Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: Learning and meta-analysis and Meta[original query] |
---|
Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases.
Ophthalmology science 2023 5 3 (3): 100288. Tomasoni Mattia, Beyeler Michael Johannes, Vela Sofia Ortin, Mounier Ninon, Porcu Eleonora, Corre Tanguy, Krefl Daniel, Button Alexander Luke, Abouzeid Hana, Lazaros Konstantinidis, Bochud Murielle, Schlingemann Reinier, Bergin Ciara, Bergmann Sv |
The effect of neurogranin on neural correlates of episodic memory encoding and retrieval. Schizophrenia bulletin 2013 Jan 39 (1): 141-50. Krug Axel, Krach Sören, Jansen Andreas, Nieratschker Vanessa, Witt Stephanie H, Shah N Jon, Nöthen Markus M, Rietschel Marcella, Kircher Ti |
A case control association study and cognitive function analysis of neuropilin and tolloid-like 1 gene and schizophrenia in the Japanese population. PloS one 2011 6 (12): e28929. Banno Masahiro, Koide Takayoshi, Aleksic Branko, Yamada Kazuo, Kikuchi Tsutomu, Kohmura Kunihiro, Adachi Yasunori, Kawano Naoko, Kushima Itaru, Ikeda Masashi, Inada Toshiya, Yoshikawa Takeo, Iwata Nakao, Ozaki Nor |
Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study. Translational psychiatry 2012 Feb 2 . Hammer C, Cichon S, Mühleisen TW, Haenisch B, Degenhardt F, Mattheisen M, Breuer R, Witt SH, Strohmaier J, Oruc L, Rivas F, Babadjanova G, Grigoroiu-Serbanescu M, Hauser J, Röth R, Rappold G, Rietschel M, Nöthen MM, Niesler B |
GSK-3ß polymorphism discriminates bipolar disorder and schizophrenia: a systematic meta-analysis. Molecular neurobiology 2013 Dec 48 (3): 404-11. Tang Hui, Shen Na, Jin Huijuan, Liu Dan, Miao Xiaoping, Zhu Ling-Qia |
The association of the BDNF Val66Met polymorphism and the hippocampal volumes in healthy humans: a joint meta-analysis of published and new data. Neuroscience and biobehavioral reviews 2014 May 42 267-78. Harrisberger F, Spalek K, Smieskova R, Schmidt A, Coynel D, Milnik A, Fastenrath M, Freytag V, Gschwind L, Walter A, Vogel T, Bendfeldt K, de Quervain D J-F, Papassotiropoulos A, Borgwardt |
aCaMKII controls the establishment of cocaine's reinforcing effects in mice and humans. Translational psychiatry 2014 4 e457. Easton A C, Lourdusamy A, Havranek M, Mizuno K, Solati J, Golub Y, Clarke T-K, Vallada H, Laranjeira R, Desrivières S, Moll G H, Mössner R, Kornhuber J, Schumann G, Giese K P, Fernandes C, Quednow B B, Müller C |
A Case-Control Study and Meta-Analysis Reveal BDNF Val66Met Is a Possible Risk Factor for PTSD. Neural plasticity 2016 2016 6979435. Bruenig Dagmar, Lurie Janine, Morris Charles P, Harvey Wendy, Lawford Bruce, Young Ross McD, Voisey Joan |
COMT Val(158) Met genotype is associated with reward learning: a replication study and meta-analysis. Genes, brain, and behavior 2016 May . Corral-Frías Nadia S, Pizzagalli Diego A, Carré Justin, Michalski Lindsay J, Nikolova Yuliya S, Perlis Roy H, Fagerness Jesen, Lee Mary R, Drabant Conley Emily, Lancaster Thomas M, Haddad Stephen, Wolf Aaron, Smoller Jordan W, Hariri Ahmad R, Bogdan Ry |
Phenome-Wide Association Study for Alcohol and Nicotine Risk Alleles in 26394 Women. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2016 May . Polimanti Renato, Kranzler Henry R, Gelernter Jo |
MEF2C rs190982 polymorphism with late-onset Alzheimer's disease in Han Chinese: A replication study and meta-analyses. Oncotarget 2016 Jun . Tang Shan-Shan, Wang Hui-Fu, Zhang Wei, Kong Ling-Li, Zheng Zhan-Jie, Tan Meng-Shan, Tan Chen-Chen, Wang Zi-Xuan, Tan Lin, Jiang Teng, Yu Jin-Tai, Tan L |
A genome-wide gene-by-trauma interaction study of alcohol misuse in two independent cohorts identifies PRKG1 as a risk locus.
