Geddes GC - Search Results

1

Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease.

Geddes GC, Basel D, Frommelt P, Kinney A, Earing M. Geddes GC, et al. Pediatr Cardiol. 2017 Oct;38(7):1465-1470. doi: 10.1007/s00246-017-1685-7. Epub 2017 Jul 19. Pediatr Cardiol. 2017. PMID: 28725922 Free PMC article.

2

FISH for 22q11.2 deletion not cost-effective for infants with congenital heart disease with microarray.

Geddes GC, Butterly M, Sajan I. Geddes GC, et al. Pediatr Cardiol. 2015 Mar;36(3):531-6. doi: 10.1007/s00246-014-1045-9. Epub 2014 Oct 11. Pediatr Cardiol. 2015. PMID: 25304247

3

Bacteremia in Patients with Heterotaxy: A Review and Implications for Management.

Loomba RS, Geddes GC, Basel D, Benson DW, Leuthner SR, Hehir DA, Ghanayem N, Shillingford AJ. Loomba RS, et al. Among authors: geddes gc. Congenit Heart Dis. 2016 Dec;11(6):537-547. doi: 10.1111/chd.12395. Epub 2016 Jul 18. Congenit Heart Dis. 2016. PMID: 27425254 Review.

4

Inheritance of a Balanced t(12;20)(q24.33;p12.2) and Unbalanced der(13)t(7;13)(p21.3;q33.2) from a Maternally Derived Double Balanced Translocation Carrier.

Peterson JF, Geddes GC, Basel DG, Schippman D, Grignon JW Jr, vanTuinen P, Kappes UP. Peterson JF, et al. Among authors: geddes gc. J Pediatr Genet. 2018 Mar;7(1):35-39. doi: 10.1055/s-0037-1605592. Epub 2017 Aug 14. J Pediatr Genet. 2018. PMID: 29441220 Free PMC article.

5

Genetic evaluation of patients with congenital heart disease.

Geddes GC, Earing MG. Geddes GC, et al. Curr Opin Pediatr. 2018 Dec;30(6):707-713. doi: 10.1097/MOP.0000000000000682. Curr Opin Pediatr. 2018. PMID: 30138133 Free PMC article. Review.

6

Three year experience of a clinical cardiovascular genetics program for infants with congenital heart disease.

Geddes GC, Syverson E, Earing MG. Geddes GC, et al. Congenit Heart Dis. 2019 Sep;14(5):832-837. doi: 10.1111/chd.12817. Epub 2019 Jun 21. Congenit Heart Dis. 2019. PMID: 31222963 Free PMC article.

7

Novel KLHL26 variant associated with a familial case of Ebstein's anomaly and left ventricular noncompaction.

Samudrala SSK, North LM, Stamm KD, Earing MG, Frommelt MA, Willes R, Tripathi S, Dsouza NR, Zimmermann MT, Mahnke DK, Liang HL, Lund M, Lin CW, Geddes GC, Mitchell ME, Tomita-Mitchell A. Samudrala SSK, et al. Among authors: geddes gc. Mol Genet Genomic Med. 2020 Apr;8(4):e1152. doi: 10.1002/mgg3.1152. Epub 2020 Jan 27. Mol Genet Genomic Med. 2020. PMID: 31985165 Free PMC article.

8

Neonatal Assessment of Infants with Heterotaxy.

Geddes GC, Samudrala SS, Earing MG. Geddes GC, et al. Clin Perinatol. 2020 Mar;47(1):171-182. doi: 10.1016/j.clp.2019.10.011. Epub 2019 Oct 31. Clin Perinatol. 2020. PMID: 32000924 Review.

9

Variants of significance: medical genetics and surgical outcomes in congenital heart disease.

Geddes GC, Przybylowski LF 3rd, Ware SM. Geddes GC, et al. Curr Opin Pediatr. 2020 Dec;32(6):730-738. doi: 10.1097/MOP.0000000000000949. Curr Opin Pediatr. 2020. PMID: 33009125 Free PMC article. Review.

10

Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease.

Landis BJ, Helm BM, Herrmann JL, Hoover MC, Durbin MD, Elmore LR, Huang M, Johansen M, Li M, Przybylowski LF, Geddes GC, Ware SM. Landis BJ, et al. Among authors: geddes gc. J Am Heart Assoc. 2022 Oct 4;11(19):e026369. doi: 10.1161/JAHA.122.026369. Epub 2022 Sep 29. J Am Heart Assoc. 2022. PMID: 36172937 Free PMC article.

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