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Aarno Palotie

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TOP 3
Aarno Palotie; Mikko Kallela; Verneri Anttila
Probing the brain of comorbidity.
Alison J Coffey; Sally Connolly; Ann Dalton; Anil Dhawan; Miranda Durkie; K Elizabeth Allen; Jennifer Emmerson; Nicola Giffin; Godfrey T Gillett; William Griffiths; Nedim Hadzic; Stephen Hague; Christopher J Joyce; Richard Kirk; Stefanie Klaffke; Christine Lo; Kirsten McLay; Giorgina Mieli-Vergani; David Nicholl; Aarno Palotie; Magnus Rattray; Basil Sharrack; Sarah Smithson; Ali Taha; Stuart Tanner; Siew Wong; Jim Bonham; Oliver Bandmann
A genetic study of Wilson's disease in the United Kingdom.
Pirkka-Pekka Laurila; Terho Lehtimäki; Daniel B Mirel; Jussi Naukkarinen; Matej Oresic; Aarno Palotie; Leena Peltonen; Olli T Raitakari; Aimo Ruokonen; Veikko Salomaa; Antti-Pekka Sarin; Sanni Söderlund; Jarkko Soronen; Ida Surakka; Jing Tang; Marja-Riitta Taskinen; Laxman Yetukuri; Christian Ehnholm; Johan G Eriksson; Tuulia Hyötyläinen; Marjo-Riitta Järvelin; Matti Jauhiainen; Antti Jula; Johannes Kettunen; Samuli Ripatti
Genomic, transcriptomic, and lipidomic profiling highlights the role of inflammation in individuals with low high-density lipoprotein cholesterol.

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All Publications

2013: Aarno Palotie; Mikko Kallela; Verneri Anttila
Probing the brain of comorbidity.
Science translational medicine 2013;5(183):183fs15.
2013: Alison J Coffey; Sally Connolly; Ann Dalton; Anil Dhawan; Miranda Durkie; K Elizabeth Allen; Jennifer Emmerson; Nicola Giffin; Godfrey T Gillett; William Griffiths; Nedim Hadzic; Stephen Hague; Christopher J Joyce; Richard Kirk; Stefanie Klaffke; Christine Lo; Kirsten McLay; Giorgina Mieli-Vergani; David Nicholl; Aarno Palotie; Magnus Rattray; Basil Sharrack; Sarah Smithson; Ali Taha; Stuart Tanner; Siew Wong; Jim Bonham; Oliver Bandmann
A genetic study of Wilson's disease in the United Kingdom.
Brain : a journal of neurology 2013;136(Pt 5):1476-87.
2013: Pirkka-Pekka Laurila; Terho Lehtimäki; Daniel B Mirel; Jussi Naukkarinen; Matej Oresic; Aarno Palotie; Leena Peltonen; Olli T Raitakari; Aimo Ruokonen; Veikko Salomaa; Antti-Pekka Sarin; Sanni Söderlund; Jarkko Soronen; Ida Surakka; Jing Tang; Marja-Riitta Taskinen; Laxman Yetukuri; Christian Ehnholm; Johan G Eriksson; Tuulia Hyötyläinen; Marjo-Riitta Järvelin; Matti Jauhiainen; Antti Jula; Johannes Kettunen; Samuli Ripatti
Genomic, transcriptomic, and lipidomic profiling highlights the role of inflammation in individuals with low high-density lipoprotein cholesterol.
Arteriosclerosis, thrombosis, and vascular biology 2013;33(4):847-57.
2013: Aarno Palotie; Elisabeth Widén; Samuli Ripatti
From genetic discovery to future personalized health research.
New biotechnology 2013;30(3):291-5.
2012: Ida Surakka; Ann-Christine Syvänen; Peter M Visscher; John B Whitfield; Elisabeth Widén; Gonneke Willemsen; Dorret I Boomsma; Kaare Christensen; Eco J C De Geus; Mario Falchi; Jaakko Kaprio; Kirsten O Kyvik; Ulrika Liljedahl; Patrik K E Magnusson; Nicholas G Martin; Grant W Montgomery; Juha Muilu; Aarno Palotie; Nancy L Pedersen; Leena Peltonen; Markus Perola; Kirsi H Pietiläinen; Iffat Rahman; Taina Rantanen; Samuli Ripatti; Kaisa Silander; Thorkild I A Sørensen; Tim Spector
A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2012;15(6):691-9.
2012: Jennifer R Harris; Robert Hewitt; Jane Kaye; Bartha Maria Knoppers; Klaus Lindpaintner; Jan-Eric Litton; Andres Metspalu; Bill Ollier; Lyle J Palmer; Aarno Palotie; Markus Pasterk; Markus Perola; Peter H J Riegman; Gert-Jan van Ommen; Martin Yuille; Marianna Bledsoe; Anthony J Brookes; Isabelle Budin-Ljøsne; Paul Burton; Rex Chisholm; David Cox; Mylène Deschênes; Isabel Fortier; Pierre Hainaut; Kurt Zatloukal
Toward a roadmap in global biobanking for health.
European journal of human genetics : EJHG 2012;20(11):1105-11.
2012: Tiia M Luukkonen; Aarno Palotie; Minna Pöyhönen; Riitta Salonen; Joseph D Terwilliger; Pekka Ellonen; Sonja Lagström; Joseph H Lee; Teppo Varilo
A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm.
Journal of medical genetics 2012;49(10):621-9.
2012: Karin J H Verweij; Jorma Viikari; Peter M Visscher; Elisabeth Widen; Jian Yang; Johan G Eriksson; Andrew C Heath; Kati Heinonen; Mirka Hintsanen; Matti Isohanni; Marjo-Riitta Järvelin; Mika Kähönen; Matthew C Keller; Liisa Keltikangas-Järvinen; Jari Lahti; Terho Lehtimäki; Nicholas G Martin; Jouko Miettunen; Grant W Montgomery; Aarno Palotie; Lars Penke; Anu-Katriina Pesonen; Anneli Pouta; Laura Pulkki-Råback; Katri Räikkönen; Olli Raitakari; Susan K Service; Anja Taanila; Juha Veijola; Brendan P Zietsch
Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding.
Evolution; international journal of organic evolution 2012;66(10):3238-51.
2012: Alison Harvey; Stephen T Holgate; Lars V Kristiansen; Hans Lehrach; Aarno Palotie; Angela Brand; Barbara Prainsack
The future of technologies for personalised medicine.
New biotechnology 2012;29(6):625-33.
2012: Thorlakur Jonsson; Augustine Kong; Yichin Liu; Yanmei Lu; Olafur T Magnusson; Janice Maloney; Aarno Palotie; Jon Snaedal; Hreinn Stefansson; Ole A Andreassen; Jasvinder K Atwal; Timothy W Behrens; Tushar Bhangale; Gyda Bjornsdottir; Sigurbjorn Bjornsson; Robert R Graham; Daniel F Gudbjartsson; Amy Gustafson; Kwame Hoyte; Johanna Huttenlocher; Erik G Jönsson; Palmi V Jonsson; Stacy Steinberg; Patrick Sulem; Unnur Thorsteinsdottir; Ryan J Watts; kari stefansson
A mutation in APP protects against Alzheimer's disease and age-related cognitive decline.
Nature 2012;488(7409):96-9.
2012: Maria Kousi; Johannes R Lemke; Liisa Myllykangas; Aarno Palotie; Erik Riesch; Angela Schulz; Meral Topçu; Michael Alber; Fusun Alehan; Verneri Anttila; Stella Calafato; Sarenur Gökben; Eveliina Jakkula; Hannu Kalimo; Outi Kopra; Anna-Elina Lehesjoki
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene.
Journal of medical genetics 2012;49(6):391-9.
2012: Aaron R Everitt; Eric M Feeley; Stephen B Gordon; David Goulding; David A Hume; Sinu P John; Leanne Kane; David J Adams; Verneri Anttila; J Kenneth Baillie; Abraham L Brass; Christopher R Chin; Simon Clare; Vincenza Colonna; Paul Digard; Gordon Dougan; Jake Dunning; Peter J Openshaw; Aarno Palotie; Thomas Pertel; Jennifer S Sims; Sarah E Smith; Rosalind L Smyth; Chris Tyler-Smith; Tim S Walsh; Rachael S Wash; Helen M Wise; Yali Xue; Kellam Paul
IFITM3 restricts the morbidity and mortality associated with influenza.
Nature 2012;484(7395):519-23.
2012: Elisabeth Widén; Diana L Cousminer; Anna-Liisa Hartikainen; Marjo-Riitta Järvelin; Jaakko Kaprio; Jaana Laitinen; Leena Peltonen; Anneli Pouta; Samuli Ripatti; Karri Silventoinen; Ulla Sovio; Aarno Palotie
Pubertal timing and growth influences cardiometabolic risk factors in adult males and females.
