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Literaturliste von Prof. Dr. Jobst Meyer

letzte Aktualisierung: 16.02.2022

Kluwe-Schiavon, B., Schote, A. B., Vonmoos, M., Hulka, L. M., Preller, K. H., Meyer, J., Baumgartner, M. R., Grünblatt, E. & Quednow, B.B. (2020). Psychiatric symptoms and expression of glucocorticoid receptor gene in cocaine users: A longitudinal study. Journal of Psychiatric Research, 121, 126-134.

Li-Tempel, T., Suer, T., Tempel, T., Larra, M. F., Winnikes, U., Meyer, J. & Schote, A. B. (2019). Promoter haplotypes of the corticotropin-releasing hormone encoding gene modulate the physiological stress response in vitro and in vivo. Stress, 22(1), 44-52.

Schote, A. B., Jäger, K., Kroll, S. L., Vonmoos, M., Hulka, L. M., Preller, K. H., Meyer, J., Grünblatt, E. & Quednow, B. B. (2019). Glucocorticoid receptor gene variants and lower expression of NR3C1 are associated with cocaine use. Addiction Biology, 24(4), 730-742.

Schote, A. B., Sayk, C. A. L., Pabst, K., Meier, J. K., Frings, C. & Meyer, J. (2019). Sex, ADHD symptoms, and CHRNA5 genotype influence reaction time but not response inhibition. Journal of Neuroscience Research, 97(2), 215-224.

Waltes, R., Freitag, C. M., Herlt, T., Lempp, T., Seitz, C., Palmason, H., Meyer, J. & Chiocchetti, A. G. (2019). Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: An exploratory pilot study. Journal of Neural Transmission, 126, 1679-1693.

Yurtsever, T., Streit, F., Foo, J. C., Trifonova, S., Kumsta, R., Muller, C. P., Turner, J. D., Meyer, J. & Schote, A. B. (2019). Temporal dynamics of cortisol-associated changes in mRNA expression of glucocorticoid responsive genes FKBP5, GILZ, SDPR, PER1, PER2 and PER3 in healthy humans. Psychoneuroendocrinology, 102, 63-67.

Freilinger, P., Kliegel, D., Hänig, S., Oehl-Jaschkowitz, B., Henn, W. & Meyer, J. (2018). Behavioral and psychological features in girls and women with triple-X syndrome. The American Journal of Medical Genetics - Part A, 176(11), 2284-2291.

Tarragon, E., Stein, J. & Meyer, J. (2017). Psychometric properties of the German translated version and adaptation of the food craving inventory. Frontiers in Psychology (Online Journal), No. 736.

Breitenstein, B., Scheuer, S., Brückl, T. M., Meyer, J., Ising, M., Uhr, M. & Holsboer, F. (2016). Association of ABCB1 gene variants, plasma antidepressant concentration, and treatment response: Results from a randomized clinical study. Journal of Psychiatric Research, 73, 86-95.

Kranz, T. M., Kopp, M., Waltes, R., Sachse, M., Duketis, E., Jarczok, T. A., Degenhardt, F., Görgen, K., Meyer, J., Freitag, C. M. & Chiocchetti, A. G. (2016). Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder. Autism Research, 9(10), 1036-1045.

Li-Tempel, T., Larra, M. F., Winnikes, U., Tempel, T., DeRijk, R. H., Schulz, A., Schächinger, H., Meyer, J. & Schote, A. B. (2016). Polymorphisms of genes related to the hypothalamic-pituitary-adrenal axis influence the cortisol awakening response as well as self-perceived stress. Biological Psychology, 119, 112-121.

Roch, S., Fydrich, T., Küch, D., Meyer, J., Rabe, K., Besch, D., Worringen, U. & Hampel, P. (2016). Erfassung von Depressivität und Ängstlichkeit in der stationären verhaltensmedizinisch orthopädischen Rehabilitation - eine Fragebogenvalidierung mithilfe des SKID. Physikalische Medizin, Rehabilitationsmedizin, Kurortmedizin, 26(3), 130-136.

Schneider, K. K., Frings, C., Meyer, J. & Schote, A. B. (2016). The role of the glucocorticoid receptor gene (NR3C1) for the processing of aversive stimuli. Neuroscience Research, 107, 8-13.

Schote, A. B., Bonenberger, M., Pálmason, H., Seitz, C., Meyer, J. & Freitag, C. M. (2016). Glucocorticoid receptor variants in childhood attention-deficit/hyperactivity disorder and comorbid psychiatric disorders. Psychiatry Research, 246, 275-283.

Yurtsever, T., Schilling, T. M., Kölsch, M., Turner, J. D., Meyer, J., Schächinger, H. & Schote, A. B. (2016). The acute and temporary modulation of PERIOD genes by hydrocortisone in healthy subjects. Chronobiology International, 33(9), 1222-1234.

Zenglein, Y., Schwenck, C., Westerwald, E., Schmidt, C., Beuth, S., Meyer, J., Palmason, H., Seitz, C., Hänig, S. & Freitag, C. M. (2016). Empirically determined, psychopathological subtypes in children with ADHD. Journal of Attention Disorders, 20(2), 96-107.

