FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Arto Mannermaa

Research Profile

Geographic Areas

Finland

Chemicals & Drugs

Disorders

Physiology

Genes & Molecular Sequences

Concepts & Ideas

Procedures

Co-author Network

Publications

TOP 3
Marjo Malinen; Arto Mannermaa; Kaisa Nieminen; Sami Heikkinen; Tiina Jääskeläinen; Veli-Matti Kosma; Mikko Pelkonen; Sami Väisänen; Jorma J Palvimo
Proto-oncogene PIM-1 is a novel estrogen receptor target associating with high grade breast tumors.
Jaana M Hartikainen; Vuokko L Kinnula; Veli-Matti Kosma; Arto Mannermaa; Maria Tengström; Ylermi Soini
Genetic polymorphisms and protein expression of NRF2 and Sulfiredoxin predict survival outcomes in breast cancer.
Szilvia Solyom; Bernadette ARESSY; Roger A Greenberg; Jaana M Hartikainen; Anne Kallioniemi; Saila Kauppila; Veli-Matti Kosma; Arto Mannermaa; Jenni Nikkilä; Jeffrey Patterson-Fortin; Katri Pylkäs; Robert Winqvist
Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Arto Mannermaa (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Marjo Malinen; Arto Mannermaa; Kaisa Nieminen; Sami Heikkinen; Tiina Jääskeläinen; Veli-Matti Kosma; Mikko Pelkonen; Sami Väisänen; Jorma J Palvimo
Proto-oncogene PIM-1 is a novel estrogen receptor target associating with high grade breast tumors.
Molecular and cellular endocrinology 2013;365(2):270-6.
2012: Jaana M Hartikainen; Vuokko L Kinnula; Veli-Matti Kosma; Arto Mannermaa; Maria Tengström; Ylermi Soini
Genetic polymorphisms and protein expression of NRF2 and Sulfiredoxin predict survival outcomes in breast cancer.
Cancer research 2012;72(21):5537-46.
2012: Szilvia Solyom; Bernadette ARESSY; Roger A Greenberg; Jaana M Hartikainen; Anne Kallioniemi; Saila Kauppila; Veli-Matti Kosma; Arto Mannermaa; Jenni Nikkilä; Jeffrey Patterson-Fortin; Katri Pylkäs; Robert Winqvist
Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions.
Science translational medicine 2012;4(122):122ra23.
2012: Bozena Berdel; Veli-Matti Kosma; Marjo Malinen; Kaisa Nieminen; Jorma J Palvimo; Ylermi Soini; Maria Tengström; Arto Mannermaa
Histone demethylase GASC1--a potential prognostic and predictive marker in invasive breast cancer.
BMC cancer 2012;12():516.
2011: Mikko Vuorela; Maarit Anttila; Maria Haanpää; Jaana M Hartikainen; Veli-Matti Kosma; Annika Lindblom; Arto Mannermaa; Ulla Puistola; Katri Pylkäs; Annika Rosengren; Karin Sundfeldt; Anna von Wachenfeldt Wäppling; Robert Winqvist
Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility.
Breast cancer research and treatment 2011;130(3):1003-10.
2011: Anna Jouppila-Mättö; Hanna Tuhkanen; Ylermi Soini; Matti Pukkila; Mervi Närkiö-Mäkelä; Reijo K Sironen; Ismo Virtanen; Arto Mannermaa; Veli-Matti Kosma
Transcription factor snail1 expression and poor survival in pharyngeal squamous cell carcinoma.
Histology and histopathology 2011;26(4):443-9.
2011: Anna Jouppila-Mättö; Arto Mannermaa; Mervi Närkiö-Mäkelä; Matti Pukkila; Reijo K Sironen; Ylermi Soini; Hanna Tuhkanen; Veli-Matti Kosma
Twist and snai1 expression in pharyngeal squamous cell carcinoma stroma is related to cancer progression.
BMC cancer 2011;11():350.
2011: Ylermi Soini; Hanna Tuhkanen; Reijo Sironen; Ismo Virtanen; Vesa Kataja; Päivi Auvinen; Arto Mannermaa; Veli-Matti Kosma
Transcription factors zeb1, twist and snai1 in breast carcinoma.
BMC cancer 2011;11():73.
2009: Saila Vepsäläinen; Seppo Helisalmi; Arto Mannermaa; Tuula Pirttilä; Hilkka Soininen; Mikko Hiltunen
Combined risk effects of IDE and NEP gene variants on Alzheimer disease.
