A citation-based method for searching scientific literature

Samuele Soraggi, Meritxell Riera, Ewa Rajpert-De Meyts, Mikkel H Schierup, Kristian Almstrup. Hum Genet 2021
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Genetics of male infertility.
Csilla Krausz, Antoni Riera-Escamilla. Nat Rev Urol 2018
221
42

The Mammalian Spermatogenesis Single-Cell Transcriptome, from Spermatogonial Stem Cells to Spermatids.
Brian P Hermann, Keren Cheng, Anukriti Singh, Lorena Roa-De La Cruz, Kazadi N Mutoji, I-Chung Chen, Heidi Gildersleeve, Jake D Lehle, Max Mayo, Birgit Westernströer,[...]. Cell Rep 2018
170
42

The adult human testis transcriptional cell atlas.
Jingtao Guo, Edward J Grow, Hana Mlcochova, Geoffrey J Maher, Cecilia Lindskog, Xichen Nie, Yixuan Guo, Yodai Takei, Jina Yun, Long Cai,[...]. Cell Res 2018
192
35

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
58
28

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
73
28

Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.
Alexandra M Lopes, Kenneth I Aston, Emma Thompson, Filipa Carvalho, João Gonçalves, Ni Huang, Rune Matthiesen, Michiel J Noordam, Inés Quintela, Avinash Ramu,[...]. PLoS Genet 2013
87
28

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
160
28

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
57
28

Novel concepts in the aetiology of male reproductive impairment.
Herman Tournaye, Csilla Krausz, Robert D Oates. Lancet Diabetes Endocrinol 2017
98
28

Cellular source and mechanisms of high transcriptome complexity in the mammalian testis.
Magali Soumillon, Anamaria Necsulea, Manuela Weier, David Brawand, Xiaolan Zhang, Hongcang Gu, Pauline Barthès, Maria Kokkinaki, Serge Nef, Andreas Gnirke,[...]. Cell Rep 2013
309
28

XRCC2 mutation causes meiotic arrest, azoospermia and infertility.
Yongjia Yang, Jihong Guo, Lei Dai, Yimin Zhu, Hao Hu, Lihong Tan, Weijian Chen, Desheng Liang, Jingliang He, Ming Tu,[...]. J Med Genet 2018
32
28

The Neonatal and Adult Human Testis Defined at the Single-Cell Level.
Abhishek Sohni, Kun Tan, Hye-Won Song, Dana Burow, Dirk G de Rooij, Louise Laurent, Tung-Chin Hsieh, Raja Rabah, Saher Sue Hammoud, Elena Vicini,[...]. Cell Rep 2019
101
28


A Comprehensive Roadmap of Murine Spermatogenesis Defined by Single-Cell RNA-Seq.
Christopher Daniel Green, Qianyi Ma, Gabriel L Manske, Adrienne Niederriter Shami, Xianing Zheng, Simone Marini, Lindsay Moritz, Caleb Sultan, Stephen J Gurczynski, Bethany B Moore,[...]. Dev Cell 2018
148
28

Single-Cell RNA Sequencing Analysis Reveals Sequential Cell Fate Transition during Human Spermatogenesis.
Mei Wang, Xixi Liu, Gang Chang, Yidong Chen, Geng An, Liying Yan, Shuai Gao, Yanwen Xu, Yueli Cui, Ji Dong,[...]. Cell Stem Cell 2018
134
28

Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest.
N van der Bijl, A Röpke, U Biswas, M Wöste, R Jessberger, S Kliesch, C Friedrich, F Tüttelmann. Hum Reprod 2019
33
21

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
71
21

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
69
21

Causes of male infertility: a 9-year prospective monocentre study on 1737 patients with reduced total sperm counts.
M Punab, O Poolamets, P Paju, V Vihljajev, K Pomm, R Ladva, P Korrovits, M Laan. Hum Reprod 2017
140
21

Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure.
Yardena Tenenbaum-Rakover, Ariella Weinberg-Shukron, Paul Renbaum, Orit Lobel, Hasan Eideh, Suleyman Gulsuner, Dvir Dahary, Amal Abu-Rayyan, Moien Kanaan, Ephrat Levy-Lahad,[...]. J Med Genet 2015
70
21


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
64
21

Point-of-care whole-exome sequencing of idiopathic male infertility.
Khalid A Fakhro, Haitham Elbardisi, Mohamed Arafa, Amal Robay, Juan L Rodriguez-Flores, Alya Al-Shakaki, Najeeb Syed, Jason G Mezey, Charbel Abi Khalil, Joel A Malek,[...]. Genet Med 2018
47
21

The X chromosome and male infertility.
Matthias Vockel, Antoni Riera-Escamilla, Frank Tüttelmann, Csilla Krausz. Hum Genet 2021
12
25

