تحصیلات
- پسا دکتری, ---, ژنتیک پزشکی, دانشگاه استنفورد
- کارشناسی ارشد, 1386, زیست شناسی سلولی و ملکولی, دانشگاه تهران
- دکتری, 1392, زیست شناسی سلولی و ملکولی, دانشگاه تهران
- کارشناسی, 1384, زیست شناسی, دانشگاه تهران
مقالات چاپ شده در نشریات بینالمللی
- MELIKA GOLOZAR, Ali Valipour motlagh, Mohammad Mahdevar, Maryam Peymani, Kolsoum Inanloorahatloo, and Kamran Ghaedi. "TBX15 and SDHB expression changes in colorectal cancer serve as potential prognostic biomarkers." EXPERIMENTAL AND MOLECULAR PATHOLOGY 136, no. 136 (2024): 104890.
- Maryam Mirzaei, Mohammadreza Monazam, Monireh Kadem, Amir Abbasi Garmaroudi, and Kolsoum Inanloorahatloo. "Intermittent white noise exposure is associated with rat cochleae damage and changes in the gene expression." Egyptian Journal of Medical Human Genetics 23, no. 1 (2022): .
- Akbar Biglarian, Enayatolah Bakhshi, Kolsoum Inanloorahatloo, and Taeibeh Kenarangi. "Identifying Gene Signature in RNA Sequencing Multiple Sclerosis Data." IRANIAN REHABILITATION JOURNAL 20, no. 2 (2022): 217-224.
- Hossein Najmabadi, Kolsoum Inanloorahatloo, Afagh Alavi, Kimia Kahrizi, and Mostafa Saghi. "Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery." BMC Medical Genomics 15, no. 1 (2022): .
- Peyman Taghizadeh, Sadegh Salehi, Iman Safari, Masoud Houshmand, Kolsoum Inanloorahatloo, Frozandeh Mahjobi, محمدحسین صنعتی , Afagh Alavi, Ali Heshmati, Saeid Amel Jamehdar, Hamid Galehdari, Mohammad Reza Haghshenas, Amir Masoud Hashemian, Abtin Heidarzadeh, Issa Jahanzad, Elham Kheyrani, Ahmad Piroozmand, Ali Mojtahedi, Hadi Razavi Nikoo, Mohammad Masoud Rahimi Bidgoli, Nayebali Rezvani, Mehdi Sepehrnejad, Arash Shakibzadeh, Gholamreza Shariati, Noorossadat Seyyedi, Seyed MohammadSaleh Zahraei, Hadi Yari, Soroosh Dabiri, and Elahe Allahi. "Study on SARS-CoV-2 strains in Iran reveals potential contribution of co-infection with and recombination between different strains to the emergence of new strains." VIROLOGY 562, no. 562 (2021): 63-73.
- Iman Safari, Kolsoum Inanloorahatloo, and Elahe Allahi. "World‐wide tracking of major SARS‐CoV‐2 genome haplotypes in sequences of June 1 to November 15, 2020 and discovery of rapid expansion of a new haplotype." JOURNAL OF MEDICAL VIROLOGY 1, no. 1 (2021): .
- seyyed Hashemi, Davood Zare-Abdollahi, Mohammad Bakhshandeh, Amirreza Vafaee, Sona Abolhassani, Kolsoum Inanloorahatloo, Fardad DanaeeFard, Niloofar Farboodi, Mohammad Rohani, and Afagh Alavi. "Clinical spectrum in multiple families with primary COQ 10 deficiency." AMERICAN JOURNAL OF MEDICAL GENETICS PART A -, no. - (2020): .
- Iman Safari, Kolsoum Inanloorahatloo, and Elahe Allahi. "Evolution of SARS‐CoV‐2 genome from December 2019 to late March 2020: Emerged haplotypes and informative Tag nucleotide variations." JOURNAL OF MEDICAL VIROLOGY -, no. - (2020): .
- Marziyeh Khani, Haniyeh Taheri, Hosein Shamshiri, [] [], john hardy, Tomas Bras, Kolsoum Inanloorahatloo, Afagh Alavi, Shahriar Nafissi, and Elahe Allahi. "Deep geno- and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutation." JOURNAL OF NEUROLOGY -, no. - (2020): .
