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Raashda Ainuddin Sulaiman

Observed names: R. A. Sulaiman, R.A. Sulaiman, Raashda A Sulaiman, Raashda A. Sulaiman, Raashda Sulaiman
ORCID: 0000-0002-6868-9823
Observed ORCID: 0000-0002-6868-9823
OpenAlex ID: A5058410527
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
2017 · Dorota Monies, Mohamed Abouelhoda, et al. · Human Genetics · 312
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Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation
2017 · Dorota Monies, Sateesh Maddirevula, et al. · Genetics in Medicine · 92
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Effect of order of draw of blood samples during phlebotomy on routine biochemistry results: Table 1
2011 · Raashda A Sulaiman, Michael P Cornes, et al. · Journal of Clinical Pathology · 41
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects
2022 · Lama AlAbdi, Muriel Desbois, et al. · Brain · 38
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Arab founder variants: Contributions to clinical genomics and precision medicine
2024 · Lama AlAbdi, Sateesh Maddirevula, et al. · Med · 23
Fibrolamellar Hepatocellular Carcinoma Mimicking Ornithine Transcarbamylase Deficiency
2014 · Raashda A. Sulaiman, Tarekegn Geberhiwot · JIMD Reports · 23
Incorrect order of draw of blood samples does not cause potassium EDTA sample contamination
2012 · M. P. Cornes, R. A. Sulaiman, et al. · British Journal of Biomedical Science · 20
A novel mutation in SLC25A46 causes optic atrophy and progressive limb spasticity, with no cerebellar atrophy or axonal neuropathy
2017 · R.A. Sulaiman, N. Patel, et al. · Clinical Genetics · 17
MYH1 is a candidate gene for recurrent rhabdomyolysis in humans
2021 · Hessa S. Alsaif, Ali Alshehri, et al. · American Journal of Medical Genetics Part A · 15
Spectrum of bone marrow pathology and hematological abnormalities in methylmalonic acidemia
2018 · Nasir A. Bakshi, Talal Al‐Anzi, et al. · American Journal of Medical Genetics Part A · 15
Ethnic differences in umbilical cord blood vitamin D and parathyroid hormone – South Asians compared to Whites born in the UK
2010 · Raashda A. Sulaiman, Caroline L. Sharratt, et al. · The Journal of Maternal-Fetal & Neonatal Medicine · 15
Pasireotide and octreotide in the treatment of severe late dumping syndrome
2017 · Alireza Mohammadi, Raashda A. Sulaiman, et al. · Clinical Case Reports · 13
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Mitigation and detection of spurious potassium and sodium results
2010 · R.A. Sulaiman, P.J. Twomey, et al. · Clinica Chimica Acta · 13
Inherited metabolic disorders and dyslipidaemia
2019 · Raashda A Sulaiman · Journal of Clinical Pathology · 12
Juvenile hemochromatosis and hepatocellular carcinoma in a patient with a novel mutation in the HJV gene
2017 · Khushnooda Ramzan, Faiqa Imtiaz, et al. · European Journal of Medical Genetics · 12
Inherited Metabolic Disorders in Adults: A view from Saudi Arabia
2018 · Raashda A. Sulaiman, Mohammed Al-Owain · European Journal of Medical Genetics · 11
Biotin treatment causing erroneous immunoassay results: A word of caution for clinicians
2016 · Raashda Ainuddin Sulaiman · Drug Discoveries & Therapeutics · 11
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Investigation and Causes of Spontaneous (Non-Diabetic) Hypoglycaemia in Adults: Pitfalls to Avoid
2023 · Maiar Elghobashy, Rousseau Gama, et al. · Diagnostics · 10
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Hemophagocytic lymphohistiocytosis: A rare cause of recurrent encephalopathy
2016 · Raashda Ainuddin Sulaiman, Marwan Yassin Shaheen, et al. · Intractable & Rare Diseases Research · 10
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Adult genomic medicine: lessons from a multisite study of 2700 patients
2025 · Khadijah Bakur, Halima Hamid, et al. · Genome Medicine · 9
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Depression in adult patients with biotin responsive basal ganglia disease
2016 · Dalal K. Bubshait, Asif Rashid, et al. · Drug Discoveries & Therapeutics · 9
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Postprandial hypoglycaemia in adults: pathogenesis, diagnosis and management
2021 · Raashda A. Sulaiman · Journal of Laboratory and Precision Medicine · 8
Emergency management of critically ill adult patients with inherited metabolic disorders
2022 · Raashda A. Sulaiman, Abdulaziz Alali, et al. · The American Journal of Emergency Medicine · 7
The neuroimaging findings of monocarboxylate transporter 1 deficiency
2020 · Manal Nicolas-Jilwan, Rita Medlej, et al. · Neuroradiology · 7
Optic neuropathy in classical methylmalonic acidemia
2019 · Mohammed AlOwain, Ola Ali Khalifa, et al. · Ophthalmic Genetics · 7
Works count: 46
Citation count: 789
H-index: 13
I10-index: 19
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