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Aberrant expression of agouti signaling protein (ASIP) as a cause of monogenic severe childhood obesity.
Kempf E, Landgraf K, Stein R, Hanschkow M, Hilbert A, Abou Jamra R, Boczki P, Herberth G, Kühnapfel A, Tseng YH, Stäubert C, Schöneberg T, Kühnen P, Rayner NW, Zeggini E, Kiess W, Blüher M, Körner A. Kempf E, et al. Among authors: abou jamra r. Nat Metab. 2022 Dec;4(12):1697-1712. doi: 10.1038/s42255-022-00703-9. Epub 2022 Dec 19. Nat Metab. 2022. PMID: 36536132 Free PMC article.
A family-based and case-control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder.
Abou Jamra R, Sircar I, Becker T, Freudenberg-Hua Y, Ohlraun S, Freudenberg J, Brockschmidt F, Schulze TG, Gross M, Spira F, Deschner M, Schmäl C, Maier W, Propping P, Rietschel M, Cichon S, Nöthen MM, Schumacher J. Abou Jamra R, et al. Mol Psychiatry. 2005 Jul;10(7):618-20. doi: 10.1038/sj.mp.4001665. Mol Psychiatry. 2005. PMID: 15852064 No abstract available.
Correction: Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial features.
Hollink IHIM, Alfadhel M, Al-Wakeel AS, Ababneh F, Pfundt R, de Man SA, Abou Jamra R, Rolfs A, Bertoli-Avella AM, van de Laar IMBH. Hollink IHIM, et al. Among authors: abou jamra r. J Hum Genet. 2018 Apr;63(4):539. doi: 10.1038/s10038-017-0373-z. Epub 2018 Mar 8. J Hum Genet. 2018. PMID: 29576627
No association between a putative functional promoter variant in the dopamine beta-hydroxylase gene and schizophrenia.
Jönsson EG, Abou Jamra R, Schumacher J, Flyckt L, Edman G, Forslund K, Mattila-Evenden M, Rylander G, Asberg M, Bjerkenstedt L, Wiesel FA, Propping P, Cichon S, Nöthen MM, Sedvall GC. Jönsson EG, et al. Among authors: abou jamra r. Psychiatr Genet. 2003 Sep;13(3):175-8. doi: 10.1097/00041444-200309000-00007. Psychiatr Genet. 2003. PMID: 12960750
Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity.
Abou Jamra R, Wohlfart S, Zweier M, Uebe S, Priebe L, Ekici A, Giesebrecht S, Abboud A, Al Khateeb MA, Fakher M, Hamdan S, Ismael A, Muhammad S, Nöthen MM, Schumacher J, Reis A. Abou Jamra R, et al. Eur J Hum Genet. 2011 Nov;19(11):1161-6. doi: 10.1038/ejhg.2011.98. Epub 2011 Jun 1. Eur J Hum Genet. 2011. PMID: 21629298 Free PMC article.
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
Schumacher J, Laje G, Abou Jamra R, Becker T, Mühleisen TW, Vasilescu C, Mattheisen M, Herms S, Hoffmann P, Hillmer AM, Georgi A, Herold C, Schulze TG, Propping P, Rietschel M, McMahon FJ, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: abou jamra r. Hum Mol Genet. 2009 Jul 15;18(14):2719-27. doi: 10.1093/hmg/ddp204. Epub 2009 May 4. Hum Mol Genet. 2009. PMID: 19414483 Free PMC article.
Association study of a functional promoter polymorphism in the XBP1 gene and schizophrenia.
Jönsson EG, Cichon S, Schumacher J, Abou Jamra R, Schulze TG, Deschner M, Forslund K, Hall H, Propping P, Czerski PM, Dmitrak-Weglarz M, Kapelski P, Driessen M, Maier W, Hauser J, Rietschel M, Nöthen MM. Jönsson EG, et al. Among authors: abou jamra r. Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):71-5. doi: 10.1002/ajmg.b.30262. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16342282
117 results