Silas J. Carlus

Uppal Road
Hyderabad, TG 500007, India

Last Updated: 09/26/2026

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Found 13 publications

In silico prediction, molecular modeling, and dynamics studies on the targeted next-generation sequencing identified genes underlying congenital heart disease in Down syndrome patients.

In silico prediction, molecular modeling, and dynamics studies on the targeted next-generation sequencing identified genes underlying congenital heart disease in Down syndrome patients.

Journal: Annals of pediatric cardiology

Published: May 09, 2023

An in silico analysis of the impact of POLE mutations on cladribine docking.

An in silico analysis of the impact of POLE mutations on cladribine docking.

Journal: European review for medical and pharmacological sciences

Published: October 31, 2022

A novel homozygous TPM1 mutation in familial pediatric hypertrophic cardiomyopathy and in silico screening of potential targeting drugs.

A novel homozygous TPM1 mutation in familial pediatric hypertrophic cardiomyopathy and in silico screening of potential targeting drugs.

Journal: European review for medical and pharmacological sciences

Published: August 04, 2020

The Polymorphism at the microRNA-155 Binding Site in the AGTR1 Gene is not Significantly Associated with Rheumatic Heart Disease in Saudi Arabia Population.

The Polymorphism at the microRNA-155 Binding Site in the AGTR1 Gene is not Significantly Associated with Rheumatic Heart Disease in Saudi Arabia Population.

Journal: MicroRNA (Shariqah, United Arab Emirates)

Published: September 12, 2019

Next-generation sequencing identifies a homozygous mutation in ACADVL associated with pediatric familial dilated cardiomyopathy.

Next-generation sequencing identifies a homozygous mutation in ACADVL associated with pediatric familial dilated cardiomyopathy.

Journal: European review for medical and pharmacological sciences

Published: March 07, 2019

Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy.

Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy.

Journal: Medicina (Kaunas, Lithuania)

Published: November 23, 2018

The peopling of Lakshadweep Archipelago.

The peopling of Lakshadweep Archipelago.

Journal: Scientific reports

Published: August 31, 2018

Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients.

Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients.

Journal: Pediatric cardiology

Published: April 17, 2018

The MTHFR C677T polymorphism is associated with mitral valve rheumatic heart disease.

The MTHFR C677T polymorphism is associated with mitral valve rheumatic heart disease.

Journal: European review for medical and pharmacological sciences

Published: January 28, 2016

Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis.

Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis.

Journal: PloS one

Published: June 09, 2015

Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation.

Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation.

Journal: The Journal of investigative dermatology

Published: April 07, 2015

SRD5A2 gene polymorphisms and the risk of benign prostatic hyperplasia but not prostate cancer.

SRD5A2 gene polymorphisms and the risk of benign prostatic hyperplasia but not prostate cancer.

Journal: Asian Pacific journal of cancer prevention : APJCP

Published: March 05, 2015

Showing 1-12 of 13

Last Updated: 09/26/2026