Works by Davis, Lea K.

Results: 56

GWAS links APOE to neuropsychiatric symptoms in mild cognitive impairment and dementia.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2025, v. 21, n. 6, p. 1, doi. 10.1002/alz.70329

By:

Vattathil, Selina M.;
Blostein, Freida;
Miller‐Fleming, Tyne W.;
Davis, Lea K.;
Wingo, Thomas S.;
Wingo, Aliza P.

Publication type:

Article

Epidemiology of Functional Seizures Among Adults Treated at a University Hospital.

Published in:

JAMA Network Open, 2020, v. 3, n. 12, p. e2027920, doi. 10.1001/jamanetworkopen.2020.27920

By:

Goleva, Slavina B.;
Lake, Allison M.;
Torstenson, Eric S.;
Haas, Kevin F.;
Davis, Lea K.

Publication type:

Article

The genetic contribution to the comorbidity of depression and anxiety: a multi-site electronic health records study of almost 178 000 people.

Published in:

Psychological Medicine, 2023, v. 53, n. 15, p. 7368, doi. 10.1017/S0033291723000983

By:

Coombes, Brandon J;
Landi, Isotta;
Choi, Karmel W;
Singh, Kritika;
Fennessy, Brian;
Jenkins, Greg D;
Batzler, Anthony;
Pendegraft, Richard;
Nunez, Nicolas A;
Gao, Y Nina;
Ryu, Euijung;
Wickramaratne, Priya;
Weissman, Myrna M;
Pathak, Jyotishman;
Mann, J John;
Smoller, Jordan W;
Davis, Lea K;
Olfson, Mark;
Charney, Alexander W;
Biernacka, Joanna M

Publication type:

Article

Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry.

Published in:

BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-09990-w

By:

Burns, Kharis;
Mullin, Benjamin H.;
Moolhuijsen, Loes M. E.;
Laisk, Triin;
Tyrmi, Jaakko S.;
Cui, Jinrui;
Actkins, Ky'Era V.;
Louwers, Yvonne V.;
Metspalu, Andres;
Milani, Lili;
Esko, Tõnu;
Nelis, Mari;
Hudjashov, Georgi;
Davis, Lea K.;
Dudbridge, Frank;
Azziz, Ricardo;
Goodarzi, Mark O.;
Laivuori, Hannele;
Mägi, Reedik;
Visser, Jenny A.

Publication type:

Article

Improving the computation efficiency of polygenic risk score modeling: faster in Julia.

Published in:

Life Science Alliance, 2022, v. 5, n. 12, p. 1, doi. 10.26508/lsa.202201382

By:

Faucon, Annika;
Samaroo, Julian;
Tian Ge;
Davis, Lea K.;
Cox, Nancy J.;
Ran Tao;
Shuey, Megan M.

Publication type:

Article

Genetic investigation of the contribution of body composition to anorexia nervosa in an electronic health record setting.

Published in:

Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02251-y

By:

Mack, Taralynn;
Sanchez-Roige, Sandra;
Davis, Lea K.

Publication type:

Article

Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization.

Published in:

Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24824-z

By:

Pathak, Gita A.;
Singh, Kritika;
Miller-Fleming, Tyne W.;
Wendt, Frank R.;
Ehsan, Nava;
Hou, Kangcheng;
Johnson, Ruth;
Lu, Zeyun;
Gopalan, Shyamalika;
Yengo, Loic;
Mohammadi, Pejman;
Pasaniuc, Bogdan;
Polimanti, Renato;
Davis, Lea K.;
Mancuso, Nicholas

Publication type:

Article

Contextualizing genetic risk score for disease screening and rare variant discovery.

Published in:

Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24387-z

By:

Zhou, Dan;
Yu, Dongmei;
Scharf, Jeremiah M.;
Mathews, Carol A.;
McGrath, Lauren;
Cook, Edwin;
Lee, S. Hong;
Davis, Lea K.;
Gamazon, Eric R.

Publication type:

Article

The physical and psychiatric health conditions related to autism genetic scores, across genetic ancestries, sexes and age-groups in electronic health records.

