| Year |
Citation |
Score |
| 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 |
0.748 |
|
| 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 |
0.711 |
|
| 2012 |
Luukkonen TM, Pöyhönen M, Palotie A, Ellonen P, Lagström S, Lee JH, Terwilliger JD, Salonen R, Varilo T. A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm. Journal of Medical Genetics. 49: 621-9. PMID 23054244 DOI: 10.1136/Jmedgenet-2012-100977 |
0.347 |
|
| 2012 |
Parmalee NL, Schubert C, Figueroa M, Bird AC, Peto T, Gillies MC, Bernstein PS, Kiryluk K, Terwilliger JD, Allikmets R. Identification of a potential susceptibility locus for macular telangiectasia type 2. Plos One. 7: e24268. PMID 22952568 DOI: 10.1371/Journal.Pone.0024268 |
0.472 |
|
| 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 |
0.76 |
|
| 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 |
0.746 |
|
| 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 |
0.786 |
|
| 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 |
0.636 |
|
| 2009 |
Terwilliger JD, Göring HH. Update to Terwilliger and Göring's "Gene mapping in the 20th and 21st centuries" (2000): gene mapping when rare variants are common and common variants are rare. Human Biology. 81: 729-33. PMID 20504192 DOI: 10.3378/027.081.0617 |
0.638 |
|
| 2009 |
Terwilliger JD, Göring HH. Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design. 2000. Human Biology. 81: 663-728. PMID 20504191 DOI: 10.3378/027.081.0615 |
0.669 |
|
| 2009 |
Mann JJ, Arango VA, Avenevoli S, Brent DA, Champagne FA, Clayton P, Currier D, Dougherty DM, Haghighi F, Hodge SE, Kleinman J, Lehner T, McMahon F, Mo?cicki EK, Oquendo MA, ... ... Terwilliger J, et al. Candidate endophenotypes for genetic studies of suicidal behavior. Biological Psychiatry. 65: 556-63. PMID 19201395 DOI: 10.1016/J.Biopsych.2008.11.021 |
0.301 |
|
| 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 |
0.744 |
|
| 2008 |
Donner J, Pirkola S, Silander K, Kananen L, Terwilliger JD, Lönnqvist J, Peltonen L, Hovatta I. An association analysis of murine anxiety genes in humans implicates novel candidate genes for anxiety disorders. Biological Psychiatry. 64: 672-80. PMID 18639233 DOI: 10.1016/J.Biopsych.2008.06.002 |
0.309 |
|
| 2008 |
Lambert BW, Terwilliger JD, Weiss KM. ForSim: a tool for exploring the genetic architecture of complex traits with controlled truth. Bioinformatics (Oxford, England). 24: 1821-2. PMID 18565989 DOI: 10.1093/Bioinformatics/Btn317 |
0.387 |
|
| 2008 |
Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, et al. Consistently replicating locus linked to migraine on 10q22-q23. American Journal of Human Genetics. 82: 1051-63. PMID 18423523 DOI: 10.1016/J.Ajhg.2008.03.003 |
0.443 |
|
| 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 |
0.72 |
|
| 2006 |
Kaunisto M, Kallela M, Hämäläinen E, Kilpikari R, Havanka H, Harno H, Nissilä M, Säkö E, Ilmavirta M, Liukkonen J, Teirmaa H, Törnwall O, Jussila M, Terwilliger J, Färkkilä M, et al. Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura Cephalalgia. 26: 1462-1472. PMID 17116097 DOI: 10.1111/J.1468-2982.2006.01228.X |
0.339 |
|
| 2006 |
Anttila V, Kallela M, Oswell G, Kaunisto M, Nyholt DR, Hämäläinen E, Havanka H, Ilmavirta M, Terwilliger J, Sobel E, Peltonen L, Kaprio J, Färkkilä M, Wessman M, Palotie A. Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine American Journal of Human Genetics. 79: 85-99. PMID 16773568 DOI: 10.1086/504814 |
0.47 |
