Morselli L, Gamazon E, Tasali E, VanCauter E, Cox NJ, and Davis LK. (in press) Univariate and bivariate heritability of quantitative sleep and metabolic traits in a large multi-generational pedigree.

Davis LK. Bridging Molecular Genetics and Epidemiology to Better Understand Sex Differences in Attention-Deficit/Hyperactivity Disorder. Biol Psychiatry. 2018 Jun 15;83(12):e55-e57. doi: 10.1016/j.biopsych.2018.04.005.

Polderman TJC, Kreukels BPC, Irwig MS, Beach L, Chan YM, Derks EM, Esteva I, Ehrenfeld J, Heijer MD Posthuma D, Raynor L, Tishelman A, Davis LK; International Gender Diversity Genomics Consortium. The Biological Contributions to Gender Identity and Gender Diversity: Bringing Data to the Table. Behavior Genetics 2018 Mar; 48(2):95-108. doi: 10.1007/s10519-018-9889-z.

Sanchez-Roige S, Fontanillas P, Elson SL, Pandit A, Schmidt EM, Foerster JR, Abecasis GR, Gray JC, de Wit H, Davis LK, MacKillop J, Palmer AA, 23andMe Research Team. Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry. Nat Neurosci. 2017 Dec 11. doi: 10.1038/s41593-017-0032-x.

Morselli LL, Gamazon ER, Tasali E, Cox NJ, Van Cauter E, Davis LK. Shared Genetic Control of Brain Activity During Sleep and Insulin Secretion: A Laboratory-Based Family Study. Diabetes. 2017 Oct 30. pii: db161229.

Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 2017 Jun 21;94(6):1101-1111.e7.

Sandra Sanchez-Roige, Pierre Fontanillas, Sarah L. Elson, the 23andMe Research Team, Joshua C. Gray, Harriet de Wit, Lea K. Davis, James MacKillop, Abraham A. Palmer. Genome-wide association study of Alcohol Use Disorder Identification Test (AUDIT) scores in 20,328 research participants of European ancestry. Addiction Biology. 2017 Oct 23. doi: 10.1111/adb.12574.

International Obsessive Compulsive Disorder Foundation Genetics Collaborative (IOCDF-GC) and OCD Collaborative Genetics Association Studies (OCGAS). Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis. Molecular Psychiatry. 2017 Aug 1. doi: 10.1038/mp.2017.154.

Alden Y Huang, Dongmei Yu, Lea K Davis, Jae-Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen, Lauren M McGrath, Cornelia Illmann, et al. De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron. 2017 May 3;94(3):486-499.e9.

Rui Chen, Lea K Davis, Stephen Guter, Qiang Wei, Suma Jacob, Melissa H Potter,Nancy J Cox, Edwin H Cook, James S Sutcliffe, Bingshan Li. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism. Molecular Autism. 2017 Mar 21;8:14.

Jianjun Gao, Lea K. Davis, Amy B. Hart, Sandra Sanchez-Roige, Lide Han, John T. Cacioppo, Abraham A. Palmer. Genome-wide Association Study of Loneliness Demonstrates a Role for Common Variation. Neuropsychopharmacology. 2017 Mar;42(4):811-821.

Sabrina Darrow, Matthew Hirschrtritt, Lea Davis, Cornelia Illmann, Lisa Osiecki, Marco Grados, Paul Sandor, Yves Dion, Robert King, David Pauls, Cathy Budman, Danielle Cath, Erica Greenberg, et al. Identification of two heritable cross-disorder endophenotypes for Tourette Syndrome. American Journal of Psychiatry. 2017 Apr 1;174(4):387-396.

Sara Hillenmeyer, Lea K. Davis, Eric R. Gamazon, Edwin H. Cook, Nancy J. Cox, Russ B. Altman. STAMS: STRING-Assisted Module Search for Genome Wide Association Studies and Application to Autism. Bioinformatics. 2016 Dec 15;32(24):3815-3822.

Eric R. Gamazon, Nancy J. Cox, Lea K. Davis. Structural dimension of SNP effects on complex traits. American Journal of Human Genetics. 2014 Nov 6;95(5):477-89.

Davis LK, Lee SH, Gamazon ER, Im H-K, Yu D, Williams S, Sullivan PF, Mathews C, Knowles J, Scharf J, Wray N, Cox NJ. Characterizing an inverse axis between orthogonal sources of genetic risk. In: Annual Meeting of the International-Genetic-Epidemiology-Society (IGES). 2015; 39(7):542–3.

de Leeuw C, Goudriaan A, Smit AB, Yu D, Mathews CA, Scharf JM, Pauls DL, Yu D, Illmann C, Osiecki L, Neale BM, Mathews CA, Reus VI, Lowe TL, Freimer NB, Cox NJ, Davis LK, et al. Involvement of astrocyte metabolic coupling in Tourette syndrome pathogenesis. European Journal of Human Genetics. 2015; 23:1519–1522.

Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette’s syndrome and OCD. American Journal of Psychiatry. 2015; 172(1):82-93.

Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, et al. Genetic association signal near NTN4 in Tourette syndrome. Annals of neurology. 2014;76(2):310–5.

Gamazon ER, Cox NJ, Davis LK. Structural architecture of SNP effects on complex traits. The American Journal of Human Genetics. 2014;95(5):477–89.

Akpudo H, Aleksic B, Alkelai A, Burton C, Roa TC, Chen DTW, Cheng M-H, Cocchi E, Davis LK, et al. Summaries of oral sessions at the XXI World Congress of Psychiatric Genetics, Boston, Massachusetts, 17–21 October 2013: state of the field. Psychiatric Genetics. 2014;24(4):125–50.

Wassink TH, Hazlett HC, Davis LK, Reiss AL, Piven J. Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome. Journal of Neurodevelopmental Disorders. 2014;6(1):1.

Trubetskoy V, Rodriguez A, Dave U, Campbell N, Crawford EL, Cook EH, Sutcliffe JS, Foster I, Madduri R, Cox NJ, Davis LK. Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes. Bioinformatics. 2014;btu591.

Davis LK. Genomic Architecture of Neuropsychiatric Phenotypes: What the Forest Can Tell Us That the Trees Cannot. In: 61st Annual Meeting. AACAP; 2014.

McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child & Adolescent Psychiatry. 2014;53(8):910–9.

Sutcliffe JS, Campbell N, Crawford EL, Li B, Davis LK, Cox NJ, et al. Leveraging Hyperserotonemia and Whole Exome Sequencing in Autism Families to Identify Genetic Risk Factors. Neuropsychopharmacology. 2013;38: S494–5.

Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Davis LK, et al. Genome-wide association study of obsessive-compulsive disorder. Molecular Psychiatry. 2013;18(7):788–98.

Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, Davis LK, et al. Genome-wide association study of Tourette’s syndrome. Molecular Psychiatry. 2013;18(6):721–8.

Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genet. 2013;9(10):e1003864.

Davis LK, Gamazon ER, Kistner-Griffin E, Badner JA, Liu C, Cook EH, et al. Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci. Molecular Autism. 2012;3(1):1.

Davis LK, Maltman N, Mosconi MW, Macmillan C, Schmitt L, Moore K, et al. Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis. American Journal of Medical Genetics Part A. 2012;158(7):1654–61.

Davis LK. In Search of Genomic Stability: Characterizing Copy Number Stable Regions. Human Mutation. 2011;32(8):v.

Davis LK, Meyer KJ, Schindler EI, Beck JS, Rudd DS, Grundstad AJ, et al. Copy number variations and primary open-angle glaucoma. Investigative Ophthalmology & Visual Science. 2011;52(10):7122–33.

Meyer KJ, Davis LK, Schindler EI, Beck JS, Rudd DS, Grundstad AJ, et al. Genome-wide analysis of copy number variants in age-related macular degeneration. Human Genetics. 2011;129(1):91–100.

Fingert JH, Robin AL, Stone JL, Roos BR, Davis LK, Scheetz TE, et al. Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. Human Molecular Genetics. 2011;20(12):2482–94.

Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson S A, Mason CE, Bilguvar K, Celestino-Soper PBS, Choi M, Crawford EL, Davis L, et al. Multiple recurrent de novo copy number variations (CNVs), including duplications of the 7q11. 23 Williams-Beuren syndrome region, are strongly associated with autism. Neuron. 2011;70(5):863.

Kistner‐Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH. Parentoforigin effects of the serotonin transporter gene associated with autism. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2011;156(2):139–44.

Celestino-Soper PB, Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, et al. Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Human Molecular Genetics. 2011;20(22):4360–70.

Urraca N, Davis L, Cook Jr EH, Schanen NC, Reiter LT. A single-tube quantitative high-resolution melting curve method for parent-of-origin determination of 15q duplications. Genetic Testing and Molecular Biomarkers. 2010;14(4):571–6.

Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PMA, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 2009;459(7246):569–73.

Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC, et al. Novel copy number variants in children with autism and additional developmental anomalies. Journal of Neurodevelopmental Disorders. 2009;1(4):292.

Davis LK, Hazlett HC, Librant AL, Nopoulos P, Sheffield VC, Piven J, et al. Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2008;147(7):1145–51.

Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC, et al. Pax6 3′ deletion results in aniridia, autism and mental retardation. Human Genetics. 2008;123(4):371–8.