Diabetes care 2012;35(4):850-6.
2012: Taru Tukiainen; Jorma Viikari; Veikko Salomaa; Antti-Pekka Sarin; Markku J Savolainen; Pasi Soininen; Marja-Riitta Taskinen; Emmi Tikkanen; Mika Ala-Korpela; Johan G Eriksson; Marjo-Riitta Järvelin; Matti Jauhiainen; Antti Jula; Mika Kähönen; Antti J Kangas; Kimmo Kaski; Johannes Kettunen; Terho Lehtimäki; Leo-Pekka Lyytikäinen; Paul F O'Reilly; Aarno Palotie; Markus Perola; Anneli Pouta; Olli Raitakari; Samuli Ripatti
Detailed metabolic and genetic characterization reveals new associations for 30 known lipid loci.
Human molecular genetics 2012;21(6):1444-55.
2012: Minna K Karjalainen; Aino Luukkonen; Louis J Muglia; Aarno Palotie; Jevon Plunkett; Jenni Sotkasiira; Kari Teramo; Johanna Ulvila; Verneri Anttila; Ritva Haataja; Johanna M Huusko; Mikko Hallman
A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers.
PloS one 2012;7(12):e51378.
2012: Christine Clark; Panos Deloukas; Elin Grundberg; Christopher J Joyce; Aarno Palotie; Priit Palta; Carol Scott; Alison J Coffey
A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profiling.
PloS one 2012;7(11):e50233.
2012: Michael Inouye; Marjo-Riitta Järvelin; Mika Kähönen; Antti J Kangas; Johannes Kettunen; Pirkka-Pekka Laurila; Terho Lehtimäki; Leo-Pekka Lyytikäinen; Niku Oksala; Aarno Palotie; Markus Perola; Olli Raitakari; Samuli Ripatti; Veikko Salomaa; Markku J Savolainen; Pasi Soininen; Marja-Riitta Taskinen; Jorma Viikari; Mika Ala-Korpela; Paul I W de Bakker
Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.
PLoS genetics 2012;8(8):e1002907.
2012: Emília Ilona Gaál; Murat Günel; Juha Hernesniemi; Juha E Jääskeläinen; Marjo-Riitta Järvelin; Antti Jula; Johannes Kettunen; Kati Kristiansson; Mitja Kurki; Terho Lehtimäki; Christopher Newton-Cheh; Mika Niemelä; Aarno Palotie; Anneli Pouta; Olli T Raitakari; Karola Rehnström; Perttu Salo; Veikko Salomaa; Antti-Pekka Sarin; Mikael von und zu Fraunberg; Elisabeth Widen; Johan G Eriksson; Markus Perola
Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure.
PLoS genetics 2012;8(3):e1002563.
2011: Katsuhito Yasuno; Hitoshi Zembutsu; Mehmet Bakırcıoğlu; Georg Auburger; Philippe Bijlenga; Kaya Bilgüvar; François Cambien; Emília Gaál; Akira Hata; Juha Hernesniemi; Ituro Inoue; Juha E Jääskeläinen; Hidetoshi Kasuya; Dietmar Krex; Boris Krischek; Richard P Lifton; Siew-Kee Low; Shrikant M Mane; Yusuke Nakamura; Mika Niemelä; Ali K Ozturk; Aarno Palotie; Gabriel J E Rinkel; Ynte M Ruigrok; Karl Schaller; Matthias Simon; Helmuth Steinmetz; Murat Günel
Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk.
Proceedings of the National Academy of Sciences of the United States of America 2011;108(49):19707-12.
2011: Annukka M Lahtinen; Eero Lehtonen; Annukka Marjamaa; Lasse Oikarinen; Aarno Palotie; Leena Peltonen; Kimmo Porthan; Veikko Salomaa; Heikki Swan; Lauri Toivonen; Tiina Heliö; Antti Jula; Maija Kaartinen; Kimmo Kontula
Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy.
Heart rhythm : the official journal of the Heart Rhythm Society 2011;8(8):1214-21.
2011: Daniel I Chasman; Boukje De Vries; Florian Ernst; Konstanze Fendrich; Michel D Ferrari; Tobias Freilinger; Lyn R Griffiths; Wolfgang Hoffmann; Mikko Kallela; Christian Kubisch; Lenore J Launer; Aarno Palotie; Paul M Ridker; Ulf Schminke; Markus Schürks; Gisela M Terwindt; Arn M J M van den Maagdenberg; Henry Völzke; Robert Y L Zee; Verneri Anttila; Julie E Buring; Tobias Kurth
Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
Nature genetics 2011;43(7):695-8.
2011: Olli P H Pietiläinen; Karola Rehnström; Samuli Ripatti; Chiara Sabatti; Susan K Service; Anja Taanila; Carola Gabriella Tilgmann; Eliza Congdon; Nelson B Freimer; Anna-Liisa Hartikainen; Ulla Heikura; Matti Isohanni; Eveliina Jakkula; Marjo-Riitta Jarvelin; Aarno Palotie; Tiina Paunio; Leena Peltonen
Phenotype mining in CNV carriers from a population cohort.
Human molecular genetics 2011;20(13):2686-95.
2011: Alison J Coffey; Eleanor Drury; Jennifer Harrow; Tim J Hubbard; Sarah Hunt; Christopher J Joyce; Felix Kokocinski; Anna-Elina Lehesjoki; Emily M Leproust; Priit Palta; Carol E Scott; Daniel J Turner; Maria S Calafato; Aarno Palotie
The GENCODE exome: sequencing the complete human exome.
European journal of human genetics : EJHG 2011;19(7):827-31.
2011: Jevon Plunkett; Scott Doniger; Guilherme Orabona; Thomas Morgan; Ritva Haataja; Mikko Hallman; Hilkka Puttonen; Ramkumar Menon; Edward Kuczynski; Errol Norwitz; Victoria Snegovskikh; Aarno Palotie; Leena Peltonen; Vineta Fellman; Emily A DeFranco; Bimal P Chaudhari; Tracy L McGregor; Jude J McElroy; Matthew T Oetjens; Kari Teramo; Ingrid Borecki; Justin Fay; Louis Muglia
An evolutionary genomic approach to identify genes involved in human birth timing.
PLoS genetics 2011;7(4):e1001365.
2011: Jingmei Li; Keith Humphreys; Tuomas Heikkinen; Kristiina Aittomäki; Carl Blomqvist; Paul D P Pharoah; Alison M Dunning; Shahana Ahmed; Maartje J Hooning; John W M Martens; Ans M W van den Ouweland; Lars Alfredsson; Aarno Palotie; Leena Peltonen-Palotie; Astrid Irwanto; Hui Qi Low; Garrett H K Teoh; Anbupalam Thalamuthu; Douglas F Easton; Heli Nevanlinna; Jianjun Liu; Kamila Czene; Per Hall
A combined analysis of genome-wide association studies in breast cancer.
Breast cancer research and treatment 2011;126(3):717-27.
2011: Michelle Luciano; Narelle K Hansell; Jari Lahti; Gail Davies; Sarah E Medland; Katri Räikkönen; Albert Tenesa; Elisabeth Widen; McGhee Kevin; Aarno Palotie; David Cherry McLachlan Liewald; David J Porteous; John M Starr; Grant W Montgomery; Nicholas G Martin; Johan G Eriksson; Margaret J Wright; Ian J Deary
Whole genome association scan for genetic polymorphisms influencing information processing speed.
Biological psychology 2011;86(3):193-202.
2011: Eleanor Raffan; David B Savage; Carol Scott; Claire Smith; Saeed Al Turki; Inês Barroso; Sanjeev Bhaskar; Gillian Carpenter; Alison Coffey; Allan Daly; Eleanor Howard; Liam A Hurst; Naz Khan; Helen Kingston; Mark O'Driscoll; Stephen O'Rahilly; Aarno Palotie; Robert K Semple
Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient.
Frontiers in endocrinology 2011;2():8.
2011: Aaron G Day-Williams; Eleanor Drury; Sarah Edkins; Kirsten McLay; Aarno Palotie; Alison J Coffey; Eleftheria Zeggini
An evaluation of different target enrichment methods in pooled sequencing designs for complex disease association studies.
PloS one 2011;6(11):e26279.
2011: Verneri Anttila; Mikko Kallela; Maija Wessman; Aarno Palotie
Towards an understanding of genetic predisposition to migraine.
Genome medicine 2011;3(3):17.
2011: Ritva Haataja; Minna K Karjalainen; Aino Luukkonen; Kari Teramo; Hilkka Puttonen; Marja Ojaniemi; Teppo Varilo; Bimal P Chaudhari; Jevon Plunkett; Jeffrey C Murray; Steven A McCarroll; Leena Peltonen; Louis J Muglia; Aarno Palotie; Mikko Hallman
Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.