|
| 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 |
0.721 |
|
| 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 |
0.706 |
|
| 2004 |
Imanishi T, Itoh T, Suzuki Y, O'Donovan C, Fukuchi S, Koyanagi KO, Barrero RA, Tamura T, Yamaguchi-Kabata Y, Tanino M, Yura K, Miyazaki S, Ikeo K, Homma K, Kasprzyk A, ... ... Terwilliger JD, et al. Integrative annotation of 21,037 human genes validated by full-length cDNA clones. Plos Biology. 2: e162. PMID 15103394 DOI: 10.1371/Journal.Pbio.0020162 |
0.339 |
|
| 2003 |
Terwilliger JD, Weiss KM. Confounding, ascertainment bias, and the blind quest for a genetic 'fountain of youth'. Annals of Medicine. 35: 532-44. PMID 14649335 DOI: 10.1080/07853890310015181 |
0.401 |
|
| 2003 |
Yonan AL, Alarcón M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, Grunn A, Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC. A genomewide screen of 345 families for autism-susceptibility loci. American Journal of Human Genetics. 73: 886-97. PMID 13680528 DOI: 10.1086/378778 |
0.603 |
|
| 2003 |
Varilo T, Paunio T, Parker A, Perola M, Meyer J, Terwilliger JD, Peltonen L. The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories. Human Molecular Genetics. 12: 51-9. PMID 12490532 DOI: 10.1093/Hmg/Ddg005 |
0.472 |
|
| 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 |
0.782 |
|
| 2002 |
Liu J, Juo SH, Holopainen P, Terwilliger J, Tong X, Grunn A, Brito M, Green P, Mustalahti K, Mäki M, Gilliam TC, Partanen J. Genomewide linkage analysis of celiac disease in Finnish families. American Journal of Human Genetics. 70: 51-9. PMID 11715113 DOI: 10.1086/338453 |
0.434 |
|
| 2001 |
Paunio T, Ekelund J, Varilo T, Parker A, Hovatta I, Turunen JA, Rinard K, Foti A, Terwilliger JD, Juvonen H, Suvisaari J, Arajärvi R, Suokas J, Partonen T, Lönnqvist J, et al. Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q Human Molecular Genetics. 10: 3037-3048. PMID 11751686 DOI: 10.1093/Hmg/10.26.3037 |
0.457 |
|
| 2001 |
Göring HH, Terwilliger JD, Blangero J. Large upward bias in estimation of locus-specific effects from genomewide scans. American Journal of Human Genetics. 69: 1357-69. PMID 11593451 DOI: 10.1086/324471 |
0.354 |
|
| 2001 |
Paavola P, Heliö T, Kiuru MH, Halme L, Turunen U, Terwilliger J, Karvonen AL, Julkunen R, Niemelä S, Nurmi H, Färkkilä M, Kontula K. Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21. European Journal of Human Genetics. 9: 328-334. PMID 11378820 DOI: 10.1038/Sj.Ejhg.5200626 |
0.47 |
|
| 2001 |
Liu J, Juo SH, Terwilliger JD, Grunn A, Tong X, Brito M, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Gilliam TC, Baron M. A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22. American Journal of Medical Genetics. 105: 189-94. PMID 11304836 DOI: 10.1002/Ajmg.1195 |
0.444 |
|
| 2001 |
Terwilliger JD. 23 On the resolution and feasibility of genome scanning approaches Advances in Genetics. 42: 351-391. PMID 11037331 DOI: 10.1016/S0065-2660(01)42032-3 |
0.434 |
|
| 2000 |
Magnusson V, Lindqvist AK, Castillejo-López C, Kristjánsdottir H, Steinsson K, Gröndal G, Sturfelt G, Truedsson L, Svenungsson E, Lundberg I, Gunnarsson I, Bolstad AI, Haga HJ, Jonsson R, Klareskog L, ... ... Terwilliger JD, et al. Fine mapping of the SLEB2 locus involved in susceptibility to systemic lupus erythematosus. Genomics. 70: 307-14. PMID 11161781 DOI: 10.1006/Geno.2000.6374 |
0.466 |
|
| 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 |
0.72 |
|
| 2000 |
Pajukanta P, Cargill M, Viitanen L, Nuotio I, Kareinen A, Perola M, Terwilliger JD, Kempas E, Daly M, Lilja H, Rioux JD, Brettin T, Viikari JS, Rönnemaa T, Laakso M, et al. Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland. American Journal of Human Genetics. 67: 1481-93. PMID 11078477 DOI: 10.1086/316902 |
0.424 |
|
| 2000 |
Moses EK, Lade JA, Guo G, Wilton AN, Grehan M, Freed K, Borg A, Terwilliger JD, North R, Cooper DW, Brennecke SP. A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2. American Journal of Human Genetics. 67: 1581-5. PMID 11035632 DOI: 10.1086/316888 |
0.463 |
|
| 2000 |
Weiss KM, Terwilliger JD. How many diseases does it take to map a gene with SNPs Nature Genetics. 26: 151-157. PMID 11017069 DOI: 10.1038/79866 |
0.326 |
|
| 2000 |
Varilo T, Laan M, Hovatta I, Wiebe V, Terwilliger JD, Peltonen L. Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo. European Journal of Human Genetics. 8: 604-612. PMID 10951523 DOI: 10.1038/Sj.Ejhg.5200482 |
0.459 |
|
| 2000 |
Terwilliger JD. Inflated False-Positive Rates in Hardy-Weinberg and Linkage-Equilibrium Tests Are Due to Sampling on the Basis of Rare Familial Phenotypes in Finite Populations American Journal of Human Genetics. 67: 258-259. PMID 10848498 DOI: 10.1086/302964 |
0.433 |
|
| 2000 |
Ekelund J, Lichtermann D, Hovatta I, Ellonen P, Suvisaari J, Terwilliger JD, Juvonen H, Varilo T, Arajärvi R, Kokko-Sahin M, Lönnqvist J, Peltonen L. Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22 Human Molecular Genetics. 9: 1049-1057. PMID 10767329 DOI: 10.1093/Hmg/9.7.1049 |
0.459 |
|
| 2000 |
Göring HHH, Terwilliger JD. Linkage Analysis in the Presence of Errors III: Marker Loci and Their Map as Nuisance Parameters American Journal of Human Genetics. 66: 1298-1309. PMID 10731467 DOI: 10.1086/302846 |
0.37 |
|
| 2000 |
Göring HHH, Terwilliger JD. Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified. American Journal of Human Genetics. 66: 1310-1327. PMID 10731466 DOI: 10.1086/302845 |
0.425 |
|
| 2000 |
Göring HHH, Terwilliger JD. Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions. American Journal of Human Genetics. 66: 1107-1118. PMID 10712221 DOI: 10.1086/302798 |
0.374 |
|
| 2000 |
Göring HHH, Terwilliger JD. Linkage Analysis in the Presence of Errors I: Complex-Valued Recombination Fractions and Complex Phenotypes American Journal of Human Genetics. 66: 1095-1106. PMID 10712220 DOI: 10.1086/302797 |
0.418 |
|
| 2000 |
Lindqvist AK, Steinsson K, Johanneson B, Kristjánsdóttir H, Arnasson A, Gröndal G, Jonasson I, Magnusson V, Sturfelt G, Truedsson L, Svenungsson E, Lundberg I, Terwilliger JD, Gyllensten UB, Alarcón-Riquelme ME. A susceptibility locus for human systemic lupus erythematosus (hSLE1) on chromosome 2q. Journal of Autoimmunity. 14: 169-78. PMID 10677248 DOI: 10.1006/Jaut.1999.0357 |
0.433 |
|
| 2000 |
Terwilliger JD. Reply to Deng and Chen American Journal of Human Genetics. 67: 261-262. DOI: 10.1086/302981 |
0.463 |
|
| 1999 |
Takashima H, Nakagawa M, Suehara M, Saito M, Saito A, Kanzato N, Matsuzaki T, Hirata K, Terwilliger JD, Osame M. Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1. Neuromuscular Disorders. 9: 368-371. PMID 10545038 DOI: 10.1016/S0960-8966(99)00021-8 |
0.437 |
|
| 1999 |
Hovatta I, Varilo T, Suvisaari J, Terwilliger JD, Ollikainen V, Arajärvi R, Juvonen H, Kokko-Sahin M, Väisänen L, Mannila H, Lönnqvist J, Peltonen L. A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci American Journal of Human Genetics. 65: 1114-1124. PMID 10486331 DOI: 10.1086/302567 |
