Early Adolescent Rai1 Reactivation Reverses Transcriptional and Social Interaction Deficits In a Mouse Model
Wei-Hsiang Huang, David C. Wang, William E. Allen, Matthew Klope, Hailan Hu, Mehrdad Shamloo, and Liqun Luo
Proceedings of National Academy of Sciences of the United States of America, 2018 August

A Conversation with SFARI Investigator Liqun Lu
Simon’s Foundation Research Initiative interview of researcher Liqun Lu

How much is too much?
Phenotypic consequences of Rai1 overexpression in mice
Girirajan S, Patel N, Slager RE, Tokarz ME, Bucan M, Wiley JL, Elsea SH
Eur J Human Genet. 2008 Aug; 16(8):941-54

Smith-Magenis syndrome
Elsea SH, Girirajan S.
Eur J Human Genet. 2008 Apr; 16(4):412-21.

Frameshift mutation hotspot identified in Smith-Magenis syndrome:
Case report and review of literature
Truong HT, Dudding T, Blanchard CL, Elsea SH.
BMC Med Genet. 2010 Oct 8;11:142.

Genomic organization of the approximately 1.5 Mb Smith-Magenis syndrome critical interval:
Transcription map, genomic contig, and candidate gene analysis
Lucas RE, Vlangos CN, Das P, Patel Pl, Elsea SH
Eur J Hum Genet. 2001 Dec;9(12):892-902.

beta(1)-adrenergic antagonists improve sleep and behavioral disturbances in a circadian disorder
Smith-Magenis Syndrome.
De Leersnyder H, de Blois MC, Vekemans M, Sidi D, Villain E, Kindermans C, Munnich A
Med Genet. 2001 Sep;38(9):586-90.

RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions
Girirajan S, Elsas LJ, 2nd, Devriendt K, Elsea SH
J Med Genet. 2005 Nov;42(11):820-8.