Search details
1.
FinnGen provides genetic insights from a well-phenotyped isolated population.
Nature
; 613(7944): 508-518, 2023 01.
Article
in English
| MEDLINE | ID: mdl-36653562
2.
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.
Nature
; 615(7952): E19, 2023 Mar.
Article
in English
| MEDLINE | ID: mdl-36829046
3.
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.
Cephalalgia
; 42(7): 631-644, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35166138
4.
PSEUDOMARKER 2.0: efficient computation of likelihoods using NOMAD.
BMC Bioinformatics
; 15: 47, 2014 Feb 17.
Article
in English
| MEDLINE | ID: mdl-24533837
5.
The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies.
BMC Endocr Disord
; 14: 9, 2014 Feb 01.
Article
in English
| MEDLINE | ID: mdl-24484869
6.
Identifying flavor preference subgroups. Genetic basis and related eating behavior traits.
Appetite
; 75: 1-10, 2014 Apr.
Article
in English
| MEDLINE | ID: mdl-24361469
7.
On the validity of the likelihood ratio test and consistency of resulting parameter estimates in joint linkage and linkage disequilibrium analysis under improperly specified parametric models.
Ann Hum Genet
; 76(1): 63-73, 2012 Jan.
Article
in English
| MEDLINE | ID: mdl-22082140
8.
Life is a simulation of life - or is it?: What we observe is just one run of a probabilistic process.
Evol Anthropol
; 26(4): 151-156, 2017 Jul.
Article
in English
| MEDLINE | ID: mdl-28815960
9.
PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals.
Hum Hered
; 71(4): 256-66, 2011.
Article
in English
| MEDLINE | ID: mdl-21811076
10.
Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen.
BMJ Open
; 12(10): e064695, 2022 10 05.
Article
in English
| MEDLINE | ID: mdl-36198465
11.
Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci.
PLoS Genet
; 3(6): e97, 2007 Jun.
Article
in English
| MEDLINE | ID: mdl-17559308
12.
An epigenome-wide association study of metabolic syndrome and its components.
Sci Rep
; 10(1): 20567, 2020 11 25.
Article
in English
| MEDLINE | ID: mdl-33239708
13.
Linkage analysis of schizophrenia controlling for population substructure.
Am J Med Genet B Neuropsychiatr Genet
; 150B(6): 827-35, 2009 Sep 05.
Article
in English
| MEDLINE | ID: mdl-19086037
14.
A bias-ed assessment of the use of SNPs in human complex traits.
Curr Opin Genet Dev
; 12(6): 726-34, 2002 Dec.
Article
in English
| MEDLINE | ID: mdl-12433588
15.
Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry).
Int J Epidemiol
; 52(4): e195-e200, 2023 08 02.
Article
in English
| MEDLINE | ID: mdl-37365732
16.
Genetic component of identification, intensity and pleasantness of odours: a Finnish family study.
Eur J Hum Genet
; 15(5): 596-602, 2007 May.
Article
in English
| MEDLINE | ID: mdl-17342154
17.
An utter refutation of the "fundamental theorem of the HapMap".
Eur J Hum Genet
; 14(4): 426-37, 2006 Apr.
Article
in English
| MEDLINE | ID: mdl-16479260
18.
A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate.
Sci Rep
; 6: 39345, 2016 12 20.
Article
in English
| MEDLINE | ID: mdl-27996024
19.
AMIGO-Kv2.1 Potassium Channel Complex Is Associated With Schizophrenia-Related Phenotypes.
Schizophr Bull
; 42(1): 191-201, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-26240432
20.
AUTOGSCAN: powerful tools for automated genome-wide linkage and linkage disequilibrium analysis.
Twin Res Hum Genet
; 8(1): 16-21, 2005 Feb.
Article
in English
| MEDLINE | ID: mdl-15836805