Rohan Singh

Mr. Rohan Singh


Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Verified
Journal Article
Open access
PDF file
RSRohan Singh
Rohan Singh
SKSindhuja Koppu
Sindhuja Koppu
PPPatrick O Perche
Patrick O Perche
Steven R. FeldmanSteven R. Feldman
Steven R. Feldman
Psoriasis is the result of uncontrolled keratinocyte proliferation, and its pathogenesis involves the dysregulation of the immune system. The interplay among cytokines released by dendritic, Th1, Th2, and Th17 cells leads to the phenotypical manifestations seen in psoriasis. Biological therapies target the cytokine-mediated pathogenesis of psoriasis and have improved patient quality of life. This review will describe the underlying molecular pathophysiology and biologics used to treat psoriasis. A review of the literature was conducted using the PubMed and Google Scholar repositories to investigate the molecular pathogenesis, clinical presentation, and current therapeutics in psoriasis. Plaque psoriasis’, the most prevalent subtype of psoriasis, pathogenesis primarily involves cytokines TNF-α, IL-17, and IL-23. Pustular psoriasis’, an uncommon variant, pathogenesis involves a mutation in IL-36RN. Currently, biological therapeutics targeted at TNF-α, IL-12/IL-23, IL-17, and IL-23/IL-39 are approved for the treatment of moderate to severe psoriasis. More studies need to be performed to elucidate the precise molecular pathology and assess efficacy between biological therapies for psoriasis. Psoriasis is a heterogenous, chronic, systemic inflammatory disease that presents in the skin with multiple types. Recognizing and understanding the underlying molecular pathways and biological therapeutics to treat psoriasis is important in treating this common disease.

19 January 2023 in Journal of Dermatological Treatment
Verified
Journal Article
Open access
JPJessica N. Pixley
Jessica N. Pixley
MCMadison K. Cook
Madison K. Cook
RSRohan Singh
Rohan Singh
JLJorge Larrondo
Jorge Larrondo
AMAmy J. McMichael
Amy J. McMichael
Platelet-Rich Plasma (PRP) offers anti-inflammatory and regenerative properties through angiogenesis, cell differentiation and proliferation. Although studied in many dermatologic conditions, its efficacy is not well-understood. Our objective is to review the use and effectiveness of PRP for dermatologic conditions. A literature search was performed through PubMed and yielded 54 articles published between January 2000 and November 2021; articles written in English were reviewed. Intradermal injections were associated with increased hair density in androgenic alopecia. Successful treatment of inflammatory nail diseases with PRP has been reported. Improvement in psoriasis was described, but only 2 studies were available. PRP was associated with higher patient self-assessment scores of photoaging and fine lines. Treatment with PRP in melasma has been associated with improved subjective satisfaction, but not with objective measures of disease improvement. PRP can serve as a safe and potentially effective adjunct for hair loss, vitiligo, non-healing wounds, photoaging, and acne scars. An important barrier to interpreting PRP research is lack of standardization of PRP preparation protocols, inconsistent clinical endpoints, and frequent combination treatments. However, PRP is relatively non-invasive, has a well-established safety profile, and patient satisfaction is often high as patients perceive great benefit from treatment with PRP.

31 October 2022 in Archives of Dermatological Research
Verified
Journal Article
Closed access
PDF file
RSRohan Singh
Rohan Singh
KKKatherine A. Kelly
Katherine A. Kelly
ASAditi Senthilnathan
Aditi Senthilnathan
SFSteven R. Feldman
Steven R. Feldman
RPRita O. Pichardo
Rita O. Pichardo

22 October 2021 in Expert Review of Clinical Immunology
Verified
Journal Article
Closed access
MFMohammad I. Fardos
Mohammad I. Fardos
RSRohan Singh
Rohan Singh
PPPatrick O Perche
Patrick O Perche
KKKatherine A. Kelly
Katherine A. Kelly
SFSteven R. Feldman
Steven R. Feldman
Atopic dermatitis (AD) is a chronic, inflammatory skin condition mediated by cytokines that utilize the Janus Kinase/Signal Transducer and Activator of Transcription (JAK-STAT) signaling cascade. T...

10 February 2022 in Expert Review of Clinical Immunology
Verified
Journal Article
Closed access
PFParker J. Funk
Parker J. Funk
PPPatrick O Perche
Patrick O Perche
RSRohan Singh
Rohan Singh
KKKatherine A. Kelly
Katherine A. Kelly
Steven R. FeldmanSteven R. Feldman
Steven R. Feldman
Cytokine blockers have revolutionized the management of psoriasis. While efficacious, not all patients respond, and treatment may lose efficacy over time. Janus kinase (JAK) inhibitors target the J...

12 September 2022 in Human Vaccines & Immunotherapeutics
Verified
Journal Article
Open access
SKSindhuja Koppu
Sindhuja Koppu
RSRohan Singh
Rohan Singh
KKKiranjit Kaur
Kiranjit Kaur
SFSteven R. Feldman
Steven R. Feldman
Bimekizumab, a selective interleukin (IL) 17 inhibitor, is an emerging systemic treatment for moderate-to-severe psoriasis. Although IL-19, IL-22, and IL-36 are implicated in the pathogenesis of psoriasis, IL-17 drives the activation of these interleukins and the formation of psoriatic plaques. This review assesses the efficacy, safety, and implications of bimekizumab in the treatment of moderate-to-severe psoriasis. A review of literature was conducted using the PubMed repository in March 2022. Articles in English discussing the use of bimekizumab in the treatment of psoriasis were included. One phase II and four phase III trials were included. During clinical trials, bimekizumab was more efficacious, when compared to placebo, ustekinumab, adalimumab, and secukinumab in the treatment of moderate to severe psoriasis. Bimekizumab is a promising, efficacious, and relatively tolerable emerging systemic treatment for moderate-to-severe plaque psoriasis.