Y. Hai

发表

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Inês Barroso, Jiyoung Heo, Beverley Balkau, 2015, Nature communications.

Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci

Robert J. Goodloe, M. Fornage, D. Absher, 2017, Human Genetics.

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits.

Sebastian M. Armasu, Christine A. Williams, Audrey Y. Chu, 2019, American journal of human genetics.

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

James M. Eales, Kyle J. Gaulton, J. Cook, 2019, Nature Communications.

Trans-ethnic genome-wide association study of kidney function provides novel insight into effector genes and causal effects on kidney-specific disease aetiologies

James M. Eales, Kyle J. Gaulton, J. Cook, 2018, bioRxiv.

Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies

James M. Eales, Kyle J. Gaulton, J. Cook, 2018 .

The Trans-Ancestral Genomic Architecture of Glycemic Traits

Stephen C. J. Parker, Tanya M. Teslovich, Anne W. Ndungu, 2020, Nature Genetics.

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

Tanya M. Teslovich, Dajiang J. Liu, Sara M. Willems, 2017, bioRxiv.

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.

Y. J. Kim, Jacob M. Keaton, Ellen M. Schmidt, 2022, Nature genetics.

Coronary Heart Disease Genetic Risk Score Predicts Cardiovascular Disease Risk in Men, Not Women: The Multi-Ethnic Study of Atherosclerosis

B. Psaty, K. Taylor, J. Rotter, 2018, Circulation. Genomic and precision medicine.

A more than four-fold sex-specific difference of autism spectrum disorders and the possible contribution of pesticide usage in China 1990–2030

Y. Hai, Guodong Leng, 2022, Frontiers in Public Health.

Clinical aggressiveness of malignant gliomas is linked to augmented metabolism of amino acids

Henry J. Lin, S. Nelson, T. Cloughesy, 2016, Journal of Neuro-Oncology.

Association of severity of primary open-angle glaucoma with serum vitamin D levels in patients of African descent

K. Taylor, J. Rotter, Xiuqing Guo, 2019, Molecular vision.

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

Giovanni Malerba, Jin Li, Rohit Varma, 2017, Nature Genetics.

Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control

Kaanan P. Shah, M. McCarthy, B. Yaspan, 2018, Diabetes.

De novo copy number variants and parental age: Is there an association?

J. Rosenfeld, J. Graham, Xiuqing Guo, 2019, European journal of medical genetics.

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Kyle J. Gaulton, Yoonjung Yoonie Joo, Cassandra N. Spracklen, 2020, Nature Genetics.

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits - the Hispanic/Latino Anthropometry Consortium

H. Hakonarson, S. Grant, G. Bedoya, 2021, bioRxiv.

Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study

R. Klein, B. Klein, A. Price, 2017, Diabetes.

Genetic Architecture of Primary Open-Angle Glaucoma in Individuals of African Descent: The African Descent and Glaucoma Evaluation Study III.

Nicholette D. Palmer, Lauren S Blieden, John P. Mitchell, 2019, Ophthalmology.

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

James M. Eales, Kyle J. Gaulton, J. Cook, 2019, Nature Communications.

Bidirectional Mendelian randomization to explore the causal relationships between body mass index and polycystic ovary syndrome

R. Krauss, J. Rotter, Xiuqing Guo, 2018, Human reproduction.

A Comprehensive Analysis of Common and Rare Variants to Identify Adiposity Loci in Hispanic Americans: The IRAS Family Study (IRASFS)

Nicholette D. Palmer, S. Kridel, R. Watanabe, 2015, PloS one.

Adiponectin, Insulin Sensitivity and Diabetic Retinopathy in Latinos With Type 2 Diabetes.

B. Klein, R. Klein, J. Rotter, 2015, Journal of Clinical Endocrinology and Metabolism.

Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH

Michael S. Reidy, Tanya M. Teslovich, Anne W. Ndungu, 2023, Diabetologia.

Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

Yoonjung Yoonie Joo, Cassandra N. Spracklen, Y. J. Kim, 2023, medRxiv.

The trans-ancestral genomic architecture of glycemic traits

Tanya M. Teslovich, Peter K. Joshi, May E. Montasser, 2021, Nature Genetics.

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

Stephen C. J. Parker, Tanya M. Teslovich, Anne W. Ndungu, 2020 .

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

Yoonjung Yoonie Joo, Cassandra N. Spracklen, Philip H. Schroeder, 2024, Nature.

Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

James M. Eales, M. Fornage, C. Rotimi, 2023, Cell genomics.

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

H. Hakonarson, S. Grant, G. Bedoya, 2022, HGG advances.

SMIM1 absence is associated with reduced energy expenditure and excess weight.

Tanya M. Teslovich, May E. Montasser, Nicholette D. Palmer, 2024, i Medicina.