Detalhe da pesquisa
1.
FinnGen provides genetic insights from a well-phenotyped isolated population.
Nature
; 613(7944): 508-518, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36653562
2.
Influence of clinical and genetic factors on propofol dose requirements: A genome-wide association study.
Anesthesiology
; 2024 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38700459
3.
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.
Nature
; 615(7952): E19, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36829046
4.
Clinical and genetic factors associated with post-operative nausea and vomiting after propofol anaesthesia.
Acta Anaesthesiol Scand
; 67(8): 1018-1027, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37156489
5.
Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder.
Pharmacogenomics J
; 22(3): 166-172, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35197553
6.
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.
Cephalalgia
; 42(7): 631-644, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35166138
7.
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families.
Cephalalgia
; 42(4-5): 345-356, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34648375
8.
A Randomized, Sham-Controlled Trial of Repetitive Transcranial Magnetic Stimulation Targeting M1 and S2 in Central Poststroke Pain: A Pilot Trial.
Neuromodulation
; 25(4): 538-548, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35670063
9.
Genetic Risk Score for Serum 25-Hydroxyvitamin D Concentration Helps to Guide Personalized Vitamin D Supplementation in Healthy Finnish Adults.
J Nutr
; 151(2): 281-292, 2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33382404
10.
First genome-wide association study on rocuronium dose requirements shows association with SLCO1A2.
Br J Anaesth
; 126(5): 949-957, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33676726
11.
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.
Cephalalgia
; 38(12): 1849-1863, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29486580
12.
Genetics and genomics in postoperative pain and analgesia.
Curr Opin Anaesthesiol
; 31(5): 569-574, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29994939
13.
Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock.
Crit Care
; 21(1): 47, 2017 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28270177
14.
High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms.
PLoS Genet
; 10(1): e1004134, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24497844
15.
Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.
Cephalalgia
; 36(7): 604-14, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25633374
16.
No Association between Genetic Loci near IRF2 and TBX1 and Acute Kidney Injury in the Critically Ill.
Am J Respir Crit Care Med
; 201(1): 109-111, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31487200
17.
Genetic predisposition to acute kidney injury--a systematic review.
BMC Nephrol
; 16: 197, 2015 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26627480
18.
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
Ann Neurol
; 73(1): 16-31, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23381943
19.
Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer.
Anesthesiology
; 119(6): 1422-33, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24343288
20.
Pain in 1,000 women treated for breast cancer: a prospective study of pain sensitivity and postoperative pain.
Anesthesiology
; 119(6): 1410-21, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24343286