Roberts W - Search Results

1

Prevalence of Creatine Deficiency Syndromes in Children With Nonsyndromic Autism.

Schulze A, Bauman M, Tsai AC, Reynolds A, Roberts W, Anagnostou E, Cameron J, Nozzolillo AA, Chen S, Kyriakopoulou L, Scherer SW, Loh A. Schulze A, et al. Among authors: roberts w. Pediatrics. 2016 Jan;137(1). doi: 10.1542/peds.2015-2672. Epub 2015 Dec 18. Pediatrics. 2016. PMID: 26684475

2

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.

Vincent JB, Herbrick JA, Gurling HM, Bolton PF, Roberts W, Scherer SW. Vincent JB, et al. Among authors: roberts w. Am J Hum Genet. 2000 Aug;67(2):510-4. doi: 10.1086/303005. Epub 2000 Jul 7. Am J Hum Genet. 2000. PMID: 10889047 Free PMC article.

3

Repeated doses of porcine secretin in the treatment of autism: a randomized, placebo-controlled trial.

Roberts W, Weaver L, Brian J, Bryson S, Emelianova S, Griffiths AM, MacKinnon B, Yim C, Wolpin J, Koren G. Roberts W, et al. Pediatrics. 2001 May;107(5):E71. doi: 10.1542/peds.107.5.e71. Pediatrics. 2001. PMID: 11331721 Clinical Trial.

4

Human chromosome 7: DNA sequence and biology.

Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R, Zhang J, Hudek AK, Li M, Haddad M, Duggan GE, Fernandez BA, Kanematsu E, Gentles S, Christopoulos CC, Choufani S, Kwasnicka D, Zheng XH, Lai Z, Nusskern D, Zhang Q, Gu Z, Lu F, Zeesman S, Nowaczyk MJ, Teshima I, Chitayat D, Shuman C, Weksberg R, Zackai EH, Grebe TA, Cox SR, Kirkpatrick SJ, Rahman N, Friedman JM, Heng HH, Pelicci PG, Lo-Coco F, Belloni E, Shaffer LG, Pober B, Morton CC, Gusella JF, Bruns GA, Korf BR, Quade BJ, Ligon AH, Ferguson H, Higgins AW, Leach NT, Herrick SR, Lemyre E, Farra CG, Kim HG, Summers AM, Gripp KW, Roberts W, Szatmari P, Winsor EJ, Grzeschik KH, Teebi A, Minassian BA, Kere J, Armengol L, Pujana MA, Estivill X, Wilson MD, Koop BF, Tosi S, Moore GE, Boright AP, Zlotorynski E, Kerem B, Kroisel PM, Petek E, Oscier DG, Mould SJ, Döhner H, Döhner K, Rommens JM, Vincent JB, Venter JC, Li PW, Mural RJ, Adams MD, Tsui LC. Scherer SW, et al. Among authors: roberts w. Science. 2003 May 2;300(5620):767-72. doi: 10.1126/science.1083423. Epub 2003 Apr 10. Science. 2003. PMID: 12690205 Free PMC article.

5

Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism.

Vincent JB, Thevarkunnel S, Kolozsvari D, Paterson AD, Roberts W, Scherer SW. Vincent JB, et al. Among authors: roberts w. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):54-6. doi: 10.1002/ajmg.b.20088. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755444

6

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.

Vincent JB, Kolozsvari D, Roberts WS, Bolton PF, Gurling HM, Scherer SW. Vincent JB, et al. Among authors: roberts ws. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):82-4. doi: 10.1002/ajmg.b.30069. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15274046

7

Type 1 diabetes and autism: is there a link?

Freeman SJ, Roberts W, Daneman D. Freeman SJ, et al. Among authors: roberts w. Diabetes Care. 2005 Apr;28(4):925-6. doi: 10.2337/diacare.28.4.925. Diabetes Care. 2005. PMID: 15793197 No abstract available.

8

Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay.

Kwasnicka-Crawford DA, Carson AR, Roberts W, Summers AM, Rehnström K, Järvelä I, Scherer SW. Kwasnicka-Crawford DA, et al. Among authors: roberts w. Genomics. 2005 Aug;86(2):182-94. doi: 10.1016/j.ygeno.2005.04.002. Genomics. 2005. PMID: 15925480

9

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW. Zeesman S, et al. Among authors: roberts w. Am J Med Genet A. 2006 Mar 1;140(5):509-14. doi: 10.1002/ajmg.a.31110. Am J Med Genet A. 2006. PMID: 16470794

10

An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.

Vincent JB, Horike SI, Choufani S, Paterson AD, Roberts W, Szatmari P, Weksberg R, Fernandez B, Scherer SW. Vincent JB, et al. Among authors: roberts w. J Med Genet. 2006 May;43(5):429-34. doi: 10.1136/jmg.2005.039693. Epub 2006 Mar 23. J Med Genet. 2006. PMID: 16556609 Free PMC article.

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