Maris Laan
19PUBLICATIONS
133CO-AUTHORS

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Publications (19)
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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
|Jan 11, 2026
Benchmarking knowledge graph embedding models for the prediction of oligogenic combinations.Inas Bosch, Barbara Gravel, Alexandre Renaux
|Dec 03, 2025
Microdeletion and microduplication syndromes, including recurrent rearrangements at 16p11.2 and 22q11.21, are enriched in unexplained male infertility.Triin Kikas, Avirup Dutta, Rain Inno
|Mar 10, 2025
Significantly increased load of hereditary cancer-linked germline variants in infertile men.Anu Valkna, Anna-Grete Juchnewitsch, Lisanna Põlluaas
|Jan 09, 2025
Introduction to androgenetics: terminology, approaches, and impactful studies across 60 years.Arvand Akbari, Laura Kasak, Maris Laan
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Frequent Collaborators
6 joint publications
Laura Kasak
4 joint publications
Donald F Conrad
4 joint publications
Margus Punab
2 joint publications
Moira K O'Bryan
2 joint publications
Kristian Almstrup
2 joint publications
Alexandre Renaux
2 joint publications
Tom Lenaerts
2 joint publications
Kenneth I Aston
2 joint publications
Kristiina Rull
2 joint publications
Liina Nagirnaja