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  1. Article ; Online: The social and winding road between inflammation and PTSD.

    Ursini, Gianluca / Punzi, Giovanna

    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

    2021  Volume 46, Issue 6, Page(s) 1064–1065

    MeSH term(s) Humans ; Inflammation ; Social Support ; Stress Disorders, Post-Traumatic
    Language English
    Publishing date 2021-02-18
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 639471-1
    ISSN 1740-634X ; 0893-133X
    ISSN (online) 1740-634X
    ISSN 0893-133X
    DOI 10.1038/s41386-021-00979-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Genetics Awakens the Complex Relationship Between Sleep and Psychiatric Disorders.

    Ursini, Gianluca / Punzi, Giovanna

    Biological psychiatry

    2021  Volume 90, Issue 9, Page(s) 588–589

    MeSH term(s) Humans ; Mental Disorders/genetics ; Sleep
    Language English
    Publishing date 2021-10-07
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 209434-4
    ISSN 1873-2402 ; 0006-3223
    ISSN (online) 1873-2402
    ISSN 0006-3223
    DOI 10.1016/j.biopsych.2021.08.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book ; Online: A FPGA-based architecture for real-time cluster finding in the LHCb silicon pixel detector

    Bassi, G. / Giambastiani, L. / Hennessy, K. / Lazzari, F. / Morello, M. J. / Pajero, T. / Prieto, A. Fernandez / Punzi, G.

    2023  

    Abstract: This article describes a custom VHDL firmware implementation of a two-dimensional cluster-finder architecture for reconstructing hit positions in the new vertex pixel detector (VELO) that is part of the LHCb Upgrade. This firmware has been deployed to ... ...

    Abstract This article describes a custom VHDL firmware implementation of a two-dimensional cluster-finder architecture for reconstructing hit positions in the new vertex pixel detector (VELO) that is part of the LHCb Upgrade. This firmware has been deployed to the existing FPGA cards that perform the readout of the VELO, as a further enhancement of the DAQ system, and will run in real time during physics data taking, reconstructing VELO hits coordinates on-the-fly at the LHC collision rate. This pre-processing allows the first level of the software trigger to accept a 11% higher rate of events, as the ready-made hits coordinates accelerate the track reconstruction and consumes significantly less electrical power. It additionally allows the raw pixel data to be dropped at the readout level, thus saving approximately 14% of the DAQ bandwidth. Detailed simulation studies have shown that the use of this real-time cluster finding does not introduce any appreciable degradation in the tracking performance in comparison to a full-fledged software implementation. This work is part of a wider effort aimed at boosting the real-time processing capability of HEP experiments by delegating intensive tasks to dedicated computing accelerators deployed at the earliest stages of the data acquisition chain.

    Comment: 13 pages, 22 figures. This work has been published on IEEE Transactions on Nuclear Science under a Creative Commons License
    Keywords Physics - Instrumentation and Detectors ; Computer Science - Hardware Architecture ; Computer Science - Computer Vision and Pattern Recognition ; High Energy Physics - Experiment
    Subject code 004
    Publishing date 2023-02-08
    Publishing country us
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Brain-derived neurotrophic factor and schizophrenia.

    Di Carlo, Pasquale / Punzi, Giovanna / Ursini, Gianluca

    Psychiatric genetics

    2019  Volume 29, Issue 5, Page(s) 200–210

    Abstract: The brain-derived neurotrophic factor (BDNF) is a secretory growth factor that promotes neuronal proliferation and survival, synaptic plasticity and long-term potentiation in the central nervous system. Brain-derived neurotrophic factor biosynthesis and ... ...

