Pisanté A - Search Results

1

Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2.

Nissenbaum J, Devor M, Seltzer Z, Gebauer M, Michaelis M, Tal M, Dorfman R, Abitbul-Yarkoni M, Lu Y, Elahipanah T, delCanho S, Minert A, Fried K, Persson AK, Shpigler H, Shabo E, Yakir B, Pisanté A, Darvasi A. Nissenbaum J, et al. Among authors: pisante a. Genome Res. 2010 Sep;20(9):1180-90. doi: 10.1101/gr.104976.110. Epub 2010 Aug 5. Genome Res. 2010. PMID: 20688780 Free PMC article.

2

pain2: A neuropathic pain QTL identified on rat chromosome 2.

Nissenbaum J, Shpigler H, Pisanté A, DelCanho S, Minert A, Seltzer Z, Devor M, Darvasi A. Nissenbaum J, et al. Among authors: pisante a. Pain. 2008 Mar;135(1-2):92-7. doi: 10.1016/j.pain.2007.05.006. Epub 2007 Jun 8. Pain. 2008. PMID: 17560719

3

Sex-specific variability and a 'cage effect' independently mask a neuropathic pain quantitative trait locus detected in a whole genome scan.

Devor M, Gilad A, Arbilly M, Nissenbaum J, Yakir B, Raber P, Minert A, Pisanté A, Darvasi A. Devor M, et al. Among authors: pisante a. Eur J Neurosci. 2007 Aug;26(3):681-8. doi: 10.1111/j.1460-9568.2007.05704.x. Eur J Neurosci. 2007. PMID: 17686043

4

An integrative approach for the identification of quantitative trait loci.

Arbilly M, Pisanté A, Devor M, Darvasi A. Arbilly M, et al. Among authors: pisante a. Anim Genet. 2006 Aug;37 Suppl 1:7-9. doi: 10.1111/j.1365-2052.2006.01472.x. Anim Genet. 2006. PMID: 16886995

5

pain1: a neuropathic pain QTL on mouse chromosome 15 in a C3HxC58 backcross.

Devor M, Gilad A, Arbilly M, Yakir B, Raber P, Pisanté A, Darvasi A. Devor M, et al. Among authors: pisante a. Pain. 2005 Aug;116(3):289-293. doi: 10.1016/j.pain.2005.04.023. Pain. 2005. PMID: 15979798

6

Type 2 diabetes susceptibility loci in the Ashkenazi Jewish population.

Bronstein M, Pisanté A, Yakir B, Darvasi A. Bronstein M, et al. Among authors: pisante a. Hum Genet. 2008 Aug;124(1):101-4. doi: 10.1007/s00439-008-0520-x. Epub 2008 May 31. Hum Genet. 2008. PMID: 18516622

7

COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

Shifman S, Bronstein M, Sternfeld M, Pisanté A, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Yakir B, Zak NB, Darvasi A. Shifman S, et al. Among authors: pisante a. Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):61-4. doi: 10.1002/ajmg.b.30032. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15211633

8

A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients.

Horowitz A, Shifman S, Rivlin N, Pisanté A, Darvasi A. Horowitz A, et al. Among authors: pisante a. Schizophr Res. 2005 Mar 1;73(2-3):263-7. doi: 10.1016/j.schres.2004.02.008. Schizophr Res. 2005. PMID: 15653270

9

Further tests of the association between schizophrenia and single nucleotide polymorphism markers at the catechol-O-methyltransferase locus in an Askenazi Jewish population using microsatellite markers.

Horowitz A, Shifman S, Rivlin N, Pisanté A, Darvasi A. Horowitz A, et al. Among authors: pisante a. Psychiatr Genet. 2005 Sep;15(3):163-9. doi: 10.1097/00041444-200509000-00005. Psychiatr Genet. 2005. PMID: 16094249

10

A variant in the reelin gene increases the risk of schizophrenia and schizoaffective disorder but not bipolar disorder.

Pisanté A, Bronstein M, Yakir B, Darvasi A. Pisanté A, et al. Psychiatr Genet. 2009 Aug;19(4):212. doi: 10.1097/YPG.0b013e32832cebe6. Psychiatr Genet. 2009. PMID: 19436241 No abstract available.

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