المؤلفون: Joanna von Berg, Patrick F. McArdle, Paavo Häppölä, Jeffrey Haessler, Charles Kooperberg, Robin Lemmens, Alessandro Pezzini, Vincent Thijs, Sara L. Pulit, Steven J. Kittner, Braxton D. Mitchell, Jeroen de Ridder, Sander W. van der Laan

المصدر: Frontiers in Genetics, Vol 15 (2024)

مصطلحات موضوعية: genome-wide association study, stroke, age at onset, APOE, atherosclerosis, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2024.1392061/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/5fe79556aa9743429be4d3f8a5445d26

المؤلفون: Joel T. Rämö, Tuomo Kiiskinen, Richard Seist, Kristi Krebs, Masahiro Kanai, Juha Karjalainen, Mitja Kurki, Eija Hämäläinen, Paavo Häppölä, Aki S. Havulinna, Heidi Hautakangas, FinnGen, Reedik Mägi, Priit Palta, Tõnu Esko, Andres Metspalu, Matti Pirinen, Konrad J. Karczewski, Samuli Ripatti, Lili Milani, Konstantina M. Stankovic, Antti Mäkitie, Mark J. Daly, Aarno Palotie

المصدر: Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2041-1723

URL الوصول: https://doaj.org/article/6c545f6161e84ab58fce429684406cdc

المؤلفون: Paavo Häppölä (4951570), Padhraig Gormley (3175580), Marjo E Nuottamo (11569658), Ville Artto (5323760), Marja-Liisa Sumelahti (5323772), Markku Nissilä (5323748), Petra Keski-Säntti (5323745), Matti Ilmavirta (5323751), Mari A Kaunisto (11569661), Eija I Hämäläinen (11569664), Samuli Ripatti (144251), Matti Pirinen (415109), Maija Wessman (207083), Aarno Palotie (41342), Mikko Kallela (5323757)

مصطلحات موضوعية: Neuroscience, Endocrinology, Psychiatry (incl. Psychotherapy), Neurology and Neuromuscular Diseases, Pharmacology and Pharmaceutical Sciences not elsewhere classified, Psychology not elsewhere classified, Migraine, headache, diagnosis criteria, polygenic risk score

Relation: https://figshare.com/articles/journal_contribution/sj-pdf-1-cep-10_1177_03331024211045651_-_Supplemental_material_for_Polygenic_risk_provides_biological_validity_for_the_ICHD-3_criteria_among_Finnish_migraine_families/16818383

الاتاحة: https://doi.org/10.25384/sage.16818383.v1

المؤلفون: Juulia Partanen, Sylvain Sebert, Priit Palta, Mykyta Artomov, Kurki M, Mark J. Daly, Paavo Häppölä, J Kaprio, Ronkainen J, Tarja Laitinen, Aoxing Liu, Myllymäki Mn, Giulio Genovese, Taru Tukiainen, Teemu Palviainen, Myllärniemi M, Juha Karjalainen, Aarno Palotie, Wei Zhou, Masahiro Kanai, Jukka Koskela, Andrea Ganna

مصطلحات موضوعية: 0303 health sciences, Mutation, Cancer, Biology, Bioinformatics, medicine.disease, medicine.disease_cause, MAD1L1, 3. Good health, Telomere, 03 medical and health sciences, Idiopathic pulmonary fibrosis, 0302 clinical medicine, 030228 respiratory system, Fibrosis, Pulmonary fibrosis, medicine, Missense mutation, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7a79faa43fea23f22c5d440f58994ad8
https://doi.org/10.1101/2021.05.07.21255988

المؤلفون: Tobias Kurth, Nadine Pelzer, Hautakangas H, Artto, O T Raitakari, Julie E. Buring, Penninx Bwjh., Christian Erikstrup, Mikko Kallela, Matti Pirinen, Christian Benner, Daniel I. Chasman, Kristian Hveem, Kristoffersen Es, Torben Hansen, Olafur A. Sveinsson, Mika Kähönen, van den Maagdenberg Amjm., Mona Ameri Chalmer, Aarno Palotie, Elisabeth Widen, Thorgeir E. Thorgeirsson, Hreinn Stefansson, Lighart L, Paul M. Ridker, de Boer I, Gisela M. Terwindt, Garbrielsen Me, Jouke J. Hottenga, Kogelman Lja., Arpo Aromaa, Bendik S. Winsvold, Dale R. Nyholt, Ikram Ma, van Dijk Kw, Harder Ave, Martin Dichgans, Rainer Malik, Mohsen Ghanbari, Marianne Bakke Johnsen, Marjo-Ritta Jarvelin, Samuli Ripatti, Paavo Häppölä, Gyda Bjornsdottir, Martti Färkkilä, Anne Heidi Skogholt, Terho Lehtimäki, Sanni Ruotsalainen, Frits R. Rosendaal, Gudrun R. Sigurdardottir, Headache Ha, Gormley P, Kari Stefansson, J.A. Zwart, Oluf Pedersen, Raymond Noordam, Ben Michael Brumpton, Laurent F. Thomas, Karina Banasik, M.G. Hrafnsdottir, Lisanne S. Vijfhuizen, Sølvsten Burgdorf K, Jes Olesen, Sigurdur H. Magnusson, T. Freilinger, Kristen Hagen, Andrea Carmine Belin, Dorret I. Boomsma, Henrik Ullum, Maija Wessman, Ran C, Anna Bjornsdottir

