Detalhe da pesquisa
1.
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Lancet Oncol
; 24(1): 91-106, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36436516
2.
Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility.
J Headache Pain
; 24(1): 78, 2023 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37380951
3.
Forensic genetics and genomics: Much more than just a human affair.
PLoS Genet
; 13(9): e1006960, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28934201
4.
Relationship between the Presence of the ApoE ε4 Allele and EEG Complexity along the Alzheimer's Disease Continuum.
Sensors (Basel)
; 20(14)2020 Jul 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32664228
5.
EEG Characterization of the Alzheimer's Disease Continuum by Means of Multiscale Entropies.
Entropy (Basel)
; 21(6)2019 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33267258
6.
Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease.
Brief Funct Genomics
; 23(2): 138-149, 2024 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37254524
7.
Microsatellites' mutation modeling through the analysis of the Y-chromosomal transmission: Results of a GHEP-ISFG collaborative study.
Forensic Sci Int Genet
; 69: 102999, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38181588
8.
The sequence of the repetitive motif influences the frequency of multistep mutations in Short Tandem Repeats.
Sci Rep
; 13(1): 10251, 2023 06 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37355683
9.
Comparative evaluation of alternative batteries of genetic markers to complement autosomal STRs in kinship investigations: autosomal indels vs. X-chromosome STRs.
Int J Legal Med
; 126(6): 917-21, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22940765
10.
Identification of species by multiplex analysis of variable-length sequences.
Nucleic Acids Res
; 38(22): e203, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20923781
11.
Estimations of Mutation Rates Depend on Population Allele Frequency Distribution: The Case of Autosomal Microsatellites.
Genes (Basel)
; 13(7)2022 07 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35886031
12.
Quantification of forensic genetic evidence: Comparison of results obtained by qualitative and quantitative software for real casework samples.
Forensic Sci Int Genet
; 59: 102715, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35490558
13.
A High Methylation Level of a Novel -284 bp CpG Island in the RAMP1 Gene Promoter Is Potentially Associated with Migraine in Women.
Brain Sci
; 12(5)2022 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35624913
14.
General derivation of the sets of pedigrees with the same kinship coefficients.
Hum Hered
; 70(3): 194-204, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20720433
15.
4SpecID: Reference DNA Libraries Auditing and Annotation System for Forensic Applications.
Genes (Basel)
; 12(1)2021 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33401773
16.
Influence of PICALM and CLU risk variants on beta EEG activity in Alzheimer's disease patients.
Sci Rep
; 11(1): 20465, 2021 10 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34650147
17.
Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG Endophenotypes.
J Alzheimers Dis
; 80(1): 209-223, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33522999
18.
Twenty Years Later: A Comprehensive Review of the X Chromosome Use in Forensic Genetics.
Front Genet
; 11: 926, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33093840
19.
APOE Variants in an Iberian Alzheimer Cohort Detected through an Optimized Sanger Sequencing Protocol.
Genes (Basel)
; 12(1)2020 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33375167
20.
Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band.
Brain Sci
; 10(11)2020 Nov 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33218114