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Page 1
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
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
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.
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
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.
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.
Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles.
Darbro BW, Mahajan VB, Gakhar L, Skeie JM, Campbell E, Wu S, Bing X, Millen KJ, Dobyns WB, Kessler JA, Jalali A, Cremer J, Segre A, Manak JR, Aldinger KA, Suzuki S, Natsume N, Ono M, Hai HD, Viet le T, Loddo S, Valente EM, Bernardini L, Ghonge N, Ferguson PJ, Bassuk AG. Darbro BW, et al. Among authors: kessler ja. Hum Mutat. 2013 Aug;34(8):1075-9. doi: 10.1002/humu.22351. Epub 2013 May 28. Hum Mutat. 2013. PMID: 23674478 Free PMC article.
294 results