المؤلفون: Meltsov, Alvin, Saare, Merli, Teder, Hindrek, Paluoja, Priit, Arffman, Riikka K., Piltonen, Terhi, Laudanski, Piotr, Wielgos, Miroslaw, Gianaroli, Luca, Koel, Mariann, Peters, Maire, Salumets, Andres, Krjutskov, Kaarel, Palta, Priit

المساهمون: Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders

مصطلحات موضوعية: Embryo-transfer, Frozen, Cycles, Window, Array, 1184 Genetics, developmental biology, physiology

وصف الملف: application/pdf

العلاقة: This research was funded by the Estonian Research Council (grant PRG1076), Horizon 2020 innovation grant (ERIN, grant no. EU952516), the EU-FP7 Marie Curie Industry-Academia Partnerships and Pathways (IAPP, grant SARM, EU324509), the Enterprise Estonia (grant no. EU48695) and by Polish Ministry of Health (grant no. 6/6/4/1/NPZ/2017/1210/1352).; Meltsov , A , Saare , M , Teder , H , Paluoja , P , Arffman , R K , Piltonen , T , Laudanski , P , Wielgos , M , Gianaroli , L , Koel , M , Peters , M , Salumets , A , Krjutskov , K & Palta , P 2023 , ' Targeted gene expression profiling for accurate endometrial receptivity testing ' , Scientific Reports , vol. 13 , no. 1 , 13959 . https://doi.org/10.1038/s41598-023-40991-zTest; ORCID: /0000-0001-9320-7008/work/153479395; 85168754103; bc8306b3-aa36-4111-a28b-8f300fa2ab2b; http://hdl.handle.net/10138/571101Test; 001138684400001

الإتاحة: http://hdl.handle.net/10138/571101Test

المؤلفون: Meltsov, Alvin, Saare, Merli, Teder, Hindrek, Paluoja, Priit, Arffman, Riikka K., Piltonen, Terhi, Laudanski, Piotr, Wielgoś, Mirosław, Gianaroli, Luca, Koel, Mariann, Peters, Maire, Salumets, Andres, Krjutškov, Kaarel, Palta, Priit

المساهمون: Enterprise Estonia, Estonian Research Council, Polish Ministry of Health, Horizon 2020 innovation grant, EU-FP7 Marie Curie Industry-Academia Partnerships and Pathways

المصدر: Scientific Reports ; volume 13, issue 1 ; ISSN 2045-2322

مصطلحات موضوعية: Multidisciplinary

الإتاحة: https://doi.org/10.1038/s41598-023-40991-zTest
https://www.nature.com/articles/s41598-023-40991-z.pdfTest
https://www.nature.com/articles/s41598-023-40991-zTest

المؤلفون: Zhytnik, Lidiia, Peters, Maire, Tilk, Kadi, Reimand, Tiia, Ilisson, Piret, Kahre, Tiina, Murumets, Ülle, Ehrenberg, Aivar, Ustav, Eva-Liina, Tõnisson, Neeme, Mölder, Signe, Teder, Hindrek, Krjutškov, Kaarel, Salumets, Andres

المصدر: Zhytnik , L , Peters , M , Tilk , K , Reimand , T , Ilisson , P , Kahre , T , Murumets , Ü , Ehrenberg , A , Ustav , E-L , Tõnisson , N , Mölder , S , Teder , H , Krjutškov , K & Salumets , A 2022 , ' Prenatal diagnosis of a 46,XY karyotype female fetus with an SRY-associated gonadal dysgenesis, conceived through an intracytoplasmic sperm injection : a case report ' , BMC Pregnancy and Childbirth , vol. 22 , no. 1 , 105 . https://doi.org/10.1186/s12884-022-04431-6Test

العلاقة: https://research.vumc.nl/en/publications/4d918de9-4aab-48c2-83ce-9987551dc743Test

الإتاحة: https://doi.org/10.1186/s12884-022-04431-6Test
https://research.vumc.nl/en/publications/4d918de9-4aab-48c2-83ce-9987551dc743Test
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85124381666&origin=inwardTest
https://www.ncbi.nlm.nih.gov/pubmed/35123446Test

المؤلفون: Paluoja, Priit, Teder, Hindrek, Ardeshirdavani, Amin, Bayindir, Baran, Vermeesch, Joris, Salumets, Andres, Krjutškov, Kaarel, Palta, Priit

المساهمون: Paluoja, Priit, Teder, Hindrek, Ardeshirdavani, Amin, Bayindir, Baran, Vermeesch, Jori, Salumets, Andre, Krjutškov, Kaarel, Palta, Priit

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34928946; info:eu-repo/semantics/altIdentifier/wos/WOS:000732531200001; volume:17; issue:12; firstpage:1; lastpage:18; numberofpages:18; journal:PLOS COMPUTATIONAL BIOLOGY; https://hdl.handle.net/11584/356298Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85122336619