مصطلحات موضوعية: Genetics, 0303 health sciences, Aura, Genome wide analysis, Specific risk, Genome-wide association study, Biology, medicine.disease, Migraine with aura, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Migraine, medicine, medicine.symptom, Allele, Gene, 030217 neurology & neurosurgery, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9e64e0da2e2c833014db37279373369e
https://doi.org/10.1101/2021.01.20.21249647

المؤلفون: Antti Mäkitie, Tuomo Kiiskinen, Juha Karjalainen, Samuli Ripatti, A. Metspalu, Tõnu Esko, Lili Milani, Kurki M, Joel T. Rämö, Masahiro Kanai, Eija Hämäläinen, Reedik Mägi, Paavo Häppölä, Hautakangas H, Matti Pirinen, Kristi Krebs, Mark J. Daly, Aki S. Havulinna, Priit Palta, A. Palotie, Konrad J. Karczewski

مصطلحات موضوعية: Genetics, 0303 health sciences, education.field_of_study, Population, Genome-wide association study, Locus (genetics), Biology, Heritability, medicine.disease, Biobank, Genome, 03 medical and health sciences, 0302 clinical medicine, medicine, Otosclerosis, Family history, 030223 otorhinolaryngology, education, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8cf1d5d721aff8b72db13f8f76573b68
https://doi.org/10.1101/2020.11.15.20227868

المؤلفون: Aarno Palotie, Samuli Ripatti, Veikko Salomaa, Nina Mars, Benjamin M. Neale, Markus Perola, Seppo Koskinen, Paavo Häppölä, Mark J. Daly, Aki S. Havulinna, Lili Milani, Mikko Kallela, Tõnis Tasa

المساهمون: Complex Disease Genetics, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, Helsinki Institute of Life Science HiLIFE, University of Helsinki, Medicum, HUS Neurocenter, Department of Neurosciences, Neurologian yksikkö, Helsinki University Hospital Area, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, Department of Public Health, Samuli Olli Ripatti / Principal Investigator, Biostatistics Helsinki, Faculty of Medicine, Clinicum

المصدر: Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports

مصطلحات موضوعية: Male, Aging, medicine.medical_specialty, Time Factors, INDEXES, MEDLINE, lcsh:Medicine, Pharmacy, Comorbidity, Type 2 diabetes, Biostatistics, 01 natural sciences, Article, 010104 statistics & probability, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Longitudinal Studies, 030212 general & internal medicine, Age of Onset, Mortality, 0101 mathematics, lcsh:Science, Aged, Public health, Multidisciplinary, business.industry, Statistical learning, Statistics, lcsh:R, Genomics, Middle Aged, medicine.disease, Coronary heart disease, 3. Good health, VARIABLE SELECTION, Risk factors, Mortality data, Charlson comorbidity index, Female, lcsh:Q, 3111 Biomedicine, business, Comorbidity index

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b73a5f6b56f9806ae16f5922511b1a06
https://doi.org/10.1038/s41598-020-72045-z

المؤلفون: Mitja I. Kurki, Mark J. Daly, Kirsi Auro, John P. Atkinson, Juha Kere, Hannele Laivuori, Anneli Pouta, Elisha D.O. Roberson, Markus Perola, A. Inkeri Lokki, Michael Triebwasser, Seppo Heinonen, Paavo Häppölä, Emma Daly, Katja Kivinen, Seppo Meri, Eero Kajantie, Jane E. Salmon

المصدر: Hypertension. 70:365-371

مصطلحات موضوعية: Adult, 0301 basic medicine, Candidate gene, Physiology, Disease, Lower risk, Article, Preeclampsia, 03 medical and health sciences, Pre-Eclampsia, Pregnancy, Internal Medicine, medicine, Humans, Finland, reproductive and urinary physiology, Genetics, Vascular Endothelial Growth Factor Receptor-1, business.industry, Genetic Variation, Odds ratio, Protective Factors, medicine.disease, female genital diseases and pregnancy complications, 3. Good health, Minor allele frequency, 030104 developmental biology, embryonic structures, Hypertension, Cohort, Female, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7595dd3182d8e3bbbfd3e7a23ead18fe
https://doi.org/10.1161/hypertensionaha.117.09406

المؤلفون: Aarno Palotie, Petra Keski-Säntti, Maija Wessman, Mari A. Kaunisto, Matti Ilmavirta, Marja-Liisa Sumelahti, Salli Vepsäläinen, Marjo Eveliina Hiekkala, Paavo Häppölä, Eija Hämäläinen, Markus Färkkilä, Elisa Häppölä, Dennis Lal, E. Cuenca-Leon, Erkki Säkö, Hannele Havanka, Mikko Kallela, Padhraig Gormley, Ville Artto, Markku Nissilä, Pietari Vuola, Hanna Harno