PLoS genetics 2011;7(2):e1001293.
2010: Michael Inouye; Johannes Kettunen; Pasi Soininen; Kaisa Silander; Samuli Ripatti; Linda S Kumpula; Eija Hämäläinen; Pekka Jousilahti; Antti J Kangas; Satu Männistö; Markku J Savolainen; Antti Jula; Jaana Leiviskä; Aarno Palotie; Veikko Salomaa; Markus Perola; Mika Ala-Korpela; Leena Peltonen
Metabonomic, transcriptomic, and genomic variation of a population cohort.
Molecular systems biology 2010;6():441.
2010: Monica Leu; Keith Humphreys; Ida Surakka; Emil Rehnberg; Juha Muilu; Päivi Rosenström; Peter Almgren; Juha Jääskeläinen; Richard P Lifton; Kirsten Ohm Kyvik; Jaakko Kaprio; Nancy L Pedersen; Aarno Palotie; Per Hall; Henrik Grönberg; Leif Groop; Leena Peltonen; Juni Palmgren; Samuli Ripatti
NordicDB: a Nordic pool and portal for genome-wide control data.
European journal of human genetics : EJHG 2010;18(12):1322-6.
2010: Ida Surakka; Kati Kristiansson; Verneri Anttila; Michael Inouye; Chris Barnes; Loukas Moutsianas; Veikko Salomaa; Mark J Daly; Aarno Palotie; Leena Peltonen; Samuli Ripatti
Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging.
Genome research 2010;20(10):1344-51.
2010: Michael Inouye; Kaisa Silander; Eija Hamalainen; Veikko Salomaa; Kennet Harald; Pekka Jousilahti; Satu Männistö; Johan G Eriksson; Janna Saarela; Samuli Ripatti; Markus Perola; Gert-Jan B van Ommen; Marja-Riitta Taskinen; Aarno Palotie; Emmanouil T Dermitzakis; Leena Peltonen
An immune response network associated with blood lipid levels.
PLoS genetics 2010;6(9):.
2010: Elisabeth Widén; Samuli Ripatti; Diana Cousminer; Ida Surakka; Tuuli Lappalainen; Marjo-Riitta Järvelin; Johan G Eriksson; Olli Raitakari; Veikko Salomaa; Ulla Sovio; Anna-Liisa Hartikainen; Anneli Pouta; Mark I McCarthy; Clive Osmond; Eero Kajantie; Terho Lehtimäki; Jorma Viikari; Mika Kähönen; Chris Tyler-Smith; Nelson Freimer; Joel N Hirschhorn; Leena Peltonen; Aarno Palotie
Distinct variants at LIN28B influence growth in height from birth to adulthood.
American journal of human genetics 2010;86(5):773-82.
2010: P Tikka-Kleemola; V Artto; S Vepsäläinen; E M Sobel; S Räty; Mari A Kaunisto; Verneri Anttila; E Hämäläinen; Marja-Liisa Sumelahti; Matti Ilmavirta; Markus Färkkilä; Mikko Kallela; Aarno Palotie; Maija Wessman
A visual migraine aura locus maps to 9q21-q22.
Neurology 2010;74(15):1171-7.
2010: Eveliina Jakkula; Virpi Leppä; Anna-Maija Sulonen; Teppo Varilo; Suvi Kallio; Anu Kemppinen; Shaun Purcell; Keijo Koivisto; Pentti J Tienari; Marja-Liisa Sumelahti; Irina Elovaara; Tuula Pirttilä; Mauri Reunanen; Arpo Aromaa; Annette Bang Oturai; Helle Bach Søndergaard; Hanne F Harbo; Inger-Lise Mero; Stacey B Gabriel; Daniel B Mirel; Stephen L Hauser; Ludwig Kappos; Chris Polman; Philip L De Jager; David A Hafler; Mark J Daly; Aarno Palotie; Janna Saarela; Leena Peltonen
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.
American journal of human genetics 2010;86(2):285-91.
2010: Jevon Plunkett; Scott Doniger; Thomas Morgan; Ritva Haataja; Mikko Hallman; Hilkka Puttonen; Ramkumar Menon; Edward Kuczynski; Errol Norwitz; Victoria Snegovskikh; Aarno Palotie; Leena Peltonen; Vineta Fellman; Emily A DeFranco; Bimal P Chaudhari; John Oates; Olivier Boutaud; Tracy L McGregor; Jude J McElroy; Kari Teramo; Ingrid Borecki; Justin C Fay; Louis J Muglia
Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth.
BMC medical genomics 2010;3():62.
2010: Jingmei Li; Keith Humphreys; Hatef Darabi; Gustaf Rosin; Ulf Hannelius; Tuomas Heikkinen; Kristiina Aittomäki; Carl Blomqvist; Paul Dp Pharoah; Alison M Dunning; Shahana Ahmed; Maartje J Hooning; Antoinette Hollestelle; Rogier A Oldenburg; Lars Alfredsson; Aarno Palotie; Leena Peltonen-Palotie; Astrid Irwanto; Hui Qi Low; Garrett Hk Teoh; Anbupalam Thalamuthu; Juha Kere; Mauro D'Amato; Douglas F Easton; Heli Nevanlinna; Jianjun Liu; Kamila Czene; Per Hall
A genome-wide association scan on estrogen receptor-negative breast cancer.
Breast cancer research : BCR 2010;12(6):R93.
2009: Steven A McCarroll; James E Bradner; Hannu Turpeinen; Liisa Volin; Paul J Martin; Shannon D Chilewski; Joseph H Antin; Stephanie J Lee; Tapani Ruutu; Barry Storer; Edus H Warren; Bo Zhang; Lue Ping Zhao; David Ginsburg; Robert J Soiffer; Jukka Partanen; John A Hansen; Jerome Ritz; Aarno Palotie; David Altshuler
Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease.
Nature genetics 2009;41(12):1341-4.
2009: P Tikka-Kleemola; Mari A Kaunisto; Eija Hämäläinen; U Todt; H Göbel; Jaakko Kaprio; C Kubisch; Markus Färkkilä; Aarno Palotie; Maija Wessman; Mikko Kallela
Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura.
Cephalalgia : an international journal of headache 2009;29(11):1224-31.
2009: Anu Kemppinen; Minna Suvela; Pentti J Tienari; Irina Elovaara; Keijo Koivisto; Tuula Pirttilä; Mauri Reunanen; Ilkka Rautakorpi; Jan Hillert; Frida Lundmark; Annette Oturai; Lars Ryder; Hanne F Harbo; Elisabeth G Celius; Aarno Palotie; Mark J Daly; Leena Peltonen; Janna Saarela
MYO9B polymorphisms in multiple sclerosis.
European journal of human genetics : EJHG 2009;17(6):840-3.
2009: Brian P McEvoy; Grant W Montgomery; Allan F McRae; Samuli Ripatti; Markus Perola; Tim D Spector; Lynn Cherkas; Kourosh R Ahmadi; Dorret Boomsma; Gonneke Willemsen; Jouke-Jan Hottenga; Nancy L Pedersen; Patrik K E Magnusson; Kirsten Ohm Kyvik; Kaare Christensen; Jaakko Kaprio; Kauko Heikkilä; Aarno Palotie; Elisabeth Widen; Juha Muilu; Ann-Christine Syvänen; Ulrika Liljedahl; Orla Hardiman; Simon Cronin; Leena Peltonen; Nicholas G Martin; Peter M Visscher
Geographical structure and differential natural selection among North European populations.
Genome research 2009;19(5):804-14.
2009: Suvi P Kallio; Eveliina Jakkula; Shaun Purcell; Minna Suvela; Keijo Koivisto; Pentti J Tienari; Irina Elovaara; Tuula Pirttilä; Mauri Reunanen; Denis Bronnikov; Markku Viander; Seppo Meri; Jan Hillert; Frida Lundmark; Hanne F Harbo; Aslaug R Lorentzen; Philip L De Jager; Mark J Daly; David A Hafler; Aarno Palotie; Leena Peltonen; Janna Saarela
Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
Human molecular genetics 2009;18(9):1670-83.
2009: Hannu Turpeinen; Liisa Volin; Lauri Nikkinen; Pauli Ojala; Aarno Palotie; Janna Saarela; Jukka Partanen
Genetic similarity of chromosome 6 between patients receiving hematopoietic stem cell transplantation and HLA matched sibling donors.
Haematologica 2009;94(4):528-35.
2009: Frances M K Williams; Angela M Carter; Bernet S Kato; Mario Falchi; Lise Bathum; Gabriela L Surdulescu; Kirsten Ohm Kyvik; Aarno Palotie; Tim D Spector; Peter J Grant
Identification of quantitative trait loci for fibrin clot phenotypes: the EuroCLOT study.
Arteriosclerosis, thrombosis, and vascular biology 2009;29(4):600-5.
