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Ali Jalali, Ph.D. - Publications

Affiliations: 
Neuroscience Institute Graduate Program Northwestern University, Evanston, IL 
Area:
Developmental Neuroscience, Spinal Cord Injury, Stem Cells
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2013 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, et al. Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles. Human Mutation. 34: 1075-9. PMID 23674478 DOI: 10.1002/Humu.22351  0.456
2011 Jalali A, Bassuk AG, Kan L, Israsena N, Mukhopadhyay A, McGuire T, Kessler JA. HeyL promotes neuronal differentiation of neural progenitor cells. Journal of Neuroscience Research. 89: 299-309. PMID 21259317 DOI: 10.1002/Jnr.22562  0.582
2009 Shrimpton AE, Kessler JA, Shaffer LG, Stack C, Jalali A, Little R, Goldstein J, Angle B, Chary A, Coppinger J, Mathison DJ, Khan S, Poznanski AK, Dobyns WB, Craig DW, et al. Variability of epilepsy, autism, brachydactyly, and other clinical features in familial and sporadic 2q37.3 deletion Journal of Pediatric Neurology. 7: 279-283. DOI: 10.3233/Jpn-2009-0312  0.484
2008 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, et al. Neuroimaging findings in children with rare or novel de novo chromosomal anomalies. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 200-10. PMID 18302267 DOI: 10.1002/Bdra.20443  0.474
2008 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, et al. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Human Genetics. 123: 237-45. PMID 18204864 DOI: 10.1007/S00439-008-0467-Y  0.492
2007 Kan L, Jalali A, Zhao LR, Zhou X, McGuire T, Kazanis I, Episkopou V, Bassuk AG, Kessler JA. Dual function of Sox1 in telencephalic progenitor cells. Developmental Biology. 310: 85-98. PMID 17719572 DOI: 10.1016/J.Ydbio.2007.07.026  0.512
2005 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. The genetics of tethered cord syndrome. American Journal of Medical Genetics. Part A. 132: 450-3. PMID 15558749 DOI: 10.1002/Ajmg.A.30439  0.507
2004 Kan L, Israsena N, Zhang Z, Hu M, Zhao LR, Jalali A, Sahni V, Kessler JA. Sox1 acts through multiple independent pathways to promote neurogenesis. Developmental Biology. 269: 580-94. PMID 15110721 DOI: 10.1016/J.Ydbio.2004.02.005  0.577
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