O\'Dushlaine, C., Rossin, L., Duncan, L., Ripke, S., Neale, B. M., Purcell, S. M., Perlis, R. H., Anttila, V., Raychaudhuri, S., Daly, M. J., Lee, P. H., Bergen, S. E., Smoller, J. W., Chambert, K., McCarroll, S. A., Moran, J. L., Scolnick, E., Parikshak, N. N., Newhouse, S., Asherson, P., Collier, D. A., Craig, I. W., Farmer, A. E., Kuntsi, J., Lewis, C. M., McGuffin, P., Breen, G., Ruderfer, D., Posthuma, D., Nurnberger, J. I., Lee, S. H., Mowry, B. J., Byrne, E. M., Wray, N. R., Faraone, S. V., Thapar, A., Fraser, C., Georgieva, L., Gordon-Smith, K., Grozeva, D., Jones, I., Kirov, G. K., Moskvina, V., Nikolov, I., Owen, M. J., Williams, N., Zammit, S., O\'Donovan, M. C., Craddock, N., Holmans, P. A., Sklar, P., Goddard, M. E., Witte, J. S., Foroud, T., Koller, D. L., Absher, D., Myers, R. M., Agartz, I., Andreassen, O. A., Djurovic, S., Mattingsdal, M., Melle, I., Akil, H., Meng, F., Thompson, R. C., Watson, S. J., Amin, F., Anjorin, A., Bass, N., Choudhury, K., Gurling, H., Kandaswamy, R., Krasucki, R., Lawrence, J., McQuillin, A., Pimm, J., Puri, V., Anney, R., Cormican, P., Corvin, A., Donohoe, G. J., Gailagher, L., Gill, M., Kenny, E., Morris, D. W., Quinn, E. M., Visscher, P. M., Arking, D. E., Chakravarti, A., Azevedo, M. H., Oliveira, G., Backlund, L., Frisen, L., Osby, U., Schalling, M., Badner, J. A., Gershon, E. S., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Battaglia, A., Bauer, M., Bayes, M., Bellivier, F., Etain, B., Jamain, S., Leboyer, M., Hultman, C. M., Kaehler, A. K., Landen, M., Laengstroem, N., Lichtenstein, P., Magnusson, P. K. E., Berrettini, W., Elia, J., Lohoff, F. W., Betancur, C., Bettecken, T., Binder, E. B., Czamara, D., Holsboer, F., Ising, M., Kohli, M. A., Lucae, S., Mueller-Myhsok, B., Uhr, M., Biederman, J., Black, D. W., Coryell, W. H., Potash, J. B., Wassink, T. H., Blackwood, D. H. R., MacIntyre, D. J., McGhee, K. A., McIntosh, A., McLean, A. W., Muir, W. J., Pickard, B. S., Bloss, C. S., Schork, N. J., Smith, E. N., Boehnke, M., Flicldnger, M., Guan, W., Kwan, P., Scott, L. J., Zhang, P., Zoellner, S., Boomsma, D. I., De Geus, E. J., Hottenga, J.-J., Middeldorp, C. M., Willemsen, G., Penninx, B. W., Smit, J. H., Van Grootheest, G., Breuer, R., Frank, J., Meier, S., Strohmaier, J., Treutlein, J., Witt, S. H., Bruggeman, R., Buccola, N. G., Buitelaar, J. K., Franke, B., Bunney, W. E., Buxbaum, J. D., Byerley, W. F., Hamilton, S. P., Weiss, L. A., Caesar, S., Jones, L., Cahn, W., Kahn, R. S., Cantor, R. M., Casas, M., Ramos-Quiroga, J. A., Cichon, S., Degenhardt, F., Herms, S., Muehleisen, T. W., Noethen, M. M., Mattheisen, M., Propping, P., Ribases, M., Schumacher, J., Hansen, T. F., Ingason, A., Jones, E. G., Olsen, L., Rasmussen, H. B., Werge, T., Cloninger, C. R., Heath, A. C., Madden, P. A. F., Pergadia, M. L., Todorov, A. A., Cook, E. H., Coon, H., McMahon, W. M., Cormand, B., Craig, D. W., Szelinger, S., Crosbie, J., Schachar, R., Cuccaro, M. L., Pericak-Vance, M. A., Curtis, D., Datta, S., Dawson, G., Piven, J., Day, R., Matthews, K., Doyle, A. E., Duan, J., Gejman, P. V., Sanders, A. R., Dudbridge, F., Duketis, E., Freitag, C. M., Poustka, F., Ebstein, R. P., Edenberg, H. J., Ennis, S., Fanous, A., Neale, M. C., Kendler, K. S., Ferrier, I. N., Parr, J. R., Young, A. H., Fombonne, E., Freedman, R., Olincy, A., Freimer, N. B., Loo, S. K., Nelson, S. F., Ophoff, R. A., Smalley, S. L., Friedl, M., Giegling, I., Hartmann, A. M., Konte, B., Rujescu, D., Gordon, S. D., Henders, A. K., Martin, N. G., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Green, E. K., Greenwood, T. A., McKinney, R., Nievergelt, C. M., Shilling, P. D., Kelsoe, J. R., Grice, D. E., Silverman, J. M., Gross, M., Hoefels, S., Maier, W., De Haan, L., Haines, J. L., Hakonarson, H., Hallmayer, J., Hamshere, M. L., Hautzinger, M., Hickie, I. B., Hipolito, M., Lawson, W. B., Nwulia, E. A., Hoogendijk, W. J., Hus, V., Tzeng, J.-Y., Keller, M. C., Kennedy, J. L., Kent, L., Kim, Y., Sullivan, P. F., Klauck, S. M., Klei, L., Devlin, B., Knowles, J. A., Medeiros, H., Pato, C. N., Pato, M. T., Korszun, A., Krabbendam, L., Myin-Germeys, I., Van Os, J., Lathrop, M., Ledbetter, D. H., Martin, C. L., Lencz, T., Malhotra, A. K., Lesch, K.-P., Levinson, D. F., Li, J., Lieberman, J. A., McGrath, P. J., Lin, D.-Y., Linszen, D. H., Liu, C., Lord, C., Lowe, J. K., Geschwind, D. H., Maestrini, E., Mahon, P. B., Schulze, T. G., Mane, S. M., McGough, J. J., McInnis, M. G., McMahon, F. J., Meyer, J., Middleton, L., Milanova, V., Miranda, A., Monaco, A. P., Moreno-De-Luca, D., Sanders, S. J., State, M., Morken, G., Morrow, E. M., Muglia, P., Tozzi, F., Murtha, M., Willsey, A. J., Nimgaonkar, V., Nolen, W. A., Oades, R. D., Palotie, A., Rehnstroem, K., Paterson, A. D., Xu, W., Quested, D. J., Reif, A., Rice, J. P., Roeder, K., Roeyers, H., Sonuga-Barke, E. J. S., Rothenberger, A., Rouleau, G., Santangelo, S. L., Sergeant, J. A., Schatzberg, A. F., Scheftner, W. A., Schellenberg, G. D., Scherer, S. W., Schwarz, M., Shi, J., Shyn, S. I., Slager, S. L., Cair, D. S., Steffens, M., Steinhausen, H.-C., Strauss, J. S., Stroup, T. S., Vincent, J. B., Sutdiffe, J. S., Szatmari, P., Thirumalai, S., Van den Oord, E. J. C. G., Vicente, A. M., Vieland, V. J., Walsh, C. A., Weissman, M. M., Wienker, T. F., Wijsman, E. M., Yu, T. W., Zandi, P. P., Zitman, F. G. & Zhao, Z. (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience, 18(2), 199-209.

Schneider, K. K., Hülße, L., Schote, A. B., Meyer, J. & Frings, C. (2015). Sex matters! Interactions of sex and polymorphisms of a cholinergic receptor gene (CHRNA5) modulate response speed. NeuroReport, 26(4), 186-191.

Schneider, K. K., Schote, A. B., Meyer, J. & Frings, C. (2015). Genes of the dopaminergic system selectively modulate top-down but not bottom-up attention. Cognitive, Affective, & Behavioral Neuroscience, 15(1), 104-116.

Schneider, K. K., Schote, A. B., Meyer, J., Markett, S., Reuter, M. & Frings, C. (2015). Individual response speed is modulated by variants of the gene encoding the alpha 4 sub-unit of the nicotinic acetylcholine receptor (CHRNA4). Behavioural Brain Research, 284, 11-18.

Gross, K. M., Schote, A. B., Meyer, J., Schneider, K. K. & Schulz, A. (2014). Elevated Social Stress Levels and Depressive Symptoms in Primary Hyperhidrosis. PLoS ONE, 9(3), No. e2412.

Jarick, I., Volckmar, A.-L., Pütter, C., Pechlivanis, S., Nguyen, T., Dauvermann, M. R., Beck, S., Albayrak, Ö., Scherag, S., Gilsbach, S., Cichon, S., Hoffmann, P., Degenhardt, F., Nöthen, M.M., Schreiber, S., Wichmann, H.-E., Jöckel, K.-H., Heinrich, J., Tiesler, C. M. T., Faraone, V., Walitza, S., Sinzig, J., Freitag, C., Meyer, J., Herpertz-Dahlmann, B., Lehmkuhl, G., Renner, T. J., Warnke, A., Romanos, M., Lesch, K.-P., Reif, A., Schimmelmann, B. G., Hebebrand, J., Scherag, A. & Hinney, A. (2014). Genome-wide analysis of rare copy n variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular Psychiatry, 19, 115-121.

