Down Syndrome: Current Status, Challenges and Future Perspectives von Kazemi, Mohammad, Salehi, Mansoor, Kheirollahi, Majid

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Sirenomelia: two case reports von Shojaee, Asiyeh, Ronnasian, Firooze, Behnam, Mahdiyeh, Salehi, Mansoor

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Novel Mutations in the MKKS, BBS7, and ALMS1 Genes in Iranian Children with Clinically Suspected Bardet–Biedl Syndrome von Dehghan, Roghayeh, Behnam, Mahdiyeh, Salehi, Mansoor, Kelishadi, Roya

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A Novel Mutation in the VPS13B Gene in a Cohen Syndrome Patient with Positive Antiphospholipid Antibodies von Dehghan, Roghayeh, Behnam, Mahdiyeh, Moafi, Alireza, Salehi, Mansoor

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Clinical Trial: CYP2D6 Related Dose Escalation of Tamoxifen in Breast Cancer Patients With Iranian Ethnic Background Resulted in Increased Concentrations of Tamoxifen and Its Metab... von Khalaj, Zahra, Baratieh, Zohreh, Nikpour, Parvaneh, Schwab, Matthias, Schaeffeler, Elke, Mokarian, Fariborz, Khanahmad, Hossein, Salehi, Rasoul, Mürdter, Thomas E, Salehi, Mansoor

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Identification of disease-causing genes using microarray data mining and Gene Ontology von Mohammadi, Azadeh, Saraee, Mohammad H, Salehi, Mansoor

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GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants von Koohiyan, Mahbobeh, Hashemzadeh-Chaleshtori, Morteza, Salehi, Mansoor, Abtahi, Hamidreza, Reiisi, Somayeh, Pourreza, Mohammad Reza, Noori-Daloii, Mohammad Reza, Tabatabaiefar, Mohammad Amin

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Effects of ABCG2 C421A and ABCG2 G34A genetic polymorphisms on clinical outcome and response to imatinib mesylate, in Iranian chronic myeloid leukemia patients von Nouri, Negar, Mehrzad, Valiollah, Khalaj, Zahra, Zaker, Erfan, Zare, Fateme, Abbasi, Elham, Khosravi, Maede

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Promising effect of rapamycin on multiple sclerosis von Bagherpour, Bahram, Salehi, Mansoor, Jafari, Rasool, Bagheri, Akram, Kiani-Esfahani, Abbas, Edalati, Masoud, Kardi, Mohammad Taghi, Shaygannejad, Vahid

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Distribution of CYP2D6 polymorphism in the Middle Eastern region von Khalaj, Zahra, Baratieh, Zohreh, Nikpour, Parvaneh, Khanahmad, Hossein, Mokarian, Fariborz, Salehi, Rasoul, Salehi, Mansoor

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Dysregulation of RNA interference components in COVID-19 patients von Mousavi, Seyyed Reza, Sajjadi, Maryam Sadat, Khosravian, Farinaz, Feizbakhshan, Sara, Salmanizadeh, Sharareh, Esfahani, Zahra Taherian, Beni, Faeze Ahmadi, Arab, Ameneh, Kazemi, Mohammad, Shahzamani, Kiana, Sami, Ramin, Hosseinzadeh, Majid, Salehi, Mansoor, Lotfi, Hajie

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A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family von Koohiyan, Mahbobeh, Noori-Daloii, Mohammad Reza, Hashemzadeh-Chaleshtori, Morteza, Salehi, Mansoor, Abtahi, Hamidreza, Tabatabaiefar, Mohammad Amin

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Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients von Komachali, Sajad Rafiee, Siahpoosh, Zakieh, Komachali, Sara Rafiee, Tamandani, Dor Mohammad Kordi, Salehi, Mansoor

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CTNS Mutations Causing Autosomal Recessive Cystinosis in a Subset of Iranian Population: Report of Two New Variants von Mohammadi Chermahini, Zahra, Salehi, Mansoor, Gheissari, Alaleh, Ahmadi Beni, Faeze, Khosravian, Farinaz, Kazemi, Mohammad

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A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23 von Koohiyan, Mahbobeh, Hashemzadeh-Chaleshtori, Morteza, Salehi, Mansoor, Abtahi, Hamidreza, Noori-Daloii, Mohammad Reza, Tabatabaiefar, Mohammad Amin

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A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel von Majidzadeh-A, Keivan, Zarinfam, Shiva, Abdoli, Nasrin, Yadegari, Fatemeh, Esmaeili, Rezvan, Farahmand, Leila, Teimourzadeh, Azin, Taghizadeh, Mahdieh, Salehi, Mansoor, Zamani, Mohamad

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Study of The Correlation between miR-106a, miR-125b, and miR-330 on Multiple Sclerosis Patients by Targeting TNFSF4 and SP1 in NF-кb/TNF-α Pathway: A Case-Control Study von Hadi, Nasrin, Seifati, Seyed Morteza, Nateghi, Behnaz, Ravaghi, Parisa, Khosravian, Farinaz, Namazi, Faezeh, Maryam Fotouhi Firouzabad, Shaygannejad, Vahid, Salehi, Mansoor

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Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants von Mianesaz, Hamidreza, Ghalamkari, Safoura, Salehi, Mansoor, Behnam, Mahdiyeh, Hosseinzadeh, Majid, Basiri, Keivan, Ghasemi, Majid, Sedghi, Maryam, Ansari, Behnaz

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A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features von Sekiguchi, Futoshi, Nasiri, Jafar, Sedghi, Maryam, Salehi, Mansoor, Hosseinzadeh, Majid, Okamoto, Nobuhiko, Mizuguchi, Takeshi, Nakashima, Mitsuko, Miyatake, Satoko, Takata, Atsushi, Miyake, Noriko, Matsumoto, Naomichi

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New long noncoding RNA biomarkers and ceRNA networks on miR-616-3p in colorectal cancer: Bioinformatics-based study von Abdolvand, Mohammad, Chermahini, Zahra Mohammadi, Bahaloo, Sahar, Emami, Mohammad Hassan, Fahim, Alireza, Rahimi, Hojjatolah, Amjadi, Elham, Maghool, Fatemeh, Rohani, Fattah, Dadkhah, Mina, Farhadian, Nooshin, Vatandoust, Nasimeh, Abdolvand, Shirin, Darehsari, Maliheh Roozbahani, Chehelgerdi, Mohammad, Beni, Faeze Ahmadi, Khodadoostan, Mahsa, Hemati, Simin, Salehi, Mansoor

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