Geddes GC - Search Results

1

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.

2

Ciliopathy variant burden and developmental delay in children with hypoplastic left heart syndrome.

Geddes GC, Stamm K, Mitchell M, Mussatto KA, Tomita-Mitchell A. Geddes GC, et al. Genet Med. 2017 Jun;19(6):711-714. doi: 10.1038/gim.2016.167. Epub 2016 Oct 27. Genet Med. 2017. PMID: 27787502 Free article.

3

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.

4

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.

5

A case of Coffin-Siris syndrome with severe congenital heart disease and a novel SMARCA4 variant.

Dsouza NR, Zimmermann MT, Geddes GC. Dsouza NR, et al. Among authors: geddes gc. Cold Spring Harb Mol Case Stud. 2019 Jun 3;5(3):a003962. doi: 10.1101/mcs.a003962. Print 2019 Jun. Cold Spring Harb Mol Case Stud. 2019. PMID: 31160358 Free PMC article.

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

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.

8

Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy.

Schubert J, Tariq M, Geddes G, Kindel S, Miller EM, Ware SM. Schubert J, et al. Hum Mutat. 2018 Dec;39(12):2083-2096. doi: 10.1002/humu.23661. Epub 2018 Oct 22. Hum Mutat. 2018. PMID: 30260051 Free article.

9

Pathogenic variants in MRPL44 cause infantile cardiomyopathy due to a mitochondrial translation defect.

Friederich MW, Geddes GC, Wortmann SB, Punnoose A, Wartchow E, Knight KM, Prokisch H, Creadon-Swindell G, Mayr JA, Van Hove JLK. Friederich MW, et al. Among authors: geddes gc. Mol Genet Metab. 2021 Aug;133(4):362-371. doi: 10.1016/j.ymgme.2021.06.001. Epub 2021 Jun 10. Mol Genet Metab. 2021. PMID: 34140213 Free PMC article.

10

Pompe disease treatment with twice a week high dose alglucoside alfa in a patient with severe dilated cardiomyopathy.

Landis JL, Hyland H, Kindel SJ, Punnoose A, Geddes GC. Landis JL, et al. Among authors: geddes gc. Mol Genet Metab Rep. 2018 May 21;16:1-4. doi: 10.1016/j.ymgmr.2018.05.002. eCollection 2018 Sep. Mol Genet Metab Rep. 2018. PMID: 29946513 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

39 results

Search Page