Steinberg, S., de Jong, S., Mattheisen, M., Costas, J., Demontis, D., Jamain, S., Pietiläinen, O. P. H., Lin, K., Papiol, S., Huttenlocher, J., Sigurdsson, E., Vassos, E., Giegling, I., Breuer, R., Fraser, G., Walker, N., Melle, I., Djurovic, S., Agartz, I., Tuulio-Henriksson, A., Suvisaari, J., Lönnqvist, J., Paunio, T., Olsen, L., Hansen, T., Ingason, A., Pirinen, M., Strengman, E., Hougaard, D. M., Ørntoft, T., Didriksen, M., Hollegaard, M. V., Nordentoft, M., Abramova, L., Kaleda, V., Arrojo, M., Sanjuán, J., Arango, C., Etain, B., Bellivier, F., Méary, A., Schürhoff, F., Szoke, A., Ribolsi, M., Magni, V., Siracusano, A., Sperling, S., Rossner, M., Christiansen, C., Kiemeney, L. A., Franke, B., van den Berg, L. H., Veldink, J., Curran, S., Bolton, P., Poot, M., Staal, W., Rehnstrom, K., Kilpinen, H., Freitag, C. M., Meyer, J., Magnusson, P., Saemundsen, E., Martsenkovsky, I., Bikshaieva, I., Martsenkovska, I., Vashchenko, O., Raleva, M., Paketchieva, K., Stefanovski, B., Durmishi, N., Milovancevic, M. P., Tosevski, D. L., Silagadze, T., Naneishvili, N., Mikeladze, N., Surguladze, S., Vincent, J. B., Farmer, A., Mitchell, P. B., Wright, A., Schofield, P. R., Fullerton, J. M., Montgomery, G. W., Martin, N. G., Rubino, I. A., van Winkel, R., Kenis, G., De Hert, M., Réthelyi, J. M., Bitter, I., Terenius, L., Jönsson, E. G., Bakker, S., van Os, J., Jablensky, A., Leboyer, M., Bramon, E., Powell, J., Murray, R., Corvin, A., Gill, M., Morris, D., O'Neill, F. A., Kendler, K., Riley, B., Craddock, N., Owen, M. J., O'Donovan, M. C., Thorsteinsdottir, U., Kong, A., Ehrenreich, H., Carracedo, A., Golimbet, V., Andreassen, O. A., Børglum, A. D., Mors, O., Mortensen, P. B., Werge, T., Ophoff, R. A., Nöthen, M. M., Rietschel, M., Cichon, S., Ruggeri, M., Tosato, S., Palotie, A., Clair, D. S., Rujescu, D., Collier, D. A., Stefansson, H. & Stefansson, K. (2014). Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19(1), 108-114.

Waltes, R., Duketis, E., Schlitt, S., Jarczok, T. A., Sachse, M., Kaempfer, L. M., Kleinboeck, T., Poustka, F., Boelte, S., Schmoetzer, G., Freitag, C. M., Chiocchetti, A. G., Knapp, M., Anney, R. J. L., Huguet, G., Bourgeron, T., Voran, A., Huy, E., Meyer, J. & Klauck, S. M. (2014). Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Human Genetics, 133(6), 781-792.

Gassert, F., Schulte, U., Husemann, M., Ulrich, W., Rödder, D., Hochkirch, A., Engel, E., Meyer, J. & Habel, J. C. (2013). From southern refugia to the northern range margin: genetic population structure of the common wall lizard, Podarcis muralis (in press). Journal of Biogeography.

Habel, J. C., Cox, S., Gassert, F., Mulwa, R. K., Meyer, J. & Lens, L. (2013). Population genetics of the East African White-eye species complex. Conservsation Genetics, 14(5), 1019-1028.

Hamshere, M. L., Langley, K., Martin, J., Agha, S. S., Stergiakouli, E., Anney, R. J. L., Buitelaar, J., Faraone, S. V., Lesch, K.-P., Neale, B. M., Franke, B., Sonuga-Barke, E., Asherson, P., Merwood, A., Kuntsi, J., Medland, S. E., Ripke, S., Steinhausen, H.-C., Freitag, C., Reif, A., Renner, T. J., Romanos, M., Romanos, J., Warnke, A., Meyer, J., Palmason, H., Arias Vasquuez, A., Lambregts-Rommelse, N., Roeyers, H., Biederman, J., Doyle, A. E., Hakonarson, H., Rothenberger, A., Banaschewski, T., Oades, R. D., McGough, J. J., Kent, L., Williams, N., Owen, M. J., Holmans, P., O'Donovan, M. C. & Thapar, A. (2013). High loading of polygenic risk for ADHD in children with comorbid aggression. American Journal of Psychiatry, 170(8), 909-916.

Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O. A., Anjorin, A., Anney, R., Anttila, V., Arking, D. E., Asherson, P., Azevedo, M. H., Backlund, L., Badner, J. A., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S. E., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J., Binder, E. B., Black, D. W., Blackwood, D. H., Bloss, C. S., Boehnke, M., Boomsma, D. I., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Buccola, N. G., Buitelaar, J. K., Bunney, W. E., Buxbaum, J. D., Byerley, W. F., Byrne, E. M., Caesar, S., Cahn, W., Cantor, R. M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Cloninger, C. R., Collier, D. A., Cook, E. H., Coon, H., Cormand, B., Corvin, A., Coryell, W. H., Craig, D. W., Craig, I. W., Crosbie, J., Cuccaro, M. L., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., De, Geus, E. J., Degenhardt, F., Djurovic, S., Donohoe, G. J., Doyle, A. E., Duan, J., Dudbridge, F., Duketis, E., Ebstein, R. P., Edenberg, H. J., Elia, J., Ennis, S., Etain, B., Fanous, A., Farmer, A. E., Ferrier, I. N., Flickinger, M., Fombonne, E., Foroud, T., Frank, J., Franke, B., Fraser, C., Freedman, R., Freimer, N. B., Freitag, C. M., Friedl, M., Frisén, L., Gallagher, L., Gejman, P. V., Georgieva, L., Gershon, E. S., Geschwind, D. H., Giegling, I., Gill, M., Gordon, S. D., Gordon-Smith, K., Green, E. K., Greenwood, T. A., Grice, D. E., Gross, M., Grozeva, D., Guan, W., Gurling, H., De, Haan, L., Haines, J. L., Hakonarson, H., Hallmayer, J., Hamilton, S. P., Hamshere, M. L., Hansen, T. F., Hartmann, A. M., Hautzinger, M., Heath, A. C., Henders, A. K., Herms, S., Hickie, I. B., Hipolito, M., Hoefels, S., Holmans, P. A., Holsboer, F., Hoogendijk, W. J., Hottenga, J.J., Hultman, C. M., Hus, V., Ingason, A., Ising, M., Jamain, S., Jones, E. G., Jones, I., Jones, L., Tzeng, J. Y., Kähler, A. K., Kahn, R. S., Kandaswamy, R., Keller, M. C., Kennedy, J. L., Kenny, E., Kent, L., Kim, Y., Kirov, G. K., Klauck, S. M., Klei, L., Knowles, J. A., Kohli, M. A., Koller, D. L., Konte, B., Korszun, A., Krabbendam, L., Krasucki, R., Kuntsi, J., Kwan, P., Landén, M., Långström, N., Lathrop, M., Lawrence, J., Lawson, W. B., Leboyer, M., Ledbetter, D. H., Lee, P. H., Lencz, T., Lesch, K. P., Levinson, D. F., Lewis, C. M., Li, J., Lichtenstein, P., Lieberman, J. A., Lin, D. Y., Linszen, D. H., Liu, C., Lohoff, F. W., Loo, S. K., Lord, C., Lowe, J. K., Lucae, S., MacIntyre, D. J., Madden, P. A., Maestrini, E., Magnusson, P. K., Mahon, P. B., Maier, W., Malhotra, A. K., Mane, S. M., Martin, C. L., Martin, N. G., Mattheisen, M., Matthews, K., Mattingsdal, M., McCarroll, S. A., McGhee, K. A., McGough, J.J., McGrath, P. J., McGuffin, P., McInnis, M. G., McIntosh, A., McKinney, R., McLean, A. W., McMahon, F. J., McMahon, W. M., McQuillin, A., Medeiros, H., Medland, S. E., Meier, S., Melle, I., Meng, F., Meyer, J., Middeldorp, C. M., Middleton, L., Milanova, V., Miranda, A., Monaco, A. P., Montgomery, G. W., Moran, J. L., Moreno-De-Luca, D., Morken, G., Morris, D. W., Morrow, E. M., Moskvina, V., Muglia, P., Mühleisen, T. W., Muir, W. J., Müller-Myhsok, B., Murtha, M., Myers, R. M., Myin-Germeys, I., Neale, M. C., Nelson, S. F., Nievergelt, C. M., Nikolov, I., Nimgaonkar, V., Nolen, W. A., Nöthen, M.M., Nurnberger, J. I., Nwulia, E. A., Nyholt, D. R., O'Dushlaine, C., Oades, R. D., Olincy, A., Oliveira, G., Olsen, L., Ophoff, R. A., Osby, U., Owen, M. J., Palotie, A., Parr, J. R., Paterson, A. D., Pato, C. N., Pato, M. T., Penninx, B. W., Pergadia, M. L., Pericak-Vance, M. A., Pickard, B. S., Pimm, J., Piven, J., Posthuma, D., Potash, J. B., Poustka, F., Propping, P., Puri, V., Quested, D. J., Quinn, E. M., Ramos-Quiroga, J. A., Rasmussen, H. B., Raychaudhuri, S., Rehnström, K., Reif, A., Ribasés, M., Rice, J. P., Rietschel, M., Roeder, K., Roeyers, H., Rossin, L., Rothenberger, A., Rouleau, G., Ruderfer, D., Rujescu, D., Sanders, A. R., Sanders, S. J., Santangelo, S. L., Sergeant, J. A., Schachar, R., Schalling, M., Schatzberg, A. F., Scheftner, W. A., Schellenberg, G. D., Scherer, S. W., Schork, N. J., Schulze, T. G., Schumacher, J., Schwarz, M., Scolnick, E., Scott, L. J., Shi, J., Shilling, P. D., Shyn, S. I., Silverman, J. M., Slager, S. L., Smalley, S. L., Smit, J. H., Smith, E. N., Sonuga-Barke, E. J., St, Clair, D., State, M., Steffens, M., Steinhausen, H. C., Strauss, J. S., Strohmaier, J., Stroup, T. S., Sutcliffe, J. S., Szatmari, P., Szelinger, S., Thirumalai, S., Thompson, R. C., Todorov, A.A., Tozzi, F., Treutlein, J., Uhr, M., van, den, Oord, E. J., Van, Grootheest, G., Van, Os, J., Vicente, A. M., Vieland, V. J., Vincent, J. B., Visscher, P. M., Walsh, C. A., Wassink, T. H., Watson, S. J., Weissman, M.M., Werge, T., Wienker, T. F., Wijsman, E. M., Willemsen, G., Williams, N., Willsey, A. J., Witt, S. H., Xu, W., Young, A. H., Yu, T. W., Zammit, S., Zandi, P.P., Zhang, P., Zitman, F. G., Zöllner, S., Devlin, B., Kelsoe, J. R., Sklar, P., Daly, M. J., O'Donovan, M. C., Craddock, N., Sullivan, P. F., Smoller, J. W., Kendler, K. S. & Wray, N. R. (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Cross-Disorder group of the psychiatric genomics consortium. Nature Genetics, 45(9), 984-994.

Lin, M. K., Freitag, C. M., Schote, A. B., Pálmason, H., Seitz, C., Renner, T. J., Romanos, M., Walitza, S., Jacob, C., Reif, A., Warnke, A., Cantor, R., Lesch, K.-P. & Meyer, J. (2013). Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated German multi-generation families. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 162(8), 855-863.

Mertins, V., Schote-Frese, A. & Meyer, J. (2013). Variants of the monoamine oxidase A gene (MAOA) predict free-riding behavior in women in a strategic public goods experiment. Journal of Neuroscience, Psychology, and Economics, 6(2), 97-114.

Trost, S., Platz, B., Usher, J., Scherk, H., Wobrock, T., Ekawardhani, S., Meyer, J., Reith, W., Falkai, P. & Gruber, O. (2013). DISC1 (disrupted-in-schizophrenia 1) is associated with cortical grey matter vs in the human brain: A voxel-based morphometry (VBM) study. Journal of Psychiatric Research, 47, 188-196.

Trost, S., Platz, B., Usher, J., Scherk, H., Wobrock, T., Ekawardhani, S., Meyer, J., Reith, W., Falkai, P. & Gruber, O. (2013). The DTNBP1 (Dysbindin-1) gene variant rs2619522 is associated with variation of hippocampal and prefrontal grey matter volumes in humans. European Archives of Psychiatry and Clinical Neuroscience, 263(1), 53-63.

Yang, L., Neale, B. M., Liu, L., Lee, S. H., Wray, N. R., Ji, N., Li, H., Qian, Q., Wang, D., Li, J., Faraone, S. V., Wang, Y. & et al. (2013). Polygenic transmission and complex neuro-developmental network for attention deficit/hyperactivity disorder: genome-wide association study of both common and rare variants. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 162(5), 419-430.

Zenglein, Y., Schwenck, C., Westerwald, E., Schmidt, C., Beuth, S., Meyer, J., Pálmason, H., Seitz, C., Hänig, S. & Freitag, C. (2013). Empirically determined, psychopathological subtypes in children with ADHD. Journal of Attention Disorders.

Elia, J., Glessner, J. T., Wang, K., Takahashi, N., Shtir, C. J., Hadley, D., Sleiman, P. M. A., Zhang, H., Kim, C. E., Robison, R., Lyon, G. J., Flory, J. H., Bradfield, J. P., Imielinski, M., Hou, C., Frackelton, E. C., Chiavacci, R. M., Sakurai, T., Rabin, C., Middleton, F. A., Thomas, K. A., Garris, M., Mentch, F., Freitag, C. M., Steinhausen, H.-C., Todorov, A. A., Reif, A., Rothenberger, A., Franke, B., Mick, E. O., Roeyers, H., Buitelaar, J., Lesch, K.-P., Banaschewski, T., Ebstein, R. P., Mulas, F., Oades, R. D., Sergeant, J., Sonuga-Barke, E., Renner, T. J., Romanos, M., Romanos, J., Warnke, A., Walitza, S., Meyer, J., Palmason, H., Seitz, C., Loo, S. K., Smalley, S. L., Biederman, J., Kent, L., Asherson, P., Anney, R. J. L., Gaynor, J. W., Shaw, P., Devoto, M., White, P. S., Grant, S. F. A., Buxbaum, J. D., Rapoport, J. L., Williams, N. M., Nelson, S. F., Faraone, S. V. & Hakonarson, H. (2012). Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics, 44(1), 78-84.

