A citation-based method for searching scientific literature

Brendan J Houston, Donald F Conrad, Moira K O'Bryan. Hum Genet 2021
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Genetics of male infertility.
Csilla Krausz, Antoni Riera-Escamilla. Nat Rev Urol 2018
234
63


Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men.
Csilla Krausz, Antoni Riera-Escamilla, Daniel Moreno-Mendoza, Kaylee Holleman, Francesca Cioppi, Ferran Algaba, Marc Pybus, Corinna Friedrich, Margot J Wyrwoll, Elena Casamonti,[...]. Genet Med 2020
35
45

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
72
36

Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease.
Biagio Cangiano, Du Soon Swee, Richard Quinton, Marco Bonomi. Hum Genet 2021
49
36

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
60
36

The genetic architecture of morphological abnormalities of the sperm tail.
Aminata Touré, Guillaume Martinez, Zine-Eddine Kherraf, Caroline Cazin, Julie Beurois, Christophe Arnoult, Pierre F Ray, Charles Coutton. Hum Genet 2021
50
36

Genetics of the congenital absence of the vas deferens.
Eric Bieth, Safouane M Hamdi, Roger Mieusset. Hum Genet 2021
21
36


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
21
36


The X chromosome and male infertility.
Matthias Vockel, Antoni Riera-Escamilla, Frank Tüttelmann, Csilla Krausz. Hum Genet 2021
15
27

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
27

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
73
27

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
27

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
167
27

Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens.
Olivier Patat, Adrien Pagin, Aurore Siegfried, Valérie Mitchell, Nicolas Chassaing, Stanislas Faguer, Laetitia Monteil, Véronique Gaston, Louis Bujan, Monique Courtade-Saïdi,[...]. Am J Hum Genet 2016
59
27

Evaluating genetic causes of azoospermia: What can we learn from a complex cellular structure and single-cell transcriptomics of the human testis?
Samuele Soraggi, Meritxell Riera, Ewa Rajpert-De Meyts, Mikkel H Schierup, Kristian Almstrup. Hum Genet 2021
14
27

Novel concepts in the aetiology of male reproductive impairment.
Herman Tournaye, Csilla Krausz, Robert D Oates. Lancet Diabetes Endocrinol 2017
110
27

Genome-wide significance testing of variation from single case exomes.
Amy B Wilfert, Katherine R Chao, Madhurima Kaushal, Sanjay Jain, Sebastian Zöllner, David R Adams, Donald F Conrad. Nat Genet 2016
23
27

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
27


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
27

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
34
27

Spermatogenic failure and the Y chromosome.
C Krausz, E Casamonti. Hum Genet 2017
64
27

Unified single-cell analysis of testis gene regulation and pathology in five mouse strains.
Min Jung, Daniel Wells, Jannette Rusch, Suhaira Ahmad, Jonathan Marchini, Simon R Myers, Donald F Conrad. Elife 2019
45
27

A genomics approach to male infertility.
Naif Alhathal, Sateesh Maddirevula, Serdar Coskun, Hamed Alali, Mirna Assoum, Thomas Morris, Hesham A Deek, Soha A Hamed, Shaheed Alsuhaibani, Abdulmalik Mirdawi,[...]. Genet Med 2020
23
27

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
52
27

Male infertility: pathogenesis and clinical diagnosis.
Csilla Krausz. Best Pract Res Clin Endocrinol Metab 2011
254
18

Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.
Mariem Ben Khelifa, Charles Coutton, Raoudha Zouari, Thomas Karaouzène, John Rendu, Marie Bidart, Sandra Yassine, Virginie Pierre, Julie Delaroche, Sylviane Hennebicq,[...]. Am J Hum Genet 2014
205
18


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
89
18

Yeast model identifies ENTPD6 as a potential non-obstructive azoospermia pathogenic gene.
Qian Wang, Chao Liu, Chaoming Tang, Huiping Guo, Yujiao Liu, Lina Wang, Haichao Zhao, Yongliang Shang, Yang Wen, Yuan Lin,[...]. Sci Rep 2015
4
50

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human.
Charles Coutton, Alexandra S Vargas, Amir Amiri-Yekta, Zine-Eddine Kherraf, Selima Fourati Ben Mustapha, Pauline Le Tanno, Clémentine Wambergue-Legrand, Thomas Karaouzène, Guillaume Martinez, Serge Crouzy,[...]. Nat Commun 2018
103
18


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
150
18

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
32
18

NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.
Ana Fernandez-Marmiesse, Sofia Gouveia, Maria L Couce. Curr Med Chem 2018
67
18

A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.
Zine-Eddine Kherraf, Amir Amiri-Yekta, Denis Dacheux, Thomas Karaouzène, Charles Coutton, Marie Christou-Kent, Guillaume Martinez, Nicolas Landrein, Pauline Le Tanno, Selima Fourati Ben Mustapha,[...]. Am J Hum Genet 2018
48
18

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
18

Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility.
D Lo Giacco, C Chianese, E Ars, E Ruiz-Castañé, G Forti, C Krausz. J Med Genet 2014
25
18

Search-and-replace genome editing without double-strand breaks or donor DNA.
Andrew V Anzalone, Peyton B Randolph, Jessie R Davis, Alexander A Sousa, Luke W Koblan, Jonathan M Levy, Peter J Chen, Christopher Wilson, Gregory A Newby, Aditya Raguram,[...]. Nature 2019
18

High resolution X chromosome-specific array-CGH detects new CNVs in infertile males.
Csilla Krausz, Claudia Giachini, Deborah Lo Giacco, Fabrice Daguin, Chiara Chianese, Elisabet Ars, Eduard Ruiz-Castane, Gianni Forti, Elena Rossi. PLoS One 2012
51
18

The androgen receptor gene mutations database: 2012 update.
Bruce Gottlieb, Lenore K Beitel, Abbesha Nadarajah, Miltiadis Paliouras, Mark Trifiro. Hum Mutat 2012
275
18

European Association of Urology guidelines on Male Infertility: the 2012 update.
Andreas Jungwirth, Aleksander Giwercman, Herman Tournaye, Thorsten Diemer, Zsolt Kopa, Gert Dohle, Csilla Krausz. Eur Urol 2012
490
18

XX SEX CHROMOSOMES IN A HUMAN MALE. FIRST CASE.
A DELACHAPELLE, H HORTLING, M NIEMI, J WENNSTROEM. Acta Med Scand 1964
102
18


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
101
18

De novo mutations in human genetic disease.
Joris A Veltman, Han G Brunner. Nat Rev Genet 2012
463
18



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.