Jenkins EC - Search Results

1

Association of autism severity with a monoamine oxidase A functional polymorphism.

Cohen IL, Liu X, Schutz C, White BN, Jenkins EC, Brown WT, Holden JJ. Cohen IL, et al. Among authors: jenkins ec. Clin Genet. 2003 Sep;64(3):190-7. doi: 10.1034/j.1399-0004.2003.00115.x. Clin Genet. 2003. PMID: 12919132

2

Autism severity is associated with child and maternal MAOA genotypes.

Cohen IL, Liu X, Lewis ME, Chudley A, Forster-Gibson C, Gonzalez M, Jenkins EC, Brown WT, Holden JJ. Cohen IL, et al. Among authors: jenkins ec. Clin Genet. 2011 Apr;79(4):355-62. doi: 10.1111/j.1399-0004.2010.01471.x. Clin Genet. 2011. PMID: 20573161

3

Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues.

Cohen IL, Sudhalter V, Pfadt A, Jenkins EC, Brown WT, Vietze PM. Cohen IL, et al. Among authors: jenkins ec. Am J Hum Genet. 1991 Feb;48(2):195-202. Am J Hum Genet. 1991. PMID: 1990832 Free PMC article.

4

Fragile X expression in short-term whole blood cultures is affected by cell density.

Krawczun MS, Jenkins EC, Brown WT, Silverman WP. Krawczun MS, et al. Among authors: jenkins ec. Am J Med Genet. 1988 May-Jun;30(1-2):435-42. doi: 10.1002/ajmg.1320300145. Am J Med Genet. 1988. PMID: 2972206

5

Folic acid treatment of fragile X males: a further study.

Fisch GS, Cohen IL, Gross AC, Jenkins V, Jenkins EC, Brown WT. Fisch GS, et al. Among authors: jenkins v, jenkins ec. Am J Med Genet. 1988 May-Jun;30(1-2):393-9. doi: 10.1002/ajmg.1320300139. Am J Med Genet. 1988. PMID: 3052065 Clinical Trial.

6

Screening developmentally disabled male populations for fragile X: the effect of sample size.

Fisch GS, Cohen IL, Jenkins EC, Brown WT. Fisch GS, et al. Among authors: jenkins ec. Am J Med Genet. 1988 May-Jun;30(1-2):655-63. doi: 10.1002/ajmg.1320300166. Am J Med Genet. 1988. PMID: 3052070 Review.

7

Fragile X and autism: a multicenter survey.

Brown WT, Jenkins EC, Cohen IL, Fisch GS, Wolf-Schein EG, Gross A, Waterhouse L, Fein D, Mason-Brothers A, Ritvo E, et al. Brown WT, et al. Among authors: jenkins ec. Am J Med Genet. 1986 Jan-Feb;23(1-2):341-52. doi: 10.1002/ajmg.1320230126. Am J Med Genet. 1986. PMID: 3513570 Review.

8

Tissue differences in fragile X mosaics: mosaicism in blood cells may differ greatly from skin.

Dobkin CS, Nolin SL, Cohen I, Sudhalter V, Bialer MG, Ding XH, Jenkins EC, Zhong N, Brown WT. Dobkin CS, et al. Among authors: jenkins ec. Am J Med Genet. 1996 Aug 9;64(2):296-301. doi: 10.1002/(SICI)1096-8628(19960809)64:2<296::AID-AJMG13>3.0.CO;2-A. Am J Med Genet. 1996. PMID: 8844069

9

Cytogenetically negative, linkage positive "fragile X" syndrome.

Sklower Brooks S, Cohen I, Ferrando C, Jenkins EC, Brown WT, Dobkin C. Sklower Brooks S, et al. Among authors: jenkins ec. Am J Med Genet. 1991 Feb-Mar;38(2-3):370-3. doi: 10.1002/ajmg.1320380242. Am J Med Genet. 1991. PMID: 1673313

10

Effects of age and communication level on eye contact in fragile X males and non-fragile X autistic males.

Cohen IL, Vietze PM, Sudhalter V, Jenkins EC, Brown WT. Cohen IL, et al. Among authors: jenkins ec. Am J Med Genet. 1991 Feb-Mar;38(2-3):498-502. doi: 10.1002/ajmg.1320380271. Am J Med Genet. 1991. PMID: 2018093

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