Detalhe da pesquisa
1.
Noninvasive prenatal diagnosis of Mendelian disorders for consanguineous couples by relative genotype dosage.
Clin Genet
; 104(5): 505-515, 2023 11.
Artigo
Inglês
| MEDLINE | ID: mdl-37434539
2.
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.
Clin Genet
; 100(4): 412-429, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34216016
3.
Genetic immune and inflammatory markers associated with diabetes in solid organ transplant recipients.
Am J Transplant
; 19(1): 238-246, 2019 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29920932
4.
Genetic and clinic predictors of new onset diabetes mellitus after transplantation.
Pharmacogenomics J
; 19(1): 53-64, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29282365
5.
Association of genetic risk scores with body mass index in Swiss psychiatric cohorts.
Pharmacogenet Genomics
; 26(5): 208-17, 2016 May.
Artigo
Inglês
| MEDLINE | ID: mdl-26918956
6.
Prediction of early weight gain during psychotropic treatment using a combinatorial model with clinical and genetic markers.
Pharmacogenet Genomics
; 26(12): 547-557, 2016 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-27741037
7.
Impact of HSD11B1 polymorphisms on BMI and components of the metabolic syndrome in patients receiving psychotropic treatments.
Pharmacogenet Genomics
; 25(5): 246-58, 2015 May.
Artigo
Inglês
| MEDLINE | ID: mdl-25751397
8.
Association of PCK1 with Body Mass Index and Other Metabolic Features in Patients With Psychotropic Treatments.
J Clin Psychopharmacol
; 35(5): 544-52, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26280835
9.
Substitution of arginine 219 by glycine compromises stability, dimerization, and catalytic activity in a G6PD mutant.
Commun Biol
; 6(1): 1245, 2023 12 09.
Artigo
Inglês
| MEDLINE | ID: mdl-38066190
10.
Genetic determinants of response to clopidogrel and cardiovascular events.
N Engl J Med
; 360(4): 363-75, 2009 Jan 22.
Artigo
Inglês
| MEDLINE | ID: mdl-19106083
11.
Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss.
Genes (Basel)
; 12(8)2021 08 20.
Artigo
Inglês
| MEDLINE | ID: mdl-34440452
12.
Pharmacogenetics in immunosuppressants: impact on dose requirement of calcineurin inhibitors in renal and liver pediatric transplant recipients.
Curr Opin Organ Transplant
; 15(5): 601-7, 2010 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-20720493
13.
Association of variants in SH2B1 and RABEP1 with worsening of low-density lipoprotein and glucose parameters in patients treated with psychotropic drugs.
Gene
; 628: 8-15, 2017 Sep 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28694205
14.
Association of CRTC1 polymorphisms with obesity markers in subjects from the general population with lifetime depression.
J Affect Disord
; 198: 43-9, 2016 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27002284
15.
Weighted Genetic Risk Scores and Prediction of Weight Gain in Solid Organ Transplant Populations.
PLoS One
; 11(10): e0164443, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27788139
16.
Influence of MCHR2 and MCHR2-AS1 Genetic Polymorphisms on Body Mass Index in Psychiatric Patients and In Population-Based Subjects with Present or Past Atypical Depression.
PLoS One
; 10(10): e0139155, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26461262
17.
Influence of CRTC1 polymorphisms on body mass index and fat mass in psychiatric patients and the general adult population.
JAMA Psychiatry
; 70(10): 1011-9, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23925723
18.
Vitamin K epoxide reductase (VKORC1) genetic polymorphism is associated to oral anticoagulant overdose.
Thromb Haemost
; 94(3): 690-1, 2005 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-16268497
19.
SLCO1B1 genetic polymorphism influences mycophenolic acid tolerance in renal transplant recipients.
Pharmacogenomics
; 11(12): 1703-13, 2010 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-21142914
20.
Impact of VKORC1 haplotypes on long-term graft function in kidney transplantation.
Transplantation
; 86(6): 779-83, 2008 Sep 27.
Artigo
Inglês
| MEDLINE | ID: mdl-18813101