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The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change.
Rehm HL, Alaimo JT, Aradhya S, Bayrak-Toydemir P, Best H, Brandon R, Buchan JG, Chao EC, Chen E, Clifford J, Cohen ASA, Conlin LK, Das S, Davis KW, Del Gaudio D, Del Viso F, DiVincenzo C, Eisenberg M, Guidugli L, Hammer MB, Harrison SM, Hatchell KE, Dyer LH, Hoang LU, Holt JM, Jobanputra V, Karbassi ID, Kearney HM, Kelly MA, Kelly JM, Kluge ML, Komala T, Kruszka P, Lau L, Lebo MS, Marshall CR, McKnight D, McWalter K, Meng Y, Nagan N, Neckelmann CS, Neerman N, Niu Z, Paolillo VK, Paolucci SA, Perry D, Pesaran T, Radtke K, Rasmussen KJ, Retterer K, Saunders CJ, Spiteri E, Stanley C, Szuto A, Taft RJ, Thiffault I, Thomas BC, Thomas-Wilson A, Thorpe E, Tidwell TJ, Towne MC, Zouk H; Medical Genome Initiative Steering Committee. Rehm HL, et al. Among authors: lau l. Genet Med. 2023 Dec;25(12):100947. doi: 10.1016/j.gim.2023.100947. Epub 2023 Jul 30. Genet Med. 2023. PMID: 37534744
Utility of SARS-CoV-2 Genomic Sequencing for Understanding Transmission and School Outbreaks.
Campigotto A, Chris A, Orkin J, Lau L, Marshall C, Bitnun A, Buchan SA, MacDonald L, Thampi N, McCready J, Juni P, Parekh RS, Science M. Campigotto A, et al. Among authors: lau l. Pediatr Infect Dis J. 2023 Apr 1;42(4):324-331. doi: 10.1097/INF.0000000000003834. Epub 2023 Jan 26. Pediatr Infect Dis J. 2023. PMID: 36795555 Free PMC article.
The Australian New Zealand Consortium in Children, Adolescents, and Young Adults Oncofertility action plan.
Lau LS, Allingham C, Anazodo A, Sullivan M, Peate M, Hunter S, Stern C, Ryan AL, Super L, Orme LM, McCarthy M, Gook D, Lewin J, Marino J, Ryan J, Downie P, Manudhane R, Winstanley M, Pettit T, Lantsberg D, Irving H, Reid S, Heath JA, Kabalan-Baeza P, Wanaguru D, Moore L, Gillam L, Zacharin M, Assis M, Rozen G, Hunter T, Julania S, Sharwood E, Ameratunga D, Jayasinghe Y; ANZCO Clinical Trial Network. Lau LS, et al. Pediatr Blood Cancer. 2024 May 7:e31041. doi: 10.1002/pbc.31041. Online ahead of print. Pediatr Blood Cancer. 2024. PMID: 38715224
An algorithm to identify patients aged 0-3 with rare genetic disorders.
Webb BD, Lau LY, Tsevdos D, Shewcraft RA, Corrigan D, Shi L, Lee S, Tyler J, Li S, Wang Z, Stolovitzky G, Edelmann L, Chen R, Schadt EE, Li L. Webb BD, et al. Among authors: lau ly. Orphanet J Rare Dis. 2024 May 2;19(1):183. doi: 10.1186/s13023-024-03188-9. Orphanet J Rare Dis. 2024. PMID: 38698482 Free PMC article.
Temporal dynamics and genomic programming of plasma cell fates.
Manakkat Vijay GK, Zhou M, Thakkar K, Rothrauff A, Chawla AS, Chen D, Lau LC, Gerges PH, Chetal K, Chhibbar P, Fan J, Das J, Joglekar A, Borghesi L, Salomonis N, Xu H, Singh H. Manakkat Vijay GK, et al. Among authors: lau lc. Nat Immunol. 2024 May 2. doi: 10.1038/s41590-024-01831-y. Online ahead of print. Nat Immunol. 2024. PMID: 38698087
Clinical management and outcome of head and neck paragangliomas (HNPGLs): A single centre retrospective study.
Darrat M, Lau L, Leonard C, Cooke S, Shahzad MA, McHenry C, McCance DR, Hunter SJ, Mullan K, Lindsay JR, Graham U, Bailie N, Hampton S, Rajendran S, Houghton F, Conkey D, Morrison PJ, Johnston PC. Darrat M, et al. Among authors: lau l. Clin Endocrinol (Oxf). 2024 May 2. doi: 10.1111/cen.15070. Online ahead of print. Clin Endocrinol (Oxf). 2024. PMID: 38696538
1,178 results