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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2002 2
2003 1
2004 1
2005 3
2006 1
2007 2
2008 5
2009 7
2010 4
2011 8
2012 7
2013 5
2014 2
2015 7
2016 8
2017 2
2018 8
2019 7
2020 2
2021 1
2022 1
2024 0

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69 results

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Page 1
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Demontis D, Walters RK, Martin J, Mattheisen M, Als TD, Agerbo E, Baldursson G, Belliveau R, Bybjerg-Grauholm J, Bækvad-Hansen M, Cerrato F, Chambert K, Churchhouse C, Dumont A, Eriksson N, Gandal M, Goldstein JI, Grasby KL, Grove J, Gudmundsson OO, Hansen CS, Hauberg ME, Hollegaard MV, Howrigan DP, Huang H, Maller JB, Martin AR, Martin NG, Moran J, Pallesen J, Palmer DS, Pedersen CB, Pedersen MG, Poterba T, Poulsen JB, Ripke S, Robinson EB, Satterstrom FK, Stefansson H, Stevens C, Turley P, Walters GB, Won H, Wright MJ; ADHD Working Group of the Psychiatric Genomics Consortium (PGC); Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium; 23andMe Research Team; Andreassen OA, Asherson P, Burton CL, Boomsma DI, Cormand B, Dalsgaard S, Franke B, Gelernter J, Geschwind D, Hakonarson H, Haavik J, Kranzler HR, Kuntsi J, Langley K, Lesch KP, Middeldorp C, Reif A, Rohde LA, Roussos P, Schachar R, Sklar P, Sonuga-Barke EJS, Sullivan PF, Thapar A, Tung JY, Waldman ID, Medland SE, Stefansson K, Nordentoft M, Hougaard DM, Werge T, Mors O, Mortensen PB, Daly MJ, Faraone SV, Børglum AD, Neale BM. Demontis D, et al. Nat Genet. 2019 Jan;51(1):63-75. doi: 10.1038/s41588-018-0269-7. Epub 2018 Nov 26. Nat Genet. 2019. PMID: 30478444 Free PMC article.
Leserbrief zu K. Knobloch: Extrakorporale Magnetotransduktionstherapie (EMTT) und hochenergetische fokussierte elektromagnetische extrakorporale Stoßwellentherapie (ESWT) zur Knochenstimulation bei metakarpaler Pseudarthrose – ein Fallbericht. Handchir Plast Chir 2021; 53: 82–86.
Meyer J. Meyer J. Handchir Mikrochir Plast Chir. 2021 Jun;53(3):332-333. doi: 10.1055/a-1440-0169. Epub 2021 Jun 16. Handchir Mikrochir Plast Chir. 2021. PMID: 34134168 German. No abstract available.
Genome-wide linkage analysis of families with primary hyperhidrosis.
Schote AB, Schiel F, Schmitt B, Winnikes U, Frank N, Gross K, Croyé MA, Tarragon E, Bekhit A, Bobbili DR, May P, Schick C, Meyer J. Schote AB, et al. Among authors: meyer j. PLoS One. 2020 Dec 30;15(12):e0244565. doi: 10.1371/journal.pone.0244565. eCollection 2020. PLoS One. 2020. PMID: 33378362 Free PMC article.
Empirically Determined, Psychopathological Subtypes in Children With ADHD.
Zenglein Y, Schwenck C, Westerwald E, Schmidt C, Beuth S, Meyer J, Palmason H, Seitz C, Hänig S, Freitag CM. Zenglein Y, et al. Among authors: meyer j. J Atten Disord. 2016 Feb;20(2):96-107. doi: 10.1177/1087054713508312. Epub 2013 Oct 22. J Atten Disord. 2016. PMID: 24149942
5-HTTLPR genotype influences amygdala volume.
Scherk H, Gruber O, Menzel P, Schneider-Axmann T, Kemmer C, Usher J, Reith W, Meyer J, Falkai P. Scherk H, et al. Among authors: meyer j. Eur Arch Psychiatry Clin Neurosci. 2009 Jun;259(4):212-7. doi: 10.1007/s00406-008-0853-4. Epub 2009 Feb 17. Eur Arch Psychiatry Clin Neurosci. 2009. PMID: 19224115 Free PMC article.
Case-control genome-wide association study of attention-deficit/hyperactivity disorder.
Neale BM, Medland S, Ripke S, Anney RJ, Asherson P, Buitelaar J, Franke B, Gill M, Kent L, Holmans P, Middleton F, Thapar A, Lesch KP, Faraone SV, Daly M, Nguyen TT, Schäfer H, Steinhausen HC, Reif A, Renner TJ, Romanos M, Romanos J, Warnke A, Walitza S, Freitag C, Meyer J, Palmason H, Rothenberger A, Hawi Z, Sergeant J, Roeyers H, Mick E, Biederman J; IMAGE II Consortium Group. Neale BM, et al. Among authors: meyer j. J Am Acad Child Adolesc Psychiatry. 2010 Sep;49(9):906-20. doi: 10.1016/j.jaac.2010.06.007. Epub 2010 Aug 5. J Am Acad Child Adolesc Psychiatry. 2010. PMID: 20732627 Free PMC article.
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder.
Martin J, Walters RK, Demontis D, Mattheisen M, Lee SH, Robinson E, Brikell I, Ghirardi L, Larsson H, Lichtenstein P, Eriksson N; 23andMe Research Team; Psychiatric Genomics Consortium: ADHD Subgroup; iPSYCH–Broad ADHD Workgroup; Werge T, Mortensen PB, Pedersen MG, Mors O, Nordentoft M, Hougaard DM, Bybjerg-Grauholm J, Wray NR, Franke B, Faraone SV, O'Donovan MC, Thapar A, Børglum AD, Neale BM. Martin J, et al. Biol Psychiatry. 2018 Jun 15;83(12):1044-1053. doi: 10.1016/j.biopsych.2017.11.026. Epub 2017 Dec 2. Biol Psychiatry. 2018. PMID: 29325848 Free PMC article.
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.
Mooney MA, McWeeney SK, Faraone SV, Hinney A, Hebebrand J; IMAGE2 Consortium; German ADHD GWAS Group; Nigg JT, Wilmot B. Mooney MA, et al. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):815-26. doi: 10.1002/ajmg.b.32446. Epub 2016 Mar 22. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 27004716 Free PMC article.
69 results