A citation-based method for searching scientific literature

O Akinloye, J Gromoll, C Callies, E Nieschlag, M Simoni. Andrologia 2007
Times Cited: 26







List of co-cited articles
410 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Abnormal sperm in mice lacking the Taf7l gene.
Yong Cheng, Mariano G Buffone, Martin Kouadio, Mary Goodheart, David C Page, George L Gerton, Irwin Davidson, Peijing Jeremy Wang. Mol Cell Biol 2007
80
50

The role of the testis-specific gene hTAF7L in the aetiology of male infertility.
K Stouffs, A Willems, W Lissens, H Tournaye, A Van Steirteghem, I Liebaers. Mol Hum Reprod 2006
22
45

Possible role of USP26 in patients with severely impaired spermatogenesis.
Katrien Stouffs, Willy Lissens, Herman Tournaye, André Van Steirteghem, Inge Liebaers. Eur J Hum Genet 2005
65
34

The intracellular localisation of TAF7L, a paralogue of transcription factor TFIID subunit TAF7, is developmentally regulated during male germ-cell differentiation.
Jean-Christophe Pointud, Gabrielle Mengus, Stefano Brancorsini, Lucia Monaco, Martti Parvinen, Paolo Sassone-Corsi, Irwin Davidson. J Cell Sci 2003
88
30

Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26.
C Ravel, B El Houate, S Chantot, D Lourenço, A Dumaine, H Rouba, A Bandyopadahyay, U Radhakrishna, B Das, S Sengupta,[...]. Mol Hum Reprod 2006
33
26

An abundance of X-linked genes expressed in spermatogonia.
P J Wang, J R McCarrey, F Yang, D C Page. Nat Genet 2001
572
26

Gene polymorphisms and male infertility--a meta-analysis and literature review.
Frank Tüttelmann, Ewa Rajpert-De Meyts, Eberhard Nieschlag, Manuela Simoni. Reprod Biomed Online 2007
149
26

Azoospermia in patients heterozygous for a mutation in SYCP3.
Toshinobu Miyamoto, Shiga Hasuike, Leah Yogev, Maria R Maduro, Mutsuo Ishikawa, Heiner Westphal, Dolores J Lamb. Lancet 2003
172
26

Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.
Hisashi Sato, Toshinobu Miyamoto, Leah Yogev, Mikio Namiki, Eitesu Koh, Hiroaki Hayashi, Yoshihito Sasaki, Mutsuo Ishikawa, Dolores J Lamb, Naomichi Matsumoto,[...]. J Hum Genet 2006
38
23

Novel mutations in testis-specific ubiquitin protease 26 gene may cause male infertility and hypogonadism.
Darius A Paduch, Anna Mielnik, Peter N Schlegel. Reprod Biomed Online 2005
55
23


The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.
Helen Skaletsky, Tomoko Kuroda-Kawaguchi, Patrick J Minx, Holland S Cordum, LaDeana Hillier, Laura G Brown, Sjoerd Repping, Tatyana Pyntikova, Johar Ali, Tamberlyn Bieri,[...]. Nature 2003
23


Maintenance of spermatogenesis requires TAF4b, a gonad-specific subunit of TFIID.
Allison E Falender, Richard N Freiman, Kenneth G Geles, Kirk C Lo, KeumSil Hwang, Dolores J Lamb, Patricia L Morris, Robert Tjian, JoAnne S Richards. Genes Dev 2005
158
23

X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
Alexander N Yatsenko, Andrew P Georgiadis, Albrecht Röpke, Andrea J Berman, Thomas Jaffe, Marta Olszewska, Birgit Westernströer, Joseph Sanfilippo, Maciej Kurpisz, Aleksandar Rajkovic,[...]. N Engl J Med 2015
146
23

Male infertility and variation in CAG repeat length in the androgen receptor gene: a meta-analysis.
Carol A Davis-Dao, Ellenie D Tuazon, Rebecca Z Sokol, Victoria K Cortessis. J Clin Endocrinol Metab 2007
77
19

Male infertility: role of genetic background.
Alberto Ferlin, Florina Raicu, Valentina Gatta, Daniela Zuccarello, Giandomenico Palka, Carlo Foresta. Reprod Biomed Online 2007
281
19

Association of a single-nucleotide polymorphism of the deleted-in-azoospermia-like gene with susceptibility to spermatogenic failure.
Yen-Ni Teng, Yung-Ming Lin, Ying-Hung Lin, Shu-Yi Tsao, Chao-Chin Hsu, Shio-Jean Lin, Wan-Ching Tsai, Pao-Lin Kuo. J Clin Endocrinol Metab 2002
69
19

Is there a role for the nuclear export factor 2 gene in male infertility?
Katrien Stouffs, Herman Tournaye, Josiane Van der Elst, Inge Liebaers, Willy Lissens. Fertil Steril 2008
11
45

Meiotic failure in male mice lacking an X-linked factor.
Fang Yang, Katarina Gell, Godfried W van der Heijden, Sigrid Eckardt, N Adrian Leu, David C Page, Ricardo Benavente, Chengtao Her, Christer Höög, K John McLaughlin,[...]. Genes Dev 2008
100
19

Molecular genetic analysis of two human sperm fibrous sheath proteins, AKAP4 and AKAP3, in men with dysplasia of the fibrous sheath.
R M Turner, M P Musse, A Mandal, K Klotz, F C Jayes, J C Herr, G L Gerton, S B Moss, H E Chemes. J Androl 2001
78
19

Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
Francesca Nuti, Csilla Krausz. Reprod Biomed Online 2008
92
19


Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia.
Anika H D M Dam, Isabelle Koscinski, Jan A M Kremer, Celine Moutou, Anne-Sophie Jaeger, Astrid R Oudakker, Herman Tournaye, Nicolas Charlet, Clotilde Lagier-Tourenne, Hans van Bokhoven,[...]. Am J Hum Genet 2007
172
19

Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
Ozlem Okutman, Jean Muller, Yoni Baert, Munevver Serdarogullari, Meral Gultomruk, Amélie Piton, Charlotte Rombaut, Moncef Benkhalifa, Marius Teletin, Valerie Skory,[...]. Hum Mol Genet 2015
66
19

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.
Sjoerd Repping, Helen Skaletsky, Laura Brown, Saskia K M van Daalen, Cindy M Korver, Tatyana Pyntikova, Tomoko Kuroda-Kawaguchi, Jan W A de Vries, Robert D Oates, Sherman Silber,[...]. Nat Genet 2003
302
15

Alterations of the USP26 gene in Caucasian men.
Katrien Stouffs, Willy Lissens, Herman Tournaye, André Van Steirteghem, Inge Liebaers. Int J Androl 2006
28
15

Multilocus analyses of estrogen-related genes reveal involvement of the ESR1 gene in male infertility and the polygenic nature of the pathology.
Jose J Galan, Belen Buch, Natalio Cruz, Ana Segura, Francisco J Moron, Lluis Bassas, Luis Martinez-Pineiro, Luis M Real, Agustin Ruiz. Fertil Steril 2005
39
15


CAG repeat length in androgen-receptor gene and reproductive variables in fertile and infertile men.
Ewa Rajpert-De Meyts, Henrik Leffers, Jørgen H Petersen, Anne Grethe Andersen, Elisabeth Carlsen, Niels Jørgensen, Niels E Skakkebaek. Lancet 2002
63
15


Association of genetic markers within the KIT and KITLG genes with human male infertility.
J J Galan, M De Felici, B Buch, M C Rivero, A Segura, J L Royo, N Cruz, L M Real, A Ruiz. Hum Reprod 2006
35
15

The mouse X chromosome is enriched for sex-biased genes not subject to selection by meiotic sex chromosome inactivation.
Pavel P Khil, Natalya A Smirnova, Peter J Romanienko, R Daniel Camerini-Otero. Nat Genet 2004
223
15

Mutational analysis of the human FATE gene in 144 infertile men.
Christian Olesen, Joachim Silber, Hans Eiberg, Erik Ernst, Karsten Petersen, Svend Lindenberg, Niels Tommerup. Hum Genet 2003
28
15

Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations.
Alberto Ferlin, Cinzia Vinanzi, Andrea Garolla, Riccardo Selice, Daniela Zuccarello, Carla Cazzadore, Carlo Foresta. Clin Endocrinol (Oxf) 2006
89
15

Novel mutations in ubiquitin-specific protease 26 gene might cause spermatogenesis impairment and male infertility.
Jie Zhang, Shu-Dong Qiu, Sheng-Bin Li, Dang-Xia Zhou, Hong Tian, Yong-Wei Huo, Ling Ge, Qiu-Yang Zhang. Asian J Androl 2007
41
15

USP26 gene variations in fertile and infertile men.
I Ribarski, O Lehavi, L Yogev, R Hauser, B Bar-Shira Maymon, A Botchan, G Paz, H Yavetz, S E Kleiman. Hum Reprod 2009
28
15


Sequence analysis of the X-linked USP26 gene in severe male factor infertility patients and fertile controls.
Greg L Christensen, Jeanine Griffin, Douglas T Carrell. Fertil Steril 2008
17
23

The mouse X chromosome is enriched for multicopy testis genes showing postmeiotic expression.
Jacob L Mueller, Shantha K Mahadevaiah, Peter J Park, Peter E Warburton, David C Page, James M A Turner. Nat Genet 2008
203
15


Gene deletions in an infertile man with sperm fibrous sheath dysplasia.
B Baccetti, G Collodel, M Estenoz, D Manca, E Moretti, P Piomboni. Hum Reprod 2005
85
15

Cytogenetics of infertile men.
E Van Assche, M Bonduelle, H Tournaye, H Joris, G Verheyen, P Devroey, A Van Steirteghem, I Liebaers. Hum Reprod 1996
329
15

Altered protamine expression and diminished spermatogenesis: what is the link?
Douglas T Carrell, Benjamin R Emery, Sue Hammoud. Hum Reprod Update 2007
210
15

Protamines and male infertility.
Rafael Oliva. Hum Reprod Update 2006
403
15

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene.
R Reijo, T Y Lee, P Salo, R Alagappan, L G Brown, M Rosenberg, S Rozen, T Jaffe, D Straus, O Hovatta. Nat Genet 1995
955
15

Natural transmission of USP9Y gene mutations: a new perspective on the role of AZFa genes in male fertility.
Csilla Krausz, Selene Degl'Innocenti, Francesca Nuti, Annamaria Morelli, Federica Felici, Mauro Sansone, Gennaro Varriale, Gianni Forti. Hum Mol Genet 2006
89
15

Testis-specific transcription mechanisms promoting male germ-cell differentiation.
Sarah Kimmins, Noora Kotaja, Irwin Davidson, Paolo Sassone-Corsi. Reproduction 2004
117
15




Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.