Sealock JM, Ziogas IA, Zhao Z, Ye F, Alexopoulos SP, Matsuoka L, Chen G, Davis LK. Proposing a Sex-Adjusted Sodium-Adjusted MELD Score for Liver Transplant Allocation. JAMA Surg. 2022 May 18. doi: 10.1001/jamasurg.2022.1548. Epub ahead of print. PMID: 35583884.

Singer EV, Niarchou M, Maxwell-Horn A, Hucks D, Johnston R, Sutcliffe JS, Davis LK, Malow BA. Characterizing sleep disorders in an autism-specific collection of electronic health records. Sleep Med. 2022 Apr;92:88-95. doi: 10.1016/j.sleep.2022.03.009. Epub 2022 Mar 17. PMID: 35367909; PMCID: PMC9018608.

Pathak GA, Singh K, Wendt FR, Fleming TW, Overstreet C, Koller D, Tylee DS, De Angelis F, Cabrera Mendoza B, Levey DF, Koenen KC, Krystal JH, Pietrzak RH, O’ Donell C, Gaziano JM, Falcone G, Stein MB, Gelernter J, Pasaniuc B, Mancuso N, Davis LK, Polimanti R. Genetically regulated multi-omics study for symptom clusters of posttraumatic stress disorder highlights pleiotropy with hematologic and cardio-metabolic traits. Mol Psychiatry. 2022 Mar;27(3):1394-1404. doi: 10.1038/s41380-022-01488-9. Epub 2022 Mar 3. PMID: 35241783.

Fox J, Goleva SB, Haas KF, Davis LK. Functional seizures are associated with cerebrovascular disease and functional stroke is more common in patients with functional seizures than epileptic seizures. Epilepsy Behav. 2022 Mar;128:108582. doi: 10.1016/j.yebeh.2022.108582. Epub 2022 Feb 3. PMID: 35123242; PMCID: PMC8898282.

Overway EM, Bosma KJ, Claxton DP, Oeser JK, Singh K, Breidenbach LB, Mchaourab HS, Davis LK, O’Brien RM. Nonsynonymous single-nucleotide polymorphisms in the G6PC2 gene affect protein expression, enzyme activity, and fasting blood glucose. J Biol Chem. 2022 Feb;298(2):101534. doi: 10.1016/j.jbc.2021.101534. Epub 2021 Dec 23. PMID: 34954144; PMCID: PMC8800118.

Rauf MA, Ziogas IA, Sealock JM, Davis LK, Izzy M, Alexopoulos SP, Matsuoka LK. Pancreatic adenocarcinoma in liver transplant recipients: a case series. Ann Pancreat Cancer. 2021 Oct;4:6. doi: 10.21037/apc-21-4. Epub 2021 Oct 30. PMID: 34825179; PMCID: PMC8612297.

Sanchez-Roige S, Fontanillas P, Jennings MV, Bianchi SB, Huang Y, Hatoum AS, Sealock J, Davis LK, Elson SL; 23andMe Research Team, Palmer AA. Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry. Mol Psychiatry. 2021 Nov;26(11):6209-6217. doi: 10.1038/s41380-021-01335-3. Epub 2021 Nov 2. PMID: 34728798; PMCID: PMC8562028.

Sealock JM, Lee YH, Moscati A, Venkatesh S, Voloudakis G, Straub P, Singh K, Feng YA, Ge T, Roussos P, Smoller JW, Chen G, Davis LK. Use of the PsycheMERGE Network to Investigate the Association Between Depression Polygenic Scores and White Blood Cell Count. JAMA Psychiatry. 2021 Dec 1;78(12):1365-1374. doi: 10.1001/jamapsychiatry.2021.2959. PMID: 34668925; PMCID: PMC8529528.

