Kraemer HC - Search Results

1

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. Among authors: kraemer hc. Am J Med Genet. 1994 Mar 15;54(1):27-35. doi: 10.1002/ajmg.1320540107. Am J Med Genet. 1994. PMID: 8178836

2

Reliability and validity of behavior problem checklists as measures of stable traits in low birth weight, premature preschoolers.

Spiker D, Kraemer HC, Constantine NA, Bryant D. Spiker D, et al. Among authors: kraemer hc. Child Dev. 1992 Dec;63(6):1481-96. Child Dev. 1992. PMID: 1446564

3

Design issues in a randomized clinical trial of a behavioral intervention: insights from the Infant Health and Development Program.

Spiker D, Kraemer HC, Scott DT, Gross RT. Spiker D, et al. Among authors: kraemer hc. J Dev Behav Pediatr. 1991 Dec;12(6):386-93. J Dev Behav Pediatr. 1991. PMID: 1723986 Clinical Trial. No abstract available.

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: kraemer hc. Am J Hum Genet. 1994 Nov;55(5):951-9. Am J Hum Genet. 1994. PMID: 7977358 Free PMC article.

5

Failure to find cytogenetic abnormalities in autistic children whose parents grew up near plastics manufacturing sites.

Spiker D, Lotspeich L, Hallmayer J, Kraemer HC, Ciaranello RD. Spiker D, et al. Among authors: kraemer hc. J Autism Dev Disord. 1993 Dec;23(4):681-2. doi: 10.1007/BF01046110. J Autism Dev Disord. 1993. PMID: 8106308 No abstract available.

6

Prediction of the development of low birth weight preterm infants by a new neonatal medical index.

Korner AF, Stevenson DK, Kraemer HC, Spiker D, Scott DT, Constantinou J, Dimiceli S. Korner AF, et al. Among authors: kraemer hc. J Dev Behav Pediatr. 1993 Apr;14(2):106-11. J Dev Behav Pediatr. 1993. PMID: 8473525

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: kraemer hc. 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

Exclusion of linkage to the HLA region in ninety multiplex sibships with autism.

Rogers T, Kalaydjieva L, Hallmayer J, Petersen PB, Nicholas P, Pingree C, McMahon WM, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Peachy T, Yang J, Hinds D, Risch N, Myers RM. Rogers T, et al. J Autism Dev Disord. 1999 Jun;29(3):195-201. doi: 10.1023/a:1023075904742. J Autism Dev Disord. 1999. PMID: 10425582

9

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. Am J Med Genet. 1999 Oct 15;88(5):551-6. Am J Med Genet. 1999. PMID: 10490715

10

Serotonin transporter polymorphism, memory and hippocampal volume in the elderly: association and interaction with cortisol.

O'Hara R, Schröder CM, Mahadevan R, Schatzberg AF, Lindley S, Fox S, Weiner M, Kraemer HC, Noda A, Lin X, Gray HL, Hallmayer JF. O'Hara R, et al. Among authors: kraemer hc. Mol Psychiatry. 2007 Jun;12(6):544-55. doi: 10.1038/sj.mp.4001978. Epub 2007 Mar 13. Mol Psychiatry. 2007. PMID: 17353910 Free PMC article.

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