Journal of neurology, neurosurgery, and psychiatry 2009;80(11):1268-70.
2009: Irina Alafuzoff; L Aho; Seppo Helisalmi; Arto Mannermaa; Hilkka Soininen
Beta-amyloid deposition in brains of subjects with diabetes.
Neuropathology and applied neurobiology 2009;35(1):60-8.
2009: Hanna Tuhkanen; Ylermi Soini; Veli-Matti Kosma; Maarit Anttila; Reijo K Sironen; Kirsi Hämäläinen; Laura Kukkonen; Ismo Virtanen; Arto Mannermaa
Nuclear expression of Snail1 in borderline and malignant epithelial ovarian tumours is associated with tumour progression.
BMC cancer 2009;9():289.
2008: Hannele Erkko; James G Dowty; Jenni Nikkilä; Kirsi Syrjäkoski; Arto Mannermaa; Katri Pylkäs; Melissa C Southey; Kaija Holli; Anne Kallioniemi; Arja Jukkola-Vuorinen; Vesa Kataja; Veli-Matti Kosma; Bing Xia; David M Livingston; Robert Winqvist; John L Hopper
Penetrance analysis of the PALB2 c.1592delT founder mutation.
Clinical cancer research : an official journal of the American Association for Cancer Research 2008;14(14):4667-71.
2008: Rainer Fagerholm; Barbara Hofstetter; Johanna Tommiska; Kirsimari Aaltonen; Radek Vrtel; Kirsi Syrjäkoski; Anne Kallioniemi; Outi Kilpivaara; Arto Mannermaa; Veli-Matti Kosma; Matti Uusitupa; Matti Eskelinen; Vesa Kataja; Kristiina Aittomäki; Karl von Smitten; Päivi Heikkilä; Jiri Lukas; Kaija Holli; Jirina Bartkova; Carl Blomqvist; Jiri Bartek; Heli Nevanlinna
NAD(P)H:quinone oxidoreductase 1 NQO1*2 genotype (P187S) is a strong prognostic and predictive factor in breast cancer.
Nature genetics 2008;40(7):844-53.
2007: Jaana M Hartikainen; Arto Mannermaa; Seppo Heinonen; Veli-Matti Kosma; Vesa Kataja
A BRCA2 mutation, 4088insA, in a Finnish breast and ovarian cancer family associated with favourable clinical course.
Anticancer research 2007;27(6C):4295-300.
2007: Jaana M Hartikainen; Vesa Kataja; Mia Pirskanen; Airi Arffman; Ulla Ristonmaa; Pia Vahteristo; Markku Ryynänen; Seppo Heinonen; Veli-Matti Kosma; Arto Mannermaa
Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families.
Clinical genetics 2007;72(4):311-20.
2007: Saila Vepsäläinen; Michele Parkinson; Seppo Helisalmi; Arto Mannermaa; Hilkka Soininen; Rudolph E Tanzi; Lars Bertram; Mikko Hiltunen
Insulin-degrading enzyme is genetically associated with Alzheimer's disease in the Finnish population.
Journal of medical genetics 2007;44(9):606-8.
2007: Hannele Erkko; Bing Xia; Jenni Nikkilä; Johanna Schleutker; Kirsi Syrjäkoski; Arto Mannermaa; Anne Kallioniemi; Katri Pylkäs; Sanna-Maria Karppinen; Katrin Rapakko; alexander miron; Qing Sheng; Guilan Li; Henna Mattila; Daphne W Bell; Daniel A Haber; Mervi Grip; Mervi Reiman; Arja Jukkola-Vuorinen; Aki Mustonen; Juha Kere; Lauri A Aaltonen; Veli-Matti Kosma; Vesa Kataja; Ylermi Soini; Ronny Drapkin; David M Livingston; Robert Winqvist
A recurrent mutation in PALB2 in Finnish cancer families.
Nature 2007;446(7133):316-9.
2006: Hanna Tuhkanen; Maarit Anttila; Veli-Matti Kosma; Seppo Heinonen; Matti Juhola; Seppo Helisalmi; Vesa Kataja; Arto Mannermaa
Frequent gene dosage alterations in stromal cells of epithelial ovarian carcinomas.
International journal of cancer. Journal international du cancer 2006;119(6):1345-53.
