S Mohsen Hosseini
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Explore the profile of S Mohsen Hosseini including associated specialties, affiliations and a list of published articles.
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32
Citations
1780
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Recent Articles
1.
Dagher S, Learned K, Dagher R, Wang J, Zhao X, Hosseini S, et al.
AJNR Am J Neuroradiol
. 2024 Nov;
PMID: 39572200
Background And Purpose: Neoadjuvant BRAF-directed therapy and immunotherapy followed by surgery improves survival in patients with BRAF-mutant anaplastic thyroid carcinoma (ATC), more so in those who have complete ATC pathologic...
2.
Hamidi S, Dadu R, Zafereo M, Ferrarotto R, Wang J, Maniakas A, et al.
JAMA Oncol
. 2024 Jul;
10(9):1264-1271.
PMID: 38990526
Importance: BRAF/MEK inhibitors revolutionized the treatment of BRAF V600E-variant anaplastic thyroid carcinoma (BRAFv-ATC), offering improved outcomes for patients with this previously incurable disease. Observations: Anaplastic thyroid carcinoma (ATC) accounts for...
3.
Ding Q, Somerville C, Manshaei R, Trost B, Reuter M, Kalbfleisch K, et al.
Hum Genet
. 2022 Nov;
142(2):201-216.
PMID: 36376761
Copy number variants (CNVs) represent major etiologic factors in rare genetic diseases. Current clinical CNV interpretation workflows require extensive back-and-forth with multiple tools and databases. This increases complexity and time...
4.
Hosseini S, Stewart J
Semin Diagn Pathol
. 2022 Aug;
39(6):389-393.
PMID: 35931593
Herein, we review the components of Rapid On-Site Evaluation (ROSE) and the mechanics of Fine Needle Aspiration (FNA) to prepare cytopathologists to assist radiologists in optimizing their diagnostic procedures. The...
5.
GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation
Manshaei R, Delong S, Andric V, Joshi E, Okello J, Dhir P, et al.
BMC Med Genomics
. 2022 Feb;
15(1):31.
PMID: 35180879
Background: Variant interpretation is the main bottleneck in medical genomic sequencing efforts. This usually involves genome analysts manually searching through a multitude of independent databases, often with the aid of...
6.
Hosseini S, Tondi Resta I, Baloch Z
Diagn Cytopathol
. 2021 Apr;
49(7):822-831.
PMID: 33823076
Background: Fine-needle aspiration (FNA) is a well-established modality for diagnosing salivary gland pathologies. The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) provides a standardized uniform framework leading to an...
7.
Hosseini S, Khanafshar E, Seeley E, Ruiz-Cordero R
Diagn Cytopathol
. 2021 Jan;
49(7):E258-E261.
PMID: 33433963
Here we report the combined cytological and molecular diagnosis of a lung mass. The cytology and extensive immunohistochemistry on an endobronchial ultrasound-guided fine needle aspiration biopsy were inconclusive. By genomic...
8.
Pollack S, Igo Jr R, Jensen R, Christiansen M, Li X, Cheng C, et al.
Diabetes
. 2020 Apr;
69(6):1306.
PMID: 32341040
No abstract available.
9.
Reuter M, Chaturvedi R, Liston E, Manshaei R, Aul R, Bowdin S, et al.
Genet Med
. 2020 Feb;
22(6):1015-1024.
PMID: 32037394
Purpose: This study investigated the diagnostic utility of nontargeted genomic testing in patients with pediatric heart disease. Methods: We analyzed genome sequencing data of 111 families with cardiac lesions for...
10.
Pollack S, Igo Jr R, Jensen R, Christiansen M, Li X, Cheng C, et al.
Diabetes
. 2018 Nov;
68(2):441-456.
PMID: 30487263
To identify genetic variants associated with diabetic retinopathy (DR), we performed a large multiethnic genome-wide association study. Discovery included eight European cohorts ( = 3,246) and seven African American cohorts...