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Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers—Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR): Molecular Cytogenetic Analysis.
Published in:
International Journal of Molecular Sciences, 2020, v. 21, n. 12, p. 4559, doi. 10.3390/ijms21124559
By:
- Olszewska, Marta;
- Stokowy, Tomasz;
- Pollock, Nijole;
- Huleyuk, Nataliya;
- Georgiadis, Andrew;
- Yatsenko, Svetlana;
- Zastavna, Danuta;
- Yatsenko, Alexander N.;
- Kurpisz, Maciej
Publication type:
Article
UBE2B mRNA alterations are associated with severe oligozoospermia in infertile men.
Published in:
Molecular Human Reproduction, 2013, v. 19, n. 6, p. 388, doi. 10.1093/molehr/gat008
By:
- Yatsenko, Alexander N.;
- Georgiadis, Andrew P.;
- Murthy, Lata J.;
- Lamb, Dolores J.;
- Matzuk, Martin M.
Publication type:
Article
Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile men.
Published in:
Molecular Human Reproduction, 2012, v. 18, n. 1, p. 14, doi. 10.1093/molehr/gar057
By:
- Yatsenko, Alexander N.;
- O'Neil, Derek S.;
- Roy, Angshumoy;
- Arias-Mendoza, Paola A.;
- Chen, Ruihong;
- Murthy, Lata J.;
- Lamb, Dolores J.;
- Matzuk, Martin M.
Publication type:
Article
Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.
Published in:
American Journal of Medical Genetics. Part A, 2017, v. 173, n. 1, p. 221, doi. 10.1002/ajmg.a.37981
By:
- Tas, Emir;
- Sebastian, Jessica;
- Madan‐Khetarpal, Suneeta;
- Sweet, Philip;
- Yatsenko, Alexander N.;
- Pollock, Nijole;
- Rajkovic, Aleksandar;
- Schneck, Francis X.;
- Yatsenko, Svetlana A.;
- Witchel, Selma Feldman
Publication type:
Article
Mendelian genetics of male infertility.
Published in:
Annals of the New York Academy of Sciences, 2010, v. 1214, n. 1, p. E1, doi. 10.1111/j.1749-6632.2010.05917.x
By:
- Hwang, Kathleen;
- Yatsenko, Alexander N.;
- Jorgez, Carolina J.;
- Mukherjee, Sarmistha;
- Nalam, Roopa Lata;
- Matzuk, Martin M.;
- Lamb, Dolores J.
Publication type:
Article
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient.
Published in:
Scientific Reports, 2015, v. 5, n. 1, p. 17408, doi. 10.1038/srep17408
By:
- Olszewska, Marta;
- Wanowska, Elzbieta;
- Kishore, Archana;
- Huleyuk, Nataliya;
- Georgiadis, Andrew P.;
- Yatsenko, Alexander N.;
- Mikula, Mariya;
- Zastavna, Danuta;
- Wiland, Ewa;
- Kurpisz, Maciej
Publication type:
Article
In vivo modeling of metastatic human high-grade serous ovarian cancer in mice.
Published in:
PLoS Genetics, 2020, v. 16, n. 6, p. 1, doi. 10.1371/journal.pgen.1008808
By:
- Kim, Olga;
- Park, Eun Young;
- Klinkebiel, David L.;
- Pack, Svetlana D.;
- Shin, Yong-Hyun;
- Abdullaev, Zied;
- Emerson, Robert E.;
- Coffey, Donna M.;
- Kwon, Sun Young;
- Creighton, Chad J.;
- Kwon, Sanghoon;
- Chang, Edmund C.;
- Chiang, Theodore;
- Yatsenko, Alexander N.;
- Chien, Jeremy;
- Cheon, Dong-Joo;
- Yang-Hartwich, Yang;
- Nakshatri, Harikrishna;
- Nephew, Kenneth P.;
- Behringer, Richard R.
Publication type:
Article
Effects of Tcte1 knockout on energy chain transportation and spermatogenesis: implications for male infertility.
Published in:
Human Reproduction Open, 2024, v. 2024, n. 2, p. 1, doi. 10.1093/hropen/hoae020
By:
- Olszewska, Marta;
- Malcher, Agnieszka;
- Stokowy, Tomasz;
- Pollock, Nijole;
- Berman, Andrea J;
- Budkiewicz, Sylwia;
- Kamieniczna, Marzena;
- Jackowiak, Hanna;
- Suszynska-Zajczyk, Joanna;
- Jedrzejczak, Piotr;
- Yatsenko, Alexander N;
- Kurpisz, Maciej
Publication type:
Article
Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4).
