Herman GE - Search Results

1

Contactin 4 as an autism susceptibility locus.

Cottrell CE, Bir N, Varga E, Alvarez CE, Bouyain S, Zernzach R, Thrush DL, Evans J, Trimarchi M, Butter EM, Cunningham D, Gastier-Foster JM, McBride KL, Herman GE. Cottrell CE, et al. Among authors: herman ge. Autism Res. 2011 Jun;4(3):189-99. doi: 10.1002/aur.184. Epub 2011 Feb 9. Autism Res. 2011. PMID: 21308999 Free PMC article.

2

Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.

McBride KL, Varga EA, Pastore MT, Prior TW, Manickam K, Atkin JF, Herman GE. McBride KL, et al. Among authors: herman ge. Autism Res. 2010 Jun;3(3):137-41. doi: 10.1002/aur.132. Autism Res. 2010. PMID: 20533527

3

Genetic testing in autism: how much is enough?

Herman GE, Henninger N, Ratliff-Schaub K, Pastore M, Fitzgerald S, McBride KL. Herman GE, et al. Genet Med. 2007 May;9(5):268-74. doi: 10.1097/gim.0b013e31804d683b. Genet Med. 2007. PMID: 17505203 Free article.

4

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.

Varga EA, Pastore M, Prior T, Herman GE, McBride KL. Varga EA, et al. Among authors: herman ge. Genet Med. 2009 Feb;11(2):111-7. doi: 10.1097/GIM.0b013e31818fd762. Genet Med. 2009. PMID: 19265751 Free article.

5

Significant contributions of the extraembryonic membranes and maternal genotype to the placental pathology in heterozygous Nsdhl deficient female embryos.

Cunningham D, Talabere T, Bir N, Kennedy M, McBride KL, Herman GE. Cunningham D, et al. Among authors: herman ge. Hum Mol Genet. 2010 Jan 15;19(2):364-73. doi: 10.1093/hmg/ddp502. Epub 2009 Oct 30. Hum Mol Genet. 2010. PMID: 19880419 Free PMC article.

6

Increasing knowledge of PTEN germline mutations: Two additional patients with autism and macrocephaly.

Herman GE, Butter E, Enrile B, Pastore M, Prior TW, Sommer A. Herman GE, et al. Am J Med Genet A. 2007 Mar 15;143A(6):589-93. doi: 10.1002/ajmg.a.31619. Am J Med Genet A. 2007. PMID: 17286265

7

Family-based clinical associations and functional characterization of the serotonin 2A receptor gene (HTR2A) in autism spectrum disorder.

Smith RM, Banks W, Hansen E, Sadee W, Herman GE. Smith RM, et al. Among authors: herman ge. Autism Res. 2014 Aug;7(4):459-67. doi: 10.1002/aur.1383. Epub 2014 Apr 17. Autism Res. 2014. PMID: 24753316 Free PMC article.

8

Analysis of hedgehog signaling in cerebellar granule cell precursors in a conditional Nsdhl allele demonstrates an essential role for cholesterol in postnatal CNS development.

Cunningham D, DeBarber AE, Bir N, Binkley L, Merkens LS, Steiner RD, Herman GE. Cunningham D, et al. Among authors: herman ge. Hum Mol Genet. 2015 May 15;24(10):2808-25. doi: 10.1093/hmg/ddv042. Epub 2015 Feb 4. Hum Mol Genet. 2015. PMID: 25652406 Free PMC article.

9

Testing genetic modifiers of behavior and response to atomoxetine in autism spectrum disorder with ADHD.

Barrie ES, Pinsonneault JK, Sadee W, Hollway JA, Handen BL, Smith T, Arnold LE, Butter E, Hansen-Kiss E, Herman GE, Aman MG. Barrie ES, et al. Among authors: herman ge. J Dev Phys Disabil. 2018 Jun;30(3):355-371. doi: 10.1007/s10882-018-9590-4. Epub 2018 Mar 5. J Dev Phys Disabil. 2018. PMID: 30197492 Free PMC article.

10

Changes in gene expression associated with loss of function of the NSDHL sterol dehydrogenase in mouse embryonic fibroblasts.

Cunningham D, Swartzlander D, Liyanarachchi S, Davuluri RV, Herman GE. Cunningham D, et al. Among authors: herman ge. J Lipid Res. 2005 Jun;46(6):1150-62. doi: 10.1194/jlr.M400462-JLR200. Epub 2005 Apr 1. J Lipid Res. 2005. PMID: 15805545 Free article.

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