Freitag, C. M., Hänig, S., Schneider, A., Seitz, C., Pálmason, H., Retz, W. & Meyer, J. (2012). Biological and psychosocial environmental risk factors influence symptom severity and psychiatric comorbidity in children with ADHD. Journal of Neural Transmission, 119, 81-94.

Gruber, O., Hasan, A., Scherk, H., Wobrock, T., Schneider-Axmann, T., Ekawardhani, S., Schmitt, A., Backens, M., Reith, W., Meyer, J. & Falkai, P. (2012). Association of the brain-derived neurotrophic factor (BDNF) val66met polymorphism with magnetic resonance spectroscopic markers in the human hippocampus: in vivo evidence for effects on the glutamate system. European Archives of Psychiatry &; Clinical Neuroscience, 262(1), 23-31.

Jain, M., Vélez, J. I., Acosta, M. T., Palacio, L. G., Balog, J., Roessler, E., Pineda, D., Londoño, A. C., Palacio, J. D., Arbelaez, A., Lopera, F., Elia, J., Hakonarson, H., Seitz, C., Freitag, C. M., Palmason, H., Meyer, J., Romanos, M., Walitza, S., Hemminger, U., Warnke, A., Romanos, J., Renner, T., Jacob, C., Lesch, K. P., Swanson, J., Castellanos, F. X., Bailey-Wilson, J. E., Arcos-Burgos, M. & Muenke, M. (2012). A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD. Molecular Psychiatry, 17(7), 741-747.

Kranz, T., Ekawardhani, S., Lin, M. K., Alt, S. R., Streit, F., Schuelter, U., Bauer, H., Henseler, D., Turner, J. D., Muller, C. P., Reif, A., Schote, A. B. & Meyer, J. (2012). The chromosome 15q14 locus for bipolar disorder and schizophrenia: Is C15orf53 a major candidate gene? Journal of Psychiatric Research, 46, 1414-1420.

Ribasés, M., Ramos-Quiroga, J. A., Hervás, A., Sánchez-Mora, C., Bosch, R., Bielsa, A., Gastaminza, X., Lesch, K.-P., Reif, A., Renner, T. J., Romanos, M., Warnke, A., Walitza, S., Freitag, C., Meyer, J., Palmason, H., Casas, M., Bayés, M. & Cormand, B. (2012). Candidate system analysis in ADHD: Evaluation of 9 genes involved in dopaminergic neurotransmission identifies association with DRD1. World Journal Biological Psychiatry, 13(4), 281-292.

Stergiakouli, E., Hamshere, M., Holmans, P., Langley, K., Zaharieva, I., deCODE Genetics, Psychiatric GWAS Consortium, Hawi, Z., Kent, L., Gill, M., Williams, N., Owen, M. J., O'Donovan, M. & Thapar, A. (2012). Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. American Journal of Psychiatry, 169, 186-194.

Williams, N. M., Franke, B., Mick, E., Anney, R. J. L., Freitag, C., Gill, M., Thapar, A., ODonovan, M., Owen, M. J., Holmans, P., Kent, L., Middleton, F., James, Y.-Z., Liu, L., Meyer, J., Nguyen, T.T., Romanos, J., Romanos, M., Schäfer, H., Seitz, C., Renner, T. J., Walitza, S., Warnke, A., Pálmason, H., Buitelaar, J., Rommelse, N., Vasquez, A.A., Hawi, Z., Langley, K., Sergeant, J., Steinhausen, H.-C., Roeyers, H., Biederman, J., Zaharieva, I., Hakonarson, H., Elia, J., Schachar, R., Scherer, S., Todorov, A., Smalley, S., Loo, S., Nelson, S., Shtir, C., Asherson, P., Reif, A., Lesch, K.-P. & Faraone, S. V. (2012). Genome-wide analysis of copy n variants in attention deficit hyperactivity disorder: The role of rare variants and duplications at 15q13.3. American Journal of Psychiatry, 169(2), 195-204.

Zilles, D., Meyer, J., Schneider-Axmann, T., Ekawardhani, S., Gruber, E., Falkai, P. & Gruber, O. (2012). Genetic polymorphisms of 5-HTT and DAT but not COMT differentially affect verbal and visuospatial working memory functioning. European Archives of Psychiatry and Clinical Neuroscience, 262(8), 667-676.

Cao-Lei, L., Leija, S. C., Kumsta, R., Wüst, S., Meyer, J., Turner, J. D. & Muller, C. P. (2011). Transcriptional control of the human glucocorticoid receptor: Identification and analysis of alternative promoter regions. Human Genetics, 129, 533-543.

Henseler, D., Turner, J. D., Eckhardt, M., van der Mark, M., Revsin, Y., Lin, M. K., Kranz, T., Muller, C. & Meyer, J. (2011). Unusual 5'-regulatory structure and regulation of the murine Mlc1 gene: Lack of promoter-specific functional elements. Journal of Nucleic Acids Investigation, 2(e11), 70-76.

Hinney, A., Scherag, A., Jarick, I., Albayrak, Ö., Pütter, C., Pechlivanis, S., Dauvermann, M. R., Beck, S., Weber, H., Scherag, S., Nguyen, T. T., Volckmar, A.-L., Knoll, N., Faraone, S. V., Neale, B. M., Franke, B., Cichon, S., Hoffmann, P., Nöthen, M. M., Schreiber, S., Jöckel, K.-H., Wichmann, H.-E., Freitag, C., Lempp, T., Meyer, J., Gilsbach, S., Herpertz-Dahlmann, B., Sinzig, J., Lehmkuhl, G., Renner, T. J., Warnke, A., Romanos, M., Lesch, K.-P., Reif, A., Schimmelmann, B. G. & Hebebrand, J. (2011). Genome-wide association study in German patients with Attention deficit/Hyperactivity disorder. American Journal of medical Genetics. Part B, Neuropsychiatric Genetics, 156(8), 888-897.

Kröger, A., Hänig, S., Seitz, C., Palmason, H., Meyer, J. & Freitag, C. M. (2011). Risk factors of autistic symptoms in children with ADHD. European Child and Adolescent Psychiatry, 20(11), 561-570.

Mertins, V., Schote, A. B., Hoffeld, W., Griessmair, M. & Meyer, J. (2011). Genetic susceptibility for individual cooperation preferences: The Role of monoamine oxidase A gene (MAOA) in the voluntary provision of public goods. PLoS ONE, 6(6), e20959.

Reif, A., Nguyen, T. T., Weissflog, L., Jacob, C. P., Romanos, M., Renner, T. J., Buttenschon, H. N., Kittel-Schneider, S., Gessner, A., Weber, H., Neuner, M., Gross-Lesch, S., Zamzow, K., Kreiker, S., Walitza, S., Meyer, J., Freitag, C. M., Bosch, R., Casas, M., Gomez, N., Ribases, M., Bayes, M., Buitelaar, J. K., Kiemeney, L. A. L. M., Kooij, J. J. S., Kan, C. C., Hoogman, M., Johansson, S., Jacobsen, K. K., Knappskog, P. M., Fasmer, O. B., Asherson, P., Warnke, A., Grabe, H.-J., Mahler, J., Teumer, A., Völzke, H., Mors, O. N., Schäfer, H., Ramos-Quiroga, J. A., Cormand, B., Haavik, J., Franke, B. & Lesch, K.-P. (2011). DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders. Neuropsychopharmacology, 36(11), 2318-2327.