Wightman DP, Jansen IE, Savage JE, Shadrin AA, Bahrami S, Holland D, Rongve A, Børte S, Winsvold BS, Drange OK, Martinsen AE, Skogholt AH, Willer C, Bråthen G, Bosnes I, Nielsen JB, Fritsche LG, Thomas LF, Pedersen LM, Gabrielsen ME, Johnsen MB, Meisingset TW, Zhou W, Proitsi P, Hodges A, Dobson R, Velayudhan L, Heilbron K, Auton A; 23andMe Research Team, Sealock JM, Davis LK, Pedersen NL, Reynolds CA, Karlsson IK, Magnusson S, Stefansson H, Thordardottir S, Jonsson PV, Snaedal J, Zettergren A, Skoog I, Kern S, Waern M, Zetterberg H, Blennow K, Stordal E, Hveem K, Zwart JA, Athanasiu L, Selnes P, Saltvedt I, Sando SB, Ulstein I, Djurovic S, Fladby T, Aarsland D, Selbæk G, Ripke S, Stefansson K, Andreassen OA, Posthuma D. A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease. Nat Genet. 2021 Sep;53(9):1276-1282. doi: 10.1038/s41588-021-00921-z. Epub 2021 Sep 7. Erratum in: Nat Genet. 2021 Dec;53(12):1722. PMID: 34493870.

Niarchou M, Lin GT, Lense MD, Gordon RL, Davis LK. Medical phenome of musicians: an investigation of health records collected on 9803 musically active individuals. Ann N Y Acad Sci. 2021 Dec;1505(1):156-168. doi: 10.1111/nyas.14671. Epub 2021 Aug 19. PMID: 34414577; PMCID: PMC8688228.

Actkins KV, Beasley HK, Faucon AB, Davis LK, Sakwe AM. Calcium-Sensing Receptor Polymorphisms at rs1801725 Are Associated with Increased Risk of Secondary Malignancies. J Pers Med. 2021 Jul 6;11(7):642. doi: 10.3390/jpm11070642. PMID: 34357109; PMCID: PMC8304025.

Bagheri M, Wang C, Shi M, Manouchehri A, Murray KT, Murphy MB, Shaffer CM, Singh K, Davis LK, Jarvik GP, Stanaway IB, Hebbring S, Reilly MP, Gerszten RE, Wang TJ, Mosley JD, Ferguson JF. The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene. Sci Rep. 2021 Aug 2;11(1):15652. doi: 10.1038/s41598-021-95154-9. PMID: 34341450; PMCID: PMC8329184.

Pathak GA, Singh K, Miller-Fleming TW, Wendt FR, Ehsan N, Hou K, Johnson R, Lu Z, Gopalan S, Yengo L, Mohammadi P, Pasaniuc B, Polimanti R, Davis LK, Mancuso N. Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization. Nat Commun. 2021 Jul 27;12(1):4569. doi: 10.1038/s41467-021-24824-z. PMID: 34315903; PMCID: PMC8316582.

Strom NI, Soda T, Mathews CA, Davis LK. A dimensional perspective on the genetics of obsessive-compulsive disorder. Transl Psychiatry. 2021 Jul 21;11(1):401. doi: 10.1038/s41398-021-01519-z. PMID: 34290223; PMCID: PMC8295308.

Zhou D, Yu D, Scharf JM, Mathews CA, McGrath L, Cook E, Lee SH, Davis LK, Gamazon ER. Contextualizing genetic risk score for disease screening and rare variant discovery. Nat Commun. 2021 Jul 20;12(1):4418. doi: 10.1038/s41467-021-24387-z. PMID: 34285202; PMCID: PMC8292385.

Mallard TT, Savage JE, Johnson EC, Huang Y, Edwards AC, Hottenga JJ, Grotzinger AD, Gustavson DE, Jennings MV, Anokhin A, Dick DM, Edenberg HJ, Kramer JR, Lai D, Meyers JL, Pandey AK, Harden KP, Nivard MG, de Geus EJC, Boomsma DI, Agrawal A, Davis LK, Clarke TK, Palmer AA, Sanchez-Roige S. Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts. Am J Psychiatry. 2022 Jan;179(1):58-70. doi: 10.1176/appi.ajp.2020.20091390. Epub 2021 May 14. PMID: 33985350.

Yengo-Kahn AM, Hibshman N, Bonfield CM, Torstenson ES, Gifford KA, Belikau D, Davis LK, Zuckerman SL, Dennis JK. Association of Preinjury Medical Diagnoses With Pediatric Persistent Postconcussion Symptoms in Electronic Health Records. J Head Trauma Rehabil. 2022 Mar-Apr 01;37(2):E80-E89. doi: 10.1097/HTR.0000000000000686. PMID: 33935230.