الإتاحة: https://doi.org/10.1371/journal.pcbi.1009684Test
https://hdl.handle.net/11584/356298Test

المؤلفون: Wedenoja, Satu, Yoshihara, Masahito, Teder, Hindrek, Sariola, Hannu, Gissler, Mika, Katayama, Shintaro, Wedenoja, Juho, Hakkinen, Inka M., Ezer, Sini, Linder, Nina, Lundin, Johan, Skoog, Tiina, Sahlin, Ellika, Iwarsson, Erik, Pettersson, Karin, Kajantie, Eero, Mokkonen, Mikael, Heinonen, Seppo, Laivuori, Hannele, Krjutskov, Kaarel, Kere, Juha

المصدر: EBioMedicine. 59

مصطلحات موضوعية: HLA-G, Interferon alpha, Sex ratio, Preeclampsia, Stillbirth, Balancing selection

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-423470Test
https://doi.org/10.1016/j.ebiom.2020.102872Test
https://uu.diva-portal.org/smash/get/diva2:1497111/FULLTEXT01.pdfTest

المؤلفون: Saare, Merli, Laisk, Triin, Teder, Hindrek, Paluoja, Priit, Palta, Priit, Koel, Mariann, Kirss, Fred, Karro, Helle, Soritsa, Deniss, Salumets, Andres, Krjutskov, Kaarel, Peters, Maire

المساهمون: Institute for Molecular Medicine Finland, University of Helsinki, Genomics of Neurological and Neuropsychiatric Disorders, HUS Gynecology and Obstetrics, Clinicum, Department of Obstetrics and Gynecology, STEMM - Stem Cells and Metabolism Research Program, Research Programs Unit

مصطلحات موضوعية: endometriosis, endometrium, menstrual cycle, 3123 Gynaecology and paediatrics

وصف الملف: application/pdf

العلاقة: Saare , M , Laisk , T , Teder , H , Paluoja , P , Palta , P , Koel , M , Kirss , F , Karro , H , Soritsa , D , Salumets , A , Krjutskov , K & Peters , M 2019 , ' A molecular tool for menstrual cycle phase dating of endometrial samples in endometriosis transcriptome studies ' , Biology of Reproduction , vol. 101 , no. 1 , pp. 1-3 . https://doi.org/10.1093/biolre/ioz072Test; ORCID: /0000-0001-9320-7008/work/64665994; 81c50981-703c-4bcf-b9ee-53d598b2f06a; http://hdl.handle.net/10138/306966Test; 000492974800001

الإتاحة: http://hdl.handle.net/10138/306966Test

المؤلفون: Teder, Hindrek, Paluoja, Priit, Rekker, Kadri, Salumets, Andres, Krjutškov, Kaarel, Palta, Priit

المساهمون: HUS Gynecology and Obstetrics, Clinicum, Department of Obstetrics and Gynecology, University of Helsinki, CAN-PRO - Translational Cancer Medicine Program, Research Programs Unit, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders

مصطلحات موضوعية: 1182 Biochemistry, cell and molecular biology, 113 Computer and information sciences, CELL-FREE DNA, DOWN-SYNDROME, MEIOTIC STAGE, MATERNAL AGE, ANEUPLOIDY, PLASMA, NONDISJUNCTION, TRISOMY-21, FRACTION, GENESIS

وصف الملف: application/pdf

العلاقة: Teder , H , Paluoja , P , Rekker , K , Salumets , A , Krjutškov , K & Palta , P 2019 , ' Computational framework for targeted high-coverage sequencing based NIPT ' , PLoS One , vol. 14 , no. 7 , 0209139 . https://doi.org/10.1371/journal.pone.0209139Test; RIS: urn:C9F4E5192F820C930DCF7421D9D92CF4; ORCID: /0000-0001-9320-7008/work/64001229; dd9da1de-0ccd-4f4a-9710-f7fcfbf71809; http://hdl.handle.net/10138/306598Test; 000484939800002

الإتاحة: http://hdl.handle.net/10138/306598Test

المؤلفون: Teder, Hindrek, Koel, Mariann, Paluoja, Priit, Jatsenko, Tatjana, Rekker, Kadri, Laisk-Podar, Triin, Kukuskina, Viktorija, Velthut-Meikas, Agne, Fjodorova, Olga, Peters, Maire, Kere, Juha, Salumets, Andres, Palta, Priit, Krjutskov, Kaarel

المساهمون: Juha Kere / Principal Investigator, Research Programs Unit, Research Programme for Molecular Neurology, University of Helsinki, Clinicum, Department of Obstetrics and Gynecology, Institute for Molecular Medicine Finland, HUS Gynecology and Obstetrics, Genomics of Neurological and Neuropsychiatric Disorders

مصطلحات موضوعية: CELL-FREE DNA, QUANTIFICATION, MUTATIONS, AMPLIFICATION, LIGATION, 3111 Biomedicine, 1184 Genetics, developmental biology, physiology

