Z. Nemoda

发表

Polymorphisms in Dopamine System Genes Are Associated with Individual Differences in Attention in Infancy Diamond and Colleagues Have Shown That Performance on a Task That Has Been Directly Associated

Mark H Johnson, Mark H. Johnson, Gergely Csibra, 2022 .

Activity-regulated RNA editing in select neuronal subfields in hippocampus

A. Penn, I. Greger, A. Balík, 2012, Nucleic acids research.

DNA methylation differences in stress-related genes, functional connectivity and gray matter volume in depressed and healthy adolescents.

L. Tozzi, M. Szyf, T. Frodl, 2020, Journal of affective disorders.

[Effects of the D4 dopamine receptor gene variation on behavior problems at 6 years of age].

Z. Nemoda, E. Birkás, J. Gervai, 2005, Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology.

Further evidence for the role of the dopamine D4 receptor (DRD4) gene in attachment disorganization: interaction of the exon III 48-bp repeat and the −521 C/T promoter polymorphisms

Z. Rónai, Z. Nemoda, J. Gervai, 2002, Molecular Psychiatry.

Investigation of de novo mutations in a schizophrenia case-parent trio by induced pluripotent stem cell-based in vitro disease modeling: convergence of schizophrenia- and autism-related cellular phenotypes

J. Réthelyi, L. Nagy, Á. Apáti, 2020, Stem cell research & therapy.

DNA methylation differences at the glucocorticoid receptor gene in depression are related to functional alterations in hypothalamic–pituitary–adrenal axis activity and to early life emotional abuse

D. Morris, L. Tozzi, M. Szyf, 2018, Psychiatry Research.

Decreased Nuclear Ascorbate Accumulation Accompanied with Altered Genomic Methylation Pattern in Fibroblasts from Arterial Tortuosity Syndrome Patients

G. Bánhegyi, Csilla E. Németh, É. Margittai, 2019, Oxidative medicine and cellular longevity.

Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

M. Daly, H. Stefánsson, R. Ophoff, 2022, Translational Psychiatry.

Potential salivary biomarkers and their genetic effects in a pilot study of adolescent boys with externalizing problems.

G. Meszaros, J. Halasz, Z. Nemoda, 2016, Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology.

Noninvasive genotyping of dopamine receptor D4 (DRD4) using nanograms of DNA from substance-dependent patients.

P. Gaszner, Z. Rónai, A. Guttman, 2002, Current medicinal chemistry.

Serotonin transporter promoter methylation in peripheral cells and neural responses to negative stimuli: A study of adolescent monozygotic twins

C. Fahim, M. Szyf, L. Booij, 2018, Translational Psychiatry.

Association of D4 dopamine receptor gene and serotonin transporter promoter polymorphisms with infants' response to novelty

Z. Rónai, Z. Nemoda, E. Birkás, 2003, Molecular Psychiatry.

Dopamine D4 receptor (DRD4) gene polymorphism is associated with attachment disorganization

Z. Nemoda, J. Gervai, K. Lakatos, 2000 .

Genetic and Biochemical Characterization of the E32del Polymorphism in Human Mesotrypsinogen

M. Sahin-Tóth, N. Teich, Z. Nemoda, 2005, Pancreatology.

Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girl

M. Sahin-Tóth, N. Teich, W. Heinritz, 2009 .

Gene conversion cetween functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six‐year‐old girl

M. Sahin-Tóth, V. Keim, N. Teich, 2005, Human mutation.

Human cationic trypsinogen is sulfated on Tyr154

M. Sahin-Tóth, Z. Nemoda, Z. Kukor, 2006, The FEBS journal.

Chymotrypsin C (Caldecrin) Stimulates Autoactivation of Human Cationic Trypsinogen*

M. Sahin-Tóth, Z. Nemoda, 2006, Journal of Biological Chemistry.

The Tetra-aspartate Motif in the Activation Peptide of Human Cationic Trypsinogen Is Essential for Autoactivation Control but Not for Enteropeptidase Recognition*

M. Sahin-Tóth, Z. Nemoda, 2005, Journal of Biological Chemistry.

The involvement of the canonical Wnt‐signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta‐analysis

K. Lesch, J. Hebebrand, A. Hinney, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Psychopathological aspects of dopaminergic gene polymorphisms in adolescence and young adulthood

A. Székely, Z. Nemoda, M. Sasvári‐Székely, 2011, Neuroscience & Biobehavioral Reviews.

Polymorphism in the Serotonin Receptor 2a (HTR2A) Gene as Possible Predisposal Factor for Aggressive Traits

T. Nánási, Z. Rónai, A. Székely, 2015, PloS one.

Serotonin transporter polymorphism and borderline or antisocial traits among low-income young adults

D. Pauls, Z. Rónai, B. Holmes, 2007, Psychiatric genetics.

Association of purinergic receptor P2RX7 gene polymorphisms with depression symptoms

