Bespalova IN[au] - Search Results

Year	Number of Results
1984	2
1986	1
1993	2
1994	1
1997	2
1998	1
1999	2
2000	2
2001	1
2002	1
2003	1
2004	1
2005	1
2010	1
2011	1
2012	4
2022	0

1

Disease susceptibility genes for autism.

Bespalova IN, Buxbaum JD. Bespalova IN, et al. Ann Med. 2003;35(4):274-81. doi: 10.1080/07853890310005966. Ann Med. 2003. PMID: 12846270 Review.

2

Non-synonymous variants in the AMACR gene are associated with schizophrenia.

Bespalova IN, Durner M, Ritter BP, Angelo GW, Rossy-Fullana E, Carrion-Baralt J, Schmeidler J, Silverman JM. Bespalova IN, et al. Schizophr Res. 2010 Dec;124(1-3):208-15. doi: 10.1016/j.schres.2010.08.040. Epub 2010 Sep 26. Schizophr Res. 2010. PMID: 20875727 Free PMC article.

3

Genetic variations in the ADAMTS12 gene are associated with schizophrenia in Puerto Rican patients of Spanish descent.

Bespalova IN, Angelo GW, Ritter BP, Hunter J, Reyes-Rabanillo ML, Siever LJ, Silverman JM. Bespalova IN, et al. Neuromolecular Med. 2012 Mar;14(1):53-64. doi: 10.1007/s12017-012-8169-y. Epub 2012 Feb 10. Neuromolecular Med. 2012. PMID: 22322903

4

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.

Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL, Buxbaum JD. Ramoz N, et al. Among authors: bespalova in. Am J Psychiatry. 2004 Apr;161(4):662-9. doi: 10.1176/appi.ajp.161.4.662. Am J Psychiatry. 2004. PMID: 15056512

5

C-reactive protein and familial risk for dementia: a phenotype for successful cognitive aging.

Silverman JM, Schmeidler J, Beeri MS, Rosendorff C, Sano M, Grossman HT, Carrión-Baralt JR, Bespalova IN, West R, Haroutunian V. Silverman JM, et al. Among authors: bespalova in. Neurology. 2012 Sep 11;79(11):1116-23. doi: 10.1212/WNL.0b013e3182698c89. Epub 2012 Aug 15. Neurology. 2012. PMID: 22895578 Free PMC article.

6

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM. Bespalova IN, et al. Hum Mol Genet. 2001 Oct 15;10(22):2501-8. doi: 10.1093/hmg/10.22.2501. Hum Mol Genet. 2001. PMID: 11709537 Free PMC article.

7

Mutation screening of PDZD2, GOLPH3, and MTMR12 genes in patients with schizophrenia.

Ritter BP, Angelo GW, Durner M, Rossy-Fullana E, Carrion-Baralt J, Silverman JM, Bespalova IN. Ritter BP, et al. Among authors: bespalova in. Psychiatr Genet. 2012 Feb;22(1):51-2. doi: 10.1097/YPG.0b013e3283463dd7. Psychiatr Genet. 2012. PMID: 21451436 No abstract available.

8

Novel cystatin B mutation and diagnostic PCR assay in an Unverricht-Lundborg progressive myoclonus epilepsy patient.

Bespalova IN, Adkins S, Pranzatelli M, Burmeister M. Bespalova IN, et al. Am J Med Genet. 1997 Sep 19;74(5):467-71. doi: 10.1002/(sici)1096-8628(19970919)74:5<467::aid-ajmg1>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9342192 Free article.

9

Fine mapping of the 5p13 locus linked to schizophrenia and schizotypal personality disorder in a Puerto Rican family.

Bespalova IN, Angelo GW, Durner M, Smith CJ, Siever LJ, Buxbaum JD, Silverman JM. Bespalova IN, et al. Psychiatr Genet. 2005 Sep;15(3):205-10. doi: 10.1097/00041444-200509000-00012. Psychiatr Genet. 2005. PMID: 16094256

10

Identification of a novel LIM domain gene, LMCD1, and chromosomal localization in human and mouse.

Bespalova IN, Burmeister M. Bespalova IN, et al. Genomics. 2000 Jan 1;63(1):69-74. doi: 10.1006/geno.1999.6049. Genomics. 2000. PMID: 10662546

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