    Abstract The brain-derived neurotrophic factor (BDNF) is a secretory growth factor that promotes neuronal proliferation and survival, synaptic plasticity and long-term potentiation in the central nervous system. Brain-derived neurotrophic factor biosynthesis and secretion are chrono-topically regulated processes at the cellular level, accounting for specific localizations and functions. Given its role in regulating brain development and activity, BDNF represents a potentially relevant gene for schizophrenia, and indeed BDNF and its non-synonymous functional variant, rs6265 (C → T, Val → Met) have been widely studied in psychiatric genetics. Human and animal studies have indicated that brain-derived neurotrophic factor is relevant for schizophrenia-related phenotypes, and that: (1) fine-tuned regulation of brain-derived neurotrophic factor secretion and activity is necessary to guarantee brain optimal development and functioning; (2) the Val → Met substitution is associated with impaired activity-dependent secretion of brain-derived neurotrophic factor; (3) disruption of brain-derived neurotrophic factor signaling is associated with altered synaptic plasticity and neurodevelopment. However, genome-wide association studies failed to associate the BDNF locus with schizophrenia, even though a sub-threshold association exists. Here, we will review studies focused on the relationship between the genetic variation of BDNF and schizophrenia, trying to fill the gap between genetic risk per se and insights from molecular biology. A deeper understanding of brain-derived neurotrophic factor biology and of the epigenetic regulation of brain-derived neurotrophic factor and its interactome during development may help clarifying the potential role of this gene in schizophrenia, thus informing development of brain-derived neurotrophic factor-based strategies of prevention and treatment of this disorder.
    MeSH term(s) Animals ; Brain-Derived Neurotrophic Factor/genetics ; Brain-Derived Neurotrophic Factor/metabolism ; Epigenesis, Genetic ; Genome-Wide Association Study ; Genotype ; Humans ; Phenotype ; Polymorphism, Single Nucleotide ; Schizophrenia/genetics
    Chemical Substances Brain-Derived Neurotrophic Factor
    Language English
    Publishing date 2019-09-20
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 1067837-2
    ISSN 1473-5873 ; 0955-8829
    ISSN (online) 1473-5873
    ISSN 0955-8829
    DOI 10.1097/YPG.0000000000000237
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Neuroepigenetics of Schizophrenia.

    Punzi, Giovanna / Bharadwaj, Rahul / Ursini, Gianluca

    Progress in molecular biology and translational science

    2018  Volume 158, Page(s) 195–226

    Abstract: Schizophrenia is a complex disorder of the brain, where genetic variants explain only a portion of risk. Neuroepigenetic mechanisms may explain the remaining share of risk, as well as the transition from susceptibility to the actual disease. Here, we ... ...

    Abstract Schizophrenia is a complex disorder of the brain, where genetic variants explain only a portion of risk. Neuroepigenetic mechanisms may explain the remaining share of risk, as well as the transition from susceptibility to the actual disease. Here, we discuss the most recent findings in the field of brain epigenetics applied to the study of schizophrenia. Methylome studies have found several candidates exhibiting methylation modifications in association with the disorder, but genes affected do not always overlap. Notably, these studies converge in that genes within the schizophrenia risk loci or genes differentially methylated in patients affected with the disorder are dynamically regulated during early life. They also imply that schizophrenia-associated genetic variation may affect DNA methylation in fetal and adult brains. Histone modifications may help mediating the effect of genetic risk variants associated with schizophrenia, and regulating chromatin higher-order structure. The 3D-organization of chromatin in the brain creates physical interactions within chromosomes, so that schizophrenia-associated genetic variants can be linked with genes distant from their loci; this suggests that chromatin conformation matters in the mechanism of risk for the disorder. Non-coding RNAs provide a novel and complex mechanism of gene regulation potentially significant for schizophrenia, as proposed by research on specific microRNAs and long non-coding RNAs (lncRNAs). Finally, a recent study in epitranscriptomics identifies RNA methylation as a further epigenetic mechanism active in human brain and specifically in a portion of the transcriptome associated with schizophrenia susceptibility. These findings indicate that, as expected from the complexity of the brain and its development, several epigenetic mechanisms may intervene in the etiopathogenesis of schizophrenia. An understanding of their roles calls for research approaches integrating the investigation of different epigenetic mechanisms and of environmental and genetic risk, in the context of development.
    MeSH term(s) Animals ; Biomarkers/blood ; Chromatin/metabolism ; DNA Methylation/genetics ; Epigenesis, Genetic ; Genetic Predisposition to Disease ; Humans ; Schizophrenia/blood ; Schizophrenia/genetics
    Chemical Substances Biomarkers ; Chromatin
    Language English
    Publishing date 2018-06-11
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 2471995-X
    ISSN 1878-0814 ; 0079-6603 ; 1877-1173
    ISSN (online) 1878-0814
    ISSN 0079-6603 ; 1877-1173
    DOI 10.1016/bs.pmbts.2018.04.010
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Prioritization of potential causative genes for schizophrenia in placenta.

    Ursini, Gianluca / Di Carlo, Pasquale / Mukherjee, Sreya / Chen, Qiang / Han, Shizhong / Kim, Jiyoung / Deyssenroth, Maya / Marsit, Carmen J / Chen, Jia / Hao, Ke / Punzi, Giovanna / Weinberger, Daniel R

    Nature communications

    2023  Volume 14, Issue 1, Page(s) 2613

    Abstract: Our earlier work has shown that genomic risk for schizophrenia converges with early life complications in affecting risk for the disorder and sex-biased neurodevelopmental trajectories. Here, we identify specific genes and potential mechanisms that, in ... ...

    Abstract Our earlier work has shown that genomic risk for schizophrenia converges with early life complications in affecting risk for the disorder and sex-biased neurodevelopmental trajectories. Here, we identify specific genes and potential mechanisms that, in placenta, may mediate such outcomes. We performed TWAS in healthy term placentae (N = 147) to derive candidate placental causal genes that we confirmed with SMR; to search for placenta and schizophrenia-specific associations, we performed an analogous analysis in fetal brain (N = 166) and additional placenta TWAS for other disorders/traits. The analyses in the whole sample and stratifying by sex ultimately highlight 139 placenta and schizophrenia-specific risk genes, many being sex-biased; the candidate molecular mechanisms converge on the nutrient-sensing capabilities of placenta and trophoblast invasiveness. These genes also implicate the Coronavirus-pathogenesis pathway and showed increased expression in placentae from a small sample of SARS-CoV-2-positive pregnancies. Investigating placental risk genes for schizophrenia and candidate mechanisms may lead to opportunities for prevention that would not be suggested by study of the brain alone.
    MeSH term(s) Pregnancy ; Female ; Humans ; Placenta/metabolism ; Schizophrenia/genetics ; Schizophrenia/metabolism ; COVID-19/metabolism ; SARS-CoV-2 ; Trophoblasts/metabolism
    Language English
    Publishing date 2023-05-15
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-38140-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Chromatic Information and Feature Detection in Fast Visual Analysis.

    Del Viva, Maria M / Punzi, Giovanni / Shevell, Steven K

    PloS one

    2016  Volume 11, Issue 8, Page(s) e0159898

    Abstract: The visual system is able to recognize a scene based on a sketch made of very simple features. This ability is likely crucial for survival, when fast image recognition is necessary, and it is believed that a primal sketch is extracted very early in the ... ...

    Abstract The visual system is able to recognize a scene based on a sketch made of very simple features. This ability is likely crucial for survival, when fast image recognition is necessary, and it is believed that a primal sketch is extracted very early in the visual processing. Such highly simplified representations can be sufficient for accurate object discrimination, but an open question is the role played by color in this process. Rich color information is available in natural scenes, yet artist's sketches are usually monochromatic; and, black-and-white movies provide compelling representations of real world scenes. Also, the contrast sensitivity of color is low at fine spatial scales. We approach the question from the perspective of optimal information processing by a system endowed with limited computational resources. We show that when such limitations are taken into account, the intrinsic statistical properties of natural scenes imply that the most effective strategy is to ignore fine-scale color features and devote most of the bandwidth to gray-scale information. We find confirmation of these information-based predictions from psychophysics measurements of fast-viewing discrimination of natural scenes. We conclude that the lack of colored features in our visual representation, and our overall low sensitivity to high-frequency color components, are a consequence of an adaptation process, optimizing the size and power consumption of our brain for the visual world we live in.
    MeSH term(s) Color Perception/physiology ; Databases, Factual ; Discriminant Analysis ; Humans ; Internet ; Pattern Recognition, Visual/physiology ; Photic Stimulation
    Language English
    Publishing date 2016
    Publishing country United States
    Document type Journal Article
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0159898
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: A multidisciplinary approach in overkill: Analysis of 13 cases and review of the literature.

    Solarino, Biagio / Punzi, Giovanna / Di Vella, Giancarlo / Carabellese, Felice / Catanesi, Roberto

    Forensic science international

    2019  Volume 298, Page(s) 402–407

    Abstract: The term overkill usually indicates the infliction of massive injuries by far exceeding the extent necessary to kill the victim. Only few articles or textbooks report this term that is mostly associated with sex-motivated homicides where injuries, ... ...