2009: A Marjamaa; Christopher Newton-Cheh; K Porthan; Antti Reunanen; Päivi Lahermo; Heikki Väänänen; Antti Jula; H Karanko; H Swan; Lauri Toivonen; Markku S Nieminen; Matti Viitasalo; Leena Peltonen; L Oikarinen; Aarno Palotie; Kimmo Kontula; Veikko Salomaa
Common candidate gene variants are associated with QT interval duration in the general population.
Journal of internal medicine 2009;265(4):448-58.
2009: Anna-Maija Sulonen; Suvi P Kallio; Pekka Ellonen; Minna Suvela; Irina Elovaara; Keijo Koivisto; Tuula Pirttilä; Mauri Reunanen; Pentti J Tienari; Aarno Palotie; Leena Peltonen; Janna Saarela
No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.
Journal of neuroimmunology 2009;206(1-2):86-90.
2009: Jevon Plunkett; Mary F Feitosa; Michelle Trusgnich; Michael F Wangler; Lisanne Palomar; Zachary A-F Kistka; Emily A DeFranco; Tammy T Shen; Adrienne E D Stormo; Hilkka Puttonen; Mikko Hallman; Ritva Haataja; Aino Luukkonen; Vineta Fellman; Leena Peltonen; Aarno Palotie; E Warwick Daw; Ping An; Kari Teramo; Ingrid Borecki; Louis J Muglia
Mother's genome or maternally-inherited genes acting in the fetus influence gestational age in familial preterm birth.
Human heredity 2009;68(3):209-19.
2009: Annukka Marjamaa; Veikko Salomaa; Christopher Newton-Cheh; Kimmo Porthan; Antti Reunanen; Hannu Karanko; Antti Jula; Päivi Lahermo; Heikki Väänänen; Lauri Toivonen; Heikki Swan; Matti Viitasalo; Markku S Nieminen; Leena Peltonen; Lasse Oikarinen; Aarno Palotie; Kimmo Kontula
High prevalence of four long QT syndrome founder mutations in the Finnish population.
Annals of medicine 2009;41(3):234-40.
2009: Beben Benyamin; Allan F McRae; Gu Zhu; Scott Gordon; Anjali K Henders; Aarno Palotie; Leena Peltonen; Nicholas G Martin; Grant W Montgomery; John B Whitfield; Peter M Visscher
Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.
American journal of human genetics 2009;84(1):60-5.
2008: Karoliina Wehkalampi; Elisabeth Widén; Tiina Laine; Aarno Palotie; Leo Dunkel
Association of the timing of puberty with a chromosome 2 locus.
The Journal of clinical endocrinology and metabolism 2008;93(12):4833-9.
2008: Per E Lundmark; Ulrika Liljedahl; Dorret I Boomsma; Heikki Mannila; Nicholas G Martin; Aarno Palotie; Leena Peltonen; Markus Perola; Tim D Spector; Ann-Christine Syvänen
Evaluation of HapMap data in six populations of European descent.
European journal of human genetics : EJHG 2008;16(9):1142-50.
2008: Mika Niemelä; Juhana Frösen; Juha Hernesniemi; Reza Dashti; Aarno Palotie
Molecular pathology of aneurysms.
Surgical neurology 2008;70(1):36-8.
2008: Verneri Anttila; Dale R Nyholt; Mikko Kallela; Ville Artto; Salli Vepsäläinen; Eveliina Jakkula; Annika Wennerström; Päivi Tikka-Kleemola; Mari A Kaunisto; Eija Hämäläinen; Elisabeth Widén; Joseph D Terwilliger; Kathleen Ries Merikangas; Grant W Montgomery; Nicholas G Martin; Mark J Daly; Jaakko Kaprio; Leena Peltonen; Markus Färkkilä; Maija Wessman; Aarno Palotie
Consistently replicating locus linked to migraine on 10q22-q23.
American journal of human genetics 2008;82(5):1051-63.
2008: Beben Benyamin; Markus Perola; Belinda K Cornes; Pamela Af Madden; Aarno Palotie; Dale R Nyholt; Grant W Montgomery; Leena Peltonen; Nicholas G Martin; Peter M Visscher
Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs.
European journal of human genetics : EJHG 2008;16(4):516-24.
2008: Karoliina Wehkalampi; Elisabeth Widén; Tiina Laine; Aarno Palotie; Leo Dunkel
Patterns of inheritance of constitutional delay of growth and puberty in families of adolescent girls and boys referred to specialist pediatric care.
The Journal of clinical endocrinology and metabolism 2008;93(3):723-8.
2008: Greg Oswell; Mari A Kaunisto; Mikko Kallela; Eija Hämäläinen; Verneri Anttila; Jaakko Kaprio; Markus Färkkilä; Maija Wessman; Aarno Palotie
No association of migraine to the GABA-A receptor complex on chromosome 15.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(1):33-6.
2008: Pille Hallast; Janna Saarela; Aarno Palotie; Maris Laan
High divergence in primate-specific duplicated regions: human and chimpanzee chorionic gonadotropin beta genes.
BMC evolutionary biology 2008;8():195.
2007: V Artto; Martti Nissilä; Maija Wessman; Aarno Palotie; Markus Färkkilä; Mikko Kallela
Treatment of hemiplegic migraine with triptans.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2007;14(9):1053-6.
2007: Kaisu Keskitalo; Antti Knaapila; Mikko Kallela; Aarno Palotie; Maija Wessman; Sampo Sammalisto; Leena Peltonen; Hely Tuorila; Markus Perola
Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16.
The American journal of clinical nutrition 2007;86(1):55-63.
2007: Markus Perola; Sampo Sammalisto; Tero Hiekkalinna; Nick G Martin; Peter M Visscher; Grant W Montgomery; Beben Benyamin; Jennifer R Harris; Dorret I Boomsma; Gonneke Willemsen; Jouke-Jan Hottenga; Kaare Christensen; Kirsten Ohm Kyvik; Thorkild I A Sørensen; Nancy L Pedersen; Patrik K E Magnusson; Tim D Spector; Elisabeth Widen; Karri Silventoinen; Jaakko Kaprio; Aarno Palotie; Leena Peltonen
Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci.
PLoS genetics 2007;3(6):e97.
2007: Maija Wessman; Gisela M Terwindt; Mari A Kaunisto; Aarno Palotie; Roel A Ophoff
Migraine: a complex genetic disorder.
Lancet neurology 2007;6(6):521-32.
2007: Päivi Tikka-Kleemola; Eija Hämäläinen; Kari Tuomainen; Minna Suvela; Agu Artma; Olev Kahre; Maija Wessman; Aarno Palotie; Kaisa Silander
The enhancement of homogenous mass extension reaction: comparison of two enzymes.
Molecular and cellular probes 2007;21(3):216-21.
2007: Antti Knaapila; Kaisu Keskitalo; Mikko Kallela; Maija Wessman; Sampo Sammalisto; Tero Hiekkalinna; Aarno Palotie; Leena Peltonen; Hely Tuorila; Markus Perola
Genetic component of identification, intensity and pleasantness of odours: a Finnish family study.
European journal of human genetics : EJHG 2007;15(5):596-602.
2007: Ker-Chau Li; Aarno Palotie; Shinsheng Yuan; Denis Bronnikov; Daniel Chen; Xuelian Wei; Oi-Wa Choi; Janna Saarela; Leena Peltonen
Finding disease candidate genes by liquid association.
Genome biology 2007;8(10):R205.
2006: Mari A Kaunisto; Mikko Kallela; Eija Hämäläinen; Riika Kilpikari; Hannele Havanka; Hanna Harno; Martti Nissilä; Erkki Säkö; Matti Ilmavirta; J Liukkonen; H Teirmaa; O Törnwall; Matti Jussila; Joseph D Terwilliger; Markus Färkkilä; Jaakko Kaprio; Aarno Palotie; Maija Wessman
Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura.
Cephalalgia : an international journal of headache 2006;26(12):1462-72.
2006: Ville Artto; Maija Wessman; Martti Nissilä; Erkki Säkö; Jarmo Liukkonen; Heikki Teirmaa; Hanna Harno; Hannele Havanka; Matti Ilmavirta; Aarno Palotie; Markus Färkkilä; Mikko Kallela
Comorbidity in Finnish migraine families.
The journal of headache and pain 2006;7(5):324-30.
2006: Päivi Lahermo; Ulrika Liljedahl; Grethe Alnaes; Tomas Axelsson; Anthony J Brookes; Pekka Ellonen; Per-Henrik Groop; Christer Halldén; Dan Holmberg; Kristina Holmberg; Mauri Keinänen; Katrin Kepp; Juha Kere; Päivi Kiviluoma; Vessela N Kristensen; Cecilia Lindgren; Jacob Odeberg; Pia Osterman; Maija Parkkonen; Janna Saarela; Maria Sterner; Linda Strömqvist; Ulvi Talas; Maija Wessman; Aarno Palotie; Ann-Christine Syvänen
A quality assessment survey of SNP genotyping laboratories.
