Samuele Soraggi, Meritxell Riera, Ewa Rajpert-De Meyts, Mikkel H Schierup, Kristian Almstrup. Hum Genet 2021
Times Cited: 14
Times Cited: 14
Times Cited
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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
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The adult human testis transcriptional cell atlas.
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Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
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Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia.
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Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.
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X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
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Mutation in TDRD9 causes non-obstructive azoospermia in infertile men.
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Novel concepts in the aetiology of male reproductive impairment.
Herman Tournaye, Csilla Krausz, Robert D Oates. Lancet Diabetes Endocrinol 2017
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Cellular source and mechanisms of high transcriptome complexity in the mammalian testis.
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XRCC2 mutation causes meiotic arrest, azoospermia and infertility.
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The Neonatal and Adult Human Testis Defined at the Single-Cell Level.
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Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives.
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A Comprehensive Roadmap of Murine Spermatogenesis Defined by Single-Cell RNA-Seq.
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Single-Cell RNA Sequencing Analysis Reveals Sequential Cell Fate Transition during Human Spermatogenesis.
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A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.
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Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine.
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Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia.
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The X chromosome and male infertility.
Matthias Vockel, Antoni Riera-Escamilla, Frank Tüttelmann, Csilla Krausz. Hum Genet 2021
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A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest.
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DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing.
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A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.
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A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family.
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Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
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Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans.
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Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1.
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TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.
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Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.
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From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia.
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A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse.
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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.