Manon S. Oud - Concepedia

Author

Manon S. Oud

Also Known As

Leendert H.J. Looijenga, M S Oud, M. S. Oud, M.S. Oud, MS Oud, Manon Oud, Manon S Oud, Manon S. Oud, Manon. S. Oud, Oud, M.

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Newcastle University University of Münster University Hospital Münster

About

Manon S. Oud is an author at Radboud University Nijmegen specializing in reproductive biology, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	48
2	Public Health	2	2	48
3	Molecular Genetics	2	2	48
4	Pathology	1	1	12
5	Developmental Biology	1	1	36

Manon S. Oud

Publications

761

Citations

H-Index

Page 1

	Year	Citations
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility Margot J. Wyrwoll, Şehime Gülsün Temel, Liina Nagirnaja, The American Journal of Human Genetics	2020	102
A de novo paradigm for male infertility Manon S. Oud, RM Smits, H E Smith, Nature Communications	2022	97
Variant <i>PNLDC1</i> , Defective piRNA Processing, and Azoospermia Liina Nagirnaja, Nina Mørup, John Nielsen, New England Journal of Medicine	2021	95
Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease Gaël Nicolas, Rocío Acuña‐Hidalgo, Michael J. Keogh, Alzheimer s & Dementia	2018	77
Diverse monogenic subforms of human spermatogenic failure Liina Nagirnaja, Alexandra M. Lopes, Wu‐Lin Charng, Nature Communications	2022	72
Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders Manon S. Oud, Brendan J. Houston, Ludmila Voložonoka, Human Reproduction	2021	70
Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia Manon S. Oud, Özlem Okutman, Linda A.J. Hendricks, Human Reproduction	2019	61
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure Jimmaline J. Hardy, Margot J. Wyrwoll, William M. McFadden, Human Genetics SpermatogenesisGerm Cell BiologyInfertilityDevelopmental BiologyGerm Cell	2021	36
Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure Antoni Riera‐Escamilla, Matthias Vockel, Liina Nagirnaja, The American Journal of Human Genetics	2022	32
TRIM71 Deficiency Causes Germ Cell Loss During Mouse Embryogenesis and Is Associated With Human Male Infertility Lucia Torres Fernández, Jana Emich, Yasmine Port, Frontiers in Cell and Developmental Biology	2021	27

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