Weiss LA - Search Results

1

Increased female autosomal burden of rare copy number variants in human populations and in autism families.

Desachy G, Croen LA, Torres AR, Kharrazi M, Delorenze GN, Windham GC, Yoshida CK, Weiss LA. Desachy G, et al. Among authors: weiss la. Mol Psychiatry. 2015 Feb;20(2):170-5. doi: 10.1038/mp.2014.179. Epub 2015 Jan 13. Mol Psychiatry. 2015. PMID: 25582617

2

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.

Weiss LA. Weiss LA. Expert Rev Mol Diagn. 2009 Nov;9(8):795-803. doi: 10.1586/erm.09.59. Expert Rev Mol Diagn. 2009. PMID: 19895225 Review.

3

An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.

Cheng Y, Quinn JF, Weiss LA. Cheng Y, et al. Among authors: weiss la. Hum Mol Genet. 2013 Jul 15;22(14):2960-72. doi: 10.1093/hmg/ddt150. Epub 2013 Apr 10. Hum Mol Genet. 2013. PMID: 23575222 Free PMC article.

4

A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.

Martin PM, Yang X, Robin N, Lam E, Rabinowitz JS, Erdman CA, Quinn J, Weiss LA, Hamilton SP, Kwok PY, Moon RT, Cheyette BN. Martin PM, et al. Among authors: weiss la. Transl Psychiatry. 2013 Sep 3;3(9):e301. doi: 10.1038/tp.2013.75. Transl Psychiatry. 2013. PMID: 24002087 Free PMC article.

5

Autism traits in the RASopathies.

Adviento B, Corbin IL, Widjaja F, Desachy G, Enrique N, Rosser T, Risi S, Marco EJ, Hendren RL, Bearden CE, Rauen KA, Weiss LA. Adviento B, et al. Among authors: weiss la. J Med Genet. 2014 Jan;51(1):10-20. doi: 10.1136/jmedgenet-2013-101951. Epub 2013 Oct 7. J Med Genet. 2014. PMID: 24101678 Free PMC article.

6

A genome-wide survey of transgenerational genetic effects in autism.

Tsang KM, Croen LA, Torres AR, Kharrazi M, Delorenze GN, Windham GC, Yoshida CK, Zerbo O, Weiss LA. Tsang KM, et al. Among authors: weiss la. PLoS One. 2013 Oct 24;8(10):e76978. doi: 10.1371/journal.pone.0076978. eCollection 2013. PLoS One. 2013. PMID: 24204716 Free PMC article.

7

Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells.

Bershteyn M, Hayashi Y, Desachy G, Hsiao EC, Sami S, Tsang KM, Weiss LA, Kriegstein AR, Yamanaka S, Wynshaw-Boris A. Bershteyn M, et al. Among authors: weiss la. Nature. 2014 Mar 6;507(7490):99-103. doi: 10.1038/nature12923. Epub 2014 Jan 12. Nature. 2014. PMID: 24413397 Free PMC article.

8

Maternal mid-pregnancy C-reactive protein and risk of autism spectrum disorders: the early markers for autism study.

Zerbo O, Traglia M, Yoshida C, Heuer LS, Ashwood P, Delorenze GN, Hansen RL, Kharrazi M, Van de Water J, Yolken RH, Weiss LA, Croen LA. Zerbo O, et al. Among authors: weiss la. Transl Psychiatry. 2016 Apr 19;6(4):e783. doi: 10.1038/tp.2016.46. Transl Psychiatry. 2016. PMID: 27093065 Free PMC article.

9

If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism.

Yeh E, Weiss LA. Yeh E, et al. Among authors: weiss la. Mol Cell Probes. 2016 Dec;30(6):346-356. doi: 10.1016/j.mcp.2016.10.007. Epub 2016 Oct 14. Mol Cell Probes. 2016. PMID: 27751841 Review.

10

Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT).

Morris SM, Acosta MT, Garg S, Green J, Huson S, Legius E, North KN, Payne JM, Plasschaert E, Frazier TW, Weiss LA, Zhang Y, Gutmann DH, Constantino JN. Morris SM, et al. Among authors: weiss la. JAMA Psychiatry. 2016 Dec 1;73(12):1276-1284. doi: 10.1001/jamapsychiatry.2016.2600. JAMA Psychiatry. 2016. PMID: 27760236 Free PMC article.

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