Yazeid Alhaidan

Publication Activity (10 Years)

Years Active: 2020-2021
Publications (10 Years): 3

Top Topics

Magnetic Resonance

Tyrosine Kinase

Top Venues

American journal of medical genetics. Part A

Molecular genetics and genomics : MGG

King Abdullah International Medical Research Center

University of Southern Denmark (PHD)

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

Affiliation History

King Abdullah International Medical Research Center May 10 2019

Saudi Arabia

Postdoctoral Research Fellow :: Medical Genomics Research Department

Odense Universitetshospital Aug 01 2015 - May 10 2019

Denmark

PhD-Student :: Klinisk Genetisk Afdeling

King Abdullah International Medical Research Center Apr 29 2011 - May 10 2019

Saudi Arabia

Supervisor :: Genomics

University of Aberdeen Institute of Medical Sciences Jul 01 2010 - Sep 01 2010

United Kingdom

Volunteer :: GI Group

Education History

University of Southern Denmark Aug 01 2015 - May 10 2019

Denmark

PHD :: Faculty of Health Sciences

University of Aberdeen Sep 01 2009 - Sep 01 2010

United Kingdom

MSC :: medical sicence

King Saud University Apr 01 2003 - Jul 07 2007

Saudi Arabia

BSC :: Collage of science

Publications

Abdulaziz Asiri, Deemah Alwadaani, Muhammad Umair, Kheloud M Alhamoudi, Mohammed H Almuhanna, Abdul Nasir, Bahauddeen M Alrfaei, Abeer Al Tuwaijri, Tlili Barhoumi, Yusra Alyafee, Bader Almuzzaini, Mohammed Aldrees, Mariam Ballow, Latifah Alayyar, Abdulkareem AlAbdulrahman, Yazeid Alhaidan, Nahlah Al Ghasham, Sulaiman Al-Ajaji, Mohammad Alsalamah, Wafa Al Suwairi, Majid Alfadhel
Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect: Expanding the Molecular and Phenotypic Spectrum. Genes 12 (2) (2021)
Anne Benner, Yazeid Alhaidan, Matthew A Lines, Klaus Brusgaard, Diva D De León, Rebecca Sparkes, Anja Lisbeth Frederiksen, Henrik Boye Thybo Christesen
PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only. American journal of medical genetics. Part A 185 (10) (2021)
Yazeid Alhaidan, Henrik Thybo Christesen, Kurt Højlund, Mohammed A Al Balwi, Klaus Brusgaard
A novel gene in early childhood diabetes: EDEM2 silencing decreases SLC2A2 and PXD1 expression, leading to impaired insulin secretion. Molecular genetics and genomics : MGG 295 (5) (2020)