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Scientific Reports (5)
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Showing 1–7 of 7 results

Advanced filters: Author: Krishna Prashanth P Clear advanced filters

Area efficient approximate multiplier based on novel 4:2 compressors and error correction logic

Krishna Prashanth P
Nithish Kumar V
ResearchOpen Access13 Dec 2025
Scientific Reports

Volume: 16, P: 1-15
Real-world data on trastuzumab emtansine (TDM1) efficacy and safety: Results of a single-centre retrospective study of HER2-positive metastatic breast cancer patients

Anuj Gupta
Bipinesh Sansar
Akhil Kapoor
ResearchOpen Access28 May 2025
Scientific Reports

Volume: 15, P: 1-8
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity

South Asia is home to almost 2 billion people but is extremely underrepresented in human genetics. This study uses genomes from ~5,000 South Asians to characterize genetic variation and help facilitate future South Asian genetic studies.

Jeffrey D. Wall
J. Fah Sathirapongsasuti
Andrew S. Peterson
ResearchOpen Access08 Jun 2023
Nature Communications

Volume: 14, P: 1-11
Whole exome sequencing reveals rare variants linked to congenital pouch colon

Praveen Mathur
Krishna Mohan Medicherla
Prashanth Suravajhala
ResearchOpen Access27 Apr 2018
Scientific Reports

Volume: 8, P: 1-8
Structural and functional analysis of the human POT1-TPP1 telomeric complex

POT1 and TTP1 are part of the shelterin complex that caps and stabilizes the ends of telomeres. Here the authors present a structural analysis of the human POT1-TTP1 complex, shedding light on how it assembles and how cancer-associated mutations impact its assembly and function.

Cory Rice
Prashanth Krishna Shastrula
Emmanuel Skordalakes
ResearchOpen Access10 Apr 2017
Nature Communications

Volume: 8, P: 1-13
An international 20 country patient and physician survey of the usability and acceptability of Stepped Care pathway in Parkinson’s disease

K. Poplawska-Domaszewicz
C. Rodriguez-Blazquez
K. Ray Chaudhuri
ResearchOpen Access13 Nov 2025
Scientific Reports

Volume: 15, P: 1-9
Author Correction: Whole exome sequencing reveals rare variants linked to congenital pouch colon

Praveen Mathur
Krishna Mohan Medicherla
Prashanth Suravajhala
Amendments and CorrectionsOpen Access11 Sept 2018
Scientific Reports

Volume: 8, P: 1-2