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Page 1
Preferences regarding Disclosure of Risk for Parkinson's Disease in a Population-based Study.
Mahlknecht P, Leiter S, Horlings C, Schwarzová K, Egner I, Stockner H, Marini K, Theyer C, Zamarian L, Djamshidian A, Seppi K, Farfan F, Garrido A, Ghosh S, Krüger R, McIntyre D, Mollenhauer B, Noyce A, Pauly C, Pilco-Janeta DF, Rege K, Satagopam VP, Schade S, Simonet C, Trenkwalder C, Poewe W; HeBA Consortium. Mahlknecht P, et al. Among authors: leiter s. Mov Disord Clin Pract. 2024 Nov 18. doi: 10.1002/mdc3.14264. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 39558636
A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor.
Mahmood S, Leiter SM, Phyu P, Craven C, Horan G, Gains J, Briggs M, Blanco E, Behjati S, Watkins J, Tadross JA, Roberts T, Trotman J, Tarpey P, Armstrong R, Murray MJ. Mahmood S, et al. Among authors: leiter sm. Pediatr Blood Cancer. 2024 Dec;71(12):e31368. doi: 10.1002/pbc.31368. Epub 2024 Oct 8. Pediatr Blood Cancer. 2024. PMID: 39380176 No abstract available.
Ertugliflozin to Reduce Arrhythmic Burden in Patients with ICDs/CRT-Ds.
Benedikt M, Oulhaj A, Rohrer U, Manninger M, Tripolt NJ, Pferschy PN, Aziz F, Wallner M, Kolesnik E, Gwechenberger M, Martinek M, Nürnberg M, Roithinger FX, Steinwender C, Widkal J, Leiter S, Zirlik A, Stühlinger M, Scherr D, Sourij H, von Lewinski D. Benedikt M, et al. Among authors: leiter s. NEJM Evid. 2024 Oct;3(10):EVIDoa2400147. doi: 10.1056/EVIDoa2400147. Epub 2024 Sep 1. NEJM Evid. 2024. PMID: 39217453 Clinical Trial.
Developing a Paired Whole Genome Sequencing Service for Children With Cancer.
Sarkies L, Thomas P, Edeko EA, Leiter S, Trotman J, Armstrong R, Vedi A. Sarkies L, et al. Among authors: leiter s. Clin Oncol (R Coll Radiol). 2024 Aug 8:S0936-6555(24)00314-5. doi: 10.1016/j.clon.2024.07.009. Online ahead of print. Clin Oncol (R Coll Radiol). 2024. PMID: 39214827
Benefits for children with suspected cancer from routine whole-genome sequencing.
Hodder A, Leiter SM, Kennedy J, Addy D, Ahmed M, Ajithkumar T, Allinson K, Ancliff P, Bailey S, Barnard G, Burke GAA, Burns C, Cano-Flanagan J, Chalker J, Coleman N, Cheng D, Clinch Y, Dryden C, Ghorashian S, Griffin B, Horan G, Hubank M, May P, McDerra J, Nagrecha R, Nicholson J, O'Connor D, Pavasovic V, Quaegebeur A, Rao A, Roberts T, Samarasinghe S, Stasevich I, Tadross JA, Trayers C, Trotman J, Vora A, Watkins J, Chitty LS, Bowdin S, Armstrong R, Murray MJ, Hook CE, Tarpey P, Vedi A, Bartram J, Behjati S. Hodder A, et al. Among authors: leiter sm. Nat Med. 2024 Jul;30(7):1905-1912. doi: 10.1038/s41591-024-03056-w. Epub 2024 Jul 2. Nat Med. 2024. PMID: 38956197 Free PMC article.
An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia.
Welters A, Leiter SM, Bachmann N, Bergmann C, Hoermann H, Korsch E, Meissner T, Payne F, Williams R, Hussain K, Semple RK, Kummer S. Welters A, et al. Among authors: leiter sm. Orphanet J Rare Dis. 2023 Nov 16;18(1):360. doi: 10.1186/s13023-023-02954-5. Orphanet J Rare Dis. 2023. PMID: 37974153 Free PMC article.
A toolbox for class I HDACs reveals isoform specific roles in gene regulation and protein acetylation.
Hess L, Moos V, Lauber AA, Reiter W, Schuster M, Hartl N, Lackner D, Boenke T, Koren A, Guzzardo PM, Gundacker B, Riegler A, Vician P, Miccolo C, Leiter S, Chandrasekharan MB, Vcelkova T, Tanzer A, Jun JQ, Bradner J, Brosch G, Hartl M, Bock C, Bürckstümmer T, Kubicek S, Chiocca S, Bhaskara S, Seiser C. Hess L, et al. Among authors: leiter s. PLoS Genet. 2022 Aug 22;18(8):e1010376. doi: 10.1371/journal.pgen.1010376. eCollection 2022 Aug. PLoS Genet. 2022. PMID: 35994477 Free PMC article.
15 results