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151 results

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Page 1
Single cell sequencing data identify distinct B cell and fibroblast populations in stricturing Crohn's disease.
Humphreys DT, Lewis A, Pan-Castillo B, Berti G, Mein C, Wozniak E, Gordon H, Gadhok R, Minicozzi A, ChinAleong J, Feakins R, Giannoulatou E, James LK, Stagg AJ, Lindsay JO, Silver A. Humphreys DT, et al. Among authors: giannoulatou e. J Cell Mol Med. 2024 May;28(9):e18344. doi: 10.1111/jcmm.18344. J Cell Mol Med. 2024. PMID: 38685679 Free PMC article.
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship.
Austin R, Brown JS, Casauria S, Madelli EO, Mattiske T, Boughtwood T, Metke A, Davis A, Horton AE, Winlaw D, Das D, Soka M, Giannoulatou E, Rath EM, Haan E, Blue GM, Vohra J, Atherton JJ, van Spaendonck-Zwarts K, Cox K, Burnett L, Wallis M, Haas M, Quinn MCJ, Pachter N, Poplawski NK, Stark Z, Bagnall RD, Weintraub RG, Pantaleo SJ, Lunke S, De Fazio P, Thompson T, James P, Chang Y, Fatkin D, Macciocca I, Ingles J, Dunwoodie SL, Semsarian C, McGaughran J; Australian Genomics Cardiovascular Disorders Flagship. Austin R, et al. Among authors: giannoulatou e. Genet Med Open. 2024 Mar 25;2:101842. doi: 10.1016/j.gimo.2024.101842. eCollection 2024. Genet Med Open. 2024. PMID: 39669597 Free PMC article.
Quantifying negative selection on synonymous variants.
Gudkov M, Thibaut L, Giannoulatou E. Gudkov M, et al. Among authors: giannoulatou e. HGG Adv. 2024 Apr 11;5(2):100262. doi: 10.1016/j.xhgg.2024.100262. Epub 2024 Jan 8. HGG Adv. 2024. PMID: 38192100 Free PMC article.
COL3A1 Variants in Spontaneous Coronary Artery Dissection.
McGrath-Cadell L, Hesselson S, Thompson JL, Iismaa SE, Tarr I, Muller DWM, Kovacic JC, Graham RM, Giannoulatou E. McGrath-Cadell L, et al. Among authors: giannoulatou e. JACC Adv. 2024 May 20;3(7):100986. doi: 10.1016/j.jacadv.2024.100986. eCollection 2024 Jul. JACC Adv. 2024. PMID: 39130004 Free PMC article. No abstract available.
Polygenic Risk in Families With Spontaneous Coronary Artery Dissection.
Tarr I, Hesselson S, Troup M, Young P, Thompson JL, McGrath-Cadell L, Fatkin D, Dunwoodie SL, Muller DWM, Iismaa SE, Kovacic JC, Graham RM, Giannoulatou E. Tarr I, et al. Among authors: giannoulatou e. JAMA Cardiol. 2024 Mar 1;9(3):254-261. doi: 10.1001/jamacardio.2023.5194. JAMA Cardiol. 2024. PMID: 38265806
Arterial dissections: Common features and new perspectives.
Bax M, Romanov V, Junday K, Giannoulatou E, Martinac B, Kovacic JC, Liu R, Iismaa SE, Graham RM. Bax M, et al. Among authors: giannoulatou e. Front Cardiovasc Med. 2022 Dec 6;9:1055862. doi: 10.3389/fcvm.2022.1055862. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 36561772 Free PMC article. Review.
Polygenic risk scores are associated with atrial electrophysiologic substrate abnormalities and outcomes after atrial fibrillation catheter ablation.
Al-Kaisey A, Wong GR, Young P, Chieng D, Hawson J, Anderson R, Sugumar H, Nalliah C, Prabhu M, Johnson R, Soka M, Tarr I, Bakshi A, Yu C, Lacaze P, Giannoulatou E, McLellan A, Lee G, Kistler PM, Fatkin D, Kalman JM. Al-Kaisey A, et al. Among authors: giannoulatou e. Heart Rhythm. 2023 Aug;20(8):1188-1194. doi: 10.1016/j.hrthm.2023.02.011. Epub 2023 Feb 16. Heart Rhythm. 2023. PMID: 36804918 Free PMC article.
Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation.
Bernkopf M, Abdullah UB, Bush SJ, Wood KA, Ghaffari S, Giannoulatou E, Koelling N, Maher GJ, Thibaut LM, Williams J, Blair EM, Kelly FB, Bloss A, Burkitt-Wright E, Canham N, Deng AT, Dixit A, Eason J, Elmslie F, Gardham A, Hay E, Holder M, Homfray T, Hurst JA, Johnson D, Jones WD, Kini U, Kivuva E, Kumar A, Lees MM, Leitch HG, Morton JEV, Németh AH, Ramachandrappa S, Saunders K, Shears DJ, Side L, Splitt M, Stewart A, Stewart H, Suri M, Clouston P, Davies RW, Wilkie AOM, Goriely A. Bernkopf M, et al. Among authors: giannoulatou e. Nat Commun. 2023 Feb 15;14(1):853. doi: 10.1038/s41467-023-36606-w. Nat Commun. 2023. PMID: 36792598 Free PMC article.
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline.
Wood KA, Tong RS, Motta M, Cordeddu V, Scimone ER, Bush SJ, Maxwell DW, Giannoulatou E, Caputo V, Traversa A, Mancini C, Ferrero GB, Benedicenti F, Grammatico P, Melis D, Steindl K, Brunetti-Pierri N, Trevisson E, Wilkie AO, Lin AE, Cormier-Daire V, Twigg SR, Tartaglia M, Goriely A. Wood KA, et al. Among authors: giannoulatou e. Am J Hum Genet. 2024 Sep 5;111(9):1953-1969. doi: 10.1016/j.ajhg.2024.07.006. Epub 2024 Aug 7. Am J Hum Genet. 2024. PMID: 39116879 Free PMC article.
151 results