Wissenschaftliche Tätigkeiten

 

Neben meiner psychotherapeutischen Tätigkeit war ich von 2008 bis 2016 als wissenschaftlicher Mitarbeiter an der Klinik für Psychiatrie und Psychotherapie der Universität Bonn angestellt. Dort habe ich zu den neurobiologischen und molekulargenetischen Grundlagen psychischer Störungen geforscht. Mein Forschungsinteresse richtete sich dabei auf die Bereiche Zwangsstörungen, Depression und Schizophrenie.

 

Publikationsverzeichnis

Leonhard Lennertz (2013). Die Serotoninhypothese der Zwangsstörung. Assoziation genetischer Varianten des serotonergen Systems mit der Zwangsstörung und kognitiven Endophänotypen. Dissertation. Universität Bonn: Bonn.

 

Leonhard Lennertz (2008). Die erinnerte elterliche Erziehung von Patienten mit Zwangsstörungen. Ergebnisse einer Familienstudie. Unveröffentlichte Diplomarbeit. Universität Bonn: Bonn.

 

The polygenic risk for obsessive-compulsive disorder is associated with the personality trait harm avoidance.

Bey K, Weinhold L, Grützmann R, Heinzel S, Kaufmann C, Klawohn J, Riesel A, Lennertz L, Schmid M, Ramirez A, Kathmann N, Wagner M. Acta Psychiatr Scand. 2020 Aug 12. doi: 10.1111/acps.13226.

 

The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia.

Richards AL, Pardiñas AF, Frizzati A, Tansey KE, Lynham AJ, Holmans P, Legge SE, Savage JE, Agartz I, Andreassen OA, Blokland GAM, Corvin A, Cosgrove D, Degenhardt F, Djurovic S, Espeseth T, Ferraro L, Gayer-Anderson C, Giegling I, van Haren NE, Hartmann AM, Hubert JJ, Jönsson EG, Konte B, Lennertz L, Olde Loohuis LM, Melle I, Morgan C, Morris DW, Murray RM, Nyman H, Ophoff RA; GROUP Investigators, van Os J; EUGEI WP2 Group; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Petryshen TL, Quattrone D, Rietschel M, Rujescu D, Rutten BPF, Streit F, Strohmaier J, Sullivan PF, Sundet K, Wagner M, Escott-Price V, Owen MJ, Donohoe G, O'Donovan MC, Walters JTR.

Schizophr Bull. 2020 Feb 26;46(2):336-344. doi: 10.1093/schbul/sbz0

 

Error-related brain activity as a transdiagnostic endophenotype for obsessive-compulsive disorder, anxiety and substance use disorder.

Riesel A, Klawohn J, Grützmann R, Kaufmann C, Heinzel S, Bey K, Lennertz L, Wagner M, Kathmann N.

Psychol Med. 2019 May;49(7):1207-1217. doi: 10.1017/S0033291719000199. Epub 2019 Feb 12.

 

Impaired Antisaccades in Obsessive-Compulsive Disorder: Evidence From Meta-Analysis and a Large Empirical Study.

Bey K, Lennertz L, Grützmann R, Heinzel S, Kaufmann C, Klawohn J, Riesel A, Meyhöfer I, Ettinger U, Kathmann N, Wagner M.

Front Psychiatry. 2018 Jun 29;9:284. doi: 10.3389/fpsyt.2018.00284. eCollection 2018.

 

Impaired planning in patients with obsessive-compulsive disorder and unaffected first-degree relatives: Evidence for a cognitive endophenotype.

Bey K, Kaufmann C, Lennertz L, Riesel A, Klawohn J, Heinzel S, Grützmann R, Kathmann N, Wagner M.

J Anxiety Disord. 2018 Jun;57:24-30. doi: 10.1016/j.janxdis.2018.05.009. Epub 2018 Jun 1.

 

Schizotypy and smooth pursuit eye movements as potential endophenotypes of obsessive-compulsive disorder.

Bey K, Meyhöfer I, Lennertz L, Grützmann R, Heinzel S, Kaufmann C, Klawohn J, Riesel A, Ettinger U, Kathmann N, Wagner M.

Eur Arch Psychiatry Clin Neurosci. 2019 Mar;269(2):235-243. doi: 10.1007/s00406-018-0899-x. Epub 2018 May 2.

