مقالات علمی چاپ شده در مجلات

1. "Identifcation of a rare variant in TNNT3 responsible for familial dilated cardiomyopathy through whole-exome sequencing and in silico analysis"
   Motahareh Jadidi, Vida Babaali, Kolsoum Inanloorahatloo, Najmeh Salehi, Reza mollazadeh
   EUROPEAN JOURNAL OF MEDICAL RESEARCH, Vol. 30, No 424, 2025
2. "Atypical presentations in an RTD patient and report of novel SLC52A3 and SLC52A2 mutations"
   Donya Sabeghi, Kolsoum Inanloorahatloo, هانیه میرزایی , Marziyeh Khani, Hosein Shamshiri, ترنم تقوی, Afagh Alavi, رضا بوستانی , Seyed Hassan Tonekaboni, Javad Akhondian, Masoomah Ebrahimi, Najmeh Salehi, شهریار نفیسی, Elaheh Elahi
   ACTA NEUROLOGICA BELGICA, Vol. 124, No 4, 2024
3. "Transcriptomic Analysis Reveals Sex-Based Differences in The Prefrontal Cortex of Autism Spectrum Disorder Patients"
   Sobhani Asma, Kolsoum Inanloorahatloo
   Cell Journal, Vol. 26, No 5, pp.320-328, 2024
4. "TBX15 and SDHB expression changes in colorectal cancer serve as potential prognostic biomarkers"
   MELIKA GOLOZAR, Ali Valipour motlagh, Mohammad Mahdevar, Maryam Peymani, Kolsoum Inanloorahatloo, Kamran Ghaedi
   EXPERIMENTAL AND MOLECULAR PATHOLOGY, Vol. 136, No 136, 2024
5. "Identification of gene signature in RNA-Seq hepatocellular carcinoma data by Pareto-optimal cluster algorithm"
   Taiebe Kenarangi, Enayatolah Bakhshi, Kolsoum Inanloorahatloo, Akbar Biglarian
   Gasteroenterology and hepatology from bed to bench, Vol. 15, No 4, 2022
6. "Intermittent white noise exposure is associated with rat cochleae damage and changes in the gene expression"
   Maryam Mirzaei, Mohammadreza Monazam, Monireh Kadem, Amir Abbasi Garmaroudi, Kolsoum Inanloorahatloo
   Egyptian Journal of Medical Human Genetics, Vol. 23, No 1, 2022
7. "Identifying Gene Signature in RNA Sequencing Multiple Sclerosis Data"
   Akbar Biglarian, Enayatolah Bakhshi, Kolsoum Inanloorahatloo, Taeibeh Kenarangi
   IRANIAN REHABILITATION JOURNAL, Vol. 20, No 2, pp.217-224, 2022
8. "Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery"
   Hossein Najmabadi, Kolsoum Inanloorahatloo, Afagh Alavi, Kimia Kahrizi, Mostafa Saghi
   BMC MEDICAL GENOMICS, Vol. 15, No 1, 2022
9. "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"
   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, Elahe Allahi
   VIROLOGY, Vol. 562, No 562, pp.63-73, 2021
10. "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"
    Iman Safari, Kolsoum Inanloorahatloo, Elahe Allahi
    JOURNAL OF MEDICAL VIROLOGY, Vol. 1, No 1, 2021
11. "Clinical spectrum in multiple families with primary COQ 10 deficiency"
    seyyed Hashemi, Davood Zare-Abdollahi, Mohammad Bakhshandeh, Amirreza Vafaee, Sona Abolhassani, Kolsoum Inanloorahatloo, Fardad DanaeeFard, Niloofar Farboodi, Mohammad Rohani, Afagh Alavi
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, Vol. -, 2020
12. "Evolution of SARS‐CoV‐2 genome from December 2019 to late March 2020: Emerged haplotypes and informative Tag nucleotide variations"
    Iman Safari, Kolsoum Inanloorahatloo, Elahe Allahi
    JOURNAL OF MEDICAL VIROLOGY, Vol. -, 2020
13. "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"
    Marziyeh Khani, Haniyeh Taheri, Hosein Shamshiri, [] [], john hardy, Tomas Bras, Kolsoum Inanloorahatloo, Afagh Alavi, Shahriar Nafissi, Elahe Allahi
    JOURNAL OF NEUROLOGY, Vol. -, 2020