Published in:

Journal of Neurodevelopmental Disorders, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s11689-023-09485-x

By:

Niarchou, Maria;
Miller-Fleming, Tyne;
Malow, Beth A.;
Davis, Lea K.

Publication type:

Article

Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture.

Published in:

PLoS Genetics, 2013, v. 9, n. 10, p. 1, doi. 10.1371/journal.pgen.1003864

By:

Davis, Lea K.;
Yu, Dongmei;
Keenan, Clare L.;
Gamazon, Eric R.;
Konkashbaev, Anuar I.;
Derks, Eske M.;
Neale, Benjamin M.;
Yang, Jian;
Lee, S. Hong;
Evans, Patrick;
Barr, Cathy L.;
Bellodi, Laura;
Benarroch, Fortu;
Berrio, Gabriel Bedoya;
Bienvenu, Oscar J.;
Bloch, Michael H.;
Blom, Rianne M.;
Bruun, Ruth D.;
Budman, Cathy L.;
Camarena, Beatriz

Publication type:

Article

Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids.

Published in:

Human Heredity, 2019, v. 84, n. 2, p. 73, doi. 10.1159/000501335

By:

Bray, Michael J.;
Davis, Lea K.;
Torstenson, Eric S.;
Jones, Sarah H.;
Edwards, Todd L.;
Velez Edwards, Digna R.

Publication type:

Article

Sexual Trauma, Polygenic Scores, and Mental Health Diagnoses and Outcomes.

Published in:

JAMA Psychiatry, 2025, v. 82, n. 1, p. 75, doi. 10.1001/jamapsychiatry.2024.3426

By:

Lake, Allison M.;
Zhou, Yu;
Wang, Bo;
Actkins, Ky'Era V.;
Zhang, Yingzhe;
Shelley, John P.;
Rajamani, Anindita;
Steigman, Michael;
Kennedy, Chris J.;
Smoller, Jordan W.;
Choi, Karmel W.;
Khankari, Nikhil K.;
Davis, Lea K.

Publication type:

Article

Genetic Liability to Posttraumatic Stress Disorder Symptoms and Its Association With Cardiometabolic and Respiratory Outcomes.

Published in:

JAMA Psychiatry, 2024, v. 81, n. 1, p. 34, doi. 10.1001/jamapsychiatry.2023.4127

By:

Pathak, Gita A.;
Singh, Kritika;
Choi, Karmel W.;
Fang, Yu;
Kouakou, Manuela R.;
Lee, Younga Heather;
Zhou, Xiang;
Fritsche, Lars G.;
Wendt, Frank R.;
Davis, Lea K.;
Polimanti, Renato

Publication type:

Article

Use of the PsycheMERGE Network to Investigate the Association Between Depression Polygenic Scores and White Blood Cell Count.

Published in:

2021

By:

Sealock, Julia M.;
Lee, Younga H.;
Moscati, Arden;
Venkatesh, Sanan;
Voloudakis, Georgios;
Straub, Peter;
Singh, Kritika;
Feng, Yen-Chen A.;
Ge, Tian;
Roussos, Panos;
Smoller, Jordan W.;
Chen, Guanhua;
Davis, Lea K.

Publication type:

journal article

Calcium-Sensing Receptor Polymorphisms at rs1801725 Are Associated with Increased Risk of Secondary Malignancies.

Published in:

Journal of Personalized Medicine, 2021, v. 11, n. 7, p. 642, doi. 10.3390/jpm11070642

By:

Actkins, Ky'Era V.;
Beasley, Heather K.;
Faucon, Annika B.;
Davis, Lea K.;
Sakwe, Amos M.

Publication type:

Article

Fate or coincidence: do COPD and major depression share genetic risk factors?

Published in:

Human Molecular Genetics, 2021, v. 30, n. 7, p. 619, doi. 10.1093/hmg/ddab068

By:

Martucci, Victoria L;
Richmond, Bradley;
Davis, Lea K;
Blackwell, Timothy S;
Cox, Nancy J;
Samuels, David;
Edwards, Digna Velez;
Aldrich, Melinda C

Publication type:

Article

Dense phenotyping from electronic health records enables machine learning-based prediction of preterm birth.

