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Page 1
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.
Arcos-Burgos M, Jain M, Acosta MT, Shively S, Stanescu H, Wallis D, Domené S, Vélez JI, Karkera JD, Balog J, Berg K, Kleta R, Gahl WA, Roessler E, Long R, Lie J, Pineda D, Londoño AC, Palacio JD, Arbelaez A, Lopera F, Elia J, Hakonarson H, Johansson S, Knappskog PM, Haavik J, Ribases M, Cormand B, Bayes M, Casas M, Ramos-Quiroga JA, Hervas A, Maher BS, Faraone SV, Seitz C, Freitag CM, Palmason H, Meyer J, Romanos M, Walitza S, Hemminger U, Warnke A, Romanos J, Renner T, Jacob C, Lesch KP, Swanson J, Vortmeyer A, Bailey-Wilson JE, Castellanos FX, Muenke M. Arcos-Burgos M, et al. Among authors: hemminger u. Mol Psychiatry. 2010 Nov;15(11):1053-66. doi: 10.1038/mp.2010.6. Epub 2010 Feb 16. Mol Psychiatry. 2010. PMID: 20157310 Free article.
A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD.
Jain M, Vélez JI, Acosta MT, Palacio LG, Balog J, Roessler E, Pineda D, Londoño AC, Palacio JD, Arbelaez A, Lopera F, Elia J, Hakonarson H, Seitz C, Freitag CM, Palmason H, Meyer J, Romanos M, Walitza S, Hemminger U, Warnke A, Romanos J, Renner T, Jacob C, Lesch KP, Swanson J, Castellanos FX, Bailey-Wilson JE, Arcos-Burgos M, Muenke M. Jain M, et al. Among authors: hemminger u. Mol Psychiatry. 2012 Jul;17(7):741-7. doi: 10.1038/mp.2011.59. Epub 2011 May 24. Mol Psychiatry. 2012. PMID: 21606926 Free PMC article.
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs.
Hebebrand J, Dempfle A, Saar K, Thiele H, Herpertz-Dahlmann B, Linder M, Kiefl H, Remschmidt H, Hemminger U, Warnke A, Knölker U, Heiser P, Friedel S, Hinney A, Schäfer H, Nürnberg P, Konrad K. Hebebrand J, et al. Among authors: hemminger u. Mol Psychiatry. 2006 Feb;11(2):196-205. doi: 10.1038/sj.mp.4001761. Mol Psychiatry. 2006. PMID: 16222334 Clinical Trial.
Children and adolescents with obsessive-compulsive disorder and comorbid attention-deficit/hyperactivity disorder: preliminary results of a prospective follow-up study.
Walitza S, Zellmann H, Irblich B, Lange KW, Tucha O, Hemminger U, Wucherer K, Rost V, Reinecker H, Wewetzer C, Warnke A. Walitza S, et al. Among authors: hemminger u. J Neural Transm (Vienna). 2008;115(2):187-90. doi: 10.1007/s00702-007-0841-2. Epub 2008 Jan 16. J Neural Transm (Vienna). 2008. PMID: 18200431
[Formal genetic findings in attention-deficit/hyperactivity-disorder].
Smidt J, Heiser P, Dempfle A, Konrad K, Hemminger U, Kathöfer A, Halbach A, Strub J, Grabarkiewicz J, Kiefl H, Linder M, Knölker U, Warnke A, Remschmidt H, Herpertz-Dahlmann B, Hebebrand J. Smidt J, et al. Among authors: hemminger u. Fortschr Neurol Psychiatr. 2003 Jul;71(7):366-77. doi: 10.1055/s-2003-40561. Fortschr Neurol Psychiatr. 2003. PMID: 12858257 Review. German.
Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.
Friedel S, Horro FF, Wermter AK, Geller F, Dempfle A, Reichwald K, Smidt J, Brönner G, Konrad K, Herpertz-Dahlmann B, Warnke A, Hemminger U, Linder M, Kiefl H, Goldschmidt HP, Siegfried W, Remschmidt H, Hinney A, Hebebrand J. Friedel S, et al. Among authors: hemminger u. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):96-9. doi: 10.1002/ajmg.b.30090. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15457498
[Children and adolescents with obsessive-compulsive disorders].
Zellmann H, Jans T, Irblich B, Hemminger U, Reinecker H, Sauer C, Lange KW, Tucha O, Wewetzer C, Warnke A, Walitza S. Zellmann H, et al. Among authors: hemminger u. Z Kinder Jugendpsychiatr Psychother. 2009 May;37(3):173-82. doi: 10.1024/1422-4917.37.3.173. Z Kinder Jugendpsychiatr Psychother. 2009. PMID: 19415602 German.
11 results