F. Niazi

发表

Neural transcriptome of constitutional Pten dysfunction in

C. Eng, G. Bebek, A. Tilot, 2015 .

Computational analysis of functional long noncoding RNAs reveals lack of peptide-coding capacity and parallels with 3' UTRs.

Saba Valadkhan, F. Niazi, S. Valadkhan, 2012, RNA.

A Novel RNA Motif Mediates the Strict Nuclear Localization of a Long Noncoding RNA

F. Niazi, L. Gunawardane, F. Jahanbani, 2014, Molecular and Cellular Biology.

Analysis of Long Noncoding RNAs in RNA-Seq Data

F. Niazi, S. Valadkhan, Farshad Niazi, 2016 .

An HIV-induced mechanism for T cell quiescence and proviral latency

J. Karn, F. Niazi, K. Leskov, 2021 .

Effects of the fruit essential oil of Cuminum cyminum Linn. (Apiaceae) on pentylenetetrazol-induced epileptiform activity in F1 neurones of Helix aspersa.

M. Janahmadi, F. Niazi, M. Kamalinejad, 2006, Journal of ethnopharmacology.

Negative regulation of the interferon response by an interferon-induced long non-coding RNA

P. Fortes, D. Anthony, F. Niazi, 2014, Nucleic acids research.

Neural transcriptome of constitutional Pten dysfunction in mice and its relevance to human idiopathic Autism Spectrum Disorder

C. Eng, G. Bebek, A. Tilot, 2015, Molecular Psychiatry.

Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer.

C. Eng, R. Keri, F. Niazi, 2015, American journal of human genetics.

Microbiomic differences in tumor and paired-normal tissue in head and neck squamous cell carcinomas

B. Burkey, C. Eng, P. Funchain, 2017, Genome Medicine.

Exome sequencing reveals germline gain-of-function EGFR mutation in an adult with Lhermitte–Duclos disease

Charis Eng, Samantha Colby, C. Eng, 2016, Cold Spring Harbor molecular case studies.

Cancer-predisposition gene KLLN maintains pericentric H3K9 trimethylation protecting genomic stability

C. Eng, F. Niazi, Madhav Sankunny, 2015, Nucleic acids research.

Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations

T. LaFramboise, C. Eng, F. Niazi, 2018, PLoS genetics.

Breast tissue, oral and urinary microbiomes in breast cancer

B. Calhoun, C. Eng, C. Sturgis, 2017, Oncotarget.

Exome Sequencing Reveals Germline SMAD9 Mutation That Reduces Phosphatase and Tensin Homolog Expression and Is Associated With Hamartomatous Polyposis and Gastrointestinal Ganglioneuromas.

L. Tucker-Kellogg, C. Eng, Haiwei Song, 2015, Gastroenterology.

Germline compound heterozygous poly-glutamine deletion in USF3 may be involved in predisposition to heritable and sporadic epithelial thyroid carcinoma

T. LaFramboise, C. Eng, M. Saji, 2016, Human molecular genetics.

Preliminary report: Late seizure recurrence years after epilepsy surgery may be associated with alterations in brain tissue transcriptome

C. Eng, I. Najm, W. Bingaman, 2018, Epilepsia open.