Liina Nagirnaja - Concepedia

Author

Liina Nagirnaja

Oregon National Primate Research Center ORCID

Also Known As

L Nagirnaja, L. Nagirnaja, Liina Nagirnaja

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Oregon National Primate Research Center University of Tartu Oregon Health & Science University University of Utah University of Münster

About

Liina Nagirnaja is an author at Oregon National Primate Research Center specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	10	572
2	Public Health	5	6	303
3	Cell Biology	2	2	113
4	Natural Sciences	1	1	29
5	Biostatistics	1	1	10

Liina Nagirnaja

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men Csilla Krausz, Antoni Riera‐Escamilla, Daniel Moreno‐Mendoza, Genetics in Medicine InfertilityAndrologyUrologyFertilityGenetics	2020	156
Genetics of Recurrent Miscarriage: Challenges, Current Knowledge, Future Directions Kristiina Rull, Liina Nagirnaja, Maris Laan Frontiers in Genetics	2012	154
Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia Laura Kasak, Margus Punab, Liina Nagirnaja, The American Journal of Human Genetics Allelic VariantGenetic DisorderMedicineGeneticsPathogenesis	2018	127
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
Segmental duplications and gene conversion: Human luteinizing hormone/chorionic gonadotropin β gene cluster Pille Hallast, Liina Nagirnaja, Tõnu Margus, Genome Research	2005	75
Diverse monogenic subforms of human spermatogenic failure Liina Nagirnaja, Alexandra M. Lopes, Wu‐Lin Charng, Nature Communications	2022	72
Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome Eisa Mahyari, Jingtao Guo, Ana C. Lima, The American Journal of Human Genetics Cell LineageKlinefelter SyndromeComparative Single-cell AnalysisCell DivisionCytogenetics	2021	69
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, Human Genetics Genome InstabilityCell DivisionGeneticsMeiosisChromosome Biology	2020	44

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