0.401 |
|
| 1999 |
Leppävuori J, Kujala U, Kinnunen J, Kaprio J, Nissilä M, Heliövaara M, Klinger N, Partanen J, Terwilliger JD, Peltonen L. Genome Scan for Predisposing Loci for Distal Interphalangeal Joint Osteoarthritis: Evidence for a Locus on 2q American Journal of Human Genetics. 65: 1060-1067. PMID 10486325 DOI: 10.1086/302569 |
0.48 |
|
| 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 |
0.746 |
|
| 1999 |
Kainulainen K, Perola M, Terwilliger J, Kaprio J, Koskenvuo M, Syvänen A, Vartiainen E, Peltonen L, Kontula K. Evidence for Involvement of the Type 1 Angiotensin II Receptor Locus in Essential Hypertension Hypertension. 33: 844-849. PMID 10082497 DOI: 10.1161/01.Hyp.33.3.844 |
0.404 |
|
| 1999 |
Aita VM, Liu J, Knowles JA, Terwilliger JD, Baltazar R, Grunn A, Loth JE, Kanyas K, Lerer B, Endicott J, Wang Z, Penchaszadeh G, Gilliam TC, Baron M. A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus. American Journal of Human Genetics. 64: 210-7. PMID 9915960 DOI: 10.1086/302185 |
0.496 |
|
| 1998 |
Terwilliger JD, Weiss KM. Linkage disequilibrium mapping of complex disease: fantasy or reality? Current Opinion in Biotechnology. 9: 578-594. PMID 9889136 DOI: 10.1016/S0958-1669(98)80135-3 |
0.422 |
|
| 1998 |
Pekkarinen P, Kestilä M, Paloneva J, Terwilliger J, Varilo T, Järvi O, Hakola P, Peltonen L. Fine-Scale Mapping of a Novel Dementia Gene, PLOSL, by Linkage Disequilibrium Genomics. 54: 307-315. PMID 9828133 DOI: 10.1006/Geno.1998.5591 |
0.462 |
|
| 1998 |
Hovatta I, Lichtermann D, Juvonen H, Suvisaari J, Terwilliger JD, Arajärvi R, Kokko-Sahin ML, Ekelund J, Lönnqvist J, Peltonen L. Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p and 22q in a population-based sampled Finnish family set. Molecular Psychiatry. 3: 452-7. PMID 9774782 DOI: 10.1038/sj.mp.4000443 |
0.301 |
|
| 1998 |
Lichtermann D, Hovatta I, Terwilliger JD, Peltonen L, Lönnqvist J. Concordance for Sex and the Pseudoautosomal Gene Hypothesis Revisited: No Evidence of Increased Sex Concordance in a Nationwide Finnish Sample of Siblings With Paternally Derived Schizophrenia American Journal of Psychiatry. 155: 1365-1375. PMID 9766768 DOI: 10.1176/Ajp.155.10.1365 |
0.318 |
|
| 1998 |
Pastinen T, Perola M, Niini P, Terwilliger J, Salomaa V, Vartiainen E, Peltonen L, Syvänen A-. Array-Based Multiplex Analysis of Candidate Genes Reveals Two Independent and Additive Genetic Risk Factors for Myocardial Infarction in the Finnish Population Human Molecular Genetics. 7: 1453-1462. PMID 9700201 DOI: 10.1093/Hmg/7.9.1453 |
0.39 |
|
| 1998 |
Terwilliger JD, Zöllner S, Laan M, Pääbo S. Mapping Genes through the Use of Linkage Disequilibrium Generated by Genetic Drift: ‘Drift Mapping’ in Small Populations with No Demographic Expansion Human Heredity. 48: 138-154. PMID 9618061 DOI: 10.1159/000022794 |
0.408 |
|
| 1998 |
Pajukanta P, Nuotio I, Terwilliger JD, Porkka KVK, Ylitalo K, Pihlajamäki J, Suomalainen AJ, Syvänen A, Lehtimäki T, Viikari JSA, Laakso M, Taskinen M, Ehnholm C, Peltonen L. Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23 Nature Genetics. 18: 369-373. PMID 9537421 DOI: 10.1038/Ng0498-369 |
0.472 |
|
| 1998 |
Kuokkanen S, Gschwend M, Rioux JD, Daly MJ, Terwilliger JD, Tienari PJ, Wikström J, Palo J, Stein LD, Hudson TJ, Lander ES, Peltonen L. Genomewide scan of multiple sclerosis in Finnish multiplex families. American Journal of Human Genetics. 61: 1379-87. PMID 9399895 DOI: 10.1086/301637 |
