Institution
Netherlands Forensic Institute
Facility•The Hague, Netherlands•
About: Netherlands Forensic Institute is a facility organization based out in The Hague, Netherlands. It is known for research contribution in the topics: Poison control & Population. The organization has 508 authors who have published 889 publications receiving 19817 citations.
Topics: Poison control, Population, Child abuse, Crime scene, DNA profiling
Papers published on a yearly basis
Papers
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TL;DR: In this article, the authors study the properties of a three-step approach to estimating the parameters of a latent structure model for categorical data and propose a simple correction for a common source of bias.
Abstract: We study the properties of a three-step approach to estimating the parameters of a latent structure model for categorical data and propose a simple correction for a common source of bias. Such models have a measurement part (essentially the latent class model) and a structural (causal) part (essentially a system of logit equations). In the three-step approach, a stand-alone measurement model is first defined and its parameters are estimated. Individual predicted scores on the latent variables are then computed from the parameter estimates of the measurement model and the individual observed scoring patterns on the indicators. Finally, these predicted scores are used in the causal part and treated as observed variables. We show that such a naive use of predicted latent scores cannot be recommended since it leads to a systematic underestimation of the strength of the association among the variables in the structural part of the models. However, a simple correction procedure can eliminate this systematic bias. This approach is illustrated on simulated and real data. A method that uses multiple imputation to account for the fact that the predicted latent variables are random variables can produce standard errors for the parameters in the structural part of the model.
683 citations
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25 Sep 2020
TL;DR: In patients with lethal CO VID-19, an extensive systemic inflammatory response was present, with a continued presence of neutrophils and NETs, which suggests a maladaptive immune response and substantiates the evidence for immunomodulation as a target in the treatment of severe COVID-19.
Abstract: Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) targets multiple organs and causes severe coagulopathy. Histopathological organ changes might not only be attributable to a direct virus-induced effect, but also the immune response. The aims of this study were to assess the duration of viral presence, identify the extent of inflammatory response, and investigate the underlying cause of coagulopathy. Methods: This prospective autopsy cohort study was done at Amsterdam University Medical Centers (UMC), the Netherlands. With informed consent from relatives, full body autopsy was done on 21 patients with COVID-19 for whom autopsy was requested between March 9 and May 18, 2020. In addition to histopathological evaluation of organ damage, the presence of SARS-CoV-2 nucleocapsid protein and the composition of the immune infiltrate and thrombi were assessed, and all were linked to disease course. Findings: Our cohort (n=21) included 16 (76%) men, and median age was 68 years (range 41-78). Median disease course (time from onset of symptoms to death) was 22 days (range 5-44 days). In 11 patients tested for SARS-CoV-2 tropism, SARS-CoV-2 infected cells were present in multiple organs, most abundantly in the lungs, but presence in the lungs became sporadic with increased disease course. Other SARS-CoV-2-positive organs included the upper respiratory tract, heart, kidneys, and gastrointestinal tract. In histological analyses of organs (sampled from nine to 21 patients per organ), an extensive inflammatory response was present in the lungs, heart, liver, kidneys, and brain. In the brain, extensive inflammation was seen in the olfactory bulbs and medulla oblongata. Thrombi and neutrophilic plugs were present in the lungs, heart, kidneys, liver, spleen, and brain and were most frequently observed late in the disease course (15 patients with thrombi, median disease course 22 days [5-44]; ten patients with neutrophilic plugs, 21 days [5-44]). Neutrophilic plugs were observed in two forms: solely composed of neutrophils with neutrophil extracellular traps (NETs), or as aggregates of NETs and platelets.. Interpretation: In patients with lethal COVID-19, an extensive systemic inflammatory response was present, with a continued presence of neutrophils and NETs. However, SARS-CoV-2-infected cells were only sporadically present at late stages of COVID-19. This suggests a maladaptive immune response and substantiates the evidence for immunomodulation as a target in the treatment of severe COVID-19. Funding: Amsterdam UMC Corona Research Fund.
385 citations
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Erasmus University Medical Center1, Life Technologies2, University of Cologne3, Netherlands Forensic Institute4, Katholieke Universiteit Leuven5, American Board of Legal Medicine6, Leiden University Medical Center7, Université de Montréal8, Université du Québec à Chicoutimi9, Charité10, Leipzig University11, Wrocław Medical University12
TL;DR: The 13 most mutable Y-STRs are analyzed in an independent sample set and empirically proved their suitability for distinguishing close and distantly related males, expected to revolutionize Y-chromosomal applications in forensic biology.
