Lohoff FW - Search Results

1

An intronic variant in OPRD1 predicts treatment outcome for opioid dependence in African-Americans.

Crist RC, Clarke TK, Ang A, Ambrose-Lanci LM, Lohoff FW, Saxon AJ, Ling W, Hillhouse MP, Bruce RD, Woody G, Berrettini WH. Crist RC, et al. Among authors: lohoff fw. Neuropsychopharmacology. 2013 Sep;38(10):2003-10. doi: 10.1038/npp.2013.99. Epub 2013 Apr 23. Neuropsychopharmacology. 2013. PMID: 23612435 Free PMC article. Clinical Trial.

2

Lack of association between temporal lobe epilepsy and a novel polymorphism in the alpha 2 subunit gene (ATP1A2) of the sodium potassium transporting ATPase.

Buono RJ, Ferraro TN, O'Connor MJ, Sperling MR, Abbey M, Finanger E, Lohoff F, Mulholland N, Berrettini WH. Buono RJ, et al. Am J Med Genet. 2000 Feb 7;96(1):79-83. Am J Med Genet. 2000. PMID: 10686557

3

Lack of association between an interleukin 1 beta (IL-1beta) gene variation and refractory temporal lobe epilepsy.

Buono RJ, Ferraro TN, O'Connor MJ, Sperling MR, Ryan SG, Scattergood T, Mulholland N, Gilmore J, Lohoff FW, Berrettini WH. Buono RJ, et al. Among authors: lohoff fw. Epilepsia. 2001 Jun;42(6):782-4. doi: 10.1046/j.1528-1157.2001.42900.x. Epilepsia. 2001. PMID: 11422336 Free article.

4

Quantitative genetic study of maximal electroshock seizure threshold in mice: evidence for a major seizure susceptibility locus on distal chromosome 1.

Ferraro TN, Golden GT, Smith GG, Longman RL, Snyder RL, DeMuth D, Szpilzak I, Mulholland N, Eng E, Lohoff FW, Buono RJ, Berrettini WH. Ferraro TN, et al. Among authors: lohoff fw. Genomics. 2001 Jul;75(1-3):35-42. doi: 10.1006/geno.2001.6577. Genomics. 2001. PMID: 11472065

5

Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.

Ferraro TN, Golden GT, Smith GG, Martin JF, Lohoff FW, Gieringer TA, Zamboni D, Schwebel CL, Press DM, Kratzer SO, Zhao H, Berrettini WH, Buono RJ. Ferraro TN, et al. Among authors: lohoff fw. Mamm Genome. 2004 Apr;15(4):239-51. doi: 10.1007/s00335-003-2270-3. Mamm Genome. 2004. PMID: 15112102

6

Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility.

Buono RJ, Lohoff FW, Sander T, Sperling MR, O'Connor MJ, Dlugos DJ, Ryan SG, Golden GT, Zhao H, Scattergood TM, Berrettini WH, Ferraro TN. Buono RJ, et al. Among authors: lohoff fw. Epilepsy Res. 2004 Feb;58(2-3):175-83. doi: 10.1016/j.eplepsyres.2004.02.003. Epilepsy Res. 2004. PMID: 15120748

7

No association between common variations in the human alpha 2 subunit gene (ATP1A2) of the sodium-potassium-transporting ATPase and idiopathic generalized epilepsy.

Lohoff FW, Ferraro TN, Sander T, Zhao H, Dahl JP, Berrettini WH, Buono RJ. Lohoff FW, et al. Neurosci Lett. 2005 Jul 1-8;382(1-2):33-8. doi: 10.1016/j.neulet.2005.02.057. Neurosci Lett. 2005. PMID: 15911117

8

Lack of association between single nucleotide polymorphisms in the corticotropin releasing hormone receptor 1 (CRHR1) gene and alcohol dependence.

Dahl JP, Doyle GA, Oslin DW, Buono RJ, Ferraro TN, Lohoff FW, Berrettini WH. Dahl JP, et al. Among authors: lohoff fw. J Psychiatr Res. 2005 Sep;39(5):475-9. doi: 10.1016/j.jpsychires.2004.12.004. Epub 2005 Jan 20. J Psychiatr Res. 2005. PMID: 15992556

9

No association between common variations in the neuronal nicotinic acetylcholine receptor alpha2 subunit gene (CHRNA2) and bipolar I disorder.

Lohoff FW, Ferraro TN, McNabb L, Schwebel C, Dahl JP, Doyle GA, Buono RJ, Berrettini WH. Lohoff FW, et al. Psychiatry Res. 2005 Jun 30;135(3):171-7. doi: 10.1016/j.psychres.2005.04.004. Psychiatry Res. 2005. PMID: 15996750

10

Lack of association between variations in the brain-derived neurotrophic factor (BDNF) gene and temporal lobe epilepsy.

Lohoff FW, Ferraro TN, Dahl JP, Hildebrandt MA, Scattergood TM, O'Connor MJ, Sperling MR, Dlugos DJ, Berrettini WH, Buono RJ. Lohoff FW, et al. Epilepsy Res. 2005 Aug-Sep;66(1-3):59-62. doi: 10.1016/j.eplepsyres.2005.06.005. Epilepsy Res. 2005. PMID: 16105728

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