Takip et
Maarja Jõeloo
Maarja Jõeloo
Diğer adlarMaarja Lepamets
PhD student, University of Tartu, Estonia
ut.ee üzerinde doğrulanmış e-posta adresine sahip
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
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
8422021
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
4962018
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
3042022
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
2432022
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
1462023
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
1042019
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
902020
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
562020
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
542019
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
472021
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
442017
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
412021
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
362019
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
202022
Chromosomal deletions on 16p11. 2 encompassing SH2B1 are associated with accelerated metabolic disease
R Hanssen, C Auwerx, M Jõeloo, MC Sadler, E Henning, J Keogh, ...
Cell Reports Medicine 4 (8), 2023
182023
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
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20