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Elina Salmela
Elina Salmela
Postdoctoral researcher, University of Helsinki, University of Turku & MPI-EVA
Verified email at eva.mpg.de - Homepage
Title
Cited by
Cited by
Year
Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environment
S Rodin, L Antonsson, C Niaudet, OE Simonson, E Salmela, EM Hansson, ...
Nature communications 5 (1), 3195, 2014
3352014
Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe
E Salmela, T Lappalainen, I Fransson, PM Andersen, K Dahlman-Wright, ...
PloS one 3 (10), e3519, 2008
1892008
Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe
TC Lamnidis, K Majander, C Jeong, E Salmela, A Wessman, V Moiseyev, ...
Nature communications 9 (1), 5018, 2018
1442018
Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe
CL Thiseas, K Majander, C Jeong, E Salmela, A Wessman, V Moiseyev, ...
BioRxiv, 2018
144*2018
Migration waves to the Baltic Sea region
T Lappalainen, V Laitinen, E Salmela, P Andersen, K Huoponen, ...
Annals of human genetics 72 (3), 337-348, 2008
1262008
Regional differences among the Finns: a Y-chromosomal perspective
T Lappalainen, S Koivumäki, E Salmela, K Huoponen, P Sistonen, ...
Gene 376 (2), 207-215, 2006
1102006
Morphological, cytogenetic, and molecular evidence for introgressive hybridization in birch
ÆHT Thórsson, E Salmela, K Anamthawat-Jónsson
Journal of Heredity 92 (5), 404-408, 2001
1062001
Skin microbiota and allergic symptoms associate with exposure to environmental microbes
J Lehtimäki, H Sinkko, A Hielm-Björkman, E Salmela, K Tiira, ...
Proceedings of the National Academy of Sciences 115 (19), 4897-4902, 2018
652018
Swedish population substructure revealed by genome-wide single nucleotide polymorphism data
E Salmela, T Lappalainen, J Liu, P Sistonen, PM Andersen, S Schreiber, ...
PLoS One 6 (2), e16747, 2011
592011
Population Structure in Contemporary Sweden—A Y‐Chromosomal and Mitochondrial DNA Analysis
T Lappalainen, U Hannelius, E Salmela, U Von Döbeln, CM Lindgren, ...
Annals of human genetics 73 (1), 61-73, 2009
562009
Genomic landscape of positive natural selection in Northern European populations
T Lappalainen, E Salmela, PM Andersen, K Dahlman-Wright, P Sistonen, ...
European Journal of Human Genetics 18 (4), 471-478, 2010
532010
Urban environment predisposes dogs and their owners to allergic symptoms
E Hakanen, J Lehtimäki, E Salmela, K Tiira, J Anturaniemi, ...
Scientific reports 8 (1), 1585, 2018
512018
Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs
U Hannelius, E Salmela, T Lappalainen, G Guillot, CM Lindgren, ...
BMC genetics 9 (1), 54, 2008
492008
Human mitochondrial DNA lineages in Iron-Age Fennoscandia suggest incipient admixture and eastern introduction of farming-related maternal ancestry
S Översti, K Majander, E Salmela, K Salo, L Arppe, S Belskiy, ...
Scientific Reports 9 (1), 16883, 2019
452019
Molecular characterization of three canine models of human rare bone diseases: Caffey, van den Ende-Gupta, and Raine syndromes
MK Hytönen, M Arumilli, AK Lappalainen, M Owczarek-Lipska, ...
PLoS genetics 12 (5), e1006037, 2016
432016
Two novel genomic regions associated with fearfulness in dogs overlap human neuropsychiatric loci
R Sarviaho, O Hakosalo, K Tiira, S Sulkama, E Salmela, MK Hytönen, ...
Translational psychiatry 9 (1), 18, 2019
392019
A woman with a sword?–weapon grave at Suontaka Vesitorninmäki, Finland
U Moilanen, T Kirkinen, NJ Saari, AB Rohrlach, J Krause, P Onkamo, ...
European Journal of Archaeology 25 (1), 42-60, 2022
332022
Genome-wide linkage analysis of human auditory cortical activation suggests distinct loci on chromosomes 2, 3, and 8
H Renvall, E Salmela, M Vihla, M Illman, E Leinonen, J Kere, R Salmelin
Journal of Neuroscience 32 (42), 14511-14518, 2012
282012
Estimating genealogies from unlinked marker data: a Bayesian approach
D Gasbarra, M Pirinen, MJ Sillanpää, E Salmela, E Arjas
Theoretical population biology 72 (3), 305-322, 2007
262007
Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers
ML Cox, JM Evans, AG Davis, LT Guo, JR Levy, AN Starr-Moss, ...
Skeletal muscle 7 (1), 1-10, 2017
222017
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