Published in:
Human Genetics, 2001, v. 108, n. 4, p. 346, doi. 10.1007/s004390100493
By:
- Yatsenko, Alexander N.;
- Shroyer, Noah F.;
- Lewis, Richard Alan;
- Lupski, James R.
Publication type:
Article
Whole‐genome sequencing identifies new candidate genes for nonobstructive azoospermia.
Published in:
Andrology, 2022, v. 10, n. 8, p. 1605, doi. 10.1111/andr.13269
By:
- Malcher, Agnieszka;
- Stokowy, Tomasz;
- Berman, Andrea;
- Olszewska, Marta;
- Jedrzejczak, Piotr;
- Sielski, Dawid;
- Nowakowski, Adam;
- Rozwadowska, Natalia;
- Yatsenko, Alexander N.;
- Kurpisz, Maciej K.
Publication type:
Article
Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male.
Published in:
Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8166-7-14
By:
- Wiland, Ewa;
- Olszewska, Marta;
- Georgiadis, Andrew;
- Huleyuk, Nataliya;
- Panasiuk, Barbara;
- Zastavna, Danuta;
- Yatsenko, Svetlana A.;
- Jedrzejczak, Piotr;
- Midro, Alina T.;
- Yatsenko, Alexander N.;
- Kurpisz, Maciej
Publication type:
Article
Reproductive genetics and the aging male.
Published in:
Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 6, p. 933, doi. 10.1007/s10815-018-1148-y
By:
- Yatsenko, Alexander N.;
- Turek, Paul J.
Publication type:
Article
Re: X-Linked TEX11 Mutations, Meiotic Arrest and Azoospermia in Infertile Men.
Published in:
2015
By:
- Yatsenko, Alexander N.;
- Georgiadis, Andrew;
- Röpke, Albercht;
- Berman, Andrea J.;
- Jaffe, Thomas;
- Olszewska, Marta;
- Westernströer, Birgit;
- Sanfilippo, Joseph;
- Kurpisz, Maciej;
- Rajkovic, Aleksandar;
- Yatsenko, Svetlana A.;
- Kliesch, Sabine;
- Schlatt, Stefan;
- Tüttelmann, Frank
Publication type:
Editorial
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Published in:
Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-34262-5
By:
- Khan, Muhammad Jaseem;
- Pollock, Nijole;
- Jiang, Huaiyang;
- Castro, Carlos;
- Nazli, Rubina;
- Ahmed, Jawad;
- Basit, Sulman;
- Rajkovic, Aleksandar;
- Yatsenko, Alexander N.
Publication type:
Article
Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure.
Published in:
Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1134849
By:
- Qureshi, Sidra;
- Hardy, Jimmaline J.;
- Pombar, Christopher;
- Berman, Andrea J.;
- Malcher, Agnieszka;
- Gingrich, Tara;
- Hvasta, Rachel;
- Kuong, Jannah;
- Munyoki, Sarah;
- Hwang, Kathleen;
- Orwig, Kyle E.;
- Ahmed, Jawad;
- Olszewska, Marta;
- Kurpisz, Maciej;
- Conrad, Donald F.;
- Khan, Muhammad Jaseem;
- Yatsenko, Alexander N.
Publication type:
Article
Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10mutations in oligozoospermic patients impair homodimerization.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 23, p. 3411, doi. 10.1093/hmg/ddl417
By:
- Yatsenko, Alexander N.;
- Roy, Angshumoy;
- Chen, Ruihong;
- Ma, Lang;
- Murthy, Lata J.;
- Yan, Wei;
- Lamb, Dolores J.;
- Matzuk, Martin M.
Publication type:
Article
ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies.
Published in:
Human Molecular Genetics, 2005, v. 14, n. 19, p. 2769, doi. 10.1093/hmg/ddi310
By:
- Wiszniewski, Wojciech;
- Zaremba, Charles M.;
- Yatsenko, Alexander N.;
- Jamrich, Milan;
- Wensel, Theodore G.;
- Lewis, Richard Alan;
- Lupski, James R.
Publication type:
Article
An ABCA4 genomic deletion in patients with Stargardt disease(Communicated by Haig H. Kazazian, Jr.).
Published in:
Human Mutation, 2003, v. 21, n. 6, p. 636, doi. 10.1002/humu.10219
By:
- Alexander N. Yatsenko
Publication type:
Article
ESX1 gene as a potential candidate responsible for male infertility in nonobstructive azoospermia.
Published in:
Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-43854-9
By:
- Malcher, Agnieszka;
- Graczyk, Zuzanna;
- Bauer, Hermann;
- Stokowy, Tomasz;
- Berman, Andrea;
- Smolibowski, Mikołaj;
- Blaszczyk, Dominika;
- Jedrzejczak, Piotr;
- Yatsenko, Alexander N.;
- Kurpisz, Maciej
Publication type:
Article

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