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Human Genetics|January 20, 2020
Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectivesLaura Kasak, Maris LaanBritish Medical Bulletin|November 10, 2021
Translational aspects of novel findings in genetics of male infertility-status quo 2021Maris Laan, Laura Kasak, Margus PunabPlacenta|March 5, 2021
Current knowledge on genetic variants shaping placental transcriptome and their link to gestational and postnatal healthTriin Kikas, Maris Laan, Laura KasakAndrology|January 9, 2025
Introduction to androgenetics: terminology, approaches, and impactful studies across 60 yearsArvand Akbari, Laura Kasak, Maris LaanScientific Reports|March 28, 2017
Copy number variation profile in the placental and parental genomes of recurrent pregnancy loss familiesLaura Kasak, Kristiina Rull, Siim Sõber, et al.Journal of Medical Genetics|March 4, 2026
<i>MGRN1</i> is linked to recessive heart and laterality defects: the first genotype-phenotype report in humansLaura Kasak, Kristiina Rull, Anu Valkna, et al.Scientific Reports|February 11, 2015
Extensive load of somatic CNVs in the human placentaLaura Kasak, Kristiina Rull, Pille Vaas, et al.Journal of the American Heart Association|August 16, 2021
Recurrent Pregnancy Loss and Concealed Long-QT SyndromeLaura Kasak, Kristiina Rull, Tao Yang, et al.Clinical Endocrinology|December 9, 2020
NR5A1 c.991-1G > C splice-site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetranceMaris Laan, Laura Kasak, Kęstutis Timinskas, et al.Human Mutation|May 16, 2014
Structural genomic variation as risk factor for idiopathic recurrent miscarriageLiina Nagirnaja, Priit Palta, Laura Kasak, et al.Pageof 2