Shi M, Manouchehri AM, Shaffer CM, Vaitinadin NS, Hellwege JN, Salem JE, Davis LK, Simmons JH, Roden DM, Shoemaker MB, Ferguson JF, Mosley JD. Genetic Thyrotropin Regulation of Atrial Fibrillation Risk Is Mediated Through an Effect on Height. J Clin Endocrinol Metab. 2021 Jun 16;106(7):2124-2132. doi: 10.1210/clinem/dgab272. PMID: 33895829; PMCID: PMC8208678.

Yang Z, Wu H, Lee PH, Tsetsos F, Davis LK, Yu D, Lee SH, Dalsgaard S, Haavik J, Barta C, Zayats T, Eapen V, Wray NR, Devlin B, Daly M, Neale B, Børglum AD, Crowley JJ, Scharf J, Mathews CA, Faraone SV, Franke B, Mattheisen M, Smoller JW, Paschou P. Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum. Biol Psychiatry. 2021 Sep 1;90(5):317-327. doi: 10.1016/j.biopsych.2020.12.028. Epub 2021 Jan 8. PMID: 33714545.

Martucci VL, Richmond B, Davis LK, Blackwell TS, Cox NJ, Samuels D, Velez Edwards D, Aldrich MC. Fate or coincidence: do COPD and major depression share genetic risk factors? Hum Mol Genet. 2021 May 12;30(7):619-628. doi: 10.1093/hmg/ddab068. PMID: 33704461; PMCID: PMC8120137.

Martin J, Khramtsova EA, Goleva SB, Blokland GAM, Traglia M, Walters RK, Hübel C, Coleman JRI, Breen G, Børglum AD, Demontis D, Grove J, Werge T, Bralten J, Bulik CM, Lee PH, Mathews CA, Peterson RE, Winham SJ, Wray N, Edenberg HJ, Guo W, Yao Y, Neale BM, Faraone SV, Petryshen TL, Weiss LA, Duncan LE, Goldstein JM, Smoller JW, Stranger BE, Davis LK; Sex Differences Cross-Disorder Analysis Group of the Psychiatric Genomics Consortium. Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits. Biol Psychiatry. 2021 Jun 15;89(12):1127-1137. doi: 10.1016/j.biopsych.2020.12.024. Epub 2021 Jan 9. PMID: 33648717; PMCID: PMC8163257.

Sanchez-Roige S, Cox NJ, Johnson EO, Hancock DB, Davis LK. Alcohol and cigarette smoking consumption as genetic proxies for alcohol misuse and nicotine dependence. Drug Alcohol Depend. 2021 Apr 1;221:108612. doi: 10.1016/j.drugalcdep.2021.108612. Epub 2021 Feb 15. PMID: 33631543; PMCID: PMC8026738.

