Kết quả tìm kiếm - Triin Laisk
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Genome-wide association study identifies five risk loci for pernicious anemia Bằng Triin Laisk, Maarja Lepamets, Mariann Koel, Erik Abner, Andres Metspalu, Mari Nelis, Lili Milani, Tõnu Esko, Reedik Mägi
Được phát hành 2021Artigo -
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Research Resource: Interactome of Human Embryo Implantation: Identification of Gene Expression Pathways, Regulation, and Integrated Regulatory Networks Bằng Signe Altmäe, Jüri Reimand, Outi Hovatta, Pu Zhang, Juha Kere, Triin Laisk, Merli Saare, Maire Peters, Jaak Vilo, Anneli Stavreus‐Evers, Andres Salumets
Được phát hành 2011Artigo -
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Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome Bằng Jaakko Tyrmi, Riikka K. Arffman, Natàlia Pujol‐Gualdo, Venla Kurra, Laure Morin‐Papunen, Eeva Sliz, Terhi Piltonen, Triin Laisk, Johannes Kettunen, Hannele Laivuori
Được phát hành 2021Revisão -
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GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer Bằng Mariann Koel, Urmo Võsa, Maarja Jõeloo, Kristi Läll, Natàlia Pujol‐Gualdo, Hannele Laivuori, Susanna Lemmelä, Mark J. Daly, Priit Palta, Reedik Mägi, Triin Laisk
Được phát hành 2023Artigo -
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Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis Bằng Eeva Sliz, Laura Huilaja, Anu Pasanen, Triin Laisk, Ene Reimann, Reedik Mägi, Katariina Hannula-Jouppi, Sirkku Peltonen, Teea Salmi, Leena Koulu, Kaisa Tasanen, Johannes Kettunen
Được phát hành 2021Revisão -
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High-Throughput Sequencing Approach Uncovers the miRNome of Peritoneal Endometriotic Lesions and Adjacent Healthy Tissues Bằng Merli Saare, Kadri Rekker, Triin Laisk, Deniss Sõritsa, Anne Mari Roost, Jaak Simm, Agne Velthut‐Meikas, Külli Samuel, Tauno Metsalu, Helle Karro, Andrei Sõritsa, Andres Salumets, Maire Peters
Được phát hành 2014Artigo -
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DNA methylation changes in endometrium and correlation with gene expression during the transition from pre-receptive to receptive phase Bằng Viktorija Kukushkina, Vijayachitra Modhukur, Marina Suhorutšenko, Maire Peters, Reedik Mägi, Nilüfer Rahmioğlu, Agne Velthut‐Meikas, Signe Altmäe, Francisco J. Esteban, Jaak Vilo, Krina T. Zondervan, Andres Salumets, Triin Laisk-Podar
Được phát hành 2017Artigo -
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Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse Bằng Natàlia Pujol‐Gualdo, Kristi Läll, Maarja Lepamets, Andres Metspalu, Mari Nelis, Lili Milani, Tõnu Esko, Georgi Hudjashov, Henna‐Riikka Rossi, Riikka K. Arffman, Terhi Piltonen, Reedik Mägi, Triin Laisk
Được phát hành 2022Revisão -
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Proteome-Wide Mendelian Randomization Identifies Causal Links Between Blood Proteins and Acute Pancreatitis Bằng Jérôme Bourgault, Erik Abner, Hasanga D. Manikpurage, Natàlia Pujol‐Gualdo, Triin Laisk, Émilie Gobeil, Éloi Gagnon, Arnaud Girard, Patricia L. Mitchell, Sébastien Thériault, Tõnu Esko, Patrick Mathieu, Benoît J. Arsenault
Được phát hành 2023Revisão -
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Endometrial receptivity revisited: endometrial transcriptome adjusted for tissue cellular heterogeneity Bằng Marina Suhorutshenko, Viktorija Kukushkina, Agne Velthut‐Meikas, Signe Altmäe, Maire Peters, Reedik Mägi, Kaarel Krjutškov, Mariann Koel, Francisco M. Codoñer, Juan F. Martínez‐Blanch, Felipe Vilella, Carlos Simón, Andres Salumets, Triin Laisk
Được phát hành 2018Artigo -