Published in:

BMC Medicine, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12916-022-02522-x

By:

Abraham, Abin;
Le, Brian;
Kosti, Idit;
Straub, Peter;
Velez-Edwards, Digna R.;
Davis, Lea K.;
Newton, J. M.;
Muglia, Louis J.;
Rokas, Antonis;
Bejan, Cosmin A.;
Sirota, Marina;
Capra, John A.

Publication type:

Article

International Society of Psychiatric Genetics Ethics Committee: Issues facing us.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 8, p. 543, doi. 10.1002/ajmg.b.32736

By:

Lázaro‐Muñoz, Gabriel;
Sabatello, Maya;
Huckins, Laura;
Peay, Holly;
Degenhardt, Franziska;
Meiser, Bettina;
Lencz, Todd;
Soda, Takahiro;
Docherty, Anna;
Crepaz‐Keay, David;
Austin, Jehannine;
Peterson, Roseann E.;
Davis, Lea K.

Publication type:

Article

Sex differences in the genetic architecture of obsessive–compulsive disorder.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 6, p. 351, doi. 10.1002/ajmg.b.32687

By:

Khramtsova, Ekaterina A.;
Heldman, Raphael;
Derks, Eske M.;
Yu, Dongmei;
Davis, Lea K.;
Stranger, Barbara E.

Publication type:

Article

The new science of sex differences in neuropsychiatric traits.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 6, p. 333, doi. 10.1002/ajmg.b.32747

By:

Davis, Lea K.;
Stranger, Barbara E.

Publication type:

Article

STAMS: STRING-assisted module search for genome wide association studies and application to autism.

Published in:

Bioinformatics, 2016, v. 32, n. 24, p. 3815, doi. 10.1093/bioinformatics/btw530

By:

Hillenmeyer, Sara;
Davis, Lea K.;
Gamazon, Eric R.;
Cook, Edwin H.;
Cox, Nancy J.;
Altman, Russ B.

Publication type:

Article

Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.

Published in:

Bioinformatics, 2015, v. 31, n. 2, p. 187, doi. 10.1093/bioinformatics/btu591

By:

Trubetskoy, Vassily;
Rodriguez, Alex;
Dave, Uptal;
Campbell, Nicholas;
Crawford, Emily L.;
Cook, Edwin H.;
Sutcliffe, James S.;
Foster, Ian;
Madduri, Ravi;
Cox, Nancy J.;
Davis, Lea K.

Publication type:

Article

Phenomewide Association Study of Health Outcomes Associated With the Genetic Correlates of 25 Hydroxyvitamin D Concentration and Vitamin D Binding Protein Concentration.

Published in:

Twin Research & Human Genetics, 2024, v. 27, n. 2, p. 69, doi. 10.1017/thg.2024.19

By:

Kresge, Hailey A.;
Blostein, Freida;
Goleva, Slavina;
Albiñana, Clara;
Revez, Joana A.;
Wray, Naomi R.;
Vilhjálmsson, Bjarni J.;
Zhu, Zhihong;
McGrath, John J.;
Davis, Lea K.

Publication type:

Article

Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.

Published in:

Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0130-3

By:

Rui Chen;
Davis, Lea K.;
Guter, Stephen;
Qiang Wei;
Jacob, Suma;
Potter, Melissa H.;
Cox, Nancy J.;
Cook, Edwin H.;
Sutcliffe, James S.;
Li, Bingshan

Publication type:

Article

Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitativet trait loci.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 3, doi. 10.1186/2040-2392-3-3

By:

Davis, Lea K.;
Gamazon, Eric R.;
Kistner-Griffin, Emily;
Badner, Judith A.;
Chunyu Liu;
Cook, Edwin H.;
Sutcliffe, James S.;
Cox, Nancy J.

Publication type:

Article

Confronting ethical and social issues related to the genetics of musicality.