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
28
21

DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing.
Wen-Bin He, Chao-Feng Tu, Qiang Liu, Lan-Lan Meng, Shi-Min Yuan, Ai-Xiang Luo, Fu-Sheng He, Juan Shen, Wen Li, Juan Du,[...]. J Med Genet 2018
53
21


A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.
Yanwei Sha, Liangkai Zheng, Zhiyong Ji, Libin Mei, Lu Ding, Shaobin Lin, Xu Wang, Xiaoyu Yang, Ping Li. BMC Med Genet 2018
30
21

A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family.
M Ben Khelifa, F Ghieh, R Boudjenah, C Hue, D Fauvert, R Dard, H J Garchon, F Vialard. Hum Reprod 2018
24
21

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
70
21

Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans.
Yue-Qiu Tan, Chaofeng Tu, Lanlan Meng, Shimin Yuan, Calvin Sjaarda, Aixiang Luo, Juan Du, Wen Li, Fei Gong, Changgao Zhong,[...]. Genet Med 2019
40
21

Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1.
Anu Bashamboo, Bruno Ferraz-de-Souza, Diana Lourenço, Lin Lin, Neil J Sebire, Debbie Montjean, Joelle Bignon-Topalovic, Jacqueline Mandelbaum, Jean-Pierre Siffroi, Sophie Christin-Maitre,[...]. Am J Hum Genet 2010
153
21

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.
Fang Yang, Sherman Silber, N Adrian Leu, Robert D Oates, Janet D Marszalek, Helen Skaletsky, Laura G Brown, Steve Rozen, David C Page, P Jeremy Wang. EMBO Mol Med 2015
96
21

Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.
Roberto Colombo, Alessandro Pontoglio, Maurizio Bini. Gynecol Obstet Invest 2017
26
21

Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations.
S Nakamura, M Miyado, K Saito, M Katsumi, A Nakamura, Y Kobori, Y Tanaka, H Ishikawa, A Yoshida, H Okada,[...]. Andrology 2017
38
21

In vitro spermatogenesis: A century-long research journey, still half way around.
Mitsuru Komeya, Takuya Sato, Takehiko Ogawa. Reprod Med Biol 2018
25
21

Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease.
Biagio Cangiano, Du Soon Swee, Richard Quinton, Marco Bonomi. Hum Genet 2021
45
21

From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia.
Csilla Krausz, Antoni Riera-Escamilla, Chiara Chianese, Daniel Moreno-Mendoza, Elisabet Ars, Osvaldo Rajmil, Roser Pujol, Massimo Bogliolo, Ignacio Blanco, Ines Rodríguez,[...]. Genet Med 2019
21
21


Molecular genetic diagnostics of hypogonadotropic hypogonadism: from panel design towards result interpretation in clinical practice.
Henriett Butz, Gábor Nyírő, Petra Anna Kurucz, István Likó, Attila Patócs. Hum Genet 2021
14
21

Genetics of the congenital absence of the vas deferens.
Eric Bieth, Safouane M Hamdi, Roger Mieusset. Hum Genet 2021
19
21

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
21

Spermatogenic failure and the Y chromosome.
C Krausz, E Casamonti. Hum Genet 2017
61
21

Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.
Frank Tüttelmann, Manuela Simoni, Sabine Kliesch, Susanne Ledig, Bernd Dworniczak, Peter Wieacker, Albrecht Röpke. PLoS One 2011
85
21

Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.
Albert Salas-Huetos, Frank Tüttelmann, Margot J Wyrwoll, Sabine Kliesch, Alexandra M Lopes, João Goncalves, Steven E Boyden, Marius Wöste, James M Hotaling, Liina Nagirnaja,[...]. Hum Genet 2021
8
37

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11.
P H Vogt, A Edelmann, S Kirsch, O Henegariu, P Hirschmann, F Kiesewetter, F M Köhn, W B Schill, S Farah, C Ramos,[...]. Hum Mol Genet 1996
910
21

Disease gene discovery in male infertility: past, present and future.
M J Xavier, A Salas-Huetos, M S Oud, K I Aston, J A Veltman. Hum Genet 2021
17
21

Chromatin and transcription transitions of mammalian adult germline stem cells and spermatogenesis.
Saher Sue Hammoud, Diana H P Low, Chongil Yi, Douglas T Carrell, Ernesto Guccione, Bradley R Cairns. Cell Stem Cell 2014
192
21

Single-cell RNA-seq uncovers dynamic processes and critical regulators in mouse spermatogenesis.
Yao Chen, Yuxuan Zheng, Yun Gao, Zhen Lin, Suming Yang, Tongtong Wang, Qiu Wang, Nannan Xie, Rong Hua, Mingxi Liu,[...]. Cell Res 2018
124
21

Staged developmental mapping and X chromosome transcriptional dynamics during mouse spermatogenesis.
Christina Ernst, Nils Eling, Celia P Martinez-Jimenez, John C Marioni, Duncan T Odom. Nat Commun 2019
68
21


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.