 

Neural correlates of working memory deficits and associations to response inhibition in obsessive compulsive disorder.

Heinzel S, Kaufmann C, Grützmann R, Hummel R, Klawohn J, Riesel A, Bey K, Lennertz L, Wagner M, Kathmann N.

Neuroimage Clin. 2017 Nov 3;17:426-434. doi: 10.1016/j.nicl.2017.10.039. eCollection 2018.

 

Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis.

International Obsessive Compulsive Disorder Foundation Genetics Collaborative (IOCDF-GC) and OCD Collaborative Genetics Association Studies (OCGAS).

Mol Psychiatry. 2018 May;23(5):1181-1188. doi: 10.1038/mp.2017.154. Epub 2017 Aug 1.

 

Frontal alpha asymmetry in OCD patients and unaffected first-degree relatives.

Grützmann R, Riesel A, Klawohn J, Heinzel S, Kaufmann C, Bey K, Lennertz L, Wagner M, Kathmann N.

J Abnorm Psychol. 2017 Aug;126(6):750-760. doi: 10.1037/abn0000283. Epub 2017 May 25.

 

Volitional saccade performance in a large sample of patients with obsessive-compulsive disorder and unaffected first-degree relatives.

Bey K, Kloft L, Lennertz L, Grützmann R, Heinzel S, Kaufmann C, Klawohn J, Riesel A, Meyhöfer I, Kathmann N, Wagner M.

Psychophysiology. 2017 Sep;54(9):1284-1294. doi: 10.1111/psyp.12884. Epub 2017 May 8.

 

Harm avoidance and childhood adversities in patients with obsessive-compulsive disorder and their unaffected first-degree relatives.

Bey K, Lennertz L, Riesel A, Klawohn J, Kaufmann C, Heinzel S, Grützmann R, Kathmann N, Wagner M.

Acta Psychiatr Scand. 2017 Apr;135(4):328-338. doi: 10.1111/acps.12707. Epub 2017 Feb 3.

 

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.

Degenhardt F, Heinemann B, Strohmaier J, Pfohl MA, Giegling I, Hofmann A, Ludwig KU, Witt SH, Ludwig M, Forstner AJ, Albus M, Schwab SG, Borrmann-Hassenbach M, Lennertz L, Wagner M, Hoffmann P, Rujescu D, Maier W, Cichon S, Rietschel M, Nöthen MM.

Psychiatr Genet. 2016 Dec;26(6):293-296.

 

Neurocognitive functioning in parents of schizophrenia patients: Attentional and executive performance vary with genetic loading.

Schulze-Rauschenbach S, Lennertz L, Ruhrmann S, Petrovsky N, Ettinger U, Pukrop R, Dreher J, Klosterkötter J, Maier W, Wagner M.Psychiatry Res. 2015 Dec 30;230(3):885-91. doi: 10.1016/j.psychres.2015.11.031. Epub 2015 Nov 19.

 

Replication of the association between CHRNA4 rs1044396 and harm avoidance in a large population-based sample.

Bey K, Lennertz L, Markett S, Petrovsky N, Gallinat J, Gründer G, Spreckelmeyer KN, Wienker TF, Mobascher A, Dahmen N, Thuerauf N, Kornhuber J, Kiefer F, Toliat MR, Nürnberg P, Winterer G, Wagner M.

Eur Neuropsychopharmacol. 2016 Jan;26(1):150-155. doi: 10.1016/j.euroneuro.2015.11.007. Epub 2015 Nov 14.

 

Smaller than expected cognitive deficits in schizophrenia patients from the population-representative ABC catchment cohort.

Lennertz L, An der Heiden W, Kronacher R, Schulze-Rauschenbach S, Maier W, Häfner H, Wagner M.

Eur Arch Psychiatry Clin Neurosci. 2016 Aug;266(5):423-31. doi: 10.1007/s00406-015-0625-x. Epub 2015 Aug 2.