Arcos-Burgos, M., Jain, M., Acosta, M. T., Shively, S., Stanescu, H., Wallis, D., Domene, S., Velez, J. I., Karkera, J. D., Balog, J., Berg, K., Kleta, R., Gahl, W. A., Roessler, E., Long, R., Lie, J., Pineda, D., Londono, A. C., Palacio, J. D., Arbelaez, A., Lopera, F., Elia, J., Hakonarson, H., Johansson, S., Knappskog, P. M., Haavik, J., Ribases, M., Cormand, B., Bayes, M., Casas, M., Ramos-Quiroga, J. A., Hervas, A., Maher, B. S., Faraone, S. V., Seitz, C., Freitag, C. M., Palmason, H., Meyer, J., Romanos, M., Walitza, S., Hemminger, U., Warnke, A., Romanos, J., Renner, T., Jacob, C., Lesch, K. P., Swanson, J., Vortmeyer, A., Bailey-Wilson, J. E., Castellanos, F. X. & Muenke, M. (2010). A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication. Molecular Psychiatry, 15(11), 1053-1066.

Freitag, C. M., Agelopoulos, K., Huy, E., Rothermundt, M., Krakowitzky, P., Meyer, J., Deckert, J., von Gontard, A. & Hohoff C (2010). Adenosine A(2A) receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder. European Child and Adolescent Psychiatry, 19, 67-74.

Freitag, C. M., Agelopoulos, K., Huy, E., Rothermundt, M., Krakowitzky, P., Meyer, J., Deckert, J., von Gontard, A. & Hohoff, C. (2010). Adenosine A sub 2A receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder. European Child & Adolescent Psychiatry, 19(1), 67-74.

Neale, B. M., Medland, S. E., Ripke, S., Asherson, P., Franke, B., Lesch, K.-P., Faraone, S. V., Nguyen, T. T., Schäfer, H., Holmans, P., Daly, M., Steinhausen, H.-C., Freitag, C., Reif, A., Renner, T. J., Romanos, M., Romanos, J., Walitza, S., Warnke, A., Meyer, J., Palmason, H., Buitelaar, J., Vasquez, A. A., Lambregts-Rommelse, N., Gill, M., Anney, R. J. L., Langely, K., O'Donovan, M., Williams, N., Owen, M., Thapar, A., Kent, L., Sergeant, J., Roeyers, H., Mick, E., Biederman, J., Doyle, A., Smalley, S., Loo, S., Hakonarson, H., Elia, J., Todorov, A., Miranda, A., Mulas, F., Ebstein, R. P., Rothenberger, A., Banaschewski, T., Oades, R. D., Sonuga-Barke, E., McGough, J., Nisenbaum, L., Middleton, F., Hu, X. & Nelson, S. (2010). Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 49(9), 884-897.

Neale, B. M., Medland, S., Ripke, S., Anney, R. J., Asherson, P., Buitelaar, J., Franke, B., Gill, M., Kent, L., Holmans, P., Middleton, F., Thapar, A., Lesch, K.-P., Faraone, S. V., Daly, M., Nguyen, T. T., Schäfer, H., Steinhausen, H.-C., Reif, A., Renner, T. J., Romanos, M., Romanos, J., Warnke, A., Walitza, S., Freitag, C., Meyer, J., Pálmason, H., Rothenberger, A., Hawi, Z., Sergeant, J., Roeyers, H., Mick, E., Biederman, J. & IMAGE II Consortium (2010). Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Acadamy of Child and Adolescent Psychiatry, 49(9), 906-920.

Palmason, H., Moser, D., Sigmund, J., Vogler, C., Hänig, S., Schneider, A., Seitz, C., Marcus, A., Meyer, J. & Freitag, C. M. (2010). Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant. Journal of Neural Transmission, 117(2), 259-267.

Freitag, C. M., Hänig, S., Palmason, H., Meyer, J., Wüst, S. & Seitz, C. (2009). Cortisol awakening response in healthy children and children with ADHD: Impact of comorbid disorders and psychosocial risk factors. Psychoneuroendocrinology, 34(7), 1019-1028.

Kumsta, R., Moser, D., Streit, F., Koper, J.W., Meyer, J. & Wüst, S. (2009). Characterization of a glucocorticoid receptor gene (GR, NR3C1) promoter polymorphism reveals functionality and extends a haplotype with putative clinical relevance. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 150(4), 476-482.

Moser, D., Ekawardhani, S., Kumsta, R., Palmason, H., Bock, C., Athanassiadou, Z., Lesch, K.-P. & Meyer, J. (2009). Functional analysis of a potassium-chloride co-transporter 3 (SLC12A6) promoter polymorphism leading to an additional DNA methylation site. Neuropsychopharmacology, 34(2), 458-467.

Scherk, H., Backens, M., Schneider-Axmann, T., Kraft, S., Kemmer, C., Usher, J., Reith, W., Falkai, P., Meyer, J. & Gruber, O. (2009). Dopamine Transporter genotype influences N-acetyl-aspartate in left putamen. World Journal of Biolical Psychiatry, 10(4), 524-530.

Scherk, H., Gruber, O., Menzel, P., Schneider-Axmann, T., Kemmer, C., Usher, J., Reith, W., Meyer, J. & Falkai, P. (2009). 5-HTTLPR genotype influences amygdala volume. European Archives of Psychiatry and Clinical Neuroscience, 259(4), 212-217.

Schimmelmann, B. G., Friedel, S., Nguyen, T.T., Sauer, S., Ganz Vogel, C. I., Konrad, K., Wilhelm, C., Sinzig, J., Renner, T. J., Romanos, M., Palmason, H., Dempfle, A., Walitza, S., Freitag, C., Meyer, J., Linder, M., Schäfer, H., Warnke, A., Lesch, K. P., Herpertz-Dahlman, B., Hinney, A. & Hebebrand, J. (2009). Exploring the genetic link between RLS and ADHD. Journal of Psychiatric Research, 43(10), 941-945.

Asherson, P., Dempfle, A., Arcos-Burgos, M., Bakker, S. C., Banaschewski, T., Biederman, J., Buitelaar, J., Castellanos, F. X., Doyle, A., Ebstein, R. P., Ekholm, J., Forabosco, P., Franke, B., Freitag, C., Friedel, S., Gill, M., Hebebrand, J., Hinney, A., Jacob, C., Lesch, K. P., Loo, S. K., Lopera, F., McCracken, J. T., McGough, J. J. & Meyer, J. (2008). Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 42(12), 1392-1398.

Lesch, K.-P., Timmesfeld, N., Renner, T. J., Halperin, R., Röser, C., Nguyen, T. T., Craig, D. W., Romanos, J., Heine, M., Meyer, J., Freitag, C., Warnke, A., Romanos, M., Schäfer, H., Walitza, S., Reif, A., Stephan, D. A. & Jacobs, C. (2008). Molecular genetics of adult ADHD: Converging evidence from genome-wide association and extended pedigree linkage studies. Journal of Neural Transmission, 115(11), 1573-1585.

