Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Attention and TH[original query] |
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A promoter nucleotide variant of the dendritic cell-specific DCNP1 associates with serum IgE levels specific for dust mite allergens among the Korean asthmatics. Genes and immunity 2007 Jul 8 (5): 369-78. Kim Y, Park C-S, Shin H D, Choi J-W, Cheong H S, Park B L, Choi Y H, Jang A S, Park S W, Lee Y M, Lee E J, Park S G, Lee J-Y, Lee J-K, Han B G, Oh B, Kimm |
[Analysis of polymorphisms in genes of insulin receptor substrate-1 and enzymes involved in estrogen biosynthesis and metabolism among breast cancer patients with BRCA1 mutations]. Voprosy onkologii 2009 55 (2): 158-64. Bershte?n L M, Ulybina Iu M, Pozharisski? K M, Imianitov E |
[The connection between Arg353Gln polymorphism of coagulation factor VII and recurrent miscarriages]. Ginekologia polska 2009 Jan 80 (1): 1. Seremak-Mrozikiewicz A, Drews K, Kurzawi?ska G, Barlik M, Mrozikiewicz PM |
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease. Human mutation 2010 Oct 31 (10): E1767-71. Bademci Güney, Edwards Todd L, Torres Andre L, Scott William K, Züchner Stephan, Martin Eden R, Vance Jeffery M, Wang Liyo |
Candidate system analysis in ADHD: evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2012 Apr 13 (4): 281-92. Ribasés Marta, Ramos-Quiroga Josep Antoni, Hervás Amaia, Sánchez-Mora Cristina, Bosch Rosa, Bielsa Anna, Gastaminza Xavier, Lesch Klaus-Peter, Reif Andreas, Renner Tobias J, Romanos Marcel, Warnke Andreas, Walitza Susanne, Freitag Christine, Meyer Jobst, Palmason Haukur, Casas Miquel, Bayés Mònica, Cormand B |
Alpha-2A adrenergic receptor gene variants are associated with increased intra-individual variability in response time. Molecular psychiatry 2014 Sep 19 (9): 1031-6. Cummins T D R, Jacoby O, Hawi Z, Nandam L S, Byrne M A V, Kim B-N, Wagner J, Chambers C D, Bellgrove M |
RHD gene polymorphisms in alloimmunized RhD-negative individuals with high rate of racial admixture. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2013 Feb 48 (1): 113-6. Martin Fábio O, de Menezes Sidnéia S, Chiba Akemi K, Langhi Dante M, Nardozza Luciano M M, Chiattone Carlos S, Bordin José |
Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal. BMC genetics 2016 06 17 (1): 92. Karmakar Arijit, Maitra Subhamita, Chakraborti Barnali, Verma Deepak, Sinha Swagata, Mohanakumar Kochupurackal P, Rajamma Usha, Mukhopadhyay Kanch |
Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies. Molecular psychiatry 2016 May . Bonvicini C, Faraone S V, Scassellati |
Pharmacogenetics of methylphenidate response and tolerability in attention-deficit/hyperactivity disorder. The pharmacogenomics journal 2016 Jan . Pagerols M, Richarte V, Sánchez-Mora C, Garcia-Martínez I, Corrales M, Corominas M, Cormand B, Casas M, Ribasés M, Ramos-Quiroga J |
Macro- and Microelement Status in Animal and Human Hypertension: the Role of the ACE Gene I/D Polymorphism. Biological trace element research 2017 Mar . Pavlyushchik Olena, Afonin Viktor, Fatykhava Svetlana, Shabunya Polina, Sarokina Viktoryia, Khapaliuk Aliaksan |
Region-Specific Regulation of Presynaptic Dopamine Homeostasis by D Autoreceptors Shapes the In Vivo Impact of the Neuropsychiatric Disease-Associated DAT Variant Val559. The Journal of neuroscience : the official journal of the Society for Neuroscience 2018 Jun 38 (23): 5302-5312. Gowrishankar Raajaram, Gresch Paul J, Davis Gwynne L, Katamish Rania M, Riele Justin R, Stewart Adele M, Vaughan Roxanne A, Hahn Maureen K, Blakely Randy |
Protective Effect of the MCP-1 Gene Haplotype against Schizophrenia. BioMed research international 2019 12 2019 4042615. Saoud Hana, Inoubli Oumaima, Ben Fredj Sihem, Hassine Mohsen, Ben Mohamed Bochra, Gaha Lotfi, Hadj Jrad Besma B |
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- Page last updated:Jun 11, 2024
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