14. "Whole-Transcriptome Analysis Reveals Dysregulation of Actin-Cytoskeleton Pathway in Intellectual Disability Patients"
    Kolsoum Inanloorahatloo, Fatemeh Peymani, Kimia Kahrizi, Hossein Najmabadi
    NEUROSCIENCE, Vol. 404, No 404, pp.423-444, 2019
15. "Sex-based differences in myocardial gene expression in recently deceased organ donors with no prior cardiovascular disease"
    Kolsoum Inanloorahatloo
    PLoS One, Vol. 12, No 8, 2017
16. "iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy"
    Kolsoum Inanloorahatloo
    NATURE CELL BIOLOGY, Vol. 18, No 10, pp.1031-1042, 2016
17. "Mutation in CYP27A1 identified in family with coronary artery"
    Kolsoum Inanloorahatloo, Amir Farhang Zand Parsa, Kalus Huse, Saeid Davaran, Matthias Platzer
    European Journal of Medical Genetics, Vol. 56, No 12, pp.655-660, 2013
18. "بررسی آلاینده های میکروبی در اسپان قارچ دکمه ای سفید (Agaricus bisporus) با استفاده از راهکار متاژنومیکس"
    شهناز شاهی، کلثوم اینانلو راحتلو، محمدعلی آموزگار
    ایمنی زیستی، نسخه 16، شماره 2، 1402
19. "بررسی اثرات ناشی از قرار گرفتن در معرض صدای سفید یکنواخت بر در حلزون گوش موش صحرایی نر SLC26A میزان بیان ژن 4"
    مریم میرزایی، کلثوم اینانلو راحتلو، منیره خادم، محمدرضا منظم، امیر عباسی
    مجله دانشگاه علوم پزشکی مازندران، نسخه 31، شماره 198، 1400
20. "استفاده از علوم اجتماعی و رفتاری برای پشتیبانی از پاسخ به همه گیری کووید-19"
    کلثوم اینانلو راحتلو
    مجله زیست شناسی ایران، نسخه 4، شماره 8، 1399
21. "بررسی پروفایل بیان ژنی در مراحل مختلف تکوین دندان در موش"
    زهره سلیمی، کلثوم اینانلو راحتلو
    مجله دندان پزشکی کودکان ایران، نسخه 15، شماره 2، 1398

مقالات علمی ارائه شده در همایش‌ها

1. "Identification of causative mutations for cardiomyopathy in two Iranian families using whole-exome sequencing and in-silico analysis"
   Motahareh Jadidi, vida babaali, Kolsoum Inanloorahatloo, reza mollazadeh
   6th international and 18th national genetic congress (GC2024), 2024
2. "Identification of homozygous mutation for hearing loss In Iranian family using Whole Exome Sequencing and in-silico analysis"
   Hora Sasani, Kolsoum Inanloorahatloo, Saeid Morovvati
   6th international and 18th national genetic congress (GC2024), 2024
3. "Identification of Genetic Variants Associated with Right Ventricular Non Compaction (RVNC)"
   mahta Hemmati Aghdam, Zahra Naghibzadeh, Kolsoum Inanloorahatloo, Motahareh Jadidi, AliHossein Sabet
   6th international and 18th national genetic congress (GC2024), 2024
4. "Identification of gene signature in RNA-Seq liver cancer data using Clustering Algorithms"
   Toktam Akbari Khalaj, Taiebe Kenarangi, Akbar Biglarian, Enayatolah Bakhshi, Kolsoum Inanloorahatloo, Mortza Lotfi
   The 1st International Biennial Conference of Artificial Intelligence and Data Science, 2024
5. "AI-Driven Variant Prioritization in Rare Genetic Disorders: Enhancing Diagnostic Accuracy and Clinical Outcomes"
   Kolsoum Inanloorahatloo
   The 1st International Biennial Conference of Artificial Intelligence and Data Science, 2024
6. "Identification of gene signatures using a Pareto-optimal cluster algorithm for multiple sclerosis RNA-Seq data"
   Taiebe Kenarangi, Akbar Biglarian, Kolsoum Inanloorahatloo, Enayatolah Bakhshi
   The 1st International Biennial Conference of Artificial Intelligence and Data Science, 2024
