Previous cancers in women diagnosed with premature ovarian insufficiency: A nationwide population‐based case–control study von Silvén, Heidi, Savukoski, Susanna M., Pesonen, Paula, Niinimäki, Riitta, Pukkala, Eero, Gissler, Mika, Suvanto, Eila, Niinimäki, Maarit

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Choice of treatment to manage early miscarriage does not affect future fertility von Savukoski, Susanna M., Niinimäki, Maarit

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Excess of severe autoimmune diseases in women with premature ovarian insufficiency: a population-based study von Savukoski, S M, Silvén, H, Pesonen, P, Pukkala, E, Gissler, M, Suvanto, E, Ollila, M-M, Niinimäki, M

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Association of genetic disorders and congenital malformations with premature ovarian insufficiency: a nationwide register-based study von Silvén, H, Savukoski, S M, Pesonen, P, Pukkala, E, Ojaniemi, M, Gissler, M, Suvanto, E, Niinimäki, M

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Incidence and familial risk of premature ovarian insufficiency in the Finnish female population von Silvén, H, Savukoski, S M, Pesonen, P, Pukkala, E, Gissler, M, Suvanto, E, Niinimäki, M

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Development and testing of an instrument to measure the collegiality competence of social and health care educators von Koskenranta, M., Kuivila, H., Pramila-Savukoski, S., Männistö, M., Mikkonen, K.

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Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses von SAVUKOSKI, M, KESTILÄ, M, WILLIAMS, R, JÄRVELÄ, I, SHARP, J, HARRIS, J, SANTAVUORI, P, GARDINER, M, PELTONEN, L

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Phenotype- genotype correlation in eight patients with Finnish variant late infantile NCL (CLN5) von HOLMBERG, V, LAURONEN, L, AUTTI, T, SANTAVUORI, P, SAVUKOSKI, M, UVEBRANT, P, HOFMAN, I, PELTONEN, L, JÄRVELÄ, I

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Women's health study (WENDY) - a protocol of a population-based study assessing gynecological and metabolic health in women in their mid-30s von Piltonen, Terhi T, Ohtamaa, Maria, Arffman, Riikka K, Vuokila, Lotta, Hurskainen, Elisa, Männikkö, Minna, Huilaja, Laura, Sinikumpu, Suvi-Päivikki, Rautio, Tero, Kilpivaara, Katariina, Jokelainen, Jari, Kiviniemi, Eetu, Pinola, Pekka, Törnävä, Minna, Komsi, Elina, Kangasniemi, Marika H, Rajecki, Maria, Luiro, Kaisu, Kinnunen, Jenni, Savukoski, Susanna M

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Loci for Classical and a Variant Late Infantile Neuronal Ceroid Lipofuscinosis Map to Chromosomes 11p15 and 15q21–23 von Sharp, J. D., Wheeler, R. B., Lake, B. D., Savukoski, M., Järvelä, I. E., Peltonen, L., Gardiner, R. M., Williams, R. E.

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The age of human mutation : Genealogical and linkage disequilibrium analysis of the CLN5 mutation in the finnish population von VARILO, T, SAVUKOSKI, M, NORIO, R, SANTAVUORI, P, PELTONEN, L, JÄRVELÄ, I

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Efficient Construction of a Physical Map by Fiber-Fish of the CLN5 Region: Refined Assignment and Long-Range Contig Covering the Critical Region on 13q22 von Klockars, T., Savukoski, M., Isosomppi, J., Laan, M., Järvelä, I., Petrukhin, K., Palotie, A., Peltonen, L.

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CLN5 , a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis von Peltonen, Leena, Savukoski, Minna, Klockars, Tuomas, Holmberg, Ville, Santavuori, Pirkko, Lander, Eric S

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Transcript identification on the CLN5 region on chromosome 13q22 von KLOCKARS, T, HOLMBERG, V, SAVUKOSKI, M, LANDER, E. S, PELTONEN, L

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Exclusion mapping of classical late infantile neuronal ceroid lipofuscinosis (Jansky-Bielschowsky disease, CLN2) von Sharp, J D, Wheeler, R B, Savukoski, M, Kestila, M, Järvelä, I E, Peltonen, L, Eiberg, H, Gardiner, R M, Williams, R

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Genetics of the neuronal ceroid lipofuscinoses von Peltonen, Leena, Savukoski, Minna, Vesa, Jouni

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MET Exon 14 Mutations in Non–Small-Cell Lung Cancer Are Associated With Advanced Age and Stage-Dependent MET Genomic Amplification and c-Met Overexpression von Awad, Mark Magdi, Oxnard, Geoffrey Raymond, Jackman, David M, Savukoski, Daniel O, Hall, Dimity, Shivdasani, Priyanka, Heng, Jennifer C, Dahlberg, Suzanne Eleanor, Janne, Pasi Antero, Verma, Suman, Christensen, James, Hammerman, Peter Seth, Sholl, Lynette Marie

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Positional Cloning of the CLN5 Gene Defective in the Finnish Variant of the LINCL von Klockars, Tuomas, Savukoski, Minna, Isosomppi, Juha, Peltonen, Leena

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Prenatally detected paternal uniparental chromosome 13 isodisomy von Järvelä, Irma, Savukoski, Minna, Ämmälä, Pirkko, Von Koskull, Harriet

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Linkage analysis of late-infantile neuronal ceroid-lipofuscinosis von Sharp, Julie, Savukoski, Minna, Wheeler, Ruth B., Harris, Juliette, Järvelä, Irma, Peltonen, Leena, Gardiner, Mark, Williams, Ruth

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