Klaus-Peter Lesch
Klaus-Peter Lesch
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Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region
KP Lesch, D Bengel, A Heils, SZ Sabol, BD Greenberg, S Petri, ...
Science 274 (5292), 1527-1531, 1996
Allelic variation of human serotonin transporter gene expression
A Heils, A Teufel, S Petri, G Stöber, P Riederer, D Bengel, KP Lesch
Journal of neurochemistry 66 (6), 2621-2624, 1996
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63-75, 2019
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Long story short: the serotonin transporter in emotion regulation and social cognition
T Canli, KP Lesch
Nature neuroscience 10 (9), 1103-1109, 2007
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
Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysis
M Hoogman, J Bralten, DP Hibar, M Mennes, MP Zwiers, LSJ Schweren, ...
The Lancet Psychiatry 4 (4), 310-319, 2017
A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders.
DA Collier, G Stöber, T Li, A Heils, M Catalano, D Di Bella, MJ Arranz, ...
Molecular psychiatry 1 (6), 453-460, 1996
Early experience and serotonin transporter gene variation interact to influence primate CNS function
AJ Bennett, KP Lesch, A Heils, JC Long, JG Lorenz, SE Shoaf, ...
Molecular psychiatry 7 (1), 118-122, 2002
Organization of the human serotonin transporter gene
KP Lesch, U Balling, J Gross, K Strauss, BL Wolozin, DL Murphy, ...
Journal of Neural Transmission/General Section JNT 95, 157-162, 1994
Altered brain serotonin homeostasis and locomotor insensitivity to 3, 4-methylenedioxymethamphetamine (“Ecstasy”) in serotonin transporter-deficient mice
D Bengel, DL Murphy, AM Andrews, CH Wichems, D Feltner, A Heils, ...
Molecular pharmacology 53 (4), 649-655, 1998
Neural stem cell proliferation is decreased in schizophrenia, but not in depression
A Reif, S Fritzen, M Finger, A Strobel, M Lauer, A Schmitt, KP Lesch
Molecular psychiatry 11 (5), 514-522, 2006
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder
J Deckert, M Catalano, YV Syagailo, M Bosi, O Okladnova, D Di Bella, ...
Human molecular genetics 8 (4), 621-624, 1999
International Union of Pharmacology. XXX. Update on chemokine receptor nomenclature
PM Murphy
Pharmacological reviews 54 (2), 227-229, 2002
Primary structure of the human platelet serotonin uptake site: identity with the brain serotonin transporter
KP Lesch, BL Wolozin, DL Murphy, P Riederer
Journal of neurochemistry 60 (6), 2319-2322, 1993
Simultaneous genotyping of four functional loci of human SLC6A4, with a reappraisal of 5-HTTLPR and rs25531
JR Wendland, BJ Martin, MR Kruse, KP Lesch, DL Murphy
Molecular psychiatry 11 (3), 224-226, 2006
Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan
B Franke, G Michelini, P Asherson, T Banaschewski, A Bilbow, ...
European Neuropsychopharmacology 28 (10), 1059-1088, 2018
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder
BM Neale, SE Medland, S Ripke, P Asherson, B Franke, KP Lesch, ...
Journal of the American Academy of Child & Adolescent Psychiatry 49 (9), 884-897, 2010
Serotonin transporter: gene, genetic disorders, and pharmacogenetics
DL Murphy, A Lerner, G Rudnick, KP Lesch
Molecular interventions 4 (2), 109, 2004
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