Feyzollah Hashemi-Gorji (Farzad Hashemi-Gorji)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 14

Top Venues

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Molecular genetics & genomic medicine

Shahid Beheshti University of Medical Sciences

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Shahid Beheshti University of Medical Sciences Oct 23 2011

Iran

Research assistant :: Genomic Research Center

Pasteur Institute of Iran Dec 16 2009 - May 20 2011

Iran

Research assistant :: Molecular Medicine Department

Publications

Shamsoulmolouk Najafi, Feyzollah Hashemi-Gorji, Hassan Roudgari, Mina Goudarzi, Amir Mohammad Jafarzadegan, Nafiseh Sheykhbahaei
Genetic change investigation in DOCK1 gene in an Iranian family with sign and symptoms of temporomandibular joint disorder (TMD). Clinical oral investigations 28 (8) (2024)
Shamsoulmolouk Najafi, Feyzollah Hashemi-Gorji, Hassan Roudgari, Mina Goudarzi, Amir Mohammad Jafarzadegan, Nafiseh Sheykhbahaei
Genetic change investigation in DOCK1 gene in an Iranian family with sign and symptoms of temporomandibular joint disorder (TMD). Clinical oral investigations 28 (8) (2024)
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Shamsoulmolouk Najafi, Feyzollah Hashemi-Gorji, Hassan Roudgari, Mina Goudarzi, Amir Mohammad Jafarzadegan, Nafiseh Sheykhbahaei
Genetic change investigation in DOCK1 gene in an Iranian family with sign and symptoms of temporomandibular joint disorder (TMD). Clinical oral investigations 28 (8) (2024)
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Feyzollah Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad Reza Ghasemi
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases. BMC medical genomics 17 (1) (2024)
Parinaz Moghimi, Feyzollah Hashemi-Gorji, Sanaz Jamshidi, Sahand Tehrani Fateh, Shadab Salehpour, Hossein Sadeghi, Fatemeh Norouzi Rostami, Reza Mirfakhraie, Mohammad Miryounesi, Mohammad Reza Ghasemi
Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort. Biochemical genetics (2024)
Aysan Moeinafshar, Sahand Tehrani Fateh, Hossein Sadeghi, Parvaneh Karimzadeh, Reza Mirfakhraie, Feyzollah Hashemi-Gorji, Pegah Larki, Mohammad Miryounesi, Mohammad Reza Ghasemi
Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Camille Engel, Stéphanie Valence, Geoffroy Delplancq, Reza Maroofian, Andrea Accogli, Emanuele Agolini, Fowzan Sami Alkuraya, Valentina Baglioni, Irene Bagnasco, Mathilde Becmeur-Lefebvre, Enrico Silvio Bertini, Ingo Borggraefe, Elise Brischoux-Boucher, Ange-Line Bruel, Alfredo Brusco, Dalal K Bubshait, Christelle Cabrol, Maria Roberta Cilio, Marie-Coralie Cornet, Christine Coubes, Olivier Danhaive, Valérie Delague, Anne Sophie Denommé-Pichon, Marilena Carmela Di Giacomo, Martine Doco-Fenzy, Hartmut Engels, Kirsten Cremer, Marion Gérard, Joseph G Gleeson, Delphine Heron, Joanna Goffeney, Anne Guimier, Frederike L Harms, Henry Houlden, Michele Iacomino, Rauan Kaiyrzhanov, Benjamin Kamien, Ehsan Ghayoor Karimiani, Dror Kraus, Paul Kuentz, Kerstin Kutsche, Damien Lederer, Lauren Massingham, Cyril Mignot, Deborah J Morris-Rosendahl, Lakshmi Nagarajan, Sylvie Odent, Clothilde Ormières, Jennifer Neil Partlow, Laurent Pasquier, Lynette Penney, Christophe Philippe, Gianluca Piccolo, Cathryn Poulton, Audrey Putoux, Marlène Rio, Christelle Rougeot, Vincenzo Salpietro, Ingrid Scheffer, Amy L Schneider, Siddharth Srivastava, Rachel Straussberg, Pasquale Striano, Enza Maria Valente, Perrine Venot, Laurent Villard, Antonio Vitobello, Johanna Wagner, Matias Wagner, Maha Saad Zaki, Federizo Zara, Gaëtan Lesca, Vahid Reza Yassaee, Mohammad Miryounesi, Feyzollah Hashemi-Gorji, Mehran Beiraghi, Farah Ashrafzadeh, Hamid Galehdari, Christopher A Walsh, Antonio Novelli, Moritz Tacke, Dinara Sadykova, Yerdan Maidyrov, Kairgali Koneev, Chingiz Shashkin, Valeria Capra, Mina Zamani, Lionel Van Maldergem, Lydie Burglen, Juliette Piard
BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients. European journal of human genetics : EJHG (2023)
Vahid Reza Yassaee, Arash Khojasteh, Feyzollah Hashemi-Gorji, Hossein Sadeghi, Hannaneh Safiaghdam, Reza Mirfakhraie
Gnathodiaphyseal dysplasia with a novel genetic variant in a large family from Iran. Molecular genetics & genomic medicine 10 (9) (2022)
Sepide Dashti, Shadab Salehpour, Mohammad Reza Ghasemi, Hossein Sadeghi, Masoumeh Rostami, Feyzollah Hashemi-Gorji, Reza Mirfakhraie, Vahid Reza Yassaee, Mohammad Miryounesi
Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 43 (4) (2022)
Krista Marie Vincent, Alison Eaton, Vahid Reza Yassaee, Mohammad Miryounesi, Feyzollah Hashemi-Gorji, Lauren Rudichuk, Helly Goez, Norma Leonard, Joanna Lazier
Delineating the expanding phenotype of HERC2-related disorders: The impact of biallelic loss of function versus missense variation. Clinical genetics 100 (5) (2021)
Feyzollah Hashemi-Gorji, Shadab Salehpour, Mohammad Miryounesi, Reza Mirfakhraie, Vahid Reza Yassaee
A novel SRD5A2 mutation in an Iranian family with sex development disorder. Andrologia 53 (1) (2020)
Feyzollah Hashemi-Gorji, Majid Fardaei, Seyed Mohammad Bagher Tabei, Mohammad Miryounesi
Novel mutation in the MED23 gene for intellectual disability: A case report and literature review. Clinical case reports 7 (2) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Feyzollah Hashemi-Gorji (Farzad Hashemi-Gorji)