0.44 |
|
| 1997 |
Julier C, Delépine M, Keavney B, Terwilliger J, Davis S, Weeks DE, Bui T, Jeunemaître X, Velho G, Froguel P, Ratcliffe P, Corvol P, Soubrier F, Lathrop GM. Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10. Human Molecular Genetics. 6: 2077-85. PMID 9328471 DOI: 10.1093/Hmg/6.12.2077 |
0.672 |
|
| 1997 |
Terwilliger JD, Shannon WD, Lathrop GM, Nolan JP, Goldin LR, Chase GA, Weeks DE. True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping. American Journal of Human Genetics. 61: 430-8. PMID 9311749 DOI: 10.1086/514855 |
0.688 |
|
| 1997 |
Hovatta I, Terwilliger JD, Lichtermann D, Mäkikyrö T, Suvisaari J, Peltonen L, Lönnqvist J. Schizophrenia in the genetic isolate of Finland American Journal of Medical Genetics. 74: 353-360. PMID 9259368 DOI: 10.1002/(Sici)1096-8628(19970725)74:4<353::Aid-Ajmg3>3.0.Co;2-Q |
0.32 |
|
| 1997 |
Trembath RC, Clough RL, Rosbotham JL, Jones AB, Camp RD, Frodsham A, Browne J, Barber R, Terwilliger J, Lathrop GM, Barker JN. Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis. Human Molecular Genetics. 6: 813-20. PMID 9158158 DOI: 10.1093/HMG/6.5.813 |
0.588 |
|
| 1997 |
Terwilliger JD. Genetic Variation and Human Disease: Principles and Evolutionary Approaches.By Kenneth M. Weiss:Genetic Variation and Human Disease: Principles and Evolutionary Approaches American Journal of Human Genetics. 60: 1565-1565. DOI: 10.1086/515477 |
0.326 |
|
| 1997 |
Lichtermann D, Hovatta I, Ekelund J, Suvisaari J, Väisänen L, Terwilliger J, Lönnqvist J, Peltonen L. Loci on chromosomes 3p, 6p, and 8p do not contribute to schizophrenia in a Finnish family sample Biological Psychiatry. 42. DOI: 10.1016/S0006-3223(97)87453-7 |
0.349 |
|
| 1996 |
Satsangi J, Parkes M, Louis E, Hashimoto L, Kato N, Welsh K, Terwilliger JD, Lathrop GM, Bell JI, Jewell DP. Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12. Nature Genetics. 14: 199-202. PMID 8841195 DOI: 10.1038/ng1096-199 |
0.546 |
|
| 1996 |
Hovatta I, Lichtermann D, Terwilliger JD, Suvisaari J, Väisänen L, Lönnqvist J, Peltonen L. Searching schizophrenia loci in a genetic isolate Psychiatric Genetics. 6: 169. DOI: 10.1097/00041444-199623000-00093 |
0.329 |
|
| 1995 |
Pekkarinen P, Terwilliger J, Bredbacka PE, Lönnqvist J, Peltonen L. Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree. Genome Research. 5: 105-115. PMID 9132265 DOI: 10.1101/Gr.5.2.105 |
0.412 |
|
| 1995 |
Speer MC, Terwilliger JD, Ott J. Data simulation for GAW9 problems 1 and 2 Genetic Epidemiology. 12: 561-564. PMID 8787973 DOI: 10.1002/Gepi.1370120606 |
0.487 |
|
| 1995 |
Raha-Chowdhury R, Bowen DJ, Stone C, Pointon JJ, Terwilliger JD, Shearman JD, Robson KJH, Bomford A, Worwood M. New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105 Human Molecular Genetics. 4: 1869-1874. PMID 8595409 DOI: 10.1093/Hmg/4.10.1869 |
0.428 |
|
| 1995 |
Vaxillaire M, Boccio V, Philippi A, Vigouroux C, Terwilliger J, Passa P, Beckmann JS, Velho G, Lathrop GM, Froguel P. A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q. Nature Genetics. 9: 418-23. PMID 7795649 DOI: 10.1038/Ng0495-418 |
0.59 |
|
| 1995 |
Pekkarinen P, Terwilliger J, Bredbacka P, Berrettini W, Lönnqvist J, Peltonen L. An X-chromosomal locus predisposing to bipolar disorder in an extended Finnish pedigree Psychiatric Genetics. 5: 137. DOI: 10.1097/00041444-199505030-00023 |
