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B. Alghamdi · SciRah

Researcher profile · Semantic Scholar

B. Alghamdi

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B. Alghamdi — researcher profile on SciRah

h-index: 8
Works: 34
Citations: 165

Most-cited papers

Lung Metastasis in Pediatric Thyroid Cancer: Radiological Pattern, Molecular Genetics, Response to Therapy, and Outcome
A. Alzahrani, Meshael M. Alswailem, Yosra Moria, Reem Almutairi +5 more
2018Journal of Clinical Endocrinology and Metabolism44 citations Open access
Semantic Scholar
Erratum to: 36th International Symposium on Intensive Care and Emergency Medicine
Author Et al, R. Bateman, M. Sharpe, J. E. Jagger +496 more
2016Critical Care21 citations Open access
Semantic Scholar
Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
A. Alzahrani, A. K. Murugan, Ebtesam Qasem, Meshael M. Alswailem +3 more
2018Endocrine15 citations
Semantic Scholar
Germline Variants in Sporadic Pituitary Adenomas
A. Alzahrani, Abdulghani Bin Nafisah, Meshael M. Alswailem, B. Alghamdi +15 more
2024Journal of the Endocrine Society12 citations
Semantic Scholar
How do BRAFV600E and TERT promoter mutations interact with the ATA and TNM staging systems in thyroid cancer?
Noha N. Mukhtar, Kheloud M. Alhamoudi, Meshael M. Alswailem, H. Alhindi +3 more
2023Frontiers in Endocrinology11 citations Open access
Semantic Scholar
Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant
Kheloud M. Alhamoudi, B. Alghamdi, Abeer Aljomaiah, Meshael M. Alswailem +2 more
2022Frontiers in Genetics11 citations Open access
Semantic Scholar
Molecular genetics of diffuse sclerosing papillary thyroid cancer.
Meshael M. Alswailem, B. Alghamdi, Anwar B Alotaibi, Abeer Aljomiah +5 more
2023Journal of Clinical Endocrinology and Metabolism9 citations
Semantic Scholar
Fumarate hydratase is a novel gene for familial non-medullary thyroid cancer.
A. Alzahrani, Meshael M. Alswailem, B. Alghamdi, H. Al-Hindi
2022Journal of Clinical Endocrinology and Metabolism8 citations Open access
Semantic Scholar
Thyroid Cancer, Neuroendocrine Tumor, Adrenal Adenoma, and Other Tumors in a Patient With a Germline PMS1 Mutation
B. Alghamdi, H. Al-Hindi, A. K. Murugan, A. Alzahrani
2023Journal of the Endocrine Society7 citations Open access
Semantic Scholar
Controversy on the management of patients carrying RET p.V804M mutation
A. Alzahrani, Meshael M. Alswailem, B. Alghamdi, Rafiullah Rafiullah +2 more
2021Endocrine5 citations Open access
Semantic Scholar
EPAS-1-related pheochromocytoma/paraganglioma: How common and how aggressive?
A. Alzahrani, Meshael M. Alswailem, A. Buffet, B. Alghamdi +4 more
2024Endocrine-Related Cancer4 citations
Semantic Scholar
A unique mechanism of a novel synonymous PHEX variant causing X-linked hypophosphatemia.
Kheloud M. Alhamoudi, B. Alghamdi, Meshael M. Alswailem, A. Nasir +3 more
2022Journal of Clinical Endocrinology and Metabolism4 citations
Semantic Scholar
A CYP11A1 homozygous exonic variant inducing an alternative splicing, frameshift and truncation in a family with congenital adrenal hyperplasia
Kheloud M. Alhamoudi, Meshael M. Alswailem, B. Alghamdi, A. Alashwal +1 more
2024Heliyon3 citations
Semantic Scholar
Papillary Thyroid Cancer and a TERT Promotor Mutation-positive Paraganglioma in a Patient With a Germline SDHB Mutation
A. Alzahrani, Meshael M. Alswailem, A. K. Murugan, B. Alghamdi +1 more
2022Journal of the Endocrine Society3 citations Open access
Semantic Scholar
A single-centre study of genetic mutations, audiology, echocardiogram and pulmonary function in Saudi children with osteogenesis imperfecta
Noman Ahmad, N. Aleysae, Mrouge Sobaihi, NisreenAbdulaziz Naitah +8 more
2021Journal of Pediatric Endocrinology & Metabolism (JPEM)2 citations
Semantic Scholar
Molecular Genetics of 1α-Hydroxylase Deficiency in the Saudi Population
Bassam Bin-Abbas, Afaf Alsagheir, B. Alghamdi, Allianah D. Benito +13 more
2025Journal of the Endocrine Society1 citations
Semantic Scholar
6408 Familial Hypoparathyroidism With Elevated Parathyroid Hormone Due To A PTH Mutation Responsive To Teriparatide
Noha N. Mukhtar, B. Alghamdi, Meshael M. Alswailem, Ali Saeed Alzahrani
2024Journal of the Endocrine Society1 citations
Semantic Scholar
Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
Noman Ahmad, S. A. Ansari, N. Aleysae, Emily L. G. Heaphy +3 more
2024Pediatric Endocrinology Diabetes and Metabolism1 citations Open access
Semantic Scholar
Pachydermoperiostosis Due to a Novel HPGD Splicing Site Mutation Masquerading as Acromegaly
Mussa H. Almalki, B. Alghamdi, Allianah D. Benito, Ahmed Alfares +1 more
2024JCEM Case Reports1 citations Open access
Semantic Scholar
Case report: Familial hypoparathyroidism with elevated parathyroid hormone due to an inactivating PTH mutation
