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Page 1
A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease.
Landis BJ, Helvaty LR, Geddes GC, Lin JI, Yatsenko SA, Lo CW, Border WL, Wechsler SB, Murali CN, Azamian MS, Lalani SR, Hinton RB, Garg V, McBride KL, Hodge JC, Ware SM. Landis BJ, et al. Among authors: geddes gc. J Am Heart Assoc. 2023 Sep 19;12(18):e029340. doi: 10.1161/JAHA.123.029340. Epub 2023 Sep 8. J Am Heart Assoc. 2023. PMID: 37681527 Free PMC article.
Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects.
Durbin MD, Fairman K, Helvaty LR, Huang M, Li M, Abreu D, Geddes GC, Helm BM, Landis BJ, McEntire A, Mitchell DK, Ware SM. Durbin MD, et al. Among authors: geddes gc. J Pediatr. 2023 Sep;260:113495. doi: 10.1016/j.jpeds.2023.113495. Epub 2023 May 20. J Pediatr. 2023. PMID: 37211210 Free PMC article.
Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart Defects.
Durbin MD, Helvaty LR, Posorske A, Zhang S, Huang M, Li M, Abreu D, Fairman K, Geddes GC, Helm BM, Landis BJ, McEntire A, Mitchell DK, Ware SM. Durbin MD, et al. Among authors: geddes gc. Res Sq [Preprint]. 2024 Mar 20:rs.3.rs-3976548. doi: 10.21203/rs.3.rs-3976548/v1. Res Sq. 2024. PMID: 38562732 Free PMC article. Preprint.
MEK Inhibition Improves Cardiomyopathy in Costello Syndrome.
Geddes GC, Parent JJ, Lander J, Jeewa A, Ware SM, Villa C, Chatfield KC, Weaver KN. Geddes GC, et al. J Am Coll Cardiol. 2023 Apr 11;81(14):1439-1441. doi: 10.1016/j.jacc.2023.02.010. J Am Coll Cardiol. 2023. PMID: 37019585 Free article. No abstract available.
Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return.
Huth EA, Zhao X, Owen N, Luna PN, Vogel I, Dorf ILH, Joss S, Clayton-Smith J, Parker MJ, Louw JJ, Gewillig M, Breckpot J, Kraus A, Sasaki E, Kini U, Burgess T, Tan TY, Armstrong R, Neas K, Ferrero GB, Brusco A, Kerstjens-Frederikse WS, Rankin J, Helvaty LR, Landis BJ, Geddes GC, McBride KL, Ware SM, Shaw CA, Lalani SR, Rosenfeld JA, Scott DA. Huth EA, et al. Among authors: geddes gc. Eur J Hum Genet. 2023 Dec;31(12):1430-1439. doi: 10.1038/s41431-023-01451-4. Epub 2023 Sep 7. Eur J Hum Genet. 2023. PMID: 37673932
Surgical History and Outcomes in Trisomy 13 and 18: A Thirty-year Review.
Hafezi N, Jensen AR, Saenz ZM, Collings AT, Colgate CL, Inanc Salih ZN, Geddes GC, Gray BW. Hafezi N, et al. Among authors: geddes gc. J Pediatr Surg. 2023 Aug;58(8):1512-1519. doi: 10.1016/j.jpedsurg.2022.10.010. Epub 2022 Oct 22. J Pediatr Surg. 2023. PMID: 36402594
A multi-disciplinary, comprehensive approach to management of children with heterotaxy.
Saba TG, Geddes GC, Ware SM, Schidlow DN, Del Nido PJ, Rubalcava NS, Gadepalli SK, Stillwell T, Griffiths A, Bennett Murphy LM, Barber AT, Leigh MW, Sabin N, Shapiro AJ. Saba TG, et al. Among authors: geddes gc. Orphanet J Rare Dis. 2022 Sep 9;17(1):351. doi: 10.1186/s13023-022-02515-2. Orphanet J Rare Dis. 2022. PMID: 36085154 Free PMC article. Review.
35 results