Tsetsos F, Yu D, Sul JH, Huang AY, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau GA, Aschauer H, Stamenkovic M, Schlögelhofer M, Sandor P, Barr CL, Grados MA, Singer HS, Nöthen MM, Hebebrand J, Hinney A, King RA, Fernandez TV, Barta C, Tarnok Z, Nagy P, Depienne C, Worbe Y, Hartmann A, Budman CL, Rizzo R, Lyon GJ, McMahon WM, Batterson JR, Cath DC, Malaty IA, Okun MS, Berlin C, Woods DW, Lee PC, Jankovic J, Robertson MM, Gilbert DL, Brown LW, Coffey BJ, Dietrich A, Hoekstra PJ, Kuperman S, Zinner SH, Wagner M, Knowles JA, Jeremy Willsey A, Tischfield JA, Heiman GA, Cox NJ, Freimer NB, Neale BM, Davis LK, Coppola G, Mathews CA, Scharf JM, Paschou P; Tourette Association of America International Consortium for Genetics, Barr CL, Batterson JR, Berlin C, Budman CL, Cath DC, Coppola G, Cox NJ, Darrow S, Davis LK, Dion Y, Freimer NB, Grados MA, Greenberg E, Hirschtritt ME, Huang AY, Illmann C, King RA, Kurlan R, Leckman JF, Lyon GJ, Malaty IA, Mathews CA, McMahon WM, Neale BM, Okun MS, Osiecki L, Robertson MM, Rouleau GA, Sandor P, Scharf JM, Singer HS, Smit JH, Sul JH, Yu D; Gilles de la Tourette GWAS Replication Initiative, Aschauer HAH, Barta C, Budman CL, Cath DC, Depienne C, Hartmann A, Hebebrand J, Konstantinidis A, Mathews CA, Müller-Vahl K, Nagy P, Nöthen MM, Paschou P, Rizzo R, Rouleau GA, Sandor P, Scharf JM, Schlögelhofer M, Stamenkovic M, Stuhrmann M, Tsetsos F, Tarnok Z, Wolanczyk T, Worbe Y; Tourette International Collaborative Genetics Study, Brown L, Cheon KA, Coffey BJ, Dietrich A, Fernandez TV, Garcia-Delgar B, Gilbert D, Grice DE, Hagstrøm J, Hedderly T, Heiman GA, Heyman I, Hoekstra PJ, Huyser C, Kim YK, Kim YS, King RA, Koh YJ, Kook S, Kuperman S, Leventhal BL, Madruga-Garrido M, Mir P, Morer A, Münchau A, Plessen KJ, Roessner V, Shin EY, Song DH, Song J, Tischfield JA, Willsey AJ, Zinner S; Psychiatric Genomics Consortium Tourette Syndrome Working Group, Aschauer H, Barr CL, Barta C, Batterson JR, Berlin C, Brown L, Budman CL, Cath DC, Coffey BJ, Coppola G, Cox NJ, Darrow S, Davis LK, Depienne C, Dietrich A, Dion Y, Fernandez T, Freimer NB, Gilbert D, Grados MA, Greenberg E, Hartmann A, Hebebrand J, Heiman G, Hirschtritt ME, Hoekstra P, Huang AY, Illmann C, Jankovic J, King RA, Kuperman S, Lee PC, Lyon GJ, Malaty IA, Mathews CA, McMahon WM, Müller-Vahl K, Nagy P, Neale BM, Nöthen MM, Okun MS, Osiecki L, Paschou P, Rizzo R, Robertson MM, Rouleau GA, Sandor P, Scharf JM, Schlögelhofer M, Singer HS, Stamenkovic M, Stuhrmann M, Sul JH, Tarnok Z, Tischfield J, Tsetsos F, Willsey AJ, Woods D, Worbe Y, Yu D, Zinner S. Synaptic processes and immune-related pathways implicated in Tourette syndrome. Transl Psychiatry. 2021 Jan 18;11(1):56. doi: 10.1038/s41398-020-01082-z. PMID: 33462189; PMCID: PMC7814139.

Dennis JK, Sealock JM, Straub P, Lee YH, Hucks D, Actkins K, Faucon A, Feng YA, Ge T, Goleva SB, Niarchou M, Singh K, Morley T, Smoller JW, Ruderfer DM, Mosley JD, Chen G, Davis LK. Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Genome Med. 2021 Jan 13;13(1):6. doi: 10.1186/s13073-020-00820-8. PMID: 33441150; PMCID: PMC7807864.

Goleva SB, Lake AM, Torstenson ES, Haas KF, Davis LK. Epidemiology of Functional Seizures Among Adults Treated at a University Hospital. JAMA Netw Open. 2020 Dec 1;3(12):e2027920. doi: 10.1001/jamanetworkopen.2020.27920. PMID: 33372972; PMCID: PMC7772716.

Tilot AK, Khramtsova EA, Liang D, Grasby KL, Jahanshad N, Painter J, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Liu S, Brotman SM, Thompson PM, Medland SE, Macciardi F, Stranger BE, Davis LK, Fisher SE, Stein JL. The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cereb Cortex. 2021 Mar 5;31(4):1873-1887. doi: 10.1093/cercor/bhaa327. PMID: 33290510; PMCID: PMC7945014.

Nayar K, Sealock JM, Maltman N, Bush L, Cook EH, Davis LK, Losh M. Elevated Polygenic Burden for Autism Spectrum Disorder Is Associated With the Broad Autism Phenotype in Mothers of Individuals With Autism Spectrum Disorder. Biol Psychiatry. 2021 Mar 1;89(5):476-485. doi: 10.1016/j.biopsych.2020.08.029. Epub 2020 Sep 12. PMID: 33229037; PMCID: PMC7901138.

