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European Journal of Human Genetics : EJHG|April 23, 2015
Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disordersRobert Brown, Hane Lee, Ascia Eskin, et al.American Journal of Human Genetics|June 15, 2006
Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failureArnaud Lacombe, Hane Lee, Laila Zahed, et al.BMC Genomics|June 15, 2007
Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expressionVincent A Funari, Allen Day, Deborah Krakow, et al.Molecular Therapy. Nucleic Acids|November 4, 2019
Targeting RyR Activity Boosts Antisense Exon 44 and 45 Skipping in Human DMD Skeletal or Cardiac Muscle Culture ModelsFlorian Barthélémy, Richard T Wang, Christopher Hsu, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 21, 2009
Osteogenic oxysterol, 20(S)-hydroxycholesterol, induces notch target gene expression in bone marrow stromal cellsWoo-Kyun Kim, Vicente Meliton, Sotirios Tetradis, et al.Human Molecular Genetics|December 7, 2005
A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneityHane Lee, Joanna C Jen, Hui Wang, et al.Physiological Genomics|December 22, 2005
Distinct gene expression profiles in adult mouse heart following targeted MAP kinase activationScherise Mitchell, Asuka Ota, William Foster, et al.Journal of the American Academy of Child and Adolescent Psychiatry|August 30, 2008
CBCL pediatric bipolar disorder profile and ADHD: comorbidity and quantitative trait loci analysisJames J McGough, Sandra K Loo, James T McCracken, et al.International Journal of Geriatric Psychiatry|October 17, 2015
Genomic predictors of remission to antidepressant treatment in geriatric depression using genome-wide expression analyses: a pilot studyHarris A Eyre, Ascia Eskin, Stanley F Nelson, et al.American Journal of Human Genetics|October 7, 2004
Evidence for sex-specific risk alleles in autism spectrum disorderJennifer L Stone, Barry Merriman, Rita M Cantor, et al.Pageof 26