Peltonen L - Search Results

1

Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases.

Feng J, Craddock N, Jones IR, Cook EH Jr, Goldman D, Heston LL, Peltonen L, DeLisi LE, Sommer SS. Feng J, et al. Among authors: peltonen l. Psychiatr Genet. 2001 Mar;11(1):45-8. doi: 10.1097/00041444-200103000-00009. Psychiatr Genet. 2001. PMID: 11409700

2

Scanning of estrogen receptor alpha (ERalpha) and thyroid hormone receptor alpha (TRalpha) genes in patients with psychiatric diseases: four missense mutations identified in ERalpha gene.

Feng J, Yan J, Michaud S, Craddock N, Jones IR, Cook EH Jr, Goldman D, Heston LL, Peltonen L, Delisi LE, Sommer SS. Feng J, et al. Among authors: peltonen l. Am J Med Genet. 2001 May 8;105(4):369-74. doi: 10.1002/ajmg.1364. Am J Med Genet. 2001. PMID: 11378852

3

An in-frame deletion in the alpha(2C) adrenergic receptor is common in African--Americans.

Feng J, Zheng J, Gelernter J, Kranzler H, Cook E, Goldman D, Jones IR, Craddock N, Heston LL, Delisi L, Peltonen L, Bennett WP, Sommer SS. Feng J, et al. Among authors: peltonen l. Mol Psychiatry. 2001 Mar;6(2):168-72. doi: 10.1038/sj.mp.4000817. Mol Psychiatry. 2001. PMID: 11317218

4

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, Mowry BJ, Brzustowicz LM, Maziade M, Sklar P, Garver DL, Abecasis GR, Lerer B, Fallin MD, Gurling HM, Gejman PV, Lindholm E, Moises HW, Byerley W, Wijsman EM, Forabosco P, Tsuang MT, Hwu HG, Okazaki Y, Kendler KS, Wormley B, Fanous A, Walsh D, O'Neill FA, Peltonen L, Nestadt G, Lasseter VK, Liang KY, Papadimitriou GM, Dikeos DG, Schwab SG, Owen MJ, O'Donovan MC, Norton N, Hare E, Raventos H, Nicolini H, Albus M, Maier W, Nimgaonkar VL, Terenius L, Mallet J, Jay M, Godard S, Nertney D, Alexander M, Crowe RR, Silverman JM, Bassett AS, Roy MA, Mérette C, Pato CN, Pato MT, Roos JL, Kohn Y, Amann-Zalcenstein D, Kalsi G, McQuillin A, Curtis D, Brynjolfson J, Sigmundsson T, Petursson H, Sanders AR, Duan J, Jazin E, Myles-Worsley M, Karayiorgou M, Lewis CM. Ng MY, et al. Among authors: peltonen l. Mol Psychiatry. 2009 Aug;14(8):774-85. doi: 10.1038/mp.2008.135. Epub 2008 Dec 30. Mol Psychiatry. 2009. PMID: 19349958 Free PMC article.

5

Dual origins of Finns revealed by Y chromosome haplotype variation.

Kittles RA, Perola M, Peltonen L, Bergen AW, Aragon RA, Virkkunen M, Linnoila M, Goldman D, Long JC. Kittles RA, et al. Among authors: peltonen l. Am J Hum Genet. 1998 May;62(5):1171-9. doi: 10.1086/301831. Am J Hum Genet. 1998. PMID: 9545401 Free PMC article.

6

The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation.

Aula N, Salomäki P, Timonen R, Verheijen F, Mancini G, Månsson JE, Aula P, Peltonen L. Aula N, et al. Among authors: peltonen l. Am J Hum Genet. 2000 Oct;67(4):832-40. doi: 10.1086/303077. Epub 2000 Aug 17. Am J Hum Genet. 2000. PMID: 10947946 Free PMC article.

7

Linkage analysis in two schizophrenic families originating from a restricted subpopulation of Finland.

Hovatta I, Seppälä J, Pekkarinen P, Tanskanen A, Lönnqvist J, Peltonen L. Hovatta I, et al. Among authors: peltonen l. Psychiatr Genet. 1994 Fall;4(3):143-52. doi: 10.1097/00041444-199400430-00004. Psychiatr Genet. 1994. PMID: 7719700

8

Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome.

Kainulainen K, Karttunen L, Puhakka L, Sakai L, Peltonen L. Kainulainen K, et al. Among authors: peltonen l. Nat Genet. 1994 Jan;6(1):64-9. doi: 10.1038/ng0194-64. Nat Genet. 1994. PMID: 8136837

9

Dissecting a population genome for targeted screening of disease mutations.

Pastinen T, Perola M, Ignatius J, Sabatti C, Tainola P, Levander M, Syvänen AC, Peltonen L. Pastinen T, et al. Among authors: peltonen l. Hum Mol Genet. 2001 Dec 15;10(26):2961-72. doi: 10.1093/hmg/10.26.2961. Hum Mol Genet. 2001. PMID: 11751678

10

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22.

Ekelund J, Lichtermann D, Hovatta I, Ellonen P, Suvisaari J, Terwilliger JD, Juvonen H, Varilo T, Arajärvi R, Kokko-Sahin ML, Lönnqvist J, Peltonen L. Ekelund J, et al. Among authors: peltonen l. Hum Mol Genet. 2000 Apr 12;9(7):1049-57. doi: 10.1093/hmg/9.7.1049. Hum Mol Genet. 2000. PMID: 10767329

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