Publications by authors named "Kristjan Pomm"

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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, Kristjan Pomm, Stanislav Tjagur

Hum Reprod· December 2025

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Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertility.
Tihana Marić, Helen Castillo-Madeen, Monika Logara Klarić, Antun Barišić, Lovro Trgovec-Greif, Kristjan Pomm

Hum Mol Genet· March 2025

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Significantly increased load of hereditary cancer-linked germline variants in infertile men.
Anu Valkna, Anna-Grete Juchnewitsch, Lisanna Põlluaas, Kristiina Lillepea, Stanislav Tjagur, Kristjan Pomm

Hum Reprod Open· February 2025

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Toward clinical exomes in diagnostics and management of male infertility.
Kristiina Lillepea, Anna-Grete Juchnewitsch, Laura Kasak, Anu Valkna, Avirup Dutta, Kristjan Pomm

Am J Hum Genet· May 2024

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Undiagnosed RASopathies in infertile men.
Anna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, Erik Tamp, Anu Valkna

Front Endocrinol (Lausanne)· April 2024

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Microdeletions and microduplications linked to severe congenital disorders in infertile men.
Triin Kikas, Anna Maria Punab, Laura Kasak, Olev Poolamets, Vladimir Vihljajev, Kristjan Pomm

Sci Rep· January 2023

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Provokes Seminal Inflammation among Infertile Males.
Stanislav Tjagur, Reet Mändar, Olev Poolamets, Kristjan Pomm, Margus Punab

Int J Mol Sci· December 2021

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A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans.
Pille Hallast, Laura Kibena, Margus Punab, Elena Arciero, Siiri Rootsi, Kristjan Pomm

Elife· March 2021

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