Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 670 Records) |
Query Trace: HTT[original query] |
---|
Association of COMT, BDNF and 5-HTT functional polymorphisms with personality characteristics. Frontiers in bioscience (Landmark edition) 2021 Nov 26 (11): 1064-1074. Tommasi Marco, Sergi Maria Rita, Konstantinidou Fani, Franzago Marica, Pesce Mirko, Fratta Irene La, Grilli Alfredo, Stuppia Liborio, Picconi Laura, Saggino Aristide, Gatta Valenti |
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1. NPJ genomic medicine 2022 9 7 (1): 53. Lobanov Sergey V, McAllister Branduff, McDade-Kumar Mia, Landwehrmeyer G Bernhard, Orth Michael, Rosser Anne E, , Paulsen Jane S, , Lee Jong-Min, MacDonald Marcy E, Gusella James F, Long Jeffrey D, Ryten Mina, Williams Nigel M, Holmans Peter, Massey Thomas H, Jones Lesl |
Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease. Human molecular genetics 2022 9 . Ruiz de Sabando Ainara, Urrutia Lafuente Edurne, Galbete Arkaitz, Ciosi Marc, García Amigot Fermín, García Solaesa Virginia, , Monckton Darren G, Ramos-Arroyo Maria |
Clinical and Molecular Findings of Intermediate Allele Carriers in the HTT Gene from the Mexican Mestizo Population. Neuro-degenerative diseases 2022 Aug . Ramírez-García Miguel Ángel, Dávila-Ortiz de Montellano David José, Martínez-Ruano Leticia, Ochoa-Morales Adriana, Romero-Hidalgo Sandra, Zenteno Juan Carlos, Yescas-Gómez Pet |
Intermediate and Expanded HTT Alleles and the Risk for ?-Synucleinopathies. Movement disorders : official journal of the Movement Disorder Society 2022 7 37 (9): 1841-1849. Pérez-Oliveira Sergio, Álvarez Ignacio, Rosas Irene, Menendez-González Manuel, Blázquez-Estrada Marta, Aguilar Miquel, Corte Daniela, Buongiorno Mariateresa, Molina-Porcel Laura, Aldecoa Iban, Martí María J, Sánchez-Juan Pascual, Infante Jon, González-Aramburu Isabel, García-González Pablo, Rosende-Roca Maitée, Boada Mercè, Ruiz Agustín, Periñán María Teresa, Macías-García Daniel, Muñoz-Delgado Laura, Gómez-Garre Pilar, Mir Pablo, Clarimón Jordi, Lleo Alberto, Alcolea Daniel, De la Casa-Fages Beatriz, Duarte Israel, Álvarez Victoria, Pastor P |
C9orf72 hexanucleotide repeat expansion found in suspected spinobulbar muscular atrophy (SBMA). Neurologia i neurochirurgia polska 2022 6 56 (3): 276-280. Radziwonik Wiktoria, Elert-Dobkowska Ewelina, Tomczuk Filip, Wozniak Aleksandra, Sobanska Anna, Stepniak Iwona, Koziorowski Dariusz, Zaremba Jacek, Su?ek An |
Polymorphism of neurodegeneration-related genes associated with Parkinson's disease risk. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 6 43 (9): 5301-5312. Li Jiaxin, Yi Minhan, Li Binbin, Yin Shujuan, Zhang Ying, Huang Zini, Shu Li, Zhang Yu |
Intermediate alleles of HTT: A new pathway in longevity. Journal of the neurological sciences 2022 5 438 120274. Ingannato Assunta, Bagnoli Silvia, Bessi Valentina, Ferrari Camilla, Mazzeo Salvatore, Sorbi Sandro, Nacmias Benedet |
Interaction effects of the 5-HTT and MAOA-uVNTR gene variants on pre-attentive EEG activity in response to threatening voices. Communications biology 2022 4 5 (1): 340. Martínez Róger Marcelo, Liao Tsai-Tsen, Fan Yang-Teng, Chen Yu-Chun, Chen Chen |
Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset. Nature neuroscience 2022 4 25 (4): 446-457. McAllister Branduff, Donaldson Jasmine, Binda Caroline S, Powell Sophie, Chughtai Uroosa, Edwards Gareth, Stone Joseph, Lobanov Sergey, Elliston Linda, Schuhmacher Laura-Nadine, Rees Elliott, Menzies Georgina, Ciosi Marc, Maxwell Alastair, Chao Michael J, Hong Eun Pyo, Lucente Diane, Wheeler Vanessa, Lee Jong-Min, MacDonald Marcy E, Long Jeffrey D, Aylward Elizabeth H, Landwehrmeyer G Bernhard, Rosser Anne E, , Paulsen Jane S, , Williams Nigel M, Gusella James F, Monckton Darren G, Allen Nicholas D, Holmans Peter, Jones Lesley, Massey Thomas |
Novel GxE effects and resilience: A case:control longitudinal study of psychosocial stress with war-affected youth. PloS one 2022 4 17 (4): e0266509. Mulligan Connie J, Clukay Christopher J, Matarazzo Anthony, Hadfield Kristin, Nevell Lisa, Dajani Rana, Panter-Brick Catheri |
CAG Repeats Within the Non-pathological Range in the HTT Gene Influence Personality Traits in Patients With Subjective Cognitive Decline: A 13-Year Follow-Up Study. Frontiers in psychiatry 2022 4 13 826135. Moschini Valentina, Mazzeo Salvatore, Bagnoli Silvia, Padiglioni Sonia, Emiliani Filippo, Giacomucci Giulia, Morinelli Carmen, Ingannato Assunta, Freni Tommaso, Belloni Laura, Ferrari Camilla, Sorbi Sandro, Nacmias Benedetta, Bessi Valenti |
5-HTT genotype and inertia of negative affect in adolescents and young adults from the general population. Journal of neural transmission (Vienna, Austria : 1996) 2022 Mar . Ollmann T M, Seidl E, Venz J, Pieper L, Voss C, Hoyer J, Kische H, Poppenhäger S R, Schiele M A, Domschke K, Beesdo-Baum |
DNA methylation age acceleration is associated with age of onset in Chinese spinocerebellar ataxia type 3 patients. Neurobiology of aging 2022 3 113 1-6. Li Jiahao, Shu Anli, Sun Yimin, Yang Wanli, Tang Xuelin, Pu Hongjiang, Peng Yun, Hu Xiaowen, Qing Ying, Wang Jian, Wan Chunling, Zhou Mingcheng, Zhang Mi |
Correction to: 5-HTT genotype and inertia of negative affect in adolescents and young adults from the general population. Journal of neural transmission (Vienna, Austria : 1996) 2022 3 129 (10): 1313-1314. Ollmann T M, Seidl E, Venz J, Pieper L, Voss C, Hoyer J, Kische H, Poppenhäger S R, Schiele M A, Domschke K, Beesdo-Baum |
Huntingtin gene intermediate alleles influence the progression from subjective cognitive decline to mild cognitive impairment: A 14-year follow-up study. European journal of neurology 2022 Feb . Mazzeo Salvatore, Emiliani Filippo, Bagnoli Silvia, Padiglioni Sonia, Conti Vittoria, Ingannato Assunta, Giacomucci Giulia, Balestrini Juri, Ferrari Camilla, Sorbi Sandro, Nacmias Benedetta, Bessi Valenti |
The OPRM1 gene and interactions with the 5-HT1a gene regulate conditioned pain modulation in fibromyalgia patients and healthy controls. PloS one 2022 11 17 (11): e0277427. Tour Jeanette, Sandström Angelica, Kadetoff Diana, Schalling Martin, Kosek E |
Brain gain-Is the cognitive performance of domestic hens affected by a functional polymorphism in the serotonin transporter gene? Frontiers in psychology 2022 13 901022. Dudde Anissa, Phi Van Loc, Schrader Lars, Obert Arnd J, Krause E Tobi |
Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis. Annals of clinical and translational neurology 2022 10 9 (11): 1820-1825. Manini Arianna, Gagliardi Delia, Meneri Megi, Antognozzi Sara, Del Bo Roberto, Scaglione Cesa, Comi Giacomo Pietro, Corti Stefania, Ronchi Dar |
Absence of a significant interaction of two common NOS1 and 5-HTT polymorphisms on sensorimotor gating in humans. Physiological research 2021 12 70 (S3): S387-S395. Rovný R, Marko M, Minárik G, Rie?anský |
Genetic contributions to brain serotonin transporter levels in healthy adults. Scientific reports 2023 9 13 (1): 16426. Silvia Elisabetta Portis Bruzzone, Arafat Nasser, Sagar Sanjay Aripaka, Marie Spies, Brice Ozenne, Peter Steen Jensen, Gitte Moos Knudsen, Vibe Gedsoe Frokjaer, Patrick MacDonald Fish |
The Huntington's Disease Gene in an Italian Cohort of Patients with Bipolar Disorder. Genes 2023 9 14 (9): . Camilla Ferrari, Elena Capacci, Silvia Bagnoli, Assunta Ingannato, Sandro Sorbi, Benedetta Nacmi |
ASSESSMENT OF THE ASSOCIATION OF SEROTONIN TRANSPORTER GENE (5-HTTVNTR & 5-HTTLPR) POLYMORPHISM IN PATIENTS WITH FIBROMYALGIA SYNDROME. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2023 7 76 (6): 1378-1384. Sidrah Parvez, Ghizal Fatima, Farzana Mahdi, Najah R Hadi, Jan Fedac |
Relationship between gene-environment interaction and obsessive-compulsive disorder: A systematic review. Journal of psychiatric research 2023 6 164 281-290. Lina Wang, Yu Chen, Miao Wang, Chaoben Zhao, Dongdong Qi |
Serotonin, ghrelin, and motilin gene/receptor/transporter polymorphisms in childhood functional constipation. Revista da Associacao Medica Brasileira (1992) 2023 3 69 (2): 279-284. Arslan Bengu, Dogan Guzide, Orenay-Boyacioglu Seda, Caliskan Metin, Elevli Mur |
A mother and her daughter carrying a pathogenic expansion of the HTT gene with a phenotype encompassing motor neuron disease and Huntington's disease. Clinical genetics 2023 12 . Antonio Canosa, Sara Cabras, Francesca Di Pede, Umberto Manera, Rosario Vasta, Cristina Moglia, Andrea Calvo, Salvatore Gallone, Adriano Ch |
Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients. International journal of molecular sciences 2023 11 24 (22): . Leon Chang, Lois Gardner, Carol House, Catherine Daly, Adrian Allsopp, Daniel Roiz de Sa, Marie-Anne Shaw, Philip M Hopki |
Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis. Journal of the Chinese Medical Association : JCMA 2023 1 86 (1): 47-51. Jih Kang-Yang, Lai Kuan-Lin, Lin Kon-Ping, Liao Yi-Chu, Lee Yi-Chu |
Phosphoproteomics implicates glutamatergic and dopaminergic signalling in the antidepressant-like properties of the iron chelator deferiprone. Neuropharmacology 2024 1 109837. Volkan Uzungil, Sandra Luza, Carlos M Opazo, Isaline Mees, Shanshan Li, Ching-Seng Ang, Nicholas A Williamson, Ashley I Bush, Anthony J Hannan, Thibault Reno |
Offspring's own serotonin transporter genotype, independently from the maternal one, increases anxiety- and depression-like behavior and alters neuroplasticity markers in rats. Journal of affective disorders 2024 1 350 89-101. Menghan Sun, Paola Brivio, Ling Shan, Sylvia Docq, Lisa C M W Heltzel, Celine A J Smits, Anthonieke Middelman, Roel Vrooman, Marcia Spoelder, Michel M M Verheij, Jan K Buitelaar, Morgane Boillot, Francesca Calabrese, Judith R Homberg, Sabrina I Hanswi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: