| Year |
Citation |
Score |
| 2023 |
Kurki MI, Karjalainen J, Palta P, Sipilä TP, Kristiansson K, Donner KM, Reeve MP, Laivuori H, Aavikko M, Kaunisto MA, Loukola A, Lahtela E, Mattsson H, Laiho P, Della Briotta Parolo P, ... ... Hiekkalinna T, et al. FinnGen provides genetic insights from a well-phenotyped isolated population. Nature. 613: 508-518. PMID 36653562 DOI: 10.1038/s41586-022-05473-8 |
0.356 |
|
| 2022 |
Nuottamo ME, Häppölä P, Artto V, Hautakangas H, Pirinen M, Hiekkalinna T, Ellonen P, Lepistö M, Hämäläinen E, Siren A, Lehesjoki AE, Kallela M, Palotie A, Kaunisto MA, Wessman M. is a novel candidate gene for migraine-epilepsy phenotype. Cephalalgia : An International Journal of Headache. 3331024211068065. PMID 35166138 DOI: 10.1177/03331024211068065 |
0.303 |
|
| 2016 |
Misiewicz Z, Hiekkalinna T, Paunio T, Varilo T, Terwilliger JD, Partonen T, Hovatta I. A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate. Scientific Reports. 6: 39345. PMID 27996024 DOI: 10.1038/Srep39345 |
0.642 |
|
| 2014 |
Gaye A, Marcon Y, Isaeva J, LaFlamme P, Turner A, Jones EM, Minion J, Boyd AW, Newby CJ, Nuotio ML, Wilson R, Butters O, Murtagh B, Demir I, Doiron D, ... ... Hiekkalinna T, et al. DataSHIELD: taking the analysis to the data, not the data to the analysis. International Journal of Epidemiology. 43: 1929-44. PMID 25261970 DOI: 10.1093/Ije/Dyu188 |
0.306 |
|
| 2014 |
Gertz EM, Hiekkalinna T, Digabel SL, Audet C, Terwilliger JD, Schäffer AA. PSEUDOMARKER 2.0: Efficient computation of likelihoods using NOMAD Bmc Bioinformatics. 15. PMID 24533837 DOI: 10.1186/1471-2105-15-47 |
0.605 |
|
| 2014 |
Törnwall O, Silventoinen K, Hiekkalinna T, Perola M, Tuorila H, Kaprio J. Identifying flavor preference subgroups. Genetic basis and related eating behavior traits. Appetite. 75: 1-10. PMID 24361469 DOI: 10.1016/J.Appet.2013.11.020 |
0.308 |
|
| 2012 |
Hiekkalinna T, Göring HH, Terwilliger JD. On the validity of the likelihood ratio test and consistency of resulting parameter estimates in joint linkage and linkage disequilibrium analysis under improperly specified parametric models. Annals of Human Genetics. 76: 63-73. PMID 22082140 DOI: 10.1111/J.1469-1809.2011.00683.X |
0.6 |
|
| 2012 |
Hiekkalinna T, Göring HH, Lambert B, Weiss KM, Norrgrann P, Schäffer AA, Terwilliger JD. On the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case-control samples. European Journal of Human Genetics : Ejhg. 20: 217-23. PMID 21934707 DOI: 10.1038/Ejhg.2011.173 |
0.665 |
|
| 2011 |
Hiekkalinna T, Schäffer AA, Lambert B, Norrgrann P, Göring HH, Terwilliger JD. PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals. Human Heredity. 71: 256-66. PMID 21811076 DOI: 10.1159/000329467 |
0.661 |
|
| 2011 |
Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM, Hiekkalinna T, Schäffer AA, Lambert B, Norrgrann P, Göring HHH, Terwilliger JD, Basu S, Pan W, Oetting WS, Andrade Md, et al. Contents Vol. 71, 2011 Human Heredity. 71. DOI: 10.1159/000331865 |
0.498 |
|
| 2009 |
Paunio T, Arajärvi R, Terwilliger JD, Hiekkalinna T, Haimi P, Partonen T, Lönnqvist J, Peltonen L, Varilo T. Linkage analysis of schizophrenia controlling for population substructure. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 827-35. PMID 19086037 DOI: 10.1002/Ajmg.B.30905 |
0.664 |
|
| 2009 |
Sammalisto S, Hiekkalinna T, Schwander K, Kardia S, Weder AB, Rodriguez BL, Doria A, Kelly JA, Bruner GR, Harley JB, Redline S, Larkin EK, Patel SR, Ewan AJ, Weber JL, et al. Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects. European Journal of Human Genetics : Ejhg. 17: 258-66. PMID 18781184 DOI: 10.1038/Ejhg.2008.152 |
0.532 |
|
| 2007 |
Perola M, Sammalisto S, Hiekkalinna T, Martin NG, Visscher PM, Montgomery GW, Benyamin B, Harris JR, Boomsma D, Willemsen G, Hottenga JJ, Christensen K, Kyvik KO, Sørensen TI, Pedersen NL, et al. Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci. Plos Genetics. 3: e97. PMID 17559308 DOI: 10.1371/Journal.Pgen.0030097 |
0.626 |
|
| 2007 |