Macedo, J. A., Hesse, J., Turner, J. D., Meyer, J., Hellhammer, D. H. & Muller, C. P. (2008). Glucocorticoid sensitivity in fibromyalgia patients: Decreased expression of corticosteroid receptors and glucocorticoid-induced leucine zipper. Psychoneuroendocrinology, 33(6), 799-809.

Romanos, M., Freitag, C., Jacob, C., Craig, D. W., Dempfle, A., Nguyen, T.T., Halperin, R., Walitza, S., Renner, T. J., Seitz, C., Romanos, J., Palmason, H., Reif, A., Heine, M., Windemuth-Kieselbach, C., Vogler, C., Sigmund, J., Warnke, A., Schäfer, H., Meyer, J., Stephan, D. A. & Lesch, K. P. (2008). Genome-wide linkage analysis of ADHD using high-density SNP arrays: Novel loci at 5q13.1 and 14q12. Molecular Psychiatry, 13(5), 522-530.

Buss, C., Schuelter, U., Hesse, J., Moser, D., Phillips, D. I., Hellhammer, D. & Meyer J (2007). Haploinsufficiency of the SERPINA6 gene is associated with severe muscle fatigue: A de novo mutation in corticosteroid-binding globulin deficiency. Journal of Neural Transmission, 114, 563-569.

Freitag, C.M., Retz-Junginger, P., Retz, W., Seitz, C., Palmason, H., Meyer, J., Rösler, M. & Gontard, A.v. (2007). AQ - Autismus-Spektrumquotient [Autism-Spectrum Quotient; Autismus-Spektrumquotient (AQ) - deutsche Kurzversion AQ-k]. Kurznachweis. Zeitschrift für Klinische Psychologie und Psychotherapie, 36(4), 280-289.

Freitag, C. M., Retz-Junginger, P., Retz, W., Seitz, C., Palmason, H., Meyer, J., Rösler, M. & von Gontard, A. (2007). Evaluation der deutschen Version des Autismus-Spektrum-Quotienten (AQ) - die Kurzversion AQ-k. Zeitschrift für Klinische Psychologie und Psychotherapie, 36(4), 280-289.

Friedel, S., Saar, K., Sauer, S., Dempfle, A., Walitza, S., Renner, T., Romanos, M., Freitag, C., Seitz, C., Palmason, H., Scherag, A., Windemuth-Kieselbach, C., Schimmelmann, B. G., Wewetzer, C., Meyer, J., Warnke, A., Lesch, K. P., Reinhardt, R., Herpertz-Dahlmann, B., Linder, M., Hinney, A., Remschmidt, H., Schäfer, H., Konrad, K., Hübner, N. & Hebebrand, J. (2007). Association and linkage of allelic variants of the dopamine transporter gene in ADHD. Molecular Psychiatry, 12, 923-933.

Moser, D., Molitor, A., Kumsta, R., Tatschner, T., Riederer, P. & Meyer, J. (2007). The glucocorticoid receptor gene exon 1-F promoter is not methylated at the NGFI-A binding site in human hippocampus. World Journal of Biological Psychiatry, 8(4), 262-268.

Schimmelmann, B. G., Friedel, S., Dempfle, A., Warnke, A., Lesch, K. P., Walitza, S., Renner, T. J., Romanos, M., Herpertz-Dahlmann, B., Linder, M., Schafer, H., Seitz, C., Palmason, H., Freitag, C., Meyer, J., Konrad, K., Hinney, A. & Hebebrand, J. (2007). No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD. Journal of Neural Transmission, 114(4), 523-526.

Selch, S., Strobel, A., Haderlein, J., Meyer, J., Jacob, C. P., Schmitt, A., Lesch, K.-P. & Reif, A. (2007). MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophrenia. Biological Psychiatry, 61, 1211-1214.

Wendland, J. R., Hampe, M., Newman, T. K., Syagailo, Y., Meyer, J., Schempp, W., Timme, A., Suomi, S. J. & Lesch, K. P. (2006). Structural variation of the monoamine oxidase A gene promoter repeat polymorphism in nonhuman primates. Genes, Brain and Behavior, 5(1), 40-45.

Bellingrath, S., Kumsta, R., Meyer, J., Moser, D., Federenko, I. S., Hellhammer, D. H. & Wüst, S. (2005). Assoziation eines Polymorphismus im H6PD Gen mit basaler Cortisolsekretion, Fettmasse und Leptinwerten. Zeitschrift für Medizinische Psychologie, 14(3), 111-117.

Lee, Y. J., Hohoff, C., Domschke, K., Sand, P., Kuhlenbäumer, G., Schirmacher, A., Freitag, C. M., Meyer, J., Stöber, G., Franke, P., Nöthen, M. M., Fritze, J., Fimmers, R., Garritsen, H. S., Stögbauer, F. & Deckert, J. (2005). Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: Association analysis in panic disorder. Neuroscience Letters, 377, 40-43.

McKeane, D. P., Meyer, J., Dobrin, S. E., Melmed, K. M., Ekawardhani, S., Tracy, N. A., Lesch, K. P. & Stephan, D. A. (2005). No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families. Schizophrenia Research, 75(1), 1-3.

Meyer, J., Johannssen, K., Freitag, C. M., Schraut, K., Teuber, I., Hahner, A., Mainhardt, C., Mössner, R., Volz, H.-P., Wienker, T. F., McKeane, D., Stephan, D. A., Rouleau, G., Reif, A. & Lesch, K.-P. (2005). Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder. International Journal of Neuropsychopharmacology, 8(4), 495-594.

Mössner, R., Weichselbaum, A., Marziniak, M., Freitag, C. M., Lesch, K.-P., Sommer, C. & Meyer, J. (2005). A highly polymorphic poly-glutamine stretch in the potassium channel KCNN3 in migraine. Headache, 45(2), 132-136.

Schmitt, A., Gofferje, V., Weber, M., Meyer, J., Mössner, R. & Lesch, K.-P. (2003). The brain-specific protein MLC1 implicated in megalencephalic leukoencephalopathy with subcortical cysts is expressed in glial cells in the murine brain. Glia, 44(3), 283-295.

Steinke, V., Meyer, J., Syagailo, Y. V., Ortega, G., Hameister, H., Mössner, R., Schmitt, A. & Lesch, K.-P. (2003). The genomic organization of the murine Mlc1 (Wkl1, KIAA0027) gene. Journal of Neural Transmission, 110(4), 333-343.

Devaney, J. M., Donarum, E. A., Brown, K. M., Meyer, J., Stöber, G., Lesch, K. P., Nestadt, G., Stephan, D. A. & Pulver, A. E. (2002). No missense mutation of WKL1 in a subgroup of probands with schizophrenia. Molecular Psychiatry, 7(4), 419-423.

Meyer, J., Ortega, G., Schraut, K., Nürnberg, G., Rüschendorf, F., Saar, K., Mössner, R., Wienker, T. F., Reis, A., Stöber, G. & Lesch, K. P. (2002). Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the 15q13-22 locus. Molecular Psychiatry, 7, 220-223.

Meyer, J., Saam, W., Mössner, R., Cangir, Ö., Ortega, G. R., Tatschner, T., Riederer, P., Wienker, T. F. & Lesch, K. P. (2002). Evolutionary conserved microsatellites in the promoter region of the 5-hydroxytryptamine receptor 2C gene (HTR2C) are not associated with bipolar disorder in females. Journal Neural Transmission, 109, 939-946.

