Youna Hu

发表

GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person

N. Eriksson, D. Hinds, J. Tung, 2016, Nature Communications.

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.

Jennifer G. Robinson, Kyle J. Gaulton, Emily H Turner, 2014, American journal of human genetics.

Identification of a Rare Coding Variant in Complement 3 Associated with Age-related Macular Degeneration

Margaret A. Pericak-Vance, David E. Larson, Elaine R. Mardis, 2013, Nature Genetics.

Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci

Andres Metspalu, Anna Murray, Till Roenneberg, 2016, PLoS genetics.

and the Role of Rare Coding Variants in Type 2 Diabetes

K. Kristiansen, T. Hansen, O. Pedersen, 2013 .

Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.

Søren Brunak, Anders Albrechtsen, Jun Wang, 2013, American journal of human genetics.

Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

He Zhang, Thomas Meitinger, Raimund Erbel, 2014, The New England journal of medicine.

Genetic Associations With Gestational Duration and Spontaneous Preterm Birth

Daniel E. Miller, Günter P. Wagner, M. Pavlicev, 2018, Obstetric Anesthesia Digest.

Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm

Britney E. Graham, Haley R. Eidem, Neil A. Miller, 2018 .

Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus

Donal N. Gorman, D. Hinds, N. Furlotte, 2016, Pain.

Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease

C. Fox, D. Girelli, N. Martinelli, 2014 .

Accurate local-ancestry inference in exome-sequenced admixed individuals via off-target sequence reads.

Hyun Min Kang, Xiaowei Zhan, Cristen Willer, 2013, American journal of human genetics.

Genetic Associations with Gestational Length and Spontaneous Preterm Birth

Xiaoting Chen, Matthew T. Weirauch, Ge Zhang, 2017, The New England journal of medicine.

GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci

Donal N. Gorman, D. Hinds, Alex Gutteridge, 2017, Human molecular genetics.

Genome-wide association analyses in > 119,000 individuals identifies thirteen morningness and two sleep duration loci

Samuel E. Jones, J. Tyrrell, T. Frayling, 2016, bioRxiv.

RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data

Xiaowei Zhan, Gonçalo R. Abecasis, Dajiang J. Liu, 2016, Bioinform..

The benefits of using genetic information to design prevention trials.

Li Li, Meena Kumari, Hyun Min Kang, 2013, American journal of human genetics.

Rare loss of function variants in candidate genes and risk of colorectal cancer

Taylor J. Maxwell, Jennifer G. Robinson, Andrew J. Sanford, 2018, Human Genetics.

Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

Scott M. Williams, Britney E. Graham, Haley R. Eidem, 2018, PLoS genetics.

GWAS of 89,283 individuals identifies genetic variants associated with being a morning person

N. Eriksson, D. Hinds, J. Tung, 2014 .

Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.

K. Kristiansen, O. Pedersen, S. Brunak, 2013, American journal of human genetics.