Showing 1–7 of 7 results
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Research | | Open
Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability
- Taimoor I. Sheikh
- , Nasim Vasli
- , Stephen Pastore
- , Kimia Kharizi
- , Ricardo Harripaul
- , Zohreh Fattahi
- , Shruti Pande
- , Farooq Naeem
- , Abrar Hussain
- , Asif Mir
- , Omar Islam
- , Katta Mohan Girisha
- , Muhammad Irfan
- , Muhammad Ayub
- , Christoph Schwarzer
- , Hossein Najmabadi
- , Anju Shukla
- , Valentina C. Sladky
- , Vincent Zoran Braun
- , Irmina Garcia-Carpio
- , Andreas Villunger
- & John B. Vincent
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Genetics of intellectual disability in consanguineous families
- Hao Hu
- , Kimia Kahrizi
- , Luciana Musante
- , Zohreh Fattahi
- , Ralf Herwig
- , Masoumeh Hosseini
- , Cornelia Oppitz
- , Seyedeh Sedigheh Abedini
- , Vanessa Suckow
- , Farzaneh Larti
- , Maryam Beheshtian
- , Bettina Lipkowitz
- , Tara Akhtarkhavari
- , Sepideh Mehvari
- , Sabine Otto
- , Marzieh Mohseni
- , Sanaz Arzhangi
- , Payman Jamali
- , Faezeh Mojahedi
- , Maryam Taghdiri
- , Elaheh Papari
- , Mohammad Javad Soltani Banavandi
- , Saeide Akbari
- , Seyed Hassan Tonekaboni
- , Hossein Dehghani
- , Mohammad Reza Ebrahimpour
- , Ingrid Bader
- , Behzad Davarnia
- , Monika Cohen
- , Hossein Khodaei
- , Beate Albrecht
- , Sarah Azimi
- , Birgit Zirn
- , Milad Bastami
- , Dagmar Wieczorek
- , Gholamreza Bahrami
- , Krystyna Keleman
- , Leila Nouri Vahid
- , Andreas Tzschach
- , Jutta Gärtner
- , Gabriele Gillessen-Kaesbach
- , Jamileh Rezazadeh Varaghchi
- , Bernd Timmermann
- , Fatemeh Pourfatemi
- , Aria Jankhah
- , Wei Chen
- , Pooneh Nikuei
- , Vera M. Kalscheuer
- , Morteza Oladnabi
- , Thomas F. Wienker
- , Hans-Hilger Ropers
- & Hossein Najmabadi
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Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration
- Zafar Iqbal
- , Lucia Püttmann
- , Luciana Musante
- , Attia Razzaq
- , Muhammad Yasir Zahoor
- , Hao Hu
- , Thomas F Wienker
- , Masoud Garshasbi
- , Zohreh Fattahi
- , Christian Gilissen
- , Lisenka ELM Vissers
- , Arjan PM de Brouwer
- , Joris A Veltman
- , Rolph Pfundt
- , Hossein Najmabadi
- , Hans-Hilger Ropers
- , Sheikh Riazuddin
- , Kimia Kahrizi
- & Hans van Bokhoven
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Research |
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
- Hossein Najmabadi
- , Hao Hu
- , Masoud Garshasbi
- , Tomasz Zemojtel
- , Seyedeh Sedigheh Abedini
- , Wei Chen
- , Masoumeh Hosseini
- , Farkhondeh Behjati
- , Stefan Haas
- , Payman Jamali
- , Agnes Zecha
- , Marzieh Mohseni
- , Lucia Püttmann
- , Leyla Nouri Vahid
- , Corinna Jensen
- , Lia Abbasi Moheb
- , Melanie Bienek
- , Farzaneh Larti
- , Ines Mueller
- , Robert Weissmann
- , Hossein Darvish
- , Klaus Wrogemann
- , Valeh Hadavi
- , Bettina Lipkowitz
- , Sahar Esmaeeli-Nieh
- , Dagmar Wieczorek
- , Roxana Kariminejad
- , Saghar Ghasemi Firouzabadi
- , Monika Cohen
- , Zohreh Fattahi
- , Imma Rost
- , Faezeh Mojahedi
- , Christoph Hertzberg
- , Atefeh Dehghan
- , Anna Rajab
- , Mohammad Javad Soltani Banavandi
- , Julia Hoffer
- , Masoumeh Falah
- , Luciana Musante
- , Vera Kalscheuer
- , Reinhard Ullmann
- , Andreas Walter Kuss
- , Andreas Tzschach
- , Kimia Kahrizi
- & H. Hilger Ropers
