Microdeletion and microduplication syndromes, including recurrent rearrangements at 16p11.2 and 22q11.21, are enriched in unexplained male infertility

Authors

Triin Kikas (ORCID: https://orcid.org/0000-0003-4698-4570)
Avirup Dutta (ORCID: https://orcid.org/0000-0002-3595-6198)
Rain Inno (ORCID: https://orcid.org/0000-0002-9205-3884)
Hanno Roomere (ORCID: https://orcid.org/0009-0002-7085-8435)
Kristjan Pomm (ORCID: https://orcid.org/0000-0002-3603-5446)
Margus Punab (ORCID: https://orcid.org/0000-0001-9601-6311)
Stanislav Tjagur (ORCID: https://orcid.org/0000-0001-9679-990X)
Maris Laan (ORCID: https://orcid.org/0000-0002-8519-243X)
Olev Poolamets

Institutions

Tartu University Hospital (EE)
University of Tartu (EE)

Publication Details

Journal: Human Reproduction
Published: 2025-11-14
DOI: https://doi.org/10.1093/humrep/deaf231
Primary Topic: Genomic variations and chromosomal abnormalities
Type: article
Field-Weighted Citation Impact: 0.00

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article

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, Hanno Roomere et al.

Nov 14, 2025

Human Reproduction

Genomic variations and chromosomal abnormalities

article

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, Hanno Roomere, Kristjan Pomm, Margus Punab, Stanislav Tjagur, Maris Laan, Olev Poolamets

November 14, 2025article en

Abstract

No abstract available for this paper.

Human ReproductionVol. 41(2)

Tartu University Hospital (EE), University of Tartu (EE)

Openalex Percentile: Top 60%

Genomic variations and chromosomal abnormalities

DOI Source OpenAlex

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