Noha N. Mukhtar, B. Alghamdi, Meshael M. Alswailem, A. Alsagheir +1 more
2024Frontiers in Endocrinology1 citations Open access
Semantic Scholar
SAT604 An Extensively Invasive Giant Prolactinoma Associated With CDH23 Mutation
B. Alghamdi, L. Alobaid, Meshael M. Alswailem, Eyas Othman +3 more
2023Journal of the Endocrine Society1 citations Open access
Semantic Scholar
Correction to: Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
A. Alzahrani, A. K. Murugan, Ebtesam Qasem, Meshael M. Alswailem +3 more
2019Endocrine1 citations Open access
Semantic Scholar
SDHB-associated paraganglioma in Saudi Arabia: High metastatic risk linked to a likely founder mutation
A. Alzahrani, B. Alghamdi, Allianah D. Benito, G. Mohamed
2026Journal of the Endocrine Society0 citations Open access
Semantic Scholar
Case Report: Three pathogenic molecular findings in a patient with myotonia congenita, pseudohypoparathyroidism, and a glaucoma-suspect phenotype
Noha N. Mukhtar, Deema Alturki, Allianah D. Benito, B. Alghamdi +2 more
2026Frontiers in Endocrinology0 citations Open access
Semantic Scholar
Germline AIP Variants Are Rare in Sporadic Unselected Pituitary Adenomas
Mohamed Rajab, B. Alghamdi, Allianah D. Benito, Burair A. Alsaihati +3 more
2026Journal of the Endocrine Society0 citations Open access
Semantic Scholar
A novel germline CDH23 variant as a likely cause of an ultra-giant prolactinoma
Eman Albasri, B. Alghamdi, A. K. Murugan, Eyas Othman +4 more
2026Orphanet Journal of Rare Diseases0 citations Open access
Semantic Scholar
Exceptional and Durable Response to Selpercatinib in a Patient with Apparently RET-Negative, HRAS-, and NF1-Mutated Metastatic Medullary Thyroid Carcinoma
A. Alzahrani, Allianah D. Benito, B. Alghamdi, A. Alqahtani +5 more
2026Thyroid0 citations
Semantic Scholar
Multiple tumours of different lineages likely related to aDNMT3Apathogenic R688H variant
Kheloud M. Alhamoudi, Meshael M. Alswailem, B. Alghamdi, Maram Alshuwaymi +4 more
2025BMJ Connections Clinical Genetics and Genomics0 citations Open access
Semantic Scholar
Germline Telomere-Regulating Gene Variants Are Not Associated with Thyroid Cancer in a Saudi Arabian Population
A. Alzahrani, Burair A. Alsaihati, Allianah D. Benito, B. Alghamdi +6 more
2025Thyroid0 citations
Semantic Scholar
THU614 Neurofibromatosis Type 1 Presenting With Pheochromocytoma And Severe Vascular And Hematological Manifestations Due To A Novel NF1 Mutation
L. Alobaid, Osamah Alsagheir, Meshael M. Alswailem, B. Alghamdi +1 more
2023Journal of the Endocrine Society0 citations Open access
Semantic Scholar
SAT631 EPAS1 Mutations In Three Adjacent Nucleotides Resulting In Different Phenotypes
Meshael M. Alswailem, B. Alghamdi, L. Alobaid, H. Al-Hindi +3 more
2023Journal of the Endocrine Society0 citations Open access
Semantic Scholar
THU683 TERT Promoter Mutations, But Not BRAFV600EMutation, Correlate With The American Thyroid Association And TNM Staging Systems And Predict Outcome Of Differentiated Thyroid Cancer
Noha N. Mukhtar, Kheloud M. Alhamoudi, Meshael M. Alswailem, H. Al-Hindi +3 more
2023Journal of the Endocrine Society0 citations Open access
Semantic Scholar
Clinical and pathological features and phenotype-genotype correlation of pheochromocytoma and paraganglioma in a highly consanguineous population
B. Alghamdi, Meshael M. Alswailem, A. Alzahrani
2022Endocrine Abstracts0 citations
Semantic Scholar
Pseudo hypoaldosteronism type 1B due to novel deletion mutation in SCNN1A gene
Noman Ahmad, Meshal Atiyah, B. Alghamdi, Halah Faleh Al Enizi +1 more
2019International Journal of Contemporary Pediatrics0 citations Open access
Semantic Scholar

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A. Alzahrani×30
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A. Alzahrani — researcher profile on SciRah
Meshael M. Alswailem×21
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Meshael M. Alswailem — researcher profile on SciRah
H. Al-Hindi×14
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A. K. Murugan×10
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Kheloud M. Alhamoudi

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Allianah D. Benito×7

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Noha N. Mukhtar×5

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Noha N. Mukhtar — researcher profile on SciRah

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Yosra Moria — researcher profile on SciRah

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H. Alhindi — researcher profile on SciRah

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L. Alobaid — researcher profile on SciRah

Osamah Alsagheir×4

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Ebtesam Qasem×3

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