Kolsoum Inanloorahatloo

1. Atypical presentations in an RTD patient and report of novel SLC52A3 and SLC52A2 mutations

Sabeghi Donya, Inanloorahatloo Kolsoum, هانیه میرزایی, Khani Marziyeh, Shamshiri Hosein, تقوی ترنم, Alavi Afagh, رضا بوستانی, Tonekaboni Seyed Hassan, Akhondian Javad, Ebrahimi Masoomah, Salehi Najmeh, نفیسی شهریار, Elahi Elaheh (2024)., ACTA NEUROLOGICA BELGICA, 124(4).

2. Identification of homozygous mutation for hearing loss In Iranian family using Whole Exome Sequencing and in-silico analysis

Sasani Hora, Inanloorahatloo Kolsoum, Morovvati Saeid (2024)., 6th international and 18th national genetic congress (GC2024), 22-24 May, Tehran, Iran.

3. Identification of causative mutations for cardiomyopathy in two Iranian families using whole-exome sequencing and in-silico analysis

Jadidi Motahareh, babaali vida, Inanloorahatloo Kolsoum, mollazadeh reza (2024)., 6th international and 18th national genetic congress (GC2024), 22-24 May, Tehran, Iran.

4. Identification of Genetic Variants Associated with Right Ventricular Non Compaction (RVNC)

Hemmati Aghdam mahta, Naghibzadeh Zahra, Inanloorahatloo Kolsoum, Jadidi Motahareh, Sabet AliHossein (2024)., 6th international and 18th national genetic congress (GC2024), 22-24 May, Tehran, Iran.

5. Transcriptomic Analysis Reveals Sex-Based Differences in The Prefrontal Cortex of Autism Spectrum Disorder Patients

Asma Sobhani, Inanloorahatloo Kolsoum (2024)., Cell Journal, 26(5), 320-328.

6. Identification of gene signature in RNA-Seq liver cancer data using Clustering Algorithms

Akbari Khalaj Toktam, Kenarangi Taiebe, Biglarian Akbar, Bakhshi Enayatolah, Inanloorahatloo Kolsoum, Lotfi Mortza (2024)., The 1st International Biennial Conference of Artificial Intelligence and Data Science, 22-23 April, Bushehr, Iran.

7. AI-Driven Variant Prioritization in Rare Genetic Disorders: Enhancing Diagnostic Accuracy and Clinical Outcomes

Inanloorahatloo Kolsoum (2024)., The 1st International Biennial Conference of Artificial Intelligence and Data Science, 22-23 April, Bushehr, Iran.

8. Identification of gene signatures using a Pareto-optimal cluster algorithm for multiple sclerosis RNA-Seq data

Kenarangi Taiebe, Biglarian Akbar, Inanloorahatloo Kolsoum, Bakhshi Enayatolah (2024)., The 1st International Biennial Conference of Artificial Intelligence and Data Science, 22-23 April, Bushehr, Iran.

9. TBX15 and SDHB expression changes in colorectal cancer serve as potential prognostic biomarkers

GOLOZAR MELIKA, Valipour motlagh Ali, Mahdevar Mohammad, Peymani Maryam, Inanloorahatloo Kolsoum, Ghaedi Kamran (2024)., EXPERIMENTAL AND MOLECULAR PATHOLOGY, 136(136), 104890.

10. predicting the impact of missense mutations on the protein structure networks: a case study of human phenylalanine hydroxylase and alfa galactosidase

Inanloorahatloo Kolsoum, Bahramali Golnaz, Ghandali Fatemeh, Marashi Sayed Amir (2024)., 3rd International & 12th Iranian Conference on Bioinformatics Partners with SilicoGene, 28-29 February, Behshahr, Iran.

11. Unveiling Microbial Contaminants in Agaricus bisporus Mushroom Spawns using metagenomics approach

Shahnaz Shahi, Inanloorahatloo Kolsoum, Amozegar Mohammad (2024)., Journal of Biosafety, 16(2).

1. Identification of Some Genes Related toSurvival in Colorectal Cancer and determination of Hubgenes Based on The Cancer Genome Atlas database

Golozar melika, Valipour Motlagh Ali, Mahdevar Mohammad, Inanloorahatloo Kolsoum, Peymani Maryam, Ghaedi Kamran (2023)., The First International Congress of Cancer Genomics, 3-5 May, Tehran, Iran.

