Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Milda Aleknonytė‐Resch"'
Autor:
Milda Aleknonytė-Resch, Joanne Trinh, Hampton Leonard, Sylvie Delcambre, Elsa Leitão, Dongbing Lai, Semra Smajić, Avi Orr-Urtreger, Avner Thaler, Cornelis Blauwendraat, Arunabh Sharma, Mary B. Makarious, Jonggeol Jeff Kim, Julie Lake, Pegah Rahmati, Sandra Freitag-Wolf, Philip Seibler, Tatiana Foroud, Andrew B. Singleton, The International Parkinson Disease Genomics Consortium, Anne Grünewald, Frank Kaiser, Christine Klein, Michael Krawczak, Astrid Dempfle
Publikováno v:
npj Parkinson's Disease, Vol 9, Iss 1, Pp 1-9 (2023)
Abstract The effects of one genetic factor upon Parkinson’s disease (PD) risk may be modified by other genetic factors. Such gene-gene interaction (G×G) could explain some of the ‘missing heritability’ of PD and the reduced penetrance of known
Externí odkaz:
https://doaj.org/article/eab9e702433b4666b815d44862487080
Autor:
Johanna Geritz, Julius Welzel, Clint Hansen, Corina Maetzler, Markus A. Hobert, Morad Elshehabi, Henrike Knacke, Milda Aleknonytė-Resch, Jennifer Kudelka, Nico Bunzeck, Walter Maetzler
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
IntroductionLinks between cognition and walking performance in patients with Parkinson’s disease (PD), which both decline with disease progression, are well known. There is lack of knowledge regarding the predictive value of cognition for changes i
Externí odkaz:
https://doaj.org/article/702174b9f1364870a34dcc1ae27d0431
Publikováno v:
European Journal of Neurology. 30:749-761
Approximately 30% of epilepsy patients develop a drug-refractory epilepsy, that is, seizures cannot be controlled with antiepileptic drugs. Surgery has been evaluated as an effective but costly form of treatment. The aim of this systematic review is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82615e00084eba19aa3ffa9e13c09743
https://doi.org/10.1111/ene.15632
https://doi.org/10.1111/ene.15632
Autor:
Astrid Dempfle, Sandra Freitag-Wolf, Silke Szymczak, Michael Krawczak, Milda Aleknonytė-Resch
Publikováno v:
Human Genetics
Case-only (CO) studies are a powerful means to uncover gene-environment (G × E) interactions for complex human diseases. Moreover, such studies may in principle also draw upon genotype imputation to increase statistical power even further. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7414a748e5a9fa8cc6ef1b823d6caa77
https://doi.org/10.21203/rs.3.rs-274423/v1
https://doi.org/10.21203/rs.3.rs-274423/v1
Autor:
Milda Aleknonytė-Resch, Stefan Schreiber, Astrid Dempfle, Sandra Freitag-Wolf, Michael Krawczak
Publikováno v:
Scandinavian journal of gastroenterology. 55(8)
Gene-gene interactions (G × G) potentially play a role in the etiology of complex human diseases, including inflammatory bowel disease (IBD), and may partially explain their 'missing heritability'.Using the largest genotype dataset available for IBD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee4707da2024a0c509652ec00d0e4acc
https://pubmed.ncbi.nlm.nih.gov/32649238
https://pubmed.ncbi.nlm.nih.gov/32649238