Laura Kasak
9PUBLICATIONS
76CO-AUTHORS
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Publications (9)
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|Mar 04, 2026
MGRN1 is linked to recessive heart and laterality defects: the first genotype-phenotype report in humans.Laura Kasak, Kristiina Rull, Anu Valkna
|Dec 26, 2022
Diverse monogenic subforms of human spermatogenic failure.Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng
|May 10, 2022
Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient management.Laura Kasak, Kristiina Lillepea, Liina Nagirnaja
|Aug 16, 2021
Recurrent Pregnancy Loss and Concealed Long-QT Syndrome.Laura Kasak, Kristiina Rull, Tao Yang
|Dec 09, 2020
NR5A1 c.991-1G > C splice-site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetrance.Maris Laan, Laura Kasak, Kęstutis Timinskas
|Jan 20, 2020
Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives.Laura Kasak, Maris Laan
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Frequent Collaborators
6 joint publications
Maris Laan
3 joint publications
Constantina Bakolitsa
3 joint publications
Zhiqiang Hu
3 joint publications
Lipika R Pal
3 joint publications
Sean D Mooney
3 joint publications
John Moult
3 joint publications
Rita Casadio
3 joint publications
Pier Luigi Martelli
3 joint publications
Olivier Lichtarge
3 joint publications
Panagiotis Katsonis
