المؤلفون: Janne Martikainen, Aku-Ville Lehtimäki, Kari Jalkanen, Piia Lavikainen, Teemu Paajanen, Heidi Marjonen, Kati Kristiansson, Jaana Lindström, Markus Perola

المصدر: Frontiers in Genetics, Vol 13 (2022)

مصطلحات موضوعية: type 2 diabetes, prevention, polygenic risk score, cost-effectiveness, QALY, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2022.880799/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/161a71b82ba74d25837af6aa1fdbc27b

المؤلفون: Heidi Marjonen, Minttu Marttila, Teemu Paajanen, Marleena Vornanen, Minna Brunfeldt, Anni Joensuu, Otto Halmesvaara, Kimmo Aro, Mervi Alanne-Kinnunen, Pekka Jousilahti, Katja Borodulin, Seppo Koskinen, Tiinamaija Tuomi, Pirjo Ilanne-Parikka, Jaana Lindström, Merja K. Laine, Kirsi Auro, Helena Kääriäinen, Markus Perola, Kati Kristiansson

المصدر: Frontiers in Genetics, Vol 12 (2021)

مصطلحات موضوعية: web portal, type 2 diabetes, coronary heart disease, venous thromboembolism, polygenic risk sore, finhealth 2017 study, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2021.763159/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/9dd10994ed42433398a786aea1f54ec1

المؤلفون: Hanna Kahila, Heidi Marjonen, Pauliina Auvinen, Kristiina Avela, Raili Riikonen, Nina Kaminen‐Ahola

المصدر: Molecular Genetics & Genomic Medicine, Vol 8, Iss 4, Pp n/a-n/a (2020)

مصطلحات موضوعية: 18q deletion syndrome, comparative genomic hybridization array, DNA methylation, fetal alcohol spectrum disorders, fetal alcohol syndrome, growth retardation, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2324-9269

URL الوصول: https://doaj.org/article/960c81911a95489f95935c6e7e1831f6

المؤلفون: Heidi Marjonen, Pauliina Auvinen, Hanna Kahila, Olga Tšuiko, Sulev Kõks, Airi Tiirats, Triin Viltrop, Timo Tuuri, Viveca Söderström-Anttila, Anne-Maria Suikkari, Andres Salumets, Aila Tiitinen, Nina Kaminen-Ahola

المصدر: Clinical Epigenetics, Vol 10, Iss 1, Pp 1-11 (2018)

مصطلحات موضوعية: Assisted reproductive technology, IVF, Fresh embryo transfer, Frozen embryo transfer, Imprinting, IGF2/H19, Medicine, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13148-018-0511-2; https://doaj.org/toc/1868-7075; https://doaj.org/toc/1868-7083

URL الوصول: https://doaj.org/article/677a4a7141614692bfa38b4d1706f4d9

المؤلفون: Heidi Marjonen, Mia Toivonen, Laura Lahti, Nina Kaminen-Ahola

المصدر: PLoS ONE, Vol 13, Iss 5, p e0197461 (2018)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC5953443?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/87af5169ddf6451499d5a768b697b33c

المؤلفون: Heidi Marjonen, Alejandra Sierra, Anna Nyman, Vladimir Rogojin, Olli Gröhn, Anni-Maija Linden, Sampsa Hautaniemi, Nina Kaminen-Ahola

المصدر: PLoS ONE, Vol 10, Iss 5, p e0124931 (2015)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC4430308?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/1be30091e6c4455f8c90355911740ca0

المؤلفون: Mariann Koel, Masoud Zamani Esteki, Heidi Marjonen, Sulev Kõks, Katre Teearu, Joris Vermeesch, Ants Kurg, Jeroen Meekels, Olga Žilina, Anne-Maria Suikkari, Andres Salumets, Airi Tiirats, Thierry Voet, Reedik Mägi, Margit Nõukas, Nina Kaminen-Ahola, Aila Tiitinen, Hanna Kahila, Viveca Söderström-Anttila, Triin Viltrop, Olga Tšuiko

المساهمون: RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Lab Centraal Lab (9)

المصدر: NATURE MEDICINE
Nature Medicine, 25(11), 1699-1705. Nature Publishing Group

مصطلحات موضوعية: 0301 basic medicine, Male, DNA Copy Number Variations, Genotype, medicine.medical_treatment, Placenta, Aneuploidy, Embryonic Development, Fertilization in Vitro, MOSAICISM, Biology, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Andrology, CHROMOSOME INSTABILITY, 03 medical and health sciences, HIDDEN-MARKOV MODEL, 0302 clinical medicine, Fetus, BLASTOCYSTS, Pregnancy, Chromosome instability, Chromosomal Instability, medicine, Humans, Cell Lineage, Blastocyst, COMMON, In vitro fertilisation, ANEUPLOIDY, ABNORMALITIES, Embryogenesis, Infant, Newborn, Embryo, General Medicine, medicine.disease, Embryo, Mammalian, female genital diseases and pregnancy complications, CONSTITUTION, GENOME, 030104 developmental biology, medicine.anatomical_structure, HUMAN-EMBRYOS, 030220 oncology & carcinogenesis, embryonic structures, Female

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bfb776eaff7ebde20a650b80a48344a
https://doi.org/10.1038/s41591-019-0620-2

