The human genetic epidemiology of COVID-19

por Niemi, Mari E. K., Daly, Mark J., Ganna, Andrea
Publicado 2022

Mosaic mutations in blood DNA sequence are associated with solid tumor cancers

por Artomov, Mykyta, Rivas, Manuel A., Genovese, Giulio, Daly, Mark J.
Publicado 2017

Network Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of Mutation

por Choi, Jinmyung, Shooshtari, Parisa, Samocha, Kaitlin E., Daly, Mark J., Cotsapas, Chris
Publicado 2016

Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

por Kanai, Masahiro, Elzur, Roy, Zhou, Wei, Daly, Mark J., Finucane, Hilary K.
Publicado 2022

Impaired Autophagy of an Intracellular Pathogen Induced by a Crohn's Disease Associated ATG16L1 Variant

por Kuballa, Petric, Huett, Alan, Rioux, John D., Daly, Mark J., Xavier, Ramnik J.
Publicado 2008

Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits

por Segrè, Ayellet V., Groop, Leif, Mootha, Vamsi K., Daly, Mark J., Altshuler, David
Publicado 2010

Burden of unique and low prevalence somatic mutations correlates with cancer survival

por Klebanov, Nikolai, Artomov, Mykyta, Goggins, William B., Daly, Emma, Daly, Mark J., Tsao, Hensin
Publicado 2019

Mendelian Randomization Analysis reveals Inverse Genetic Risks between Skin Cancers and Vitiligo

por Rashid, Sarem, Molotkov, Ivan, Klebanov, Nikolai, Shaughnessy, Michael, Daly, Mark J., Artomov, Mykyta, Tsao, Hensin
Publicado 2023

Genetic variants in cellular transport do not affect mesalamine response in ulcerative colitis

por Moran, Christopher J., Huang, Hailiang, Rivas, Manuel, Kaplan, Jess L., Daly, Mark J., Winter, Harland S.
Publicado 2018

Profiling the inflammatory bowel diseases using genetics, serum biomarkers, and smoking information

por Liu, Ruize, Li, Dalin, Haritunians, Talin, Ruan, Yunfeng, Daly, Mark J., Huang, Hailiang, McGovern, Dermot P.B.
Publicado 2023

Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function

por Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J.
Publicado 2010

Autosomal monoallelic expression in the mouse

por Zwemer, Lillian M, Zak, Alexander, Thompson, Benjamin R, Kirby, Andrew, Daly, Mark J, Chess, Andrew, Gimelbrant, Alexander A
Publicado 2012

The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell Symposium

por Rasmussen, Sonja A., Abul-Husn, Noura S., Casanova, Jean-Laurent, Daly, Mark J., Rehm, Heidi L., Murray, Michael F.
Publicado 2021

Proteins Encoded in Genomic Regions Associated with Immune-Mediated Disease Physically Interact and Suggest Underlying Biology

por Rossin, Elizabeth J., Lage, Kasper, Raychaudhuri, Soumya, Xavier, Ramnik J., Tatar, Diana, Benita, Yair, Cotsapas, Chris, Daly, Mark J.
Publicado 2011

Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder

por Bahl, Samira, Chiang, Colby, Beauchamp, Roberta L, Neale, Benjamin M, Daly, Mark J, Gusella, James F, Talkowski, Michael E, Ramesh, Vijaya
Publicado 2013

ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease

por Helkkula, Pyry, Kiiskinen, Tuomo, Havulinna, Aki S., Karjalainen, Juha, Koskinen, Seppo, Salomaa, Veikko, Daly, Mark J., Palotie, Aarno, Surakka, Ida, Ripatti, Samuli
Publicado 2021

Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD

por Wagner, Erin K., Raychaudhuri, Soumya, Villalonga, Mercedes B., Java, Anuja, Triebwasser, Michael P., Daly, Mark J., Atkinson, John P., Seddon, Johanna M.
Publicado 2016

Host genetic variation and its microbiome interactions within the Human Microbiome Project

por Kolde, Raivo, Franzosa, Eric A., Rahnavard, Gholamali, Hall, Andrew Brantley, Vlamakis, Hera, Stevens, Christine, Daly, Mark J., Xavier, Ramnik J., Huttenhower, Curtis
Publicado 2018

Association of APOE Haplotypes With Common Age-Related Ocular Diseases in 412,171 Individuals

por Liuska, Perttu J., Rämö, Joel T., Lemmelä, Susanna, Kaarniranta, Kai, Uusitalo, Hannu, Lahtela, Elisa, Daly, Mark J., Harju, Mika, Palotie, Aarno, Turunen, Joni A.
Publicado 2023

Genetic mapping of a modifier locus affecting hypertension in soluble guanylate cyclase α(1) deficient mice

por Buys, Emmanuel S, Raher, Michael J, Kirby, Andrew, Hayton, Sarah R, Tainsh, Laurel T, Sips, Patrick Y, Brouckaert, Peter, Daly, Mark J, Bloch, Kenneth D
Publicado 2011