Crider KS - Search Results

1

The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: an update.

Grosse SD, Khoury MJ, Greene CL, Crider KS, Pollitt RJ. Grosse SD, et al. Among authors: crider ks. Genet Med. 2006 Apr;8(4):205-12. doi: 10.1097/01.gim.0000204472.25153.8d. Genet Med. 2006. PMID: 16617240 Free article. Review.

2

Genetic variation associated with preterm birth: a HuGE review.

Crider KS, Whitehead N, Buus RM. Crider KS, et al. Genet Med. 2005 Nov-Dec;7(9):593-604. doi: 10.1097/01.gim.0000187223.69947.db. Genet Med. 2005. PMID: 16301860 Free article. Review.

3

Factors affecting maternal participation in the genetic component of the National Birth Defects Prevention Study-United States, 1997-2007.

Glidewell J, Reefhuis J, Rasmussen SA, Woomert A, Hobbs C, Romitti PA, Crider KS. Glidewell J, et al. Among authors: crider ks. Genet Med. 2014 Apr;16(4):329-37. doi: 10.1038/gim.2013.143. Epub 2013 Sep 26. Genet Med. 2014. PMID: 24071796 Free PMC article.

4

Epigenome-wide association studies of prenatal maternal mental health and infant epigenetic profiles: a systematic review.

Drzymalla E, Crider KS, Wang A, Marta G, Khoury MJ, Rasooly D. Drzymalla E, et al. Among authors: crider ks. Transl Psychiatry. 2023 Dec 7;13(1):377. doi: 10.1038/s41398-023-02620-1. Transl Psychiatry. 2023. PMID: 38062042 Free PMC article.

5

Trisomies 13 and 18: population prevalences, characteristics, and prenatal diagnosis, metropolitan Atlanta, 1994-2003.

Crider KS, Olney RS, Cragan JD. Crider KS, et al. Am J Med Genet A. 2008 Apr 1;146A(7):820-6. doi: 10.1002/ajmg.a.32200. Am J Med Genet A. 2008. PMID: 18348276

6

Trends in cytogenetic testing and identification of chromosomal abnormalities among pregnancies and children with birth defects, metropolitan Atlanta, 1968-2005.

Jackson JM, Crider KS, Rasmussen SA, Cragan JD, Olney RS. Jackson JM, et al. Among authors: crider ks. Am J Med Genet A. 2012 Jan;158A(1):116-23. doi: 10.1002/ajmg.a.34385. Epub 2011 Dec 2. Am J Med Genet A. 2012. PMID: 22140020

7

Frequency of prenatal cytogenetic diagnosis and pregnancy outcomes by maternal race-ethnicity, and the effect on the prevalence of trisomy 21, Metropolitan Atlanta, 1996-2005.

Jackson JM, Crider KS, Cragan JD, Rasmussen SA, Olney RS. Jackson JM, et al. Among authors: crider ks. Am J Med Genet A. 2014 Jan;164A(1):70-6. doi: 10.1002/ajmg.a.36247. Epub 2013 Nov 22. Am J Med Genet A. 2014. PMID: 24273106 Free PMC article.

8

Population-based surveillance for rare congenital and inherited disorders: models and challenges.

Jackson JM, Crider KS, Olney RS. Jackson JM, et al. Among authors: crider ks. Adv Exp Med Biol. 2010;686:133-50. doi: 10.1007/978-90-481-9485-8_9. Adv Exp Med Biol. 2010. PMID: 20824444 Review.

9

Folate-related gene variants in Irish families affected by neural tube defects.

Fisk Green R, Byrne J, Crider KS, Gallagher M, Koontz D, Berry RJ. Fisk Green R, et al. Among authors: crider ks. Front Genet. 2013 Nov 6;4:223. doi: 10.3389/fgene.2013.00223. eCollection 2013. Front Genet. 2013. PMID: 24223580 Free PMC article.

10

Racial and ethnic disparity in participation in DNA collection at the Atlanta site of the National Birth Defects Prevention Study.

Crider KS, Reefhuis J, Woomert A, Honein MA. Crider KS, et al. Am J Epidemiol. 2006 Oct 15;164(8):805-12. doi: 10.1093/aje/kwj264. Epub 2006 Jul 28. Am J Epidemiol. 2006. PMID: 16877537

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