A defect in the structure of type I procollagen in a patient who had osteogenesis imperfecta: excess mannose in the COOH-terminal propeptide.

Por Peltonen, L, Palotie, A, Prockop, D J
Publicado em 1980

Diagnosis of pancreatic lesions using fine needle aspiration cytology: detection of K-ras point mutations using solid phase minisequencing.

Por Ihalainen, J, Taavitsainen, M, Salmivaara, T, Palotie, A
Publicado em 1994

Thermal stability of type I and type III procollagens from normal human fibroblasts and from a patient with osteogenesis imperfecta.

Por Peltonen, L, Palotie, A, Hayashi, T, Prockop, D J
Publicado em 1980

Systematic review of genome-wide expression studies in multiple sclerosis

Por Kemppinen, A K, Kaprio, J, Palotie, A, Saarela, J
Publicado em 2011

Osteoporosis-pseudoglioma syndrome: clinical, morphological, and biochemical studies.

Por Somer, H, Palotie, A, Somer, M, Hoikka, V, Peltonen, L
Publicado em 1988

Abnormal copper metabolism and deficient lysyl oxidase activity in a heritable connective tissue disorder.

Por Kuivaniemi, H, Peltonen, L, Palotie, A, Kaitila, I, Kivirikko, K I
Publicado em 1982

Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37.

Por Visapää, I, Fellman, V, Varilo, T, Palotie, A, Raivio, K O, Peltonen, L
Publicado em 1998

Multiallelic polymorphism of the cartilage collagen gene: no association with osteoarthrosis.

Por Vikkula, M, Nissilä, M, Hirvensalo, E, Nuotio, P, Palotie, A, Aho, K, Peltonen, L
Publicado em 1993

Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus.

Por Ikonen, E, Palo, J, Ott, J, Gusella, J, Somer, H, Karila, L, Palotie, A, Peltonen, L
Publicado em 1990

Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals.

Por Mäkelä-Bengs, P, Järvinen, N, Vuopala, K, Suomalainen, A, Ignatius, J, Sipilä, M, Herva, R, Palotie, A, Peltonen, L
Publicado em 1998

Genome-wide association study of antisocial personality disorder

Por Rautiainen, M-R, Paunio, T, Repo-Tiihonen, E, Virkkunen, M, Ollila, H M, Sulkava, S, Jolanki, O, Palotie, A, Tiihonen, J
Publicado no Transl Psychiatry (2016)

Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptides.

Por Kainulainen, K, Sakai, L Y, Child, A, Pope, F M, Puhakka, L, Ryhänen, L, Palotie, A, Kaitila, I, Peltonen, L
Publicado em 1992

Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3

Por Polvi, A., Siren, A., Kallela, M., Rantala, H., Artto, V., Sobel, E.M., Palotie, A., Lehesjoki, A.-E., Wessman, M.
Publicado em 2012

Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population.

Por Laiho, E, Ignatius, J, Mikkola, H, Yee, V C, Teller, D C, Niemi, K M, Saarialho-Kere, U, Kere, J, Palotie, A
Publicado em 1997

Genetic association study of Endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura

Por Tikka-Kleemola, P, Kaunisto, MA, Hämäläinen, E, Todt, U, Göbel, H, Kaprio, J, Kubisch, C, Färkkilä, M, Palotie, A, Wessman, M, Kallela, M
Publicado em 2009

Comorbidity in Finnish migraine families

Por Artto, V., Wessman, M., Nissilä, M., Säkö, E., Liukkonen, J., Teirmaa, H., Harno, H., Havanka, H., Ilmavirta, M., Palotie, A., Färkkilä, M., Kallela, M.
Publicado em 2006

A visual migraine aura locus maps to 9q21-q22

Por Tikka-Kleemola, P., Artto, V., Vepsäläinen, S., Sobel, E.M., Räty, S., Kaunisto, M.A., Anttila, V., Hämäläinen, E., Sumelahti, M.-L., Ilmavirta, M., Färkkilä, M., Kallela, M., Palotie, A., Wessman, M.
Publicado em 2010

Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine

Por Anttila, V., Kallela, M., Oswell, G., Kaunisto, M. A., Nyholt, D. R., Hämäläinen, E., Havanka, H., Ilmavirta, M., Terwilliger, J., Sobel, E., Peltonen, L., Kaprio, J., Färkkilä, M., Wessman, M., Palotie, A.
Publicado em 2006

Genetic background of extreme violent behavior

Por Tiihonen, J, Rautiainen, M-R, Ollila, HM, Repo-Tiihonen, E, Virkkunen, M, Palotie, A, Pietiläinen, O, Kristiansson, K, Joukamaa, M, Lauerma, H, Saarela, J, Tyni, S, Vartiainen, H, Paananen, J, Goldman, D, Paunio, T
Publicado no Mol Psychiatry (2014)

Hostility in adolescents and adults: a genome-wide association study of the Young Finns

Por Merjonen, P, Keltikangas-Järvinen, L, Jokela, M, Seppälä, I, Lyytikäinen, L-P, Pulkki-Råback, L, Kivimäki, M, Elovainio, M, Kettunen, J, Ripatti, S, Kähönen, M, Viikari, J, Palotie, A, Peltonen, L, Raitakari, O T, Lehtimäki, T
Publicado em 2011