 

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, Illmann C, McGrath LM, Mayerfeld C, Arepalli S, Barlassina C, Barr CL, Bellodi L, Benarroch F, Berrió GB, Bienvenu OJ, Black DW, Bloch MH, Brentani H, Bruun RD, Budman CL, Camarena B, Campbell DD, Cappi C, Silgado JC, Cavallini MC, Chavira DA, Chouinard S, Cook EH, Cookson MR, Coric V, Cullen B, Cusi D, Delorme R, Denys D, Dion Y, Eapen V, Egberts K, Falkai P, Fernandez T, Fournier E, Garrido H, Geller D, Gilbert DL, Girard SL, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Grünblatt E, Hardy J, Heiman GA, Hemmings SM, Herrera LD, Hezel DM, Hoekstra PJ, Jankovic J, Kennedy JL, King RA, Konkashbaev AI, Kremeyer B, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Liu C, Lochner C, Lowe TL, Lupoli S, Macciardi F, Maier W, Manunta P, Marconi M, McCracken JT, Mesa Restrepo SC, Moessner R, Moorjani P, Morgan J, Muller H, Murphy DL, Naarden AL, Nurmi E, Ochoa WC, Ophoff RA, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Rauch SL, Renner T, Reus VI, Richter MA, Riddle MA, Robertson MM, Romero R, Rosário MC, Rosenberg D, Ruhrmann S, Sabatti C, Salvi E, Sampaio AS, Samuels J, Sandor P, Service SK, Sheppard B, Singer HS, Smit JH, Stein DJ, Strengman E, Tischfield JA, Turiel M, Valencia Duarte AV, Vallada H, Veenstra-VanderWeele J, Walitza S, Wang Y, Weale M, Weiss R, Wendland JR, Westenberg HG, Shugart YY, Hounie AG, Miguel EC, Nicolini H, Wagner M, Ruiz-Linares A, Cath DC, McMahon W, Posthuma D, Oostra BA, Nestadt G, Rouleau GA, Purcell S, Jenike MA, Heutink P, Hanna GL, Conti DV, Arnold PD, Freimer NB, Stewart SE, Knowles JA, Cox NJ, Pauls DL.

Am J Psychiatry. 2015 Jan;172(1):82-93. doi: 10.1176/appi.ajp.2014.13101306. Epub 2014 Oct 31.

 

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.

McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, Gallagher P, Fagerness JA, Barr CL, Bellodi L, Benarroch F, Bienvenu OJ, Black DW, Bloch MH, Bruun RD, Budman CL, Camarena B, Cath DC, Cavallini MC, Chouinard S, Coric V, Cullen B, Delorme R, Denys D, Derks EM, Dion Y, Rosário MC, Eapen V, Evans P, Falkai P, Fernandez TV, Garrido H, Geller D, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Grünblatt E, Heiman GA, Hemmings SM, Herrera LD, Hounie AG, Jankovic J, Kennedy JL, King RA, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Lochner C, Lowe TL, Lyon GJ, Macciardi F, Maier W, McCracken JT, McMahon W, Murphy DL, Naarden AL, Neale BM, Nurmi E, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Reus VI, Richter MA, Riddle M, Robertson MM, Rosenberg D, Rouleau GA, Ruhrmann S, Sampaio AS, Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Tischfield JA, Vallada H, Veenstra-VanderWeele J, Walitza S, Wang Y, Wendland JR, Shugart YY, Miguel EC, Nicolini H, Oostra BA, Moessner R, Wagner M, Ruiz-Linares A, Heutink P, Nestadt G, Freimer N, Petryshen T, Posthuma D, Jenike MA, Cox NJ, Hanna GL, Brentani H, Scherer SW, Arnold PD, Stewart SE, Mathews CA, Knowles JA, Cook EH, Pauls DL, Wang K, Scharf JM.

J Am Acad Child Adolesc Psychiatry. 2014 Aug;53(8):910-9. doi: 10.1016/j.jaac.2014.04.022. Epub 2014 Jun 24.

 

Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, Bloch MH, Blom RM, Bruun RD, Budman CL, Camarena B, Campbell D, Cappi C, Cardona Silgado JC, Cath DC, Cavallini MC, Chavira DA, Chouinard S, Conti DV, Cook EH, Coric V, Cullen BA, Deforce D, Delorme R, Dion Y, Edlund CK, Egberts K, Falkai P, Fernandez TV, Gallagher PJ, Garrido H, Geller D, Girard SL, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Haddad S, Heiman GA, Hemmings SM, Hounie AG, Illmann C, Jankovic J, Jenike MA, Kennedy JL, King RA, Kremeyer B, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Liu C, Lochner C, Lowe TL, Macciardi F, McCracken JT, McGrath LM, Mesa Restrepo SC, Moessner R, Morgan J, Muller H, Murphy DL, Naarden AL, Ochoa WC, Ophoff RA, Osiecki L, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Rauch SL, Renner TJ, Reus VI, Richter MA, Riddle MA, Robertson MM, Romero R, Rosàrio MC, Rosenberg D, Rouleau GA, Ruhrmann S, Ruiz-Linares A, Sampaio AS, Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Strengman E, Tischfield JA, Valencia Duarte AV, Vallada H, Van Nieuwerburgh F, Veenstra-Vanderweele J, Walitza S, Wang Y, Wendland JR, Westenberg HG, Shugart YY, Miguel EC, McMahon W, Wagner M, Nicolini H, Posthuma D, Hanna GL, Heutink P, Denys D, Arnold PD, Oostra BA, Nestadt G, Freimer NB, Pauls DL, Wray NR, Stewart SE, Mathews CA, Knowles JA, Cox NJ, Scharf JM.
PLoS Genet. 2013 Oct;9(10):e1003864. doi: 10.1371/journal.pgen.1003864. Epub 2013 Oct 24.

 

Characterization of SLITRK1 variation in obsessive-compulsive disorder.
Ozomaro U, Cai G, Kajiwara Y, Yoon S, Makarov V, Delorme R, Betancur C, Ruhrmann S, Falkai P, Grabe HJ, Maier W, Wagner M, Lennertz L, Moessner R, Murphy DL, Buxbaum JD, Züchner S, Grice DE.

PLoS One. 2013 Aug 21;8(8):e70376. doi: 10.1371/journal.pone.0070376. eCollection 2013.

 

5-HT3 receptor influences the washing phenotype and visual organization in obsessive-compulsive disorder supporting 5-HT3 receptor antagonists as novel treatment option.
Lennertz L, Wagner M, Grabe HJ, Franke PE, Guttenthaler V, Rampacher F, Schulze-Rauschenbach S, Vogeley A, Benninghoff J, Ruhrmann S, Pukrop R, Klosterkötter J, Falkai P, Maier W, Mössner R.

Eur Neuropsychopharmacol. 2014 Jan;24(1):86-94. doi: 10.1016/j.euroneuro.2013.07.003. Epub 2013 Aug 6.

 

The functional coding variant Asn107Ile of the neuropeptide S receptor gene (NPSR1) influences age at onset of obsessive-compulsive disorder.
Lennertz L, Franke PE, Grabe HJ, Rampacher F, Schulze-Rauschenbach S, Guttenthaler V, Ruhrmann S, Pukrop R, Klosterkötter J, Falkai P, Maier W, Wagner M, Mössner R.
Int J Neuropsychopharmacol. 2013 Oct;16(9):1951-8. doi: 10.1017/S1461145713000382. Epub 2013 May 17.

 

Nicotine enhances antisaccade performance in schizophrenia patients and healthy controls.
Petrovsky N, Ettinger U, Quednow BB, Landsberg MW, Drees J, Lennertz L, Frommann I, Heilmann K, Sträter B, Kessler H, Dahmen N, Mössner R, Maier W, Wagner M.
Int J Neuropsychopharmacol. 2013 Aug;16(7):1473-81. doi: 10.1017/S1461145713000011. Epub 2013 Feb 11.

 

[Serotonin transporter gene and stress reactivity in unipolar depression : Role of the HPA system as endophenotype of the SLC6A4 gene.]
Welper H, Aller A, Guttenthaler V, Höfels S, Lennertz L, Pfeiffer U, Schwab SG, Zobel A.
Nervenarzt.
2013 Jan 18. [Epub ahead of print] German.