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Variability of genome-wide DNA methylation and mRNA expression profiles in reproductive and endocrine disease related tissues Bằng Nilüfer Rahmioğlu, Alexander Drong, Helen Lockstone, Thomas T. Tapmeier, Karin Hellner, Merli Saare, Triin Laisk-Podar, Christine Dew, Emily Tough, Geoffrey C. Nicholson, Maire Peters, Andrew P. Morris, Cecilia M. Lindgren, Christian M. Becker, Krina T. Zondervan
Được phát hành 2017Artigo -
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Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency Bằng Ilpo Huhtaniemi, Outi Hovatta, Antonio La Marca, Gabriel Livera, Danielle Monniaux, Luca Persani, Abdelkader Heddar, Katarzyna Jarząbek, Triin Laisk-Podar, Andres Salumets, Juha S. Tapanainen, Reiner A. Veitia, Jenny A. Visser, Peter Wieacker, Sławomir Wołczyński, Micheline Misrahi
Được phát hành 2018Revisão -
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Meta-signature of human endometrial receptivity: a meta-analysis and validation study of transcriptomic biomarkers Bằng Signe Altmäe, Mariann Koel, Urmo Võsa, Priit Adler, Marina Suhorutšenko, Triin Laisk-Podar, Viktorija Kukushkina, Merli Saare, Agne Velthut‐Meikas, Kaarel Krjutškov, Lusine Aghajanova, Parameswaran Grace Lalitkumar, Kristina Gemzell‐Danielsson, Linda C. Giudice, Carlos Simón, Andres Salumets
Được phát hành 2017Revisão -
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GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology Bằng Jonas Bovijn, Leigh Jackson, Jenny C. Censin, Chia‐Yen Chen, Triin Laisk, Samantha Laber, Teresa Ferreira, Sara L. Pulit, Craig A. Glastonbury, Jordan W. Smoller, James Harrison, Katherine S. Ruth, Robin N. Beaumont, Samuel E. Jones, Jessica Tyrrell, Andrew R. Wood, Michael N. Weedon, Reedik Mägi, Benjamin M. Neale, Cecilia M. Lindgren, Anna Murray, Michael V. Holmes
Được phát hành 2018Artigo -
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Polygenic prediction of preeclampsia and gestational hypertension Bằng Michael C. Honigberg, Buu Truong, Raiyan R. Khan, Brenda Xiao, Laxmi Bhatta, Ha My T. Vy, Rafael F. Guerrero, Art Schuermans, Margaret Sunitha Selvaraj, Aniruddh P. Patel, Satoshi Koyama, So Mi Jemma Cho, Shamsudheen Karuthedath Vellarikkal, Mark Trinder, Sarah Urbut, Kathryn J. Gray, Ben Brumpton, Snehal Patil, Sebastian Zöllner, Mariah C. Antopia, Richa Saxena, Girish N. Nadkarni, Ron Do, Qi Yan, Itsik Pe’er, Shefali S. Verma, Rajat M. Gupta, David M. Haas, Hilary C. Martin, David A. van Heel, Triin Laisk, Pradeep Natarajan
Được phát hành 2023Revisão -
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Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria Bằng Felix R. Day, Tugce Karaderi, Michelle R. Jones, Cindy Meun, Chunyan He, Alex Drong, Peter Kraft, Nan Lin, Hongyan Huang, Linda Broer, Reedik Mägi, Richa Saxena, Triin Laisk, Margrit Urbanek, M. Geoffrey Hayes, Guðmar Þorleifsson, Juan Fernández‐Tajes, Anubha Mahajan, Benjamin H. Mullin, Bronwyn Stuckey, Timothy D. Spector, Scott G. Wilson, Mark O. Goodarzi, Lea K. Davis, Barbara Obermayer‐Pietsch, André G. Uitterlinden, Verneri Anttila, Benjamin M. Neale, Marjo‐Riitta Järvelin, Bart C.J.M. Fauser, Irina Kowalska, Jenny A. Visser, Marianne Andersen, Ken K. Ong, Elisabet Stener‐Victorin, David A. Ehrmann, Richard S. Legro, Andres Salumets, Mark I. McCarthy, Laure Morin‐Papunen, Unnur Þorsteinsdóttir, Kāri Stefánsson, Unnur Styrkársdóttir, John R. B. Perry, Andrea Dunaif, Joop S.E. Laven, Steve Franks, Cecilia M. Lindgren, Corrine K. Welt
Được phát hành 2018Revisão
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Các môn học liên quan
Biology
Gene
Genetics
Medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Bioinformatics
Internal medicine
Computational biology
Endocrinology
Genetic association
Pregnancy
Biobank
Population
Disease
Gene expression
Allele
Environmental health
Insulin resistance
Pathology
Polycystic ovary
Endometrium
Phenotype
Diabetes mellitus
Genome
Infertility
Locus (genetics)
Obesity
1000 Genomes Project