All papers authored by Ranad Shaheen
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2022
Mary E. McQuaid 
,
Kashif Ahmed,
Stephanie Tran,
Justine Rousseau ,
Ranad Shaheen ,
Kristin D. Kernohan,
Kyoko E. Yuki ,
Prerna Grover ,
Ema S. Dreseris,
Sameen Ahmed,
Lucie Dupuis ,
Jennifer Stimec,
Mary Shago,
Zuhair N. Al-Hassnan ,
Roch Tremblay
and 14 other authors
,
Kashif Ahmed,
Stephanie Tran,
Justine Rousseau ,
Ranad Shaheen ,
Kristin D. Kernohan,
Kyoko E. Yuki ,
Prerna Grover ,
Ema S. Dreseris,
Sameen Ahmed,
Lucie Dupuis ,
Jennifer Stimec,
Mary Shago,
Zuhair N. Al-Hassnan ,
Roch Tremblay
and 14 other authors
Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome
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2021
Reem Saleh,
Varun Sasidharan Nair,
Khaled Murshed ,
Mohamed Abu Nada,
Eyad Elkord ,
Ranad Shaheen
Download from link.springer.com
,
Mohamed Abu Nada,
Eyad Elkord ,
Ranad Shaheen
Download from link.springer.com
Reem Saleh,
Varun Sasidharan Nair,
Khaled Murshed ,
Mohamed Abu Nada,
Eyad Elkord ,
Ranad Shaheen
,
Mohamed Abu Nada,
Eyad Elkord ,
Ranad Shaheen
Transcriptome of CD8+ tumor-infiltrating T cells: a link between diabetes and colorectal cancer
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2017
Dorota Monies ,
Sateesh Maddirevula,
Wesam Kurdi ,
Mohammed H. Alanazy ,
Hisham Alkhalidi ,
Mohammed Al-Owain,
Raashda A. Sulaiman ,
Eissa Faqeih,
Ewa Goljan,
Niema Ibrahim,
Firdous Abdulwahab,
Mais Hashem,
Mohamed Abouelhoda,
Ranad Shaheen ,
Stefan T. Arold
and 1 other authors
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,
Sateesh Maddirevula,
Wesam Kurdi ,
Mohammed H. Alanazy ,
Hisham Alkhalidi ,
Mohammed Al-Owain,
Raashda A. Sulaiman ,
Eissa Faqeih,
Ewa Goljan,
Niema Ibrahim,
Firdous Abdulwahab,
Mais Hashem,
Mohamed Abouelhoda,
Ranad Shaheen ,
Stefan T. Arold
and 1 other authors
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Mohamed Abouelhoda,
Turki Sobahy,
Mohamed El-Kalioby ,
Nisha Patel ,
Hanan Shamseldin ,
Dorota Monies ,
Nada Al-Tassan ,
Khushnooda Ramzan,
Faiqa Imtiaz ,
Ranad Shaheen ,
Fowzan S. Alkuraya
,
Nisha Patel ,
Hanan Shamseldin ,
Dorota Monies ,
Nada Al-Tassan ,
Khushnooda Ramzan,
Faiqa Imtiaz ,
Ranad Shaheen ,
Fowzan S. Alkuraya
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden
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