2006: Katri Heikkinen; Katrin Rapakko; Sanna-Maria Karppinen; Hannele Erkko; Sakari Knuutila; Tuija Lundán; Arto Mannermaa; Anne-Lise Børresen-Dale; Ake Borg; Rosa B Barkardottir; John H J Petrini; Robert Winqvist
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability.
Carcinogenesis 2006;27(8):1593-9.
2006: Jaana M Hartikainen; Hanna Tuhkanen; Vesa Kataja; Matti Eskelinen; Matti Uusitupa; Veli-Matti Kosma; Arto Mannermaa
Refinement of the 22q12-q13 breast cancer--associated region: evidence of TMPRSS6 as a candidate gene in an eastern Finnish population.
Clinical cancer research : an official journal of the American Association for Cancer Research 2006;12(5):1454-62.
2006: Seppo Helisalmi; Saila Vepsäläinen; Anne Maria Koivisto; Arto Mannermaa; Susan Iivonen; Mikko Hiltunen; V Kiviniemi; Hilkka Soininen
Association of CYP46 intron 2 polymorphism in Finnish Alzheimer's disease samples and a global scale summary.
Journal of neurology, neurosurgery, and psychiatry 2006;77(3):421-2.
2005: Mia Pirskanen; Mikko Hiltunen; Arto Mannermaa; Seppo Helisalmi; Maarit Lehtovirta; Tuomo Hänninen; Hilkka Soininen
Estrogen receptor beta gene variants are associated with increased risk of Alzheimer's disease in women.
European journal of human genetics : EJHG 2005;13(9):1000-6.
2005: Saila Vepsäläinen; Eero Castren; Seppo Helisalmi; Susan Iivonen; Arto Mannermaa; Maarit Lehtovirta; Tuomo Hänninen; Hilkka Soininen; Mikko Hiltunen
Genetic analysis of BDNF and TrkB gene polymorphisms in Alzheimer's disease.
Journal of neurology 2005;252(4):423-8.
2005: Jaana M Hartikainen; Hanna Tuhkanen; Vesa Kataja; Alison M Dunning; Antonis Antoniou; Paula Smith; Airi Arffman; Mia Pirskanen; Douglas F Easton; Matti Eskelinen; Matti Uusitupa; Veli-Matti Kosma; Arto Mannermaa
An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005;14(1):75-80.
2004: Seppo Helisalmi; Mikko Hiltunen; Saila Vepsäläinen; Susan Iivonen; Arto Mannermaa; Maarit Lehtovirta; Anne Maria Koivisto; Irina Alafuzoff; Hilkka Soininen
Polymorphisms in neprilysin gene affect the risk of Alzheimer's disease in Finnish patients.
Journal of neurology, neurosurgery, and psychiatry 2004;75(12):1746-8.
2004: Seppo Helisalmi; Mikko Hiltunen; Saila Vepsäläinen; Susan Iivonen; Elizabeth H Corder; Maarit Lehtovirta; Arto Mannermaa; Anne Maria Koivisto; Hilkka Soininen
Genetic variation in apolipoprotein D and Alzheimer's disease.
Journal of neurology 2004;251(8):951-7.
2004: Hanna Tuhkanen; Maarit Anttila; Veli-Matti Kosma; Jukka Puolakka; Matti Juhola; Seppo Heinonen; Arto Mannermaa
Marked allelic imbalance on chromosome 5q31 does not explain alpha-catenin expression in epithelial ovarian cancer.
Gynecologic oncology 2004;94(2):416-21.
2004: Seppo Helisalmi; Bart Dermaut; Mikko Hiltunen; Arto Mannermaa; Marleen Van den Broeck; Maarit Lehtovirta; Anne Maria Koivisto; Susan Iivonen; Marc Cruts; Hilkka Soininen; Christine Van Broeckhoven
Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population.
Neurology 2004;63(1):173-5.
2004: Jaana M Autere; Jukka S Moilanen; Saara Finnilä; Hilkka Soininen; Arto Mannermaa; Päivi Hartikainen; Merja Hallikainen; Kari Majamaa
Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia.
Human genetics 2004;115(1):29-35.
2004: Susan Iivonen; E Corder; Maarit Lehtovirta; Seppo Helisalmi; Arto Mannermaa; Saila Vepsäläinen; Tuomo Hänninen; Hilkka Soininen; Mikko Hiltunen
Polymorphisms in the CYP19 gene confer increased risk for Alzheimer disease.
