P01 HD39420/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2001	1
2002	5
2003	8
2004	9
2005	8
2006	8
2007	8
2008	3
2009	3
2024	0

1

Genome architecture, rearrangements and genomic disorders.

Stankiewicz P, Lupski JR. Stankiewicz P, et al. Trends Genet. 2002 Feb;18(2):74-82. doi: 10.1016/s0168-9525(02)02592-1. Trends Genet. 2002. PMID: 11818139 Review.

2

Molecular mechanisms for genomic disorders.

Inoue K, Lupski JR. Inoue K, et al. Annu Rev Genomics Hum Genet. 2002;3:199-242. doi: 10.1146/annurev.genom.3.032802.120023. Epub 2002 Apr 15. Annu Rev Genomics Hum Genet. 2002. PMID: 12142364 Review.

3

Molecular-evolutionary mechanisms for genomic disorders.

Stankiewicz P, Lupski JR. Stankiewicz P, et al. Curr Opin Genet Dev. 2002 Jun;12(3):312-9. doi: 10.1016/s0959-437x(02)00304-0. Curr Opin Genet Dev. 2002. PMID: 12076675 Review.

4

Genetics and genomics of behavioral and psychiatric disorders.

Inoue K, Lupski JR. Inoue K, et al. Curr Opin Genet Dev. 2003 Jun;13(3):303-9. doi: 10.1016/s0959-437x(03)00057-1. Curr Opin Genet Dev. 2003. PMID: 12787794 Review.

5

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease.

Shaw CJ, Lupski JR. Shaw CJ, et al. Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R57-64. doi: 10.1093/hmg/ddh073. Epub 2004 Feb 5. Hum Mol Genet. 2004. PMID: 14764619 Review.

6

Increased LIS1 expression affects human and mouse brain development.

Bi W, Sapir T, Shchelochkov OA, Zhang F, Withers MA, Hunter JV, Levy T, Shinder V, Peiffer DA, Gunderson KL, Nezarati MM, Shotts VA, Amato SS, Savage SK, Harris DJ, Day-Salvatore DL, Horner M, Lu XY, Sahoo T, Yanagawa Y, Beaudet AL, Cheung SW, Martinez S, Lupski JR, Reiner O. Bi W, et al. Nat Genet. 2009 Feb;41(2):168-77. doi: 10.1038/ng.302. Epub 2009 Jan 11. Nat Genet. 2009. PMID: 19136950 Free PMC article.

7

Cognitive and adaptive behavior profiles in Smith-Magenis syndrome.

Madduri N, Peters SU, Voigt RG, Llorente AM, Lupski JR, Potocki L. Madduri N, et al. J Dev Behav Pediatr. 2006 Jun;27(3):188-92. doi: 10.1097/00004703-200606000-00002. J Dev Behav Pediatr. 2006. PMID: 16775514

8

Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications.

Yatsenko SA, Treadwell-Deering D, Krull K, Lewis RA, Glaze D, Stankiewicz P, Lupski JR, Potocki L. Yatsenko SA, et al. Am J Med Genet A. 2005 Oct 1;138A(2):175-80. doi: 10.1002/ajmg.a.30948. Am J Med Genet A. 2005. PMID: 16152635 Review.

9

Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardation.

Borg K, Nowakowska B, Obersztyn E, Cheung SW, Brycz-Witkowska J, Korniszewski L, Mazurczak T, Stankiewicz P, Bocian E. Borg K, et al. Am J Med Genet A. 2007 Nov 15;143A(22):2738-43. doi: 10.1002/ajmg.a.32017. Am J Med Genet A. 2007. PMID: 17937435

10

Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome.

Yatsenko SA, Yatsenko AN, Szigeti K, Craigen WJ, Stankiewicz P, Cheung SW, Lupski JR. Yatsenko SA, et al. Clin Genet. 2004 Aug;66(2):128-36. doi: 10.1111/j.1399-0004.2004.00290.x. Clin Genet. 2004. PMID: 15253763

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