- Kolsoum Inanloorahatloo, Fatemeh Peymani, Kimia Kahrizi, and Hossein Najmabadi. "Whole-Transcriptome Analysis Reveals Dysregulation of Actin-Cytoskeleton Pathway in Intellectual Disability Patients." NEUROSCIENCE 404, no. 404 (2019): 423-444.
- Kolsoum Inanloorahatloo, Elahe Allahi, and Saeid Davaran. "Lack of association between the MEF2A gene and coronary artery disease in iranian families." Iranian Journal of Basic Medical Sciences 16, no. 8 (2018): 950-954.
- Kolsoum Inanloorahatloo. "Sex-based differences in myocardial gene expression in recently deceased organ donors with no prior cardiovascular disease." PLoS One 12, no. 8 (2017): e0183874.
- Kolsoum Inanloorahatloo. "iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy." NATURE CELL BIOLOGY 18, no. 10 (2016): 1031-1042.
- Kolsoum Inanloorahatloo. "Polymorphisms of cystathionine beta-synthase gene are associated with susceptibility to sepsis." EUROPEAN JOURNAL OF HUMAN GENETICS 24, no. 7 (2015): 1041-1048.
- Kolsoum Inanloorahatloo, Amir Farhang Zand Parsa, Kalus Huse, Saeid Davaran, and Matthias Platzer. "Mutation in CYP27A1 identified in family with coronary artery." European Journal of Medical Genetics 56, no. 12 (2013): 655-660.
- Kolsoum Inanloorahatloo, and Ali Farazmand. "Expression of Dmrt Family Genes During Gonadal Differentiation in Two Species of Artemia (Branchiopoda, Anostraca) from Urmia Lake (Iran)." CRUSTACEANA 83, no. 10 (2010): 1153-1165.
- Kolsoum Inanloorahatloo, and Ali Farazmand. "Comparison of protein profile between bisexual and parthenogenetic species of Artemia (BRANCHIOPODA, ANOSTRACA).." CRUSTACEANA 82, no. 10 (2009): 1237-1248.
مقالات چاپ شده در نشریات داخلی
همایشهای بینالمللی
- Negin Mohammadi, Kolsoum Inanloorahatloo, Kimia Kahrizi, and Hossein Najmabadi. "Whole-Transcriptome Analysis Reveals Dysregulation of Extracellular Matrix Pathway in Intellectual Disability Patients." 22th National and 10th International Congress In Biology, Shahrekord.
- Motahareh Jadidi, Vida Babaali, Kolsoum Inanloorahatloo, and Reza Mollazadeh. "Mutation in TNNT3 gene identified in family with Left ventricular non-compaction." 22th National and 10th International Congress on Biology, Shahrekord.
- Mahboobe RezaviYekta, and Kolsoum Inanloorahatloo. "KDM6A mutation deregulatestranslation and nonsense mediated decaypathways in Intellectual disability patients." 4th International and 16th Iranian Genetics Congress, Tehran.
- Kolsoum Inanloorahatloo. "Molecular Signatures of iPSC Derived Cardiomyocytes Highlight Sex-Specific Differences." The 3rd National Festival and International Congress on Stem Cell and Regenerative Medicine, Tehran.
- Kolsoum Inanloorahatloo, Fatemeh Peymani, Kimia Kahrizi, and Hossein Najmabadi. "A splice-site mutation and overexpression of CCNT2 in autosomal recessive intellectual disability patients." ASHG 2018, San Diego.
- Kolsoum Inanloorahatloo, Fatemeh Peymani, Kimia Kahrizi, and Hossein Najmabadi. "Downregulation of SHTN1 gene in intellectual disability patients with mutation in CCNT2, CDK9 and TAF2 transcription factors." European Human Genetics Conference, Milan.
- Fatemeh Peymani, Kolsoum Inanloorahatloo, Kimia Kahrizi, and Hossein Najmabadi. "Identification of molecular pathways involved in Intellectual disability in family with mutation in CDK9 gene using RNA-seq." 3th internatinal and 15th Iranian Genetics Congress, Tehran.
- Kolsoum Inanloorahatloo. "Abnormal Activation of TGFβ Signaling as a Pathogenesis of Left Ventricular Non-compaction Cardiomyopathy." American Heart Association (AHA), orlando,FL.
- Kolsoum Inanloorahatloo. "Aberrant TGFβ Signaling as an Etiology of Left Ventricular Non-compaction Cardiomyopathy." American Heart Association's Basic Cardiovascular Sciences, New Orleans.
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