Johnson EC, Demontis D, Thorgeirsson TE, Walters RK, Polimanti R, Hatoum AS, Sanchez-Roige S, Paul SE, Wendt FR, Clarke TK, Lai D, Reginsson GW, Zhou H, He J, Baranger DAA, Gudbjartsson DF, Wedow R, Adkins DE, Adkins AE, Alexander J, Bacanu SA, Bigdeli TB, Boden J, Brown SA, Bucholz KK, Bybjerg-Grauholm J, Corley RP, Degenhardt L, Dick DM, Domingue BW, Fox L, Goate AM, Gordon SD, Hack LM, Hancock DB, Hartz SM, Hickie IB, Hougaard DM, Krauter K, Lind PA, McClintick JN, McQueen MB, Meyers JL, Montgomery GW, Mors O, Mortensen PB, Nordentoft M, Pearson JF, Peterson RE, Reynolds MD, Rice JP, Runarsdottir V, Saccone NL, Sherva R, Silberg JL, Tarter RE, Tyrfingsson T, Wall TL, Webb BT, Werge T, Wetherill L, Wright MJ, Zellers S, Adams MJ, Bierut LJ, Boardman JD, Copeland WE, Farrer LA, Foroud TM, Gillespie NA, Grucza RA, Harris KM, Heath AC, Hesselbrock V, Hewitt JK, Hopfer CJ, Horwood J, Iacono WG, Johnson EO, Kendler KS, Kennedy MA, Kranzler HR, Madden PAF, Maes HH, Maher BS, Martin NG, McGue M, McIntosh AM, Medland SE, Nelson EC, Porjesz B, Riley BP, Stallings MC, Vanyukov MM, Vrieze S; Psychiatric Genomics Consortium Substance Use Disorders Workgroup, Davis LK, Bogdan R, Gelernter J, Edenberg HJ, Stefansson K, Børglum AD, Agrawal A. A large-scale genome-wide association study meta-analysis of cannabis use disorder. Lancet Psychiatry. 2020 Dec;7(12):1032-1045. doi: 10.1016/S2215-0366(20)30339-4. Epub 2020 Oct 20. Erratum in: Lancet Psychiatry. 2022 Apr;9(4):e12. PMID: 33096046; PMCID: PMC7674631.

Actkins KV, Singh K, Hucks D, Velez Edwards DR, Aldrich M, Cha J, Wellons M, Davis LK. Characterizing the Clinical and Genetic Spectrum of Polycystic Ovary Syndrome in Electronic Health Records. J Clin Endocrinol Metab. 2021 Jan 1;106(1):153-167. doi: 10.1210/clinem/dgaa675. PMID: 32961557; PMCID: PMC7765638.

Walters CE Jr, Nitin R, Margulis K, Boorom O, Gustavson DE, Bush CT, Davis LK, Below JE, Cox NJ, Camarata SM, Gordon RL. Automated Phenotyping Tool for Identifying Developmental Language Disorder Cases in Health Systems Data (APT-DLD): A New Research Algorithm for Deployment in Large-Scale Electronic Health Record Systems. J Speech Lang Hear Res. 2020 Sep 15;63(9):3019-3035. doi: 10.1044/2020_JSLHR-19-00397. Epub 2020 Aug 11. PMID: 32791019; PMCID: PMC7890229.

Zhou H, Sealock JM, Sanchez-Roige S, Clarke TK, Levey DF, Cheng Z, Li B, Polimanti R, Kember RL, Smith RV, Thygesen JH, Morgan MY, Atkinson SR, Thursz MR, Nyegaard M, Mattheisen M, Børglum AD, Johnson EC, Justice AC, Palmer AA, McQuillin A, Davis LK, Edenberg HJ, Agrawal A, Kranzler HR, Gelernter J. Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. Nat Neurosci. 2020 Jul;23(7):809-818. doi: 10.1038/s41593-020-0643-5. Epub 2020 May 25. PMID: 32451486; PMCID: PMC7485556.

