Tobias R - Search Results

1

Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.

Lodha N, Bonfield S, Orton NC, Doering CJ, McRory JE, Mema SC, Rehak R, Sauvé Y, Tobias R, Stell WK, Bech-Hansen NT. Lodha N, et al. Among authors: tobias r. Adv Exp Med Biol. 2010;664:549-58. doi: 10.1007/978-1-4419-1399-9_63. Adv Exp Med Biol. 2010. PMID: 20238058

2

A novel CACNA1F gene mutation causes Aland Island eye disease.

Jalkanen R, Bech-Hansen NT, Tobias R, Sankila EM, Mäntyjärvi M, Forsius H, de la Chapelle A, Alitalo T. Jalkanen R, et al. Among authors: tobias r. Invest Ophthalmol Vis Sci. 2007 Jun;48(6):2498-502. doi: 10.1167/iovs.06-1103. Invest Ophthalmol Vis Sci. 2007. PMID: 17525176

3

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.

Jalkanen R, Mäntyjärvi M, Tobias R, Isosomppi J, Sankila EM, Alitalo T, Bech-Hansen NT. Jalkanen R, et al. Among authors: tobias r. J Med Genet. 2006 Aug;43(8):699-704. doi: 10.1136/jmg.2006.040741. Epub 2006 Feb 27. J Med Genet. 2006. PMID: 16505158 Free PMC article.

4

Serotonin transporter gene promoter region polymorphism associated with poststroke major depression.

Ramasubbu R, Tobias R, Buchan AM, Bech-Hansen NT. Ramasubbu R, et al. Among authors: tobias r. J Neuropsychiatry Clin Neurosci. 2006 Winter;18(1):96-9. doi: 10.1176/jnp.18.1.96. J Neuropsychiatry Clin Neurosci. 2006. PMID: 16525076

5

Extended evaluation of serotonin transporter gene functional polymorphisms in subjects with post-stroke depression.

Ramasubbu R, Tobias R, Bech-Hansen NT. Ramasubbu R, et al. Among authors: tobias r. Can J Psychiatry. 2008 Mar;53(3):197-201. doi: 10.1177/070674370805300310. Can J Psychiatry. 2008. PMID: 18441666

6

Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP).

Cummings KJ, Klotz C, Liu WQ, Weese-Mayer DE, Marazita ML, Cooper ME, Berry-Kravis EM, Tobias R, Goldie C, Bech-Hansen NT, Wilson RJ. Cummings KJ, et al. Among authors: tobias r. Acta Paediatr. 2009 Mar;98(3):482-9. doi: 10.1111/j.1651-2227.2008.01131.x. Epub 2008 Dec 17. Acta Paediatr. 2009. PMID: 19120039

7

Nonsyndromic cleft lip with or without cleft palate in China: assessment of candidate regions.

Marazita ML, Field LL, Cooper ME, Tobias R, Maher BS, Peanchitlertkajorn S, Liu YE. Marazita ML, et al. Among authors: tobias r. Cleft Palate Craniofac J. 2002 Mar;39(2):149-56. doi: 10.1597/1545-1569_2002_039_0149_nclwow_2.0.co_2. Cleft Palate Craniofac J. 2002. PMID: 11879070

8

Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families.

Marazita ML, Field LL, Cooper ME, Tobias R, Maher BS, Peanchitlertkajorn S, Liu YE. Marazita ML, et al. Among authors: tobias r. Am J Hum Genet. 2002 Aug;71(2):349-64. doi: 10.1086/341944. Epub 2002 Jun 26. Am J Hum Genet. 2002. PMID: 12087515 Free PMC article.

9

Association mapping of disease loci, by use of a pooled DNA genomic screen.

Barcellos LF, Klitz W, Field LL, Tobias R, Bowcock AM, Wilson R, Nelson MP, Nagatomi J, Thomson G. Barcellos LF, et al. Among authors: tobias r. Am J Hum Genet. 1997 Sep;61(3):734-47. doi: 10.1086/515512. Am J Hum Genet. 1997. PMID: 9326338 Free PMC article.

10

Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31.

Field LL, Tobias R, Thomson G, Plon S. Field LL, et al. Among authors: tobias r. Genomics. 1996 Apr 1;33(1):1-8. doi: 10.1006/geno.1996.0153. Genomics. 1996. PMID: 8617492

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