Archiwum Publications - Institute of Human Genetics Polish Academy of Sciences

Whole-genome sequencing identifies a potentially causative homozygous splicing variant in RAD54 like in non-obstructive azoospermia.

Askari RE, Malcher A, Sadeghzadeh S, Ibrahim R, Pastuszak K, Srivastava A, Kalantar SM, Vahidi S, Ghasemi N, Kurpisz M.

International Journal of Reproductive Biomedicine; 2026, 24(7): 617-626; doi: 10.18502/ijrm.v24i7.21585

IF-1,4 MNiSW-70

The association between the MCM6 LCT-13910C>T variant and bone mineral density in patients with inflammatory bowel disease.

Picher A, Ratajczak-Pawłowska AE, Skrzypczak-Zielińska M, Dobrowolska A, Krela-Kaźmierczak I.

Front Genet. 2026 Jul 24;17:1822823. doi: 10.3389/fgene.2026.1822823

IF-3,0 MNiSW-100

Are head and neck versus abdominal paragangliomas driven by different single nucleotide events?

Kotlarz K, Ziemnicka K, Budny B, Mielczarek M, Liu J, Wrotkowska E, Kaznowski J, Suchocki T, Kałużny J, Wierzbicka M, Dobosz P, Ruchała M, Szyda J.

J Appl Genet. 2026 Sep;67(3):661-667. doi: 10.1007/s13353-025-00994-0.

IF-2,1 MNiSW-140

Advanced Biological Therapies: Principles, Mechanisms and Medical Applications

Brozek R, Lorenz A, Dorocka-Bobkowska B, Kurpisz M.

J Clin Med (MDPI) 2026; 15: 6523 (25 stron) https://doi.org/10.3390/jcm15176523

IF-3,3 MNiSW-140

Differential Regulation of Inflammatory and Pro-Resolving Lipid Mediators in Chronic Coronary Syndrome Across Cardiometabolic Phenotypes.

Krasińska B, Urbanowicz T, Gabriel K, Kurpisz M, Grywalska E, Mertowska P, Spasenenko I, Raffa GM, Manca P, Pisano C, Olasińska-Wiśniewska A, Filipiak KJ, Kowalewski M, Mertowski S, Suwalski P, Krasiński Z, Tykarski A.

Int J Mol Sci (MDPI) 2026; 27(15): 6667 (24 strony) doi: 10.3390/ijms27156667

IF-5,6 MNiSW-140

Selective dysfunction of E-series inflammation resolution in diabetes: E-series resolution dysfunction index as a novel biomarker in chronic coronary syndrome.

Krasińska B, Urbanowicz T, Grywalska E, Kurpisz M, Tykarski A.

Pol Arch Intern Med. 2026; 136(7-8): 17343. (6 stron) doi: 10.20452/pamw.17343

IF-4,8 MNiSW-200

Genomic context of mutations in MIR142 in blood cancers: summary and integrative analysis.

Wegorek W, Tire A, Kuznicki D, Richter J, Giefing M, Klapper W, Kozlowski P, Galka-Marciniak P.

Cell Mol Biol Lett, 2026; 31(1): 127(14 stron) doi: 10.1186/s11658-026-00933-9.

IF-12,2 MNiSW-100

Whole-Genome Sequencing Identifies Potentially Causative Variants in SOX30, AKAP4, and RNF220 in Non-Obstructive Azoospermia.

Ebrahimi Askari R, Malcher A, Sefid F, Sadeghzadeh S, Ibrahim R, Pastuszak K, Srivastava A, Mehdi Kalantar S, Vahidi S, Ghasemi N, Kurpisz M.

Int J Mol Sci, 2026; 27: 7230 (11 stron) https://doi.org/10.3390/ijms27167230

IF-5,6 MNiSW-140

Multi-omic screening identifies RBMXL3 as a primate-specific RNA-binding protein and candidate regulator of RNA metabolism in human spermatogenesis.

Barszcz AJ, Tutak K, Zyprych-Walczak J, Dassi E, Ilaslan E, Dąbrowska M, Malcher A, Olszewska M, Cysewski D, Nadel A, Kolanowski T, Madeja ZE, Hrab M, Yatsenko AN, Kurpisz M, Warkocki Z, Rozwadowska N.

Cell Mol Biol Lett, 2026; 31(1):122 (30 stron) doi: 10.1186/s11658-026-00959-z.

IF-12,2 MNiSW-100

The Growth Supporting Role of ZDHHC11 Is Linked to the MEF2B-BCL6 Regulatory Circuit in Burkitt Lymphoma.

Lotteke J, Ziel-Swier LJYM, Rassek K, Liu Y, Seitz A, Koerts J, de Jong D, Rutgers B, Kompaniiets A, Przybył J, Chamuleau MED, van den Berg A, Dzikiewicz-Krawczyk A, Kluiver J.

Int J Cancer, 2026; 159(6): 1535-1545. (11 stron) doi: 10.1002/ijc.70506

IF-4,9 MNiSW-140

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