Impact of genetic variants within serotonin turnover enzymes on human cerebral monoamine oxidase A in vivo.
Translational Psychiatry
Spies, Marie M; Murgaš, Matej M; Vraka, Chrysoula C; Philippe, Cecile C; Gryglewski, Gregor G; Nics, Lukas L; Balber, Theresa T; Baldinger-Melich, Pia P; Hartmann, Annette M AM; Rujescu, Dan D; Hacker, Marcus M; Winkler-Pjrek, Edda E; Winkler, Dietmar D; Lanzenberger, Rupert R
The MAOA rs979605 Genetic Polymorphism Is Differentially Associated with Clinical Improvement Following Antidepressant Treatment between Male and Female Depressed Patients.
MAOA uVNTR Genetic Variant and Major Depressive Disorder: A Systematic Review.
Cells
Castro Gonçalves, Ana Beatriz AB; Ferreira Fratelli, Caroline C; Saraiva Siqueira, Jhon Willatan JW; Canongia de Abreu Cardoso Duarte, Ligia L; Ribeiro Barros, Aline A; Possatti, Isabella I; Lima Dos Santos, Maurício M; de Souza Silva, Calliandra Maria CM; Rodrigues da Silva, Izabel Cristina IC
Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.
Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.
Npj Parkinson'S Disease
Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD
Publication Date: 2022-06-29
Variant appearance in text: MAOA: D470D; rs1137070
Bacillus Calmette-Guérin Treatment Changes the Tumor Microenvironment of Non-Muscle-Invasive Bladder Cancer.
Frontiers In Oncology
Su, Fei F; Liu, Ming M; Zhang, Wei W; Tang, Min M; Zhang, Jinsong J; Li, Hexin H; Zou, Lihui L; Zhang, Rui R; Liu, Yudong Y; Li, Lin L; Ma, Jie J; Zhang, Yaqun Y; Chen, Meng M; Xiao, Fei F
A systematic review of common genetic variation and biological pathways in autism spectrum disorder.
Bmc Neuroscience
Rodriguez-Gomez, Diego Alejandro DA; Garcia-Guaqueta, Danna Paola DP; Charry-Sánchez, Jesús David JD; Sarquis-Buitrago, Elias E; Blanco, Mariana M; Velez-van-Meerbeke, Alberto A; Talero-Gutiérrez, Claudia C
Genetic Determinants Highlight the Existence of Shared Etiopathogenetic Mechanisms Characterizing Age-Related Macular Degeneration and Neurodegenerative Disorders.
Frontiers In Neurology
Strafella, Claudia C; Caputo, Valerio V; Termine, Andrea A; Fabrizio, Carlo C; Ruffo, Paola P; Potenza, Saverio S; Cusumano, Andrea A; Ricci, Federico F; Caltagirone, Carlo C; Giardina, Emiliano E; Cascella, Raffaella R
Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder.
Translational Psychiatry
Yadav, Santosh K SK; Bhat, Ajaz A AA; Hashem, Sheema S; Nisar, Sabah S; Kamal, Madeeha M; Syed, Najeeb N; Temanni, Mohamed-Ramzi MR; Gupta, Rakesh K RK; Kamran, Saddat S; Azeem, Muhammad Waqar MW; Srivastava, Amit K AK; Bagga, Puneet P; Chawla, Sanjeev S; Reddy, Ravinder R; Frenneaux, Michael P MP; Fakhro, Khalid K; Haris, Mohammad M
Fatigue in Women with Fibromyalgia: A Gene-Physical Activity Interaction Study.
Journal Of Clinical Medicine
Estévez-López, Fernando F; Salazar-Tortosa, Diego F DF; Camiletti-Moirón, Daniel D; Gavilán-Carrera, Blanca B; Aparicio, Virginia A VA; Acosta-Manzano, Pedro P; Segura-Jiménez, Víctor V; Álvarez-Gallardo, Inmaculada C IC; Carbonell-Baeza, Ana A; Munguía-Izquierdo, Diego D; Geenen, Rinie R; Lacerda, Eliana E; Delgado-Fernández, Manuel M; Martínez-González, Luis J LJ; Ruiz, Jonatan R JR; Álvarez-Cubero, María J MJ
Patients Stratification Strategies to Optimize the Effectiveness of Scavenging Biogenic Aldehydes: Towards a Neuroprotective Approach for Parkinson's Disease.
Current Neuropharmacology
Masato, Anna A; Sandre, Michele M; Antonini, Angelo A; Bubacco, Luigi L
Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.
Npj Systems Biology And Applications
Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A
Publication Date: 2021-01-08
Variant appearance in text: MAOA: 1410T>C; D470D; rs1137070
Effects of Childhood Adversity and Its Interaction with the MAOA, BDNF, and COMT Polymorphisms on Subclinical Attention Deficit/Hyperactivity Symptoms in Generally Healthy Youth.
Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.
Communications Biology
Perrino, Peter A PA; Talbot, Lidiya L; Kirkland, Rose R; Hill, Amanda A; Rendall, Amanda R AR; Mountford, Hayley S HS; Taylor, Jenny J; , ; Buscarello, Alexzandrea N AN; Lahiri, Nayana N; Saggar, Anand A; Fitch, R Holly RH; Newbury, Dianne F DF
Cross-Sectional Survey of Mental Health Risk Factors and Comparison of the Monoamine oxidase A Gene DNA Methylation Level in Different Mental Health Conditions among Oilfield Workers in Xinjiang, China.
International Journal Of Environmental Research And Public Health
Highly Variable Pharmacokinetics of Tyramine in Humans and Polymorphisms in OCT1, CYP2D6, and MAO-A.
Frontiers In Pharmacology
Rafehi, Muhammad M; Faltraco, Frank F; Matthaei, Johannes J; Prukop, Thomas T; Jensen, Ole O; Grytzmann, Aileen A; Blome, Felix G FG; Berger, Ralf Günter RG; Krings, Ulrich U; Vormfelde, Stefan V SV; Tzvetkov, Mladen V MV; Brockmöller, Jürgen J
Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.
Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09
Variant appearance in text: MAOA: D470D; rs1137070
A pharmacogenetic study of patients with schizophrenia from West Siberia gets insight into dopaminergic mechanisms of antipsychotic-induced hyperprolactinemia.
Bmc Medical Genetics
Osmanova, Diana Z DZ; Freidin, Maxim B MB; Fedorenko, Olga Yu OY; Pozhidaev, Ivan V IV; Boiko, Anastasiia S AS; Vyalova, Natalia M NM; Tiguntsev, Vladimir V VV; Kornetova, Elena G EG; Loonen, Anton J M AJM; Semke, Arkadiy V AV; Wilffert, Bob B; Bokhan, Nikolay A NA; Ivanova, Svetlana A SA
A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.
Brain imaging genetics in ADHD and beyond - Mapping pathways from gene to disorder at different levels of complexity.
Neuroscience And Biobehavioral Reviews
Klein, Marieke M; Onnink, Marten M; van Donkelaar, Marjolein M; Wolfers, Thomas T; Harich, Benjamin B; Shi, Yan Y; Dammers, Janneke J; Arias-Vásquez, Alejandro A; Hoogman, Martine M; Franke, Barbara B