    Abstract The term overkill usually indicates the infliction of massive injuries by far exceeding the extent necessary to kill the victim. Only few articles or textbooks report this term that is mostly associated with sex-motivated homicides where injuries, generally stabbing, are directed to significant sexual parts of the body. The aim of this study is to shed light on the phenomenon of overkill by reviewing some cases personally analyzed by the authors from both a forensic pathology rather than forensic psychiatry views. The reported results coupled with the literature revision confirmed the importance of a complete analysis of all criminological elements for better defining overkill cases.
    MeSH term(s) Adolescent ; Adult ; Female ; Forensic Psychiatry ; Homicide/psychology ; Humans ; Insanity Defense ; Intelligence ; Male ; Mental Disorders/psychology ; Motivation ; Multiple Trauma/psychology ; Substance-Related Disorders/psychology ; Weapons ; Wounds, Stab/psychology
    Language English
    Publishing date 2019-03-22
    Publishing country Ireland
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 424042-x
    ISSN 1872-6283 ; 0379-0738
    ISSN (online) 1872-6283
    ISSN 0379-0738
    DOI 10.1016/j.forsciint.2019.03.029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Reduced community viral load does not coincide with a reduction in the rate of new HIV diagnoses and recent infections: data from a region of southern Italy.

    Monno, L / Saracino, A / Scudeller, L / Santoro, C / Brindicci, G / Punzi, G / Lagioia, A / Lo Caputo, S / Angarano, G

    HIV medicine

    2017  Volume 18, Issue 10, Page(s) 711–723

    Abstract: Objectives: We assessed whether changes in community viral load (CVL) over time were associated with the rate of new HIV diagnoses (NDs).: Methods: HIV-1-positive individuals referred to our institute and permanently residing in our province were ... ...

    Abstract Objectives: We assessed whether changes in community viral load (CVL) over time were associated with the rate of new HIV diagnoses (NDs).
    Methods: HIV-1-positive individuals referred to our institute and permanently residing in our province were considered for inclusion in the study. A total of 861 HIV-infected adults with at least one HIV RNA measurement (12 530 measurements in total) between 2008 and 2014 were included. Viraemia copy-years were calculated from all HIV RNA values for each patient using the trapezoidal rule; multiple CVL indicators were considered. Total NDs and recent infections (< 1 year) were analysed separately. The association between NDs and CVL was tested by means of mixed Poisson models, with CVL as a fixed effect and year as a random effect.
    Results: The incidence of NDs was 2.28 per 100 000 residents in 2008 and 2.52 per 100 000 residents in 2014. Total numbers of NDs and recent infections did not vary significantly over time (P for trend 0.879 and 0.39, respectively). Mean HIV RNA decreased from 31 095.8 HIV-1 RNA copies/mL in 2008 to 21 231.5 copies/mL in 2014 (P < 0.001); a downward trend was always observed regardless of the CVL indicator considered. Depending on the indicator, there were some differences in CVL by patient characteristics. The most substantial contributors to CVL appeared to be male individuals, men who have sex with men (MSM), non-Italians, and untreated subjects (all P < 0.05). The relative risk of ND increased among Italians and MSM with an increasing proportion of subjects having an undetectable HIV RNA, and decreased in the same population with increasing levels of CVL.
    Conclusions: In our setting, CVL represented a good marker of access to care and treatment; however, reduced CVL did not coincide with a reduction in the rate of NDs.
    MeSH term(s) Adolescent ; Adult ; Aged ; Female ; HIV Infections/diagnosis ; HIV Infections/drug therapy ; HIV Infections/epidemiology ; HIV Infections/virology ; HIV-1/isolation & purification ; Humans ; Incidence ; Italy/epidemiology ; Male ; Middle Aged ; RNA, Viral/blood ; Viral Load ; Young Adult
    Chemical Substances RNA, Viral
    Language English
    Publishing date 2017-04-26
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2001932-4
    ISSN 1468-1293 ; 1464-2662
    ISSN (online) 1468-1293
    ISSN 1464-2662
    DOI 10.1111/hiv.12515
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Increased expression of MARCKS in post-mortem brain of violent suicide completers is related to transcription of a long, noncoding, antisense RNA.

    Punzi, G / Ursini, G / Shin, J H / Kleinman, J E / Hyde, T M / Weinberger, D R

    Molecular psychiatry

    2014  Volume 19, Issue 10, Page(s) 1057–1059

    MeSH term(s) Biomarkers/blood ; Humans ; Male ; Suicidal Ideation
    Chemical Substances Biomarkers
    Language English
    Publishing date 2014-05-13
    Publishing country England
    Document type Journal Article ; Comment
    ZDB-ID 1330655-8
    ISSN 1476-5578 ; 1359-4184
    ISSN (online) 1476-5578
    ISSN 1359-4184
    DOI 10.1038/mp.2014.41
    Database MEDical Literature Analysis and Retrieval System OnLINE

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