 

Genome-wide association study of obsessive-compulsive disorder.
Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Davis LK, Osiecki L, McGrath L, Haddad S, Crane J, Hezel D, Illman C, Mayerfeld C, Konkashbaev A, Liu C, Pluzhnikov A, Tikhomirov A, Edlund CK, Rauch SL, Moessner R, Falkai P, Maier W, Ruhrmann S, Grabe HJ, Lennertz L, Wagner M, Bellodi L, Cavallini MC, Richter MA, Cook EH Jr, Kennedy JL, Rosenberg D, Stein DJ, Hemmings SM, Lochner C, Azzam A, Chavira DA, Fournier E, Garrido H, Sheppard B, Umaña P, Murphy DL, Wendland JR, Veenstra-VanderWeele J, Denys D, Blom R, Deforce D, Van Nieuwerburgh F, Westenberg HG, Walitza S, Egberts K, Renner T, Miguel EC, Cappi C, Hounie AG, Conceição do Rosário M, Sampaio AS, Vallada H, Nicolini H, Lanzagorta N, Camarena B, Delorme R, Leboyer M, Pato CN, Pato MT, Voyiaziakis E, Heutink P, Cath DC, Posthuma D, Smit JH, Samuels J, Bienvenu OJ, Cullen B, Fyer AJ, Grados MA, Greenberg BD, McCracken JT, Riddle MA, Wang Y, Coric V, Leckman JF, Bloch M, Pittenger C, Eapen V, Black DW, Ophoff RA, Strengman E, Cusi D, Turiel M, Frau F, Macciardi F, Gibbs JR, Cookson MR, Singleton A; North American Brain Expression Consortium, Hardy J; UK Brain Expression Database, Crenshaw AT, Parkin MA, Mirel DB, Conti DV, Purcell S, Nestadt G, Hanna GL, Jenike MA, Knowles JA, Cox N, Pauls DL.
Mol Psychiatry. 2013 Jul;18(7):788-98. doi: 10.1038/mp.2012.85. Epub 2012 Aug 14. Erratum in: Mol Psychiatry. 2013 Jul;18(7):843. Davis, L K [added].

 

Association of amygdala volumes with cortisol secretion in unipolar depressed patients.
Schuhmacher A, Mössner R, Jessen F, Scheef L, Block W, Belloche AC, Lennertz L, Welper H, Höfels S, Pfeiffer U, Wagner M, Maier W, Schwab S, Zobel A.
Psychiatry Res. 2012 May 31;202(2):96-103. doi: 10.1016/j.pscychresns.2011.09.007. Epub 2012 Jun 13.

 

Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics.
Schuhmacher A, Becker T, Rujescu D, Quednow BB, Lennertz L, Wagner M, Benninghoff J, Rietschel M, Häfner H, Franke P, Wölwer W, Gaebel W, Maier W, Mössner R.
J Psychiatr Res. 2012 Aug;46(8):1073-80. doi: 10.1016/j.jpsychires.2012.04.021. Epub 2012 May 30.

 

A variant of the neuronal amino acid transporter SLC6A15 is associated with ACTH and cortisol responses and cognitive performance in unipolar depression.
Schuhmacher A, Lennertz L, Wagner M, Höfels S, Pfeiffer U, Guttenthaler V, Maier W, Zobel A, Mössner R.
Int J Neuropsychopharmacol. 2013 Feb;16(1):83-90. doi: 10.1017/S1461145712000223. Epub 2012 Apr 4.

 

Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating.
Quednow BB, Brinkmeyer J, Mobascher A, Nothnagel M, Musso F, Gründer G, Savary N, Petrovsky N, Frommann I, Lennertz L, Spreckelmeyer KN, Wienker TF, Dahmen N, Thuerauf N, Clepce M, Kiefer F, Majic T, Mössner R, Maier W, Gallinat J, Diaz-Lacava A, Toliat MR, Thiele H, Nürnberg P, Wagner M, Winterer G.
Proc Natl Acad Sci U S A. 2012 Apr 17;109(16):6271-6. doi: 10.1073/pnas.1118051109. Epub 2012 Mar 26.

 

Antisaccade performance in patients with obsessive-compulsive disorder and unaffected relatives: further evidence for impaired response inhibition as a candidate endophenotype.
Lennertz L, Rampacher F, Vogeley A, Schulze-Rauschenbach S, Pukrop R, Ruhrmann S, Klosterkötter J, Maier W, Falkai P, Wagner M.
Eur Arch Psychiatry Clin Neurosci. 2012 Oct;262(7):625-34. doi: 10.1007/s00406-012-0311-1. Epub 2012 Mar

 

The functional coding variant Asn107Ile of the neuropeptide S receptor gene (NPSR1) is associated with schizophrenia and modulates verbal memory and the acoustic startle response.
Lennertz L, Quednow BB, Schuhmacher A, Petrovsky N, Frommann I, Schulze-Rauschenbach S, Landsberg MW, Steinbrecher A, Höfels S, Pukrop R, Klosterkötter J, Franke PE, Wölwer W, Gaebel W, Häfner H, Maier W, Wagner M, Mössner R.
Int J Neuropsychopharmacol. 2012 Oct;15(9):1205-15. doi: 10.1017/S1461145711001623. Epub 2011 Nov 14.