Zhang Y, Ho K, Keaton JM, Hartzel DN, Day F, Justice AE, Josyula NS, Pendergrass SA, Actkins K, Davis LK, Velez Edwards DR, Holohan B, Ramirez A, Stanaway IB, Crosslin DR, Jarvik GP, Sleiman P, Hakonarson H, Williams MS, Lee MTM. A genome-wide association study of polycystic ovary syndrome identified from electronic health records. Am J Obstet Gynecol. 2020 Oct;223(4):559.e1-559.e21. doi: 10.1016/j.ajog.2020.04.004. Epub 2020 Apr 11. PMID: 32289280.

Dennis J, Sealock J, Levinson RT, Farber-Eger E, Franco J, Fong S, Straub P, Hucks D, Song WL, Linton MF, Fontanillas P, Elson SL, Ruderfer D, Abdellaoui A, Sanchez-Roige S, Palmer AA, Boomsma DI, Cox NJ, Chen G, Mosley JD, Wells QS, Davis LK. Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease. Mol Psychiatry. 2021 Aug;26(8):4254-4264. doi: 10.1038/s41380-019-0614-y. Epub 2019 Dec 3. PMID: 31796895; PMCID: PMC7266730.

Lázaro-Muñoz G, Sabatello M, Huckins L, Peay H, Degenhardt F, Meiser B, Lencz T, Soda T, Docherty A, Crepaz-Keay D, Austin J, Peterson RE, Davis LK; ISPG Ethics Committee. International Society of Psychiatric Genetics Ethics Committee: Issues facing us. Am J Med Genet B Neuropsychiatr Genet. 2019 Dec;180(8):543-554. doi: 10.1002/ajmg.b.32736. Epub 2019 May 23. PMID: 31124312; PMCID: PMC6861601.

Yilmaz Z, Halvorsen M, Bryois J, Yu D, Thornton LM, Zerwas S, Micali N, Moessner R, Burton CL, Zai G, Erdman L, Kas MJ, Arnold PD, Davis LK, Knowles JA, Breen G, Scharf JM, Nestadt G, Mathews CA, Bulik CM, Mattheisen M, Crowley JJ; Eating Disorders Working Group of the Psychiatric Genomics Consortium, Tourette Syndrome/Obsessive–Compulsive Disorder Working Group of the Psychiatric Genomics Consortium. Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. Mol Psychiatry. 2020 Sep;25(9):2036-2046. doi: 10.1038/s41380-018-0115-4. Epub 2018 Aug 7. PMID: 30087453; PMCID: PMC6367065.

Leu C, Stevelink R, Smith AW, Goleva SB, Kanai M, Ferguson L, Campbell C, Kamatani Y, Okada Y, Sisodiya SM, Cavalleri GL, Koeleman BPC, Lerche H, Jehi L, Davis LK, Najm IM, Palotie A, Daly MJ, Busch RM; Epi25 Consortium, Lal D. Polygenic burden in focal and generalized epilepsies. Brain. 2019 Nov 1;142(11):3473-3481. doi: 10.1093/brain/awz292. PMID: 31608925

Abdellaoui A, Sanchez-Roige S, Sealock J, Treur JL, Dennis J, Fontanillas P, Elson S; 23andme Research Team, Nivard MG, Ip HF, van der Zee M, Baselmans BML, Hottenga JJ, Willemsen G, Mosing M, Lu Y, Pedersen NL, Denys D, Amin N, M van Duijn C, Szilagyi I, Tiemeier H, Neumann A, Verweij KJH, Cacioppo S, Cacioppo JT, Davis LK, Palmer AA, Boomsma DI. Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness. Hum Mol Genet. 2019 Nov 15;28(22):3853-3865. doi: 10.1093/hmg/ddz219. PMID: 31518406

Bray MJ, Davis LK, Torstenson ES, Jones SH, Edwards TL, Velez Edwards DR. Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids. Hum Hered. 2019;84(2):73-81. doi: 10.1159/000501335. Epub 2019 Sep 3. PMID: 31480066

Zheutlin AB, Dennis J, Karlsson Linnér R, Moscati A, Restrepo N, Straub P, Ruderfer D, Castro VM, Chen CY, Ge T, Huckins LM, Charney A, Kirchner HL, Stahl EA, Chabris CF, Davis LK, Smoller JW. Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems. Am J Psychiatry. 2019 Oct 1;176(10):846-855. doi: 10.1176/appi.ajp.2019.18091085. Epub 2019 Aug 16. PMID: 31416338

Davis LK, Stranger BE. The new science of sex differences in neuropsychiatric traits. Am J Med Genet B Neuropsychiatr Genet. 2019 Sep;180(6):333-334. doi: 10.1002/ajmg.b.32747. Epub 2019 Jun 24. PMID: 31237066

Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, Aschauer H, Stamenkovic M, Schlögelhofer M, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, Hinney A, King RA, Fernandez TV, Barta C, Tarnok Z, Nagy P, Depienne C, Worbe Y, Hartmann A, Budman CL, Rizzo R, Lyon GJ, McMahon WM, Batterson JR, Cath DC, Malaty IA, Okun MS, Berlin C, Woods DW, Lee PC, Jankovic J, Robertson MM, Gilbert DL, Brown LW, Coffey BJ, Dietrich A, Hoekstra PJ, Kuperman S, Zinner SH, Luðvigsson P, Sæmundsen E, Thorarensen Ó, Atzmon G, Barzilai N, Wagner M, Moessner R, Ophoff R, Pato CN, Pato MT, Knowles JA, Roffman JL, Smoller JW, Buckner RL, Willsey AJ, Tischfield JA, Heiman GA, Stefansson H, Stefansson K, Posthuma D, Cox NJ, Pauls DL, Freimer NB, Neale BM, Davis LK, Paschou P, Coppola G, Mathews CA, Scharf JM; Tourette Association of America International Consortium for Genetics, the Gilles de la Tourette GWAS Replication Initiative, the Tourette International Collaborative Genetics Study, and the Psychiatric Genomics Consortium Tourette Syndrome Working Group. Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. Am J Psychiatry. 2019 Mar 1;176(3):217-227. doi: 10.1176/appi.ajp.2018.18070857. PMID: 30818990

Salem JE, Shoemaker MB, Bastarache L, Shaffer CM, Glazer AM, Kroncke B, Wells QS, Shi M, Straub P, Jarvik GP, Larson EB, Velez Edwards DR, Edwards TL, Davis LK, Hakonarson H, Weng C, Fasel D, Knollmann BC, Wang TJ, Denny JC, Ellinor PT, Roden DM, Mosley JD. Association of Thyroid Function Genetic Predictors With Atrial Fibrillation: A Phenome-Wide Association Study and Inverse-Variance Weighted Average Meta-analysis. JAMA Cardiol. 2019 Feb 1;4(2):136-143. doi: 10.1001/jamacardio.2018.4615. PMID: 30673079

Jansen IE, Savage JE, Watanabe K, Bryois J, Williams DM, Steinberg S, Sealock J, Karlsson IK, Hägg S, Athanasiu L, Voyle N, Proitsi P, Witoelar A, Stringer S, Aarsland D, Almdahl IS, Andersen F, Bergh S, Bettella F, Bjornsson S, Brækhus A, Bråthen G, de Leeuw C, Desikan RS, Djurovic S, Dumitrescu L, Fladby T, Hohman TJ, Jonsson PV, Kiddle SJ, Rongve A, Saltvedt I, Sando SB, Selbæk G, Shoai M, Skene NG, Snaedal J, Stordal E, Ulstein ID, Wang Y, White LR, Hardy J, Hjerling-Leffler J, Sullivan PF, van der Flier WM, Dobson R, Davis LK, Stefansson H, Stefansson K, Pedersen NL, Ripke S, Andreassen OA, Posthuma D. Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk. Nat Genet. 2019 Mar;51(3):404-413. doi: 10.1038/s41588-018-0311-9. PMID: 30617256

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 (2019) Genome-wide association study of Alcohol Use Disorder Identification Test (AUDIT) scores in 20,328 research participants of European ancestry. Addiction Biology. Jan;24(1):121-131. PubMed PMID: 29058377.

Khramtsova E.A., Heldman R., Derks E.M., Yu D., Tourette Syndrome/Obsessive‐Compulsive Disorder Working Group of the Psychiatric Genomics Consortium, Davis LK* and Stranger BE*. (2018) Sex differences in the genetic architecture of obsessive-compulsive disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. Nov 20. doi: 10.1002/ajmg.b.32687. [Epub ahead of print]. PubMed PMID: 30456828.

Ekaterina Khramtsova, Lea K. Davis* & Barbara Stranger*. (2018) The role of sex in the genomics of human complex traits. Nature Genetics Reviews. Dec 23. DOI: 10.1038/s41576-018-0083-1. [Epub ahead of print]. PubMed PMID: 30581192.

Felix Day, Tugce Karaderi, Michelle R Jones, Cindy Meun, Chunyan He, Alex Drong,  Peter Kraft, Nan Lin, Hongyan Huang, Linda Broer, Reedik Magi, Richa Saxena, Triin Laisk-Podar, Margrit Urbanek, Geoffrey MHayes, Gudmar Thorleifsson, Juan Fernandez-Tajes, Anubha Mahajan, Benjamin H Mullin, Bronwyn G.A.Stuckey, Timothy D. Spector, Scott G Wilson, Mark O Goodarzi, Lea Davis, Barbara Obermeyer-Pietsch, Andre G Uitterlinden, Verneri Anttila, Benjamin M Neale, Marjo-Riitta Jarvelin, Bart Fauser, Irina Kowalska, Jenny A Visser, Marianne Anderson, Ken Ong, Elisabet Stener-Victorin, David Ehrmann, Richard S Legro, Andres Salumets, Mark I McCarthy, Laure Morin-Papunen, Unnur Thorsteinsdottir, Kari Stefansson, 23andMe Research Team, Unnur Styrkarsdottir, John Perry, Andrea Dunaif, Joop S.E. Laven, Steve Franks, Cecilia M Lindgren, Corrine K Welt. (2018) Large-Scale Genome-Wide Meta Analysis of Polycystic Ovary Syndrome Suggests Shared Genetic Architecture for Different Diagnosis Criteria. PLoS Genetics. Dec 19;14(12):e1007813. PubMed Central PMCID: PMC6300389.

Joelle A. Pasman, Karin J.H. Verweij, Zachary Gerring, Sven Stringer, Sandra Sanchez-Roige, Jorien L. Treur, Abdel Abdellaoui, Michel G. Nivard, Bart M.L. Baselmans, Jue-Sheng Ong, Hill F. Ip, Matthijs D. van der Zee, Meike Bartels, Felix R. Day, Pierre Fontanillas, Sarah L. Elson, the 23andMe Research Team, Harriet de Wit, Lea K. Davis, James MacKillop, International Cannabis Consortium, Jaime L. Derringer, Susan J.T. Branje, Catharina A. Hartman, Andrew C. Heath, Pol A.C. van Lier, Pamela A.F. Madden, Reedik Magi, WimMeeus, Grant W. Montgomery, A. J. Oldehinkel, Zdenka Pausova, Josep A. Ramos Quiroga, Thomas Paus, Marta Ribases, Jaakko Kaprio, Marco P.M. Boks, Jordana T. Bell, Tim D. Spector, Joel Gelernter, Dorret I.Boomsma, Nicholas G. Martin, Stuart MacGregor, John R.B. Perry, Abraham A. Palmer, Danielle Posthuma, Marcus R. Munafo, Nathan A. Gillespie, Eske M. Derks, Jacqueline M. Vink (2018) GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia. Nature Neuroscience. Sep;21(9):1161-1170. PubMed PMID: 30150663.

Erik Pettersson, Paul Lichtenstein, Henrik Larsson, Jie Song, Attention Deficit/Hyperactivity Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Autism Spectrum Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Bipolar Disorder Working Group of the PGC, Eating Disorder Working Group of the PGC, Major Depressive Disorder Working Group of the PGC, Obsessive Compulsive Disorders and Tourette Syndrome Working Group of the PGC, Schizophrenia CLOZUK, Substance Use Disorder Working Group of the PGC, Arpana Agrawal, Anders D Børglum, Cynthia M Bulik, Mark J Daly, Lea K Davis, Ditte Demontis, Howard J. Edenberg, Jakob Grove, Joel Gelernter, Ben M Neale, Antonio F. Pardiñas, Eli Stahl, James TR Walters, Raymond Walters, Patrick F Sullivan, Danielle Posthuma, Tinca JC Polderman. (2018) Genetic influences on eight psychiatric disorders based on family data of 4,408,646 full and half-siblings, and genetic data of 333,748 cases and controls. Psychological Medicine. Sep 17:1-8. PubMed PMID: 30221610.

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.