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H. Al-Hindi · SciRah

Researcher profile · Semantic Scholar

H. Al-Hindi

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H. Al-Hindi — researcher profile on SciRah

h-index: 19
Works: 71
Citations: 1,339

Most-cited papers

Curcumin inhibits the Sonic Hedgehog signaling pathway and triggers apoptosis in medulloblastoma cells
M. Elamin, Z. Shinwari, Siti‐Faujiah Hendrayani, H. Al-Hindi +4 more
2009Molecular Carcinogenesis131 citations
Semantic Scholar
Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay.
M. Al-Sayed, H. Alzaidan, Albandary Albakheet, Hana A. Hakami +12 more
2013American Journal of Human Genetics103 citations Open access
Semantic Scholar
ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder
Z. Al-Hassnan, M. Aldosary, M. Alfadhel, E. Faqeih +17 more
2014Journal of Medical Genetics97 citations
Semantic Scholar
S100A4 (Mts1) gene overexpression is associated with invasion and metastasis of papillary thyroid carcinoma
M. Zou, R. Al-Baradie, H. Al-Hindi, N. Farid +1 more
2005British Journal of Cancer97 citations Open access
Semantic Scholar
Comparison of differentiated thyroid cancer in children and adolescents (≤20 years) with young adults
A. Alzahrani, Dania Alkhafaji, M. Tuli, H. Al-Hindi +1 more
2016Clinical Endocrinology56 citations
Semantic Scholar
Single Point Mutations in Pediatric Differentiated Thyroid Cancer
A. Alzahrani, A. K. Murugan, Ebtesam Qasem, Meshael M. Alswailem +2 more
2017Thyroid53 citations
Semantic Scholar
TERT promoter mutations in thyroid cancer: a report from a Middle Eastern population.
Ebtesam Qasem, A. K. Murugan, H. Al-Hindi, M. Xing +3 more
2015Endocrine-Related Cancer49 citations Open access
Semantic Scholar
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
Genetic Alterations in Pediatric Thyroid Cancer Using a Comprehensive Childhood Cancer Gene Panel.
A. Alzahrani, Meshael M. Alswailem, A. Alswailem, H. Al-Hindi +3 more
2020Journal of Clinical Endocrinology and Metabolism41 citations Open access
Semantic Scholar
Uncommon TERT Promoter Mutations in Pediatric Thyroid Cancer
A. Alzahrani, Ebtesam Qasem, A. K. Murugan, H. Al-Hindi +5 more
2016Thyroid37 citations
Semantic Scholar
Clinical and biochemical features associated with BCS1L mutation
M. Al-Owain, D. Çolak, Albandary Albakheet, B. Al‐Younes +11 more
2013Journal of Inherited Metabolic Disease37 citations Open access
Semantic Scholar
Vici syndrome associated with unilateral lung hypoplasia and myopathy
M. Al-Owain, Amal Al-Hashem, M. Al-Muhaizea, H. Humaidan +3 more
2010American Journal of Medical Genetics. Part A37 citations
Semantic Scholar
A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype
H. Raef, M. Zou, E. Baitei, Roua A. Al-Rijjal +8 more
2011Clinical Endocrinology35 citations Open access
Semantic Scholar
HABP2 Gene Mutations Do Not Cause Familial or Sporadic Non-Medullary Thyroid Cancer in a Highly Inbred Middle Eastern Population
A. Alzahrani, A. K. Murugan, Ebtesam Qasem, H. Al-Hindi
2016Thyroid33 citations
Semantic Scholar
Juvenile Hyaline Fibromatosis: Morphologic, Immunohistochemical, and Ultrastructural Study of Three Siblings
A. Haleem, H. Al-Hindi, M. al Juboury, H. Al Husseini +1 more
2002American journal of dermatopathology33 citations
Semantic Scholar
Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer
A. K. Murugan, Ebtesam Qasem, H. Al-Hindi, Yu-Fei Shi +1 more
2016Journal of Translational Medicine32 citations Open access
Semantic Scholar
Mature (Benign) Cystic Retroperitoneal Teratoma Involving the Left Adrenal Gland in a 22-Year-Old Male: A Case Report and Literature Review
A. Bhatti, H. Al-Hindi, A. Azzam, Tarek Amin +1 more
2013Case Reports in Oncological Medicine32 citations Open access
Semantic Scholar
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome.
D. Monies, H. Al-Hindi, M. Al-Muhaizea, Dyala Jaroudi +5 more
2014Neuromuscular Disorders30 citations
Semantic Scholar
Novel homozygous mutation in DSP causing skin fragility–woolly hair syndrome: report of a large family and review of the desmoplakin‐related phenotypes
M. Al-Owain, S. Wakil, F. Shareef, A. Al-Fatani +8 more
2011Clinical Genetics28 citations
Semantic Scholar
Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy
M. Al-Owain, N. Kaya, H. Alzaidan, Ibrahim Bin Hussain +9 more
2010Clinical and Developmental Immunology19 citations Open access
Semantic Scholar
Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paraganglioma
Shatha Albattal, Meshael M. Alswailem, Yosra Moria, H. Al-Hindi +5 more
2019OncoTarget18 citations Open access
Semantic Scholar
Unusual cause of ectopic secretion of adrenocorticotropic hormone: Cushing syndrome attributable to small cell prostate cancer.
Omalkhaire M. Alshaikh, Abdulraof Al-Mahfouz, H. Al-Hindi, Ali Bin Mahfouz +1 more
2010Endocrine Practice18 citations
Semantic Scholar
Central Nervous System Brucellosis Granuloma and White Matter Disease in Immunocompromised Patient
M. Alqwaifly, F. Al-Ajlan, H. Al-Hindi, A. Al-Semari
2017Emerging Infectious Diseases16 citations Open access
Semantic Scholar
A novel syndromic form of sensory‐motor polyneuropathy is linked to chromosome 22q13.31‐q13.33
