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Laura Raffield
Laura Raffield
Assistant Professor, Department of Genetics, University of North Carolina at Chapel Hill
在 unc.edu 的电子邮件经过验证
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A catalog of genetic loci associated with kidney function from analyses of a million individuals
M Wuttke, Y Li, M Li, KB Sieber, MF Feitosa, M Gorski, A Tin, L Wang, ...
Nature genetics 51 (6), 957-972, 2019
6252019
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
4652020
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
4632020
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
4262020
The trans-ancestral genomic architecture of glycemic traits
J Chen, CN Spracklen, G Marenne, A Varshney, LJ Corbin, J Luan, ...
Nature genetics 53 (6), 840-860, 2021
4092021
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
3582022
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ...
Nature genetics 54 (5), 560-572, 2022
3192022
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
A Tin, J Marten, VL Halperin Kuhns, Y Li, M Wuttke, H Kirsten, KB Sieber, ...
Nature genetics 51 (10), 1459-1474, 2019
2972019
Use of> 100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in …
MH Kowalski, H Qian, Z Hou, JD Rosen, AL Tapia, Y Shan, D Jain, ...
PLoS genetics 15 (12), e1008500, 2019
2272019
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
PK Joshi, N Pirastu, KA Kentistou, K Fischer, E Hofer, KE Schraut, ...
Nature communications 8 (1), 910, 2017
1652017
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
A Teumer, Y Li, S Ghasemi, BP Prins, M Wuttke, T Hermle, A Giri, ...
Nature communications 10 (1), 4130, 2019
1592019
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
N Franceschini, C Giambartolomei, PS De Vries, C Finan, JC Bis, ...
Nature communications 9 (1), 5141, 2018
1432018
Comparison of proteomic assessment methods in multiple cohort studies
LM Raffield, H Dang, KA Pratte, S Jacobson, LA Gillenwater, E Ampleford, ...
Proteomics 20 (12), 1900278, 2020
1212020
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
DL McCartney, JL Min, RC Richmond, AT Lu, MK Sobczyk, G Davies, ...
Genome biology 22, 1-25, 2021
1202021
Association of clonal hematopoiesis with incident heart failure
B Yu, MB Roberts, LM Raffield, SM Zekavat, NQH Nguyen, ML Biggs, ...
Journal of the American College of Cardiology 78 (1), 42-52, 2021
1162021
Clonal hematopoiesis is associated with higher risk of stroke
R Bhattacharya, SM Zekavat, J Haessler, M Fornage, L Raffield, ...
Stroke, 2022
1042022
Platelet-related variants identified by exomechip meta-analysis in 157,293 individuals
JD Eicher, N Chami, T Kacprowski, A Nomura, MH Chen, LR Yanek, ...
The American Journal of Human Genetics 99 (1), 40-55, 2016
972016
Clonal hematopoiesis associated with epigenetic aging and clinical outcomes
D Nachun, AT Lu, AG Bick, P Natarajan, J Weinstock, MD Szeto, ...
Aging Cell 20 (6), e13366, 2021
822021
APOL1 associations with nephropathy, atherosclerosis, and all-cause mortality in African Americans with type 2 diabetes
BI Freedman, CD Langefeld, L Lu, ND Palmer, SC Smith, BM Bagwell, ...
Kidney international 87 (1), 176-181, 2015
772015
Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism
N Matoba, D Liang, H Sun, N Aygün, JC McAfee, JE Davis, LM Raffield, ...
Translational psychiatry 10 (1), 265, 2020
732020
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