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.
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer.
Hum Mol Genet
; 32(12): 2103-2116, 2023 06 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36929174
3.
Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5.
Gastroenterology
; 165(4): 861-873, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37453564
4.
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
5.
Primary age-related tauopathy in a Finnish population-based study of the oldest old (Vantaa 85+).
Neuropathol Appl Neurobiol
; 48(3): e12788, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34927275
6.
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples.
PLoS Comput Biol
; 17(12): e1009684, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34928946
7.
Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health.
Eur Respir J
; 57(5)2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33243845
8.
De novo mutations in schizophrenia implicate synaptic networks.
Nature
; 506(7487): 179-84, 2014 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-24463507
9.
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.
Proc Natl Acad Sci U S A
; 114(3): E327-E336, 2017 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28031487
10.
Creating basis for introducing non-invasive prenatal testing in the Estonian public health setting.
Prenat Diagn
; 39(13): 1262-1268, 2019 12.
Artigo
em Alemão
| MEDLINE | ID: mdl-31691324
11.
Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study.
Cephalalgia
; 38(2): 312-322, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28103696
12.
Distribution and medical impact of loss-of-function variants in the Finnish founder population.
PLoS Genet
; 10(7): e1004494, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25078778
13.
Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regions.
Blood
; 122(25): e52-60, 2013 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-24159175
14.
Structural genomic variation as risk factor for idiopathic recurrent miscarriage.
Hum Mutat
; 35(8): 972-82, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24827138
15.
A molecular tool for menstrual cycle phase dating of endometrial samples in endometriosis transcriptome studies.
Biol Reprod
; 101(1): 1-3, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31004479
16.
A molecular tool for menstrual cycle phase dating of endometrial samples in endometriosis transcriptome studies.
Biol Reprod
; 101(4): 868, 2019 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31687746
17.
Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes.
Nat Genet
; 56(3): 377-382, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38182742
18.
Targeted gene expression profiling for accurate endometrial receptivity testing.
Sci Rep
; 13(1): 13959, 2023 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37633957
19.
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.
Nat Commun
; 14(1): 157, 2023 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36653343
20.
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration.
JAMA Ophthalmol
; 141(5): 449-457, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37079300