7. "predicting the impact of missense mutations on the protein structure networks: a case study of human phenylalanine hydroxylase and alfa galactosidase"
   Kolsoum Inanloorahatloo, Golnaz Bahramali, Fatemeh Ghandali, Sayed Amir Marashi
   3rd International & 12th Iranian Conference on Bioinformatics Partners with SilicoGene, 2024
8. "Identification of Some Genes Related toSurvival in Colorectal Cancer and determination of Hubgenes Based on The Cancer Genome Atlas database"
   melika Golozar, Ali Valipour Motlagh, Mohammad Mahdevar, Kolsoum Inanloorahatloo, Maryam Peymani, Kamran Ghaedi
   The First International Congress of Cancer Genomics, 2023
9. "Mutation in TNNT3 gene identified in family with Left ventricular non-compaction"
   Motahareh Jadidi, Vida Babaali, Kolsoum Inanloorahatloo, Reza Mollazadeh
   22th National and 10th International Congress on Biology, 2022
10. "Whole-Transcriptome Analysis Reveals Dysregulation of Extracellular Matrix Pathway in Intellectual Disability Patients"
    Negin Mohammadi, Kolsoum Inanloorahatloo, Kimia Kahrizi, Hossein Najmabadi
    22th National and 10th International Congress In Biology, 2022
11. "KDM6A mutation deregulatestranslation and nonsense mediated decaypathways in Intellectual disability patients"
    Mahboobe RezaviYekta, Kolsoum Inanloorahatloo
    4th International and 16th Iranian Genetics Congress, 2020
12. "Sex Differences in Health and Disease: Cardiovascular Disease and Cognitive Impairment"
    Kolsoum Inanloorahatloo
    4th International & 16th Iranian Genetics Congress, 2020
13. "Gene expression profile analysis during mouse tooth development"
    زهره سلیمی, Kolsoum Inanloorahatloo
    CInternational Congress of Isfahan Biomedical Sciences ICIBS –2020, 2020
14. "Differentially expressed genes and molecularpathways in Intellectual disability patients with mutation in Polr3b gene"
    Mostafa Saghi, Kolsoum Inanloorahatloo, Afagh Alavi, Hossein Najmabadi, Kimia Kahrizi
    International Congress of Isfahan Biomedical Sciences ICIBS –2020, 2020
15. "Identification the role of TUB in Intellectual disability using RNA-Seq"
    Fatemeh Peymani, Kolsoum Inanloorahatloo
    ESHG, 2020
16. "Molecular Signatures of iPSC Derived Cardiomyocytes Highlight Sex-Specific Differences"
    Kolsoum Inanloorahatloo
    The 3rd National Festival and International Congress on Stem Cell and Regenerative Medicine, 2018
17. "A splice-site mutation and overexpression of CCNT2 in autosomal recessive intellectual disability patients"
    Kolsoum Inanloorahatloo, Fatemeh Peymani, Kimia Kahrizi, Hossein Najmabadi
    ASHG 2018, 2018
18. "Downregulation of SHTN1 gene in intellectual disability patients with mutation in CCNT2, CDK9 and TAF2 transcription factors"
    Kolsoum Inanloorahatloo, Fatemeh Peymani, Kimia Kahrizi, Hossein Najmabadi
    European Human Genetics Conference, 2018
19. "Identification of molecular pathways involved in Intellectual disability in family with mutation in CDK9 gene using RNA-seq"
    Fatemeh Peymani, Kolsoum Inanloorahatloo, Kimia Kahrizi, Hossein Najmabadi
    3th internatinal and 15th Iranian Genetics Congress, 2018
20. "Application of whole exome sequencing (WES) in clinical diagnosis; An example"
    Seyed Saleh Hashemi, Afagh Alavi, Davood Zare-Abdollahi, Kolsoum Inanloorahatloo, Fardad DanaeeFard
    International Congress of Isfahan Biomedical Sciences ICIBS –2020, 2017