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Mutation Research. Reviews in Mutation Research|June 11, 2022
Postzygotic mutations and where to find them - Recent advances and future implications in the field of non-neoplastic somatic mosaicismKrystyna Wasilewska, Tomasz Gambin, Małgorzata Rydzanicz, et al.
Molecular Syndromology|April 14, 2022
Aicardi-Goutières Syndrome due to a <i>SAMHD1</i> Mutation Presenting with Deep White Matter CystsBarbara Oleksy, Hanna Mierzewska, Jolanta Tryfon, et al.
The American Journal on Addictions|May 31, 2017
An association between genetic variation in the glutamatergic system and suicide attempts in alcohol-dependent individualsSylwia Fudalej, Anna Klimkiewicz, Anna Mach, et al.
Plos One|September 30, 2014
Inverse association between obesity predisposing FTO genotype and completed suicideIzabela Chojnicka, Sylwia Fudalej, Anna Walczak, et al.
Journal of the Peripheral Nervous System : JPNS|November 19, 2014
Exome sequencing reveals mutations in MFN2 and GDAP1 in severe Charcot-Marie-Tooth diseaseAnna Kostera-Pruszczyk, Joanna Kosinska, Agnieszka Pollak, et al.
Neuropsychobiology|December 3, 2015
Association between FKBP5 Functional Polymorphisms and Completed SuicideSylwia Fudalej, Maciej Kopera, Dorota Wołyńczyk-Gmaj, et al.
Psychoneuroendocrinology|December 27, 2016
OXTR polymorphism in depression and completed suicide-A study on a large population sampleKrystyna Wasilewska, Aleksandra Pawlak, Grażyna Kostrzewa, et al.
Journal of Studies on Alcohol and Drugs|March 22, 2016
DISC1 as a Possible Genetic Contribution to Opioid Dependence in a Polish SampleSylwia Fudalej, Andrzej Jakubczyk, Maciej Kopera, et al.
Clinical Genetics|December 15, 2018
A study in a Polish ataxia cohort indicates genetic heterogeneity and points to MTCL1 as a novel candidate geneMagdalena Krygier, Mariusz Kwarciany, Krystyna Wasilewska, et al.
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