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 | 1083 | 2019 |
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 | 284 | 2019 |
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 | 242 | 2014 |
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 | 210 | 2014 |
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 | 203 | 2013 |
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 | 179 | 2017 |
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 | 167 | 2012 |
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 | 121 | 2018 |
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 | 119 | 2013 |
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 | 118 | 2007 |
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 | 93 | 2013 |
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 | 84 | 2010 |
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 | 83 | 2014 |
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 | 82 | 2012 |
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 | 80 | 2013 |
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 | 73 | 2014 |
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 | 70 | 2010 |
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 | 70 | 1999 |
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 | 67 | 2020 |
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 | 66 | 2002 |