Meyer, J., Mai, M., Ortega, G., Mössner, R. & Lesch, K.-P. (2002). Mutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree. Schizophrenia Research, 58(1), 87-91.

Syagailo, Y. V., Okladnova, O., Reimer, E., Grässle, M., Mössner, R., Gattenlöhner, S., Marx, A., Meyer, J. & Lesch, K.-P. (2002). Structural and functional characterization of the PAX7 5-flanking regulatory region. Gene, 294(1-2), 259-268.

Gross, J., Grimm, O., Ortega, G., Teuber, I., Lesch, K.-P. & Meyer, J. (2001). Mutational analysis of the neuronal cadherin gene CELSR1 and exclusion as a candidate for catatonic schizophrenia in a large family. Psychiatric Genetics, 11(4), 197-200.

Meyer, J., Huberth, A., Ortega, G., Syagailo, Y. V., Jatzke, S., Mössner, R., Strom, T. M., Ulzheimer-Teuber, I., Stöber, G., Schmitt, A. & Lesch, K. P. (2001). A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree. Molecular Psychiatry, 6(3), 302-306.

Rubie, C., Schmidt, F., Knapp, M., Sprandel, J., Wiegand, C., Meyer, J., Jungkunz, G., Riederer, P. & Stöber, G. (2001). The human dopamine transporter gene: The 5'-flanking region reveals five diallelic polymorphic sites in a Caucasian population sample. Neuroscience Letters, 297, 125-128.

Stöber, G., Saar, K., Rüschendorf, F., Meyer, J., Nürnberg, G., Jatzke, S., Franzek, E., Reis, A., Lesch, K.-P., Wienker, T. F. & Beckmann, H. (2001). Splitting schizophrenia: Periodic catatonia susceptibility locus on chromosome 15q15. American Journal of Human Genetics, 67(5), 1201-1207.

Syagailo, Y. V., Stöber, G., Gräßle, M., Reimer, E., Knapp, M., Jungkunz, G., Okladnova, O., Meyer, J. & Lesch, K.-P. (2001). Association analysis of the functional monoamine oxidase a gene promoter polymorphism in psychiatric disorders. American Journal of Medical Genetics, 105(2), 168-171.

Arranz, M. J., Munro, J., Birkett, J., Bolonna, A., Mancama, D., Sodhi, M., Lesch, K. P., Meyer, J. F., Sham, P., Collier, D. A., Murray, R. M. & Kerwin, R. W. (2000). Pharmacogenetic prediction of clozapine response. The Lancet, 355(9215), 1615-1616.

Deckert, J., Meyer, J., Catalano, M., Bosi, M., Sand, P., DiBella, D., Ortega, G., Stöber, G., Franke, P., Nöthen, M. M., Fritze, J., Maier, W., Beckmann, H., Propping, P., Bellodi, L. & Lesch, K.-P. (2000). Novel 5'-regulatory region polymorphisms of the 5-HT sub 2C receptor gene: Association study with panic disorder. International Journal of Neuropsychopharmacology, 3(4), 321-325.

Stöber, G., Meyer, J., Nanda, I., Wienker, T. F., Saar, K., Knapp, M., Jatzke, S., Schmid, M., Lesch, K. P. & Beckmann, H. (2000). Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13. American Journal of Medical Genetics, 96(3), 392-397.

Stöber, G., Meyer, J., Nanda, I., Wienker, T. F., Saar, K., Jatzke, S., Schmid, M., Lesch, K.-P. & Beckmann, H. (2000). hKCNN3, which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia. European Archives of Psychiatry and Clinical Neuroscience, 250(4), 163-168.

Lesch, K. P., Jatzke, S., Meyer, J., Stöber, G., Okladnova, O., Mössner, R. & Riederer, P. (1999). Mosaicism for a serotonin transporter gene promoter-associated deletion: Decreased recombination in depression. Journal of Neural Transmission, 106(11-12), 1223-1230.

Meyer, J., Wiedemann, P., Okladnova, O., Brüss, M., Staab, T., Stöber, G., Riederer, P., Bönisch, H. & Lesch, K.-P. (1998). Cloning and functional characterization of the human norepinephrine transporter gene promoter. Journal of Neural Transmission, 105(11-12), 1341-1350.

Stöber, G., Jatzke, S., Meyer, J., Okladnova, O., Knapp, M., Beckmann, H. & Lesch, K.-P. (1998). Short CAG repeats within the hSKCa3 gene associated with schizophrenia: Results of a family-based study. NeuroReport, 9(16), 3595-3599.

Lesch, K. P., Meyer, J., Glatz, K., Flügge, G., Hinney, A., Hebebrand, J., Klauck, S. M., Poustka, A., Poustka, F., Bengel, D., Mössner, R., Riederer, P. & Heils, A. (1997). The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: Alternative biallelic variation in rhesus monkeys. Journal of Neural Transmission, 104(11-12), 1259-1266.

Lorenz, M., Leipert, K.-P., Wilhelm, H., Backmund, B., Prosiegel, M., Meyer, J. & Zihl, J. (1997). Zerebrale Funktionsstörungen und Blindheit - Teil 1. Der Augenarzt, 61, 25-28, 93-95.

Meyer, J., Südbeck, P., Held, M., Wagner, T., Schmitz, M. L., Bricarelli, F. D., Eggermont, E., Friedrich, U., Haas, O. A., Kobelt, A., Leroy, J. G., Van Maldergem, L., Michel, E., Mitulla, B., Pfeiffer, R. A., Schinzel, A., Schmidt, H. & Scherer, G. (1997). Mutational analysis of the "SOX9" gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations. Human Molecular Genetics, 6(1), 91-98.

Meyer, J., Wirth, J., Held, M., Schempp, W. & Scherer, G. (1996). SOX20, a new member of the SOX gene family, is located on chromosome 17p13. Cytogenetics and Cell Genetics, 72(2-3), 246-249.

Wirth, J., Wagner, T., Meyer, J., Pfeiffer, R. A., Tietze, H.-U., Schempp, W. & Scherer, G. (1996). Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9. Human Genetics, 97, 186-193.

Wagner, T., Wirth, J., Meyer, J., Zabel, B., Held, M., Zimmer, J., Pasantes, J., Bricarelli, F. D., Keutel, J., Hustert, E., Wolf, U., Tommerup, N., Schempp, W. & Scherer, G. (1994). Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related Gene SOX9. Cell, 79(6), 1111-1120.

Eder, C., Maercker, C., Meyer, J. & Lipps, H. J. (1993). The processing of macronuclear DNA sequences during macronuclear development of the hypotrichous ciliate Stylonychia lemnae. International Journal of Developmental Biology, 37, 473-477.

Meyer, J., Nick, S., Stamminger, T., Grummt, F., Jahn, G. & Lipps, H. J. (1993). Inhibition of HIV-1 replication by a high-copy-number vector expressing antisense RNA for reverse transcriptase. Gene, 129(2), 263-268.

Weber, S., Schmid, M., Meyer, J., Cooke, H. J. & Lipps, H. J. (1993). A linear vector carrying human telomeres is replicated in unfertilized eggs of Xenopus laevis. Cell Biology International, 17, 623-624.

Hameister, H., Schulz, W. A., Meyer, J., Thoma, S., Adolph, S., Gaa, A. & von Deimling, O. (1992). Gene order and genetic distance of 13 loci spanning murine chromosome 15. Genomics, 14(2), 417-422.



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