A citation-based method for searching scientific literature

Jimmaline J Hardy, Margot J Wyrwoll, William Mcfadden, Agnieszka Malcher, Nadja Rotte, Nijole C Pollock, Sarah Munyoki, Maria V Veroli, Brendan J Houston, Miguel J Xavier, Laura Kasak, Margus Punab, Maris Laan, Sabine Kliesch, Peter Schlegel, Thomas Jaffe, Kathleen Hwang, Josip Vukina, Miguel A Brieño-Enríquez, Kyle Orwig, Judith Yanowitz, Michael Buszczak, Joris A Veltman, Manon Oud, Liina Nagirnaja, Marta Olszewska, Moira K O'Bryan, Donald F Conrad, Maciej Kurpisz, Frank Tüttelmann, Alexander N Yatsenko. Hum Genet 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10 mutations in oligozoospermic patients impair homodimerization.
Alexander N Yatsenko, Angshumoy Roy, Ruihong Chen, Lang Ma, Lata J Murthy, Wei Yan, Dolores J Lamb, Martin M Matzuk. Hum Mol Genet 2006
88
100

Adaptive Evolution Leads to Cross-Species Incompatibility in the piRNA Transposon Silencing Machinery.
Swapnil S Parhad, Shikui Tu, Zhiping Weng, William E Theurkauf. Dev Cell 2017
34
100

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
100

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
100

Trimmomatic: a flexible trimmer for Illumina sequence data.
Anthony M Bolger, Marc Lohse, Bjoern Usadel. Bioinformatics 2014
100

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
150
100


SUMOylation promotes protective responses to DNA-protein crosslinks.
Nikoline Borgermann, Leena Ackermann, Petra Schwertman, Ivo A Hendriks, Karen Thijssen, Julio Cy Liu, Hannes Lans, Michael L Nielsen, Niels Mailand. EMBO J 2019
38
100

Molecular histology of spermatogenesis in the Japanese macaque monkey (Macaca fuscata).
Sawako Okada, Kota Kuroki, Cody A Ruiz, Anthony J Tosi, Masanori Imamura. Primates 2021
1
100

Mutation in TDRD9 causes non-obstructive azoospermia in infertile men.
Maram Arafat, Iris Har-Vardi, Avi Harlev, Eliahu Levitas, Atif Zeadna, Maram Abofoul-Azab, Victor Dyomin, Val C Sheffield, Eitan Lunenfeld, Mahmoud Huleihel,[...]. J Med Genet 2017
51
100

A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.
Moran Gershoni, Ron Hauser, Leah Yogev, Ofer Lehavi, Foad Azem, Haim Yavetz, Shmuel Pietrokovski, Sandra E Kleiman. Genet Med 2017
65
100

CUA Guideline: The workup of azoospermic males.
Keith Jarvi, Kirk Lo, Anthony Fischer, John Grantmyre, Armand Zini, Victor Chow, Victor Mak. Can Urol Assoc J 2010
48
100

Piwi and potency: PIWI proteins in animal stem cells and regeneration.
Josien C van Wolfswinkel. Integr Comp Biol 2014
32
100



A systematic review and standardized clinical validity assessment of male infertility genes.
Manon S Oud, Ludmila Volozonoka, Roos M Smits, Lisenka E L M Vissers, Liliana Ramos, Joris A Veltman. Hum Reprod 2019
59
100

Mouse models of male infertility.
Howard J Cooke, Philippa T K Saunders. Nat Rev Genet 2002
202
100

The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses.
Gil Stelzer, Naomi Rosen, Inbar Plaschkes, Shahar Zimmerman, Michal Twik, Simon Fishilevich, Tsippi Iny Stein, Ron Nudel, Iris Lieder, Yaron Mazor,[...]. Curr Protoc Bioinformatics 2016
801
100

Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Margot J Wyrwoll, Şehime G Temel, Liina Nagirnaja, Manon S Oud, Alexandra M Lopes, Godfried W van der Heijden, James S Heald, Nadja Rotte, Joachim Wistuba, Marius Wöste,[...]. Am J Hum Genet 2020
11
100

PNLDC1, mouse pre-piRNA Trimmer, is required for meiotic and post-meiotic male germ cell development.
Toru Nishimura, Ippei Nagamori, Tsunetoshi Nakatani, Natsuko Izumi, Yukihide Tomari, Satomi Kuramochi-Miyagawa, Toru Nakano. EMBO Rep 2018
31
100

The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease.
Janan T Eppig, Judith A Blake, Carol J Bult, James A Kadin, Joel E Richardson. Nucleic Acids Res 2015
253
100

Spermatogonial kinetics in humans.
Sara Di Persio, Rossana Saracino, Stefania Fera, Barbara Muciaccia, Valentina Esposito, Carla Boitani, Bartolomeo P Berloco, Francesco Nudo, Gustavo Spadetta, Mario Stefanini,[...]. Development 2017
36
100