Abstract: Nonrecombining Y-chromosomal microsatellites (Y-STRs) are widely used to infer population histories, discover genealogical relationships, and identify males for criminal justice purposes. Although a key requirement for their application is reliable mutability knowledge, empirical data are only available for a small number of Y-STRs thus far. To rectify this, we analyzed a large number of 186 Y-STR markers in nearly 2000 DNA-confirmed father-son pairs, covering an overall number of 352,999 meiotic transfers. Following confirmation by DNA sequence analysis, the retrieved mutation data were modeled via a Bayesian approach, resulting in mutation rates from 3.78 × 10−4 (95% credible interval [CI], 1.38 × 10−5 − 2.02 × 10−3) to 7.44 × 10−2 (95% CI, 6.51 × 10−2 − 9.09 × 10−2) per marker per generation. With the 924 mutations at 120 Y-STR markers, a nonsignificant excess of repeat losses versus gains (1.16:1), as well as a strong and significant excess of single-repeat versus multirepeat changes (25.23:1), was observed. Although the total repeat number influenced Y-STR locus mutability most strongly, repeat complexity, the length in base pairs of the repeated motif, and the father's age also contributed to Y-STR mutability. To exemplify how to practically utilize this knowledge, we analyzed the 13 most mutable Y-STRs in an independent sample set and empirically proved their suitability for distinguishing close and distantly related males. This finding is expected to revolutionize Y-chromosomal applications in forensic biology, from previous male lineage differentiation toward future male individual identification.
366 citations
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TL;DR: In this paper, the authors show which forces play a role in impact and spreading, and obtain an expression relating impact velocity to droplet volume and maximum diameter of the resulting pattern, which offers important insight for the analysis of bloodstains in forensic science.
Abstract: The impact velocity of a liquid droplet can be deduced from its spatter pattern, but there has been controversy concerning details of how droplets respond after impact. The authors show which forces play a role in impact and spreading, and obtain an expression relating impact velocity to droplet volume and maximum diameter of the resulting pattern. This offers important insight for the analysis of bloodstains in forensic science, as well as for inkjet printing and other applications.
270 citations
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TL;DR: It is suggested that genetic variants regulating expression of the OCA2 gene exist in the HERC2 gene or, alternatively, within the 11.7 kb of sequence between OCA1 and HERC1, and that most iris color variation in Europeans is explained by those two genes.
Abstract: Human iris color was one of the first traits for which Mendelian segregation was established. To date, the genetics of iris color is still not fully understood and is of interest, particularly in view of forensic applications. In three independent genome-wide association (GWA) studies of a total of 1406 persons and a genome-wide linkage study of 1292 relatives, all from the Netherlands, we found that the 15q13.1 region is the predominant region involved in human iris color. There were no other regions showing consistent genome-wide evidence for association and linkage to iris color. Single nucleotide polymorphisms (SNPs) in the HERC2 gene and, to a lesser extent, in the neighboring OCA2 gene were independently associated to iris color variation. OCA2 has been implicated in iris color previously. A replication study within two populations confirmed that the HERC2 gene is a new and significant determinant of human iris color variation, in addition to OCA2. Furthermore, HERC2 rs916977 showed a clinal allele distribution across 23 European populations, which was significantly correlated to iris color variation. We suggest that genetic variants regulating expression of the OCA2 gene exist in the HERC2 gene or, alternatively, within the 11.7 kb of sequence between OCA2 and HERC2, and that most iris color variation in Europeans is explained by those two genes. Testing markers in the HERC2-OCA2 region may be useful in forensic applications to predict eye color phenotypes of unknown persons of European genetic origin.
253 citations
Authors
Showing all 510 results
Name | H-index | Papers | Citations |
---|---|---|---|
Titia Sijen | 41 | 113 | 8726 |
Oscar Lao | 40 | 81 | 7001 |
Rick R. van Rijn | 30 | 179 | 3064 |
Reinoud D. Stoel | 25 | 65 | 2033 |
Arnout C.C. Ruifrok | 23 | 49 | 4162 |
Ate D. Kloosterman | 22 | 49 | 1571 |
Robert C. Janaway | 22 | 46 | 1277 |
R.R. van Rijn | 21 | 63 | 1454 |
Cor J. Veenman | 20 | 60 | 3698 |
Charles E.H. Berger | 19 | 67 | 1353 |
Kristiaan J. van der Gaag | 19 | 29 | 1460 |
Eric Lock | 18 | 20 | 846 |
Hinda Haned | 17 | 43 | 1123 |
Marjan Sjerps | 17 | 57 | 870 |
Silke Brauer | 17 | 22 | 2531 |