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Page 1
Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.
Boyles AL, Billups AV, Deak KL, Siegel DG, Mehltretter L, Slifer SH, Bassuk AG, Kessler JA, Reed MC, Nijhout HF, George TM, Enterline DS, Gilbert JR, Speer MC; NTD Collaborative Group. Boyles AL, et al. Among authors: kessler ja. Environ Health Perspect. 2006 Oct;114(10):1547-52. doi: 10.1289/ehp.9166. Environ Health Perspect. 2006. PMID: 17035141 Free PMC article.
Autosomal dominant occipital cephalocele.
Bassuk AG, McLone D, Bowman R, Kessler JA. Bassuk AG, et al. Among authors: kessler ja. Neurology. 2004 May 25;62(10):1888-90. doi: 10.1212/01.wnl.0000125255.90915.5c. Neurology. 2004. PMID: 15159504
TERC is not a major gene in human neural tube defects.
Benz LP, Swift FE, Graham FL, Enterline DS, Melvin EC, Hammock P, Gilbert JR, Speer MC, Bassuk AG, Kessler JA, George TM; NTD Collaborative Group. Benz LP, et al. Among authors: kessler ja. Birth Defects Res A Clin Mol Teratol. 2004 Aug;70(8):531-3. doi: 10.1002/bdra.20057. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15329831
SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects.
Deak KL, Boyles AL, Etchevers HC, Melvin EC, Siegel DG, Graham FL, Slifer SH, Enterline DS, George TM, Vekemans M, McClay D, Bassuk AG, Kessler JA, Linney E, Gilbert JR, Speer MC. Deak KL, et al. Among authors: kessler ja. Hum Genet. 2005 Jul;117(2-3):133-42. doi: 10.1007/s00439-005-1299-7. Epub 2005 May 10. Hum Genet. 2005. PMID: 15883837 Free PMC article.
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2.
Deak KL, Dickerson ME, Linney E, Enterline DS, George TM, Melvin EC, Graham FL, Siegel DG, Hammock P, Mehltretter L, Bassuk AG, Kessler JA, Gilbert JR, Speer MC; NTD Collaborative Group. Deak KL, et al. Among authors: kessler ja. Birth Defects Res A Clin Mol Teratol. 2005 Nov;73(11):868-75. doi: 10.1002/bdra.20183. Birth Defects Res A Clin Mol Teratol. 2005. PMID: 16237707
HeyL promotes neuronal differentiation of neural progenitor cells.
Jalali A, Bassuk AG, Kan L, Israsena N, Mukhopadhyay A, McGuire T, Kessler JA. Jalali A, et al. Among authors: kessler ja. J Neurosci Res. 2011 Mar;89(3):299-309. doi: 10.1002/jnr.22562. Epub 2011 Jan 5. J Neurosci Res. 2011. PMID: 21259317 Free PMC article.
Dual function of Sox1 in telencephalic progenitor cells.
Kan L, Jalali A, Zhao LR, Zhou X, McGuire T, Kazanis I, Episkopou V, Bassuk AG, Kessler JA. Kan L, et al. Among authors: kessler ja. Dev Biol. 2007 Oct 1;310(1):85-98. doi: 10.1016/j.ydbio.2007.07.026. Epub 2007 Jul 27. Dev Biol. 2007. PMID: 17719572 Free PMC article.
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.
Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, Dobyns WB, Millen KJ, Pina-Neto JM, Kessler JA, Bassuk AG. Jalali A, et al. Among authors: kessler ja. Hum Genet. 2008 Apr;123(3):237-45. doi: 10.1007/s00439-008-0467-y. Epub 2008 Jan 19. Hum Genet. 2008. PMID: 18204864 Free PMC article.
The genetics of tethered cord syndrome.
Bassuk AG, Craig D, Jalali A, Mukhopadhyay A, Kim F, Charrow J, Gulbu U, Epstein LG, Bowman R, McLone D, Yagi H, Matsuoka R, Stephan DA, Kessler JA. Bassuk AG, et al. Among authors: kessler ja. Am J Med Genet A. 2005 Feb 1;132A(4):450-3. doi: 10.1002/ajmg.a.30439. Am J Med Genet A. 2005. PMID: 15558749 No abstract available.
Neuroimaging findings in children with rare or novel de novo chromosomal anomalies.
Epstein LG, Jalali A, Chary AN, Khan S, Ross J, Coppinger J, Carlson K, Charrow J, Burton B, Zimmerman D, Curran J, Kim F, Nguyen P, Burrowes D, Angle B, Stack C, Shaffer L, Kessler JA, Bassuk AG. Epstein LG, et al. Among authors: kessler ja. Birth Defects Res A Clin Mol Teratol. 2008 Apr;82(4):200-10. doi: 10.1002/bdra.20443. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18302267
296 results