Authors:
Ikonen, Elina
Palo, Jorma
Ott, jurg
Gusella, James
Somer, Hannu
Karila, Leena
Palotie, Aarno
Peltonen, Leena
Citation: Ikonen, Elina et al., Huntington disease in finland: linkage disequilibrium of chromosome 4 RELP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus, American journal of human genetics , 46-I(1), 1990, pp. 5-11
Authors:
Lewis, Cathryn M.
Levinson, Douglas F.
Wise, Lesley H.
DeLisi, Lynn E.
Straub, Richard E.
Hovatta, Iiris
Williams, Nigel M.
Schwab, Sibylle G.
Pulver, Ann E.
Faraone, Stephen V.
Brzustowicz, Linda M.
Kaufmann, Charles A.
Garver, David L.
Gurling, Hugh M.D.
Lindholm, Eva
Coon, Hilary
Moises, Hans W.
Byerley, William
Shaw, Sarah H.
Mesen, Andrea
Sherrington, Robin
O'Neill, F. Anthony
Walsh, Dermot
Kendler, Kenneth S.
Ekelund, Jesper
Paunio, Tiina
Lönnqvist, Jouko
Peltonen, Leena
O'Donovan, Michael C.
Owen, Michael J.
Wildenauer, Dieter B.
Maier, Wolfgang
Nestadt, Gerald
Blouin, Jean-Louis
Antonarakis, Stylianos E.
Mowry, Bryan J.
Silverman, Jeremy M.
Crowe, Raymond R.
Cloninger, Robert C.
Tsuang, Jeremy M.
Malaspina, Dolores
Harkavy-Friedman, Jill M.
Svrakic, Dragan M.
Bassett, Anne S.
Holcomb, Jennifer
Kalsi, Gursharan
McQuillin, Andrew
Brynjolfson, Jon
Sigmundsson, Thordur
Petursson, Hannes
Jazin, Elena
Zoëga, Tomas
Helgason, Tomas
Citation: M. Lewis, Cathryn et al., Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia, American journal of human genetics , 73(1), 2003, pp. 34-48
Authors:
Segurado, Ricardo
Detera-Wadleigh, Sevilla D.
Levinson, Douglas F.
Lewis, Cathryn M.
Gil, Michael
Nurnberger, John I., Jr.
Craddock, Nick
DePaulo, Raymond J.
Baron, Miron
Gershon, Elliot S.
Ekhoolm, Jenny
Cichon, Sven
Turecki, Gustavo
Claes, Stephan
Kelsoe, John R.
Badenhop, Renee F.
Morissette, J.
Coon, Hilary
Blackwood, Douglas
McInnes, L.Allison
Foroud, Tatiana
Edenberg, Howard J.
Reich, Theodore
Rice, John P.
Goate, Alison
McInnis, Melvin G.
McMahon, Francis J.
Badner, Judith A.
Goldin, Lynn R.
Bennett, Phil
Willour, Virginia L.
Zandi, Peter P.
Liu, Jianjun
Gillam, Conrad
Juo, Suh-Hang
Berrettini, Wade H.
Yoshikawa, Takeo
Peltonen, Leena
Lönnqvist, Juoko
Nöthen, Markus M.
Schumacher, Johannes
Windemuth, Christine
Rietschel, Marcella
Proppin, Peter
Maier, Wolfgang
Alda, Martin
Grof, Paul
Rouleau, Guy A.
Del-Favero, Jurgen
Van Broeckhoven, Christine
Mendlewicz, Julien
Adolfsson, Rolf
Spence, M. Anne
Luebbert, Hermann
Adams, Linda J.
Donald, Jennifer A.
Mitchell, Philip B.
Barden, Nicholas
Shink, Eric
Byerley, William
Muir, Walter
Visscher, Peter M.
Macgregor, Stuart
Gurling, Hugh
Kalsi, Gursharan
McQuillin, Andrew
Escamilla, Michael A.
Reus, Victor I.
Leon, Pedro
Freimer, Nelson B.
Ewald, Henrik
Kruse, Torben A.
