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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2013 6
2014 1
2015 1
2016 1
2017 2
2018 5
2019 2
2020 3
2021 3
2022 3
2023 2
2024 0

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Reply of the authors.
Malcher A, Kurpisz MK. Malcher A, et al. Fertil Steril. 2014 May;101(5):e32-3. doi: 10.1016/j.fertnstert.2014.02.031. Epub 2014 Mar 26. Fertil Steril. 2014. PMID: 24680365 Free article. No abstract available.
Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure.
Qureshi S, Hardy JJ, Pombar C, Berman AJ, Malcher A, Gingrich T, Hvasta R, Kuong J, Munyoki S, Hwang K, Orwig KE, Ahmed J, Olszewska M, Kurpisz M, Conrad DF, Jaseem Khan M, Yatsenko AN. Qureshi S, et al. Among authors: malcher a. Front Genet. 2023 May 10;14:1134849. doi: 10.3389/fgene.2023.1134849. eCollection 2023. Front Genet. 2023. PMID: 37234866 Free PMC article.
New mutation causing androgen insensitivity syndrome - a case report and review of literature.
Maciejewska-Jeske M, Rojewska-Madziala P, Broda K, Drabek K, Szeliga A, Czyzyk A, Malinger S, Kostrzak A, Podfigurna A, Bala G, Meczekalski B, Malcher A, Kurpisz M. Maciejewska-Jeske M, et al. Among authors: malcher a. Gynecol Endocrinol. 2019 Apr;35(4):294-297. doi: 10.1080/09513590.2018.1529160. Epub 2018 Nov 19. Gynecol Endocrinol. 2019. PMID: 30449224 Review.
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure.
Hardy JJ, Wyrwoll MJ, Mcfadden W, Malcher A, Rotte N, Pollock NC, Munyoki S, Veroli MV, Houston BJ, Xavier MJ, Kasak L, Punab M, Laan M, Kliesch S, Schlegel P, Jaffe T, Hwang K, Vukina J, Brieño-Enríquez MA, Orwig K, Yanowitz J, Buszczak M, Veltman JA, Oud M, Nagirnaja L, Olszewska M, O'Bryan MK, Conrad DF, Kurpisz M, Tüttelmann F, Yatsenko AN; GEMINI Consortium. Hardy JJ, et al. Among authors: malcher a. Hum Genet. 2021 Aug;140(8):1169-1182. doi: 10.1007/s00439-021-02287-y. Epub 2021 May 7. Hum Genet. 2021. PMID: 33963445 Free PMC article.
26 results