Neurology 2004;62(7):1170-6.
2004: Hanna Tuhkanen; Maarit Anttila; Veli-Matti Kosma; Seppo Ylä-Herttuala; Seppo Heinonen; Arja Kuronen; Matti Juhola; Raija Tammi; Markku Tammi; Arto Mannermaa
Genetic alterations in the peritumoral stromal cells of malignant and borderline epithelial ovarian tumors as indicated by allelic imbalance on chromosome 3p.
International journal of cancer. Journal international du cancer 2004;109(2):247-52.
2004: Susanna Tervo; Miia Kivipelto; Tuomo Hänninen; Matti Vanhanen; Merja Hallikainen; Arto Mannermaa; Hilkka Soininen
Incidence and risk factors for mild cognitive impairment: a population-based three-year follow-up study of cognitively healthy elderly subjects.
Dementia and geriatric cognitive disorders 2004;17(3):196-203.
2003: Susan Iivonen; Seppo Helisalmi; Arto Mannermaa; Irina Alafuzoff; Maarit Lehtovirta; Hilkka Soininen; Mikko Hiltunen
Heparan sulfate proteoglycan 2 polymorphism in Alzheimer's disease and correlation with neuropathology.
Neuroscience letters 2003;352(2):146-50.
2003: Alison M Dunning; Peter D Ellis; Simon McBride; Heidi L Kirschenlohr; Catherine S Healey; Paul R Kemp; Robert N Luben; Jenny Chang-Claude; Arto Mannermaa; Vesa Kataja; Paul D P Pharoah; Douglas F Easton; Bruce A J Ponder; James C Metcalfe
A transforming growth factorbeta1 signal peptide variant increases secretion in vitro and is associated with increased incidence of invasive breast cancer.
Cancer research 2003;63(10):2610-5.
2003: Jaana Laasanen; Mikko Hiltunen; Eeva-Liisa Romppanen; Kari Punnonen; Arto Mannermaa; Seppo Heinonen
Microsatellite marker association at chromosome region 2p13 in Finnish patients with preeclampsia and obstetric cholestasis suggests a common risk locus.
European journal of human genetics : EJHG 2003;11(3):232-6.
2003: Kari M Mattila; Mikko Hiltunen; Juha O Rinne; Arto Mannermaa; Matias Röyttä; Irina Alafuzoff; Pekka Laippala; Hilkka Soininen; Terho Lehtimäki
Absence of association between an intercellular adhesion molecule 1 gene E469K polymorphism and Alzheimer's disease in Finnish patients.
Neuroscience letters 2003;337(1):61-3.
2002: Marja-Lissa Eloranta; Jaana T M Heiskanen; Mikko J Hiltunen; Arto Mannermaa; Kari Punnonen; Seppo Heinonen
Multidrug resistance 3 gene mutation 1712delT and estrogen receptor alpha gene polymorphisms in Finnish women with obstetric cholestasis.
European journal of obstetrics, gynecology, and reproductive biology 2002;105(2):132-5.
2002: Jaana Laasanen; Seppo Heinonen; Mikko Hiltunen; Arto Mannermaa; Markku Laakso
Polymorphism in the peroxisome proliferator-activated receptor-gamma gene in women with preeclampsia.
Early human development 2002;69(1-2):77-82.
2002: T Anttila; Eeva-Liisa Helkala; Miia Kivipelto; Merja Hallikainen; Kari Alhainen; H Heinonen; Arto Mannermaa; Jaakko Tuomilehto; Hilkka Soininen; Aulikki Nissinen
Midlife income, occupation, APOE status, and dementia: a population-based study.
Neurology 2002;59(6):887-93.
2002: Marja-Lissa Eloranta; Jaana T M Heiskanen; Mikko J Hiltunen; Arto Mannermaa; Kari Punnonen; Seppo Heinonen
Multidrug resistance 3 gene mutation 1712delT and estrogen receptor alpha gene polymorphisms in Finnish women with obstetric cholestasis.
European journal of obstetrics, gynecology, and reproductive biology 2002;104(2):109-12.
2002: Jaana M Autere; Mikko J Hiltunen; Arto Mannermaa; Pekka Jäkälä; Päivi Hartikainen; Kari Majamaa; Irina Alafuzoff; Hilkka Soininen
Molecular genetic analysis of the alpha-synuclein and the parkin gene in Parkinson's disease in Finland.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2002;9(5):479-83.