Human mutation 2006;27(7):711-4.
2006: Verneri Anttila; Mikko Kallela; Greg Oswell; Mari A Kaunisto; Dale R Nyholt; E Hamalainen; Hannele Havanka; Matti Ilmavirta; Joseph D Terwilliger; Eric Sobel; Leena Peltonen; Jaakko Kaprio; M Farkkila; Maija Wessman; Aarno Palotie
Trait components provide tools to dissect the genetic susceptibility of migraine.
American journal of human genetics 2006;79(1):85-99.
2006: Leena Peltonen; Markus Perola; Jussi Naukkarinen; Aarno Palotie
Lessons from studying monogenic disease for common disease.
Human molecular genetics 2006;15 Spec No 1():R67-74.
2006: Janna Saarela; Suvi P Kallio; Daniel Chen; Alexandre Montpetit; Anne Jokiaho; Eva Choi; Rosanna Asselta; Denis Bronnikov; Matthew R Lincoln; A Dessa Sadovnick; Pentti J Tienari; Keijo Koivisto; Aarno Palotie; George C Ebers; Thomas J Hudson; Leena Peltonen
PRKCA and multiple sclerosis: association in two independent populations.
PLoS genetics 2006;2(3):e42.
2005: H M F Riise Stensland; Janna Saarela; Denis O Bronnikov; Maija Parkkonen; Anne Jokiaho; Aarno Palotie; Pentti J Tienari; Marja-Liisa Sumelahti; Irina Elovaara; Keijo Koivisto; Tuula Pirttilä; Mauri Reunanen; Eric Sobel; Leena Peltonen
Fine mapping of the multiple sclerosis susceptibility locus on 5p14-p12.
Journal of neuroimmunology 2005;170(1-2):122-33.
2005: Eun Hwa Choi; James G Taylor; Charles B Foster; THOMAS WALSH; Veli-Jukka Anttila; Tapani Ruutu; Aarno Palotie; STEPHEN CHANOCK
Common polymorphisms in critical genes of innate immunity do not contribute to the risk for chronic disseminated candidiasis in adult leukemia patients.
Medical mycology : official publication of the International Society for Human and Animal Mycology 2005;43(4):349-53.
2005: Tao Shi; David Seligson; Arie S Belldegrun; Aarno Palotie; Steve Horvath
Tumor classification by tissue microarray profiling: random forest clustering applied to renal cell carcinoma.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2005;18(4):547-57.
2005: Mari A Kaunisto; Päivi J Tikka; Mikko Kallela; Suzanne M Leal; Jeanette C Papp; Arja Korhonen; Eija Hämäläinen; Hanna Harno; Hannele Havanka; Martti Nissilä; Erkki Säkö; Matti Ilmavirta; Jaakko Kaprio; Markus Färkkilä; Roel A Ophoff; Aarno Palotie; Maija Wessman
Chromosome 19p13 loci in Finnish migraine with aura families.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;132B(1):85-9.
2004: Laura Segall; Rosemarie Scanzano; Mari A Kaunisto; Maija Wessman; Aarno Palotie; J Jay Gargus; Rhoda Blostein
Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.
The Journal of biological chemistry 2004;279(42):43692-6.
2004: Daniel C Chen; Janna Saarela; Royden A Clark; Timo Miettinen; Anthony Chi; Evan E Eichler; Leena Peltonen; Aarno Palotie
Segmental duplications flank the multiple sclerosis locus on chromosome 17q.
Genome research 2004;14(8):1483-92.
2004: Mari A Kaunisto; Hanna Harno; Kaate R J Vanmolkot; J Jay Gargus; G Sun; Eija Hämäläinen; Elina Liukkonen; Mikko Kallela; Arn van den Maagdenberg; Rune R Frants; Markus Färkkilä; Aarno Palotie; Maija Wessman
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
Neurogenetics 2004;5(2):141-6.
2004: Matthew H T Bui; Harri Visapaa; David Seligson; Hyung Kim; Ken-Ryu Han; Yunda Huang; Steve Horvath; Eric J Stanbridge; Aarno Palotie; Robert A Figlin; Arie S Belldegrun
Prognostic value of carbonic anhydrase IX and KI67 as predictors of survival for renal clear cell carcinoma.
The Journal of urology 2004;171(6 Pt 1):2461-6.
2004: Hanna Harno; Timo Hirvonen; Mari A Kaunisto; Heikki Aalto; Hilla Levo; Elina Isotalo; Hannu Somer; Mikko Kallela; Aarno Palotie; Maija Wessman; Markus Färkkilä
Acetazolamide improves neurotological abnormalities in a family with episodic ataxia type 2 (EA-2).
Journal of neurology 2004;251(2):232-4.
2004: Mari A Kaunisto; Hanna Harno; Mikko Kallela; Hannu Somer; Riitta Sallinen; Eija Hämäläinen; Päivi J Miettinen; J Vesa; Arto Orpana; Aarno Palotie; Markus Färkkilä; Maija Wessman
Novel splice site CACNA1A mutation causing episodic ataxia type 2.
Neurogenetics 2004;5(1):69-73.
2004: Maija Wessman; Mari A Kaunisto; Mikko Kallela; Aarno Palotie
The molecular genetics of migraine.
Annals of medicine 2004;36(6):462-73.
2004: Aarno Palotie; Leena Peltonen-Palotie
[Do we need a Finnish biobank? Availability of epidemiologic data should benefit everybody].
Duodecim; lääketieteellinen aikakauskirja 2004;120(14):1710-2.
2003: Hanna Harno; Timo Hirvonen; Mari A Kaunisto; Heikki Aalto; Hilla Levo; Elina Isotalo; Mikko Kallela; Jaakko Kaprio; Aarno Palotie; Maija Wessman; Markus Färkkilä
Subclinical vestibulocerebellar dysfunction in migraine with and without aura.
Neurology 2003;61(12):1748-52.
2003: Daniel C Chen; Janna Saarela; Ilpo Nuotio; Anne Jokiaho; Leena Peltonen; Aarno Palotie
Comparison of GenFlex Tag array and Pyrosequencing in SNP genotyping.
The Journal of molecular diagnostics : JMD 2003;5(4):243-9.
2003: Elles J C M Mulder; Caroline Van Baal; David Gaist; Mikko Kallela; Jaakko Kaprio; Dan A Svensson; Dale R Nyholt; Nicholas G Martin; Alex J MacGregor; Lynn F Cherkas; Dorret I Boomsma; Aarno Palotie
Genetic and environmental influences on migraine: a twin study across six countries.
Twin research : the official journal of the International Society for Twin Studies 2003;6(5):422-31.
2003: Kaisa Silander; Tomas Axelsson; Elisabeth Widén; Andreas Dahlgren; Aarno Palotie; Ann-Christine Syvänen
Analysis of genetic variation in the GenomEUtwin project.
Twin research : the official journal of the International Society for Twin Studies 2003;6(5):391-8.
2003: Mark O Goodarzi; Xiuqing Guo; Kent D Taylor; Manuel J Quiñones; Carlos Samayoa; Huiying Yang; Mohammed F Saad; Aarno Palotie; Ronald M Krauss; Willa A Hsueh; Jerome I Rotter
Determination and use of haplotypes: ethnic comparison and association of the lipoprotein lipase gene and coronary artery disease in Mexican-Americans.
Genetics in medicine : official journal of the American College of Medical Genetics 2003;5(4):322-7.
2003: Gheeyoung Choe; Steve Horvath; Timothy F Cloughesy; Katherine Crosby; David Seligson; Aarno Palotie; Landon Inge; Bradley L Smith; Charles L Sawyers; Paul S Mischel
Analysis of the phosphatidylinositol 3'-kinase signaling pathway in glioblastoma patients in vivo.
Cancer research 2003;63(11):2742-6.
2003: Paul S Mischel; Ruty Shai; Tao Shi; Steve Horvath; Kan V Lu; Gheeyoung Choe; David Seligson; Thomas J Kremen; Aarno Palotie; Linda M Liau; Timothy F Cloughesy; Stanley F Nelson
Identification of molecular subtypes of glioblastoma by gene expression profiling.
Oncogene 2003;22(15):2361-73.
2003: Cromwell Espineda; David Seligson; William James Ball; JianYu Rao; Aarno Palotie; Steve Horvath; Yunda Huang; Tao Shi; Ayyappan K Rajasekaran
Analysis of the Na,K-ATPase alpha- and beta-subunit expression profiles of bladder cancer using tissue microarrays.
Cancer 2003;97(8):1859-68.
2003: Robert J Agate; William Grisham; Juli Wade; Suzanne Mann; John Wingfield; Carolyn Schanen; Aarno Palotie; Arthur P Arnold
Neural, not gonadal, origin of brain sex differences in a gynandromorphic finch.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(8):4873-8.