S. Bohlega, AM Alazami, E. Cupler, H. Al-Hindi +2 more
2011Clinical Genetics16 citations
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
MYH1 is a candidate gene for recurrent rhabdomyolysis in humans
H. Alsaif, A. Alshehri, R. Sulaiman, H. Al-Hindi +3 more
2021American Journal of Medical Genetics. Part A14 citations
Semantic Scholar
Absence of somatic mutations of the mTOR gene in differentiated thyroid cancer
A. K. Murugan, Eman A. Humudh, Ebtesam Qasem, H. Al-Hindi +3 more
2015Meta Gene14 citations Open access
Semantic Scholar
Response of medulloblastoma cells to vincristine and lomustine: role of TRKC, CTNNB1 and STK15.
Z. Shinwari, H. Al-Hindi, E. Al-Shail, Y. Khafaga +3 more
2011Anticancer Research14 citations
Semantic Scholar
Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia
N. Alharbi, R. Matar, E. Cupler, H. Al-Hindi +7 more
2022Frontiers in Neuroscience13 citations Open access
Semantic Scholar
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation
S. Bohlega, S. Alfawaz, H. Abou-Al-Shaar, H. Al-Hindi +4 more
2018Acta myologica12 citations
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
Analysis of ALK, IDH1, IDH2 and MMP8 somatic mutations in differentiated thyroid cancers
A. K. Murugan, Ebtesam Qasem, H. Al-Hindi, A. Alzahrani
2021Molecular and clinical oncology11 citations Open access
Semantic Scholar
Isolated renal hydatid disease in a non-endemic country: a single centre experience.
A. Mokhtar, Ahmed A. Alsayyah, H. Al-Hindi, R. Seyam +1 more
2012Canadian Urological Association journal = Journal de l'Association des urologues du Canada11 citations Open access
Semantic Scholar
GPCR-mediated PI3K pathway mutations in pediatric and adult thyroid cancer
A. K. Murugan, Ebtesam Qasem, H. Al-Hindi, A. Alzahrani
2019OncoTarget10 citations Open access
Semantic Scholar
Large‐scale mitochondrial DNA deletion underlying familial multiple system atrophy of the cerebellar subtype
Abdulaziz Alsemari, H. Al-Hindi
2015Clinical Case Reports10 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
Clinical and genetic features of Calpainopathies in Saudi Arabia - a descriptive cross-sectional study.
N. Alharbi, E. Shosha, E. Cupler, H. Al-Hindi +6 more
2021European Review for Medical and Pharmacological Sciences9 citations
Semantic Scholar
Surgical Outcome of Thyroid Nodules with Atypia of Undetermined Significance and Follicular Lesion of Undetermined Significance in Fine Needle Aspiration Biopsy
Saad Alqahtani, S. Alsobhi, R. AlSalloum, S. Najjar +2 more
20179 citations Open access
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
A molecular study of pediatric pilomyxoid and pilocytic astrocytomas: Genome-wide copy number screening, retrospective analysis of clinicopathological features and long-term clinical outcome
E. Alshail, A. Alahmari, A. Dababo, M. Alsagob +8 more
2023Frontiers in Oncology7 citations Open access
Semantic Scholar
January 1997 ‐ 7 Year Old Girl with Seizures
H. Al-Hindi, B. Subach, Ronald Hamilton
1997Brain Pathology7 citations Open access
Semantic Scholar
Clinicopathologic and genomic characterizations of brain metastases using a comprehensive genomic panel
Duna Barakeh, Ebtehal Alsolme, Fatimah Alqubaishi, Amal Almutairi +14 more
2022Frontiers in Medicine6 citations Open access
Semantic Scholar
Appendiceal spirochetosis: a light and electron microscope study of two cases.
A. Haleem, H. Al-Hindi, H. Al Husseini, M. al Juboury
2003Annals of Saudi Medicine6 citations Open access
Semantic Scholar
An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline SDHB pathogenic variant in the absence of paraganglioma or pheochromocytoma
A. Alzahrani, Abdulghani Bin Nafisah, Meshael M. Alswailem, Yosra Moria +3 more
2023Frontiers in Endocrinology5 citations Open access
Semantic Scholar
The impact of thyroid imaging reporting and data system on the management of Bethesda III thyroid nodules
Saad M. Alqahtani, S. Al-Sobhi, Mohammed A. Alturiqy, R. AlSalloum +1 more
2022Journal of Taibah University Medical Sciences5 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
Cauda equina syndrome as the initial presenting clinical feature of medulloblastoma: a case report
Faisal Al-Otaibi, A. ul-Haq, H. Al-Hindi, Amani Al-Kofide +1 more
2012Journal of Medical Case Reports5 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

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A. Alzahrani×22
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A. Alzahrani — researcher profile on SciRah
Meshael M. Alswailem×14
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Meshael M. Alswailem — researcher profile on SciRah
A. K. Murugan×12
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A. K. Murugan — researcher profile on SciRah
Ebtesam Qasem×10
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Ebtesam Qasem — researcher profile on SciRah

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B. Alghamdi — researcher profile on SciRah

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Yu-Fei Shi — researcher profile on SciRah

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M. Al-Owain — researcher profile on SciRah

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