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Masoud Dehghan Tezerjani

Showing results (1-10 of 19) with videos related to

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International Journal of Reproductive Biomedicine|December 22, 2020
Unraveling the dark matter, long non-coding RNAs, in male reproductive diseases: A narrative reviewMasoud Dehghan Tezerjani, Seyed Mehdi Kalantar
Scientific Reports|April 27, 2026
MetaXVP: an interpretable machine learning framework for deep insight into variant pathogenicity and VUS classificationMasoud Dehghan Tezerjani, Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar
International Journal of Reproductive Biomedicine|November 16, 2022
Association study of <i>ESR1</i> rs9340799, rs2234693, and <i>MMP2</i> rs243865 variants in Iranian women with premature ovarian insufficiency: A case-control studyFarzaneh Sadat Eshaghi, Masoud Dehghan Tezerjani, Nasrin Ghasemi, et al.
Acta Neurologica Belgica|October 17, 2024
Repurposing doxycycline for a case of CONDSIAS Syndrome with a novel ADPRHL2 missense mutationHosein Eslamiyeh, Mohammad Yahya Vahidi Mehrjardi, Negareh Poursalehi, et al.
International Journal of General Medicine|June 18, 2020
Association of <i>GSTP1, GSTT1</i> and <i>GSTM1</i> Gene Variants with Coronary Artery Disease in Iranian Population: A Case-Control StudyAlemeh Pourkeramati, Ehsan Zare Mehrjardi, Masoud Dehghan Tezerjani, et al.
Frontiers in Pediatrics|July 17, 2020
A Novel <i>PCNT</i> Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)Masoud Dehghan Tezerjani, Mohammad Yahya Vahidi Mehrjardi, Hossein Hozhabri, et al.
International Journal of Molecular and Cellular Medicine|September 12, 2017
A Novel Missense Mutation in the ALDH13 Gene Causes Anophthalmia in Two Unrelated Iranian Consanguineous FamiliesMohammadreza Dehghani, Masoud Dehghan Tezerjani, Zahra Metanat, et al.
Ophthalmic Genetics|July 21, 2021
Incomplete penetrance of autosomal recessive anophthalmia in a large consanguineous familyMasoud Dehghan Tezerjani, Behdokht Fathi Dizaji, Zahra Metanat, et al.
Medical Journal of the Islamic Republic of Iran|July 4, 2020
Molecular biomarkers in diabetes mellitus (DM)Seyed Mohsen Aghaei Zarch, Masoud Dehghan Tezerjani, Mehrdad Talebi, et al.
Frontiers in Immunology|September 11, 2024
Exploring potential roles of long non-coding RNAs in cancer immunotherapy: a comprehensive reviewAsghar Arshi, Esmaeil Mahmoudi, Farzaneh Raeisi, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
International Journal of Reproductive Biomedicine|December 22, 2020
Unraveling the dark matter, long non-coding RNAs, in male reproductive diseases: A narrative reviewMasoud Dehghan Tezerjani, Seyed Mehdi Kalantar
Scientific Reports|April 27, 2026
MetaXVP: an interpretable machine learning framework for deep insight into variant pathogenicity and VUS classificationMasoud Dehghan Tezerjani, Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar
International Journal of Reproductive Biomedicine|November 16, 2022
Association study of <i>ESR1</i> rs9340799, rs2234693, and <i>MMP2</i> rs243865 variants in Iranian women with premature ovarian insufficiency: A case-control studyFarzaneh Sadat Eshaghi, Masoud Dehghan Tezerjani, Nasrin Ghasemi, et al.
Acta Neurologica Belgica|October 17, 2024
Repurposing doxycycline for a case of CONDSIAS Syndrome with a novel ADPRHL2 missense mutationHosein Eslamiyeh, Mohammad Yahya Vahidi Mehrjardi, Negareh Poursalehi, et al.
International Journal of General Medicine|June 18, 2020
Association of <i>GSTP1, GSTT1</i> and <i>GSTM1</i> Gene Variants with Coronary Artery Disease in Iranian Population: A Case-Control StudyAlemeh Pourkeramati, Ehsan Zare Mehrjardi, Masoud Dehghan Tezerjani, et al.
Frontiers in Pediatrics|July 17, 2020
A Novel <i>PCNT</i> Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)Masoud Dehghan Tezerjani, Mohammad Yahya Vahidi Mehrjardi, Hossein Hozhabri, et al.
International Journal of Molecular and Cellular Medicine|September 12, 2017
A Novel Missense Mutation in the ALDH13 Gene Causes Anophthalmia in Two Unrelated Iranian Consanguineous FamiliesMohammadreza Dehghani, Masoud Dehghan Tezerjani, Zahra Metanat, et al.
Ophthalmic Genetics|July 21, 2021
Incomplete penetrance of autosomal recessive anophthalmia in a large consanguineous familyMasoud Dehghan Tezerjani, Behdokht Fathi Dizaji, Zahra Metanat, et al.
Medical Journal of the Islamic Republic of Iran|July 4, 2020
Molecular biomarkers in diabetes mellitus (DM)Seyed Mohsen Aghaei Zarch, Masoud Dehghan Tezerjani, Mehrdad Talebi, et al.
Frontiers in Immunology|September 11, 2024
Exploring potential roles of long non-coding RNAs in cancer immunotherapy: a comprehensive reviewAsghar Arshi, Esmaeil Mahmoudi, Farzaneh Raeisi, et al.
Pageof 2