Spiker D - Search Results

1

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.

Li J, Tabor HK, Nguyen L, Gleason C, Lotspeich LJ, Spiker D, Risch N, Myers RM. Li J, et al. Among authors: spiker d. Am J Med Genet. 2002 Jan 8;114(1):24-30. doi: 10.1002/ajmg.1618. Am J Med Genet. 2002. PMID: 11840501

2

Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient.

Spiker D, Lotspeich LJ, Dimiceli S, Myers RM, Risch N. Spiker D, et al. Am J Med Genet. 2002 Mar 8;114(2):129-36. doi: 10.1002/ajmg.10188. Am J Med Genet. 2002. PMID: 11857572

3

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism.

Li J, Nguyen L, Gleason C, Lotspeich L, Spiker D, Risch N, Myers RM. Li J, et al. Among authors: spiker d. Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):51-7. doi: 10.1002/ajmg.b.20122. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15048648

4

Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families.

Hallmayer J, Pintado E, Lotspeich L, Spiker D, McMahon W, Petersen PB, Nicholas P, Pingree C, Kraemer HC, Wong DL, et al. Hallmayer J, et al. Among authors: spiker d. Am J Hum Genet. 1994 Nov;55(5):951-9. Am J Hum Genet. 1994. PMID: 7977358 Free PMC article.

5

Genetics of autism: characteristics of affected and unaffected children from 37 multiplex families.

Spiker D, Lotspeich L, Kraemer HC, Hallmayer J, McMahon W, Petersen PB, Nicholas P, Pingree C, Wiese-Slater S, Chiotti C, et al. Spiker D, et al. Am J Med Genet. 1994 Mar 15;54(1):27-35. doi: 10.1002/ajmg.1320540107. Am J Med Genet. 1994. PMID: 8178836

6

Male-to-male transmission in extended pedigrees with multiple cases of autism.

Hallmayer J, Spiker D, Lotspeich L, McMahon WM, Petersen PB, Nicholas P, Pingree C, Ciaranello RD. Hallmayer J, et al. Among authors: spiker d. Am J Med Genet. 1996 Feb 16;67(1):13-8. doi: 10.1002/(SICI)1096-8628(19960216)67:1<13::AID-AJMG2>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8678108

7

A genomic screen of autism: evidence for a multilocus etiology.

Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Petersen PB, Pingree C, McMahon W, Wong DL, Cavalli-Sforza LL, Kraemer HC, Myers RM. Risch N, et al. Among authors: spiker d. Am J Hum Genet. 1999 Aug;65(2):493-507. doi: 10.1086/302497. Am J Hum Genet. 1999. PMID: 10417292 Free PMC article.

8

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.

Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, Yang J, Hinds D, Myers RM, Risch N. Salmon B, et al. Among authors: spiker d. Am J Med Genet. 1999 Oct 15;88(5):551-6. Am J Med Genet. 1999. PMID: 10490715

9

Birth order effects on nonverbal IQ scores in autism multiplex families.

Spiker D, Lotspeich LJ, Dimiceli S, Szatmari P, Myers RM, Risch N. Spiker D, et al. J Autism Dev Disord. 2001 Oct;31(5):449-60. doi: 10.1023/a:1012217807469. J Autism Dev Disord. 2001. PMID: 11794410

10

Brief report: effect of maternal age on severity of autism.

Baxter AC, Lotspeich LJ, Spiker D, Martin JL, Grether JK, Hallmayer JF. Baxter AC, et al. Among authors: spiker d. J Autism Dev Disord. 2007 May;37(5):976-82. doi: 10.1007/s10803-006-0217-8. J Autism Dev Disord. 2007. PMID: 17013673

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