A. Székely, A. Somogyi, Z. Nemoda, 2019, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Association analysis of norepinephrine transporter polymorphisms and methylphenidate response in ADHD patients

Z. Tarnok, Z. Nemoda, K. Lakatos, 2018, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Association of the tumor necrosis factor ‐308 A/G promoter polymorphism with Tourette syndrome

G. Keszler, Z. Tarnok, Z. Nemoda, 2014, International journal of immunogenetics.

Association between dopaminergic polymorphisms and borderline personality traits among at-risk young adults and psychiatric inpatients

A. Székely, K. Lyons-Ruth, Z. Nemoda, 2010, Behavioral and Brain Functions.

Ankyrin-3 as a molecular marker of early-life stress and vulnerability to psychiatric disorders

M. Rietschel, M. Szyf, G. Blasi, 2016, Translational psychiatry.

Analysis of a polymorphic microRNA target site in the purinergic receptor P2RX7 gene

A. Székely, A. Guttman, Z. Nemoda, 2010, Electrophoresis.

Epigenetic Changes of FKBP5 as a Link Connecting Genetic and Environmental Risk Factors with Structural and Functional Brain Changes in Major Depression

L. Tozzi, M. Szyf, T. Frodl, 2018, Neuropsychopharmacology.

Rapid and sensitive genotyping of dopamine D4 receptor tandem repeats by automated ultrathin‐layer gel electrophoresis

Z. Rónai, A. Guttman, Z. Nemoda, 2000, Electrophoresis.

Genome-wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

H. Stefánsson, B. Leventhal, W. McMahon, 2023, Biological Psychiatry.

Genome-wide Association Study identifies two novel loci for Gilles de la Tourette Syndrome

H. Stefánsson, J. Stamatoyannopoulos, Y. Worbe, 2021, medRxiv.

Alterations in DNA Methylation and Hydroxymethylation Due to Parental Care in Rhesus Macaques

S. Suomi, Z. Nemoda, R. Massart, 2016 .

Epigenetic Alterations and Prenatal Maternal Depression

M. Szyf, Z. Nemoda, 2017, Birth defects research.

Infant genotype may moderate sensitivity to maternal affective communications: Attachment disorganization, quality of care, and the DRD4 polymorphism

Z. Rónai, K. Lyons-Ruth, J. Bureau, 2007, Social neuroscience.

Carboxylesterase 1 gene polymorphism and methylphenidate response in ADHD

J. Gádoros, Z. Tarnok, Z. Nemoda, 2009, Neuropharmacology.

The Signature of Maternal Social Rank in Placenta Deoxyribonucleic Acid Methylation Profiles in Rhesus Monkeys.

M. Szyf, S. Suomi, A. Dettmer, 2017, Child development.

The Use of Saliva for Genetic and Epigenetic Research

Z. Nemoda, 2020 .

Serotonin transporter gene promoter methylation in peripheral cells in healthy adults: Neural correlates and tissue specificity

M. Szyf, L. Booij, R. Tremblay, 2017, European Neuropsychopharmacology.

Maternal depression is associated with DNA methylation changes in cord blood T lymphocytes and adult hippocampi

M. Szyf, M. Hallett, G. Turecki, 2015, Translational Psychiatry.

Dopamine D4 receptor and serotonin transporter gene effects on the longitudinal development of infant temperament

Mark H. Johnson, M. H. Johnson, K. Holmboe, 2011, Genes, brain, and behavior.

Catechol‐O‐methyltransferase Val158Met polymorphism is associated with methylphenidate response in ADHD children

J. Gádoros, Z. Tarnok, Z. Nemoda, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Association between the 120‐bp duplication of the dopamine D4 receptor gene and attention deficit hyperactivity disorder: Genetic and molecular analyses

J. Gádoros, Z. Tarnok, Z. Nemoda, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Linkage analysis and molecular haplotyping of the dopamine D4 receptor gene promoter region

Z. Rónai, Z. Nemoda, E. Szántai, 2005, Psychiatric genetics.

Association between Novelty Seeking and the −521 C/T polymorphism in the promoter region of the DRD4 gene

Z. Rónai, A. Székely, Z. Nemoda, 2001, Molecular Psychiatry.

Dopaminergic candidate genes in Tourette syndrome: Association between tic severity and 3′ UTR polymorphism of the dopamine transporter gene

J. Gádoros, Z. Rónai, Z. Tarnok, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Dopamine D4 receptor (DRD4) gene polymorphism is associated with attachment disorganization in infants

Z. Nemoda, J. Gervai, K. Lakatos, 2000, Molecular Psychiatry.

Association between dopamine D4 receptor (DRD4) gene polymorphisms and novelty-elicited auditory event-related potentials in preschool children

I. Winkler, J. Horváth, Z. Nemoda, 2006, Brain Research.

Transmission disequilibrium tests confirm the link between DRD4 gene polymorphism and infant attachment