2002: Jaana Laasanen; Eeva-Liisa Romppanen; Mikko Hiltunen; Seppo Helisalmi; Arto Mannermaa; Kari Punnonen; Seppo Heinonen
Two exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are jointly associated with preeclampsia.
European journal of human genetics : EJHG 2002;10(9):569-73.
2002: Miia Kivipelto; Eeva-Liisa Helkala; Mikko P Laakso; Tuomo Hänninen; Merja Hallikainen; Kari Alhainen; Susan Iivonen; Arto Mannermaa; Jaakko Tuomilehto; Aulikki Nissinen; Hilkka Soininen
Apolipoprotein E epsilon4 allele, elevated midlife total cholesterol level, and high midlife systolic blood pressure are independent risk factors for late-life Alzheimer disease.
Annals of internal medicine 2002;137(3):149-55.
2002: Seija Korhonen; Eeva-Liisa Romppanen; Mikko Hiltunen; Arto Mannermaa; Kari Punnonen; Maritta Hippeläinen; Seppo Heinonen
Lack of association between C-850T polymorphism of the gene encoding tumor necrosis factor-alpha and polycystic ovary syndrome.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2002;16(4):271-4.
2002: Jaana Laasanen; Mikko Hiltunen; Kari Punnonen; Arto Mannermaa; Seppo Heinonen
Fibrinogen and factor VII promoter polymorphisms in women with preeclampsia.
Obstetrics and gynecology 2002;100(2):317-20.
2002: Jaana T M Heiskanen; Eeva-Liisa Romppanen; Mikko Hiltunen; Susan Iivonen; Arto Mannermaa; Kari Punnonen; Seppo Heinonen
Polymorphism in the tumor necrosis factor-alpha gene in women with preeclampsia.
Journal of assisted reproduction and genetics 2002;19(5):220-3.
2002: Mia Pirskanen; Mikko Hiltunen; Arto Mannermaa; Susan Iivonen; Seppo Helisalmi; Maarit Lehtovirta; Anne Maria Koivisto; Markku Laakso; Hilkka Soininen; Irina Alafuzoff
Interleukin 1 alpha gene polymorphism as a susceptibility factor in Alzheimer's disease and its influence on the extent of histopathological hallmark lesions of Alzheimer's disease.
Dementia and geriatric cognitive disorders 2002;14(3):123-7.
2002: Susan Iivonen; Mikko Hiltunen; Irina Alafuzoff; Arto Mannermaa; Petri Kerokoski; Jukka Puoliväli; Antero Salminen; Seppo Helisalmi; Hilkka Soininen
Seladin-1 transcription is linked to neuronal degeneration in Alzheimer's disease.
Neuroscience 2002;113(2):301-10.
2001: Mikko Hiltunen; Arto Mannermaa; D Thompson; D Easton; Mia Pirskanen; Seppo Helisalmi; Anne Maria Koivisto; Maarit Lehtovirta; Markku Ryynänen; Hilkka Soininen
Genome-wide linkage disequilibrium mapping of late-onset Alzheimer's disease in Finland.
Neurology 2001;57(9):1663-8.
2001: Jaana T M Heiskanen; Mia Pirskanen; Mikko J Hiltunen; Arto Mannermaa; Kari Punnonen; Seppo Heinonen
Insertion-deletion polymorphism in the gene for angiotensin-converting enzyme is associated with obstetric cholestasis but not with preeclampsia.
American journal of obstetrics and gynecology 2001;185(3):600-3.
2001: Mia Pirskanen; Irina Alafuzoff; Mikko Hiltunen; Arto Mannermaa; Seppo Helisalmi; Maarit Lehtovirta; Anne Maria Koivisto; M Laakso; Hilkka Soininen
An association between a subset of Finnish late-onset Alzheimer's disease and alpha2-macroglobulin.
Neurogenetics 2001;3(3):171-2.
2001: Seppo Heinonen; Marja-Lissa Eloranta; Jaana T M Heiskanen; Kari Punnonen; Seppo Helisalmi; Arto Mannermaa; Mikko Hiltunen
Maternal susceptibility locus for obstetric cholestasis maps to chromosome region 2p13 in Finnish patients.
Scandinavian journal of gastroenterology 2001;36(7):766-70.
2001: Saara Finnilä; Jaana M Autere; M Lehtovirta; Päivi Hartikainen; Arto Mannermaa; Hilkka Soininen; Kari Majamaa
Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln.
