Aboulfazl Rad (Abolfazl Rad)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 9

Top Venues

cellular and molecular research center

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

Affiliation History

cellular and molecular research center Sep 06 2014

Iran

Academic member

Publications

Asuman Koparir, Caroline Lekszas, Kemal Keseroğlu, Thalia Rose, Lena Rappl, Aboulfazl Rad, Reza Maroofian, Nakul Narendran, Atefeh Hasanzadeh, Ehsan Ghayoor Karimiani, Felix Boschann, Uwe Kornak, Eva Klopocki, Ertuğrul M Özbudak, Barbara Vona, Thomas Haaf, Daniel Liedtke
Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome. Human genomics 18 (1) (2024)
Asuman Koparir, Caroline Lekszas, Kemal Keseroğlu, Thalia Rose, Lena Rappl, Aboulfazl Rad, Reza Maroofian, Nakul Narendran, Atefeh Hasanzadeh, Ehsan Ghayoor Karimiani, Felix Boschann, Uwe Kornak, Eva Klopocki, Ertuğrul M Özbudak, Barbara Vona, Thomas Haaf, Daniel Liedtke
Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome. Human genomics 18 (1) (2024)
Asuman Koparir, Caroline Lekszas, Kemal Keseroğlu, Thalia Rose, Lena Rappl, Aboulfazl Rad, Reza Maroofian, Nakul Narendran, Atefeh Hasanzadeh, Ehsan Ghayoor Karimiani, Felix Boschann, Uwe Kornak, Eva Klopocki, Ertuğrul M Özbudak, Barbara Vona, Thomas Haaf, Daniel Liedtke
Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome. Human genomics 18 (1) (2024)
Barbara Vona, Neda Mazaheri, Sheng-Jia Lin, Lucy A Dunbar, Reza Maroofian, Hela Azaiez, Kevin T A Booth, Sandrine Vitry, Aboulfazl Rad, Franz Rüschendorf, Pratishtha Varshney, Ben Fowler, Christian Beetz, Kumar N Alagramam, David P Murphy, Gholamreza Shariati, Alireza Sedaghat, Henry Houlden, Cassidy Petree, Shruthi VijayKumar, Richard J H Smith, Thomas Haaf, Aziz El-Amraoui, Michael R Bowl, Guarav K Varshney, Hamid Galehdari
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans. Human genetics 140 (6) (2021)
Barbara Vona, Aboulfazl Rad, Ellen Reisinger
The Many Faces of DFNB9: Relating OTOF Variants to Hearing Impairment. Genes 11 (12) (2020)
Lauretta El Hayek, Islam Oguz Tuncay, Nadine Nijem, Jamie Russell, Sara Ludwig, Kiran Kaur, Xiaohong Li, Priscilla Anderton, Miao Tang, Amanda Gerard, Anja Heinze, Pia Zacher, Hessa S Alsaif, Aboulfazl Rad, Kazem Hassanpour, Mohammad Reza Abbaszadegan, Camerun Washington, Barbara R DuPont, Raymond J Louie, null null, Madeline Couse, Maha Faden, R Curtis Rogers, Rami Abou Jamra, Ellen R Elias, Reza Maroofian, Henry Houlden, Anna Lehman, Bruce Beutler, Maria H Chahrour
KDM5A mutations identified in autism spectrum disorder using forward genetics. eLife 9 (2020)
Julia Doll, Susanne Kolb, Linda Schnapp, Aboulfazl Rad, Franz Rüschendorf, Imran Khan, Abolfazl Adli, Atefeh Hasanzadeh, Daniel Liedtke, Sabine Knaup, Michaela Ah Hofrichter, Tobias Müller, Marcus Dittrich, Il-Keun Kong, Hyung-Goo Kim, Thomas Haaf, Barbara Vona
Novel Loss-of-Function Variants in CDC14A are Associated with Recessive Sensorineural Hearing Loss in Iranian and Pakistani Patients. International journal of molecular sciences 21 (1) (2020)
Aboulfazl Rad, Thore Schade-Mann, Philipp Gamerdinger, Grigoriy A Yanus, Björn Schulte, Marcus Müller, Evgeny N Imyanitov, Saskia Biskup, Hubert Löwenheim, Anke Tropitzsch, Barbara Vona
Aberrant COL11A1 splicing causes prelingual autosomal dominant nonsyndromic hearing loss in the DFNA37 locus. Human mutation 42 (1) (2020)
Seyed Elyas Meshkani, Narges Kooshan, Arezoo Baradaran Moghadam, Farahnaz Falanji, Abolfazl Adli, Fahimeh Baghbani-Arani, Alireza Ghasemi Arian, Aboulfazl Rad
Signaling roadmap to epithelial-mesenchymal transition in pterygium, TWIST1 centralized. Journal of cellular physiology 234 (10) (2019)

Aboulfazl Rad.css-eqlu8i{font-size:small;padding-left:4px;} (Abolfazl Rad)

Publication Activity (10 Years)

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Aboulfazl Rad (Abolfazl Rad)