Detalhe da pesquisa
1.
Spitting in the wind?-The challenges of RNA sequencing for biomarker discovery from saliva.
Int J Legal Med
; 138(2): 401-412, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37847308
2.
Targeted S5 RNA sequencing assay for the identification and direct association of common body fluids with DNA donors in mixtures.
Int J Legal Med
; 137(1): 13-32, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36333511
3.
Analytical description of adolescent binge drinking patients.
BMC Pediatr
; 23(1): 512, 2023 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37845619
4.
Genetic variants in eleven central and peripheral chemoreceptor genes in sudden infant death syndrome.
Pediatr Res
; 92(4): 1026-1033, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35102300
5.
Re-evaluation of single nucleotide variants and identification of structural variants in a cohort of 45 sudden unexplained death cases.
Int J Legal Med
; 135(4): 1341-1349, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33895855
6.
Functional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death.
Int J Legal Med
; 133(6): 1733-1742, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31455979
7.
Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes.
Int J Legal Med
; 132(4): 1057-1065, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29350269
8.
2,000 Year old ß-thalassemia case in Sardinia suggests malaria was endemic by the Roman period.
Am J Phys Anthropol
; 164(2): 362-370, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28681914
9.
Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.
Int J Legal Med
; 130(4): 1011-1021, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26846766
10.
Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.
Mol Cell Probes
; 29(1): 31-4, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25449952
11.
Toward male individualization with rapidly mutating y-chromosomal short tandem repeats.
Hum Mutat
; 35(8): 1021-32, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24917567
12.
Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS).
Pediatr Res
; 76(1): 41-5, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24727946
13.
Sodium/proton exchanger 3 (NHE3) and sudden infant death syndrome (SIDS).
Int J Legal Med
; 128(6): 939-43, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24590378
14.
Selecting mRNA markers in blood for age estimation of the donor of a biological stain.
Forensic Sci Int Genet
; 68: 102976, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38000161
15.
mRNA profiling using a minimum of five mRNA markers per body fluid and a novel scoring method for body fluid identification.
Int J Legal Med
; 127(4): 707-21, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23254458
16.
Exome analysis focusing on epilepsy-related genes in children and adults with sudden unexplained death.
Seizure
; 113: 66-75, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37995443
17.
Quantitative PCR analysis of bloodstains of different ages.
Forensic Sci Int
; 350: 111785, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37527614
18.
Body Fluid Identification in Samples Collected after Intimate and Social Contact: A Comparison of Two mRNA Profiling Methods and the Additional Information Gained by cSNP Genotypes.
Genes (Basel)
; 14(3)2023 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36980908
19.
Comparative evaluation of the MAPlex, Precision ID Ancestry Panel, and VISAGE Basic Tool for biogeographical ancestry inference.
Forensic Sci Int Genet
; 64: 102850, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36924679
20.
19th century family saga re-told by DNA recovered from postcard stamps.
Forensic Sci Int
; 330: 111129, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34883299