Detalhe da pesquisa
1.
Genetic insights into biological mechanisms governing human ovarian ageing.
Nature
; 596(7872): 393-397, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34349265
2.
Correction: Obesity and risk of female reproductive conditions: A Mendelian randomisation study.
PLoS Med
; 19(9): e1004095, 2022 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-36054878
3.
Obesity and risk of female reproductive conditions: A Mendelian randomisation study.
PLoS Med
; 19(2): e1003679, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35104295
4.
Genetic insight into sick sinus syndrome.
Eur Heart J
; 42(20): 1959-1971, 2021 05 21.
Artigo
Inglês
| MEDLINE | ID: mdl-36282123
5.
Genetic insight into sick sinus syndrome.
Eur Heart J
; 42(20): 1959-1971, 2021 05 21.
Artigo
Inglês
| MEDLINE | ID: mdl-33580673
6.
Sequence variants associating with urinary biomarkers.
Hum Mol Genet
; 28(7): 1199-1211, 2019 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30476138
7.
Profile of common prostate cancer risk variants in an unscreened Romanian population.
J Cell Mol Med
; 22(3): 1574-1582, 2018 03.
Artigo
Inglês
| MEDLINE | ID: mdl-29266682
8.
Identification of Lynch syndrome risk variants in the Romanian population.
J Cell Mol Med
; 22(12): 6068-6076, 2018 12.
Artigo
Inglês
| MEDLINE | ID: mdl-30324682
9.
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA.
BMC Med Genet
; 18(1): 129, 2017 11 14.
Artigo
Inglês
| MEDLINE | ID: mdl-29137621
10.
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters.
BMC Med Genet
; 18(1): 103, 2017 10 02.
Artigo
Inglês
| MEDLINE | ID: mdl-28965491
11.
Studying the genetics of participation using footprints left on the ascertained genotypes.
Nat Genet
; 55(8): 1413-1420, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37443256
12.
Mendelian imputation of parental genotypes improves estimates of direct genetic effects.
Nat Genet
; 54(6): 897-905, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35681053
13.
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.
Commun Biol
; 4(1): 706, 2021 06 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34108613
14.
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis.
Nat Commun
; 11(1): 393, 2020 01 20.
Artigo
Inglês
| MEDLINE | ID: mdl-31959851
15.
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.
Commun Biol
; 3(1): 189, 2020 04 23.
Artigo
Inglês
| MEDLINE | ID: mdl-32327693
16.
Deconstructing the sources of genotype-phenotype associations in humans.
Science
; 365(6460): 1396-1400, 2019 09 27.
Artigo
Inglês
| MEDLINE | ID: mdl-31604265
17.
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.
Nat Commun
; 10(1): 1284, 2019 03 20.
Artigo
Inglês
| MEDLINE | ID: mdl-30894546
18.
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy.
Nat Commun
; 10(1): 1777, 2019 04 16.
Artigo
Inglês
| MEDLINE | ID: mdl-30992453
19.
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis.
Nat Genet
; 51(2): 267-276, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30643255
20.
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.
Nat Commun
; 10(1): 2358, 2019 May 24.
Artigo
Inglês
| MEDLINE | ID: mdl-31127096