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Developmental Biology|August 28, 2003
Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networksStanislav L Karsten, Lili C Kudo, Robert Jackson, et al.American Journal of Medical Genetics|February 22, 2002
Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradientDonna Spiker, Linda J Lotspeich, Sue Dimiceli, et al.Nature|October 2, 2009
Robust discrimination between self and non-self neurites requires thousands of Dscam1 isoformsDaisuke Hattori, Yi Chen, Benjamin J Matthews, et al.Human Heredity|April 3, 2009
Markov Models for inferring copy number variations from genotype data on Illumina platformsHui Wang, Jan H Veldink, Hylke Blauw, et al.Science (New York, N.Y.)|February 22, 2003
Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamideUn-kyung Kim, Eric Jorgenson, Hilary Coon, et al.The Journal of Allergy and Clinical Immunology|August 2, 2019
Genetic ancestry does not explain increased atopic dermatitis susceptibility or worse disease control among African American subjects in 2 large US cohortsKatrina Abuabara, Yue You, David J Margolis, 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.Genetics|October 22, 2022
A large genome-wide association study of QT interval length utilizing electronic health recordsThomas J Hoffmann, Meng Lu, Akinyemi Oni-Orisan, et al.Paediatric Anaesthesia|April 22, 2026
Association Between High-Risk Preexisting Substance Use and Increased Postoperative Opioid Dose Use Among Adolescents Undergoing Ambulatory Orthopedic SurgeryCornelius B Groenewald, Jennifer A Rabbitts, Amber N Borucki, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2004
Lack of evidence for an association between WNT2 and RELN polymorphisms and autismJun Li, Loan Nguyen, Christopher Gleason, et al.Pageof 24