Molecular psychiatry 2017 Mar . Polimanti R, Kaufman J, Zhao H, Kranzler H R, Ursano R J, Kessler R C, Gelernter J, Stein M |
Stress-Dependent Association Between Polygenic Risk for Schizophrenia and Schizotypal Traits in Young Army Recruits. Schizophrenia bulletin 2018 02 44 (2): 338-347. Hatzimanolis Alex, Avramopoulos Dimitrios, Arking Dan E, Moes Anna, Bhatnagar Pallav, Lencz Todd, Malhotra Anil K, Giakoumaki Stella G, Roussos Panos, Smyrnis Nikolaos, Bitsios Panos, Stefanis Nicholas |
A Meta-Prediction of Methylenetetrahydrofolate-Reductase Polymorphisms and Air Pollution Increased the Risk of Ischemic Heart Diseases Worldwide. International journal of environmental research and public health 2018 Jul 15 (7): . Chen Zhao-Feng, Young Lufei, Yu Chong Ho, Shiao S Pamela |
Evaluation of parameters affecting performance and reliability of machine learning-based antibiotic susceptibility testing from whole genome sequencing data. PLoS computational biology 2019 9 15 (9): e1007349. Hicks Allison L, Wheeler Nicole, Sánchez-Busó Leonor, Rakeman Jennifer L, Harris Simon R, Grad Yonatan |
A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders.
Translational psychiatry 2019 05 9 (1): 150. Rayner Christopher, Coleman Jonathan R I, Purves Kirstin L, Hodsoll John, Goldsmith Kimberley, Alpers Georg W, Andersson Evelyn, Arolt Volker, Boberg Julia, Bögels Susan, Creswell Cathy, Cooper Peter, Curtis Charles, Deckert Jürgen, Domschke Katharina, El Alaoui Samir, Fehm Lydia, Fydrich Thomas, Gerlach Alexander L, Grocholewski Anja, Hahlweg Kurt, Hamm Alfons, Hedman Erik, Heiervang Einar R, Hudson Jennifer L, Jöhren Peter, Keers Robert, Kircher Tilo, Lang Thomas, Lavebratt Catharina, Lee Sang-Hyuck, Lester Kathryn J, Lindefors Nils, Margraf Jürgen, Nauta Maaike, Pané-Farré Christiane A, Pauli Paul, Rapee Ronald M, Reif Andreas, Rief Winfried, Roberts Susanna, Schalling Martin, Schneider Silvia, Silverman Wendy K, Ströhle Andreas, Teismann Tobias, Thastum Mikael, Wannemüller Andre, Weber Heike, Wittchen Hans-Ulrich, Wolf Christiane, Rück Christian, Breen Gerome, Eley Thalia |
Orexin in the anxiety spectrum: association of a HCRTR1 polymorphism with panic disorder/agoraphobia, CBT treatment response and fear-related intermediate phenotypes. Translational psychiatry 2019 Feb 9 (1): 75. Gottschalk Michael G, Richter Jan, Ziegler Christiane, Schiele Miriam A, Mann Julia, Geiger Maximilian J, Schartner Christoph, Homola György A, Alpers Georg W, Büchel Christian, Fehm Lydia, Fydrich Thomas, Gerlach Alexander L, Gloster Andrew T, Helbig-Lang Sylvia, Kalisch Raffael, Kircher Tilo, Lang Thomas, Lonsdorf Tina B, Pané-Farré Christiane A, Ströhle Andreas, Weber Heike, Zwanzger Peter, Arolt Volker, Romanos Marcel, Wittchen Hans-Ulrich, Hamm Alfons, Pauli Paul, Reif Andreas, Deckert Jürgen, Neufang Susanne, Höfler Michael, Domschke Kathari |
Anxiety risk SNPs on chromosome 2 modulate arousal in children in a fear generalization paradigm. European child & adolescent psychiatry 2019 12 29 (9): 1301-1310. Reinhard Julia, Drepper Carsten, Weber Heike, Schiele Miriam A, Kneer Katharina, Mittermeier Anna, Frey Lillien, Reif Andreas, Pauli Paul, Domschke Katharina, Deckert Jürgen, Romanos Marc |
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.
JAMA psychiatry 2019 Oct . Greenwood Tiffany A, Lazzeroni Laura C, Maihofer Adam X, Swerdlow Neal R, Calkins Monica E, Freedman Robert, Green Michael F, Light Gregory A, Nievergelt Caroline M, Nuechterlein Keith H, Radant Allen D, Siever Larry J, Silverman Jeremy M, Stone William S, Sugar Catherine A, Tsuang Debby W, Tsuang Ming T, Turetsky Bruce I, Gur Ruben C, Gur Raquel E, Braff David |
Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease.
