Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Yaira Z. Nunez"'
Autor:
Aislinn Low, Brendan Stiltner, Yaira Z. Nunez, Keyrun Adhikari, Joseph D. Deak, Robert H. Pietrzak, Henry R. Kranzler, Joel Gelernter, Renato Polimanti
Publikováno v:
Translational Psychiatry, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract There is a high prevalence of antisocial personality disorder (ASPD) in individuals affected by substance use disorders (SUD). However, there is limited information on the specific patterns of association of ASPD with SUD severity and specif
Externí odkaz:
https://doaj.org/article/5a613867b9114907a851b62aed383662
Autor:
Brendan Stiltner, Robert H. Pietrzak, Daniel S. Tylee, Yaira Z. Nunez, Keyrun Adhikari, Henry R. Kranzler, Joel Gelernter, Renato Polimanti
Publikováno v:
iScience, Vol 26, Iss 8, Pp 107336- (2023)
Summary: To characterize polysubstance addiction (PSA) patterns of cocaine use disorder (CoUD), we performed a latent class analysis (LCA) in 7,989 participants with a lifetime DSM-5 diagnosis of CoUD. This analysis identified three PSA subgroups amo
Externí odkaz:
https://doaj.org/article/c2aecbf616f04aa380ab9bbc556c6079
Autor:
Renato Polimanti, Daniel F. Levey, Gita A. Pathak, Frank R. Wendt, Yaira Z. Nunez, Robert J. Ursano, Ronald C. Kessler, Henry R. Kranzler, Murray B. Stein, Joel Gelernter
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Substance dependence diagnoses (SDs) are important risk factors for suicidality. We investigated the associations of multiple SDs with different suicidality outcomes, testing how genetic background moderates these associations. The Yale-Penn
Externí odkaz:
https://doaj.org/article/944b6cdf80384367ae276ca756ef7895
Autor:
Brendan Stiltner, Robert H. Pietrzak, Daniel S. Tylee, Yaira Z. Nunez, Keyrun Adhikari, Henry R. Kranzler, Joel Gelernter, Renato Polimanti
Publikováno v:
medRxiv
AimsWe performed a latent class analysis (LCA) in a sample ascertained for addiction phenotypes to investigate cocaine use disorder (CoUD) subgroups related to polysubstance addiction (PSA) patterns and characterized their differences with respect to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3141a579fcf99bf5fa09d03874bb0a5
https://doi.org/10.1101/2023.02.08.23285653
https://doi.org/10.1101/2023.02.08.23285653
Autor:
Joseph D. Deak, Hang Zhou, Marco Galimberti, Daniel F. Levey, Frank R. Wendt, Sandra Sanchez-Roige, Alexander S. Hatoum, Emma C. Johnson, Yaira Z. Nunez, Ditte Demontis, Anders D. Børglum, Veera M. Rajagopal, Mariela V. Jennings, Rachel L. Kember, Amy C. Justice, Howard J. Edenberg, Arpana Agrawal, Renato Polimanti, Henry R. Kranzler, Joel Gelernter
Publikováno v:
Molecular psychiatry, vol 27, iss 10
Despite the large toll of opioid use disorder (OUD), genome-wide association studies (GWAS) of OUD to date have yielded few susceptibility loci. We performed a large-scale GWAS of OUD in individuals of European (EUR) and African (AFR) ancestry, optim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84447b01a4935a388bc4db22e043f92d
https://escholarship.org/uc/item/4ff2m3s5
https://escholarship.org/uc/item/4ff2m3s5
Autor:
Yaira Z. Nunez, Chih-Ken Chen, Yu-Chi Huang, Joel Gelernter, Sheng-Chang Wang, Ming-Chyi Huang, Mei-Hing Ng, Henry R. Kranzler, Meng-Chang Tsai, Bao-Zhu Yang, Liang-Jen Wang
Publikováno v:
Complex Psychiatry
The Semi-Structured Assessment for Drug Dependence and Alcoholism (SSADDA) is a polydiagnostic instrument for substance use and psychiatric disorders. We translated the SSADDA English version into Chinese (SSADDA-Chinese) and report here our examinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94f4a51b0005369ff35d61b948161b6f
https://doi.org/10.1159/000511606
https://doi.org/10.1159/000511606
Autor:
Joseph D. Deak, Hang Zhou, Marco Galimberti, Daniel Levey, Frank R. Wendt, Sandra Sanchez-Roige, Alexander Hatoum, Emma C. Johnson, Yaira Z. Nunez, Ditte Demontis, Anders D. Børglum, Veera M. Rajagopal, Mariela V. Jennings, Rachel L. Kember, Amy C. Justice, Howard J. Edenberg, Arpana Agrawal, Renato Polimanti, Henry R. Kranzler, Joel Gelernter
BackgroundDespite the large toll of opioid use disorder (OUD), genome-wide association studies (GWAS) of OUD to date have yielded few susceptibility loci.MethodsWe performed a large-scale GWAS of OUD in individuals of European (EUR) and African (AFR)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8749b11588b02b6f5fefa3c6a6c18818
https://doi.org/10.1101/2021.12.04.21267094
https://doi.org/10.1101/2021.12.04.21267094
Autor:
Lin Lu, Amy C. Justice, Suhua Chang, Joel Gelernter, Henry R. Kranzler, Kittipong Sanichwankul, Robert T. Malison, Rasmon Kalayasiri, Xiang-Ding Chen, Yan Sun, Apiwat Mutirangura, Jie Shi, Hang Zhou, Hong-Wen Deng, Yaira Z. Nunez
BACKGROUNDAlcohol use disorder (AUD) is a leading cause of death and disability worldwide. Genome-wide association studies (GWAS) have identified ∼30 AUD risk genes in European populations, but many fewer in East Asians.METHODSWe conducted GWAS and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce78843cab2513e41a7b5dcc4fdb116f
https://doi.org/10.1101/2021.09.17.21263732
https://doi.org/10.1101/2021.09.17.21263732
Autor:
Frank R. Wendt, Flavio De Angelis, Antonella De Lillo, Joel Gelernter, Aranyak Goswami, Henry R. Kranzler, Yaira Z. Nunez, Maria Fuciarelli, Gita A. Pathak, Renato Polimanti
Publikováno v:
Circulation: Genomic and Precision Medicine. 14
Background: The Val122Ile mutation in Transthyretin ( TTR ) gene causes a rare, difficult to diagnose hereditary form of cardiac amyloidosis. This mutation is most common in the United States and mainly present in people of African descent. The carri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7a3b57fe77fa8514b9f88bffc6c9212
https://doi.org/10.1161/circgen.120.003011
https://doi.org/10.1161/circgen.120.003011
Autor:
Gita A, Pathak, Frank R, Wendt, Antonella, De Lillo, Yaira Z, Nunez, Aranyak, Goswami, Flavio, De Angelis, Maria, Fuciarelli, Henry R, Kranzler, Joel, Gelernter, Renato, Polimanti
Publikováno v:
Circ Genom Precis Med
BACKGROUND -: The Val122Ile mutation in Transthyretin (TTR) gene causes a rare, difficult to diagnose hereditary form of cardiac amyloidosis. This mutation is most common in the United States and mainly present in people of African descent. The carri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c4b812b1cc60046bb51e7b8253debbb
https://pubmed.ncbi.nlm.nih.gov/33428857
https://pubmed.ncbi.nlm.nih.gov/33428857