Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MAR, Green T et al..  2008.  Association between microdeletion and microduplication at 16p11.2 and autism.. The New England journal of medicine. 358:667-75.

Kim H-G, Kishikawa S, Higgins AW, Seong I-S, Donovan DJ, Shen Y, Lally E, Weiss LA, Najm J, Kutsche K et al..  2008.  Disruption of neurexin 1 associated with autism spectrum disorder.. American journal of human genetics. 82:199-207.

Cross S, Kim S-J, Weiss LA, Delahanty RJ, Sutcliffe JS, Leventhal BL, Cook EH, Veenstra-Vanderweele J.  2008.  Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism.. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. 33:353-60.

Weiss LA, Purcell S, Waggoner S, Lawrence K, Spektor D, Daly MJ, Sklar P, Skuse D.  2007.  Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome.. Human molecular genetics. 16:107-13.

Thompson EE, Pan L, Ostrovnaya I, Weiss LA, Gern JE, Lemanske RF, Nicolae DL, Ober C.  2007.  Integrin beta 3 genotype influences asthma and allergy phenotypes in the first 6 years of life.. The Journal of allergy and clinical immunology. 119:1423-9.

Weiss LA, Ober C, Cook EH.  2006.  ITGB3 shows genetic and expression interaction with SLC6A4.. Human genetics. 120:93-100.

Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS.  2006.  Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility.. European journal of human genetics : EJHG. 14:923-31.

Kurina LM, Weiss LA, Graves SW, Parry R, Williams GH, Abney M, Ober C.  2005.  Sex differences in the genetic basis of morning serum cortisol levels: genome-wide screen identifies two novel loci specific to women.. The Journal of clinical endocrinology and metabolism. 90:4747-52.

Weiss LA, Abney M, Cook EH, Ober C.  2005.  Sex-specific genetic architecture of whole blood serotonin levels.. American journal of human genetics. 76:33-41.

Weiss LA, Abney M, Parry R, Scanu AM, Cook EH, Ober C.  2005.  Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample.. Human genetics. 117:81-7.

Weiss LA, Lester LA, Gern JE, Wolf RL, Parry R, Lemanske RF, Solway J, Ober C.  2005.  Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations.. American journal of respiratory and critical care medicine. 172:67-73.

Weiss LA, Veenstra-Vanderweele J, Newman DL, Kim S-J, Dytch H, McPeek MSara, Cheng S, Ober C, Cook EH, Abney M.  2004.  Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin.. European journal of human genetics : EJHG. 12:949-54.