Author

Peter N. Schlegel

Weill Cornell MedicineORCID 0000-0002-7129-8137Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Developmental Biology· 1 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 3 Organism:human· 3 Approach:statistical model· 3 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:gene regulatory network inference· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Alberto BarrosiD· 2 shared Alexandra Manuel LopesiD· 2 shared Antoni Riera‐EscamillaiD· 2 shared Corinna FriedrichiD· 2 shared Csilla Gabriella KrausziD· 2 shared Donald F. ConradiD· 2 shared Douglas T. CarrelliD· 2 shared Emily S. JungheimiD· 2 shared

Activity by Year

2018-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Alberto BarrosORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Diverse Monogenic Subforms of Human Spermatogenic Failure

Liina Nagirnaja, Alexandra Manuel Lopes, Wu‐Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Golubickaitė, Alexandra M. Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka A. Vigh‐Conrad, Manon S. Oud, Miguel Joao Xavier, , Donald F. Conrad

This study identifies genetic subforms of non-obstructive azoospermia using exome sequencing and single-cell RNA sequencing, revealing molecular groups of genes involved in spermatogenesis.

Nature Communications · Dec 26, 2022Peer-reviewedGenetic & Genomic Medicine

A de novo paradigm for male infertility

Manon S. Oud, RM Smits, H E Smith, Francesco Kumara Mastrorosa, Giles S. Holt, Brendan J. Houston, Petra F. de Vries, B. Alobaidi, Lois E. Batty, H. Ismail, J. Greenwood, Harsh J. Sheth, Aneta Mikulášová, Galuh Astuti, Christian Gilissen, , Joris Andre Veltman

The paper identifies de novo mutations as a significant genetic cause of male infertility, finding several candidate genes and an enrichment of loss-of-function and missense mutations in intolerant genes.

Nature Communications · Jan 10, 2022Peer-reviewedGenetics

YBX2 Dysregulation is a Potential Cause for Late Maturation Arrest in Men with Non-Obstructive Azoospermia

Ryan Kendrick Flannigan, Anna Mielnik, Brian D. Robinson, Francesca Khani, Alexander Bolyakov, Peter N. Schlegel, Darius A. Paduch

The paper investigates YBX2 dysregulation in human testis samples and finds reduced YBX2 and PRM1/2 mRNA in maturation arrest, linked to COMP levels and impaired spermatogenesis.

bioRxiv · Jul 8, 2018 · PreprintDevelopmental Biology