2003: Harri Visapää; Matthew H T Bui; Yunda Huang; David Seligson; Henry Tsai; Allan J Pantuck; Robert Figlin; Jian Yu Rao; Arie Belldegrun; Steve Horvath; Aarno Palotie
Correlation of Ki-67 and gelsolin expression to clinical outcome in renal clear cell carcinoma.
Urology 2003;61(4):845-50.
2003: Eun Hwa Choi; Charles B Foster; James G Taylor; Hans Christian Erichsen; Renee A Chen; THOMAS WALSH; Veli-Jukka Anttila; Tapani Ruutu; Aarno Palotie; STEPHEN CHANOCK
Association between chronic disseminated candidiasis in adult acute leukemia and common IL4 promoter haplotypes.
The Journal of infectious diseases 2003;187(7):1153-6.
2003: Harri Visapää; David Seligson; Mervi Eeva; Flora Gaber; JianYu Rao; Arie Belldegrun; Aarno Palotie
8q24 amplification in transitional cell carcinoma of bladder.
Applied immunohistochemistry & molecular morphology : AIMM / official publication of the Society for Applied Immunohistochemistry 2003;11(1):33-6.
2003: Harri Visapää; David Seligson; Yunda Huang; Jian Yu Rao; Arie Belldegrun; Steve Horvath; Aarno Palotie
Ki67, gelsolin and PTEN expression in sarcomatoid renal tumors.
Urological research 2003;30(6):387-9.
2003: Matthew H T Bui; David Seligson; Ken-Ryu Han; Allan J Pantuck; Frederick J Dorey; Yunda Huang; Steve Horvath; Bradley C Leibovich; Shefali Chopra; Shu-Yuan Liao; Eric J Stanbridge; Michael I Lerman; Aarno Palotie; Robert A Figlin; Arie S Belldegrun
Carbonic anhydrase IX is an independent predictor of survival in advanced renal clear cell carcinoma: implications for prognosis and therapy.
Clinical cancer research : an official journal of the American Association for Cancer Research 2003;9(2):802-11.
2002: Hisamitsu Ide; David Seligson; Sanaz Memarzadeh; Li Xin; Steve Horvath; Purnima Dubey; Maryann B Flick; Barry M Kacinski; Aarno Palotie; Owen N Witte
Expression of colony-stimulating factor 1 receptor during prostate development and prostate cancer progression.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(22):14404-9.
2002: Janna Saarela; Marlena Schoenberg Fejzo; Daniel Chen; Saara Finnilä; Maija Parkkonen; Satu Kuokkanen; Eric Sobel; Pentti J Tienari; Marja-Liisa Sumelahti; Juhani Wikström; Irina Elovaara; Keijo Koivisto; Tuula Pirttilä; Mauri Reunanen; Aarno Palotie; Leena Peltonen
Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24.
Human molecular genetics 2002;11(19):2257-67.
2002: JianYu Rao; David Seligson; Harri Visapaa; Steve Horvath; Mervi Eeva; Kia Michel; Allan J Pantuck; Arie Belldegrun; Aarno Palotie
Tissue microarray analysis of cytoskeletal actin-associated biomarkers gelsolin and E-cadherin in urothelial carcinoma.
Cancer 2002;95(6):1247-57.
2002: Maija Wessman; Mikko Kallela; Mari A Kaunisto; Pia Marttila; Eric Sobel; Jaana Hartiala; Greg Oswell; Suzanne M Leal; Jeanette C Papp; Eija Hämäläinen; Petra Broas; Geoffrey Joslyn; Iiris Hovatta; Tero Hiekkalinna; Jaakko Kaprio; Jürg Ott; Rita M Cantor; John-Anker Zwart; Matti Ilmavirta; Hannele Havanka; Markus Färkkilä; Leena Peltonen; Aarno Palotie
A susceptibility locus for migraine with aura, on chromosome 4q24.
American journal of human genetics 2002;70(3):652-62.
2002: Heikki Repo; Krista Anttonen; Sami K Kilpinen; Aarno Palotie; Petri Salven; Arto Orpana; Marjatta Leirisalo-Repo
CD14 and TNfa promoter polymorphisms in patients with acute arthritis. Special reference to development of chronic spondyloarthropathy.
Scandinavian journal of rheumatology 2002;31(6):355-61.
2001: Mikko Kallela; Maija Wessman; Hannele Havanka; Aarno Palotie; Markus Färkkilä
Familial migraine with and without aura: clinical characteristics and co-occurrence.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2001;8(5):441-9.
2001: Iiro Rajantie; Niklas Ekman; Kristina Iljin; Elena Arighi; Y Gunji; Juha-Pekka Kaukonen; Aarno Palotie; M Dewerchin; Peter Carmeliet; Kari Alitalo
Bmx tyrosine kinase has a redundant function downstream of angiopoietin and vascular endothelial growth factor receptors in arterial endothelium.
Molecular and cellular biology 2001;21(14):4647-55.
2001: Markus Perola; Miina Ohman; Tero Hiekkalinna; J Leppävuori; Päivi Pajukanta; Maija Wessman; M Koskenvuo; Aarno Palotie; Kenneth Lange; Jaakko Kaprio; Leena Peltonen
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups.
American journal of human genetics 2001;69(1):117-23.
2001: Riitta Sallinen; Anne Latvanlehto; Ari-Pekka Kvist; Marko Rehn; I Eerola; M L Chu; Paolo Bonaldo; B Saitta; Giorgio M Bressan; Taina Pihlajaniemi; Eero Vuorio; Aarno Palotie; Maija Wessman; Nina Horelli-Kuitunen
Physical mapping of mouse collagen genes on chromosome 10 by high-resolution FISH.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(5):340-6.
2001: Päivi Pajukanta; Jackie S Bodnar; Riitta Sallinen; M Chu; T Airaksinen; Q Xiao; Lawrence W Castellani; Sonal S Sheth; Maija Wessman; Aarno Palotie; Janet S Sinsheimer; Peter Demant; Aldons J Lusis; Leena Peltonen
Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(3):238-45.
2000: Ulla Wartiovaara; H Mikkola; G Szôke; Gizella Haramura; Levente Kárpáti; Istvan Balogh; Riitta Lassila; László Muszbek; Aarno Palotie
Effect of Val34Leu polymorphism on the activation of the coagulation factor XIII-A.
Thrombosis and haemostasis 2000;84(4):595-600.
2000: Jussi Mikkelsson; Markus Perola; Ulla Wartiovaara; L Peltonen; Aarno Palotie; Antti Penttilä; Pekka J Karhunen
Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle-aged Finnish men who died suddenly.
Thrombosis and haemostasis 2000;84(1):78-82.
2000: E Virolainen; Maija Wessman; Iiris Hovatta; Katri Niemi; Jaakko Ignatius; Juha Kere; Leena Peltonen; Aarno Palotie
Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.
American journal of human genetics 2000;66(3):1132-7.
1999: Nina Horelli-Kuitunen; N Gahmberg; Mervi Eeva; Aarno Palotie; I Järvelä
Interstitial deletion of bands 11q21-->22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes.
American journal of medical genetics 1999;86(5):416-9.
1999: Mikko Kallela; Maija Wessman; Markus Färkkilä; Aarno Palotie; Markku Koskenvuo; Marja-Liisa Honkasalo; Jaakko Kaprio
Clinical characteristics of migraine concordant monozygotic twin pairs.
Acta neurologica Scandinavica 1999;100(4):254-9.
1999: E Laiho; Katri Niemi; Jaakko Ignatius; Juha Kere; Aarno Palotie; Ulpu Saarialho-Kere
Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis.
European journal of human genetics : EJHG 1999;7(6):625-32.
1999: Ari-Pekka Kvist; Anne Latvanlehto; Malin Sund; Nina Horelli-Kuitunen; Marko Rehn; Aarno Palotie; D Beier; Taina Pihlajaniemi
Complete exon-intron organization and chromosomal location of the gene for mouse type XIII collagen (col13a1) and comparison with its human homologue.
Matrix biology : journal of the International Society for Matrix Biology 1999;18(3):261-74.
1999: Mikko Kallela; Maija Wessman; Markus Färkkilä; Aarno Palotie; Markku Koskenvuo; Marja-Liisa Honkasalo; Jaakko Kaprio
Clinical characteristics of migraine in a population-based twin sample: similarities and differences between migraine with and without aura.
Cephalalgia : an international journal of headache 1999;19(3):151-8.
1999: P Paavola; Kristiina Avela; Nina Horelli-Kuitunen; Maarit Bärlund; Anne Kallioniemi; N Idänheimo; M Kyttälä; Albert de La Chapelle; Aarno Palotie; Anna-Elina Lehesjoki; Leena Peltonen
High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23.