Published in:

Annals of the New York Academy of Sciences, 2023, v. 1522, n. 1, p. 5, doi. 10.1111/nyas.14972

By:

Gordon, Reyna L.;
Martschenko, Daphne O.;
Nayak, Srishti;
Niarchou, Maria;
Morrison, Matthew D.;
Bell, Eamonn;
Jacoby, Nori;
Davis, Lea K.

Publication type:

Article

Medical phenome of musicians: an investigation of health records collected on 9803 musically active individuals.

Published in:

Annals of the New York Academy of Sciences, 2021, v. 1505, n. 1, p. 156, doi. 10.1111/nyas.14671

By:

Niarchou, Maria;
Lin, George T.;
Lense, Miriam D.;
Gordon, Reyna L.;
Davis, Lea K.

Publication type:

Article

Sex-Adjusted Model for End-stage Liver Disease Scores for Liver Transplant Allocation—Reply.

Published in:

JAMA Surgery, 2022, v. 157, n. 12, p. 1167, doi. 10.1001/jamasurg.2022.4150

By:

Sealock, Julia M.;
Davis, Lea K.

Publication type:

Article

Proposing a Sex-Adjusted Sodium-Adjusted MELD Score for Liver Transplant Allocation.

Published in:

2022

By:

Sealock, Julia M.;
Ziogas, Ioannis A.;
Zhao, Zhiguo;
Ye, Fei;
Alexopoulos, Sophoclis P.;
Matsuoka, Lea;
Chen, Guanhua;
Davis, Lea K.

Publication type:

journal article

Strength of Genetic Associations with Thyrotropin Values Differs Between Populations with Similarity to African and European Reference Populations.

Published in:

Thyroid, 2025, v. 35, n. 2, p. 131, doi. 10.1089/thy.2024.0525

By:

Wade, Alisha N.;
Guare, Lindsay;
Hayat, Mahtaab;
Straub, Peter;
Gao, Ziyue;
Medici, Marco;
Teumer, Alexander;
Davis, Lea K.;
Ramsay, Michèle;
Ritchie, Marylyn D.;
BioBank, Penn Medicine;
Cappola, Anne R.

Publication type:

Article

Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease.

Published in:

Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-020-00820-8

By:

Dennis, Jessica K.;
Sealock, Julia M.;
Straub, Peter;
Lee, Younga H.;
Hucks, Donald;
Actkins, Ky'Era;
Faucon, Annika;
Feng, Yen-Chen Anne;
Ge, Tian;
Goleva, Slavina B.;
Niarchou, Maria;
Singh, Kritika;
Morley, Theodore;
Smoller, Jordan W.;
Ruderfer, Douglas M.;
Mosley, Jonathan D.;
Chen, Guanhua;
Davis, Lea K.

Publication type:

Article

Weldon, Bateson, and the origins of genetics: Reflections on the unraveling and rebuilding of a scientific community.

Published in:

PLoS Genetics, 2022, v. 18, n. 10, p. 1, doi. 10.1371/journal.pgen.1010379

By:

Davis, Lea K.

Publication type:

Article

Genome-wide analysis of copy number variants in age-related macular degeneration.

Published in:

Human Genetics, 2011, v. 129, n. 1, p. 91, doi. 10.1007/s00439-010-0904-6

By:

Meyer, Kacie J.;
Davis, Lea K.;
Schindler, Emily I.;
Beck, John S.;
Rudd, Danielle S.;
Grundstad, A. Jason;
Scheetz, Todd E.;
Braun, Terry A.;
Fingert, John H.;
Alward, Wallace L.;
Kwon, Young H.;
Folk, James C.;
Russell, Stephen R.;
Wassink, Thomas H.;
Stone, Edwin M.;
Sheffield, Val C.

Publication type:

Article

A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.

Published in:

Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05624-4

By:

Mosley, Jonathan D.;
Feng, QiPing;
Wells, Quinn S.;
Van Driest, Sara L.;
Shaffer, Christian M.;
Edwards, Todd L.;
Bastarache, Lisa;
Wei, Wei-Qi;
Davis, Lea K.;
McCarty, Catherine A.;
Thompson, Will;
Chute, Christopher G.;
Jarvik, Gail P.;
Gordon, Adam S.;
Palmer, Melody R.;
Crosslin, David R.;
Larson, Eric B.;
Carrell, David S.;
Kullo, Iftikhar J.;
Pacheco, Jennifer A.

