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Mari Niemi
Mari Niemi
Novartis Institutes for BioMedical Research
Verified email at novartis.com
Title
Cited by
Cited by
Year
FinnGen provides genetic insights from a well-phenotyped isolated population
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ...
Nature 613 (7944), 508-518, 2023
7482023
Mapping the human genetic architecture of COVID-19
MEK Niemi, J Karjalainen, RG Liao, BM Neale, M Daly, A Ganna, ...
Nature 600 (7889), 472-477, 2021
715*2021
COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets
TM Delorey, CGK Ziegler, G Heimberg, R Normand, Y Yang, ...
Nature, 1-32, 2021
5952021
FinnGen: Unique genetic insights from combining isolated population and national health register data
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ...
medRxiv, 2022
3492022
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
MEK Niemi, HC Martin, DL Rice, G Gallone, S Gordon, M Kelemen, ...
Nature 562 (7726), 268-271, 2018
2972018
Quantifying the contribution of recessive coding variation to developmental disorders
HC Martin, WD Jones, R McIntyre, G Sanchez-Andrade, M Sanderson, ...
Science 362 (6419), 1161-1164, 2018
1682018
Cognitive impairment and health-related quality of life following traumatic brain injury
N Gorgoraptis, J Zaw-Linn, C Feeney, C Tenorio-Jimenez, M Niemi, ...
NeuroRehabilitation 44 (3), 321-331, 2019
1092019
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
T Nakanishi, S Pigazzini, F Degenhardt, M Cordioli, G Butler-Laporte, ...
MedRxiv, 2021
1022021
The human genetic epidemiology of COVID-19
MEK Niemi, MJ Daly, A Ganna
Nature Reviews Genetics 23 (9), 533-546, 2022
972022
Mapping the human genetic architecture of COVID-19 by worldwide meta-analysis
COVID-19 Host Genetics Initiative
MedRxiv, 2021
69*2021
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
F Degenhardt, D Ellinghaus, S Juzenas, J Lerga-Jaso, M Wendorff, ...
Human molecular genetics 31 (23), 3945-3966, 2022
552022
Prevalence and correlates of vitamin D deficiency in adults after traumatic brain injury
OA Jamall, C Feeney, J Zaw‐Linn, A Malik, MEK Niemi, ...
Clinical endocrinology 85 (4), 636-644, 2016
432016
Reduced reproductive success is associated with selective constraint on human genes
EJ Gardner, MDC Neville, KE Samocha, K Barclay, M Kolk, MEK Niemi, ...
Nature, 1-6, 2022
402022
The contribution of X-linked coding variation to severe developmental disorders
HC Martin, EJ Gardner, KE Samocha, J Kaplanis, N Akawi, A Sifrim, ...
Nature communications 12 (1), 1-13, 2021
392021
A single-cell and spatial atlas of autopsy tissues reveals pathology and cellular targets of SARS-CoV-2
TM Delorey, CGK Ziegler, G Heimberg, R Normand, Y Yang, ...
bioRxiv, 2021
392021
New susceptibility loci for severe COVID-19 by detailed GWAS analysis in European populations
F Degenhardt, D Ellinghaus, S Juzenas, J Lerga-Jaso, M Wendorff, ...
medRxiv, 2021
142021
Genetic determinants of mannose-binding lectin activity predispose to thromboembolic complications in critical COVID-19
M Hultström, R Frithiof, J Grip, L Lindelöf, O Rooijackers, S Pigazzini, ...
Nature Immunology 23 (6), 861-864, 2022
82022
Sex-biased reduction in reproductive success drives selective constraint on human genes
EJ Gardner, MDC Neville, KE Samocha, K Barclay, M Kolk, MEK Niemi, ...
bioRxiv, 2020
62020
Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen
RS Rodosthenous, MEK Niemi, L Kallio, M Perala, P Terho, T Knopp, ...
BMJ open 12 (10), e064695, 2022
32022
Autosomal recessive coding variants explain only a small proportion of undiagnosed developmental disorders in the British Isles
HC Martin, WD Jones, J Stephenson, J Handsaker, G Gallone, JF McRae, ...
bioRxiv, 201533, 2017
22017
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