Genome research 1999;9(3):267-76.
1999: Tiina Heliö; Ulla Wartiovaara; Leena Halme; Ulla Turunen; H Mikkola; Aarno Palotie; Markus Färkkilä; Kimmo Kontula
Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease.
Scandinavian journal of gastroenterology 1999;34(2):170-4.
1999: Juha-Pekka Kaukonen; Eeva-Riitta Savolainen; Aarno Palotie
Human Emt tyrosine kinase is specifically expressed both in mature T-lymphocytes and T-cell associated hematopoietic malignancies.
Leukemia & lymphoma 1999;32(5-6):513-22.
1999: Ulla Wartiovaara; Markus Perola; H Mikkola; K Tötterman; Vesa Savolainen; Antti Penttilä; P J Grant; Matti J Tikkanen; Erkki Vartiainen; Pekka J Karhunen; Leena Peltonen; Aarno Palotie
Association of FXIII Val34Leu with decreased risk of myocardial infarction in Finnish males.
Atherosclerosis 1999;142(2):295-300.
1999: Riitta Sallinen; W Kuang; E Engvall; Aarno Palotie; Maija Wessman; Nina Horelli-Kuitunen
Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1999;87(3-4):195-6.
1999: Nina Horelli-Kuitunen; Jaakko Aaltonen; Marie-Laure Yaspo; Mervi Eeva; Maija Wessman; Leena Peltonen; Aarno Palotie
Mapping ESTs by fiber-FISH.
Genome research 1999;9(1):62-71.
1999: P Paavola; Nina Horelli-Kuitunen; Aarno Palotie; Leena Peltonen
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene.
Genomics 1999;55(1):122-5.
1998: Ilona Visapää; Vineta Fellman; Teppo Varilo; Aarno Palotie; Kari O Raivio; Leena Peltonen
Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37.
American journal of human genetics 1998;63(5):1396-403.
1998: Nina Järvinen; P Mäkelä-Bengs; Anu Suomalainen; Katri Vuopala; Riitta Herva; Aarno Palotie; Leena Peltonen
LCCS: a lethal motoneuron disease of the fetus maps to chromosome 9q34.
Annals of the New York Academy of Sciences 1998;857():260-2.
1998: P Mäkelä-Bengs; Nina Järvinen; Katri Vuopala; Anu Suomalainen; Jaakko Ignatius; M Sipilä; Riitta Herva; Aarno Palotie; Leena Peltonen
Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals.
American journal of human genetics 1998;63(2):506-16.
1998: Ulla Wartiovaara; Petri Salven; H Mikkola; Riitta Lassila; Juha-Pekka Kaukonen; V Joukov; Arto Orpana; Ari Ristimäki; Markku Heikinheimo; Heikki Joensuu; Kari Alitalo; Aarno Palotie
Peripheral blood platelets express VEGF-C and VEGF which are released during platelet activation.
Thrombosis and haemostasis 1998;80(1):171-5.
1998: Tiina Heliö; Markus Färkkilä; Leena Halme; M Karlsson; Aarno Palotie; Kimmo Kontula
[Genetic background and DNA diagnostics of hemochromatosis].
Duodecim; lääketieteellinen aikakauskirja 1998;114(14):1404-9.
1997: Nina Horelli-Kuitunen; Ari-Pekka Kvist; T Helaakoski; Kari I Kivirikko; Taina Pihlajaniemi; Aarno Palotie
The order and transcriptional orientation of the human COL13A1 and P4HA genes on chromosome 10 long arm determined by high-resolution FISH.
Genomics 1997;46(2):299-302.
1997: D Chilov; E Kukk; Suvi Taira; Michael Jeltsch; Juha-Pekka Kaukonen; Aarno Palotie; V Joukov; Kari Alitalo
Genomic organization of human and mouse genes for vascular endothelial growth factor C.
The Journal of biological chemistry 1997;272(40):25176-83.
1997: Pasi Hägg; Nina Horelli-Kuitunen; Lauri Eklund; Aarno Palotie; Taina Pihlajaniemi
Cloning of mouse type XV collagen sequences and mapping of the corresponding gene to 4B1-3. Comparison of mouse and human alpha 1 (XV) collagen sequences indicates divergence in the number of small collagenous domains.
Genomics 1997;45(1):31-41.
1997: T Klockars; Juha Isosomppi; Maris Laan; N Kakko; Aarno Palotie; Leena Peltonen
The visual assignment of genes by fiber-fish: BTF3 protein homologue gene (BTF3) and a novel pseudogene of human RNA helicase A (DDX9P) on 13q22.
Genomics 1997;44(3):355-7.
1997: E Laiho; Jaakko Ignatius; H Mikkola; Vivien C Yee; David C Teller; Katri Niemi; Ulpu Saarialho-Kere; Juha Kere; Aarno Palotie
Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population.
American journal of human genetics 1997;61(3):529-38.
1997: Jaakko Aaltonen; Nina Horelli-Kuitunen; J B Fan; P Björses; Jaakko Perheentupa; Richard Myers; Aarno Palotie; Leena Peltonen
High-resolution physical and transcriptional mapping of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy locus on chromosome 21q22.3 by FISH.
Genome research 1997;7(8):820-9.
1997: P Suvanto; Kirmo Wartiovaara; Maria Lindahl; Urmas Arumae; M Moshnyakov; Nina Horelli-Kuitunen; Matti S Airaksinen; Aarno Palotie; Hannu Sariola; Mart Saarma
Cloning, mRNA distribution and chromosomal localisation of the gene for glial cell line-derived neurotrophic factor receptor beta, a homologue to GDNFR-alpha.
Human molecular genetics 1997;6(8):1267-73.
1997: E Kukk; Ulla Wartiovaara; Y Gunji; Juha-Pekka Kaukonen; H J Bühring; I Rappold; M T Matikainen; P Vihko; J Partanen; Aarno Palotie; Kari Alitalo; Riitta Alitalo
Analysis of Tie receptor tyrosine kinase in haemopoietic progenitor and leukaemia cells.
British journal of haematology 1997;98(1):195-203.
1997: Peppi Koivunen; Nina Horelli-Kuitunen; T Helaakoski; P Karvonen; M Jaakkola; Aarno Palotie; Kari I Kivirikko
Structures of the human gene for the protein disulfide isomerase-related polypeptide ERp60 and a processed gene and assignment of these genes to 15q15 and 1q21.
Genomics 1997;42(3):397-404.
1997: H Mikkola; László Muszbek; Gizella Haramura; Eija Hämäläinen; Anu Jalanko; Aarno Palotie
Molecular mechanisms of mutations in factor XIII A-subunit deficiency: in vitro expression in COS-cells demonstrates intracellular degradation of the mutant proteins.
Thrombosis and haemostasis 1997;77(6):1068-72.
1997: Juha-Pekka Kaukonen; L Alanen-Kurki; M Jalkanen; Aarno Palotie
The mapping and visual ordering of the human syndecan-1 and N-myc genes near the telomeric region of chromosome 2p.
Human genetics 1997;99(3):295-7.
1997: H Mikkola; László Muszbek; E Laiho; Martti Syrjälä; Eija Hämäläinen; Gizella Haramura; T Salmi; Leena Peltonen; Aarno Palotie
Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency: a splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA.
Blood 1997;89(4):1279-87.
1996: M Laan; Juha Isosomppi; T Klockars; Leena Peltonen; Aarno Palotie
Utilization of FISH in positional cloning: an example on 13q22.
Genome research 1996;6(10):1002-12.
1996: Juha-Pekka Kaukonen; I Lahtinen; Seppo Laine; Kari Alitalo; Aarno Palotie
BMX tyrosine kinase gene is expressed in granulocytes and myeloid leukaemias.
British journal of haematology 1996;94(3):455-60.
1996: T Klockars; M Savukoski; Juha Isosomppi; M Laan; Irma Järvelä; K Petrukhin; Aarno Palotie; Leena Peltonen
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.
Genomics 1996;35(1):71-8.
1996: Kristian J Paavonen; N Horelli-Kuitunen; D Chilov; E Kukk; S Pennanen; Olli Kallioniemi; K Pajusola; B Olofsson; Ulf Eriksson; V Joukov; Aarno Palotie; Kari Alitalo
Novel human vascular endothelial growth factor genes VEGF-B and VEGF-C localize to chromosomes 11q13 and 4q34, respectively.
Circulation 1996;93(6):1079-82.
1996: M Heiskanen; Olli Kallioniemi; Aarno Palotie
Fiber-FISH: experiences and a refined protocol.
Genetic analysis : biomolecular engineering 1996;12(5-6):179-84.
1996: H Mikkola; Aarno Palotie
Gene defects in congenital factor XIII deficiency.
Seminars in thrombosis and hemostasis 1996;22(5):393-8.