Journal of medical genetics 2001;38(6):400-5.
2001: J Kallinen; K Marin; Seppo Heinonen; Arto Mannermaa; A Palotie; Markku Ryynänen
Wide scope prenatal diagnosis at Kuopio University Hospital 1997-1998: integration of gene tests and fetal karyotyping.
BJOG : an international journal of obstetrics and gynaecology 2001;108(5):505-9.
2001: J Kallinen; Seppo Heinonen; A Palotie; Arto Mannermaa; M Ryynanen
Antenatal gene tests in low-risk pregnancies: molecular screening for aspartylglucosaminuria (AGU) and infantile neuronal ceroid lipofuscinosis (INCL) in Finland.
Prenatal diagnosis 2001;21(5):409-12.
2001: Seppo Heinonen; Seija Korhonen; Maritta Hippeläinen; Mikko Hiltunen; Arto Mannermaa; S Saarikoski
Apolipoprotein E alleles in women with polycystic ovary syndrome.
Fertility and sterility 2001;75(5):878-80.
2001: J Kallinen; Seppo Heinonen; Markku Ryynänen; L Pulkkinen; Arto Mannermaa
Antenatal genetic screening for congenital nephrosis.
Prenatal diagnosis 2001;21(2):81-4.
2000: Alison M Dunning; Francine Durocher; Catherine S Healey; M Dawn Teare; Simon McBride; F Carlomagno; Chun-Fang Xu; Elisabeth Dawson; S Rhodes; S Ueda; E Lai; Robert N Luben; E J Van Rensburg; Arto Mannermaa; Vesa Kataja; G Rennart; Carl Bruder; Ian Purvis; Douglas Easton; Bruce A J Ponder
The extent of linkage disequilibrium in four populations with distinct demographic histories.
American journal of human genetics 2000;67(6):1544-54.
2000: W F Reynolds; Mikko Hiltunen; Mia Pirskanen; Arto Mannermaa; Seppo Helisalmi; Maarit Lehtovirta; Irina Alafuzoff; Hilkka Soininen
MPO and APOEepsilon4 polymorphisms interact to increase risk for AD in Finnish males.
Neurology 2000;55(9):1284-90.
2000: Catherine S Healey; Alison M Dunning; M Dawn Teare; D Chase; L Parker; J Burn; Jenny Chang-Claude; Arto Mannermaa; Vesa Kataja; David Huntsman; Paul D P Pharoah; Robert N Luben; Douglas F Easton; Bruce A J Ponder
A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability.
Nature genetics 2000;26(3):362-4.
2000: Virpi Launonen; Arto Mannermaa; Frej Stenbäck; V M Kosma; Ulla Puistola; Pia Huusko; M Anttila; Risto Bloigu; S Saarikoski; Antti Kauppila; Robert Winqvist
Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer: correlation to clinicopathological variables.
Cancer genetics and cytogenetics 2000;122(1):49-54.
2000: Laura Sarantaus; Pia Huusko; Hannaleena Eerola; Virpi Launonen; Paula Vehmanen; Katrin Rapakko; Elizabeth M Gillanders; Kirsi Syrjäkoski; Tommi Kainu; Pia Vahteristo; Ralf Krahe; Kimmo Pääkkönen; J Hartikainen; Carl Blomqvist; T Löppönen; Kaija Holli; Markku Ryynänen; Ralf Bützow; Ake Borg; B Wasteson Arver; E Holmberg; Arto Mannermaa; Juha Kere; Olli Kallioniemi; Robert Winqvist; Heli Nevanlinna
Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.
European journal of human genetics : EJHG 2000;8(10):757-63.
2000: Marja-Lissa Eloranta; Jaana T M Heiskanen; Mikko Hiltunen; Seppo Helisalmi; Arto Mannermaa; Seppo Heinonen
Apolipoprotein E alleles in women with intrahepatic cholestasis of pregnancy.
Scandinavian journal of gastroenterology 2000;35(9):966-8.
2000: J Kallinen; Seppo Heinonen; Arto Mannermaa; Markku Ryynänen
Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation.
Clinical genetics 2000;58(2):111-5.
2000: Seppo Helisalmi; RH Valve; Matti K Karvonen; Mikko Hiltunen; Mia Pirskanen; Arto Mannermaa; Markku Koulu; Ullamari Pesonen; Matti Uusitupa; Hilkka Soininen
The leucine (7)-to-proline (7) polymorphism in the signal peptide of neuropeptide Y is not associated with Alzheimer's disease or the link apolipoprotein E.