Mors, Ole
Radhakrishna, Uppala
Blouin, Jean-Louis
Antonarakis, Stylianos
Akarsu, Nurten
Citation: Segurado, Ricardo et al., Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder, American journal of human genetics , 73(1), 2003, pp. 49-62
Citation: Enattah, Nabil Sabri et al., Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture, American journal of human genetics , 82(1), 2008, pp. 57-72
Authors:
Hackman, Peter
Vihola, Anna
Haravouri, Henna
Marchand, Sylvie
Sarparanta, Jaakko
de Seze, Jerome
Labeit, Siegfried
Witt, Christian
Peltonen, Leena
Richard, Isabelle
Udd, Bjarne
Citation: Hackman, Peter et al., Tibial Muscular Dystrophy Is a Titinopathy Caused by Mutations in TTN, the Gene Encoding the Giant Skeletal-Muscle Protein Titin, American journal of human genetics , 71(3), 2002, pp. 492-500
Authors:
Kainulainen, Katariina
Steinmann, Beat
Collins, Francis
Dietz, Harry C.
Francomano, Clair A.
Child, Anne.
Kilpatrick, Michael W.
Brock, David J. H.
Keston, Marion
Pyeritz, Reed E.
Peltonen, Leena
Citation: Kainulainen, Katariina et al., Marfan syndrome: No evidence for heterogeneity in different populations, and more precise mapping of the gene, American journal of human genetics , 49-I(3), 1991, pp. 662-667
Authors:
Auranen, Mari
Vanhala, Raija
Varilo, Teppo
Ayers, Kristin
Kempas, Elli
Ylisaukko-oja, Tero
Sinsheimer, Janet S.
Peltonen, Leena
Järvelä, Irma
Citation: Auranen, Mari et al., A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27, American journal of human genetics , 71(4), 2002, pp. 777-790
Authors:
Sajantila, Antti
Budowle, Bruce
M Ström, Marjanne
Johnsson, Vivian
Lukka, Matti
Peltonen, Leena
Ehnholm, Christian
Citation: Sajantila, Antti et al., PCR amplification of alleles at the DIS80 locus: comparison of a Finnish and a North American Caucasian population sample, and forensic casework evaluation., American journal of human genetics , 50-II(4), 1992, pp. 816-825
Authors:
Saccone, Scott F.
Pergadia, Michele L.
Loukola, Anu
Broms, Ulla
Montgomery, Grant W.
Wang, Jen C
Agrawal, Arpana
Dick, Danielle M.
Heath, Andrew C.
Todorov, Alexandre A.
Maunu, Heidi
Heikkilä, Kauko
Morley, Katherine I.
Rice, John P.
Todd, Richard D.
Kaprio, Jaakko
Peltonen, Leena
Martin, Nicholas G.
Goate, Alison M.
Madden, Pamela A.F.
Citation: F. Saccone, Scott et al., Genetic Linkage to Chromosome 22q12 for a Heavy-Smoking Quantitative Trait in Two Independent Samples, American journal of human genetics , 80(5), 2007, pp. 856-866
Authors:
Visapää, Ilona
Fellman, Vineta
Vesa, Jouni
Dasvarma, Ayan
Hutton, Jenna L.
Kumar, Vijay
Payne, Gregory S.
Makarow, Marja
Van Coster, Rudy
Taylor, Robert W.
Turnbull, Douglass
Suomalainen, Anu
Peltonen, Leena
Citation: Visapää, Ilona et al., GRACILE Syndrome, a Lethal Metabolic Disorder with Iron Overload, Is Caused by a Point Mutation in BCS1L, American journal of human genetics , 71(4), 2002, pp. 863-876
Authors:
Pajukanta, Päivi
Allayee, Hooman
Krass, Kelly L.
Kuraishy, Ali
Soro, Aino
Lilja, Heidi E.
Mar, Rebecca
Taskinen, Marja-Riitta
Nuotio, Ilpo
Laakso, Markku
Rotter, Jerome I.
de Bruin Tjerk, W.A.
Cantor, M. Rita
Aldons Lusis, J.
Peltonen, Leena
Citation: Pajukanta, Päivi et al., Combined Analysis of Genome Scans of Dutch and Finnish Families Reveals a Susceptibility Locus for High-Density Lipoprotein Cholesterol on Chromosome 16q, American journal of human genetics , 72(4), 2003, pp. 903-917
Authors:
Palmer, Christina G.S.
Turunen, Joni A.
Sinsheimer, Janet S.
Minassian, Sonia
Paunio, Tiina
Lönnqvist, Jouko
Peltonen, Leena
Woodward, J. Arthur
Citation: Palmer, Christina G.s et al., RHD Maternal-Fetal Genotype Incompatibility Increases Schizophrenia Susceptibility, American journal of human genetics , 71(6), 2002, pp. 1312-1319