Author

Muhammad Arif Nadeem Saqib

Pakistan Health Research CouncilORCID 0000-0001-6365-5520Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Aida Bytyci TelegrafiiD· 1 shared Ana PetracoviciiD· 1 shared Boris KereniD· 1 shared Chongsheng HeiD· 1 shared Cyril MignotiD· 1 shared David B. BeckiD· 1 shared Dustin BaldridgeiD· 1 shared Eleanor G. SeabyiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Aida Bytyci TelegrafiORCID

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintJul 31, 2019

Delineation of the First Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency

David B. Beck, Ana Petracovici, Chongsheng He…·Jill A. Fahrner

This study identifies and characterizes 11 cases of TET3 deficiency, a new Mendelian disorder of DNA demethylation, associated with intellectual disability and developmental delays.

2 citations

humanDNA methylation

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