BMC medical genomics 2020 08 13 (1): 120. Winkler Thomas W, Grassmann Felix, Brandl Caroline, Kiel Christina, Günther Felix, Strunz Tobias, Weidner Lorraine, Zimmermann Martina E, Korb Christina A, Poplawski Alicia, Schuster Alexander K, Müller-Nurasyid Martina, Peters Annette, Rauscher Franziska G, Elze Tobias, Horn Katrin, Scholz Markus, Cañadas-Garre Marisa, McKnight Amy Jayne, Quinn Nicola, Hogg Ruth E, Küchenhoff Helmut, Heid Iris M, Stark Klaus J, Weber Bernhard H |
Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples. Scientific reports 2020 5 10 (1): 8622. Esteller-Cucala Paula, Maceda Iago, Børglum Anders D, Demontis Ditte, Faraone Stephen V, Cormand Bru, Lao Osc |
Association between diabetic retinopathy and interleukin-related gene polymorphisms: a machine learning aided meta-analysis. Ophthalmic genetics 2020 Apr 1-7. Sun Xiaojun, Guo Shil |
Identifying genetic risk variants associated with noise-induced hearing loss based on a novel strategy for evaluating individual susceptibility. Hearing research 2021 6 407 108281. Jiang Zhuang, Fa Botao, Zhang Xunmiao, Wang Jiping, Feng Yanmei, Shi Haibo, Zhang Yue, Sun Daoyuan, Wang Hui, Yin Shank |
Investigating the association of CD36 gene polymorphisms (rs1761667 and rs1527483) with T2DM and dyslipidemia: Statistical analysis, machine learning based prediction, and meta-analysis. PloS one 2021 16 (10): e0257857. Hatmal Ma'mon M, Alshaer Walhan, Mahmoud Ismail S, Al-Hatamleh Mohammad A I, Al-Ameer Hamzeh J, Abuyaman Omar, Zihlif Malek, Mohamud Rohimah, Darras Mais, Al Shhab Mohammad, Abu-Raideh Rand, Ismail Hilweh, Al-Hamadi Ali, Abdelhay A |
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis. Neurology. Genetics 2022 9 8 (5): e200011. Grassano Maurizio, Brodini Giorgia, De Marco Giovanni, Casale Federico, Fuda Giuseppe, Salamone Paolina, Brunetti Maura, Sbaiz Luca, Gallone Salvatore, Cugnasco Paolo, Bombaci Alessandro, Vasta Rosario, Manera Umberto, Canosa Antonio, Moglia Cristina, Calvo Andrea, Traynor Bryan J, Chio Adria |
Exploring polygenic contributors to subgroups of comorbid conditions in autism spectrum disorder. Scientific reports 2022 Mar 12 (1): 3416. Klein Louis, D'Urso Shannon, Eapen Valsamma, Hwang Liang-Dar, Lin Ping |
Thirty novel sequence variants impacting human intracranial volume. Brain communications 2022 11 4 (6): fcac271. Nawaz Muhammad Sulaman, Einarsson Gudmundur, Bustamante Mariana, Gisladottir Rosa S, Walters G Bragi, Jonsdottir Gudrun A, Skuladottir Astros Th, Bjornsdottir Gyda, Magnusson Sigurdur H, Asbjornsdottir Bergrun, Unnsteinsdottir Unnur, Sigurdsson Engilbert, Jonsson Palmi V, Palmadottir Vala Kolbrun, Gudjonsson Sigurjon A, Halldorsson Gisli H, Ferkingstad Egil, Jonsdottir Ingileif, Thorleifsson Gudmar, Holm Hilma, Thorsteinsdottir Unnur, Sulem Patrick, Gudbjartsson Daniel F, Stefansson Hreinn, Thorgeirsson Thorgeir E, Ulfarsson Magnus O, Stefansson Ka |
LLM-PBC: Logic Learning Machine-Based Explainable Rules Accurately Stratify the Genetic Risk of Primary Biliary Cholangitis. Journal of personalized medicine 2022 10 12 (10): . Gerussi Alessio, Verda Damiano, Cappadona Claudio, Cristoferi Laura, Bernasconi Davide Paolo, Bottaro Sandro, Carbone Marco, Muselli Marco, Invernizzi Pietro, Asselta Rosanna, On Behalf Of The Italian Pbc Genetics Study Grou |
Machine Learning Identifies Six Genetic Variants and Alterations in the Heart Atrial Appendage as Key Contributors to PD Risk Predictivity. Frontiers in genetics 2021 12 785436. Ho Daniel, Schierding William, Farrow Sophie L, Cooper Antony A, Kempa-Liehr Andreas W, O'Sullivan Justin |
Association of apolipoprotein E epsilon 4 and cognitive impairment in adults living with human immunodeficiency virus: a meta-analysis. Chinese medical journal 2023 1 135 (22): 2677-2686. Mu Tingting, Wei Jiaqi, Sun Jun, Jin Junyan, Zhang Tong, Wu Hao, Su B |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: