Theo dõi
Maarja Jõeloo
Maarja Jõeloo
Tên khácMaarja Lepamets
PhD student, University of Tartu, Estonia
Email được xác minh tại ut.ee
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
8462021
Primer3_masker: integrating masking of template sequence with primer design software
T Kõressaar, M Lepamets, L Kaplinski, K Raime, R Andreson, M Remm
Bioinformatics 34 (11), 1937-1938, 2018
4992018
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
3062022
A cross-disorder dosage sensitivity map of the human genome
RL Collins, JT Glessner, E Porcu, M Lepamets, R Brandon, C Lauricella, ...
Cell 185 (16), 3041-3055. e25, 2022
2422022
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
N Rahmioglu, S Mortlock, M Ghiasi, PL Møller, L Stefansdottir, ...
Nature genetics 55 (3), 423-436, 2023
1562023
Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions
S Reisberg, K Krebs, M Lepamets, M Kals, R Mägi, K Metsalu, ...
Genetics in Medicine 21 (6), 1345-1354, 2019
1062019
Identification of ALK in Thinness
M Orthofer, A Valsesia, R Mägi, QP Wang, J Kaczanowska, I Kozieradzki, ...
Cell 181 (6), 1246-1262. e22, 2020
982020
The genetic architecture of sporadic and multiple consecutive miscarriage
T Laisk, ALG Soares, T Ferreira, JN Painter, JC Censin, S Laber, J Bacelis, ...
Nature communications 11 (1), 5980, 2020
912020
The individual and global impact of copy-number variants on complex human traits
C Auwerx, M Lepamets, MC Sadler, M Patxot, M Stojanov, D Baud, ...
The American Journal of Human Genetics 109 (4), 647-668, 2022
692022
Genome-wide study identifies association between HLA-B∗ 55: 01 and self-reported penicillin allergy
K Krebs, J Bovijn, N Zheng, M Lepamets, JC Censin, T Jürgenson, D Särg, ...
The American Journal of Human Genetics 107 (4), 612-621, 2020
572020
Genome-wide study identifies association between HLA-B* 55: 01 and penicillin allergy
K Krebs, J Bovijn, M Lepamets, JC Censin, T Jürgenson, D Särg, Y Luo, ...
bioRxiv, 2020.02. 27.967497, 2020
57*2020
Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification
K Läll, M Lepamets, M Palover, T Esko, A Metspalu, N Tõnisson, P Padrik, ...
BMC cancer 19, 1-9, 2019
552019
StrainSeeker: fast identification of bacterial strains from raw sequencing reads using user-provided guide trees
M Roosaare, M Vaher, L Kaplinski, M Möls, R Andreson, M Lepamets, ...
PeerJ 5, e3353, 2017
542017
Genome-wide association study identifies five risk loci for pernicious anemia
T Laisk, M Lepamets, M Koel, E Abner, ...
Nature Communications 12 (1), 3761, 2021
452021
GenomeTester4: a toolkit for performing basic set operations-union, intersection and complement on k-mer lists
L Kaplinski, M Lepamets, M Remm
Gigascience 4 (1), s13742-015-0097-y, 2015
452015
FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads
FD Pajuste, L Kaplinski, M Möls, T Puurand, M Lepamets, M Remm
Scientific reports 7 (1), 2537, 2017
432017
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
M D’Antonio, JP Nguyen, TD Arthur, H Matsui, BM Neale, M Daly, ...
Cell reports 37 (7), 2021
422021
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility
AS Lee, J Rusch, AC Lima, A Usmani, N Huang, M Lepamets, ...
Nature communications 10 (1), 4626, 2019
352019
Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse
N Pujol-Gualdo, K Läll, M Lepamets, ...
Nature Communications 13 (1), 3584, 2022
222022
Rare copy-number variants as modulators of common disease susceptibility
C Auwerx, M Jõeloo, MC Sadler, N Tesio, S Ojavee, CJ Clark, R Mägi, ...
Genome Medicine 16 (1), 5, 2024
172024
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