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Reproduction (Cambridge, England)|April 22, 2022
A systematic review and standardized clinical validity assessment of genes involved in female reproductive failureLudmila Volozonoka, Anna Miskova, Liene Kornejeva, et al.
Systems Biology in Reproductive Medicine|October 16, 2020
Reducing misdiagnosis caused by maternal cell contamination in genetic testing for early pregnancy lossLudmila Volozonoka, Linda Gailite, Dmitrijs Perminov, et al.
Diagnostics (Basel, Switzerland)|November 26, 2022
Clinical and Genetic Characterisation of Cystic Fibrosis Patients in Latvia: A Twenty-Five-Year ExperienceMadara Auzenbaha, Elina Aleksejeva, Gita Taurina, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|December 11, 2020
The outcomes after transfers of embryos with chromosomal mosaicism: a single reproductive medicine center experience at iVF Riga clinicBaiba Alksere, Ieva Grinfelde, Liene Kornejeva, et al.
Molecular Genetics and Metabolism Reports|September 29, 2021
A novel <i>EDA</i> variant causing X-linked hypohidrotic ectodermal dysplasia: Case reportBaiba Alksere, Liene Kornejeva, Ieva Grinfelde, et al.
Neurology. Genetics|November 16, 2022
Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of LatviaBaiba Lace, Ieva Micule, Viktorija Kenina, et al.
Plos Genetics|March 29, 2014
Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndromeMichael F Wangler, Claudia Gonzaga-Jauregui, Tomasz Gambin, et al.
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