Mary E. Haas

发表

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations

Apekshya Panda, Sarah E. Calvo, Vamsi K. Mootha, 2020, Nucleic Acids Res..

Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease

Sekar Kathiresan, Pradeep Natarajan, Amit V. Khera, 2017, bioRxiv.

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease

Mary E. Haas, J. Danesh, S. Gabriel, 2018, Nature Communications.

Cardiometabolic Polygenic Risk Scores and Osteoarthritis Outcomes: A Mendelian Randomization Study Using Data From the Malmö Diet and Cancer Study and the UK Biobank

Mary E. Haas, O. Melander, P. Nilsson, 2019, Arthritis & rheumatology.

Association of Habitual Alcohol Intake With Risk of Cardiovascular Disease

Mary E. Haas, P. Ellinor, S. Kathiresan, 2022, JAMA network open.

Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes

Johnathon R. Walls, Mary E. Haas, R. Collins, 2022, Nature Communications.

DNA Sequence Variation in ACVR1C Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes

Mary E. Haas, J. Danesh, S. Gabriel, 2018, Diabetes.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Andrew D. Johnson, May E. Montasser, Nicholette D. Palmer, 2020, Nature Genetics.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2020, Nature Genetics.

Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure.

Mary E. Haas, S. Kathiresan, G. Davey Smith, 2018, American journal of human genetics.

for Blood Pressure Genome-Wide Association Studies, (2018). Genetic association of albuminuria with cardiometabolic disease and blood pressure. Human Genetics

Mary E. Haas, S. Kathiresan, A. Bick, 2018 .

Association of genetic variation with cirrhosis: a multi-trait genome-wide association and gene-environment interaction study.

Mary E. Haas, A. Khera, S. Kathiresan, 2020, Gastroenterology.

Genetic Association of Arterial Stiffness Index with Blood Pressure and Coronary Artery Disease

Mary E. Haas, Hongyu Zhao, A. Khera, 2018, bioRxiv.

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

Mary E. Haas, E. Lander, A. Khera, 2018, Nature Genetics.

Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling

Mary E. Haas, J. Danesh, S. Gabriel, 2018, Circulation.

Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery

Mary E. Haas, P. Ellinor, D. Roden, 2019, Circulation.

Lipid nanoparticle-mediated codelivery of Cas9 mRNA and single-guide RNA achieves liver-specific in vivo genome editing of Angptl3

Mary E. Haas, Feng Zhang, Qiaobing Xu, 2021, Proceedings of the National Academy of Sciences.

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

Mary E. Haas, E. Lander, P. Ellinor, 2018, Nature Genetics.

Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood

Matthew S. Lebo, Marina T. DiStefano, Mary E. Haas, 2019, Cell.

Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease

Yan V. Sun, Donald R. Miller, Mary E. Haas, 2019, Nature Genetics.

Role of Insulin in the Regulation of Proprotein Convertase Subtilisin/Kexin Type 9.

Mary E. Haas, Ji Miao, Jingwen Liu, 2015, Arteriosclerosis, thrombosis, and vascular biology.

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

Mary E. Haas, J. Danesh, S. Gabriel, 2019, bioRxiv.

Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease

Yan V. Sun, Donald R. Miller, Mary E. Haas, 2019, Nature Genetics.

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease

Mary E. Haas, J. Danesh, S. Gabriel, 2018, Nature Communications.

The regulation of ApoB metabolism by insulin

Mary E. Haas, A. Attie, S. Biddinger, 2013, Trends in Endocrinology & Metabolism.

Framework From a Multidisciplinary Approach for Transitioning Variants of Unknown Significance From Clinical Genetic Testing in Kidney Disease to a Definitive Classification

Mary E. Haas, P. Igarashi, K. Patel, 2022, Kidney international reports.

A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

Christopher D. Brown, Henry J. Lin, Yan V. Sun, 2021, Nature Genetics.

A genome-wide association study for nonalcoholic fatty liver disease identifies novel genetic loci and trait-relevant candidate genes in the Million Veteran Program.

Christopher D. Brown, Liu, Sun, 2021, medRxiv.

The beta secretase BACE1 regulates the expression of insulin receptor in the liver

Mary E. Haas, C. Desbois-Mouthon, S. Biddinger, 2018, Nature Communications.

Insulin Dissociates the Effects of Liver X Receptor on Lipogenesis, Endoplasmic Reticulum Stress, and Inflammation*

Mary E. Haas, Ji Miao, M. Graham, 2015, The Journal of Biological Chemistry.

Hepatic insulin signaling is required for obesity-dependent expression of SREBP-1c mRNA but not for feeding-dependent expression.

Robert V Farese, Mary E. Haas, Ji Miao, 2012, Cell metabolism.

University of Dundee The beta secretase BACE 1 regulates the expression of the insulin receptor in the liver

Mary E. Haas, C. Desbois-Mouthon, S. Biddinger, 2018 .

Machine learning enables new insights into genetic contributions to liver fat accumulation

Mary E. Haas, A. Philippakis, M. Budoff, 2021, Cell genomics.

Electronic health record-based genome-wide meta-analysis provides insights on the genetic architecture of non-alcoholic fatty liver disease

Mary E. Haas, Y. Bossé, A. Khera, 2021, Cell reports. Medicine.

Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) in Secondary Hyperlipidemias

Mary E. Haas, M. Haas, 2016 .

Effect of Leptin Replacement on PCSK9 in ob/ob Mice and Female Lipodystrophic Patients.

Mary E. Haas, Ji Miao, R. Muniyappa, 2016, Endocrinology.

Machine learning enables new insights into clinical significance of and genetic contributions to liver fat accumulation

Mary E. Haas, A. Philippakis, A. Khera, 2020, medRxiv.

A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

Christopher D. Brown, Henry J. Lin, Yan V. Sun, 2022, Nature Genetics.

Electronic Health Record-Based Genome-Wide Meta-Analysis Provides New Insights on the Genetic Architecture of Non-Alcoholic Fatty Liver Disease

Mary E. Haas, Y. Bossé, A. Khera, 2021, SSRN Electronic Journal.

The Role of Proprotein Convertase Subtilisin/Kexin Type 9 in Nephrotic Syndrome-Associated Hypercholesterolemia

Mary E. Haas, D. Salant, S. D. de Ferranti, 2016, Circulation.

Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis

Mary E. Haas, J. Pankow, H. Ullum, 2022, The Journal of clinical investigation.