Terwilliger J - Search Results

1

Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population.

Pastinen T, Perola M, Niini P, Terwilliger J, Salomaa V, Vartiainen E, Peltonen L, Syvänen A. Pastinen T, et al. Among authors: terwilliger j. Hum Mol Genet. 1998 Sep;7(9):1453-62. doi: 10.1093/hmg/7.9.1453. Hum Mol Genet. 1998. PMID: 9700201

2

The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories.

Varilo T, Paunio T, Parker A, Perola M, Meyer J, Terwilliger JD, Peltonen L. Varilo T, et al. Among authors: terwilliger jd. Hum Mol Genet. 2003 Jan 1;12(1):51-9. doi: 10.1093/hmg/ddg005. Hum Mol Genet. 2003. PMID: 12490532

3

AUTOGSCAN: powerful tools for automated genome-wide linkage and linkage disequilibrium analysis.

Hiekkalinna T, Terwilliger JD, Sammalisto S, Peltonen L, Perola M. Hiekkalinna T, et al. Twin Res Hum Genet. 2005 Feb;8(1):16-21. doi: 10.1375/1832427053435382. Twin Res Hum Genet. 2005. PMID: 15836805

4

Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.

Hennah W, Tomppo L, Hiekkalinna T, Palo OM, Kilpinen H, Ekelund J, Tuulio-Henriksson A, Silander K, Partonen T, Paunio T, Terwilliger JD, Lönnqvist J, Peltonen L. Hennah W, et al. Among authors: terwilliger jd. Hum Mol Genet. 2007 Mar 1;16(5):453-62. doi: 10.1093/hmg/ddl462. Epub 2006 Dec 21. Hum Mol Genet. 2007. PMID: 17185386

5

Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus.

Nikali K, Suomalainen A, Terwilliger J, Koskinen T, Weissenbach J, Peltonen L. Nikali K, et al. Among authors: terwilliger j. Am J Hum Genet. 1995 May;56(5):1088-95. Am J Hum Genet. 1995. PMID: 7726163 Free PMC article.

6

Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension.

Kainulainen K, Perola M, Terwilliger J, Kaprio J, Koskenvuo M, Syvänen AC, Vartiainen E, Peltonen L, Kontula K. Kainulainen K, et al. Among authors: terwilliger j. Hypertension. 1999 Mar;33(3):844-9. doi: 10.1161/01.hyp.33.3.844. Hypertension. 1999. PMID: 10082497

7

Two-locus linkage analysis in multiple sclerosis (MS).

Tienari PJ, Terwilliger JD, Ott J, Palo J, Peltonen L. Tienari PJ, et al. Among authors: terwilliger jd. Genomics. 1994 Jan 15;19(2):320-5. doi: 10.1006/geno.1994.1064. Genomics. 1994. PMID: 7514567 Free article.

8

Genomewide scan of multiple sclerosis in Finnish multiplex families.

Kuokkanen S, Gschwend M, Rioux JD, Daly MJ, Terwilliger JD, Tienari PJ, Wikström J, Palo J, Stein LD, Hudson TJ, Lander ES, Peltonen L. Kuokkanen S, et al. Among authors: terwilliger jd. Am J Hum Genet. 1997 Dec;61(6):1379-87. doi: 10.1086/301637. Am J Hum Genet. 1997. PMID: 9399895 Free PMC article.

9

Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.

Pekkarinen P, Hovatta I, Hakola P, Järvi O, Kestilä M, Lenkkeri U, Adolfsson R, Holmgren G, Nylander PO, Tranebjaerg L, Terwilliger JD, Lönnqvist J, Peltonen L. Pekkarinen P, et al. Among authors: terwilliger jd. Am J Hum Genet. 1998 Feb;62(2):362-72. doi: 10.1086/301722. Am J Hum Genet. 1998. PMID: 9463329 Free PMC article.

10

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23.

Pajukanta P, Nuotio I, Terwilliger JD, Porkka KV, Ylitalo K, Pihlajamäki J, Suomalainen AJ, Syvänen AC, Lehtimäki T, Viikari JS, Laakso M, Taskinen MR, Ehnholm C, Peltonen L. Pajukanta P, et al. Among authors: terwilliger jd. Nat Genet. 1998 Apr;18(4):369-73. doi: 10.1038/ng0498-369. Nat Genet. 1998. PMID: 9537421

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