Dr Kolsoum InanlooRahatloo Dr Kolsoum InanlooRahatloo

Ph.D., Assistant Professor

Contact Information

Department of Cell and Molecular Biology (Genetic), Enghelab Avenue, Tehran 14155-6955, Iran

Email  inanloo@ut.ac.ir

            inanloo@khayam.ut.ac.ir
   

 

Education

Ph.D. Cell and Molecular Biology. University of Tehran/Fritz Lipmann Institute -2013

M.Sc. Cell and Molecular Biology. University of Tehran-2007

B.A. Zoology. University of Tehran-2005

 

Research

Postdoc Fellow. Cardiovascular disease (Genetics, Stem Cell and Epigenetics) - Stanford University-2015

Postdoc Fellow. Identification of Molecular pathways underlying Intellectual disability disease – Genetic Research Center-2018

Visiting student. Fritz Lipmann Institute - 2011

 

Current research and research goals

  • Whole transcriptome analysis of intellectual disability patients
  • Sex differences in gene expression
  • Stem cell biology, genomics, transcriptomics and proteomics of cardiovascular disease
  • Meta-analysis using public data

 

Selected Publications

InanlooRahatloo K, Liang G, Vo D, Ebert A, Nguyen I, et al. (2017) Sex-based differences in myocardial gene expression in recently deceased organ donors with no prior cardiovascular disease. PLOS ONE 12(8): e0183874. https://doi.org/10.1371/journal.pone.0183874

Kodo, K., Ong, S., Jahanbani, F., Termglinchan, V., InanlooRahatloo, K., Ebert, A., Shukla, P., Abilez, O., Churko, J., Karakikes, I., Jung, G., Ichida, F., Wu, S., Snyder, M., Bernstein, D., Wu, J. iPSC-derived cardiomyocytes reveal abnormal TGF-βsignalling in left ventricular non-compaction cardiomyopathy. Nature Cell Biology. Accepted.

Wilson, K.D., Shen, P., Fung, E., Karakikes, I., Zhang, A., InanlooRahatloo, K., Odegaard, J., Sallam, K., Davis, R.W., Lui, G.K., Ashley, E.A., Scharfe, C., Wu, J.C. A Rapid, High-Quality, Cost-Effective, Comprehensive and Expandable Targeted Next-Generation Sequencing Assay for Inherited Heart Diseases. Circ Res. 2015 Sep 11;117(7):603-11. doi: 10.1161/CIRCRESAHA.115.306723.

Sponholz, C., Kramer, M., Schöneweck, F., Menzel, U., InanlooRahatloo, K., Giamarellos-Bourboulis E., Papavassileiou, V., Lymberopoulou, K., Pavlaki, M., Koutelidakis, I., Perdios, I., Bauer, M., Platzer. M., Huse, K. Splice donor polymorphisms of cystathionine beta-synthase gene are associated with susceptibility and outcome of sepsis. European Journal of Human Genetics. 2015 Oct 28. doi: 10.1038/ejhg.2015.231.

InanlooRahatloo K., Zand-parsa A. F., Huse K., Rasooli P., Davaran S., Platzer M., Kramer M., Fun J.B., Amini S., Steemers F. & Elahi H. 2014. Mutation in ST6GALNAC5 identified in family with coronary artery disease. Scientific Reports 4: 3595 doi:10.1038/srep03595.

InanlooRahatloo K., Zand-parsa A. F., Huse K., Rasooli P., Davaran S., Platzer M. Fun J.B., Amini S., Steemers F. & Elahi H. 2013. Mutation in CYP27A1 identified in family with coronary artery disease. Eur J Med Genet. 28;56(12):655-60.

 

Selected Conferences

Peymani, F., InanlooRahatloo K., Kahrizi K., Najmabadi H. Identification of molecular pathways involved in Intellectual disability in family with mutation in CDK9 gene using RNA-seq. 3rd international and 15th Iranian Genetics congress.  May15-18, 2018. Tehran.Iran. Poster

InanlooRahatloo, K, Liang G, Vo D, Nguyen I, Elbert A.D, Wu J.C, Nguyen P. Sexually dimorphic gene expression in human left ventricle tissue. OSSD Ninth Annual Meeting. April 21-23, 2015.Stanford, CA. Poster

Kodo K., Ong S.G., Jahanbani F., Termglinchan V., Inanloorahatloo K., Elbert A., Shukla P., Wu JC. Abnormal Activation of TGFβ Signaling as a Pathogenesis of Left Ventricular Non-compaction Cardiomyopathy. Circulation. 2015; 132; A12501-A12501.

Kodo K., Ong S.G., Jahanbani F., Termglinchan V., InanlooRahatloo K., Ebert A., Shukla P., Abilez O., Churko J., Karakikes I., Jung G., Snyder M.P., Bernstein D., Wu J.C. Aberrant TGFβ Signaling as an Etiology of Left Ventricular Non-compaction Cardiomyopathy. Circulation Research. 117; A248.

InanlooRahatloo, K., Zand-parsa A.F., E. Elahi, S. Davaran. 2014. Mutation in ST6GALNAC5 identified in family with coronary artery disease. 19th WORLD CONGRESS ON HEART DISEASE. BOSTON, MA, USA, JULY 25-28, 2014. Oral.

InanlooRahatloo, K., E. Elahi, S. Davaran, J. Bing-Fan. 2012. Whole exome sequencing combined with linkage analysis identifies novel variations in a large Coronary Artery Disease family. European Conference of Human Genetics, Nurenberg, Germany, June 23-26 Poster