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Page 1
Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder.
LaBianca S, Brikell I, Helenius D, Loughnan R, Mefford J, Palmer CE, Walker R, Gådin JR, Krebs M, Appadurai V, Vaez M, Agerbo E, Pedersen MG, Børglum AD, Hougaard DM, Mors O, Nordentoft M, Mortensen PB, Kendler KS, Jernigan TL, Geschwind DH, Ingason A, Dahl AW, Zaitlen N, Dalsgaard S, Werge TM, Schork AJ. LaBianca S, et al. Among authors: zaitlen n. Nat Genet. 2024 Feb;56(2):234-244. doi: 10.1038/s41588-023-01593-7. Epub 2023 Nov 30. Nat Genet. 2024. PMID: 38036780
SLIViT: a general AI framework for clinical-feature diagnosis from limited 3D biomedical-imaging data.
Avram O, Durmus B, Rakocz N, Corradetti G, An U, Nitalla MG, Rudas A, Wakatsuki Y, Hirabayashi K, Velaga S, Tiosano L, Corvi F, Verma A, Karamat A, Lindenberg S, Oncel D, Almidani L, Hull V, Fasih-Ahmad S, Esmaeilkhanian H, Wykoff CC, Rahmani E, Arnold CW, Zhou B, Zaitlen N, Gronau I, Sankararaman S, Chiang JN, Sadda SR, Halperin E. Avram O, et al. Among authors: zaitlen n. Res Sq [Preprint]. 2023 Nov 21:rs.3.rs-3044914. doi: 10.21203/rs.3.rs-3044914/v2. Res Sq. 2023. PMID: 38045283 Free PMC article. Preprint.
Brain cell-type shifts in Alzheimer's disease, autism, and schizophrenia interrogated using methylomics and genetics.
Yap CX, Vo DD, Heffel MG, Bhattacharya A, Wen C, Yang Y, Kemper KE, Zeng J, Zheng Z, Zhu Z, Hannon E, Vellame DS, Franklin A, Caggiano C, Wamsley B, Geschwind DH, Zaitlen N, Gusev A, Pasaniuc B, Mill J, Luo C, Gandal MJ. Yap CX, et al. Among authors: zaitlen n. Sci Adv. 2024 May 24;10(21):eadn7655. doi: 10.1126/sciadv.adn7655. Epub 2024 May 23. Sci Adv. 2024. PMID: 38781333 Free PMC article.
Author Correction: Multi-ancestry polygenic mechanisms of type 2 diabetes.
Smith K, Deutsch AJ, McGrail C, Kim H, Hsu S, Huerta-Chagoya A, Mandla R, Schroeder PH, Westerman KE, Szczerbinski L, Majarian TD, Kaur V, Williamson A, Zaitlen N, Claussnitzer M, Florez JC, Manning AK, Mercader JM, Gaulton KJ, Udler MS. Smith K, et al. Among authors: zaitlen n. Nat Med. 2024 May 17. doi: 10.1038/s41591-024-03066-8. Online ahead of print. Nat Med. 2024. PMID: 38760590 No abstract available.
Tissue informative cell-free DNA methylation sites in amyotrophic lateral sclerosis.
Caggiano C, Morselli M, Qian X, Celona B, Thompson M, Wani S, Tosevska A, Taraszka K, Heuer G, Ngo S, Steyn F, Nestor P, Wallace L, McCombe P, Heggie S, Thorpe K, McElligott C, English G, Henders A, Henderson R, Lomen-Hoerth C, Wray N, McRae A, Pellegrini M, Garton F, Zaitlen N. Caggiano C, et al. Among authors: zaitlen n. medRxiv [Preprint]. 2024 Apr 10:2024.04.08.24305503. doi: 10.1101/2024.04.08.24305503. medRxiv. 2024. PMID: 38645132 Free PMC article. Preprint.
Multi-ancestry polygenic mechanisms of type 2 diabetes.
Smith K, Deutsch AJ, McGrail C, Kim H, Hsu S, Huerta-Chagoya A, Mandla R, Schroeder PH, Westerman KE, Szczerbinski L, Majarian TD, Kaur V, Williamson A, Zaitlen N, Claussnitzer M, Florez JC, Manning AK, Mercader JM, Gaulton KJ, Udler MS. Smith K, et al. Among authors: zaitlen n. Nat Med. 2024 Apr;30(4):1065-1074. doi: 10.1038/s41591-024-02865-3. Epub 2024 Mar 5. Nat Med. 2024. PMID: 38443691
143 results