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Disclosure of Genetic Risk Revealed in a Research Study
Castellanos, Angela, Phimister, Elizabeth G, Stefánsson, Kári, Clayton, Ellen W
Published in The New England journal of medicine (20.02.2020)
Published in The New England journal of medicine (20.02.2020)
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Informed Consent and Subject Motivation to Participate in a Large, Population-Based Genomics Study: The Marshfield Clinic Personalized Medicine Research Project
McCarty, Catherine A., Nair, Anuradha, Austin, Diane M., Giampietro, Philip F.
Published in Community genetics (01.01.2007)
Published in Community genetics (01.01.2007)
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Complement C3 Associates With Incidence of Diabetes, but No Evidence of a Causal Relationship
Borné, Yan, Muhammad, Iram Faqir, Lorés-Motta, Laura, Hedblad, Bo, Nilsson, Peter M, Melander, Olle, de Jong, Eiko K, Blom, Anna M, den Hollander, Anneke I, Engström, Gunnar
Published in The journal of clinical endocrinology and metabolism (01.12.2017)
Published in The journal of clinical endocrinology and metabolism (01.12.2017)
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Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland
Clark, Jeremy S. C., van de Wetering, Thierry, Marciniak, Błażej, Żądzińska, Elżbieta, Ciechanowicz, Andrzej, Kaczmarczyk, Mariusz, Boroń, Agnieszka, Rydzewska, Kamila, Posiadło, Konrad, Strapagiel, Dominik
Published in Scientific reports (07.11.2022)
Published in Scientific reports (07.11.2022)
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Overinterpretation of high throughput sequencing data in medical genetics: first evidence against TMPRSS3/GJB2 digenic inheritance of hearing loss
Ołdak, Monika, Lechowicz, Urszula, Pollak, Agnieszka, Oziębło, Dominika, Skarżyński, Henryk
Published in Journal of translational medicine (14.08.2019)
Published in Journal of translational medicine (14.08.2019)
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Identification of Siglec-1 null individuals infected with HIV-1
Martinez-Picado, Javier, McLaren, Paul J., Erkizia, Itziar, Martin, Maureen P., Benet, Susana, Rotger, Margalida, Dalmau, Judith, Ouchi, Dan, Wolinsky, Steven M., Penugonda, Sudhir, Günthard, Huldrych F., Fellay, Jacques, Carrington, Mary, Izquierdo-Useros, Nuria, Telenti, Amalio
Published in Nature communications (11.08.2016)
Published in Nature communications (11.08.2016)
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Exosomal MicroRNAs: Biomarkers of moyamoya disease and involvement in vascular cytoskeleton reconstruction
Wang, Mengjie, Zhang, Bin, Jin, Feng, Li, Genhua, Cui, Changmeng, Feng, Song
Published in Heliyon (15.06.2024)
Published in Heliyon (15.06.2024)
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Genetic and environmental risk factors for extramacular drusen
Altay, Lebriz, Subiras, Xavier, Lorés de Motta, Laura, Schick, Tina, Berghold, Aileen, Hoyng, Carel B, den Hollander, Anneke I, Fauser, Sascha, Sadda, Srinivas R, Liakopoulos, Sandra
Published in Molecular vision (04.10.2020)
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Published in Molecular vision (04.10.2020)
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Clinical Characteristics of Familial and Sporadic Age-Related Macular Degeneration: Differences and Similarities
Saksens, Nicole T. M., Kersten, Eveline, Groenewoud, Joannes M. M., van Grinsven, Mark J. J. P., van de Ven, Johannes P. H., Sánchez, Clara I., Schick, Tina, Fauser, Sascha, den Hollander, Anneke I., Hoyng, Carel B., Boon, Camiel J. F.
Published in Investigative ophthalmology & visual science (09.10.2014)
Published in Investigative ophthalmology & visual science (09.10.2014)
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