0.305 |
|
| 1994 |
James MR, Richard CW, Schott J-, Yousry C, Clark K, Bell J, Terwilliger JD, Kazan J, Dubay C, Vignal A, Agrapart M, Imai T, Nakamura Y, Polymeropoulos M, Weissenbach J, et al. A radiation hybrid map of 506 STS markers spanning human chromosome 11. Nature Genetics. 8: 70-76. PMID 7987395 DOI: 10.1038/Ng0994-70 |
0.37 |
|
| 1994 |
Tienari PJ, Terwilliger JD, Ott J, Palo J, Peltonen L. Two-locus linkage analysis in multiple sclerosis (MS). Genomics. 19: 320-5. PMID 7514567 DOI: 10.1006/Geno.1994.1064 |
0.605 |
|
| 1993 |
Terwilliger JD, Ott J. A novel polylocus method for linkage analysis using the lod-score or affected sib-pair method. Genetic Epidemiology. 10: 477-82. PMID 8314047 DOI: 10.1002/Gepi.1370100625 |
0.545 |
|
| 1993 |
Terwilliger JD, Speer M, Ott J. Chromosome-based method for rapid computer simulation in human genetic linkage analysis. Genetic Epidemiology. 10: 217-24. PMID 8224802 DOI: 10.1002/Gepi.1370100402 |
0.546 |
|
| 1993 |
Schork NJ, Boehnke M, Terwilliger JD, Ott J. Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. American Journal of Human Genetics. 53: 1127-36. PMID 8213836 |
0.588 |
|
| 1992 |
Terwilliger JD, Ott J. A multisample bootstrap approach to the estimation of maximized-over-models lod score distributions. Cytogenetics and Cell Genetics. 59: 142-4. PMID 1737483 DOI: 10.1159/000133228 |
0.456 |
|
| 1992 |
Terwilliger JD, Ding Y, Ott J. On the relative importance of marker heterozygosity and intermarker distance in gene mapping. Genomics. 13: 951-6. PMID 1505986 DOI: 10.1016/0888-7543(92)90006-E |
0.56 |
|
| 1992 |
Terwilliger JD, Ott J. A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. Human Heredity. 42: 337-46. PMID 1493912 DOI: 10.1159/000154096 |
0.551 |
|
| 1992 |
Terwilliger JD, Ott J, Mamolini E, Beretta M, Cappellozza G, Moncinelli R, Scapoli C, Barale R, Barrai I, El-Hazmi MAF, Warsy AS, Saha N, Juneja RK, Gahne B, Tay JSH, et al. Subject Index, Vol. 42, 1992 Human Heredity. 42: 389-390. DOI: 10.1159/000154104 |
0.417 |
|
| 1992 |
Terwilliger JD, Ott J, Mamolini E, Beretta M, Cappellozza G, Moncinelli R, Scapoli C, Barale R, Barrai I, El-Hazmi MAF, Warsy AS, Saha N, Juneja RK, Gahne B, Tay JSH, et al. Contents, Vol. 42, 1992 Human Heredity. 42. DOI: 10.1159/000154094 |
0.428 |
|
| 1991 |
Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence. American Journal of Medical Genetics. 38: 140-6. PMID 2012126 DOI: 10.1002/Ajmg.1320380130 |
0.55 |
|
| 1991 |
Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27. Journal of the Neurological Sciences. 102: 206-8. PMID 1883411 DOI: 10.1016/0022-510X(91)90070-N |
0.531 |
|
| 1991 |
Delisi LE, Crow TJ, Davies KE, Terwilliger JD, Ott J, Ram R, Flint T, Boccio A. No genetic linkage detected for schizophrenia to Xq27-q28. The British Journal of Psychiatry : the Journal of Mental Science. 158: 630-4. PMID 1677599 DOI: 10.1192/Bjp.158.5.630 |
0.524 |
|
| 1990 |
Kwan SP, Terwilliger J, Parmley R, Raghu G, Sandkuyl LA, Ott J, Ochs H, Wedgwood R, Rosen F. Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus Genomics. 6: 238-242. PMID 2307467 DOI: 10.1016/0888-7543(90)90562-9 |
0.589 |
|
| 1989 |
Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, Westaway D, Ott J, Prusiner SB. Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome. Nature. 338: 342-5. PMID 2564168 DOI: 10.1038/338342A0 |
0.492 |
|
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