Saeed Talebi

school of medicine

H指数:17

被引数:1,014

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荣誉奖项

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Inherited metabolic disorder-related genes and mutation spectrum in Iranians: an 11-year analysis using next-generation sequencing and sanger sequencing

伊朗人遗传代谢病相关基因及突变谱：一项基于下一代测序和Sanger测序的11年分析

Orphanet Journal of Rare Diseases

IF3.5

2026-10-020

OAAI

Parnian Alagha; Negar Molaei; Maryam Beheshtian; Fatemeh Ahangari; Shima Dehdahsi; Mahsa Fadaee; Mehri Ashki; Zhila Ghaderi; Zohreh Elahi; Raheleh Vazehan; Maryam Mozaffarpour Nouri; Parishad Saei; Khadijeh Noudehi; Fatemeh Fatehi; Shima Zamanian Najafabadi; Fariba Afroozan; Banafsheh Salmani; Mahdieh kooshki; Armita Ghaderi; Zohreh Vahidi; Mina Makvand; Atiyeh Ahmadpour; Mahsa Tahmasebivand; Elmira Shiuokhi; Saeed Talebi; Reza Shervin Badv; Babak Zamani; Farhad Mahvelati-Shamsabadi; Bahram Haghi Ashtiani; Payam Sarraf; Haleh Habibi; Afshin Fayyazi; Ali Asghar Okhovat; Mahmoud Reza Ashrafi; Farzad Fatehi; Parvaneh Karimzadeh; Shahriar Nafissi; Kimia Kahrizi; Ariana Kariminejad; Hossein Najmabadi

Exome Sequencing and Molecular Modeling Reveal Novel Loci in Familial Multiple Sclerosis: The Importance of BTNL3 and BTNL8 in Disease Pathogenesis

外显子测序和分子建模揭示家族性多发性硬化中的新型位点：BTNL3和BTNL8在疾病发病机制中的重要性

Molecular Neurobiology

IF4.3

2025-12-010

PRE

DNA REPAIR

IF2.7

2024-04-010

PRE

Integrated genomic sequencing in myeloid blast crisis chronic myeloid leukemia (MBC-CML), identified potentially important findings in the context of leukemogenesis model (vol 12, pg.no: 12816, 2022)

SCIENTIFIC REPORTS

IF3.9

2023-01-130

OAAI

Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency

KIDNEY INTERNATIONAL

IF12.6

2022-09-0133

Drovandi, Stefania; Lipska-Zietkiewicz, Beata S.; Ozaltin, Fatih; Emma, Francesco; Gulhan, Bora; Boyer, Olivia; Trautmann, Agnes; Xu, Hong; Shen, Qian; Rao, Jia; Riedhammer, Korbinian M.; Heemann, Uwe; Hoefele, Julia; Stenton, Sarah L.; Tsygin, Alexey N.; Ng, Kar-Hui; Fomina, Svitlana; Benetti, Elisa; Aurelle, Manon; Prikhodina, Larisa; Schreuder, Michiel F.; Tabatabaeifar, Mansoureh; Jankowski, Maciej; Baiko, Sergey; Mao, Jianhua; Feng, Chunyue; Liu, Cuihua; Sun, Shuzhen; Deng, Fang; Wang, Xiaowen; Clave, Stephanie; Stanczyk, Malgorzata; Balasz-Chmielewska, Irena; Fila, Marc; Durkan, Anne M.; Levart, Tanja Kersnik; Dursun, Ismail; Esfandiar, Nasrin; Haas, Dorothea; Bjerre, Anna; Anarat, Ali; Benz, Marcus R.; Talebi, Saeed; Hooman, Nakysa; Ariceta, Gema; Schaefer, Franz

Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy

KIDNEY INTERNATIONAL

IF12.6

2022-09-0126

Drovandi, Stefania; Lipska-Zietkiewicz, Beata S.; Ozaltin, Fatih; Emma, Francesco; Gulhan, Bora; Boyer, Olivia; Trautmann, Agnes; Zietkiewicz, Szymon; Xu, Hong; Shen, Qian; Rao, Jia; Riedhammer, Korbinian M.; Heemann, Uwe; Hoefele, Julia; Stenton, Sarah L.; Tsygin, Alexey N.; Ng, Kar-Hui; Fomina, Svitlana; Benetti, Elisa; Aurelle, Manon; Prikhodina, Larisa; Schijvens, Anne M.; Tabatabaeifar, Mansoureh; Jankowski, Maciej; Baiko, Sergey; Mao, Jianhua; Feng, Chunyue; Deng, Fang; Rousset-Rouviere, Caroline; Stanczyk, Malgorzata; Balasz-Chmielewska, Irena; Fila, Marc; Durkan, Anne M.; Levart, Tanja Kersnik; Dursun, Ismail; Esfandiar, Nasrin; Haas, Dorothea; Bjerre, Anna; Anarat, Ali; Benz, Marcus R.; Talebi, Saeed; Hooman, Nakysa; Ariceta, Gema; Serna Higuita, Lina Maria; Schaefer, Franz; Trautmann, Agnes; Tabatabaeifar, Mansoureh; Gheissari, Alaleh; Hooman, Nakysa; Benetti, Elisa; Emma, Francesco; Nigmatullina, Nazym; Tkaczyk, Marcin; Borzecka, Halina; Tsygin, Alexey N.; Prikhodina, Larisa; Bogdanovic, Radovan; Mir, Sevgi; Fomina, Svitlana; Klopstock, Thomas; Prokisch, Holger; Kornblum, Cornelia; Liu, Cui-Hua; Sun, Shu-Zhen; Dong, Yang; Wang, Xiao-Wen; Luan, Jiang-Wei; Schaefer, Franz

Integrated genomic sequencing in myeloid blast crisis chronic myeloid leukemia (MBC-CML), identified potentially important findings in the context of leukemogenesis model

SCIENTIFIC REPORTS

IF3.9

2022-07-272

OAAI

Exome sequencing reveals novel rare variants in Iranian familial multiple sclerosis: The importance of POLD2 in the disease pathogenesis

GENOMICS

IF3

2021-07-018

OAAI

The importance of CDC27 in cancer: molecular pathology and clinical aspects

CANCER CELL INTERNATIONAL