De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, A Cicek E, Kou Y, Liu L, Fromer M, Walker S et al..  2014.  Synaptic, transcriptional and chromatin genes disrupted in autism.. Nature. 515:209-15.

Cheng Y, Quinn JFrancis, Weiss LAnne.  2013.  An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.. Human molecular genetics. 22:2960-72.

Tsang KM, Croen LA, Torres AR, Kharrazi M, DeLorenze GN, Windham GC, Yoshida CK, Zerbo O, Weiss LA.  2013.  A genome-wide survey of transgenerational genetic effects in autism.. PloS one. 8:e76978.

Martin P-M, Yang X, Robin N, Lam E, Rabinowitz JS, Erdman CA, Quinn J, Weiss LA, Hamilton SP, Kwok P-Y et al..  2013.  A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.. Translational psychiatry. 3:e301.

Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A.  2013.  SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).. Molecular autism. 4:36.

Chow ML, Pramparo T, Winn ME, Barnes CCarter, Li H-R, Weiss L, Fan J-B, Murray S, April C, Belinson H et al..  2012.  Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages.. PLoS genetics. 8:e1002592.

Weiss LA.  2009.  Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.. Expert review of molecular diagnostics. 9:795-803.

Weiss LA, Arking DE, Hopkins GDiscovery, Consortium theAutism, Daly MJ, Chakravarti A.  2009.  A genome-wide linkage and association scan reveals novel loci for autism.. Nature. 461:802-8.

Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ et al..  2009.  Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.. Journal of medical genetics. 46:242-8.

Blaya C, Moorjani P, Salum GAbrahão, Gonçalves L, Weiss LA, Leistner-Segal S, Manfro GG, Smoller JW.  2009.  Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance.. Neuroscience letters. 452:84-6.

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.

Prado RAlves do, Panzeri H, Neto AJulio Fern, Neves FDomingues, da Silva MRibeiro, Mendonça G.  2005.  Shear bond strength of dental porcelains to nickel-chromium alloys.. Brazilian dental journal. 16:202-6.

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.

Weiss LA, Escayg A, Kearney JA, Trudeau M, MacDonald BT, Mori M, Reichert J, Buxbaum JD, Meisler MH.  2003.  Sodium channels SCN1A, SCN2A and SCN3A in familial autism.. Molecular psychiatry. 8:186-94.