1996: H Mikkola; Vivien C Yee; Martti Syrjälä; R Seitz; R Egbring; P Petrini; Rolf Ljung; Jørgen Ingerslev; David C Teller; Leena Peltonen; Aarno Palotie
Four novel mutations in deficiency of coagulation factor XIII: consequences to expression and structure of the A-subunit.
Blood 1996;87(1):141-51.
1995: Tomi Mäkelä; E Hellsten; Jouni Vesa; H Hirvonen; Aarno Palotie; Leena Peltonen; Kari Alitalo
The rearranged L-myc fusion gene (RLF) encodes a Zn-15 related zinc finger protein.
Oncogene 1995;11(12):2699-704.
1995: K Tenhunen; M Laan; T Manninen; Aarno Palotie; Leena Peltonen; Anu Jalanko
Molecular cloning, chromosomal assignment, and expression of the mouse aspartylglucosaminidase gene.
Genomics 1995;30(2):244-50.
1995: M Heiskanen; E Hellsten; Olli Kallioniemi; Tomi Mäkelä; Kari Alitalo; Leena Peltonen; Aarno Palotie
Visual mapping by fiber-FISH.
Genomics 1995;30(1):31-6.
1995: M Heiskanen; B Saitta; Aarno Palotie; M L Chu
Head to tail organization of the human COL6A1 and COL6A2 genes by fiber-FISH.
Genomics 1995;29(3):801-3.
1995: Maritta Ilmonen; T Heliö; R Bütler; Aarno Palotie; P Pietinen; J K Huttunen; Matti J Tikkanen
Two new immunogenetic polymorphisms of the apoB gene and their effect on serum lipid levels and responses to changes in dietary fat intake.
Arteriosclerosis, thrombosis, and vascular biology 1995;15(9):1287-93.
1995: M Laan; K Grön-Virta; A Salo; Pertti Aula; Leena Peltonen; Aarno Palotie; Ann-Christine Syvänen
Solid-phase minisequencing confirmed by FISH analysis in determination of gene copy number.
Human genetics 1995;96(3):275-80.
1995: M Laan; Olli Kallioniemi; E Hellsten; Kari Alitalo; Leena Peltonen; Aarno Palotie
Mechanically stretched chromosomes as targets for high-resolution FISH mapping.
Genome research 1995;5(1):13-20.
1995: Pekka Anttila; J Ihalainen; A Salo; M Heiskanen; E Juvonen; Aarno Palotie
Idiopathic macrocytic anaemia in the aged: molecular and cytogenetic findings.
British journal of haematology 1995;90(4):797-803.
1995: E Hellsten; Jouni Vesa; M Heiskanen; Tomi Mäkelä; Irma Järvelä; John Kenneth Cowell; S Mead; Kari Alitalo; Aarno Palotie; Leena Peltonen
Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus.
Genomics 1995;25(2):404-12.
1995: E M Rytkönen; R Halila; M Laan; M Saksela; Olli Kallioniemi; Aarno Palotie; Kari O Raivio
The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22.
Cytogenetics and cell genetics 1995;68(1-2):61-3.
1994: J Ihalainen; Matti Taavitsainen; T Salmivaara; Aarno Palotie
Diagnosis of pancreatic lesions using fine needle aspiration cytology: detection of K-ras point mutations using solid phase minisequencing.
Journal of clinical pathology 1994;47(12):1082-4.
1994: M Heiskanen; Ritva Karhu; E Hellsten; Leena Peltonen; Olli Kallioniemi; Aarno Palotie
High resolution mapping using fluorescence in situ hybridization to extended DNA fibers prepared from agarose-embedded cells.
BioTechniques 1994;17(5):928-9, 932-3.
1994: Tiina Heliö; Aarno Palotie; Timo Sane; Matti J Tikkanen; Kimmo Kontula
No evidence for linkage between familial hypertriglyceridemia and apolipoprotein B, apolipoprotein C-III or lipoprotein lipase genes.
Human genetics 1994;94(3):271-8.
1994: M Heiskanen; Ann-Christine Syvänen; H Siitari; Seppo Laine; Aarno Palotie
A novel method to quantitate methylation of specific genomic regions.
PCR methods and applications 1994;4(1):26-30.
1994: H Mikkola; Martti Syrjälä; Vesa Rasi; Elina Vahtera; Eija Hämäläinen; Leena Peltonen; Aarno Palotie
Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levels.
Blood 1994;84(2):517-25.
1994: M Kämäräinen; L Riittinen; Markku Seppala; Aarno Palotie; Leif C Andersson
Progesterone-associated endometrial protein--a constitutive marker of human erythroid precursors.
Blood 1994;84(2):467-73.
1994: J Ihalainen; H Siitari; Seppo Laine; Ann-Christine Syvänen; Aarno Palotie
Towards automatic detection of point mutations: use of scintillating microplates in solid-phase minisequencing.
BioTechniques 1994;16(5):938-43.
1994: J Ihalainen; E Juvonen; Eeva-Riitta Savolainen; Tapani Ruutu; Aarno Palotie
Calcitonin gene methylation in chronic myeloproliferative disorders.
Leukemia 1994;8(2):230-5.
1994: Maritta Ilmonen; T Heliö; T Ebeling; K Pyörälä; M Uusitupa; Aarno Palotie; Matti J Tikkanen
Screening for mutations in the exon 26 of the apolipoprotein B gene in hypercholesterolemic Finnish families by the single-strand conformation polymorphism method.
Human mutation 1994;4(3):217-23.
1993: A Salo; Seppo Pakkala; Sten-Erik Jansson; P Helminen; Aarno Palotie
Monitoring of adult B-cell lineage acute lymphoblastic leukemia: validation of a simple method for detecting immunoglobulin heavy chain gene clonality.
Leukemia 1993;7(9):1459-65.
1993: N E Enomaa; P L Lukinmaa; E M Ikonen; J C Waltimo; Aarno Palotie; A E Paetau; Leena Peltonen
Expression of aspartylglucosaminidase in human tissues from normal individuals and aspartylglucosaminuria patients.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1993;41(7):981-9.
1993: J Ihalainen; Seppo Pakkala; Eeva-Riitta Savolainen; Sten-Erik Jansson; Aarno Palotie
Hypermethylation of the calcitonin gene in the myelodysplastic syndromes.
Leukemia 1993;7(2):263-7.
1993: Aarno Palotie; Ann-Christine Syvänen
Development of molecular genetic methods for monitoring myeloid malignancies.
Scandinavian journal of clinical and laboratory investigation. Supplementum 1993;213():29-38.
1993: Jaakko Aaltonen; J Komulainen; A Vikman; Aarno Palotie; C Wadelius; J Perheentupa; Leena Peltonen
Autoimmune polyglandular disease type I. Exclusion map using amplifiable multiallelic markers in a microtiter well format.
European journal of human genetics : EJHG 1993;1(2):164-71.
1992: K Kainulainen; L Y Sakai; A Child; F Michael Pope; L Puhakka; L Ryhänen; Aarno Palotie; Ilkka Kaitila; Leena Peltonen
Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptides.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(13):5917-21.
1992: L Haataja; J Schleutker; M Renlund; Aarno Palotie; Leena Peltonen; Pertti Aula
Exclusion map of Salla disease: attempts to localize the disease gene using a computer program.
Human genetics 1992;88(3):298-300.
1992: Tiina Heliö; Aarno Palotie; K J Tötterman; J Ott; R Kauppinen-Mäkelin; Matti J Tikkanen
Lack of association between the apolipoprotein B gene 3' hypervariable region alleles and coronary artery disease in Finnish patients with angiographically documented coronary artery disease.
Journal of internal medicine 1992;231(1):49-57.
1991: T Malinen; Aarno Palotie; Seppo Pakkala; Leena Peltonen; Tapani Ruutu; Sten-Erik Jansson
Acceleration of chronic myeloid leukemia correlates with calcitonin gene hypermethylation.
Blood 1991;77(11):2435-40.
1991: Irma Järvelä; J Schleutker; L Haataja; P Santavuori; L Puhakka; T Manninen; Aarno Palotie; L A Sandkuijl; M Renlund; Raymond White
Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1.
Genomics 1991;9(1):170-3.
1990: T Hämäläinen; Aarno Palotie; K Aalto-Setälä; Kimmo Kontula; Matti J Tikkanen
Absence of familial defective apolipoprotein B-100 in Finnish patients with elevated serum cholesterol.
Atherosclerosis 1990;82(3):177-83.
1990: K Kainulainen; A Savolainen; Aarno Palotie; Ilkka Kaitila; J Rosenbloom; Leena Peltonen
Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2.
Human genetics 1990;84(3):233-6.
1990: E Ikonen; Jukka U Palo; J Ott; James Gusella; Hannu Somer; L Karila; Aarno Palotie; Leena Peltonen
Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus.
American journal of human genetics 1990;46(1):5-11.