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Paul Auer
Paul Auer
Professor of Biostatistics, Medical College of Wisconsin
Bestätigte E-Mail-Adresse bei mcw.edu
Titel
Zitiert von
Zitiert von
Jahr
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
9532017
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
7102014
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
6672015
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
5892021
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
5642019
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
5152017
Statistical design and analysis of RNA sequencing data
PL Auer, RW Doerge
Genetics 185 (2), 405-416, 2010
4842010
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
NO Stitziel, HH Won, AC Morrison, GM Peloso, R Do, LA Lange, ...
The New England Journal of Medicine 371, 2072-2082, 2014
415*2014
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
4112017
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
3962015
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
3542016
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
GM Peloso, PL Auer, JC Bis, A Voorman, AC Morrison, NO Stitziel, ...
The American Journal of Human Genetics 94 (2), 223-232, 2014
3442014
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
2992016
The fate of duplicated genes in a polyploid plant genome
A Roulin, PL Auer, M Libault, J Schlueter, A Farmer, G May, G Stacey, ...
The Plant Journal 73 (1), 143-153, 2013
2612013
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
2592017
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
2432018
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
2262021
Rare variant association studies: considerations, challenges and opportunities
PL Auer, G Lettre
Genome medicine 7 (1), 1-11, 2015
2182015
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ...
The American Journal of Human Genetics 94 (2), 233-245, 2014
2162014
Meta-analysis of gene-level tests for rare variant association
DJ Liu, GM Peloso, X Zhan, OL Holmen, M Zawistowski, S Feng, ...
Nature genetics 46 (2), 200-204, 2014
2112014
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