Author

Niloofar Serajpour

Iran University of Medical Sciences

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Azadeh ShojaeiiD· 1 shared Behnaz Karimi· 1 shared Hila Milo RasoulyiD· 1 shared Nakysa HoomaniD· 1 shared Pedram KhosraviiD· 1 shared Rozita Hosseini· 1 shared

Activity by Year

2018-2018 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 15 mutual co-author links

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1 shared paperGenetics

Azadeh ShojaeiORCID

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1 paper

Recent·Most cited

Molecular genetic analysis of Steroid Resistant Nephrotic Syndrome: Detection of a novel mutation

Niloofar Serajpour, Behnaz Karimi, Nakysa Hooman, Rozita Hosseini, Pedram Khosravi, Hila Milo Rasouly, Azadeh Shojaei

The paper identifies a novel mutation in FAT1 and pathogenic mutations in NPHS2 among SRNS patients, suggesting the need for WES after NPHS2 screening.

bioRxiv · Apr 22, 2018 · PreprintGenetics