Mohamed H Al-Hamed (Mohamed Alhamed)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 9

Top Venues

Genes

Human mutation

Scientific reports

Journal of nephrology

Newcastle University (PHD)

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

Education History

Newcastle University

United Kingdom

PHD :: Genetics Medicine

Publications

Mohamed H Al-Hamed, John Andrew Sayer, Nada Alsahan, Noel Edwards, Wafaa Ali, Maha Tulbah, Faiqa Imtiaz
Missense Variants in <i>GFRA1</i> and <i>NPNT</i> Are Associated with Congenital Anomalies of the Kidney and Urinary Tract. Genes 13 (10) (2022)
Mohamed H Al-Hamed, Norah Altuwaijri, Nada Alsahan, Wafaa Ali, Firdous Abdulwahab, Fatema Alzahrani, Nada Majrashi, Fowzan Sami Alkuraya
A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis. Clinical genetics 102 (1) (2022)
Mohamed H Al-Hamed, Maged H Hussein, Yaser Shah, Hamad Al-Mojalli, Essam Alsabban, Turki Alshareef, Ali Altayyar, Samir Elshouny, Wafaa Ali, Mai Abduljabbar, Afaf AlOtaibi, Amal AlShammasi, Rana Akili, Mohamed Abouelhoda, John A Sayer, Majed J Dasouki, Faiqa Imtiaz
Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients. Human mutation (2022)
Mohamed H Al-Hamed, Wesam Kurdi, Rubina Khan, Maha Tulbah, Maha AlNemer, Nada AlSahan, Maisoon AlMugbel, Rafiullah Rafiullah, Mirna Assoum, Dorota Monies, Zeeshan Shah, Zuhair Rahbeeni, Nada Derar, Fahad Hakami, Gawaher Almutairi, Afaf AlOtaibi, Wafaa Ali, Amal AlShammasi, Wardah AlMubarak, Samia AlDawoud, Saja AlAmri, Bashayer Saeed, Hanifa Bukhari, Mohannad Ali, Rana Akili, Laila Alquayt, Samia Hagos, Hadeel Elbardisy, Asma Akilan, Nora Almuhana, Abrar AlKhalifah, Mohamed Abouelhoda, Khushnooda Ramzan, John A Sayer, Faiqa Imtiaz
Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes. Human genetics (2021)
Mohamed H Al-Hamed, John Andrew Sayer, Nada Alsahan, Maha Tulbah, Wesam Kurdi, Qamariya Ambusaidi, Wafaa Ali, Faiqa Imtiaz
Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families. Journal of nephrology 34 (3) (2020)
Mohamed H Al-Hamed, Nada Alsahan, Huda I Tulbah, Wesam Kurdi, Wafa'a Ali, John Andrew Sayer, Faiqa Imtiaz
Fetal Anomalies Associated with Novel Pathogenic Variants in TMEM94. Genes 11 (9) (2020)
Mohamed H Al-Hamed, Hamad Alzaidan, Maged Hussein, Lina Albaik, Alya Qari, John Andrew Sayer, Faiqa Imtiaz
Novel pathogenic MAPKBP1 variant in a family with nephronophthisis. Clinical kidney journal 14 (2) (2020)
Eman Al Yemni, Dorota Monies, Thamer Alkhairallah, Saeed Bohlega, Mohamed Abouelhoda, Amna Magrashi, Abeer Mustafa, Basma AlAbdulaziz, Mohamed H Al-Hamed, Batoul Baz, Ewa Goljan, Renad Albar, Amjad Jabaan, Tariq Faquih, Shazia Subhani, Wafa Ali, Jameela Shinwari, Bashayer Al-Mubarak, Nada A Al-Tassan
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease. Scientific reports 9 (1) (2019)
Mohamed H Al-Hamed, Nada Alsahan, Sarah J Rice, Noel Edwards, Eman Nooreddeen, Maha Alotaibi, Wesam Kurdi, Maha Alnemer, Naderah Altaleb, Wafa Ali, Nouf Al-Numair, Najd Almejaish, John A Sayer, Faiqa Imtiaz
Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families. Pediatric nephrology (Berlin, Germany) 34 (9) (2019)

Mohamed H Al-Hamed.css-eqlu8i{font-size:small;padding-left:4px;} (Mohamed Alhamed)

Publication Activity (10 Years)

Top Topics

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Mohamed H Al-Hamed (Mohamed Alhamed)