وصف الملف: application/pdf

العلاقة: This work was supported by the Estonian Ministry of Education and Research (grant no. IUT34-16), by the Enterprise Estonia (grant no. EU48695), by the EU FP7-PEOPLE-2012-IAPP, SARM (grant no. EU324509), by the European Commission Horizon 2020 research and innovation program under grant agreement 692065 (project WIDENLIFE) and MSCA-RISE-2015 project MOMENDO (grant no. 691058). We thank S. Vuoristo for helpful discussions and M. Saare for providing information on housekeeping genes. We also thank the Karolinska Institutet Bioinformatics and Expression Analysis (BEA) core facility and High Performance Computing Center of the University of Tartu.; Teder , H , Koel , M , Paluoja , P , Jatsenko , T , Rekker , K , Laisk-Podar , T , Kukuskina , V , Velthut-Meikas , A , Fjodorova , O , Peters , M , Kere , J , Salumets , A , Palta , P & Krjutskov , K 2018 , ' TAC-seq : targeted DNA and RNA sequencing for precise biomarker molecule counting ' , Npj genomic medicine , vol. 3 , 34 . https://doi.org/10.1038/s41525-018-0072-5Test; ORCID: /0000-0001-9320-7008/work/52695920; 85058842481; d4bc4c87-2e3e-4f73-ad18-1c7257cfd4d0; http://hdl.handle.net/10138/288721Test; 000454051200001

الإتاحة: http://hdl.handle.net/10138/288721Test

المؤلفون: Soritsa, Deniss, Teder, Hindrek, Roosipuu, Retlav, Tamm, Hannes, Laisk-Podar, Triin, Soplepmann, Pille, Altraja, Alan, Salumets, Andres, Peters, Maire

المساهمون: Department of Obstetrics and Gynecology, Clinicum, University of Helsinki, HUS Gynecology and Obstetrics

مصطلحات موضوعية: Benign metastasizing leiomyoma, BMP8B, Endometriosis, GnRH agonists, Pulmonary lesion, Somatic gene mutation, OF-THE-LITERATURE, UTERINE LEIOMYOMA, GASTRIC-CANCER, UTERUS, OOPHORECTOMY, PROGRESSION, CLONALITY, 3111 Biomedicine

وصف الملف: application/pdf

العلاقة: The research was funded by grant IUT34-16 from the Estonian Ministry of Education and Research, by Enterprise Estonia, grant no EU48695, and by the European Commission Horizon 2020 research and innovation programme under grant agreements 692065 (project WIDENLIFE) and 691058 (MSCA-RISE-2015 project MOMENDO).; Soritsa , D , Teder , H , Roosipuu , R , Tamm , H , Laisk-Podar , T , Soplepmann , P , Altraja , A , Salumets , A & Peters , M 2018 , ' Whole exome sequencing of benign pulmonary metastasizing leiomyoma reveals mutation in the BMP8B gene ' , BMC Medical Genetics , vol. 19 , 20 . https://doi.org/10.1186/s12881-018-0537-5Test; 85041482140; a5f7a225-09a0-455c-9b24-f2964b308e84; http://hdl.handle.net/10138/233503Test; 000423749400001

الإتاحة: http://hdl.handle.net/10138/233503Test

المؤلفون: Sauk, Martin, Zilina, Olga, Kurg, Ants, Ustav, Eva-Liina, Peters, Maire, Paluoja, Priit, Roost, Anne Mari, Teder, Hindrek, Palta, Priit, Brison, Nathalie, Vermeesch, Joris R., Krjutskov, Kaarel, Salumets, Andres, Kaplinski, Lauris

المساهمون: Research Programme for Molecular Neurology, Research Programs Unit, Department of Obstetrics and Gynecology, HUS Gynecology and Obstetrics

مصطلحات موضوعية: MATERNAL PLASMA, DNA, FRACTION, 3111 Biomedicine, 3123 Gynaecology and paediatrics

وصف الملف: application/pdf

العلاقة: This study was supported by the Estonian Research Council [institutional research funding IUT34-16]; by the EU FP7-PEOPLE-2012-IAPP grant SARM [grant no 324509]; by Enterprise Estonia [grant no EU48695]; and by Horizon 2020 innovation programme [WIDENLIFE, 692065].; Sauk , M , Zilina , O , Kurg , A , Ustav , E-L , Peters , M , Paluoja , P , Roost , A M , Teder , H , Palta , P , Brison , N , Vermeesch , J R , Krjutskov , K , Salumets , A & Kaplinski , L 2018 , ' NIPTmer : rapid k-mer-based software package for detection of fetal aneuploidies ' , Scientific Reports , vol. 8 , 5616 . https://doi.org/10.1038/s41598-018-23589-8Test; 85044938385; 5ea82774-6f62-4996-a083-c87d43b9c83e; http://hdl.handle.net/10138/234563Test; 000429095600025

الإتاحة: http://hdl.handle.net/10138/234563Test