Detalhe da pesquisa
1.
Rare coding variants in ten genes confer substantial risk for schizophrenia.
Nature
; 604(7906): 509-516, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396579
2.
Accounting for age of onset and family history improves power in genome-wide association studies.
Am J Hum Genet
; 109(3): 417-432, 2022 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35139346
3.
Genome-Wide Association study of susceptibility to respiratory syncytial virus hospitalization in young children < 5 years of age.
J Infect Dis
; 2023 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37666001
4.
Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study.
Psychol Med
; 53(1): 217-226, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33949298
5.
DNA-methylation and immunological response in medication overuse headache.
Cephalalgia
; 43(3): 3331024221147482, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36786322
6.
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes.
Brain
; 145(2): 555-568, 2022 04 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35022648
7.
Methylation microarray-based detection of clinical copy-number aberrations in CLL benchmarked to standard FISH analysis.
Genomics
; 114(6): 110510, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36272495
8.
Genome-wide study of early and severe childhood asthma identifies interaction between CDHR3 and GSDMB.
J Allergy Clin Immunol
; 150(3): 622-630, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35381269
9.
The Duffy-null genotype and risk of infection.
Hum Mol Genet
; 29(20): 3341-3349, 2020 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32959868
10.
IGHV-associated methylation signatures more accurately predict clinical outcomes of chronic lymphocytic leukemia patients than IGHV mutation load.
Haematologica
; 107(4): 877-886, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34092057
11.
A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions.
Behav Brain Funct
; 18(1): 14, 2022 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36457050
12.
Increased transmission of SARS-CoV-2 in Denmark during UEFA European championships.
Epidemiol Infect
; 150: e123, 2022 03 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35317884
13.
Molecular epidemiology of the SARS-CoV-2 variant Omicron BA.2 sub-lineage in Denmark, 29 November 2021 to 2 January 2022.
Euro Surveill
; 27(10)2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35272746
14.
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.
Hum Mol Genet
; 28(2): 332-340, 2019 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30281099
15.
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.
Am J Hum Genet
; 102(6): 1204-1211, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29861106
16.
Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.
Mol Psychiatry
; 25(10): 2410-2421, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30116032
17.
A major role for common genetic variation in anxiety disorders.
Mol Psychiatry
; 25(12): 3292-3303, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31748690
18.
Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.
Childs Nerv Syst
; 37(3): 819-830, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33226468
19.
Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021.
Euro Surveill
; 26(50)2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34915977
20.
Idiopathic early ovarian aging: is there a relation with premenopausal accelerated biological aging in young women with diminished response to ART?
J Assist Reprod Genet
; 38(11): 3027-3038, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34599460