المؤلفون: Heidi Marjonen, Kristiina Avela, Nina Kaminen-Ahola, Hanna Kahila, Pauliina Auvinen, Raili Riikonen

المساهمون: Department of Obstetrics and Gynecology, HUS Gynecology and Obstetrics, Helsinki University Hospital Area, University of Helsinki, Medicum, Department of Medical and Clinical Genetics, Doctoral Programme in Biomedicine, HUSLAB, Clinicum, Environmental Epigenetics Laboratory

المصدر: Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 4, Pp n/a-n/a (2020)

مصطلحات موضوعية: 18q deletion syndrome, 0301 basic medicine, comparative genomic hybridization array, Microarray, Developmental Disabilities, Bisulfite sequencing, 030105 genetics & heredity, Twins, Dizygotic, Imprinting (psychology), Genetics (clinical), Genetics, Comparative Genomic Hybridization, DNA methylation, IGF2, twins, Phenotype, Fetal Alcohol Spectrum Disorders, Original Article, RNA, Long Noncoding, Chromosome Deletion, MRI, IGF2/H19, Adult, lcsh:QH426-470, Dizygotic twin, Fetal alcohol syndrome, growth retardation, Locus (genetics), Biology, Genomic Imprinting, 03 medical and health sciences, Insulin-Like Growth Factor II, medicine, Humans, Genetic Testing, Molecular Biology, prenatal alcohol exposure, H19, Original Articles, medicine.disease, INDIVIDUALS, lcsh:Genetics, 030104 developmental biology, 18Q DELETIONS, 1182 Biochemistry, cell and molecular biology, 3111 Biomedicine, fetal alcohol syndrome, Chromosomes, Human, Pair 18, Comparative genomic hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1905009e308c69d9c216c4c83663e62f
https://doi.org/10.1002/mgg3.1192

المؤلفون: Andres Salumets, Anne-Maria Suikkari, Sulev Kõks, Olga Tšuiko, Airi Tiirats, Nina Kaminen-Ahola, Triin Viltrop, Hanna Kahila, Aila Tiitinen, Timo Tuuri, Viveca Söderström-Anttila, Pauliina Auvinen, Heidi Marjonen

المساهمون: Department of Medical and Clinical Genetics, Doctoral Programme in Biomedicine, Department of Obstetrics and Gynecology, HUS Gynecology and Obstetrics, University of Helsinki, Clinicum, Environmental Epigenetics Laboratory, 'European Union (EU)' and 'Horizon 2020'

المصدر: Clinical Epigenetics, Vol 10, Iss 1, Pp 1-11 (2018)
Clinical Epigenetics

مصطلحات موضوعية: 0301 basic medicine, Male, CCCTC-Binding Factor, PERINATAL OUTCOMES, medicine.medical_treatment, Placenta, Bisulfite sequencing, lcsh:Medicine, 0302 clinical medicine, Pregnancy, 3123 Gynaecology and paediatrics, Genotype, Genetics (clinical), Finland, Genetics & Heredity, 030219 obstetrics & reproductive medicine, DNA methylation, Frozen embryo transfer, Imprinting, Assisted reproductive technology, Embryo transfer, 3. Good health, Oncology, IVF, embryonic structures, Female, RNA, Long Noncoding, medicine.symptom, SINGLETON PREGNANCIES, Life Sciences & Biomedicine, Maternal Age, IGF2/H19, Adult, Estonia, Reproductive Techniques, Assisted, lcsh:QH426-470, Birth weight, Biology, EMBRYO-TRANSFER, Polymorphism, Single Nucleotide, Andrology, 03 medical and health sciences, Genomic Imprinting, Insulin-Like Growth Factor II, Genetics, medicine, Humans, COHORT, FROZEN, Allele, Molecular Biology, rs10732516, METAANALYSIS, Science & Technology, In vitro fertilisation, Binding Sites, Research, IVF/ICSI, Fresh embryo transfer, lcsh:R, Infant, Newborn, BECKWITH-WIEDEMANN-SYNDROME, Low birth weight, lcsh:Genetics, 030104 developmental biology, Case-Control Studies, IN-VITRO FERTILIZATION, CHILDREN BORN, Developmental Biology

وصف الملف: application/pdf; Electronic-eCollection

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7837a2e20eb56cdf3b14242932130002
http://link.springer.com/article/10.1186/s13148-018-0511-2

المؤلفون: Ilkka Lappalainen, Valérie Barbié, Sarah E. Hunt, Heidi Marjonen, Enni Makkonen, Fiona Cunningham, Michael J.E. Sternberg, Alessia David, Mats Lindstedt, Kati Kristiansson, Marcella Attimonelli, Roberto Preste

المصدر: F1000Research. 9:1207

مصطلحات موضوعية: General Immunology and Microbiology, Computer science, media_common.quotation_subject, International survey, General Medicine, Key features, Data science, General Biochemistry, Genetics and Molecular Biology, Annotation, Training material, Research environment, Quality (business), Elixir (programming language), General Pharmacology, Toxicology and Pharmaceutics, computer, Cloud storage, computer.programming_language, media_common

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::010930ee7c0a187eab3f8736436b3f07
https://doi.org/10.12688/f1000research.24427.1