About: Renato Polimanti

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl)
rdfs:label	Renato Polimanti (en) Renato Polimanti (es) Renato Polimanti (it) Renato Polimanti (nl) Renato Polimanti (sl) Renato Polimanti (ast)
skos:prefLabel	Renato Polimanti (en) Renato Polimanti (es) Renato Polimanti (it) Renato Polimanti (nl) Renato Polimanti (sl) Renato Polimanti (ast)
name	Renato Polimanti (en) Renato Polimanti (es) Renato Polimanti (it) Renato Polimanti (nl) Renato Polimanti (sl) Renato Polimanti (ast)
Scopus author ID	wds:Q40700619-BEC0638D-5E6A-46AD-A326-2F09EE3F445F
Scopus author ID	36061883800
given name	wds:Q40700619-A781191D-4C39-47DF-A961-7A3D85EA18C2
given name	Renato
instance of	wds:Q40700619-4C1FC80B-D5A5-4DB4-AF1A-6A2AFF463E44
instance of	Homo sapiens
occupation	wds:Q40700619-EDDC3DD2-DCB0-4678-B67C-420921BFBE29
employer	wds:Q40700619-2570A12A-16CE-4E7A-BD28-41CC1E682323
sex or gender	wds:Q40700619-9AAC5C89-1DC6-4DF6-9495-BACD67B2E0B0
VIAF ID	wds:Q40700619-2fb690bf-f2df-4c95-bd82-48f83c9ff579
GND ID	wds:Q40700619-7ce95878-91c0-4a5a-b6df-8bc1e5d903da
family name	wds:Q40700619-75ABE4CC-57E4-4F02-9964-677113355D22
official website	wds:Q40700619-85B65AF4-FB7D-4849-98AF-C54DE0E4B943
VIAF ID	http://viaf.org/viaf/884157527421827300003
GND ID	https://d-nb.info/gnd/1200596366
occupation	researcher
employer	Yale School of Medicine
sex or gender	male
VIAF ID	884157527421827300003
GND ID	1200596366
family name	Polimanti
official website	http://medicine.yale.edu/psychiatry/people/renato_polimanti-1.profile?source=news
ORCID iD	wds:Q40700619-BD8770A1-9378-4A16-8808-2B871A4B4D43
ORCID iD	https://orcid.org/0000-0003-0745-6046
ORCID iD	0000-0003-0745-6046
IRIS UNIROMA2 author ID	wds:Q40700619-B07B1F7C-EB8D-4841-9DA5-B4A518E405AD
IRIS UNIROMA2 author ID	08487
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q40700619
is author of	HapMap-based study of human soluble glutathione S-transferase enzymes: the role of natural selection in shaping the single nucleotide polymorphism diversity of xenobiotic-metabolizing genes GSTO1E155del polymorphism associated with increased risk for late-onset Alzheimer's disease: association hypothesis for an uncommon genetic variant. Antioxidant status and APOE genotype as susceptibility factors for neurodegeneration in Alzheimer's disease and vascular dementia Metal-score as a potential non-invasive diagnostic test for Alzheimer's disease GSTM1 null genotype as risk factor for late-onset Alzheimer's disease in Italian patients. S100A10 identified in a genome-wide gene × cannabis dependence interaction analysis of risky sexual behaviours Dissecting ancestry genomic background in substance dependence genome-wide association studies Genetic factor common to schizophrenia and HIV infection is associated with risky sexual behavior: antagonistic vs. synergistic pleiotropic SNPs enriched for distinctly different biological functions The Interplay Between Risky Sexual Behaviors and Alcohol Dependence: Genome-Wide Association and Neuroimaging Support for LHPP as a Risk Gene Intronic rs2147363 variant in ATP7B transcription factor-binding site associated with Alzheimer's disease ADH1B: From alcoholism, natural selection, and cancer to the human phenome Glutathione S-transferase variants as risk factor for essential hypertension in Italian patients. Low-copper diet as a preventive strategy for Alzheimer's disease. Glutathione S-transferase ω class (GSTO) polymorphisms in a sample from Rome (Central Italy). Human genetic variation of CYP450 superfamily: analysis of functional diversity in worldwide populations. Glutathione S-transferase genes and the risk of recurrent miscarriage in Italian women. Functional polymorphisms of GSTA1 and GSTO2 genes associated with asthma in Italian children ATP7B variants as modulators of copper dyshomeostasis in Alzheimer's disease Copper status in Alzheimer's disease and other neurodegenerative disorders 2013. GSTT1 and GSTM1 gene polymorphisms in European and African populations Glutaredoxin 1 is a major player in copper metabolism in neuroblastoma cells. GSTA1, GSTO1 and GSTO2 gene polymorphisms in Italian asthma patients Glutathione S-transferase gene polymorphisms and air pollution as interactive risk factors for asthma in a multicentre Italian field study: A preliminary study Haplotype differences for copy number variants in the 22q11.23 region among human populations: a pigmentation-based model for selective pressure Explorative genetic association study of GSTT2B copy number variant in complex disease risks GSTO2N142D gene polymorphism associated with hypothyroidism in Italian patients Functional variability of glutathione S-transferases in Basque populations. Genome-wide Association Studies of Posttraumatic Stress Disorder in 2 Cohorts of US Army Soldiers A genome-wide gene-by-trauma interaction study of alcohol misuse in two independent cohorts identifies PRKG1 as a risk locus Cross-Phenotype Polygenic Risk Score Analysis of Persistent Post-Concussive Symptoms in U.S. Army Soldiers with Deployment-Acquired Traumatic Brain Injury Phenome-Wide Association Study for Alcohol and Nicotine Risk Alleles in 26394 Women Genome-wide association study of body mass index in subjects with alcohol dependence Phenome-wide association study for CYP2A6 alleles: rs113288603 is associated with hearing loss symptoms in elderly smokers Human GST loci as markers of evolutionary forces: GSTO1E155del and GSTO1E208K polymorphisms may be under natural selection induced by environmental arsenic Copper hypothesis in the missing hereditability of sporadic Alzheimer's disease: ATP7B gene as potential harbor of rare variants. A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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