V, Chan AY, Lin JJ, Jeon BS, Song K, Tham CC, Pang CP, Ahn J, Park KH, Wiggs JL, Aung T, Tan AH, Ahmad Annuar A, Makarious MB, Blauwendraat C, Nalls MA, Robak LA, Alcalay RN, Gan-Or Z, Reynolds R, Lim SY, Xia Y, Khor CC, Tan EK, Wang Z, Foo JN. Chew EG, et al. Among authors: tan ah. Nat Aging. 2024 Nov 21. doi: 10.1038/s43587-024-00760-7. Online ahead of print. Nat Aging. 2024. PMID: 39572736
4,903 results