1. Identification of gene signature in RNA-Seq hepatocellular carcinoma data by Pareto-optimal cluster algorithm

Kenarangi Taiebe, Bakhshi Enayatolah, Inanloorahatloo Kolsoum, Biglarian Akbar (2022)., Gasteroenterology and hepatology from bed to bench, 15(4).

2. Whole-Transcriptome Analysis Reveals Dysregulation of Extracellular Matrix Pathway in Intellectual Disability Patients

Mohammadi Negin, Inanloorahatloo Kolsoum, Kahrizi Kimia, Najmabadi Hossein (2022)., 22th National and 10th International Congress In Biology, 31 August-2 September, Shahrekord, Iran.

3. Mutation in TNNT3 gene identified in family with Left ventricular non-compaction

Jadidi Motahareh, Babaali Vida, Inanloorahatloo Kolsoum, Mollazadeh Reza (2022)., 22th National and 10th International Congress on Biology, 31 August-2 September, Shahrekord, Iran.

4. Intermittent white noise exposure is associated with rat cochleae damage and changes in the gene expression

Mirzaei Maryam, Monazam Mohammadreza, Kadem Monireh, Abbasi Garmaroudi Amir, Inanloorahatloo Kolsoum (2022)., Egyptian Journal of Medical Human Genetics, 23(1).

5. Identifying Gene Signature in RNA Sequencing Multiple Sclerosis Data

Biglarian Akbar, Bakhshi Enayatolah, Inanloorahatloo Kolsoum, Kenarangi Taeibeh (2022)., IRANIAN REHABILITATION JOURNAL, 20(2), 217-224.

6. Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery

Najmabadi Hossein, Inanloorahatloo Kolsoum, Alavi Afagh, Kahrizi Kimia, Saghi Mostafa (2022)., BMC MEDICAL GENOMICS, 15(1).

1. 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

Taghizadeh Peyman, Salehi Sadegh, Safari Iman, Houshmand Masoud, Inanloorahatloo Kolsoum, Mahjobi Frozandeh, محمدحسین صنعتی, Alavi Afagh, Heshmati Ali, Amel Jamehdar Saeid, Galehdari Hamid, Haghshenas Mohammad Reza, Hashemian Amir Masoud, Heidarzadeh Abtin, Jahanzad Issa, Kheyrani Elham, Piroozmand Ahmad, Mojtahedi Ali, Razavi Nikoo Hadi, Rahimi Bidgoli Mohammad Masoud, Rezvani Nayebali, Sepehrnejad Mehdi, Shakibzadeh Arash, Shariati Gholamreza, Seyyedi Noorossadat, Zahraei Seyed MohammadSaleh, Yari Hadi, Dabiri Soroosh, Allahi Elahe (2021)., VIROLOGY, 562(562), 63-73.

2. Investigating the Effects of Exposure to Continuous White Noise on SLC26A4 Gene Expression Levels in Male Rat Cochlea

Mirzaei Maryam, Inanloorahatloo Kolsoum, Kadem Monireh, Monazam Mohammadreza, Abbasi Amir (2021)., Journal of Mazandaran University of Medical Sciences, 31(198).

3. 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

Safari Iman, Inanloorahatloo Kolsoum, Allahi Elahe (2021)., JOURNAL OF MEDICAL VIROLOGY, 1(1).

1. Use of Social and Behavioral Science for Support of COVID-19 Pandemy responses

Inanloorahatloo Kolsoum (2020)., Biological Science Promotion, 4(8).

2. Clinical spectrum in multiple families with primary COQ 10 deficiency

Hashemi seyyed, Zare-Abdollahi Davood, Bakhshandeh Mohammad, Vafaee Amirreza, Abolhassani Sona, Inanloorahatloo Kolsoum, DanaeeFard Fardad, Farboodi Niloofar, Rohani Mohammad, Alavi Afagh (2020)., AMERICAN JOURNAL OF MEDICAL GENETICS PART A, -(-).

3. Evolution of SARS‐CoV‐2 genome from December 2019 to late March 2020: Emerged haplotypes and informative Tag nucleotide variations

Safari Iman, Inanloorahatloo Kolsoum, Allahi Elahe (2020)., JOURNAL OF MEDICAL VIROLOGY, -(-).

4. Life: The science of biology

Inanloorahatloo Kolsoum, رحیمی گلنوش (2020).