Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Galuh Astuti"'
Autor:
Annechien E.G. Haarman, MD, Caroline C.W. Klaver, MD, PhD, Milly S. Tedja, MD, Susanne Roosing, PhD, Galuh Astuti, MSc, Christian Gilissen, PhD, Lies H. Hoefsloot, MD, PhD, Marianne van Tienhoven, BSc, Tom Brands, Ing, Frank J. Magielsen, Ing, Bert H.J.F.M.M. Eussen, Ing, Annelies de Klein, PhD, Erwin Brosens, PhD, Virginie J.M. Verhoeven, MD, PhD
Publikováno v:
Ophthalmology Science, Vol 3, Iss 4, Pp 100303- (2023)
Purpose: Myopia (nearsightedness) is a condition in which a refractive error (RE) affects vision. Although common variants explain part of the genetic predisposition (18%), most of the estimated 70% heritability is missing. Here, we investigate the c
Externí odkaz:
https://doaj.org/article/1d1f755f75e7485baa103613d1e9e1b0
Autor:
Isabel Quintana, Mariona Terradas, Pilar Mur, Iris B.A.W. te Paske, Sophia Peters, Isabel Spier, Verena Steinke-Lange, Claudia Maestro, David Torrents, Montserrat Puiggròs, Romina Royo, Raul Tonda, Genís Parra, Davide Piscia, Sergi Beltrán, Matilde Navarro, Virginia Piñol, Joan Brunet, Noemi Gonzalez-Abuin, Gemma Aiza, Anna Sommer, Yasmijn van Herwaarden, Galuh Astuti, Elke Holinski-Feder, Nicoline Hoogerbrugge, Richarda M. de Voer, Stefan Aretz, Gabriel Capellá, Laura Valle
Publikováno v:
Genes and Diseases, Vol 10, Iss 3, Pp 753-757 (2023)
Externí odkaz:
https://doaj.org/article/6d5ba9489029433d87b24a830388dc13
Autor:
Rebekkah J. Hitti-Malin, Daan M. Panneman, Zelia Corradi, Erica G. M. Boonen, Galuh Astuti, Claire-Marie Dhaenens, Heidi Stöhr, Bernhard H. F. Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Sandro Banfi, Tamar Ben-Yosef, Damjan Glavač, G. Jane Farrar, Carmen Ayuso, Petra Liskova, Lubica Dudakova, Marie Vajter, Monika Ołdak, Jacek P. Szaflik, Anna Matynia, Michael B. Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfride De Baere, Carel B. Hoyng, Catherina H. Z. Li, Caroline C. W. Klaver, Chris F. Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L. Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeina, Gita Taurina, Andrea L. Vincent, Lisa Roberts, Raj Ramesar, Giovanna Sartor, Elena Luppi, Susan M. Downes, L. Ingeborgh van den Born, Terri L. McLaren, John N. De Roach, Tina M. Lamey, Jennifer A. Thompson, Fred K. Chen, Anna M. Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J. Bolz, Hülya Kayserili, Susanne Roosing, Frans P. M. Cremers
Publikováno v:
Biomolecules, Vol 14, Iss 3, p 367 (2024)
Inherited macular dystrophies (iMDs) are a group of genetic disorders, which affect the central region of the retina. To investigate the genetic basis of iMDs, we used single-molecule Molecular Inversion Probes to sequence 105 maculopathy-associated
Externí odkaz:
https://doaj.org/article/a59ac914048b4e7daf70faf03534c762
Autor:
Timo A Kumpula, Sandra Vorimo, Taneli T Mattila, Luke O'Gorman, Galuh Astuti, Anna Tervasmäki, Susanna Koivuluoma, Tiina M Mattila, Mervi Grip, Robert Winqvist, Outi Kuismin, Jukka Moilanen, Alexander Hoischen, Christian Gilissen, Tuomo Mantere, Katri Pylkäs
Publikováno v:
PLoS Genetics, Vol 19, Iss 8, p e1010889 (2023)
Copy number variants (CNVs) are a major source of genetic variation and can disrupt genes or affect gene dosage. They are known to be causal or underlie predisposition to various diseases. However, the role of CNVs in inherited breast cancer suscepti
Externí odkaz:
https://doaj.org/article/39bcaeff36374f21a232d35722e005e7
Autor:
Anita de Breuk, Yara T. E. Lechanteur, Galuh Astuti, Jordi Corominas Galbany, Caroline C. W. Klaver, Carel B. Hoyng, Anneke I. den Hollander
Publikováno v:
Clinical Genetics, 102, 414-423
Clinical Genetics, 102(5), 414-423. Wiley-Blackwell Publishing Ltd
Clinical Genetics, 102, 5, pp. 414-423
Clinical Genetics, 102(5), 414-423. Wiley-Blackwell Publishing Ltd
Clinical Genetics, 102, 5, pp. 414-423
Contains fulltext : 288257.pdf (Publisher’s version ) (Open Access) Early onset drusen maculopathy (EODM) can lead to advanced macular degeneration at a young age, affecting quality of life. However, the genetic causes of EODM are not well studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f628d6f7591df7c809b1fce1c11bd9c3
http://www.scopus.com/inward/record.url?scp=85137974462&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85137974462&partnerID=8YFLogxK
Autor:
Caspar I. van der Made, Annet Simons, Janneke Schuurs-Hoeijmakers, Guus van den Heuvel, Tuomo Mantere, Simone Kersten, Rosanne C. van Deuren, Marloes Steehouwer, Simon V. van Reijmersdal, Martin Jaeger, Tom Hofste, Galuh Astuti, Jordi Corominas Galbany, Vyne van der Schoot, Hans van der Hoeven, Wanda Hagmolen of ten Have, Eva Klijn, Catrien van den Meer, Jeroen Fiddelaers, Quirijn de Mast, Chantal P. Bleeker-Rovers, Leo A. B. Joosten, Helger G. Yntema, Christian Gilissen, Marcel Nelen, Jos W. M. van der Meer, Han G. Brunner, Mihai G. Netea, Frank L. van de Veerdonk, Alexander Hoischen
Publikováno v:
Jama : Journal of the American Medical Association, 324, 7, pp. 663-673
Jama : Journal of the American Medical Association, 324, 663-673
JAMA-Journal of the American Medical Association, 324(7), 663-673. American Medical Association
JAMA
Jama : Journal of the American Medical Association, 324, 663-673
JAMA-Journal of the American Medical Association, 324(7), 663-673. American Medical Association
JAMA
Severe coronavirus disease 2019 (COVID-19) can occur in younger, predominantly male, patients without preexisting medical conditions. Some individuals may have primary immunodeficiencies that predispose to severe infections caused by severe acute res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::200155b69006dec2e09eb1bfe979005f
https://hdl.handle.net/2066/222168
https://hdl.handle.net/2066/222168