Z. Rónai, Z. Nemoda, J. Gervai, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A novel A/G SNP in the −615th position of the dopamine D4 receptor promoter region as a source of misgenotyping of the −616 C/G SNP

Z. Rónai, A. Székely, R. Szmola, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic factors of reaction time performance: DRD4 7‐repeat allele associated with slower responses

D. Balota, J. Duchek, A. Székely, 2011, Genes, brain, and behavior.

Human personality dimensions of persistence and harm avoidance associated with DRD4 and 5‐HTTLPR polymorphisms

Z. Rónai, A. Székely, Z. Nemoda, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Additive effects of serotonergic and dopaminergic polymorphisms on trait impulsivity

Peter Antal, Peter Sarkozy, Zsolt Demetrovics, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A loss of function polymorphism (G191R) of anionic trypsinogen (PRSS2) confers protection against chronic pancreatitis.

T. Molnár, J. Drenth, J. Jansen, 2008, Pancreas.

Assessing genetic polymorphisms using DNA extracted from cells present in saliva samples

D. Granger, C. Fortunato, E. Beltzer, 2011, BMC medical research methodology.

Early life adversity alters normal sex-dependent developmental dynamics of DNA methylation

M. Szyf, S. Suomi, A. Dettmer, 2016, Development and Psychopathology.

Analysis of dopamine D4 receptor gene polymorphism using microchip electrophoresis.

Z. Rónai, A. Székely, A. Guttman, 2001, Journal of Chromatography A.

Attachment and temperament revisited: infant distress, attachment disorganisation and the serotonin transporter polymorphism

K. Lyons-Ruth, J. Bureau, Z. Nemoda, 2016, Journal of reproductive and infant psychology.

Peripheral DNA methylation of HPA axis-related genes in humans: Cross-tissue convergence, two-year stability and behavioural and neural correlates

M. Szyf, L. Booij, R. Tremblay, 2018, Psychoneuroendocrinology.

Associations between depression severity and purinergic receptor P2RX7 gene polymorphisms.

A. Székely, X. Gonda, P. Dome, 2013, Journal of affective disorders.

Differential Genetic Effect of the Norepinephrine Transporter Promoter Polymorphisms on Attention Problems in Clinical and Non-clinical Samples

Z. Tarnok, Z. Nemoda, E. Birkás, 2019, Front. Neurosci..

A pilot study of early onset obsessive-compulsive disorder: Symptom dimensions and association analysis with polymorphisms of the serotonin transporter gene

Z. Nemoda, K. Lakatos, M. Sasvári‐Székely, 2018, Psychiatry Research.

The domain-variant indirect association between electrophysiological response to reward and ADHD presentations is moderated by dopaminergic polymorphisms.

I. Ulbert, J. Réthelyi, R. Fiáth, 2023, Comprehensive psychiatry.

[Modeling neurological and psychiatric disorders in vitro using induced pluripotent stem cells: highlighting findings in Alzheimer's disease and schizophrenia].

J. Réthelyi, Á. Apáti, Z. Nemoda, 2016, Neuropsychopharmacologia Hungarica.

Association between depression and the Gln460Arg polymorphism of P2RX7 Gene: A dimensional approach

A. Székely, Z. Nemoda, G. Faludi, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

P2RX7 Gln460Arg polymorphism is associated with depression among diabetic patients

Z. Rónai, T. Varga, A. Somogyi, 2008, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Differential neurocognitive profiles in adult attention-deficit/hyperactivity disorder subtypes revealed by the Cambridge Neuropsychological Test Automated Battery.

S. Bálint, T. Kilencz, A. Pulay, 2023, European archives of psychiatry and clinical neuroscience.

[Analysis of the dopamine D4 receptor gene variants in attention deficit hyperactivity disorder].

J. Gádoros, Z. Tarnok, Z. Nemoda, 2007, Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology.

High‐throughput genotyping of repeat polymorphism in the regulatory region of serotonin transporter gene by gel microchip electrophoresis

Z. Rónai, A. Székely, A. Guttman, 2001, Electrophoresis.

MicroRNA-Mediated Suppression of Glial Cell Line-Derived Neurotrophic Factor Expression Is Modulated by a Schizophrenia-Associated Non-Coding Polymorphism

G. Keszler, Z. Rónai, Z. Nemoda, 2024, International journal of molecular sciences.

Polymorphisms in dopamine system genes are associated with individual differences in attention in infancy.

G. Csibra, Z. Nemoda, Karla Holmboe, 2010, Developmental psychology.

Psychometric properties of the Hungarian childhood trauma questionnaire short form and its validity in patients with adult attention-deficit hyperactivity disorder or borderline personality disorder

Z. Unoka, B. Czéh, Z. Nemoda, 2023, Borderline Personality Disorder and Emotion Dysregulation.

Direct haplotype detection of adjacent polymorphic sites in the regulatory region of the dopamine D4 receptor (DRD4) gene

Z. Rónai, A. Guttman, Z. Nemoda, 2002, Electrophoresis.