Publication type:

Article

Polygenic burden in focal and generalized epilepsies.

Published in:

2019

By:

Leu, Costin;
Stevelink, Remi;
Smith, Alexander W;
Goleva, Slavina B;
Kanai, Masahiro;
Ferguson, Lisa;
Campbell, Ciaran;
Kamatani, Yoichiro;
Okada, Yukinori;
Sisodiya, Sanjay M;
Cavalleri, Gianpiero L;
Koeleman, Bobby P C;
Lerche, Holger;
Jehi, Lara;
Davis, Lea K;
Najm, Imad M;
Palotie, Aarno;
Daly, Mark J;
Busch, Robyn M;
Consortium, Epi25

Publication type:

journal article

Genetic association signal near NTN4 in Tourette syndrome.

Published in:

2014

By:

Paschou, Peristera;
Yu, Dongmei;
Gerber, Gloria;
Evans, Patrick;
Tsetsos, Fotis;
Davis, Lea K;
Karagiannidis, Iordanis;
Chaponis, Jonathan;
Gamazon, Eric;
Mueller-Vahl, Kirsten;
Stuhrmann, Manfred;
Schloegelhofer, Monika;
Stamenkovic, Mara;
Hebebrand, Johannes;
Noethen, Markus;
Nagy, Peter;
Barta, Csaba;
Tarnok, Zsanett;
Rizzo, Renata;
Depienne, Christel

Publication type:

journal article

Genetic association signal near NTN 4 in Tourette syndrome.

Published in:

Annals of Neurology, 2014, v. 76, n. 2, p. 310, doi. 10.1002/ana.24215

By:

Paschou, Peristera;
Yu, Dongmei;
Gerber, Gloria;
Evans, Patrick;
Tsetsos, Fotis;
Davis, Lea K.;
Karagiannidis, Iordanis;
Chaponis, Jonathan;
Gamazon, Eric;
Mueller‐Vahl, Kirsten;
Stuhrmann, Manfred;
Schloegelhofer, Monika;
Stamenkovic, Mara;
Hebebrand, Johannes;
Noethen, Markus;
Nagy, Peter;
Barta, Csaba;
Tarnok, Zsanett;
Rizzo, Renata;
Depienne, Christel

Publication type:

Article

Shared Genetic Control of Brain Activity During Sleep and Insulin Secretion: A Laboratory-Based Family Study.

Published in:

2018

By:

Morselli, Lisa L.;
Gamazon, Eric R.;
Tasali, Esra;
Cox, Nancy J.;
Van Cauter, Eve;
Davis, Lea K.

Publication type:

journal article

Identification of Transdiagnostic Childhood Externalizing Pathology Within an Electronic Medical Records Database and Application to the Analysis of Rare Copy Number Variation.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2025, v. 198, n. 4, p. 1, doi. 10.1002/ajmg.b.33020

By:

Reddy, India A.;
Han, Lide;
Sanchez‐Roige, Sandra;
Niarchou, Maria;
Ruderfer, Douglas M.;
Davis, Lea K.

Publication type:

Article

Life is pain: Fibromyalgia as a nexus of multiple liability distributions.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2023, v. 192, n. 7/8, p. 171, doi. 10.1002/ajmg.b.32949

By:

Moscati, Arden;
Faucon, Annika B.;
Arnaiz‐Yépez, Cayetana;
Lönn, Sara Larsson;
Sundquist, Jan;
Sundquist, Kristina;
Belbin, Gillian M.;
Nadkarni, Girish;
Cho, Judy H.;
Loos, Ruth J. F.;
Davis, Lea K.;
Kendler, Kenneth S.

Publication type:

Article

A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2022, v. 189, n. 6, p. 185, doi. 10.1002/ajmg.b.32911

By:

Niarchou, Maria;
Sealock, Julia M.;
Straub, Peter;
Sanchez‐Roige, Sandra;
Sutcliffe, James S.;
Davis, Lea K.

Publication type:

Article

Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry.

Published in:

2019

By:

Sanchez‐Roige, Sandra;
Fontanillas, Pierre;
Elson, Sarah L.;
Gray, Joshua C.;
Wit, Harriet;
Davis, Lea K.;
MacKillop, James;
Palmer, Abraham A.;
Sanchez-Roige, Sandra;
23andMe Research Team;
de Wit, Harriet

Publication type:

journal article

LGBTQ+ Perspectives on Conducting Genomic Research on Sexual Orientation and Gender Identity.

Published in:

Behavior Genetics, 2022, v. 52, n. 4/5, p. 246, doi. 10.1007/s10519-022-10105-y

By:

Hammack-Aviran, Catherine;
Eilmus, Ayden;
Diehl, Carolyn;
Gottlieb, Keanan Gabriel;
Gonzales, Gilbert;
Davis, Lea K.;
Clayton, Ellen Wright

Publication type:

Article

The Biological Contributions to Gender Identity and Gender Diversity: Bringing Data to the Table.

Published in:

Behavior Genetics, 2018, v. 48, n. 2, p. 95, doi. 10.1007/s10519-018-9889-z

By:

Polderman, Tinca J. C.;
Kreukels, Baudewijntje P. C.;
Irwig, Michael S.;
Beach, Lauren;
Yee-Ming Chan;
Derks, Eske M.;
Esteva, Isabel;
Ehrenfeld, Jesse;
Den Heijer, Martin;
Posthuma, Danielle;
Raynor, Lewis;
Tishelman, Amy;
Davis, Lea K.

Publication type:

Article

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.

Published in:

Journal of Speech, Language & Hearing Research, 2020, v. 63, n. 9, p. 3019, doi. 10.1044/2020_JSLHR-19-00397

By:

Walters Jr., Courtney E.;
Nitin, Rachana;
Margulis, Katherine;
Boorom, Olivia;
Gustavson, Daniel E.;
Bush, Catherine T.;
Davis, Lea K.;
Below, Jennifer E.;
Cox, Nancy J.;
Camarata, Stephen M.;
Gordon, Reyna L.

Publication type:

Article

Sex modifies the effect of genetic risk scores for polycystic ovary syndrome on metabolic phenotypes.

Published in:

PLoS Genetics, 2023, v. 19, n. 5, p. 1, doi. 10.1371/journal.pgen.1010764

By:

Actkins, Ky'Era V.;
Jean-Pierre, Genevieve;
Aldrich, Melinda C.;
Velez Edwards, Digna R.;
Davis, Lea K.

Publication type:

Article

The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-95154-9

By:

Bagheri, Minoo;
Wang, Chuan;
Shi, Mingjian;
Manouchehri, Ali;
Murray, Katherine T.;
Murphy, Matthew B.;
Shaffer, Christian M.;
Singh, Kritika;
Davis, Lea K.;
Jarvik, Gail P.;
Stanaway, Ian B.;
Hebbring, Scott;
Reilly, Muredach P.;
Gerszten, Robert E.;
Wang, Thomas J.;
Mosley, Jonathan D.;
Ferguson, Jane F.

Publication type:

Article

In Search of Genomic Stability: Characterizing Copy Number Stable Regions.

Published in:

Human Mutation, 2011, v. 32, n. 8, p. v, doi. 10.1002/humu.21572

By:

Davis, Lea K.

Publication type:

Article

Developing a phenotype risk score for tic disorders in a large, clinical biobank.

Published in:

Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-03011-w

By:

Miller-Fleming, Tyne W.;
Allos, Annmarie;
Gantz, Emily;
Yu, Dongmei;
Isaacs, David A.;
Mathews, Carol A.;
Scharf, Jeremiah M.;
Davis, Lea K.

Publication type:

Article

Medical and genetic correlates of long-term buprenorphine treatment in the electronic health records.

Published in:

Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-023-02713-x

By:

Niarchou, Maria;
Sanchez-Roige, Sandra;
Reddy, India A.;
Reese, Thomas J.;
Marcovitz, David;
Davis, Lea K.

Publication type:

Article