A widely employed germ cell marker is an ancient disordered protein with reproductive functions in diverse eukaryotes.
Michelle A Carmell, Gregoriy A Dokshin, Helen Skaletsky, Yueh-Chiang Hu, Josien C van Wolfswinkel, Kyomi J Igarashi, Daniel W Bellott, Michael Nefedov, Peter W Reddien, George C Enders,[...]. Elife 2016
32
100

Effects of heme oxygenase isozymes on Leydig cells steroidogenesis.
Barbara Piotrkowski, Casandra M Monzón, Romina M Pagotto, Cecilia G Reche, Marcos Besio, Cora B Cymeryng, Omar P Pignataro. J Endocrinol 2009
5
100



Variable termination sites of DNA polymerases encountering a DNA-protein cross-link.
Anna V Yudkina, Antonina P Dvornikova, Dmitry O Zharkov. PLoS One 2018
9
100

GCNA Interacts with Spartan and Topoisomerase II to Regulate Genome Stability.
Gregoriy A Dokshin, Gregory M Davis, Ashley D Sawle, Matthew D Eldridge, Peter K Nicholls, Taylin E Gourley, Katherine A Romer, Luke W Molesworth, Hannah R Tatnell, Ahmet R Ozturk,[...]. Dev Cell 2020
17
100

Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
Laura Kasak, Margus Punab, Liina Nagirnaja, Marina Grigorova, Ave Minajeva, Alexandra M Lopes, Anna Maria Punab, Kenneth I Aston, Filipa Carvalho, Eve Laasik,[...]. Am J Hum Genet 2018
53
100

Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia.
Esther Maor-Sagie, Yuval Cinnamon, Barak Yaacov, Avraham Shaag, Hannoch Goldsmidt, Shamir Zenvirt, Neri Laufer, Carmelit Richler, Ayala Frumkin. J Assist Reprod Genet 2015
58
100

Mechanism and Regulation of DNA-Protein Crosslink Repair by the DNA-Dependent Metalloprotease SPRTN.
Julian Stingele, Roberto Bellelli, Ferdinand Alte, Graeme Hewitt, Grzegorz Sarek, Sarah L Maslen, Susan E Tsutakawa, Annabel Borg, Svend Kjær, John A Tainer,[...]. Mol Cell 2016
109
100

Multiple testicular sampling in non-obstructive azoospermia--is it necessary?
R Hauser, A Botchan, A Amit, D Ben Yosef, R Gamzu, G Paz, J B Lessing, L Yogev, H Yavetz. Hum Reprod 1998
101
100

Male infertility.
Ashok Agarwal, Saradha Baskaran, Neel Parekh, Chak-Lam Cho, Ralf Henkel, Sarah Vij, Mohamed Arafa, Manesh Kumar Panner Selvam, Rupin Shah. Lancet 2021
45
100

SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility.
Samantha L P Schilit, Shreya Menon, Corinna Friedrich, Tammy Kammin, Ellen Wilch, Carrie Hanscom, Sizun Jiang, Sabine Kliesch, Michael E Talkowski, Frank Tüttelmann,[...]. Am J Hum Genet 2020
21
100

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
174
100

A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest.
Moran Gershoni, Ron Hauser, Shimi Barda, Ofer Lehavi, Eli Arama, Shmuel Pietrokovski, Sandra E Kleiman. Hum Reprod 2019
26
100

'How to count sperm properly': checklist for acceptability of studies based on human semen analysis.
Lars Björndahl, Christopher L R Barratt, David Mortimer, Pierre Jouannet. Hum Reprod 2016
91
100

Genetics of male infertility.
Csilla Krausz, Antoni Riera-Escamilla. Nat Rev Urol 2018
188
100

The genetics of human infertility by functional interrogation of SNPs in mice.
Priti Singh, John C Schimenti. Proc Natl Acad Sci U S A 2015
40
100

Mutation in CATIP (C2orf62) causes oligoteratoasthenozoospermia by affecting actin dynamics.
Maram Arafat, Avi Harlev, Iris Har-Vardi, Eliahu Levitas, Tsvia Priel, Moran Gershoni, Charles Searby, Val C Sheffield, Eitan Lunenfeld, Ruti Parvari. J Med Genet 2020
2
100

GCNA Preserves Genome Integrity and Fertility Across Species.
Varsha Bhargava, Courtney D Goldstein, Logan Russell, Lin Xu, Murtaza Ahmed, Wei Li, Amanda Casey, Kelly Servage, Rahul Kollipara, Zachary Picciarelli,[...]. Dev Cell 2020
25
100

Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia.
Özgecan Ayhan, Mahmut Balkan, Ayse Guven, Renin Hazan, Murat Atar, Atalay Tok, Aslıhan Tolun. J Med Genet 2014
68
100

Gene ontology: tool for the unification of biology. The Gene Ontology Consortium.
M Ashburner, C A Ball, J A Blake, D Botstein, H Butler, J M Cherry, A P Davis, K Dolinski, S S Dwight, J T Eppig,[...]. Nat Genet 2000
100

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
100


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.