Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Lotta L. E. Koskinen"'
Autor:
Manuel A. Rivas, Daniel Graham, Patrick Sulem, Christine Stevens, A. Nicole Desch, Philippe Goyette, Daniel Gudbjartsson, Ingileif Jonsdottir, Unnur Thorsteinsdottir, Frauke Degenhardt, Sören Mucha, Mitja I. Kurki, Dalin Li, Mauro D’Amato, Vito Annese, Severine Vermeire, Rinse K. Weersma, Jonas Halfvarson, Paulina Paavola-Sakki, Maarit Lappalainen, Monkol Lek, Beryl Cummings, Taru Tukiainen, Talin Haritunians, Leena Halme, Lotta L. E. Koskinen, Ashwin N. Ananthakrishnan, Yang Luo, Graham A. Heap, Marijn C. Visschedijk, UK IBD Genetics Consortium, NIDDK IBD Genetics Consortium, Daniel G. MacArthur, Benjamin M. Neale, Tariq Ahmad, Carl A. Anderson, Steven R. Brant, Richard H. Duerr, Mark S. Silverberg, Judy H Cho, Aarno Palotie, Päivi Saavalainen, Kimmo Kontula, Martti Färkkilä, Dermot P. B. McGovern, Andre Franke, Kari Stefansson, John D. Rioux, Ramnik J. Xavier, Mark J. Daly
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-8 (2016)
While hundreds of loci are linked with inflammatory bowel diseases (IBDs), the functional consequences of the associated variants remain unclear. Here, the authors screened in ulcerative colitis (UC) patients’ genomes for protein-truncating variant
Externí odkaz:
https://doaj.org/article/7ec515461747449295bc0f9f7b59f420
Autor:
A. Inkeri Lokki, Tea Kaartokallio, Ville Holmberg, Päivi Onkamo, Lotta L. E. Koskinen, Päivi Saavalainen, Seppo Heinonen, Eero Kajantie, Juha Kere, Katja Kivinen, Anneli Pouta, Pia M. Villa, Leena Hiltunen, Hannele Laivuori, Seppo Meri
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
Preeclampsia (PE) is a common vascular disease of pregnancy with genetic predisposition. Dysregulation of the complement system has been implicated, but molecular mechanisms are incompletely understood. In this study, we determined the potential link
Externí odkaz:
https://doaj.org/article/0c984d3effe643e7adb55a4e699b159b
Autor:
Manuel A. Rivas, Daniel Graham, Patrick Sulem, Christine Stevens, A. Nicole Desch, Philippe Goyette, Daniel Gudbjartsson, Ingileif Jonsdottir, Unnur Thorsteinsdottir, Frauke Degenhardt, Sören Mucha, Mitja I. Kurki, Dalin Li, Mauro D’Amato, Vito Annese, Severine Vermeire, Rinse K. Weersma, Jonas Halfvarson, Paulina Paavola-Sakki, Maarit Lappalainen, Monkol Lek, Beryl Cummings, Taru Tukiainen, Talin Haritunians, Leena Halme, Lotta L. E. Koskinen, Ashwin N. Ananthakrishnan, Yang Luo, Graham A. Heap, Marijn C. Visschedijk, UK IBD Genetics Consortium, NIDDK IBD Genetics Consortium, Daniel G. MacArthur, Benjamin M. Neale, Tariq Ahmad, Carl A. Anderson, Steven R. Brant, Richard H. Duerr, Mark S. Silverberg, Judy H. Cho, Aarno Palotie, Päivi Saavalainen, Kimmo Kontula, Martti Färkkilä, Dermot P. B. McGovern, Andre Franke, Kari Stefansson, John D. Rioux, Ramnik J. Xavier, Mark J. Daly
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-1 (2016)
Nature Communications 7 Article number: 12342 (2016); Published 9 August 2016; Updated 13 September 2016 The HTML version of this Article incorrectly listed the authors of the UK IBD Genetics Consortium and the NIDDK IBD Genetics Consortium individua
Externí odkaz:
https://doaj.org/article/750183ef44f04abe937a2d55611517af
Autor:
Dawit A. Yohannes, Katri Kaukinen, Katri Lindfors, Matti Nykter, Päivi Saavalainen, Aarno Palotie, Juliana X. M. Cerqueira, Kalle Kurppa, Lotta L. E. Koskinen, Elina Kilpeläinen, Anastasia Shcherban, Pilvi Laurikka, Heini Huhtala
Publikováno v:
Journal of Human Genetics
The phenotype of coeliac disease varies considerably for incompletely understood reasons. We investigated whether established coeliac disease susceptibility variants (SNPs) are individually or cumulatively associated with distinct phenotypes. We also
Autor:
Kim Gall, Tero-Pekka Alastalo, Inka Saarinen, Elina Hirvonen, Emma Mårtensson, Joe Jacher, Hatice Duzkale, Päivi Kokkonen, Johanna Sistonen, Juha Koskenvuo, Lotta L. E. Koskinen, Alicia Scocchia, Zöe Powis
Publikováno v:
Molecular Genetics and Metabolism. 132:S233-S234
Autor:
Lotta L. E. Koskinen, Emanuela Izzo, Eija H. Seppälä, Tero-Pekka Alastalo, Kirsi Alakurtti, Kimberly Gall, Akashdeep Singh, Juha Koskenvuo
Publikováno v:
Molecular Genetics and Metabolism. 132:S100-S101
Autor:
Emanuela Izzo, Samuel Myllykangas, Inka Saarinen, Kimberly Gall, Kirsi Alakurtti, Lotta L. E. Koskinen, Tero-Pekka Alastalo, Eija H. Seppälä, Akashdeep Singh, Juha Koskenvuo
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0255933 (2021)
PLoS ONE
PLoS ONE
Epilepsy is one of the most common childhood-onset neurological conditions with a genetic etiology. Genetic diagnosis provides potential for etiologically-based management and treatment. Existing research has focused on early-onset (
Autor:
Kirsi Alakurtti, Eija H. Seppälä, Lotta L. E. Koskinen, Khalida Liaquat, Tero-Pekka Alastalo, Juha Koskenvuo, Akashdeep Singh, Kim Gall, Emmanuela Izzo
Publikováno v:
Molecular Genetics and Metabolism. 132:S59
Autor:
Lotta L. E. Koskinen, Emanuela Izzo, Kirsi Alakurtti, Eija H. Seppälä, Tero-Pekka Alastalo, Kimberly Gall, Juha Koskenvuo
Publikováno v:
Molecular Genetics and Metabolism. 129:S80
Autor:
Jaana Vuopio, Päivi Saavalainen, T. Sakari Jokiranta, Pekka Jousilahti, Richard C. Trembath, Jari Suvilehto, Sari Suomela, Lotta L. E. Koskinen, Karita Haapasalo, Annika Wolin, Jonathan Barker, Juha Kere
Pharyngeal tonsillitis is one of the most common upper respiratory tract infections, and group A streptococcus is the most important bacterial pathogen causing it. While most patients experience tonsillitis only rarely, a subset of patients suffers f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4522fe496b868a781819ee6ca6379a8d
http://hdl.handle.net/10138/248075
http://hdl.handle.net/10138/248075