Articles with public access mandates - Paul AuerLearn more
Not available anywhere: 5
Review
Unraveling the influence of common von Willebrand factor variants on von Willebrand disease phenotype: an exploratory study on the molecular and clinical profile of von …
N Borràs, I Garcia-Martínez, J Batlle, A Pérez-Rodríguez, R Parra, ...
Thrombosis and Haemostasis 120 (03), 437-448, 2020
Mandates: Government of Spain
Review
A unified linear mixed model for familial relatedness and population structure in genetic association studies
N DeVogel, PL Auer, R Manansala, A Rau, T Wang
Genetic Epidemiology 45 (3), 305-315, 2021
Mandates: UK Medical Research Council
Review
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels
PS de Vries, P Reventun, MR Brown, AS Heath, JE Huffman, NQ Le, ...
Blood 143 (18), 1845-1855, 2024
Mandates: UK Medical Research Council
Review
Convent of the Sacred Heart Libraries
Y Hu, SA Bien, KK Nishimura, J Haessler, CJ Hodonsky, AR Baldassari, ...
Mandates: US National Institutes of Health
Review
Nonlinear Estimation Methods for Mendelian Randomization in Genetic Studies
Y Cho, PL Auer, D Ghosh
Sankhya B, 1-39, 2023
Mandates: US National Science Foundation
Available somewhere: 128
Review
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
Mandates: US National Institutes of Health, US Department of Veterans Affairs
Review
Association analysis identifies 65 new breast cancer risk loci
K Michailidou, S Lindström, J Dennis, J Beesley, S Hui, S Kar, A Lemaçon, ...
Nature 551 (7678), 92-94, 2017
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Polygenic risk scores for prediction of breast cancer and breast cancer subtypes
N Mavaddat, K Michailidou, J Dennis, M Lush, L Fachal, A Lee, JP Tyrer, ...
The American Journal of Human Genetics 104 (1), 21-34, 2019
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
JC Crosby, GM Peloso, PL Auer, et al.
New England Journal of Medicine 371, 22-31, 2014
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, P Angelica Merlini, ...
Nature 518 (7537), 102-106, 2015
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
Mandates: US National Institutes of Health, UK Biotechnology and Biological Sciences …
Review
A population-based study of genes previously implicated in breast cancer
C Hu, SN Hart, R Gnanaolivu, H Huang, KY Lee, J Na, C Gao, J Lilyquist, ...
New England Journal of Medicine 384 (5), 440-451, 2021
Mandates: US National Institutes of Health, State of Califonia, Susan G. Komen
Review
Exome-wide association study of plasma lipids in> 300,000 individuals
DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ...
Nature genetics 49 (12), 1758-1766, 2017
Mandates: US National Institutes of Health, British Heart Foundation, UK Medical …
Review
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture
HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ...
Nature 526 (7571), 112-117, 2015
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ...
Nature 586 (7831), 763-768, 2020
Mandates: US National Institutes of Health, American Heart Association, Leducq …
Review
The polygenic and monogenic basis of blood traits and diseases
D Vuckovic, EL Bao, P Akbari, CA Lareau, A Mousas, T Jiang, MH Chen, ...
Cell 182 (5), 1214-1231. e11, 2020
Mandates: US National Institutes of Health, US Department of Veterans Affairs, UK …
Review
Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations
MH Chen, LM Raffield, A Mousas, S Sakaue, JE Huffman, A Moscati, ...
Cell 182 (5), 1198-1213. e14, 2020
Mandates: US National Institutes of Health, US Department of Veterans Affairs …
Review
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
Mandates: US National Institutes of Health, American Heart Association, German …
Review
Breast cancer risk from modifiable and nonmodifiable risk factors among white women in the United States
P Maas, M Barrdahl, AD Joshi, PL Auer, MM Gaudet, RL Milne, ...
JAMA oncology 2 (10), 1295-1302, 2016
Mandates: US National Institutes of Health
Review
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
RL Milne, KB Kuchenbaecker, K Michailidou, J Beesley, S Kar, ...
Nature genetics 49 (12), 1767-1778, 2017
Mandates: US National Institutes of Health, National Health and Medical Research …
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