 Print previewpersonal data approved: 2023. III. 27. | Publications |
2020
 from data base, 2023. III. 27. |
Chiarella J., Schumann L., Pomares F.B., Frodl T., Tozzi L., Nemoda Z., Yu P., Szyf M., Khalid-Khan S., Booij L.: DNA methylation differences in stress-related genes, functional connectivity and gray matter volume in depressed and healthy adolescents, JOURNAL OF AFFECTIVE DISORDERS 271: pp. 160-168.
type of document: Journal paper/Article
number of independent citations: 5
language: English
URL |
2019
from data base, 2023. III. 27. |
Vereczkei Andrea, Abdul-Rahman Omar, Halmai Zsuzsa, Nagy Geza, Szekely Anna, Somogyi Aniko, Faludi Gabor, Nemoda Zsofia: Association of purinergic receptor P2RX7 gene polymorphisms with depression symptoms, PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY 92: pp. 207-216.
type of document: Journal paper/Article
number of independent citations: 18
language: English
URL |
2019
from data base, 2023. III. 27. |
Grünblatt E., Nemoda Z., Werling A.M., Roth A., Angyal N., Tarnok Z., Thomsen H., Peters T., Hinney A., Hebebrand J., Lesch K.-P., Romanos M., Walitza S.: The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis, AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 180: (6) pp. 365-376.
type of document: Journal paper/Article
number of independent citations: 7
language: English
URL |
2019
from data base, 2023. III. 27. |
Németh Csilla E., Nemoda Zsófia, Lőw Péter, Szabó Pál, Horváth Erzsébet Z., Willaert Andy, Boel Annekatrien, Callewaert Bert L., Coucke Paul J., Colombi Marina, Bánhegyi Gábor, Margittai Éva: Decreased Nuclear Ascorbate Accumulation Accompanied with Altered Genomic Methylation Pattern in Fibroblasts from Arterial Tortuosity Syndrome Patients, OXIDATIVE MEDICINE AND CELLULAR LONGEVITY 2019: 8156592
type of document: Journal paper/Article
number of independent citations: 2
language: English
URL |
2019
from data base, 2023. III. 27. |
Nemoda Zsofia, Angyal Nora, Tarnok Zsanett, Birkas Emma, Bognar Emese, Sasvari-Szekely Maria, Gervai Judit, Lakatos Krisztina: Differential genetic effect of the norepinephrine transporter promoter polymorphisms on attention problems in clinical and non-clinical samples, FRONTIERS IN NEUROSCIENCE 12: 1051
type of document: Journal paper/Article
number of independent citations: 1
language: English
URL |
2015
from data base, 2023. III. 27. |
Nemoda Z, Massart R, Suderman M, Hallett M, Li T, Coote M, Cody N, Sun ZS, Soares CN, Turecki G, Steiner M, Szyf M: Maternal depression is associated with DNA methylation changes in cord blood T lymphocytes and adult hippocampi, TRANSLATIONAL PSYCHIATRY 5: e545
type of document: Journal paper/Article
number of independent citations: 71
language: English
URL |
2010
from data base, 2023. III. 27. |
Nemoda Z, Lyons-Ruth K, Szekely A, Bertha E, Faludi G, Sasvari-Szekely M: Association between dopaminergic polymorphisms and borderline personality traits among at-risk young adults and psychiatric inpatients, BEHAVIORAL AND BRAIN FUNCTIONS 6: 4
type of document: Journal paper/Article
number of independent citations: 66
language: English
URL |
2009
from data base, 2023. III. 27. |
Nemoda Z, Angyal N, Tarnok Z, Gadoros J, Sasvari-Szekely M: Carboxylesterase 1 gene polymorphism and methylphenidate response in ADHD, NEUROPHARMACOLOGY 57: (7-8) pp. 731-733.
type of document:
number of independent citations: 76
language: English
URL |
2007
from data base, 2023. III. 27. |
Tarnok Z, Ronai Z, Gervai J, Kereszturi E, Gadoros J, Sasvari-Szekely M, Nemoda Z: Dopaminergic candidate genes in Tourette syndrome: association between tic severity and 3' UTR polymorphism of the dopamine transporter gene., AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 144B: (7) pp. 900-905.
type of document: Journal paper/Article
number of independent citations: 44
language: English
URL |
2002
from data base, 2023. III. 27. |
Lakatos K, Nemoda Z, Toth I, Ronai Z, Ney K, Sasvari-Szekely M, Gervai J: Further evidence for the role of the dopamine D4 receptor (DRD4) gene in attachment disorganisation: interaction of the exon III 48-bp repeat and the -521 C/T promoter polymorphisms, MOLECULAR PSYCHIATRY 7: (1) pp. 27-31.
type of document: Journal paper/Article
number of independent citations: 128
language: English
URL |
| | Number of independent citations to these publications: | 418 |
|
|
Login
puskin.sote.hu