Neuroscience letters 2000;287(1):25-8.
2000: Mikko Hiltunen; Seppo Helisalmi; Arto Mannermaa; Irina Alafuzoff; Anne Maria Koivisto; Maarit Lehtovirta; Mia Pirskanen; Raimo Sulkava; Auli Verkkoniemi; Hilkka Soininen
Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?
European journal of human genetics : EJHG 2000;8(4):259-66.
2000: Irina Alafuzoff; Seppo Helisalmi; Arto Mannermaa; Hilkka Soininen
Severity of cardiovascular disease, apolipoprotein E genotype, and brain pathology in aging and dementia.
Annals of the New York Academy of Sciences 2000;903():244-51.
2000: Seppo Helisalmi; Mikko Hiltunen; Arto Mannermaa; Anne Maria Koivisto; Maarit Lehtovirta; Irina Alafuzoff; Markku Ryynänen; Hilkka Soininen
Is the presenilin-1 E318G missense mutation a risk factor for Alzheimer's disease?
Neuroscience letters 2000;278(1-2):65-8.
1999: Seppo Helisalmi; Mikko Hiltunen; Piia Valonen; Arto Mannermaa; Anne Maria Koivisto; Maarit Lehtovirta; Markku Ryynänen; Hilkka Soininen
Promoter polymorphism (-491A/T) in the APOE gene of Finnish Alzheimer's disease patients and control individuals.
Journal of neurology 1999;246(9):821-4.
1999: Mikko Hiltunen; Arto Mannermaa; Anne Maria Koivisto; Maarit Lehtovirta; Seppo Helisalmi; Markku Ryynänen; PJ Riekkinen; Hilkka Soininen
Linkage disequilibrium in the 13q12 region in Finnish late onset Alzheimer's disease patients.
European journal of human genetics : EJHG 1999;7(6):652-8.
1999: Markku Ryynänen; Seppo Heinonen; M Makkonen; E Kajanoja; Arto Mannermaa; K Pertti
Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies.
European journal of human genetics : EJHG 1999;7(2):212-6.
1998: Mikko Hiltunen; Arto Mannermaa; Seppo Helisalmi; Anne Maria Koivisto; Maarit Lehtovirta; Markku Ryynänen; PJ Riekkinen; Hilkka Soininen
Butyrylcholinesterase K variant and apolipoprotein E4 genes do not act in synergy in Finnish late-onset Alzheimer's disease patients.
Neuroscience letters 1998;250(1):69-71.
1998: Maarit Lehtovirta; Jyrki Kuikka; Seppo Helisalmi; Päivi Hartikainen; Arto Mannermaa; Markku Ryynänen; Hilkka Soininen
Longitudinal SPECT study in Alzheimer's disease: relation to apolipoprotein E polymorphism.
Journal of neurology, neurosurgery, and psychiatry 1998;64(6):742-6.
1998: Markku Ryynänen; Seppo Heinonen; M Makkonen; Arto Mannermaa; Pertti Kirkinen
[Screening for Fragile X syndrome mutations during early pregnancy--results and mothers' opinions about the gene test].
Duodecim; lääketieteellinen aikakauskirja 1998;22(114):2323-9.
1997: Seppo Helisalmi; Arto Mannermaa; Maarit Lehtovirta; Markku Ryynänen; PJ Riekkinen; Hilkka Soininen
No association between alpha1-antichymotrypsin polymorphism, apolipoprotein E and patients with late-onset Alzheimer's disease.
Neuroscience letters 1997;231(1):56-8.
1997: Pekka Jäkälä; Tuomo Hänninen; Markku Ryynänen; Markku Laakso; Kaarina Partanen; Arto Mannermaa; Hilkka Soininen
Fragile-X: neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes.
The Journal of clinical investigation 1997;100(2):331-8.
1996: Arto Mannermaa; L Pulkkinen; E Kajanoja; Markku Ryynänen; S Saarikoski
Deletion in the FMR1 gene in a fragile-X male.
American journal of medical genetics 1996;64(2):293-5.
1996: Maarit Lehtovirta; J Partanen; M Könönen; Hilkka Soininen; Seppo Helisalmi; Arto Mannermaa; Markku Ryynänen; Päivi Hartikainen; PJ Riekkinen
Spectral analysis of EEG in Alzheimer's disease: relation to apolipoprotein E polymorphism.