Knaapila A, Keskitalo K, Kallela M, Wessman M, Sammalisto S, Hiekkalinna T, Palotie A, Peltonen L, Tuorila H, Perola M. Genetic component of identification, intensity and pleasantness of odours: a Finnish family study. European Journal of Human Genetics : Ejhg. 15: 596-602. PMID 17342154 DOI: 10.1038/Sj.Ejhg.5201804 |
0.434 |
|
| 2007 |
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. Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1. Human Molecular Genetics. 16: 453-62. PMID 17185386 DOI: 10.1093/Hmg/Ddl462 |
0.631 |
|
| 2006 |
Terwilliger JD, Hiekkalinna T. An utter refutation of the "fundamental theorem of the HapMap". European Journal of Human Genetics : Ejhg. 14: 426-37. PMID 16479260 DOI: 10.1038/Sj.Ejhg.5201583 |
0.627 |
|
| 2005 |
Hiekkalinna T, Terwilliger JD, Sammalisto S, Peltonen L, Perola M. AUTOGSCAN: powerful tools for automated genome-wide linkage and linkage disequilibrium analysis. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 8: 16-21. PMID 15836805 DOI: 10.1375/1832427053435382 |
0.612 |
|
| 2005 |
Sammalisto S, Hiekkalinna T, Suviolahti E, Sood K, Metzidis A, Pajukanta P, Lilja HE, Soro-Paavonen A, Taskinen MR, Tuomi T, Almgren P, Orho-Melander M, Groop L, Peltonen L, Perola M. A male-specific quantitative trait locus on 1p21 controlling human stature. Journal of Medical Genetics. 42: 932-9. PMID 15827092 DOI: 10.1136/Jmg.2005.031278 |
0.424 |
|
| 2005 |
Ekelund J, Hennah W, Hiekkalinna T, Parker A, Meyer J, Lönnqvist J, Peltonen L. Replication of 1q42 linkage in Finnish schizophrenia pedigrees. Molecular Psychiatry. 9: 1037-41. PMID 15197400 DOI: 10.1038/Sj.Mp.4001536 |
0.449 |
|
| 2004 |
Lilja HE, Suviolahti E, Soro-Paavonen A, Hiekkalinna T, Day A, Lange K, Sobel E, Taskinen MR, Peltonen L, Perola M, Pajukanta P. Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia. Journal of Lipid Research. 45: 1876-84. PMID 15258200 DOI: 10.1194/Jlr.M400141-Jlr200 |
0.417 |
|
| 2004 |
Paunio T, Tuulio-Henriksson A, Hiekkalinna T, Perola M, Varilo T, Partonen T, Cannon TD, Lönnqvist J, Peltonen L. Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q. Human Molecular Genetics. 13: 1693-702. PMID 15198991 DOI: 10.1093/Hmg/Ddh184 |
0.4 |
|
| 2003 |
Ekholm JM, Kieseppä T, Hiekkalinna T, Partonen T, Paunio T, Perola M, Ekelund J, Lönnqvist J, Pekkarinen-Ijäs P, Peltonen L. Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder. Human Molecular Genetics. 12: 1907-15. PMID 12874110 DOI: 10.1093/Hmg/Ddg199 |
0.466 |
|
| 2002 |
Terwilliger JD, Haghighi F, Hiekkalinna TS, Göring HH. A bias-ed assessment of the use of SNPs in human complex traits. Current Opinion in Genetics & Development. 12: 726-34. PMID 12433588 DOI: 10.1016/S0959-437X(02)00357-X |
0.62 |
|
| 2002 |
Soro A, Pajukanta P, Lilja HE, Ylitalo K, Hiekkalinna T, Perola M, Cantor RM, Viikari JS, Taskinen MR, Peltonen L. Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families. American Journal of Human Genetics. 70: 1333-40. PMID 11891617 DOI: 10.1086/339988 |
0.46 |
|
| 2002 |
Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hämäläinen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, et al. A susceptibility locus for migraine with aura, on chromosome 4q24. American Journal of Human Genetics. 70: 652-62. PMID 11836652 DOI: 10.1086/339078 |
0.599 |
|
| 2001 |
Perola M, Ohman M, Hiekkalinna T, Leppävuori J, Pajukanta P, Wessman M, Koskenvuo M, Palotie A, Lange K, Kaprio J, Peltonen L. Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups. American Journal of Human Genetics. 69: 117-23. PMID 11410840 DOI: 10.1086/321286 |
0.51 |
|
| 2000 |
Perola M, Kainulainen K, Pajukanta P, Terwilliger JD, Hiekkalinna T, Ellonen P, Kaprio J, Koskenvuo M, Kontula K, Peltonen L. Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings. Journal of Hypertension. 18: 1579-85. PMID 11081770 DOI: 10.1097/00004872-200018110-00008 |
0.624 |
|
| 1999 |
Pajukanta P, Terwilliger JD, Perola M, Hiekkalinna T, Nuotio I, Ellonen P, Parkkonen M, Hartiala J, Ylitalo K, Pihlajamäki J, Porkka K, Laakso M, Viikari J, Ehnholm C, Taskinen MR, et al. Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels. American Journal of Human Genetics. 64: 1453-63. PMID 10205279 DOI: 10.1086/302365 |
0.652 |
|
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