المساهمون: Neurologian yksikkö, Clinicum, Institute for Molecular Medicine Finland, Helsinki Institute of Life Science HiLIFE, University of Helsinki, Department of Neurosciences, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, HUS Neurocenter, Complex Disease Genetics, Genomics of Neurological and Neuropsychiatric Disorders

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Aura, PROTEINS, FEBRILE SEIZURES PLUS, GENERALIZED EPILEPSY, VARIANTS, 3124 Neurology and psychiatry, 03 medical and health sciences, TYPE-2, 0302 clinical medicine, pathogenic variant, CHANNEL, ATP1A2, Internal medicine, medicine, Humans, Generalized epilepsy, ICHD-3 beta criteria, clinical characteristics, Exome sequencing, Finland, SPECTRUM, CONSEQUENCES, Genetic heterogeneity, business.industry, 3112 Neurosciences, General Medicine, Middle Aged, medicine.disease, Migraine with aura, 3. Good health, NAV1.1 Voltage-Gated Sodium Channel, 030104 developmental biology, Migraine, Mutation, ion channel, International Classification of Headache Disorders, Female, Neurology (clinical), Calcium Channels, medicine.symptom, Sodium-Potassium-Exchanging ATPase, business, exome sequencing, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::303866426aa32b7939ccbb7178d33b76
http://hdl.handle.net/10138/306611

المؤلفون: Aarno Palotie, Paavo Häppölä, Andres Metspalu, Priit Palta, Timo Sipilä, Mart Kals

المصدر: eScience

مصطلحات موضوعية: End user, business.industry, Computer science, education, Sorting, Genomics, World Wide Web, Chromosome (genetic algorithm), population characteristics, Web application, Web resource, business, Exome, Graphical user interface

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::22c9f1f053c38a7a7bdac78c130fed9b
https://doi.org/10.1109/escience.2018.00116

المؤلفون: Maija Wessman, Mitja I. Kurki, Aarno Palotie, Matti Ilmavirta, Salli Vepsäläinen, Hanna Harno, Mark J. Daly, Paavo Häppölä, Pekka Jousilahti, Verneri Anttila, Liisa Metsähonkala, Marja-Liisa Sumelahti, Markus Färkkilä, Mikko Kallela, Padhraig Gormley, Erkki Säkö, Marjo Eveliina Hiekkala, Benjamin M. Neale, Markku Nissilä, Priit Palta, Kumar Veerapen, Dennis Lal, Eija Hämäläinen, Jarmo Liukkonen, Hannele Havanka, Matti Sillanpää, Ville Artto, Heiko Runz, Adele A. Mitchell, Ida Surakka, Veikko Salomaa, Mari A. Kaunisto, Samuli Ripatti

مصطلحات موضوعية: 0303 health sciences, medicine.medical_specialty, education.field_of_study, business.industry, Aura, Population, Family aggregation, medicine.disease, Migraine with aura, 03 medical and health sciences, 0302 clinical medicine, Migraine, Internal medicine, Medicine, Outpatient clinic, Migraine treatment, medicine.symptom, business, education, 030217 neurology & neurosurgery, Familial hemiplegic migraine, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2309e8e697b8bab658edf5f03b9c5883

المؤلفون: Johanna M. Seddon, Soumya Raychaudhuri, Eric H. Souied, Ilkka Immonen, Mark J. Daly, Sanna Seitsonen, Yi Yu, Erin K. Wagner, Paavo Häppölä

مصطلحات موضوعية: 0301 basic medicine, Collagen Type IV, Male, Genotype, Ubiquitin-Protein Ligases, Genome-wide association study, Disease, Biology, Autoantigens, Polymorphism, Single Nucleotide, 03 medical and health sciences, Macular Degeneration, 0302 clinical medicine, Polymorphism (computer science), Risk Factors, medicine, Genetics, Beta 2-Glycoprotein I, Chymotrypsin, Humans, Genetic Predisposition to Disease, Allele, Molecular Biology, Genetics (clinical), 030304 developmental biology, Genetic association, 0303 health sciences, Association Studies Articles, Case-control study, Genetic Variation, General Medicine, Odds ratio, Macular degeneration, Heritability, medicine.disease, Complement system, 030104 developmental biology, Case-Control Studies, Complement Factor H, Etiology, 030221 ophthalmology & optometry, Female, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5f87f2470ef0c172382dafc13fc3177
https://europepmc.org/articles/PMC6078639/

المؤلفون: Maija Wessman, Marjo Nuottamo, Mari Kaunisto, Paavo Häppölä, Ville Artto, Mikko Kallela, Verneri Anttila, Aarno Palotie

المصدر: University of Helsinki

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0b236b31dfff560c4c8751a69e2fc5e5
https://researchportal.helsinki.fi/en/publications/d0902136-b40c-4c26-b8b2-81ba02e4ec43