Neurobiology of aging 1996;17(4):523-6.
1996: Maarit Lehtovirta; Hilkka Soininen; Mikko P Laakso; Kaarina Partanen; Seppo Helisalmi; Arto Mannermaa; Markku Ryynänen; Jyrki Kuikka; Päivi Hartikainen; PJ Riekkinen
SPECT and MRI analysis in Alzheimer's disease: relation to apolipoprotein E epsilon 4 allele.
Journal of neurology, neurosurgery, and psychiatry 1996;60(6):644-9.
1996: Seppo Helisalmi; Arto Mannermaa; Maarit Lehtovirta; Markku Ryynänen; PJ Riekkinen; Hilkka Soininen
Screening for amyloid beta precursor protein codon 665, 670/671 and 717 mutations in Finnish patients with Alzheimer's disease.
Neuroscience letters 1996;205(1):68-70.
1996: Seppo Helisalmi; K Linnaranta; Maarit Lehtovirta; Arto Mannermaa; Outi Kopra; Markku Ryynänen; PJ Riekkinen; Hilkka Soininen
Apolipoprotein E polymorphism in patients with different neurodegenerative disorders.
Neuroscience letters 1996;205(1):61-4.
1996: Maarit Lehtovirta; Hilkka Soininen; Seppo Helisalmi; Arto Mannermaa; Eeva-Liisa Helkala; Päivi Hartikainen; Tuomo Hänninen; Markku Ryynänen; PJ Riekkinen
Clinical and neuropsychological characteristics in familial and sporadic Alzheimer's disease: relation to apolipoprotein E polymorphism.
Neurology 1996;46(2):413-9.
1995: Outi Kopra; Maarit Lehtovirta; Hilkka Soininen; Seppo Helisalmi; Arto Mannermaa; H Sorvari; O Kosunen; Leo Paljärvi; Markku Ryynänen; PJ Riekkinen
Alzheimer pathology of patients carrying apolipoprotein E epsilon 4 allele.
Neurobiology of aging 1995;16(4):505-13.
1995: Maarit Lehtovirta; Mikko P Laakso; Hilkka Soininen; Seppo Helisalmi; Arto Mannermaa; Eeva-Liisa Helkala; Kaarina Partanen; Markku Ryynänen; Pauli Vainio; Päivi Hartikainen
Volumes of hippocampus, amygdala and frontal lobe in Alzheimer patients with different apolipoprotein E genotypes.
Neuroscience 1995;67(1):65-72.
1995: O Kosunen; S Talasniemi; Maarit Lehtovirta; Outi Kopra; Seppo Helisalmi; Arto Mannermaa; Leo Paljärvi; Markku Ryynänen; PJ Riekkinen; Hilkka Soininen
Relation of coronary atherosclerosis and apolipoprotein E genotypes in Alzheimer patients.
Stroke; a journal of cerebral circulation 1995;26(5):743-8.
1995: Markku Ryynänen; Pertti Kirkinen; Arto Mannermaa; S Saarikoski
Carrier diagnosis of the fragile X syndrome--a challenge in antenatal clinics.
American journal of obstetrics and gynecology 1995;172(4 Pt 1):1236-9.
1995: Hilkka Soininen; O Kosunen; Seppo Helisalmi; Arto Mannermaa; Leo Paljärvi; S Talasniemi; Markku Ryynänen; PJ Riekkinen
A severe loss of choline acetyltransferase in the frontal cortex of Alzheimer patients carrying apolipoprotein epsilon 4 allele.
Neuroscience letters 1995;187(2):79-82.
1995: Maarit Lehtovirta; Seppo Helisalmi; Arto Mannermaa; Hilkka Soininen; Keijo Koivisto; Markku Ryynänen; PJ Riekkinen
Apolipoprotein E polymorphism and Alzheimer's disease in eastern Finland.
Neuroscience letters 1995;185(1):13-5.
1995: Hilkka Soininen; Kaarina Partanen; Asla Pitkänen; Merja Hallikainen; Tuomo Hänninen; Seppo Helisalmi; Arto Mannermaa; Markku Ryynänen; Keijo Koivisto; PJ Riekkinen
Decreased hippocampal volume asymmetry on MRIs in nondemented elderly subjects carrying the apolipoprotein E epsilon 4 allele.
Neurology 1995;45(2):391-2.