Pericak-Vance MA - Search Results

1

A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis.

Griswold AJ, Ma D, Sacharow SJ, Robinson JL, Jaworski JM, Wright HH, Abramson RK, Lybaek H, Øyen N, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Griswold AJ, et al. Autism Res. 2011 Jun;4(3):221-7. doi: 10.1002/aur.186. Epub 2011 Feb 28. Autism Res. 2011. PMID: 21360829 Free PMC article.

2

Genomic screen and follow-up analysis for autistic disorder.

Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, Bass MP, McClain C, von Wendt L, Vance JM, Abramson RH, Wright HH, Ashley-Koch A, Gilbert JR, DeLong RG, Cuccaro ML, Pericak-Vance MA. Shao Y, et al. Am J Med Genet. 2002 Jan 8;114(1):99-105. doi: 10.1002/ajmg.10153. Am J Med Genet. 2002. PMID: 11840513

3

No association between the WNT2 gene and autistic disorder.

McCoy PA, Shao Y, Wolpert CM, Donnelly SL, Ashley-Koch A, Abel HL, Ravan SA, Abramson RK, Wright HH, DeLong GR, Cuccaro ML, Gilbert JR, Pericak-Vance MA. McCoy PA, et al. Am J Med Genet. 2002 Jan 8;114(1):106-9. doi: 10.1002/ajmg.10182. Am J Med Genet. 2002. PMID: 11840514

4

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.

Shao Y, Raiford KL, Wolpert CM, Cope HA, Ravan SA, Ashley-Koch AA, Abramson RK, Wright HH, DeLong RG, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Shao Y, et al. Am J Hum Genet. 2002 Apr;70(4):1058-61. doi: 10.1086/339765. Epub 2002 Mar 1. Am J Hum Genet. 2002. PMID: 11875756 Free PMC article.

5

Behavioral comparisons in autistic individuals from multiplex and singleton families.

Cuccaro ML, Shao Y, Bass MP, Abramson RK, Ravan SA, Wright HH, Wolpert CM, Donnelly SL, Pericak-Vance MA. Cuccaro ML, et al. J Autism Dev Disord. 2003 Feb;33(1):87-91. doi: 10.1023/a:1022286622534. J Autism Dev Disord. 2003. PMID: 12708583

6

Identification of MeCP2 mutations in a series of females with autistic disorder.

Carney RM, Wolpert CM, Ravan SA, Shahbazian M, Ashley-Koch A, Cuccaro ML, Vance JM, Pericak-Vance MA. Carney RM, et al. Pediatr Neurol. 2003 Mar;28(3):205-11. doi: 10.1016/s0887-8994(02)00624-0. Pediatr Neurol. 2003. PMID: 12770674

7

Detailed analysis of allelic variation in the ABCA4 gene in age-related maculopathy.

Schmidt S, Postel EA, Agarwal A, Allen IC Jr, Walters SN, De la Paz MA, Scott WK, Haines JL, Pericak-Vance MA, Gilbert JR. Schmidt S, et al. Invest Ophthalmol Vis Sci. 2003 Jul;44(7):2868-75. doi: 10.1167/iovs.02-0957. Invest Ophthalmol Vis Sci. 2003. PMID: 12824224

8

The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease.

Oliveira SA, Martin ER, Scott WK, Nicodemus KK, Small GW, Schmechel DE, Doraiswamy PM, Roses AD, Saunders AM, Gilbert JR, Haines JL, Vance JM, Pericak-Vance MA. Oliveira SA, et al. Neurosci Lett. 2003 Aug 28;347(3):143-6. doi: 10.1016/s0304-3940(03)00670-0. Neurosci Lett. 2003. PMID: 12875906

9

Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R.

Cuccaro ML, Shao Y, Grubber J, Slifer M, Wolpert CM, Donnelly SL, Abramson RK, Ravan SA, Wright HH, DeLong GR, Pericak-Vance MA. Cuccaro ML, et al. Child Psychiatry Hum Dev. 2003 Fall;34(1):3-17. doi: 10.1023/a:1025321707947. Child Psychiatry Hum Dev. 2003. PMID: 14518620

10

Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.

Scott WK, Hauser ER, Schmechel DE, Welsh-Bohmer KA, Small GW, Roses AD, Saunders AM, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA. Scott WK, et al. Am J Hum Genet. 2003 Nov;73(5):1041-51. doi: 10.1086/379083. Epub 2003 Oct 16. Am J Hum Genet. 2003. PMID: 14564669 Free PMC article.

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