S. Subhani

发表

Diabetic Foot Complications and Their Risk Factors from a Large Retrospective Cohort Study

K. Al-Rubeaan, Khalid Al-Rubeaan, Mohammad Al Derwish, 2015, PloS one.

Ischemic Stroke and Its Risk Factors in a Registry-Based Large Cross-Sectional Diabetic Cohort in a Country Facing a Diabetes Epidemic

K. Al-Rubeaan, F. Al-Hussain, A. Youssef, 2016, Journal of diabetes research.

Diabetic Nephropathy and Its Risk Factors in a Society with a Type 2 Diabetes Epidemic: A Saudi National Diabetes Registry-Based Study

K. Al-Rubeaan, D. Alnaqeb, A. Youssef, 2014, PloS one.

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

F. Alkuraya, S. AlKhater, T. Algoufi, 2019, American journal of human genetics.

Estimation of Modified Concordance Ratio in Sib-Pairs: Effect of Consanguinity on the Risk of Congenital Heart Diseases

Allan Donner, Shazia Subhani, Futwan Al-Mohanna, 2010, The international journal of biostatistics.

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families

M. Abouelhoda, D. Monies, S. Subhani, 2017, Scientific Reports.

Maternal obesity and neonatal congenital cardiovascular defects

S. Subhani, Hala S. Khalil, A. M. Saleh, 2008, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Design and development of an Internet registry for congenital heart defects.

S. Subhani, W. Greer, W. Mitri, 2002, Teratology.

Design and Development of a Web-Based Saudi National Diabetes Registry

K. Al-Rubeaan, S. Subhani, 2010, Journal of diabetes science and technology.

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

F. Alkuraya, E. Faqeih, K. Al-Thihli, 2017, Human Genetics.

A Web-Based Interactive Diabetes Registry for Health Care Management and Planning in Saudi Arabia

K. Al-Rubeaan, A. Youssef, S. Subhani, 2013, Journal of medical Internet research.

Diabetic retinopathy and its risk factors in a society with a type 2 diabetes epidemic: a Saudi National Diabetes Registry‐based study

K. Al-Rubeaan, A. A. Abu El-Asrar, A. Youssef, 2015, Acta ophthalmologica.

Sugar-sweetened carbonated beverage consumption correlates with BMI, waist circumference, and poor dietary choices in school children

F. Al-Mohanna, K. Al-Rubeaan, M. Shoukri, 2010, BMC public health.

A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies

A. Alazami, B. Meyer, S. Bohlega, 2016, Human Genomics.

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

F. Alkuraya, E. Faqeih, K. Al-Thihli, 2017, Human Genetics.

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families

M. Abouelhoda, D. Monies, S. Subhani, 2017, Scientific Reports.

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

S. Bohlega, M. Abouelhoda, D. Monies, 2019, Scientific Reports.

Whole-Genome Sequencing Reveals Exonic Variation of ASIC5 Gene Results in Recurrent Pregnancy Loss

M. Abouelhoda, J. Borgio, H. S. Alsuwat, 2021, Frontiers in Medicine.

Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.

A. Al-ghonaium, S. Al‐Muhsen, M. Dasouki, 2016, The Journal of allergy and clinical immunology.

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

F. Alkuraya, S. AlKhater, T. Algoufi, 2019, American journal of human genetics.

Genetic profiling of children with advanced cholestatic liver disease

F. Alkuraya, M. Abouelhoda, D. Monies, 2017, Clinical genetics.

Pattern of Cleft Lip and Palate in Hospital-Based Population in Saudi Arabia: Retrospective Study

S. Subhani, K. Ravichandran, A. Aljohar, 2008, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

The clinical utility of rapid exome sequencing in a consanguineous population

M. Temsah, F. Alkuraya, E. Faqeih, 2023, Genome Medicine.

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease

S. Bohlega, M. Abouelhoda, D. Monies, 2019, Scientific Reports.

A web-based cleft lip and palate registry.

S. Subhani, S. Becker, W. Mitri, 2002, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.