Rupesh Mishra
Overview
Explore the profile of Rupesh Mishra including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
8
Citations
152
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Joshi P, Riley P, Mishra R, Azizi Machekposhti S, Narayan R
Biosensors (Basel)
. 2022 Apr;
12(4).
PMID: 35448258
Opioid drugs are extremely potent synthetic analytes, and their abuse is common around the world. Hence, a rapid and point-of-need device is necessary to assess the presence of this compound...
2.
Paudel B, Paudel B, Mishra R, Karki O, Shahi R, Poudyal B
JNMA J Nepal Med Assoc
. 2020 Sep;
58(228):560-563.
PMID: 32968288
Introduction: Distress is a major concern during diagnosis and treatment of hematological malignancies. The Distress Thermometer is a commonly used screening tool to detect distress. The objectives of this study...
3.
Kruszka P, Addissie Y, Tekendo-Ngongang C, Jones K, Savage S, Gupta N, et al.
Am J Med Genet A
. 2019 Dec;
182(2):303-313.
PMID: 31854143
Turner syndrome (TS) is a common multiple congenital anomaly syndrome resulting from complete or partial absence of the second X chromosome. In this study, we explore the phenotype of TS...
4.
Poudyal B, Mishra R
Natl Med J India
. 2019 Mar;
31(2):115-116.
PMID: 30829233
No abstract available.
5.
Kruszka P, Porras A, de Souza D, Moresco A, Huckstadt V, Gill A, et al.
Am J Med Genet A
. 2018 Apr;
176(5):1128-1136.
PMID: 29681090
Williams-Beuren syndrome (WBS) is a common microdeletion syndrome characterized by a 1.5Mb deletion in 7q11.23. The phenotype of WBS has been well described in populations of European descent with not...
6.
Kruszka P, Porras A, Addissie Y, Moresco A, Medrano S, Mok G, et al.
Am J Med Genet A
. 2017 Jul;
173(9):2323-2334.
PMID: 28748642
Noonan syndrome (NS) is a common genetic syndrome associated with gain of function variants in genes in the Ras/MAPK pathway. The phenotype of NS has been well characterized in populations...
7.
Kruszka P, Addissie Y, McGinn D, Porras A, Biggs E, Share M, et al.
Am J Med Genet A
. 2017 Mar;
173(4):879-888.
PMID: 28328118
22q11.2 deletion syndrome (22q11.2 DS) is the most common microdeletion syndrome and is underdiagnosed in diverse populations. This syndrome has a variable phenotype and affects multiple systems, making early recognition...
8.
Ocana C, Hayat A, Mishra R, Vasilescu A, Del Valle M, Marty J
Analyst
. 2015 Apr;
140(12):4148-53.
PMID: 25905497
In this paper, we have reported a novel electrochemical aptamer-antibody based sandwich biosensor for the detection of lysozyme. In the sensing strategy, an anti-lysozyme aptamer was immobilized onto the carbon...