Sugirthan J. Sivalingam

Bonn, NW, Germany

Last Updated: 09/26/2026

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Found 40 publications

Diagnostic Utility of Non-contrast Thoracic Computed Tomography in the Detection of Anemia and Its Severity: A Cross-Sectional Analytical Study.

Diagnostic Utility of Non-contrast Thoracic Computed Tomography in the Detection of Anemia and Its Severity: A Cross-Sectional Analytical Study.

Journal: Cureus

Published: August 12, 2025

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Journal: Nature genetics

Published: June 24, 2025

Estimation of Fetal Foot Length and Femur-to-Foot Length Ratio in Indian Population for Estimating Gestational Age on Sonography During Second Trimester (17-25 Weeks).

Estimation of Fetal Foot Length and Femur-to-Foot Length Ratio in Indian Population for Estimating Gestational Age on Sonography During Second Trimester (17-25 Weeks).

Journal: Cureus

Published: May 20, 2025

Blood-based DNA methylation profiles in major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders.

Blood-based DNA methylation profiles in major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders.

Journal: Comprehensive psychiatry

Published: January 24, 2025

NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling.

NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling.

Journal: F1000Research

Published: August 27, 2024

Benchmarking whole exome sequencing in the German network for personalized medicine.

Benchmarking whole exome sequencing in the German network for personalized medicine.

Journal: European journal of cancer (Oxford, England : 1990)

Published: June 20, 2024

Structural variation in 1,019 diverse humans based on long-read sequencing.

Structural variation in 1,019 diverse humans based on long-read sequencing.

Journal: Nature

Published: April 22, 2024

Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distal.

Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distal.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Published: April 17, 2024

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Journal: Nature genetics

Published: July 19, 2023

Altered Notch signalling in Dowling-Degos disease: a transcriptomic insight into disease pathogenesis.

Altered Notch signalling in Dowling-Degos disease: a transcriptomic insight into disease pathogenesis.

Journal: The British journal of dermatology

Published: April 28, 2023

Gene-based burden scores identify rare variant associations for 28 blood biomarkers.

Gene-based burden scores identify rare variant associations for 28 blood biomarkers.

Journal: BMC genomic data

Published: November 14, 2022

Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss.

Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss.

Journal: Nature communications

Published: September 21, 2022

Showing 1-12 of 40

Last Updated: 09/26/2026