 

Impact of TCF4 on the genetics of schizophrenia.
Lennertz L, Quednow BB, Benninghoff J, Wagner M, Maier W, Mössner R.
Eur Arch Psychiatry Clin Neurosci. 2011 Nov;261 Suppl 2:S161-5. doi: 10.1007/s00406-011-0256-9. Epub 2011 Sep 20. Review.

 

A promoter variant of SHANK1 affects auditory working memory in schizophrenia patients and in subjects clinically at risk for psychosis.
Lennertz L, Wagner M, Wölwer W, Schuhmacher A, Frommann I, Berning J, Schulze-Rauschenbach S, Landsberg MW, Steinbrecher A, Alexander M, Franke PE, Pukrop R, Ruhrmann S, Bechdolf A, Gaebel W, Klosterkötter J, Häfner H, Maier W, Mössner R.
Eur Arch Psychiatry Clin Neurosci. 2012 Mar;262(2):117-24. doi: 10.1007/s00406-011-0233-3. Epub 2011 Sep 7.

 

The schizophrenia risk gene ZNF804A influences the antipsychotic response of positive schizophrenia symptoms.
Mössner R, Schuhmacher A, Wagner M, Lennertz L, Steinbrecher A, Quednow BB, Rujescu D, Rietschel M, Maier W.
Eur Arch Psychiatry Clin Neurosci. 2012 Apr;262(3):193-7. doi: 10.1007/s00406-011-0235-1. Epub 2011 Sep 4.

 

Novel schizophrenia risk gene TCF4 influences verbal learning and memory functioning in schizophrenia patients.
Lennertz L, Rujescu D, Wagner M, Frommann I, Schulze-Rauschenbach S, Schuhmacher A, Landsberg MW, Franke P, Möller HJ, Wölwer W, Gaebel W, Häfner H, Maier W, Mössner R.
Neuropsychobiology. 2011;63(3):131-6. doi: 10.1159/000317844. Epub 2011 Jan 13.

 

Evidence for specific cognitive deficits in visual information processing in patients with OCD compared to patients with unipolar depression.
Rampacher F, Lennertz L, Vogeley A, Schulze-Rauschenbach S, Kathmann N, Falkai P, Wagner M.
Prog Neuropsychopharmacol Biol Psychiatry.
2010 Aug 16;34(6):984-91. doi: 10.1016/j.pnpbp.2010.05.008. Epub 2010 May 18.

 

A coding variant of the novel serotonin receptor subunit 5-HT3E influences sustained attention in schizophrenia patients.
Lennertz L, Wagner M, Frommann I, Schulze-Rauschenbach S, Schuhmacher A, Kühn KU, Pukrop R, Klosterkötter J, Wölwer W, Gaebel W, Rietschel M, Häfner H, Maier W, Mössner R.
Eur Neuropsychopharmacol.
2010 Jun;20(6):414-20. doi: 10.1016/j.euroneuro.2010.02.012. Epub 2010 Mar 30.

 

Perceived parental rearing in subjects with obsessive-compulsive disorder and their siblings.
Lennertz L, Grabe HJ, Ruhrmann S, Rampacher F, Vogeley A, Schulze-Rauschenbach S, Ettelt S, Meyer K, Kraft S, Reck C, Pukrop R, John U, Freyberger HJ, Klosterkötter J, Maier W, Falkai P, Wagner M.
Acta Psychiatr Scand.
2010 Apr;121(4):280-8. doi: 10.1111/j.1600-0447.2009.01469.x. Epub 2009 Aug 19.

 

Praxis für Psychotherapie

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50996 Köln

 

Katrin Lennertz

Diplom Psychologin

Psychologische Psychotherapeutin

praxis[at]psychotherapie-lennertz[dot]de

Tel.: 0221-98048348

 

Dr. phil. Leonhard Lennertz

Diplom Psychologe

Psychologischer Psychotherapeut

info[at]psychotherapie-lennertz[dot]de

Tel.: 0221-98048350