Follow
Csaba Barta, MD, PhD
Csaba Barta, MD, PhD
Associate Professor, Semmelweis University
Verified email at med.semmelweis-univ.hu
Title
Cited by
Cited by
Year
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
10272019
Interrogating the genetic determinants of Tourette’s syndrome and other tic disorders through genome-wide association studies
D Yu, JH Sul, F Tsetsos, MS Nawaz, AY Huang, I Zelaya, C Illmann, ...
American Journal of Psychiatry 176 (3), 217-227, 2019
2542019
Variability in the prevalence of adult ADHD in treatment seeking substance use disorder patients: results from an international multi-center study exploring DSM-IV and DSM-5 …
G van de Glind, M Konstenius, MWJ Koeter, ...
Drug and alcohol dependence 134, 158-166, 2014
2342014
Psychiatric comorbidity in treatment‐seeking substance use disorder patients with and without attention deficit hyperactivity disorder: results of the IASP study
K van Emmerik‐van Oortmerssen, G van de Glind, MWJ Koeter, S Allsop, ...
Addiction 109 (2), 262-272, 2014
2072014
Validity of the Adult ADHD Self-Report Scale (ASRS) as a screener for adult ADHD in treatment seeking substance use disorder patients
G Van de Glind, W van den Brink, MWJ Koeter, PJ Carpentier, ...
Drug and alcohol dependence 132 (3), 587-596, 2013
1982013
Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome
AY Huang, D Yu, LK Davis, JH Sul, F Tsetsos, V Ramensky, I Zelaya, ...
Neuron 94 (6), 1101-1111. e7, 2017
1722017
A global view of the OCA2-HERC2 region and pigmentation
MP Donnelly, P Paschou, E Grigorenko, D Gurwitz, C Barta, RB Lu, ...
Human genetics 131, 683-696, 2012
1632012
Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families
I Karagiannidis, S Dehning, P Sandor, Z Tarnok, R Rizzo, T Wolanczyk, ...
Journal of medical genetics 50 (11), 760-764, 2013
1182013
Geographically separate increases in the frequency of the derived ADH1B* 47His allele in eastern and western Asia
H Li, N Mukherjee, U Soundararajan, Z Tárnok, C Barta, S Khaliq, ...
The American Journal of Human Genetics 81 (4), 842-846, 2007
1182007
De novo sequence and copy number variants are strongly associated with tourette disorder and implicate cell polarity in pathogenesis
S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ...
Cell reports 24 (13), 3441-3454. e12, 2018
1162018
Multivariate analysis of dopaminergic gene variants as risk factors of heroin dependence
A Vereczkei, Z Demetrovics, A Szekely, P Sarkozy, P Antal, A Szilagyi, ...
PLoS One 8 (6), e66592, 2013
912013
The genetics of problem and pathological gambling: a systematic review
Á Gyollai, M D Griffiths, C Barta, A Vereczkei, R Urbán, B Kun, G Kokonyei, ...
Current pharmaceutical design 20 (25), 3993-3999, 2014
822014
The distribution and most recent common ancestor of the 17q21 inversion in humans
MP Donnelly, P Paschou, E Grigorenko, D Gurwitz, SQ Mehdi, ...
The American Journal of Human Genetics 86 (2), 161-171, 2010
822010
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families
I Karagiannidis, R Rizzo, Z Tarnok, T Wolanczyk, J Hebebrand, ...
Molecular psychiatry 17 (7), 665-668, 2012
812012
The International ADHD in Substance Use Disorders Prevalence (IASP) study: background, methods and study population
G Van De Glind, K Van Emmerik‐van Oortmerssen, PJ Carpentier, ...
International journal of methods in psychiatric research 22 (3), 232-244, 2013
772013
Genetic association signal near NTN4 in Tourette syndrome
P Paschou, D Yu, G Gerber, P Evans, F Tsetsos, LK Davis, I Karagiannidis, ...
Annals of neurology 76 (2), 310-315, 2014
712014
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase
N Mukherjee, KK Kidd, AJ Pakstis, WC Speed, H Li, Z Tarnok, C Barta, ...
Molecular psychiatry 15 (2), 216-225, 2010
702010
Screening for mutations of 21-hydroxylase gene in Hungarian patients with congenital adrenal hyperplasia
A Ferenczi, M Garami, E Kiss, M Pék, M Sasvári-Székely, C Barta, ...
The Journal of Clinical Endocrinology & Metabolism 84 (7), 2369-2372, 1999
691999
Hormonal evaluation and mutation screening for steroid 21-hydroxylase deficiency in patients with unilateral and bilateral adrenal incidentalomas
A Patócs, M Tóth, C Barta, M Sasvári-Székely, I Varga, N Szücs, C Jakab, ...
European journal of endocrinology 147 (3), 349-355, 2002
662002
Co-occurrences of substance use and other potentially addictive behaviors: Epidemiological results from the Psychological and Genetic Factors of the Addictive Behaviors (PGA) Study
E Kotyuk, A Magi, A Eisinger, O Király, A Vereczkei, C Barta, MD Griffiths, ...
Journal of Behavioral Addictions 9 (2), 272-288, 2020
642020
The system can't perform the operation now. Try again later.
Articles 1–20